Lander, Eric

Publication with MATCHING institution:

Khera AV, Won HH, Peloso GM, ..., Kathiresan S (2017) Association of Rare and Common Variation in the Lipoprotein Lipase
Gene With Coronary Artery Disease. None. [IF=None, Cited=80, 28267856].
Adelmann CH, Wang T, Sabatini DM, Lander E (2019) Genome-Wide CRISPR/Cas9 Screening for Identification of Cancer Genes
in Cell Lines. Methods in Molecular Biology. [IF=0.413, Cited=9, 30542996].
Lander E, Lodish H (1990) Mitochondrial diseases: gene mapping and gene therapy. Cell. [IF=8.479, Cited=28, 2190693].
Vallabh SM, Minikel EV, Schreiber SL, Lander E (2020) Towards a treatment for genetic prion disease: trials and
biomarkers. The Lancet Neurology. [IF=13.538, Cited=30, 32199098].
Ulirsch JC, Verboon JM, Kazerounian S, ..., Gazda HT (2018) The Genetic Landscape of Diamond-Blackfan Anemia. American
Journal of Human Genetics. [IF=2.607, Cited=120, 30503522].
Lander E (2019) 2018 William Allan Award: Discovering the Genes for Common Disease: From Families to Populations.
American Journal of Human Genetics. [IF=2.607, Cited=0, 30849323].
Landau DA, Clement K, Ziller MJ, ..., Wu CJ (2014) Locally disordered methylation forms the basis of intratumor
methylome variation in chronic lymphocytic leukemia. Cancer Cell. [IF=5.274, Cited=225, 25490447].
Gupta PB, Onder TT, Jiang G, ..., Lander E (2009) Identification of selective inhibitors of cancer stem cells by high-
throughput screening. Cell. [IF=8.479, Cited=1000, 19682730].
Hsu PD, Lander E, Zhang F (2014) Development and applications of CRISPR-Cas9 for genome engineering. Cell. [IF=8.479,
Cited=1000, 24906146].
Engreitz JM, Sirokman K, McDonel P, ..., Lander E (2014) RNA-RNA interactions enable specific targeting of noncoding
RNAs to nascent Pre-mRNAs and chromatin sites. Cell. [IF=8.479, Cited=293, 25259926].
Schwartz S, Bernstein DA, Mumbach MR, ..., Regev A (2014) Transcriptome-wide mapping reveals widespread dynamic-
regulated pseudouridylation of ncRNA and mRNA. Cell. [IF=8.479, Cited=543, 25219674].
Rao SSP, Huntley MH, Durand NC, ..., Aiden EL (2014) A 3D map of the human genome at kilobase resolution reveals
principles of chromatin looping. Cell. [IF=8.479, Cited=1000, 25497547].
Cacchiarelli D, Trapnell C, Ziller MJ, ..., Mikkelsen TS (2015) Integrative Analyses of Human Reprogramming Reveal
Dynamic Nature of Induced Pluripotency. Cell. [IF=8.479, Cited=132, 26186193].
Andersen KG, Shapiro BJ, Matranga CB, ..., Sabeti PC (2015) Clinical Sequencing Uncovers Origins and Evolution of Lassa
Virus. Cell. [IF=8.479, Cited=161, 26276630].
Lander E (2016) The Heroes of CRISPR. Cell. [IF=8.479, Cited=167, 26771483].
Tewhey R, Kotliar D, Park DS, ..., Sabeti PC (2016) Direct Identification of Hundreds of Expression-Modulating Variants
using a Multiplexed Reporter Assay. Cell. [IF=8.479, Cited=232, 27259153].
Dixit A, Parnas O, Li B, ..., Regev A (2016) Perturb-Seq: Dissecting Molecular Circuits with Scalable Single-Cell RNA
Profiling of Pooled Genetic Screens. Cell. [IF=8.479, Cited=663, 27984732].
Wang T, Yu H, Hughes NW, ..., Sabatini DM (2017) Gene Essentiality Profiling Reveals Gene Networks and Synthetic Lethal
Interactions with Oncogenic Ras. Cell. [IF=8.479, Cited=340, 28162770].
Kim AR, Ulirsch JC, Wilmes S, ..., Sankaran VG (2017) Functional Selectivity in Cytokine Signaling Revealed Through a
Pathogenic EPO Mutation. Cell. [IF=8.479, Cited=74, 28283061].
Rusu V, Hoch E, Mercader JM, ..., Lander E (2017) Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two
Distinct Mechanisms. Cell. [IF=8.479, Cited=70, 28666119].
Rao SSP, Huang SC, Glenn St Hilaire B, ..., Aiden EL (2017) Cohesin Loss Eliminates All Loop Domains. Cell. [IF=8.479,
Cited=839, 28985562].
Cleary B, Cong L, Cheung A, ..., Regev A (2017) Efficient Generation of Transcriptomic Profiles by Random Composite
Measurements. Cell. [IF=8.479, Cited=46, 29153835].
Khajuria RK, Munschauer M, Ulirsch JC, ..., Sankaran VG (2018) Ribosome Levels Selectively Regulate Translation and
Lineage Commitment in Human Hematopoiesis. Cell. [IF=8.479, Cited=211, 29551269].
Schiebinger G, Shu J, Tabaka M, ..., Lander ES (2019) Optimal-Transport Analysis of Single-Cell Gene Expression
Identifies Developmental Trajectories in Reprogramming. Cell. [IF=8.479, Cited=191, 30712874].
Khera AV, Chaffin M, Wade KH, ..., Kathiresan S (2019) Polygenic Prediction of Weight and Obesity Trajectories from
Birth to Adulthood. Cell. [IF=8.479, Cited=276, 31002795].
Dvela-Levitt M, Kost-Alimova M, Emani M, ..., Greka A (2019) Small Molecule Targets TMED9 and Promotes Lysosomal
Degradation to Reverse Proteinopathy. Cell. [IF=8.479, Cited=72, 31348885].
Qiu X, Zhang Y, Martin-Rufino JD, ..., Weissman JS (2022) Mapping transcriptomic vector fields of single cells. Cell.
[IF=8.479, Cited=98, 35108499].
Martin-Rufino JD, Castano N, Pang M, ..., Sankaran VG (2023) Massively parallel base editing to map variant effects in
human hematopoiesis. Cell. [IF=8.479, Cited=20, 37137305].
Sandoval-Velasco M, Dudchenko O, Rodríguez JA, ..., Aiden EL (2024) Three-dimensional genome architecture persists in a
52,000-year-old woolly mammoth skin sample. Cell. [IF=8.479, Cited=0, 38996487].
Schwartz S, Mumbach MR, Jovanovic M, ..., Regev A (2014) Perturbation of m6A writers reveals two distinct classes of
mRNA methylation at internal and 5' sites. Cell Reports. [IF=1.738, Cited=720, 24981863].
Giannakis M, Mu XJ, Shukla SA, ..., Garraway LA (2016) Genomic Correlates of Immune-Cell Infiltrates in Colorectal
Carcinoma. Cell Reports. [IF=1.738, Cited=413, 27149842].
Hoch E, Florez JC, Lander E, Jacobs SBR (2019) Gain-of-Function Claims for Type-2-Diabetes-Associated Coding Variants in
SLC16A11 Are Not Supported by the Experimental Data. Cell Reports. [IF=1.738, Cited=4, 31618643].
Durand NC, Robinson JT, Shamim MS, ..., Aiden EL (2016) Juicebox Provides a Visualization System for Hi-C Contact Maps
with Unlimited Zoom. Cell Systems. [IF=1.971, Cited=805, 27467250].
Durand NC, Shamim MS, Machol I, ..., Aiden EL (2016) Juicer Provides a One-Click System for Analyzing Loop-Resolution
Hi-C Experiments. Cell Systems. [IF=1.971, Cited=1000, 27467249].
Yassour M, Jason E, Hogstrom LJ, ..., Xavier RJ (2018) Strain-Level Analysis of Mother-to-Child Bacterial Transmission
during the First Few Months of Life. None. [IF=None, Cited=202, 30001517].
Sinnott-Armstrong N, Sousa IS, Laber S, ..., Claussnitzer M (2021) A regulatory variant at 3q21.1 confers an increased
pleiotropic risk for hyperglycemia and altered bone mineral density. None. [IF=None, Cited=20, 33513366].
Khera AV, Won HH, Peloso GM, ..., Kathiresan S (2016) Diagnostic Yield and Clinical Utility of Sequencing Familial
Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia. Journal of the American College of Cardiology.
[IF=6.424, Cited=382, 27050191].
Emdin CA, Khera AV, Natarajan P, ..., Kathiresan S (2016) Phenotypic Characterization of Genetically Lowered Human
Lipoprotein(a) Levels. Journal of the American College of Cardiology. [IF=6.424, Cited=100, 28007139].
Stitziel NO, Khera AV, Wang X, ..., Kathiresan S (2017) ANGPTL3 Deficiency and Protection Against Coronary Artery
Disease. Journal of the American College of Cardiology. [IF=6.424, Cited=213, 28385496].
Khera AV, Mason-Suares H, Brockman D, ..., Kathiresan S (2019) Rare Genetic Variants Associated With Sudden Cardiac
Death in Adults. Journal of the American College of Cardiology. [IF=6.424, Cited=20, 31727422].
Blumenstiel B, DeFelice M, Birsoy O, ..., Lennon NJ (2016) Development and Validation of a Mass Spectrometry-Based Assay
for the Molecular Diagnosis of Mucin-1 Kidney Disease. Journal of Molecular Diagnostics. [IF=1.058, Cited=18, 27157321].
Mitchell CM, Mazzoni C, Hogstrom L, ..., Yassour M (2020) Delivery Mode Affects Stability of Early Infant Gut
Microbiota. Cell Reports Medicine. [IF=1.969, Cited=92, 33377127].
Crowdis J, Balch S, Sterlin L, ..., Van Allen EM (2022) A patient-driven clinicogenomic partnership for metastatic
prostate cancer. Cell Genomics. [IF=2.669, Cited=3, 36177448].
Mitt M, Kals M, Pärn K, ..., Palta P (2017) Improved imputation accuracy of rare and low-frequency variants using
population-specific high-coverage WGS-based imputation reference panel. European Journal of Human Genetics. [IF=1.676,
Cited=109, 28401899].
Tiao G, Improgo MR, Kasar S, ..., Brown JR (2017) Rare germline variants in ATM are associated with chronic lymphocytic
leukemia. Leukemia. [IF=2.198, Cited=16, 28652578].
Lander E (2011) Initial impact of the sequencing of the human genome. Nature. [IF=11.591, Cited=500, 21307931].
Lawrence MS, Stojanov P, Polak P, ..., Getz G (2013) Mutational heterogeneity in cancer and the search for new cancer-
associated genes. Nature. [IF=11.591, Cited=1000, 23770567].
Lawrence MS, Stojanov P, Mermel CH, ..., Getz G (2014) Discovery and saturation analysis of cancer genes across 21
tumour types. Nature. [IF=11.591, Cited=1000, 24390350].
Purcell SM, Moran JL, Fromer M, ..., Sklar P (2014) A polygenic burden of rare disruptive mutations in schizophrenia.
Nature. [IF=11.591, Cited=871, 24463508].
Brawand D, Wagner CE, Li YI, ..., Di Palma F (2014) The genomic substrate for adaptive radiation in African cichlid
fish. Nature. [IF=11.591, Cited=448, 25186727].
Do R, Stitziel NO, Won HH, ..., Kathiresan S (2014) Exome sequencing identifies rare LDLR and APOA5 alleles conferring
risk for myocardial infarction. Nature. [IF=11.591, Cited=387, 25487149].
McHugh CA, Chen CK, Chow A, ..., Guttman M (2015) The Xist lncRNA interacts directly with SHARP to silence transcription
through HDAC3. Nature. [IF=11.591, Cited=640, 25915022].
Landau DA, Tausch E, Taylor-Weiner AN, ..., Wu CJ (2015) Mutations driving CLL and their evolution in progression and
relapse. Nature. [IF=11.591, Cited=583, 26466571].
Fuchsberger C, Flannick J, Teslovich TM, ..., McCarthy MI (2016) The genetic architecture of type 2 diabetes. Nature.
[IF=11.591, Cited=592, 27398621].
Engreitz JM, Haines JE, Perez EM, ..., Lander E (2016) Local regulation of gene expression by lncRNA promoters,
transcription and splicing. Nature. [IF=11.591, Cited=694, 27783602].
Saleheen D, Natarajan P, Armean IM, ..., Kathiresan S (2017) Human knockouts and phenotypic analysis in a cohort with a
high rate of consanguinity. Nature. [IF=11.591, Cited=164, 28406212].
Ott PA, Hu Z, Keskin DB, ..., Wu CJ (2017) An immunogenic personal neoantigen vaccine for patients with melanoma.
Nature. [IF=11.591, Cited=1000, 28678778].
Rheinbay E, Parasuraman P, Grimsby J, ..., Getz G (2017) Recurrent and functional regulatory mutations in breast cancer.
Nature. [IF=11.591, Cited=154, 28658208].
Joung J, Engreitz JM, Konermann S, ..., Zhang F (2017) Genome-scale activation screen identifies a lncRNA locus
regulating a gene neighbourhood. Nature. [IF=11.591, Cited=235, 28792927].
Abudayyeh OO, Gootenberg JS, Essletzbichler P, ..., Zhang F (2017) RNA targeting with CRISPR-Cas13. Nature. [IF=11.591,
Cited=842, 28976959].
Burger JA, Landau DA, Taylor-Weiner A, ..., Wu CJ (2016) Clonal evolution in patients with chronic lymphocytic leukaemia
developing resistance to BTK inhibition. Nature Communications. [IF=3.268, Cited=199, 27199251].
Kasar S, Kim J, Improgo R, ..., Brown JR (2015) Whole-genome sequencing reveals activation-induced cytidine deaminase
signatures during indolent chronic lymphocytic leukaemia evolution. Nature Communications. [IF=3.268, Cited=154, 26638776].
Weisenfeld NI, Yin S, Sharpe T, ..., Jaffe DB (2014) Comprehensive variation discovery in single human genomes. Nature
Genetics. [IF=6.89, Cited=112, 25326702].
Giannakis M, Hodis E, Jasmine Mu X, ..., Garraway LA (2014) RNF43 is frequently mutated in colorectal and endometrial
cancers. Nature Genetics. [IF=6.89, Cited=286, 25344691].
Stachler MD, Taylor-Weiner A, Peng S, ..., Bass AJ (2015) Paired exome analysis of Barrett's esophagus and
adenocarcinoma. Nature Genetics. [IF=6.89, Cited=212, 26192918].
