Walsh, Christopher A

Publication with MATCHING institution:

Khoshkhoo S, Wang Y, Chahine Y, ..., Kahle KT (2023) Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase
Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy. JAMA Neurology. [IF=5.982, Cited=11, 37126322].
Akula SK, Chen AY, Neil JE, ..., Walsh CA (2023) Exome Sequencing and the Identification of New Genes and Shared
Mechanisms in Polymicrogyria. JAMA Neurology. [IF=5.982, Cited=3, 37486637].
Thomas AX, Link N, Robak LA, ..., Mirzaa GM (2022) ANKLE2-related microcephaly: A variable microcephaly syndrome
resembling Zika infection. Annals of Clinical and Translational Neurology. [IF=1.383, Cited=2, 35871307].
Imitola J, Khurana DS, Teplyuk NM, ..., Carvalho KS (2015) A novel 2q37 microdeletion containing human neural
progenitors genes including STK25 results in severe developmental delay, epilepsy, and microcephaly. American Journal of
Medical Genetics, Part A. [IF=1.165, Cited=5, 26238961].
Al-Maawali A, Barry BJ, Rajab A, ..., Stoler JM (2015) Novel loss-of-function variants in DIAPH1 associated with
syndromic microcephaly, blindness, and early onset seizures. American Journal of Medical Genetics, Part A. [IF=1.165,
Cited=19, 26463574].
Chen MH, Choudhury S, Hirata M, ..., Walsh CA (2018) Thoracic aortic aneurysm in patients with loss of function Filamin
A mutations: Clinical characterization, genetics, and recommendations. American Journal of Medical Genetics, Part A.
[IF=1.165, Cited=21, 29334594].
Amrom D, Poduri A, Goldman JS, ..., Dobyns WB (2019) Duplication 2p16 is associated with perisylvian polymicrogyria.
American Journal of Medical Genetics, Part A. [IF=1.165, Cited=1, 31660690].
Dias C, Pfundt R, Kleefstra T, ..., Rodan LH (2021) De novo variants in TCF7L2 are associated with a syndromic
neurodevelopmental disorder. American Journal of Medical Genetics, Part A. [IF=1.165, Cited=6, 34003604].
Khalil R, Kenny C, Hill RS, ..., Chahrour MH (2018) PSMD12 haploinsufficiency in a neurodevelopmental disorder with
autistic features. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. [IF=0.858, Cited=15, 30421579].
Poduri A, Heinzen EL, Chitsazzadeh V, ..., Walsh CA (2013) SLC25A22 is a novel gene for migrating partial seizures in
infancy. Annals of Neurology. [IF=2.769, Cited=45, 24596948].
Poduri A, Salih M, Walsh CA (2014) Reply: To PMID 24243345. Annals of Neurology. [IF=2.769, Cited=0, 24242934].
D'Gama AM, Geng Y, Couto JA, ..., Poduri A (2015) Mammalian target of rapamycin pathway mutations cause
hemimegalencephaly and focal cortical dysplasia. Annals of Neurology. [IF=2.769, Cited=142, 25599672].
Shao DD, Achkar CM, Lai A, ..., Walsh CA (2020) Polymicrogyria is Associated With Pathogenic Variants in PTEN. Annals of
Neurology. [IF=2.769, Cited=6, 32959437].
Chaste P, Sanders SJ, Mohan KN, ..., Kim SJ (2014) Modest impact on risk for autism spectrum disorder of rare copy
number variants at 15q11.2, specifically breakpoints 1 to 2. Autism Research. [IF=1.588, Cited=38, 24821083].
Marsh APL, Edwards TJ, Galea C, ..., Lockhart PJ (2017) DCC mutation update: Congenital mirror movements, isolated
agenesis of the corpus callosum, and developmental split brain syndrome. Human Mutation. [IF=1.507, Cited=19, 29068161].
Wang P, Roider E, Coulter ME, ..., Giese RW (2021) DNA Adductomics by mass tag prelabeling. Rapid Communications in Mass
Spectrometry. [IF=0.653, Cited=1, 33821547].
McDonough GA, Cheng Y, Morillo KS, ..., Miller MB (2024) Neuropathologically directed profiling of PRNP somatic and
germline variants in sporadic human prion disease. Acta Neuropathologica. [IF=2.769, Cited=0, 39048735].
Andersen RE, Alkuraya IF, Ajeesh A, ..., Morton CC (2024) Chromosomal structural rearrangements implicate long non-
coding RNAs in rare germline disorders. Human Genetics. [IF=1.653, Cited=0, 39060644].
Zhang X, Ling J, Barcia G, ..., Nabbout R (2014) Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause
progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures. American Journal of Human Genetics.
[IF=2.607, Cited=78, 24656866].
Dias CM, Punetha J, Zheng C, ..., Maroofian R (2019) Homozygous Missense Variants in NTNG2, Encoding a Presynaptic
Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. American Journal of Human Genetics.
[IF=2.607, Cited=22, 31668703].
Maia N, Potelle S, Yildirim H, ..., Foulquier F (2022) Impaired catabolism of free oligosaccharides due to MAN2C1
variants causes a neurodevelopmental disorder. American Journal of Human Genetics. [IF=2.607, Cited=3, 35045343].
Tepe B, Macke EL, Niceta M, ..., Bellen HJ (2023) Bi-allelic variants in INTS11 are associated with a complex
neurological disorder. American Journal of Human Genetics. [IF=2.607, Cited=7, 37054711].
Lemire G, Sanchis-Juan A, Russell K, ..., O'Donnell-Luria A (2024) Exome copy number variant detection, analysis, and
classification in a large cohort of families with undiagnosed rare genetic disease. American Journal of Human Genetics.
[IF=2.607, Cited=0, 38565148].
Dias C, Mo A, Cai C, ..., Walsh CA (2024) Cell-type-specific effects of autism-associated 15q duplication syndrome in
the human brain. American Journal of Human Genetics. [IF=2.607, Cited=0, 39079538].
Chaste P, Klei L, Sanders SJ, ..., Devlin B (2014) A genome-wide association study of autism using the Simons Simplex
Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? Biological Psychiatry.
[IF=2.412, Cited=82, 25534755].
Zhang X, Chen MH, Wu X, ..., Walsh CA (2016) Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing
Cerebral Cortex. Cell. [IF=8.479, Cited=169, 27565344].
Doan RN, Bae BI, Cubelos B, ..., Walsh CA (2016) Mutations in Human Accelerated Regions Disrupt Cognition and Social
Behavior. Cell. [IF=8.479, Cited=145, 27667684].
Ganz J, Luquette LJ, Bizzotto S, ..., Walsh CA (2024) Contrasting somatic mutation patterns in aging human neurons and
oligodendrocytes. Cell. [IF=8.479, Cited=0, 38503282].
Manzini MC, Xiong L, Shaheen R, ..., Walsh CA (2014) CC2D1A regulates human intellectual and social function as well as
NF-κB signaling homeostasis. Cell Reports. [IF=1.738, Cited=43, 25066123].
Cai X, Evrony GD, Lehmann HS, ..., Walsh CA (2014) Single-cell, genome-wide sequencing identifies clonal somatic copy-
number variation in the human brain. Cell Reports. [IF=1