Park RJ, Wang T, Koundakjian D, ..., Walker BD (2016) A genome-wide CRISPR screen identifies a restricted set of HIV
host dependency factors. Nature Genetics. [IF=6.89, Cited=181, 27992415].
Polak P, Kim J, Braunstein LZ, ..., Getz G (2017) A mutational signature reveals alterations underlying deficient
homologous recombination repair in breast cancer. Nature Genetics. [IF=6.89, Cited=277, 28825726].
Bass AJ, Lawrence MS, Brace LE, ..., Meyerson M (2011) Genomic sequencing of colorectal adenocarcinomas identifies a
recurrent VTI1A-TCF7L2 fusion. Nature Genetics. [IF=6.89, Cited=211, 21892161].
Ludwig LS, Gazda HT, Eng JC, ..., Sankaran VG (2014) Altered translation of GATA1 in Diamond-Blackfan anemia. Nature
Medicine. [IF=11.877, Cited=192, 24952648].
Van Allen EM, Wagle N, Stojanov P, ..., Garraway LA (2014) Whole-exome sequencing and clinical interpretation of
formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. Nature Medicine. [IF=11.877,
Cited=347, 24836576].
Hacisuleyman E, Goff LA, Trapnell C, ..., Rinn JL (2014) Topological organization of multichromosomal regions by the
long intergenic noncoding RNA Firre. Nature Structural and Molecular Biology. [IF=2.542, Cited=373, 24463464].
Bis JC, Jian X, Kunkle BW, ..., Farrer LA (2018) Whole exome sequencing study identifies novel rare and common
Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry.
[IF=2.603, Cited=131, 30108311].
Bis JC, Jian X, Kunkle BW, ..., Farrer LA (2020) Correction: Whole exome sequencing study identifies novel rare and
common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry.
[IF=2.603, Cited=5, 31636380].
Alver M, Palover M, Saar A, ..., Esko T (2018) Recall by genotype and cascade screening for familial
hypercholesterolemia in a population-based biobank from Estonia. Genetics in Medicine. [IF=2.761, Cited=23, 30270359].
Natarajan P, Peloso GM, Zekavat SM, ..., Kathiresan S (2018) Deep-coverage whole genome sequences and blood lipids among
16,324 individuals. Nature Communications. [IF=3.268, Cited=79, 30140000].
Ray JP, de Boer CG, Fulco CP, ..., Hacohen N (2020) Prioritizing disease and trait causal variants at the TNFAIP3 locus
using functional and genomic features. Nature Communications. [IF=3.268, Cited=25, 32144282].
Fahed AC, Wang M, Homburger JR, ..., Khera AV (2020) Polygenic background modifies penetrance of monogenic variants for
tier 1 genomic conditions. Nature Communications. [IF=3.268, Cited=162, 32820175].
Schmidt N, Lareau CA, Keshishian H, ..., Munschauer M (2020) The SARS-CoV-2 RNA-protein interactome in infected human
cells. Nature Microbiology. [IF=4.448, Cited=173, 33349665].
Kotliar D, Raju S, Tabrizi S, ..., Sabeti PC (2024) Genome-wide association study identifies human genetic variants
associated with fatal outcome from Lassa fever. Nature Microbiology. [IF=4.448, Cited=0, 38326571].
Munschauer M, Nguyen CT, Sirokman K, ..., Lander E (2018) The NORAD lncRNA assembles a topoisomerase complex critical
for genome stability. Nature. [IF=11.591, Cited=203, 30150775].
Munschauer M, Nguyen CT, Sirokman K, ..., Lander E (2018) Publisher Correction: The NORAD lncRNA assembles a
topoisomerase complex critical for genome stability. Nature. [IF=11.591, Cited=11, 30279576].
Keskin DB, Anandappa AJ, Sun J, ..., Reardon DA (2018) Neoantigen vaccine generates intratumoral T cell responses in
phase Ib glioblastoma trial. Nature. [IF=11.591, Cited=661, 30568305].
Johnson EO, LaVerriere E, Office E, ..., Hung DT (2019) Large-scale chemical-genetics yields new M. tuberculosis
inhibitor classes. Nature. [IF=11.591, Cited=69, 31217586].
Collins RL, Brand H, Karczewski KJ, ..., Talkowski ME (2021) Author Correction: A structural variation reference for
medical and population genetics. Nature. [IF=11.591, Cited=1, 33536627].
Collins RL, Brand H, Karczewski KJ, ..., Talkowski ME (2020) A structural variation reference for medical and population
genetics. Nature. [IF=11.591, Cited=386, 32461652].
Abel HJ, Larson DE, Regier AA, ..., Hall IM (2020) Mapping and characterization of structural variation in 17,795 human
genomes. Nature. [IF=11.591, Cited=127, 32460305].
Bick AG, Weinstock JS, Nandakumar SK, ..., Natarajan P (2020) Inherited causes of clonal haematopoiesis in 97,691 whole
genomes. Nature. [IF=11.591, Cited=258, 33057201].
Bick AG, Weinstock JS, Nandakumar SK, ..., Natarajan P (2021) Author Correction: Inherited causes of clonal
haematopoiesis in 97,691 whole genomes. Nature. [IF=11.591, Cited=2, 33707633].
Nasser J, Bergman DT, Fulco CP, ..., Engreitz JM (2021) Genome-wide enhancer maps link risk variants to disease genes.
Nature. [IF=11.591, Cited=199, 33828297].
Bergman DT, Jones TR, Liu V, ..., Engreitz JM (2022) Compatibility rules of human enhancer and promoter sequences.
Nature. [IF=11.591, Cited=48, 35594906].
Schnitzler GR, Kang H, Fang S, ..., Engreitz JM (2024) Convergence of coronary artery disease genes onto endothelial
cell programs. Nature. [IF=11.591, Cited=2, 38326615].
Cleary B, Simonton B, Bezney J, ..., Regev A (2021) Compressed sensing for highly efficient imaging transcriptomics.
Nature Biotechnology. [IF=8.861, Cited=14, 33859401].
Khera AV, Chaffin M, Aragam KG, ..., Kathiresan S (2018) Genome-wide polygenic scores for common diseases identify
individuals with risk equivalent to monogenic mutations. Nature Genetics. [IF=6.89, Cited=1000, 30104762].
Fulco CP, Nasser J, Jones TR, ..., Engreitz JM (2019) Activity-by-contact model of enhancer-promoter regulation from
thousands of CRISPR perturbations. Nature Genetics. [IF=6.89, Cited=386, 31784727].
Basak A, Munschauer M, Lareau CA, ..., Sankaran VG (2020) Control of human hemoglobin switching by LIN28B-mediated
regulation of BCL11A translation. Nature Genetics. [IF=6.89, Cited=47, 31959994].
Dietlein F, Weghorn D, Taylor-Weiner A, ..., Sunyaev SR (2020) Identification of cancer driver genes based on nucleotide
context. Nature Genetics. [IF=6.89, Cited=109, 32015527].
Weeks EM, Ulirsch JC, Cheng NY, ..., Finucane HK (2023) Leveraging polygenic enrichments of gene features to predict
genes underlying complex traits and diseases. Nature Genetics. [IF=6.89, Cited=39, 37443254].
Salehi Nowbandegani P, Wohns AW, Ballard JL, ..., O'Connor LJ (2023) Extremely sparse models of linkage disequilibrium
in ancestrally diverse association studies. Nature Genetics. [IF=6.89, Cited=5, 37640881].
Painter CA, Jain E, Tomson BN, ..., Wagle N (2020) The Angiosarcoma Project: enabling genomic and clinical discoveries
in a rare cancer through patient-partnered research. Nature Medicine. [IF=11.877, Cited=109, 32042194].
Hsu JY, Fulco CP, Cole MA, ..., Pinello L (2018) CRISPR-SURF: discovering regulatory elements by deconvolution of CRISPR
tiling screen data. Nature Methods. [IF=10.009, Cited=18, 30504875].
Flannick J, Fuchsberger C, Mahajan A, ..., McCarthy MI (2017) Sequence data and association statistics from 12,940 type
2 diabetes cases and controls. Scientific data. [IF=2.887, Cited=19, 29257133].
Lander E (2015) Cutting the Gordian helix--regulating genomic testing in the era of precision medicine. New England
Journal of Medicine. [IF=17.194, Cited=36, 25689017].
Lander E (2015) Brave New Genome. New England Journal of Medicine. [IF=17.194, Cited=53, 26039524].
Collins FS, Doudna JA, Lander E, ..., Rotimi CN (2021) Human Molecular Genetics and Genomics - Important Advances and
Exciting Possibilities. New England Journal of Medicine. [IF=17.194, Cited=10, 33393745].
Nau GJ, Richmond JFL, Schlesinger A, ..., Young RA (2002) Human macrophage activation programs induced by bacterial
pathogens. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=424, 11805289].
Mootha V, Mootha VK, Handschin C, ..., Spiegelman BM (2004) Erralpha and Gabpa/b specify PGC-1alpha-dependent oxidative
phosphorylation gene expression that is altered in diabetic muscle. Proceedings of the National Academy of Sciences of
the United States of America. [IF=2.765, Cited=447, 15100410].
Margulies EH, Vinson JP, Miller W, ..., Clamp M (2005) An initial strategy for the systematic identification of
functional elements in the human genome by low-redundancy comparative sequencing. Proceedings of the National Academy of
Sciences of the United States of America. [IF=2.765, Cited=78, 15778292].
Waterston RH, Lander E, Sulston JE (2002) On the sequencing of the human genome. Proceedings of the National Academy of
Sciences of the United States of America. [IF=2.765, Cited=76, 11880605].
Subramanian A, Tamayo P, Mootha V, ..., Mesirov JP (2005) Gene set enrichment analysis: a knowledge-based approach for
interpreting genome-wide expression profiles. Proceedings of the National Academy of Sciences of the United States of
America. [IF=2.765, Cited=1000, 16199517].
Kamal M, Xie X, Lander E (2006) A large family of ancient repeat elements in the human genome is under strong selection.
Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=61, 16477033].
Hong KH, Bonventre JC, O'Leary E, ..., Lander E (2001) Deletion of cytosolic phospholipase A(2) suppresses
Apc(Min)-induced tumorigenesis. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=74, 11274413].
Xie X, Kamal M, Lander E (2006) A family of conserved noncoding elements derived from an ancient transposable element.
Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=49, 16864796].
Waterston RH, Lander E, Sulston JE (2003) More on the sequencing of the human genome. Proceedings of the National
Academy of Sciences of the United States of America. [IF=2.765, Cited=14, 12631699].
Xie X, Mikkelsen TS, Gnirke A, ..., Lander E (2007) Systematic discovery of regulatory motifs in conserved regions of
the human genome, including thousands of CTCF insulator sites. Proceedings of the National Academy of Sciences of the
United States of America. [IF=2.765, Cited=211, 17442748].
Clamp M, Fry B, Kamal M, ..., Lander E (2007) Distinguishing protein-coding and noncoding genes in the human genome.
Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=303, 18040051].
Beroukhim R, Getz G, Nghiemphu L, ..., Sellers WR (2007) Assessing the significance of chromosomal aberrations in
cancer: methodology and application to glioma. Proceedings of the National Academy of Sciences of the United States of
America. [IF=2.765, Cited=686, 18077431].
Shao H, Burrage LC, Sinasac DS, ..., Nadeau JH (2008) Genetic architecture of complex traits: large phenotypic effects
and pervasive epistasis. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765,
Cited=171, 19066216].
Luo B, Cheung HW, Subramanian A, ..., Sabatini DM (2008) Highly parallel identification of essential genes in cancer
cells. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=365, 19091943].
Khalil AM, Guttman M, Huarte M, ..., Rinn JL (2009) Many human large intergenic noncoding RNAs associate with chromatin-
modifying complexes and affect gene expression. Proceedings of the National Academy of Sciences of the United States of
America. [IF=2.765, Cited=1000, 19571010].
Taube JH, Herschkowitz JI, Komurov K, ..., Mani SA (2010) Core epithelial-to-mesenchymal transition interactome gene-
expression signature is associated with claudin-low and metaplastic breast cancer subtypes. Proceedings of the National
Academy of Sciences of the United States of America. [IF=2.765, Cited=683, 20713713].
Fillmore CM, Gupta PB, Rudnick JA, ..., Kuperwasser C (2010) Estrogen expands breast cancer stem-like cells through
paracrine FGF/Tbx3 signaling. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=184, 21098263].
Gnerre S, Maccallum I, Przybylski D, ..., Jaffe DB (2010) High-quality draft assemblies of mammalian genomes from
massively parallel sequence data. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=966, 21187386].
Sankaran VG, Menne TF, Šćepanović D, ..., Lodish HF (2011) MicroRNA-15a and -16-1 act via MYB to elevate fetal
hemoglobin expression in human trisomy 13. Proceedings of the National Academy of Sciences of the United States of
America. [IF=2.765, Cited=144, 21205891].
Cheung HW, Cowley GS, Weir BA, ..., Hahn WC (2011) Systematic investigation of genetic vulnerabilities across cancer
cell lines reveals lineage-specific dependencies in ovarian cancer. Proceedings of the National Academy of Sciences of
the United States of America. [IF=2.765, Cited=279, 21746896].
Zuk O, Hechter E, Sunyaev SR, Lander E (2012) The mystery of missing heritability: Genetic interactions create phantom
heritability. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=839, 22223662].
Lohr JG, Stojanov P, Lawrence MS, ..., Golub TR (2012) Discovery and prioritization of somatic mutations in diffuse
large B-cell lymphoma (DLBCL) by whole-exome sequencing. Proceedings of the National Academy of Sciences of the United
States of America. [IF=2.765, Cited=621, 22343534].
Grad YH, Lipsitch M, Feldgarden M, ..., Hanage WP (2012) Genomic epidemiology of the Escherichia coli O104:H4 outbreaks
in Europe, 2011. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=159, 22315421].
Grad YH, Lipsitch M, Griggs AD, ..., Hanage WP (2012) Reply to Guy et al.: Support for a bottleneck in the 2011
Escherichia coli O104:H4 outbreak in Germany. Proceedings of the National Academy of Sciences of the United States of
America. [IF=2.765, Cited=3, 23479789].
Zuk O, Schaffner SF, Samocha K, ..., Lander E (2014) Searching for missing heritability: designing rare variant
association studies. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765,
Cited=364, 24443550].
Golan D, Lander E, Rosset S (2014) Measuring missing heritability: inferring the contribution of common variants.
Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=155, 25422463].
Perry JA, Kiezun A, Tonzi P, ..., Janeway KA (2014) Complementary genomic approaches highlight the PI3K/mTOR pathway as
a common vulnerability in osteosarcoma. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=259, 25512523].
Golan D, Rosset S, Lander E (2015) Reply to Lee: Downward bias in heritability estimation is not due to simplified
linkage equilibrium SNP simulation. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=0, 26417112].
Kamburov A, Lawrence MS, Polak P, ..., Getz G (2015) Comprehensive assessment of cancer missense mutation clustering in
protein structures. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765,
Cited=125, 26392535].
Sanborn AL, Rao SSP, Huang SC, ..., Aiden EL (2015) Chromatin extrusion explains key features of loop and domain
formation in wild-type and engineered genomes. Proceedings of the National Academy of Sciences of the United States of
America. [IF=2.765, Cited=849, 26499245].
Darrow EM, Huntley MH, Dudchenko O, ..., Aiden EL (2016) Deletion of DXZ4 on the human inactive X chromosome alters
higher-order genome architecture. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=149, 27432957].
Guo MH, Nandakumar SK, Ulirsch JC, ..., Sankaran VG (2016) Comprehensive population-based genome sequencing provides
insight into hematopoietic regulatory mechanisms. Proceedings of the National Academy of Sciences of the United States
of America. [IF=2.765, Cited=31, 28031487].
Grossman SR, Zhang X, Wang L, ..., Lander E (2017) Systematic dissection of genomic features determining transcription
factor binding and enhancer function. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=91, 28137873].
Grossman SR, Engreitz J, Ray JP, ..., Lander E (2018) Positional specificity of different transcription factor classes
within enhancers. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=46, 29987030].
Poulsen BE, Yang R, Clatworthy AE, ..., Hung DT (2019) Defining the core essential genome of Pseudomonas
aeruginosa. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=85, 31036669].
Staunton JE, Slonim DK, Coller HA, ..., Golub TR (2001) Chemosensitivity prediction by transcriptional profiling.
Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=340, 11553813].
Bhattacharjee A, Richards WG, Staunton J, ..., Meyerson M (2001) Classification of human lung carcinomas by mRNA
expression profiling reveals distinct adenocarcinoma subclasses. Proceedings of the National Academy of Sciences of the
United States of America. [IF=2.765, Cited=1000, 11707567].
Humpherys D, Eggan K, Akutsu H, ..., Jaenisch R (2002) Abnormal gene expression in cloned mice derived from embryonic
stem cell and cumulus cell nuclei. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=240, 12235366].
Marshall JL, Doughty BR, Subramanian V, ..., Engreitz JM (2020) HyPR-seq: Single-cell quantification of chosen RNAs via
hybridization and sequencing of DNA probes. Proceedings of the National Academy of Sciences of the United States of
America. [IF=2.765, Cited=14, 33376219].
Chen CZ, Li M, de Graaf D, ..., Lodish HF (2002) Identification of endoglin as a functional marker that defines long-
term repopulating hematopoietic stem cells. Proceedings of the National Academy of Sciences of the United States of
America. [IF=2.765, Cited=100, 12438646].
Hirschhorn JN, Sklar P, Lindblad-Toh K, ..., Lander E (2000) SBE-TAGS: an array-based method for efficient single-
nucleotide polymorphism genotyping. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=80, 11035790].
Ramaswamy S, Tamayo P, Rifkin R, ..., Golub TR (2001) Multiclass cancer diagnosis using tumor gene expression
signatures. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765, Cited=816, 11742071].
Gupta A, Martin-Rufino JD, Jones TR, ..., Lander E (2022) Inferring gene regulation from stochastic transcriptional
variation across single cells at steady state. Proceedings of the National Academy of Sciences of the United States of
America. [IF=2.765, Cited=7, 35969771].
Mootha V, Mootha VK, Lepage P, ..., Lander ES (2003) Identification of a gene causing human cytochrome c oxidase
deficiency by integrative genomics. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=366, 12529507].
Dietrich WF, Radany EH, Smith JS, ..., Lander E (1994) Genome-wide search for loss of heterozygosity in transgenic mouse
tumors reveals candidate tumor suppressor genes on chromosomes 9 and 16. Proceedings of the National Academy of Sciences
of the United States of America. [IF=2.765, Cited=40, 7937788].
Radany EH, Hong K, Kesharvarzi S, ..., Bishop JM (1997) Mouse mammary tumor virus/v-Ha-ras transgene-induced mammary
tumors exhibit strain-specific allelic loss on mouse chromosome 4. Proceedings of the National Academy of Sciences of
the United States of America. [IF=2.765, Cited=22, 9238034].
Fazeli A, Steen RG, Dickinson SL, ..., Weinberg RA (1997) Effects of p53 mutations on apoptosis in mouse intestinal and
human colonic adenomas. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765,
Cited=45, 9294187].
Madhani HD, Galitski T, Lander E, Fink GR (1999) Effectors of a developmental mitogen-activated protein kinase cascade
revealed by expression signatures of signaling mutants. Proceedings of the National Academy of Sciences of the United
States of America. [IF=2.765, Cited=125, 10535956].
Tamayo P, Slonim D, Mesirov J, ..., Golub TR (1999) Interpreting patterns of gene expression with self-organizing maps:
methods and application to hematopoietic differentiation. Proceedings of the National Academy of Sciences of the United
States of America. [IF=2.765, Cited=1000, 10077610].
Coller HA, Grandori C, Tamayo P, ..., Golub TR (2000) Expression analysis with oligonucleotide microarrays reveals that
MYC regulates genes involved in growth, cell cycle, signaling, and adhesion. Proceedings of the National Academy of
Sciences of the United States of America. [IF=2.765, Cited=512, 10737792].
Pachter L, Batzoglou S, Spitkovsky VI, ..., Berger B (1999) A dictionary-based approach for gene annotation. Journal of
Computational Biology. [IF=0.499, Cited=8, 10582576].
Causton HC, Ren B, Koh SS, ..., Young RA (2001) Remodeling of yeast genome expression in response to environmental
changes. Molecular Biology of the Cell. [IF=0.848, Cited=825, 11179418].
Gould KA, Dietrich WF, Borenstein N, ..., Dove WF (1996) Mom1 is a semi-dominant modifier of intestinal adenoma size and
multiplicity in Min/+ mice. Genetics. [IF=1.102, Cited=53, 8978062].
Lennon NJ, Bhattacharyya RP, Mina MJ, ..., Gabriel SB (2021) Cross-Sectional Assessment of SARS-CoV-2 Viral Load by
Symptom Status in Massachusetts Congregate Living Facilities. Journal of Infectious Diseases. [IF=1.292, Cited=2, 34255846].
Costello M, Pugh TJ, Fennell TJ, ..., Getz G (2013) Discovery and characterization of artifactual mutations in deep
coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation. Nucleic Acids Research.
[IF=4.663, Cited=276, 23303777].
Martyn GE, Montgomery MT, Jones H, ..., Engreitz JM (2023) Rewriting regulatory DNA to dissect and reprogram gene
expression. None. [IF=None, Cited=0, 38187584].
Siraj L, Castro RI, Dewey H, ..., Tewhey R (2024) Functional dissection of complex and molecular trait variants at
single nucleotide resolution. None. [IF=None, Cited=0, 38766054].
Kim H, Zheng S, Amini SS, ..., Verhaak RGW (2015) Whole-genome and multisector exome sequencing of primary and post-
treatment glioblastoma reveals patterns of tumor evolution. Genome Research. [IF=1.745, Cited=251, 25650244].
Wang T, Lander E, Sabatini DM (2016) Single Guide RNA Library Design and Construction. Cold Spring Harbor Protocols.
[IF=0.733, Cited=17, 26933249].
Wang T, Lander E, Sabatini DM (2016) Viral Packaging and Cell Culture for CRISPR-Based Screens. Cold Spring Harbor
Protocols. [IF=0.733, Cited=18, 26933250].
Wang T, Lander E, Sabatini DM (2016) Large-Scale Single Guide RNA Library Construction and Use for CRISPR-Cas9-Based
Genetic Screens. Cold Spring Harbor Protocols. [IF=0.733, Cited=13, 26933254].
Gabriel SB, Schaffner SF, Nguyen H, ..., Altshuler D (2002) The structure of haplotype blocks in the human genome.
Science. [IF=7.729, Cited=1000, 12029063].
Singer JB, Hill AE, Burrage LC, ..., Nadeau JH (2004) Genetic dissection of complex traits with chromosome substitution
strains of mice. Science. [IF=7.729, Cited=231, 15031436].
Sabeti PC, Schaffner SF, Fry B, ..., Lander E (2006) Positive natural selection in the human lineage. Science.
[IF=7.729, Cited=687, 16778047].
Lamb J, Crawford ED, Peck D, ..., Golub TR (2006) The Connectivity Map: using gene-expression signatures to connect
small molecules, genes, and disease. Science. [IF=7.729, Cited=1000, 17008526].
Getz G, Höfling H, Mesirov JP, ..., Lander E (2007) Comment on "The consensus coding sequences of human breast and
colorectal cancers". Science. [IF=7.729, Cited=86, 17872428].
Altshuler D, Daly MJ, Lander E (2008) Genetic mapping in human disease. Science. [IF=7.729, Cited=793, 18988837].
Wade CM, Giulotto E, Sigurdsson S, ..., Lindblad-Toh K (2009) Genome sequence, comparative analysis, and population
genetics of the domestic horse. Science. [IF=7.729, Cited=448, 19892987].
Lieberman-Aiden E, van Berkum NL, Williams L, ..., Dekker J (2009) Comprehensive mapping of long-range interactions
reveals folding principles of the human genome. Science. [IF=7.729, Cited=1000, 19815776].
Grossman SR, Shlyakhter I, Karlsson EK, ..., Sabeti PC (2010) A composite of multiple signals distinguishes causal
variants in regions of positive selection. Science. [IF=7.729, Cited=327, 20056855].
Green RE, Krause J, Briggs AW, ..., Pääbo S (2010) A draft sequence of the Neandertal genome. Science. [IF=7.729,
Cited=1000, 20448178].
Neafsey DE, Lawniczak MKN, Park DJ, ..., Muskavitch MAT (2010) SNP genotyping defines complex gene-flow boundaries among
African malaria vector mosquitoes. Science. [IF=7.729, Cited=122, 20966254].
Lander E (2011) Genome-sequencing anniversary. The accelerator. Science. [IF=7.729, Cited=5, 21350161].
Reshef DN, Reshef YA, Finucane HK, ..., Sabeti PC (2011) Detecting novel associations in large data sets. Science.
[IF=7.729, Cited=552, 22174245].
Stransky N, Egloff AM, Tward AD, ..., Grandis JR (2011) The mutational landscape of head and neck squamous cell
carcinoma. Science. [IF=7.729, Cited=1000, 21798893].
Gire SK, Stremlau M, Andersen KG, ..., Sabeti PC (2012) Epidemiology. Emerging disease or diagnosis? Science. [IF=7.729,
Cited=17, 23139320].
Engreitz JM, Pandya-Jones A, McDonel P, ..., Guttman M (2013) The Xist lncRNA exploits three-dimensional genome
architecture to spread across the X chromosome. Science. [IF=7.729, Cited=594, 23828888].
Wang T, Wei JJ, Sabatini DM, Lander E (2013) Genetic screens in human cells using the CRISPR-Cas9 system. Science.
[IF=7.729, Cited=1000, 24336569].
Carneiro M, Rubin CJ, Di Palma F, ..., Andersson L (2014) Rabbit genome analysis reveals a polygenic basis for
phenotypic change during domestication. Science. [IF=7.729, Cited=211, 25170157].
Gire SK, Goba A, Andersen KG, ..., Sabeti PC (2014) Genomic surveillance elucidates Ebola virus origin and transmission
during the 2014 outbreak. Science. [IF=7.729, Cited=668, 25214632].
Lander E (1996) The new genomics: global views of biology. Science. [IF=7.729, Cited=564, 8928008].
Hawkins TL, McKernan KJ, Jacotot LB, ..., Lander E (1997) A magnetic attraction to high-throughput genomics. Science.
[IF=7.729, Cited=19, 9206843].
Wang DG, Fan JB, Siao CJ, ..., Lander E (1998) Large-scale identification, mapping, and genotyping of single-nucleotide
polymorphisms in the human genome. Science. [IF=7.729, Cited=1000, 9582121].
Pardes H, Manton KG, Lander E, ..., Palmer H (1999) Effects of medical research on health care and economy. Science.
[IF=7.729, Cited=24, 9917262].
Galitski T, Saldanha AJ, Styles CA, ..., Fink GR (1999) Ploidy regulation of gene expression. Science. [IF=7.729,
Cited=389, 10398601].
Golub TR, Slonim DK, Tamayo P, ..., Lander E (1999) Molecular classification of cancer: class discovery and class
prediction by gene expression monitoring. Science. [IF=7.729, Cited=1000, 10521349].
Lander E, Weinberg RA (2000) Genomics: journey to the center of biology. Science. [IF=7.729, Cited=55, 10755930].
Lander E, Botstein D (1987) Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children.
Science. [IF=7.729, Cited=518, 2884728].
Huang Q, Liu D, Majewski P, ..., Hacohen N (2001) The plasticity of dendritic cell responses to pathogens and their
components. Science. [IF=7.729, Cited=453, 11679675].
Cox DR, Green ED, Lander E, ..., Myers RM (1994) Assessing mapping progress in the Human Genome Project. Science.
[IF=7.729, Cited=20, 8091223].
Lander E, Schork NJ (1994) Genetic dissection of complex traits. Science. [IF=7.729, Cited=1000, 8091226].
Lander E (1993) DNA fingerprinting: the NRC report. Science. [IF=7.729, Cited=3, 8493559].
Wang T, Birsoy K, Hughes NW, ..., Sabatini DM (2015) Identification and characterization of essential genes in the human
genome. Science. [IF=7.729, Cited=891, 26472758].
Abudayyeh OO, Gootenberg JS, Konermann S, ..., Zhang F (2016) C2c2 is a single-component programmable RNA-guided RNA-
targeting CRISPR effector. Science. [IF=7.729, Cited=911, 27256883].
Fulco CP, Munschauer M, Anyoha R, ..., Engreitz JM (2016) Systematic mapping of functional enhancer-promoter connections
with CRISPR interference. Science. [IF=7.729, Cited=315, 27708057].
Dudchenko O, Batra SS, Omer AD, ..., Aiden EL (2017) De novo assembly of the Aedes aegypti genome using Hi-C
yields chromosome-length scaffolds. Science. [IF=7.729, Cited=1000, 28336562].
Zhou Y, Castonguay P, Sidhom EH, ..., Greka A (2017) A small-molecule inhibitor of TRPC5 ion channels suppresses
progressive kidney disease in animal models. Science. [IF=7.729, Cited=87, 29217578].
Yassour M, Vatanen T, Siljander H, ..., Xavier RJ (2016) Natural history of the infant gut microbiome and impact of
antibiotic treatment on bacterial strain diversity and stability. Science Translational Medicine. [IF=2.778, Cited=469, 27306663].
De Sanctis GT, Singer JB, Jiao A, ..., Drazen JM (1999) Quantitative trait locus mapping of airway responsiveness to
chromosomes 6 and 7 in inbred mice. None. [IF=None, Cited=29, 10600881].
Michalkiewicz M, Michalkiewicz T, Ettinger RA, ..., Lernmark A (2004) Transgenic rescue demonstrates involvement of the
Ian5 gene in T cell development in the rat. Physiological Genomics. [IF=0.843, Cited=28, 15328390].
Onder TT, Gupta PB, Mani SA, ..., Weinberg RA (2008) Loss of E-cadherin promotes metastasis via multiple downstream
transcriptional pathways. Cancer Research. [IF=1.624, Cited=951, 18483246].
Wagle N, Grabiner BC, Van Allen EM, ..., Rosenberg JE (2014) Activating mTOR mutations in a patient with an
extraordinary response on a phase I trial of everolimus and pazopanib. Cancer Discovery. [IF=3.608, Cited=185, 24625776].
Brastianos PK, Carter SL, Santagata S, ..., Hahn WC (2015) Genomic Characterization of Brain Metastases Reveals Branched
Evolution and Potential Therapeutic Targets. Cancer Discovery. [IF=3.608, Cited=553, 26410082].
Grasso CS, Giannakis M, Wells DK, ..., Peters U (2018) Genetic Mechanisms of Immune Evasion in Colorectal Cancer. Cancer
Discovery. [IF=3.608, Cited=264, 29510987].
Hacohen N, Fritsch EF, Carter TA, ..., Wu CJ (2013) Getting personal with neoantigen-based therapeutic cancer vaccines.
Cancer Immunology Research. [IF=1.693, Cited=104, 24777245].
Khera AV, Wang M, Chaffin M, ..., Kathiresan S (2022) Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling
as a Nonlipid Molecular Subtype of Coronary Artery Disease. Circulation. Genomic and precision medicine. [IF=1.275,
Cited=5, 36215124].
Khera AV, Chaffin M, Zekavat SM, ..., Kathiresan S (2019) Whole-Genome Sequencing to Characterize Monogenic and
Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction. Circulation. [IF=6.144,
Cited=113, 30586733].
Wang L, Shalek AK, Lawrence M, ..., Wu CJ (2014) Somatic mutation as a mechanism of Wnt/β-catenin pathway activation in
CLL. Blood. [IF=2.983, Cited=46, 24778153].
Rajasagi M, Shukla SA, Fritsch EF, ..., Wu CJ (2014) Systematic identification of personal tumor-specific neoantigens in
chronic lymphocytic leukemia. Blood. [IF=2.983, Cited=196, 24891321].
Yassour M, Lim MY, Yun HS, ..., Huttenhower C (2016) Sub-clinical detection of gut microbial biomarkers of obesity and
type 2 diabetes. Genome Medicine. [IF=2.422, Cited=132, 26884067].
Hall AB, Yassour M, Sauk J, ..., Huttenhower C (2017) A novel Ruminococcus gnavus clade enriched in inflammatory bowel
disease patients. Genome Medicine. [IF=2.422, Cited=305, 29183332].
Thormaehlen AS, Schuberth C, Won HH, ..., Runz H (2015) Systematic cell-based phenotyping of missense alleles empowers
rare variant association studies: a case for LDLR and myocardial infarction. PLoS Genetics. [IF=1.236, Cited=34, 25647241].
Tonomura N, Elvers I, Thomas R, ..., Lindblad-Toh K (2015) Genome-wide association study identifies shared risk loci
common to two malignancies in golden retrievers. PLoS Genetics. [IF=1.236, Cited=44, 25642983].
Paranjpe MD, Chaffin M, Zahid S, ..., Khera AV (2022) Neurocognitive trajectory and proteomic signature of inherited
risk for Alzheimer's disease. PLoS Genetics. [IF=1.236, Cited=2, 36048760].
Hoeppner MP, Lundquist A, Pirun M, ..., Grabherr MG (2014) An improved canine genome and a comprehensive catalogue of
coding genes and non-coding transcripts. PLoS ONE. [IF=1.253, Cited=144, 24625832].
Singer JB, Hill AE, Nadeau JH, Lander E (2004) Mapping quantitative trait loci for anxiety in chromosome substitution
strains of mice. Genetics. [IF=1.102, Cited=70, 15371360].
Poirier C, Qin Y, Adams CP, ..., Bishop CE (2004) A complex interaction of imprinted and maternal-effect genes modifies
sex determination in Odd Sex (Ods) mice. Genetics. [IF=1.102, Cited=12, 15579706].
Regev A, Teichmann SA, Lander E, ..., Yosef N (2017) The Human Cell Atlas. eLife. [IF=1.743, Cited=923, 29206104].
Lander E (None) Genes and genomes. None. [IF=None, Cited=0, 10941417].

Publication with MISSING institution:

McCarthy MI, Kruglyak L, Lander E (1998) Sib-pair collection strategies for complex diseases. Genetic Epidemiology.
[IF=0.668, Cited=34, 9671984].
Rioux JD, Karinen H, Kocher K, ..., Laakso M (2004) Genomewide search and association studies in a Finnish celiac
disease population: Identification of a novel locus and replication of the HLA and CTLA4 loci. American Journal of
Medical Genetics, Part A. [IF=1.165, Cited=25, 15386476].
Yeo TW, De Jager PL, Gregory SG, ..., Sawcer S (2007) A second major histocompatibility complex susceptibility locus for
multiple sclerosis. Annals of Neurology. [IF=2.769, Cited=104, 17252545].
Lindblad-Toh K, Lander E, McPherson JD, ..., Birney E (2001) Progress in sequencing the mouse genome. Genesis (United
States). [IF=0.583, Cited=14, 11783003].
Accili D, Frapier C, Mosthaf L, ..., Taylor SI (1989) A mutation in the insulin receptor gene that impairs transport of
the receptor to the plasma membrane and causes insulin-resistant diabetes. EMBO Journal. [IF=2.114, Cited=68, 2573522].
Yi TM, Lander E (1994) Recognition of related proteins by iterative template refinement (ITR). Protein Science.
[IF=1.97, Cited=30, 7987226].
Luongo C, Gould KA, Su LK, ..., Moser AR (1993) Mapping of multiple intestinal neoplasia (Min) to proximal chromosome 18
of the mouse. Genomics. [IF=1.012, Cited=32, 8094372].
Haldi M, Perrot V, Saumier M, ..., Lander E (1994) Large human YACs constructed in a rad52 strain show a reduced rate of
chimerism. Genomics. [IF=1.012, Cited=22, 7713499].
Segre JA, Nemhauser JL, Taylor BA, ..., Lander E (1995) Positional cloning of the nude locus: genetic, physical, and
transcription maps of the region and mutations in the mouse and rat. Genomics. [IF=1.012, Cited=80, 7490093].
Navin A, Prekeris R, Lisitsyn NA, ..., Simpson EM (1996) Mouse Y-specific repeats isolated by whole chromosome
representational difference analysis. Genomics. [IF=1.012, Cited=19, 8812464].
Shi YP, Mohapatra G, Miller J, ..., Gray J (1997) FISH probes for mouse chromosome identification. Genomics. [IF=1.012,
Cited=30, 9339359].
Zhong TP, Kaphingst K, Akella U, ..., Fishman MC (1998) Zebrafish genomic library in yeast artificial chromosomes.
Genomics. [IF=1.012, Cited=8, 9503028].
Bartoloni L, Blouin JL, Maiti AK, ..., Antonarakis SE (2001) Axonemal beta heavy chain dynein DNAH9: cDNA sequence,
genomic structure, and investigation of its role in primary ciliary dyskinesia. Genomics. [IF=1.012, Cited=29, 11247663].
Yi TM, Lander E (1993) Protein secondary structure prediction using nearest-neighbor methods. Journal of Molecular
Biology. [IF=1.281, Cited=64, 8371270].
Engreitz J, Lander E, Guttman M (2015) RNA antisense purification (RAP) for mapping RNA interactions with chromatin.
Methods in Molecular Biology. [IF=0.413, Cited=51, 25555582].
Truett GE, Jacob HJ, Miller J, ..., Leibel RL (1995) Genetic map of rat chromosome 5 including the fatty (fa) locus.
Mammalian Genome. [IF=0.583, Cited=15, 7719022].
Kusumi K, Smith JS, Segre JA, ..., Lander E (1993) Construction of a large-insert yeast artificial chromosome library of
the mouse genome. Mammalian Genome. [IF=0.583, Cited=68, 8358173].
Burrage LC, Baskin-Hill AE, Sinasac DS, ..., Nadeau JH (2010) Genetic resistance to diet-induced obesity in chromosome
substitution strains of mice. Mammalian Genome. [IF=0.583, Cited=27, 20127486].
Haldi ML, Strickland C, Lim P, ..., Lander E (1996) A comprehensive large-insert yeast artificial chromosome library for
physical mapping of the mouse genome. Mammalian Genome. [IF=0.583, Cited=48, 8854865].
Haldi ML, Lim P, Kaphingst K, ..., Lander E (1997) Construction of a large-insert yeast artificial chromosome library of
the rat genome. Mammalian Genome. [IF=0.583, Cited=5, 9096113].
Bieg S, Koike G, Jiang J, ..., Lernmark A (1998) Genetic isolation of iddm 1 on chromosome 4 in the biobreeding (BB)
rat. Mammalian Genome. [IF=0.583, Cited=30, 9530633].
Brown DM, Matise TC, Koike G, ..., Jacob HJ (1998) An integrated genetic linkage map of the laboratory rat. Mammalian
Genome. [IF=0.583, Cited=32, 9657848].
Szpirer C, Szpirer J, Van Vooren P, ..., Levan G (1998) Gene-based anchoring of the rat genetic linkage and cytogenetic
maps: new regional localizations, orientation of the linkage groups, and insights into mammalian chromosome evolution.
Mammalian Genome. [IF=0.583, Cited=17, 9716657].
Klaff LS, Koike G, Jiang J, ..., Lernmark A (1999) BB rat diabetes susceptibility and body weight regulation genes
colocalize on chromosome 2. Mammalian Genome. [IF=0.583, Cited=21, 10441739].
Walsh EC, Sabeti P, Hutcheson HB, ..., Altshuler D (2005) Searching for signals of evolutionary selection in 168 genes
related to immune function. Human Genetics. [IF=1.653, Cited=47, 16362345].
Klockars T, Holmberg V, Savukoski M, ..., Peltonen L (1999) Transcript identification on the CLN5 region on chromosome
13q22. Human Genetics. [IF=1.653, Cited=4, 10480355].
Donis-Keller H, Green P, Helms C, ..., Lander E (1987) A genetic linkage map of the human genome. Cell. [IF=8.479,
Cited=541, 3664638].
Jacob HJ, Lindpaintner K, Lincoln SE, ..., Lander E (1991) Genetic mapping of a gene causing hypertension in the stroke-
prone spontaneously hypertensive rat. Cell. [IF=8.479, Cited=410, 1655275].
Dietrich WF, Lander E, Smith JS, ..., Dove W (1993) Genetic identification of Mom-1, a major modifier locus affecting
Min-induced intestinal neoplasia in the mouse. Cell. [IF=8.479, Cited=413, 8242739].
Dzau VJ, Jacob HJ, Lindpainter K, ..., Lander E (1992) Genetic mapping in hypertension. Journal of Vascular Surgery.
[IF=2.095, Cited=3, 1578573].
Arratia R, Lander E, Tavaré S, Waterman MS (1991) Genomic mapping by anchoring random clones: a mathematical analysis.
Genomics. [IF=1.012, Cited=40, 1783390].
Dietrich WF, Damron DM, Isberg RR, ..., Swanson MS (1995) Lgn1, a gene that determines susceptibility to Legionella
pneumophila, maps to mouse chromosome 13. Genomics. [IF=1.012, Cited=42, 7607666].
Pettersson A, Wilson D, Daniels T, ..., Lernmark A (1995) Thyroiditis in the BB rat is associated with lymphopenia but
occurs independently of diabetes. Journal of Autoimmunity. [IF=2.537, Cited=20, 7492346].
Ulirsch JC, Verboon JM, Kazerounian S, ..., Gazda HT (2019) The Genetic Landscape of Diamond-Blackfan Anemia. American
Journal of Human Genetics. [IF=2.607, Cited=12, 30735661].
Germain AR, Carmody LC, Morgan B, ..., Munoz B (2012) Identification of a selective small molecule inhibitor of breast
cancer stem cells. Bioorganic and Medicinal Chemistry Letters. [IF=0.704, Cited=20, 22503247].
Germain AR, Carmody LC, Nag PP, ..., Munoz B (2013) Cinnamides as selective small-molecule inhibitors of a cellular
model of breast cancer stem cells. Bioorganic and Medicinal Chemistry Letters. [IF=0.704, Cited=6, 23403082].
Vasudevan KM, Barbie DA, Rabinovsky R, ..., Garraway LA (2009) AKT-independent signaling downstream of oncogenic PIK3CA
mutations in human cancer. Cancer Cell. [IF=5.274, Cited=351, 19573809].
Bernstein BE, Kamal M, Lindblad-Toh K, ..., Lander E (2005) Genomic maps and comparative analysis of histone
modifications in human and mouse. Cell. [IF=8.479, Cited=1000, 15680324].
Moffat J, Grueneberg DA, Yang X, ..., Sabatini DM (2006) A lentiviral RNAi library for human and mouse genes applied to
an arrayed viral high-content screen. Cell. [IF=8.479, Cited=1000, 16564017].
Bernstein BE, Mikkelsen TS, Xie X, ..., Lander ES (2006) A bivalent chromatin structure marks key developmental genes in
embryonic stem cells. Cell. [IF=8.479, Cited=1000, 16630819].
Bernstein BE, Meissner A, Lander E (2007) The mammalian epigenome. Cell. [IF=8.479, Cited=1000, 17320505].
Boehm JS, Zhao JJ, Yao J, ..., Hahn WC (2007) Integrative genomic approaches identify IKBKE as a breast cancer oncogene.
Cell. [IF=8.479, Cited=413, 17574021].
Huarte M, Guttman M, Feldser D, ..., Rinn JL (2010) A large intergenic noncoding RNA induced by p53 mediates global gene
repression in the p53 response. Cell. [IF=8.479, Cited=1000, 20673990].
Mikkelsen TS, Xu Z, Zhang X, ..., Rosen ED (2010) Comparative epigenomic analysis of murine and human adipogenesis.
Cell. [IF=8.479, Cited=360, 20887899].
Gupta PB, Fillmore CM, Jiang G, ..., Lander E (2011) Stochastic state transitions give rise to phenotypic equilibrium in
populations of cancer cells. Cell. [IF=8.479, Cited=874, 21854987].
Hodis E, Watson IR, Kryukov GV, ..., Chin L (2012) A landscape of driver mutations in melanoma. Cell. [IF=8.479,
Cited=1000, 22817889].
Imielinski M, Berger AH, Hammerman PS, ..., Meyerson M (2012) Mapping the hallmarks of lung adenocarcinoma with
massively parallel sequencing. Cell. [IF=8.479, Cited=1000, 22980975].
Landau DA, Carter SL, Stojanov P, ..., Wu CJ (2013) Evolution and impact of subclonal mutations in chronic lymphocytic
leukemia. Cell. [IF=8.479, Cited=895, 23415222].
Grossman SR, Andersen KG, Shlyakhter I, ..., Sabeti PC (2013) Identifying recent adaptations in large-scale genomic
data. Cell. [IF=8.479, Cited=221, 23415221].
Garraway LA, Lander E (2013) Lessons from the cancer genome. Cell. [IF=8.479, Cited=758, 23540688].
Baca SC, Prandi D, Lawrence MS, ..., Garraway LA (2013) Punctuated evolution of prostate cancer genomes. Cell.
[IF=8.479, Cited=762, 23622249].
Gifford CA, Ziller MJ, Gu H, ..., Meissner A (2013) Transcriptional and epigenetic dynamics during specification of
human embryonic stem cells. Cell. [IF=8.479, Cited=280, 23664763].
Guttman M, Russell P, Ingolia NT, ..., Lander ES (2013) Ribosome profiling provides evidence that large noncoding RNAs
do not encode proteins. Cell. [IF=8.479, Cited=457, 23810193].
Brennan CW, Verhaak RGW, McKenna A, ..., Chin L (2013) The somatic genomic landscape of glioblastoma. Cell. [IF=8.479,
Cited=1000, 24120142].
Schwartz S, Agarwala SD, Mumbach MR, ..., Regev A (2013) High-resolution mapping reveals a conserved, widespread,
dynamic mRNA methylation program in yeast meiosis. Cell. [IF=8.479, Cited=361, 24269006].
Tewhey R, Kotliar D, Park DS, ..., Sabeti PC (2018) Direct Identification of Hundreds of Expression-Modulating Variants
using a Multiplexed Reporter Assay. Cell. [IF=8.479, Cited=29, 29474912].
Schiebinger G, Shu J, Tabaka M, ..., Lander ES (2019) Optimal-Transport Analysis of Single-Cell Gene Expression
Identifies Developmental Trajectories in Reprogramming. Cell. [IF=8.479, Cited=43, 30849376].
Giannakis M, Mu XJ, Shukla SA, ..., Garraway LA (2016) Genomic Correlates of Immune-Cell Infiltrates in Colorectal
Carcinoma. Cell Reports. [IF=1.738, Cited=123, 27760322].
Aiden AP, Rivera MN, Rheinbay E, ..., Bernstein BE (2010) Wilms tumor chromatin profiles highlight stem cell properties
and a renal developmental network. None. [IF=None, Cited=59, 20569696].
Proia TA, Keller PJ, Gupta PB, ..., Kuperwasser C (2011) Genetic predisposition directs breast cancer phenotype by
dictating progenitor cell fate. None. [IF=None, Cited=250, 21295272].
Rioux JD, Daly MJ, Green T, ..., Siminovitch KA (1998) Absence of linkage between inflammatory bowel disease and
selected loci on chromosomes 3, 7, 12, and 16. Gastroenterology. [IF=5.156, Cited=39, 9797358].
Szpirer C, Szpirer J, Van Vooren P, ..., Levan G (1999) Gene-based anchoring of the rat genetic linkage and cytogenetic
maps. Transplantation Proceedings. [IF=0.445, Cited=1, 10330994].
Yi TM, Lander E (1996) Iterative template refinement: protein-fold prediction using iterative search and hybrid
sequence/structure templates. None. [IF=None, Cited=3, 8743692].
Fambrough D, McClure K, Kazlauskas A, Lander E (1999) Diverse signaling pathways activated by growth factor receptors
induce broadly overlapping, rather than independent, sets of genes. Cell. [IF=8.479, Cited=269, 10380925].
Holstege FC, Jennings EG, Wyrick JJ, ..., Young RA (1998) Dissecting the regulatory circuitry of a eukaryotic genome.
Cell. [IF=8.479, Cited=1000, 9845373].
Lowe CJ, Wu M, Salic A, ..., Kirschner M (2003) Anteroposterior patterning in hemichordates and the origins of the
chordate nervous system. Cell. [IF=8.479, Cited=285, 12837244].
Mootha V, Mootha VK, Bunkenborg J, ..., Mann M (2003) Integrated analysis of protein composition, tissue diversity, and
gene regulation in mouse mitochondria. Cell. [IF=8.479, Cited=565, 14651853].
Reich DE, Lander E (2001) On the allelic spectrum of human disease. Trends in Genetics. [IF=2.117, Cited=668, 11525833].
Xu Y, Stange-Thomann N, Weber G, ..., Meyerson M (2003) Pathogen discovery from human tissue by sequence-based
computational subtraction. Genomics. [IF=1.012, Cited=30, 12659816].
Lincoln SE, Lander E (1992) Systematic detection of errors in genetic linkage data. Genomics. [IF=1.012, Cited=217, 1427888].
Goff DJ, Galvin K, Katz H, ..., Tabin CJ (1992) Identification of polymorphic simple sequence repeats in the genome of
the zebrafish. Genomics. [IF=1.012, Cited=29, 1427829].
Hamilton BA, Smith DJ, Mueller KL, ..., Lander E (1997) The vibrator mutation causes neurodegeneration via reduced
expression of PITP alpha: positional complementation cloning and extragenic suppression. Neuron. [IF=3.346, Cited=119, 9182797].
Moralejo DH, Park HA, Speros SJ, ..., Lernmark A (2003) Genetic dissection of lymphopenia from autoimmunity by
introgression of mutated Ian5 gene onto the F344 rat. Journal of Autoimmunity. [IF=2.537, Cited=26, 14624755].
Ferrando AA, Neuberg DS, Staunton J, ..., Look AT (2002) Gene expression signatures define novel oncogenic pathways in T
cell acute lymphoblastic leukemia. Cancer Cell. [IF=5.274, Cited=694, 12086890].
Singh D, Febbo PG, Ross K, ..., Sellers WR (2002) Gene expression correlates of clinical prostate cancer behavior.
Cancer Cell. [IF=5.274, Cited=886, 12086878].
Cargill M, Altshuler D, Ireland J, ..., Lander E (1999) Characterization of single-nucleotide polymorphisms in coding
regions of human genes. Nature Genetics. [IF=6.89, Cited=1000, 10391209].
Van Etten WJ, Steen RG, Nguyen H, ..., Hudson TJ (1999) Radiation hybrid map of the mouse genome. Nature Genetics.
[IF=6.89, Cited=63, 10431245].
Nusbaum C, Slonim DK, Harris KL, ..., Lander E (1999) A YAC-based physical map of the mouse genome. Nature Genetics.
[IF=6.89, Cited=38, 10431246].
Sidow A, Bulotsky MS, Kerrebrock AW, ..., Lander E (1999) A novel member of the F-box/WD40 gene family, encoding
dactylin, is disrupted in the mouse dactylaplasia mutant. Nature Genetics. [IF=6.89, Cited=67, 10471509].
Lander E, Ellis JJ (1998) Founding father. Nature. [IF=11.591, Cited=3, 9817195].
Paterson AH, Lander E, Hewitt JD, ..., Tanksley SD (1988) Resolution of quantitative traits into Mendelian factors by
using a complete linkage map of restriction fragment length polymorphisms. Nature. [IF=11.591, Cited=639, 2902517].
Lander E (1988) Splitting schizophrenia. Nature. [IF=11.591, Cited=44, 2903447].
Clark EA, Golub TR, Lander E, Hynes RO (2000) Genomic analysis of metastasis reveals an essential role for RhoC. Nature.
[IF=11.591, Cited=895, 10952316].
Altshuler D, Pollara VJ, Cowles CR, ..., Lander E (2000) An SNP map of the human genome generated by reduced
representation shotgun sequencing. Nature. [IF=11.591, Cited=412, 11029002].
Sachidanandam R, Weissman D, Schmidt SC, ..., Altshuler D (2001) A map of human genome sequence variation containing
1.42 million single nucleotide polymorphisms. Nature. [IF=11.591, Cited=1000, 11237013].
Reich DE, Cargill M, Bolk S, ..., Lander E (2001) Linkage disequilibrium in the human genome. Nature. [IF=11.591,
Cited=961, 11346797].
Hamilton BA, Frankel WN, Kerrebrock AW, ..., Lander E (1996) Disruption of the nuclear hormone receptor RORalpha in
staggerer mice. Nature. [IF=11.591, Cited=326, 8602221].
Sidow A, Bulotsky MS, Kerrebrock AW, ..., Lander E (1997) Serrate2 is disrupted in the mouse limb-development mutant
syndactylism. Nature. [IF=11.591, Cited=70, 9338782].
Pomeroy SL, Tamayo P, Gaasenbeek M, ..., Golub TR (2002) Prediction of central nervous system embryonal tumour outcome
based on gene expression. Nature. [IF=11.591, Cited=1000, 11807556].
Wyrick JJ, Holstege FC, Jennings EG, ..., Young RA (1999) Chromosomal landscape of nucleosome-dependent gene expression
and silencing in yeast. Nature. [IF=11.591, Cited=285, 10586882].
Engert JC, Bérubé P, Mercier J, ..., Richter A (2000) ARSACS, a spastic ataxia common in northeastern Québec, is caused
by mutations in a new gene encoding an 11.5-kb ORF. Nature Genetics. [IF=6.89, Cited=222, 10655055].
Nadeau JH, Singer JB, Matin A, Lander E (2000) Analysing complex genetic traits with chromosome substitution strains.
Nature Genetics. [IF=6.89, Cited=266, 10700173].
Lindblad-Toh K, Winchester E, Daly MJ, ..., Lander E (2000) Large-scale discovery and genotyping of single-nucleotide
polymorphisms in the mouse. Nature Genetics. [IF=6.89, Cited=239, 10742102].
Bulman MP, Kusumi K, Frayling TM, ..., Turnpenny PD (2000) Mutations in the human delta homologue, DLL3, cause axial
skeletal defects in spondylocostal dysostosis. Nature Genetics. [IF=6.89, Cited=224, 10742114].
Altshuler D, Hirschhorn JN, Klannemark M, ..., Lander E (2000) The common PPARgamma Pro12Ala polymorphism is associated
with decreased risk of type 2 diabetes. Nature Genetics. [IF=6.89, Cited=905, 10973253].
Lindblad-Toh K, Tanenbaum DM, Daly MJ, ..., Meyerson M (2000) Loss-of-heterozygosity analysis of small-cell lung
carcinomas using single-nucleotide polymorphism arrays. Nature Biotechnology. [IF=8.861, Cited=150, 10973224].
Jackson-Grusby L, Beard C, Possemato R, ..., Jaenisch R (2001) Loss of genomic methylation causes p53-dependent
apoptosis and epigenetic deregulation. Nature Genetics. [IF=6.89, Cited=442, 11137995].
Sklar P, Schwab SG, Williams NM, ..., Wildenauer DB (2001) Association analysis of NOTCH4 loci in schizophrenia using
family and population-based controls. Nature Genetics. [IF=6.89, Cited=46, 11381257].
Kusumi K, Sun ES, Kerrebrock AW, ..., Lander E (1998) The mouse pudgy mutation disrupts Delta homologue Dll3 and
initiation of early somite boundaries. Nature Genetics. [IF=6.89, Cited=182, 9662403].
Hacia JG, Fan JB, Ryder O, ..., Collins FS (1999) Determination of ancestral alleles for human single-nucleotide
polymorphisms using high-density oligonucleotide arrays. Nature Genetics. [IF=6.89, Cited=207, 10369258].
Savukoski M, Klockars T, Holmberg V, ..., Peltonen L (1998) CLN5, a novel gene encoding a putative transmembrane protein
mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis. Nature Genetics. [IF=6.89, Cited=156, 9662406].
Lander E, Lander ES, Baylis F, ..., Winnacker EL (2019) Adopt a moratorium on heritable genome editing. Nature.
[IF=11.591, Cited=99, 30867611].
Sabeti PC, Reich DE, Higgins JM, ..., Lander E (2002) Detecting recent positive selection in the human genome from
haplotype structure. Nature. [IF=11.591, Cited=1000, 12397357].
Wade CM, Kulbokas EJ, Kirby AW, ..., Daly MJ (2002) The mosaic structure of variation in the laboratory mouse genome.
Nature. [IF=11.591, Cited=321, 12466852].
Waterston RH, Lindblad-Toh K, Birney E, ..., Lander E (2002) Initial sequencing and comparative analysis of the mouse
genome. Nature. [IF=11.591, Cited=1000, 12466850].
Okazaki Y, Furuno M, Kasukawa T, ..., Hayashizaki Y (2002) Analysis of the mouse transcriptome based on functional
annotation of 60,770 full-length cDNAs. Nature. [IF=11.591, Cited=1000, 12466851].
Galagan JE, Calvo SE, Borkovich KA, ..., Birren B (2003) The genome sequence of the filamentous fungus Neurospora
crassa. Nature. [IF=11.591, Cited=919, 12712197].
Kellis M, Patterson N, Endrizzi M, ..., Lander E (2003) Sequencing and comparison of yeast species to identify genes and
regulatory elements. Nature. [IF=11.591, Cited=1000, 12748633].
Kellis M, Birren BW, Lander E (2004) Proof and evolutionary analysis of ancient genome duplication in the yeast
Saccharomyces cerevisiae. Nature. [IF=11.591, Cited=910, 15004568].
Harbison CT, Gordon DB, Lee TI, ..., Young RA (2004) Transcriptional regulatory code of a eukaryotic genome. Nature.
[IF=11.591, Cited=1000, 15343339].
Jaillon O, Aury JM, Brunet F, ..., Roest Crollius H (2004) Genome duplication in the teleost fish Tetraodon nigroviridis
reveals the early vertebrate proto-karyotype. Nature. [IF=11.591, Cited=1000, 15496914].
Xie X, Lu J, Kulbokas EJ, ..., Kellis M (2005) Systematic discovery of regulatory motifs in human promoters and 3' UTRs
by comparison of several mammals. Nature. [IF=11.591, Cited=1000, 15735639].
Nusbaum C, Zody MC, Borowsky ML, ..., Lander E (2005) DNA sequence and analysis of human chromosome 18. Nature.
[IF=11.591, Cited=30, 16177791].
Lindblad-Toh K, Wade CM, Mikkelsen TS, ..., Lander E (2005) Genome sequence, comparative analysis and haplotype
structure of the domestic dog. Nature. [IF=11.591, Cited=1000, 16341006].
Nusbaum C, Mikkelsen TS, Zody MC, ..., Lander E (2006) DNA sequence and analysis of human chromosome 8. Nature.
[IF=11.591, Cited=73, 16421571].
Zody MC, Garber M, Sharpe T, ..., Nusbaum C (2006) Analysis of the DNA sequence and duplication history of human
chromosome 15. Nature. [IF=11.591, Cited=49, 16572171].
Taylor TD, Noguchi H, Totoki Y, ..., Sakaki Y (2006) Human chromosome 11 DNA sequence and analysis including novel gene
identification. Nature. [IF=11.591, Cited=45, 16554811].
Houstis N, Rosen ED, Lander E (2006) Reactive oxygen species have a causal role in multiple forms of insulin resistance.
Nature. [IF=11.591, Cited=1000, 16612386].
Zody MC, Garber M, Adams DJ, ..., Nusbaum C (2006) DNA sequence of human chromosome 17 and analysis of rearrangement in
the human lineage. Nature. [IF=11.591, Cited=96, 16625196].
Patterson N, Richter DJ, Gnerre S, ..., Reich D (2006) Genetic evidence for complex speciation of humans and
chimpanzees. Nature. [IF=11.591, Cited=277, 16710306].
Bourlat SJ, Juliusdottir T, Lowe CJ, ..., Telford MJ (2006) Deuterostome phylogeny reveals monophyletic chordates and
the new phylum Xenoturbellida. Nature. [IF=11.591, Cited=282, 17051155].
Mikkelsen TS, Wakefield MJ, Aken B, ..., Lindblad-Toh K (2007) Genome of the marsupial Monodelphis domestica reveals
innovation in non-coding sequences. Nature. [IF=11.591, Cited=463, 17495919].
Birney E, Stamatoyannopoulos JA, Dutta A, ..., de Jong PJ (2007) Identification and analysis of functional elements in
1% of the human genome by the ENCODE pilot project. Nature. [IF=11.591, Cited=1000, 17571346].
Mikkelsen TS, Ku M, Jaffe DB, ..., Bernstein BE (2007) Genome-wide maps of chromatin state in pluripotent and lineage-
committed cells. Nature. [IF=11.591, Cited=1000, 17603471].
Sabeti PC, Fry B, Lohmueller J, ..., Stewart J (2007) Genome-wide detection and characterization of positive selection
in human populations. Nature. [IF=11.591, Cited=1000, 17943131].
Daily JP, Scanfeld D, Pochet N, ..., Regev A (2007) Distinct physiological states of Plasmodium falciparum in malaria-
infected patients. Nature. [IF=11.591, Cited=157, 18046333].
Clark AG, Eisen MB, Smith DR, ..., MacCallum I (2007) Evolution of genes and genomes on the Drosophila phylogeny.
Nature. [IF=11.591, Cited=1000, 17994087].
Weir BA, Woo MS, Getz G, ..., Meyerson M (2007) Characterizing the cancer genome in lung adenocarcinoma. Nature.
[IF=11.591, Cited=734, 17982442].
Mikkelsen TS, Hanna J, Zhang X, ..., Meissner A (2008) Dissecting direct reprogramming through integrative genomic
analysis. Nature. [IF=11.591, Cited=938, 18509334].
Meissner A, Mikkelsen TS, Gu H, ..., Lander ES (2008) Genome-scale DNA methylation maps of pluripotent and
differentiated cells. Nature. [IF=11.591, Cited=1000, 18600261].
Ding L, Getz G, Wheeler DA, ..., Wilson RK (2008) Somatic mutations affect key pathways in lung adenocarcinoma. Nature.
[IF=11.591, Cited=1000, 18948947].
Miller W, Drautz DI, Ratan A, ..., Schuster SC (2008) Sequencing the nuclear genome of the extinct woolly mammoth.
Nature. [IF=11.591, Cited=151, 19020620].
Guttman M, Amit I, Garber M, ..., Lander ES (2009) Chromatin signature reveals over a thousand highly conserved large
non-coding RNAs in mammals. Nature. [IF=11.591, Cited=1000, 19182780].
Barbie DA, Tamayo P, Boehm JS, ..., Hahn WC (2009) Systematic RNA interference reveals that oncogenic KRAS-driven
cancers require TBK1. Nature. [IF=11.591, Cited=1000, 19847166].
Beroukhim R, Mermel CH, Porter D, ..., Meyerson M (2010) The landscape of somatic copy-number alteration across human
cancers. Nature. [IF=11.591, Cited=1000, 20164920].
Artez A, Bernabé RR, Eerola I, ..., Yang H (2010) International network of cancer genome projects. Nature. [IF=11.591,
Cited=1000, 20393554].
Berger MF, Lawrence MS, Demichelis F, ..., Garraway LA (2011) The genomic complexity of primary human prostate cancer.
Nature. [IF=11.591, Cited=829, 21307934].
Chapman MA, Lawrence MS, Keats JJ, ..., Golub TR (2011) Initial genome sequencing and analysis of multiple myeloma.
Nature. [IF=11.591, Cited=984, 21430775].
Alföldi J, Di Palma F, Grabherr M, ..., Lindblad-Toh K (2011) The genome of the green anole lizard and a comparative
analysis with birds and mammals. Nature. [IF=11.591, Cited=367, 21881562].
Guttman M, Donaghey J, Carey BW, ..., Lander E (2011) lincRNAs act in the circuitry controlling pluripotency and
differentiation. Nature. [IF=11.591, Cited=1000, 21874018].
Lindblad-Toh K, Garber M, Zuk O, ..., Kellis M (2011) A high-resolution map of human evolutionary constraint using 29
mammals. Nature. [IF=11.591, Cited=693, 21993624].
Jones FC, Grabherr MG, Chan YF, ..., Kingsley DM (2012) The genomic basis of adaptive evolution in threespine
sticklebacks. Nature. [IF=11.591, Cited=1000, 22481358].
Onder TT, Kara N, Cherry A, ..., Daley GQ (2012) Chromatin-modifying enzymes as modulators of reprogramming. Nature.
[IF=11.591, Cited=429, 22388813].
Berger MF, Hodis E, Heffernan TP, ..., Garraway LA (2012) Melanoma genome sequencing reveals frequent PREX2 mutations.
Nature. [IF=11.591, Cited=486, 22622578].
Banerji S, Cibulskis K, Rangel-Escareno C, ..., Meyerson M (2012) Sequence analysis of mutations and translocations
across breast cancer subtypes. Nature. [IF=11.591, Cited=773, 22722202].
Amemiya CT, Alföldi J, Lee AP, ..., Lindblad-Toh K (2013) The African coelacanth genome provides insights into tetrapod
evolution. Nature. [IF=11.591, Cited=376, 23598338].
Joung J, Engreitz JM, Konermann S, ..., Zhang F (2017) Erratum: Genome-scale activation screen identifies a lncRNA locus
regulating a gene neighbourhood. Nature. [IF=11.591, Cited=5, 28933431].
Ott PA, Hu Z, Keskin DB, ..., Wu CJ (2018) Corrigendum: An immunogenic personal neoantigen vaccine for patients with
melanoma. Nature. [IF=11.591, Cited=9, 29542692].
Gnirke A, Melnikov A, Maguire J, ..., Nusbaum C (2009) Solution hybrid selection with ultra-long oligonucleotides for
massively parallel targeted sequencing. Nature Biotechnology. [IF=8.861, Cited=837, 19182786].
Guttman M, Garber M, Levin JZ, ..., Regev A (2010) Ab initio reconstruction of cell type-specific transcriptomes in
mouse reveals the conserved multi-exonic structure of lincRNAs. Nature Biotechnology. [IF=8.861, Cited=780, 20436462].
Robinson JT, Thorvaldsdóttir H, Winckler W, ..., Mesirov JP (2011) Integrative genomics viewer. Nature Biotechnology.
[IF=8.861, Cited=1000, 21221095].
Melnikov A, Murugan A, Zhang X, ..., Mikkelsen TS (2012) Systematic dissection and optimization of inducible enhancers
in human cells using a massively parallel reporter assay. Nature Biotechnology. [IF=8.861, Cited=395, 22371084].
Carter SL, Cibulskis K, Helman E, ..., Getz G (2012) Absolute quantification of somatic DNA alterations in human cancer.
Nature Biotechnology. [IF=8.861, Cited=1000, 22544022].
Cibulskis K, Lawrence MS, Carter SL, ..., Getz G (2013) Sensitive detection of somatic point mutations in impure and
heterogeneous cancer samples. Nature Biotechnology. [IF=8.861, Cited=1000, 23396013].
Bernstein BE, Stamatoyannopoulos JA, Costello JF, ..., Thomson JA (2010) The NIH Roadmap Epigenomics Mapping Consortium.
Nature Biotechnology. [IF=8.861, Cited=1000, 20944595].
Karlsson EK, Baranowska I, Wade CM, ..., Lindblad-Toh K (2007) Efficient mapping of mendelian traits in dogs through
genome-wide association. Nature Genetics. [IF=6.89, Cited=360, 17906626].
Barbieri CE, Baca SC, Lawrence MS, ..., Garraway LA (2012) Exome sequencing identifies recurrent SPOP, FOXA1 and MED12
mutations in prostate cancer. Nature Genetics. [IF=6.89, Cited=968, 22610119].
Pugh TJ, Morozova O, Attiyeh EF, ..., Maris JM (2013) The genetic landscape of high-risk neuroblastoma. Nature Genetics.
[IF=6.89, Cited=702, 23334666].
Kirby A, Gnirke A, Jaffe DB, ..., Daly MJ (2013) Mutations causing medullary cystic kidney disease type 1 lie in a large
VNTR in MUC1 missed by massively parallel sequencing. Nature Genetics. [IF=6.89, Cited=149, 23396133].
Dulak AM, Stojanov P, Peng S, ..., Bass AJ (2013) Exome and whole-genome sequencing of esophageal adenocarcinoma
identifies recurrent driver events and mutational complexity. Nature Genetics. [IF=6.89, Cited=491, 23525077].
Farhat MR, Shapiro BJ, Kieser KJ, ..., Murray M (2013) Genomic analysis identifies targets of convergent positive
selection in drug-resistant Mycobacterium tuberculosis. Nature Genetics. [IF=6.89, Cited=255, 23995135].
Barretina J, Taylor BS, Banerji S, ..., Singer S (2010) Subtype-specific genomic alterations define new targets for
soft-tissue sarcoma therapy. Nature Genetics. [IF=6.89, Cited=466, 20601955].
Loewer S, Cabili MN, Guttman M, ..., Rinn JL (2010) Large intergenic non-coding RNA-RoR modulates reprogramming of human
induced pluripotent stem cells. Nature Genetics. [IF=6.89, Cited=622, 21057500].
Lisitsyn NA, Segre JA, Kusumi K, ..., Lander E (1994) Direct isolation of polymorphic markers linked to a trait by
genetically directed representational difference analysis. Nature Genetics. [IF=6.89, Cited=61, 8136836].
Superti-Furga A, Hästbacka J, Wilcox WR, ..., Gitzelmann R (1996) Achondrogenesis type IB is caused by mutations in the
diastrophic dysplasia sulphate transporter gene. Nature Genetics. [IF=6.89, Cited=113, 8528239].
Galli J, Li LS, Glaser A, ..., Luthman H (1996) Genetic analysis of non-insulin dependent diabetes mellitus in the GK
rat. Nature Genetics. [IF=6.89, Cited=161, 8528247].
Brown DM, Provoost AP, Daly MJ, ..., Jacob HJ (1996) Renal disease susceptibility and hypertension are under independent
genetic control in the fawn-hooded rat. Nature Genetics. [IF=6.89, Cited=158, 8528250].
Laitinen T, Daly MJ, Rioux JD, ..., Kere J (2001) A susceptibility locus for asthma-related traits on chromosome 7
revealed by genome-wide scan in a founder population. Nature Genetics. [IF=6.89, Cited=105, 11326283].
Lander E (1993) Finding similarities and differences among genomes. Nature Genetics. [IF=6.89, Cited=19, 8513322].
Jacob HJ, Pettersson A, Wilson D, ..., Lander E (1992) Genetic dissection of autoimmune type I diabetes in the BB rat.
Nature Genetics. [IF=6.89, Cited=141, 1303251].
Mahtani MM, Widén E, Lehto M, ..., Groop LC (1996) Mapping of a gene for type 2 diabetes associated with an insulin
secretion defect by a genome scan in Finnish families. Nature Genetics. [IF=6.89, Cited=182, 8782826].
Cormier RT, Hong KH, Halberg RB, ..., Lander E (1997) Secretory phospholipase Pla2g2a confers resistance to intestinal
tumorigenesis. Nature Genetics. [IF=6.89, Cited=186, 9288104].
Hudson TJ, Church DM, Greenaway S, ..., Denny P (2001) A radiation hybrid map of mouse genes. Nature Genetics. [IF=6.89,
Cited=37, 11586302].
Rioux JD, Daly MJ, Silverberg MS, ..., Hudson TJ (2001) Genetic variation in the 5q31 cytokine gene cluster confers
susceptibility to Crohn disease. Nature Genetics. [IF=6.89, Cited=517, 11586304].
Daly MJ, Rioux JD, Schaffner SF, ..., Lander E (2001) High-resolution haplotype structure in the human genome. Nature
Genetics. [IF=6.89, Cited=926, 11586305].
Ramaswamy S, Ross KN, Lander E, Golub TR (2002) A molecular signature of metastasis in primary solid tumors. Nature
Genetics. [IF=6.89, Cited=1000, 12469122].
Lohmueller KE, Pearce CL, Pike M, ..., Hirschhorn JN (2003) Meta-analysis of genetic association studies supports a
contribution of common variants to susceptibility to common disease. Nature Genetics. [IF=6.89, Cited=1000, 12524541].
De Sanctis GT, Merchant M, Beier DR, ..., Drazen JM (1995) Quantitative locus analysis of airway hyperresponsiveness in
A/J and C57BL/6J mice. Nature Genetics. [IF=6.89, Cited=165, 7550342].
Daly MJ, Lander E (1996) The importance of being independent: sib pair analysis in diabetes. Nature Genetics. [IF=6.89,
Cited=14, 8841179].
Kong A, Frigge M, Bell GI, ..., Cox NJ (1997) Diabetes, dependence, asymptotics, selection and significance. Nature
Genetics. [IF=6.89, Cited=6, 9326932].
Mootha V, Mootha VK, Lindgren CM, ..., Groop LC (2003) PGC-1alpha-responsive genes involved in oxidative phosphorylation
are coordinately downregulated in human diabetes. Nature Genetics. [IF=6.89, Cited=1000, 12808457].
Hästbacka J, de la Chapelle A, Kaitila I, ..., Lander E (1992) Linkage disequilibrium mapping in isolated founder
populations: diastrophic dysplasia in Finland. Nature Genetics. [IF=6.89, Cited=333, 1345170].
Freedman ML, Reich D, Penney KL, ..., Altshuler D (2004) Assessing the impact of population stratification on genetic
association studies. Nature Genetics. [IF=6.89, Cited=515, 15052270].
Volkman SK, Sabeti PC, DeCaprio D, ..., Wirth DF (2006) A genome-wide map of diversity in Plasmodium falciparum. Nature
Genetics. [IF=6.89, Cited=219, 17159979].
Manolio TA, Rodriguez LL, Brooks L, ..., Collins FS (2007) New models of collaboration in genome-wide association
studies: the Genetic Association Information Network. Nature Genetics. [IF=6.89, Cited=214, 17728769].
Armstrong SA, Staunton JE, Silverman LB, ..., Korsmeyer SJ (2001) MLL translocations specify a distinct gene expression
profile that distinguishes a unique leukemia. Nature Genetics. [IF=6.89, Cited=916, 11731795].
Reich DE, Schaffner SF, Daly MJ, ..., Altshuler D (2002) Human genome sequence variation and the influence of gene
history, mutation and recombination. Nature Genetics. [IF=6.89, Cited=175, 12161752].
Cowles CR, Hirschhorn JN, Altshuler D, Lander E (2002) Detection of regulatory variation in mouse genes. Nature
Genetics. [IF=6.89, Cited=256, 12410233].
Shipp MA, Ross KN, Tamayo P, ..., Golub TR (2002) Diffuse large B-cell lymphoma outcome prediction by gene-expression
profiling and supervised machine learning. Nature Medicine. [IF=11.877, Cited=1000, 11786909].
Chiang DY, Getz G, Jaffe DB, ..., Lander E (2008) High-resolution mapping of copy-number alterations with massively
parallel sequencing. Nature Methods. [IF=10.009, Cited=318, 19043412].
Nusbaum C, Ohsumi TK, Gomez J, ..., Jaffe DB (2008) Sensitive, specific polymorphism discovery in bacteria using
massively parallel sequencing. Nature Methods. [IF=10.009, Cited=51, 19079253].
Gu H, Bock C, Mikkelsen TS, ..., Meissner A (2010) Genome-scale DNA methylation mapping of clinical samples at single-
nucleotide resolution. Nature Methods. [IF=10.009, Cited=198, 20062050].
Hacohen N, Hahn WC, Lander E, Sabatini DM (2006) Genome-scale loss-of-function screening with a lentiviral RNAi library.
Nature Methods. [IF=10.009, Cited=266, 16929317].
Lander E (2004) Eric S. Lander. Nature Reviews Drug Discovery. [IF=18.471, Cited=4, 15368656].
Flannick J, Fuchsberger C, Mahajan A, ..., McCarthy MI (2018) Erratum: Sequence data and association statistics from
12,940 type 2 diabetes cases and controls. Scientific data. [IF=2.887, Cited=1, 29360107].
Hästbacka J, Kerrebrock A, Mokkala K, ..., Lander E (1999) Identification of the Finnish founder mutation for
diastrophic dysplasia (DTD). European Journal of Human Genetics. [IF=1.676, Cited=24, 10482955].
Tello-Ruiz MK, Curley C, DelMonte T, ..., Rioux JD (2006) Haplotype-based association analysis of 56 functional
candidate genes in the IBD6 locus on chromosome 19. European Journal of Human Genetics. [IF=1.676, Cited=17, 16570073].
Sklar P, Gabriel SB, McInnis MG, ..., Lander E (2002) Family-based association study of 76 candidate genes in bipolar
disorder: BDNF is a potential risk locus. Brain-derived neutrophic factor. Molecular Psychiatry. [IF=2.603, Cited=379, 12140781].
Sklar P, Pato MT, Kirby A, ..., Pato CN (2004) Genome-wide scan in Portuguese Island families identifies 5q31-5q35 as a
susceptibility locus for schizophrenia and psychosis. Molecular Psychiatry. [IF=2.603, Cited=81, 14699422].
Cormier RT, Bilger A, Lillich AJ, ..., Dove WF (2000) The Mom1AKR intestinal tumor resistance region consists of Pla2g2a
and a locus distal to D4Mit64. Oncogene. [IF=1.523, Cited=67, 10918573].
Altshuler D, Kruglyak L, Lander E (1998) Genetic polymorphisms and disease. New England Journal of Medicine. [IF=17.194,
Cited=58, 9606122].
Hafler DA, Compston A, Sawcer S, ..., Hauser SL (2007) Risk alleles for multiple sclerosis identified by a genomewide
study. New England Journal of Medicine. [IF=17.194, Cited=1000, 17660530].
Wang L, Lawrence MS, Wan Y, ..., Wu CJ (2011) SF3B1 and other novel cancer genes in chronic lymphocytic leukemia. New
England Journal of Medicine. [IF=17.194, Cited=712, 22150006].
Brat DJ, Verhaak RGW, Aldape KD, ..., Zhang J (2015) Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade
Gliomas. New England Journal of Medicine. [IF=17.194, Cited=1000, 26061751].
Stitziel NO, Won HH, Morrison AC, ..., Kathiresan S (2014) Inactivating mutations in NPC1L1 and protection from coronary
heart disease. New England Journal of Medicine. [IF=17.194, Cited=226, 25390462].
Genovese G, Kähler AK, Handsaker RE, ..., McCarroll SA (2014) Clonal hematopoiesis and blood-cancer risk inferred from
blood DNA sequence. New England Journal of Medicine. [IF=17.194, Cited=1000, 25426838].
Lander E (2011) QnAs with Eric S. Lander. Interview by Prashant Nair. Proceedings of the National Academy of Sciences of
the United States of America. [IF=2.765, Cited=3, 21606349].
Lander E, Botstein D (1986) Strategies for studying heterogeneous genetic traits in humans by using a linkage map of
restriction fragment length polymorphisms. Proceedings of the National Academy of Sciences of the United States of
America. [IF=2.765, Cited=80, 2876423].
Lander E, Green P (1987) Construction of multilocus genetic linkage maps in humans. Proceedings of the National Academy
of Sciences of the United States of America. [IF=2.765, Cited=799, 3470801].
Sweeney C, Fambrough D, Huard C, ..., Carraway KL (2001) Growth factor-specific signaling pathway stimulation and gene
expression mediated by ErbB receptors. Journal of Biological Chemistry. [IF=1.122, Cited=69, 11297548].
Wei BQ, Mikkelsen TS, McKinney MK, ..., Cravatt BF (2006) A second fatty acid amide hydrolase with variable distribution
among placental mammals. Journal of Biological Chemistry. [IF=1.122, Cited=184, 17015445].
Kuokkanen S, Gschwend M, Rioux JD, ..., Peltonen L (1997) Genomewide scan of multiple sclerosis in Finnish multiplex
families. American Journal of Human Genetics. [IF=2.607, Cited=174, 9399895].
Rioux JD, Stone VA, Daly MJ, ..., Lin AY (1998) Familial eosinophilia maps to the cytokine gene cluster on human
chromosomal region 5q31-q33. American Journal of Human Genetics. [IF=2.607, Cited=65, 9758611].
Pfeifer D, Kist R, Dewar K, ..., Scherer G (1999) Campomelic dysplasia translocation breakpoints are scattered over 1 Mb
proximal to SOX9: evidence for an extended control region. American Journal of Human Genetics. [IF=2.607, Cited=124, 10364523].
Rioux JD, Silverberg MS, Daly MJ, ..., Siminovitch KA (2000) Genomewide search in Canadian families with inflammatory
bowel disease reveals two novel susceptibility loci. American Journal of Human Genetics. [IF=2.607, Cited=324, 10777714].
Pajukanta P, Cargill M, Viitanen L, ..., Peltonen L (2000) Two loci on chromosomes 2 and X for premature coronary heart
disease identified in early- and late-settlement populations of Finland. American Journal of Human Genetics. [IF=2.607,
Cited=100, 11078477].
Lee N, Daly MJ, Delmonte T, ..., Rioux JD (2001) A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-
Saint-Jean cytochrome oxidase deficiency to 2p16. American Journal of Human Genetics. [IF=2.607, Cited=22, 11156535].
Hirschhorn JN, Lindgren CM, Daly MJ, ..., Lander E (2001) Genomewide linkage analysis of stature in multiple populations
reveals several regions with evidence of linkage to adult height. American Journal of Human Genetics. [IF=2.607,
Cited=122, 11410839].
Ardlie K, Liu-Cordero SN, Eberle MA, ..., Kruglyak L (2001) Lower-than-expected linkage disequilibrium between tightly
linked markers in humans suggests a role for gene conversion. American Journal of Human Genetics. [IF=2.607, Cited=77, 11473344].
Lindgren CM, Mahtani MM, Widén E, ..., Lander E (2002) Genomewide search for type 2 diabetes mellitus susceptibility
loci in Finnish families: the Botnia study. American Journal of Human Genetics. [IF=2.607, Cited=94, 11791216].
Giallourakis C, Stoll M, Miller K, ..., Rioux JD (2003) IBD5 is a general risk factor for inflammatory bowel disease:
replication of association with Crohn disease and identification of a novel association with ulcerative colitis.
American Journal of Human Genetics. [IF=2.607, Cited=114, 12776251].
Walsh EC, Mather KA, Schaffner SF, ..., Rioux JD (2003) An integrated haplotype map of the human major
histocompatibility complex. American Journal of Human Genetics. [IF=2.607, Cited=111, 12920676].
Miretti MM, Walsh EC, Ke X, ..., Deloukas P (2005) A high-resolution linkage-disequilibrium map of the human major
histocompatibility complex and first generation of tag single-nucleotide polymorphisms. American Journal of Human
Genetics. [IF=2.607, Cited=178, 15747258].
Sawcer S, Ban M, Maranian M, ..., Haines JL (2005) A high-density screen for linkage in multiple sclerosis. American
Journal of Human Genetics. [IF=2.607, Cited=184, 16080120].
Slonim D, Kruglyak L, Stein L, Lander E (1997) Building human genome maps with radiation hybrids. Journal of
Computational Biology. [IF=0.499, Cited=76, 9385541].
Kruglyak L, Lander E (1998) Faster multipoint linkage analysis using Fourier transforms. Journal of Computational
Biology. [IF=0.499, Cited=144, 9541867].
Hulbert SH, Ilott TW, Legg EJ, ..., Michelmore RW (1988) Genetic analysis of the fungus, Bremia lactucae, using
restriction fragment length polymorphisms. Genetics. [IF=1.102, Cited=130, 2906309].
Paterson AH, Damon S, Hewitt JD, ..., Tanksley SD (1991) Mendelian factors underlying quantitative traits in tomato:
comparison across species, generations, and environments. Genetics. [IF=1.102, Cited=373, 1673106].
Dietrich W, Katz H, Lincoln SE, ..., Lander E (1992) A genetic map of the mouse suitable for typing intraspecific
crosses. Genetics. [IF=1.102, Cited=676, 1353738].
Stuber CW, Lincoln SE, Wolff DW, ..., Lander E (1992) Identification of genetic factors contributing to heterosis in a
hybrid from two elite maize inbred lines using molecular markers. Genetics. [IF=1.102, Cited=337, 1468633].
Kruglyak L, Lander E (1995) A nonparametric approach for mapping quantitative trait loci. Genetics. [IF=1.102,
Cited=174, 7768449].
Lehesjoki AE, Koskiniemi M, Norio R, ..., de la Chapelle A (1993) Localization of the EPM1 gene for progressive
myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping. Human Molecular Genetics.
[IF=1.158, Cited=90, 8104628].
Laitinen T, Kauppi P, Ignatius J, ..., Kere J (1997) Genetic control of serum IgE levels and asthma: linkage and linkage
disequilibrium studies in an isolated population. Human Molecular Genetics. [IF=1.158, Cited=54, 9328470].
Ober C, Cox NJ, Abney M, ..., Parry R (1998) Genome-wide search for asthma susceptibility loci in a founder population.
The Collaborative Study on the Genetics of Asthma. Human Molecular Genetics. [IF=1.158, Cited=223, 9700192].
Tantisira KG, Lake S, Silverman ES, ..., Weiss ST (2004) Corticosteroid pharmacogenetics: association of sequence
variants in CRHR1 with improved lung function in asthmatics treated with inhaled corticosteroids. Human Molecular
Genetics. [IF=1.158, Cited=190, 15128701].
Sawcer SJ, Maranian M, Singlehurst S, ..., Haines JL (2004) Enhancing linkage analysis of complex disorders: an
evaluation of high-density genotyping. Human Molecular Genetics. [IF=1.158, Cited=48, 15238506].
Kurooka H, Segre JA, Hirano Y, ..., Honjo T (1996) Rescue of the hairless phenotype in nude mice by transgenic insertion
of the wild-type Hfh11 genomic locus. International Immunology. [IF=0.92, Cited=10, 8671685].
MacMurray AJ, Weaver A, Shin HS, Lander E (1991) An automated method for DNA preparation from thousands of YAC clones.
Nucleic Acids Research. [IF=4.663, Cited=5, 2014175].
Meissner A, Gnirke A, Bell GW, ..., Jaenisch R (2005) Reduced representation bisulfite sequencing for comparative high-
resolution DNA methylation analysis. Nucleic Acids Research. [IF=4.663, Cited=649, 16224102].
Pato CN, Lander E, Schulz SC (1989) Prospects for the genetic analysis of schizophrenia. Schizophrenia Bulletin.
[IF=1.951, Cited=6, 2683037].
Strohl KP, Gallaugher L, Lynn A, ..., Nadeau J (2007) Sleep-related epilepsy in the A/J mouse. Sleep. [IF=1.591,
Cited=15, 17326542].
Williams CN, Kocher K, Lander E, ..., Rioux JD (2002) Using a genome-wide scan and meta-analysis to identify a novel IBD
locus and confirm previously identified IBD loci. Inflammatory Bowel Diseases. [IF=1.468, Cited=37, 12454612].
Guckelberger P, Doughty BR, Munson G, ..., Engreitz JM (2024) Cohesin-mediated 3D contacts tune enhancer-promoter
regulation. None. [IF=None, Cited=0, 39026740].
Sankaran VG, Ludwig LS, Sicinska E, ..., Lodish HF (2012) Cyclin D3 coordinates the cell cycle during differentiation to
regulate erythrocyte size and number. Genes and Development. [IF=1.985, Cited=85, 22929040].
Brockman W, Alvarez P, Young S, ..., Jaffe DB (2008) Quality scores and SNP detection in sequencing-by-synthesis
systems. Genome Research. [IF=1.745, Cited=171, 18212088].
Batzoglou S, Pachter L, Mesirov JP, ..., Lander E (2000) Human and mouse gene structure: comparative analysis and
application to exon prediction. Genome Research. [IF=1.745, Cited=178, 10899144].
Berger MF, Levin JZ, Vijayendran K, ..., Garraway LA (2010) Integrative analysis of the melanoma transcriptome. Genome
Research. [IF=1.745, Cited=182, 20179022].
Drier Y, Lawrence MS, Carter SL, ..., Getz G (2012) Somatic rearrangements across cancer reveal classes of samples with
distinct patterns of DNA breakage and rearrangement-induced hypermutability. Genome Research. [IF=1.745, Cited=96, 23124520].
Inoue K, Dewar K, Katsanis N, ..., Birren B (2001) The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals
unique genome architectural features and provides insights into the recent evolution of new genes. Genome Research.
[IF=1.745, Cited=94, 11381029].
Batzoglou S, Jaffe DB, Stanley K, ..., Lander E (2002) ARACHNE: a whole-genome shotgun assembler. Genome Research.
[IF=1.745, Cited=232, 11779843].
Galagan JE, Nusbaum C, Roy A, ..., Birren B (2002) The genome of M. acetivorans reveals extensive metabolic and
physiological diversity. Genome Research. [IF=1.745, Cited=339, 11932238].
Vinson JP, Jaffe DB, O'Neill K, ..., Lander E (2005) Assembly of polymorphic genomes: algorithms and application to
Ciona savignyi. Genome Research. [IF=1.745, Cited=111, 16077012].
MacMurray AJ, Moralejo DH, Kwitek AE, ..., Lernmark A (2002) Lymphopenia in the BB rat model of type 1 diabetes is due
to a mutation in a novel immune-associated nucleotide (Ian)-related gene. Genome Research. [IF=1.745, Cited=162, 12097339].
Schork NJ, Krieger JE, Trolliet MR, ..., Jacob HJ (1995) A biometrical genome search in rats reveals the multigenic
basis of blood pressure variation. Genome Research. [IF=1.745, Cited=75, 9132270].
Margulies EH, Cooper GM, Asimenos G, ..., Sidow A (2007) Analyses of deep mammalian sequence alignments and constraint
predictions for 1% of the human genome. Genome Research. [IF=1.745, Cited=140, 17567995].
Miller W, Rosenbloom K, Hardison RC, ..., Kent WJ (2007) 28-way vertebrate alignment and conservation track in the UCSC
Genome Browser. Genome Research. [IF=1.745, Cited=189, 17984227].
Butler J, MacCallum I, Kleber M, ..., Jaffe DB (2008) ALLPATHS: de novo assembly of whole-genome shotgun microreads.
Genome Research. [IF=1.745, Cited=459, 18340039].
Jaffe DB, Butler J, Gnerre S, ..., Lander E (2003) Whole-genome sequence assembly for mammalian genomes: Arachne 2.
Genome Research. [IF=1.745, Cited=174, 12529310].
Batzoglou S, Berger B, Mesirov J, Lander E (1999) Sequencing a genome by walking with clone-end sequences: a
mathematical analysis. Genome Research. [IF=1.745, Cited=14, 10613838].
Lander E, Botstein D (1986) Mapping complex genetic traits in humans: new methods using a complete RFLP linkage map.
Cold Spring Harbor Symposia on Quantitative Biology. [IF=0.889, Cited=83, 2884068].
Aihara H, Alston-Garnjost n, Avery a, ..., McNeil a (1987) Exclusive production of proton-antiproton pairs in two-photon
collisions. None. [IF=None, Cited=3, 9958125].
Hästbacka J, Superti-Furga A, Wilcox WR, ..., Lander E (1996) Sulfate transport in chondrodysplasia. Annals of the New
York Academy of Sciences. [IF=1.878, Cited=7, 8702119].
Superti-Furga A, Hästbacka J, Rossi A, ..., Gitzelmann R (1996) A family of chondrodysplasias caused by mutations in the
diastrophic dysplasia sulfate transporter gene and associated with impaired sulfation of proteoglycans. Annals of the
New York Academy of Sciences. [IF=1.878, Cited=10, 8702127].
Green P, Lander E (1991) Forensic DNA tests and hardy-weinberg equilibrium. Science. [IF=7.729, Cited=5, 17775346].
Goodman N, Lander E, Oberai-Soltz R (1995) Software availability. Science. [IF=7.729, Cited=1, 7809601].
Ross RK, Coetzee GA, Pearce CL, ..., Daley G (1999) Androgen metabolism and prostate cancer: establishing a model of
genetic susceptibility. European Urology. [IF=6.8, Cited=18, 10325489].
Nomura A, Won HH, Khera AV, ..., Kathiresan S (2017) Protein-Truncating Variants at the Cholesteryl Ester Transfer
Protein Gene and Risk for Coronary Heart Disease. Circulation Research. [IF=3.534, Cited=46, 28506971].
Lehto M, Tuomi T, Mahtani MM, ..., Groop L (1997) Characterization of the MODY3 phenotype. Early-onset diabetes caused
by an insulin secretion defect. Journal of Clinical Investigation. [IF=2.423, Cited=102, 9045858].
Sankaran VG, Ghazvinian R, Do R, ..., Gazda HT (2012) Exome sequencing identifies GATA1 mutations resulting in Diamond-
Blackfan anemia. Journal of Clinical Investigation. [IF=2.423, Cited=224, 22706301].
Moses AM, Chiang DY, Kellis M, ..., Eisen MB (2003) Position specific variation in the rate of evolution in
transcription factor binding sites. None. [IF=None, Cited=99, 12946282].
Cho J, Bass AJ, Lawrence MS, ..., Meyerson M (2014) Colon cancer-derived oncogenic EGFR G724S mutant identified by whole
genome sequence analysis is dependent on asymmetric dimerization and sensitive to cetuximab. Molecular Cancer. [IF=5.74,
Cited=18, 24894453].
Chiang DY, Moses AM, Kellis M, ..., Eisen MB (2003) Phylogenetically and spatially conserved word pairs associated with
gene-expression changes in yeasts. None. [IF=None, Cited=34, 12844359].
Neafsey DE, Schaffner SF, Volkman SK, ..., Wirth DF (2008) Genome-wide SNP genotyping highlights the role of natural
selection in Plasmodium falciparum population divergence. None. [IF=None, Cited=82, 19077304].
Gnerre S, Lander E, Lindblad-Toh K, Jaffe DB (2009) Assisted assembly: how to improve a de novo genome assembly by using
related species. None. [IF=None, Cited=31, 19712469].
Karlsson EK, Sigurdsson S, Ivansson E, ..., Lindblad-Toh K (2013) Genome-wide analyses implicate 33 loci in heritable
dog osteosarcoma, including regulatory variants near CDKN2A/B. None. [IF=None, Cited=91, 24330828].
Krewson TD, Supelak PJ, Hill AE, ..., Palmert MR (2004) Chromosomes 6 and 13 harbor genes that regulate pubertal timing
in mouse chromosome substitution strains. Endocrinology. [IF=1.146, Cited=35, 15284200].
Sabeti PC, Walsh E, Schaffner SF, ..., Lander E (2005) The case for selection at CCR5-Delta32. PLoS Biology. [IF=2.285,
Cited=112, 16248677].
Lowe CJ, Terasaki M, Wu M, ..., Gerhart J (2006) Dorsoventral patterning in hemichordates: insights into early chordate
evolution. PLoS Biology. [IF=2.285, Cited=181, 16933975].
Markljung E, Jiang L, Jaffe JD, ..., Andersson L (2009) ZBED6, a novel transcription factor derived from a domesticated
DNA transposon regulates IGF2 expression and muscle growth. PLoS Biology. [IF=2.285, Cited=112, 20016685].
Lowe CJ, Terasaki M, Wu M, ..., Gerhart J (2015) Correction: Dorsoventral Patterning in Hemichordates: Insights into
Early Chordate Evolution. PLoS Biology. [IF=2.285, Cited=0, 26714185].
Pedersen JS, Bejerano G, Siepel A, ..., Haussler D (2006) Identification and classification of conserved RNA secondary
structures in the human genome. PLoS Computational Biology. [IF=1.278, Cited=309, 16628248].
Ku M, Koche RP, Rheinbay E, ..., Bernstein BE (2008) Genomewide analysis of PRC1 and PRC2 occupancy identifies two
classes of bivalent domains. PLoS Genetics. [IF=1.236, Cited=701, 18974828].
Van Tyne D, Park DJ, Schaffner SF, ..., Sabeti PC (2011) Identification and functional validation of the novel
antimalarial resistance locus PF10_0355 in Plasmodium falciparum. PLoS Genetics. [IF=1.236, Cited=67, 21533027].
Kim SY, Dunn IF, Firestein R, ..., Hahn WC (2010) CK1epsilon is required for breast cancers dependent on beta-catenin
activity. PLoS ONE. [IF=1.253, Cited=59, 20126544].
Hill AE, Lander E, Nadeau JH (2006) Chromosome substitution strains: a new way to study genetically complex traits.
None. [IF=None, Cited=15, 17071995].
Barclay J, Balaguero N, Mione M, ..., Rees M (2001) Ducky mouse phenotype of epilepsy and ataxia is associated with
mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells. Journal of
Neuroscience. [IF=1.471, Cited=196, 11487633].
Lander E, Nybo K (2014) Scientists. Excitement for a new era. BioTechniques. [IF=0.626, Cited=0, 24779058].
Freeman RM, Wu M, Cordonnier-Pratt MM, ..., Kirschner M (2008) cDNA sequences for transcription factors and signaling
proteins of the hemichordate Saccoglossus kowalevskii: efficacy of the expressed sequence tag (EST) approach for
evolutionary and developmental studies of a new organism. Biological Bulletin. [IF=0.58, Cited=29, 18574105].
van Berkum NL, Lieberman-Aiden E, Williams L, ..., Lander E (2010) Hi-C: a method to study the three-dimensional
architecture of genomes. Journal of Visualized Experiments. [IF=0.398, Cited=192, 20461051].
Lander E, Jiang G, Tao K (2009) Taking aim at aggressive cancer cells. Cancer Biology and Therapy. [IF=0.866, Cited=0, 19830887].
Lander E (2000) Genomics: launching a revolution in medicine. Journal of Law, Medicine and Ethics. [IF=1.076, Cited=0, 11244841].
Dracopoli NC, Stanger BZ, Ito CY, ..., Housman DE (1988) A genetic linkage map of 27 loci from PND to FY on the short
arm of human chromosome I. American Journal of Human Genetics. [IF=2.607, Cited=0, 2902785].
Lander E, Botstein D (1986) Consanguinity and heterogeneity: cystic fibrosis need not be homogeneous in Italy. American
Journal of Human Genetics. [IF=2.607, Cited=0, 3752091].
Lander E, Krohn E, Kramer P (1973) [Treatment of cardiac insufficiency using alpha-acetyldigitoxin]. None. [IF=None,
Cited=0, 4765769].
Lander E (1968) [Effect of thio-TEPA on mice ovaries]. Zhurnal Obshchei Biologii. [IF=0.299, Cited=0, 4988679].
Lander E (1970) We went back to O.R. rotation, and we're glad. None. [IF=None, Cited=0, 5202663].
Jaursch U, Lander E, Schmidt R, ..., Simon KH (1969) [Simultaneous increase of drug effect on the heart and tolerance of
digoxin by combination of electrolytes, flavones and purines]. None. [IF=None, Cited=0, 5816435].
Kruglyak L, Lander E (1995) Complete multipoint sib-pair analysis of qualitative and quantitative traits. American
Journal of Human Genetics. [IF=2.607, Cited=0, 7668271].
Kruglyak L, Lander E (1995) High-resolution genetic mapping of complex traits. American Journal of Human Genetics.
[IF=2.607, Cited=0, 7726179].
Kruglyak L, Daly MJ, Lander E (1995) Rapid multipoint linkage analysis of recessive traits in nuclear families,
including homozygosity mapping. American Journal of Human Genetics. [IF=2.607, Cited=0, 7847388].
Hegi ME, Devereux TR, Dietrich WF, ..., Wiseman RW (1994) Allelotype analysis of mouse lung carcinomas reveals frequent
allelic losses on chromosome 4 and an association between allelic imbalances on chromosome 6 and K-ras activation.
Cancer Research. [IF=1.624, Cited=0, 7954475].
Hsu LC, Kennan WS, Shepel LA, ..., Gould MN (1994) Genetic identification of Mcs-1, a rat mammary carcinoma suppressor
gene. Cancer Research. [IF=1.624, Cited=0, 8168109].
Parangi S, Dietrich W, Christofori G, ..., Hanahan D (1995) Tumor suppressor loci on mouse chromosomes 9 and 16 are lost
at distinct stages of tumorigenesis in a transgenic model of islet cell carcinoma. Cancer Research. [IF=1.624, Cited=0, 8521395].
Hästbacka J, Superti-Furga A, Wilcox WR, ..., Lander E (1996) Atelosteogenesis type II is caused by mutations in the
diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three
chondrodysplasias. American Journal of Human Genetics. [IF=2.607, Cited=0, 8571951].
Kruglyak L, Lander E (1996) Limits on fine mapping of complex traits. American Journal of Human Genetics. [IF=2.607,
Cited=0, 8651271].
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander E (1996) Parametric and nonparametric linkage analysis: a unified multipoint
approach. American Journal of Human Genetics. [IF=2.607, Cited=0, 8651312].
Gschwend M, Levran O, Kruglyak L, ..., Botstein D (1996) A locus for Fanconi anemia on 16q determined by homozygosity
mapping. American Journal of Human Genetics. [IF=2.607, Cited=0, 8755924].
Schuler GD, Boguski MS, Stewart EA, ..., Hudson TJ (1996) A gene map of the human genome. Science. [IF=7.729, Cited=0, 8849440].
Schuler GD, Boguski MS, Hudson TJ, ..., Hudson JR (1996) Genome maps 7. The human transcript map. Wall chart. Science.
[IF=7.729, Cited=0, 8928009].

Lander, Eric

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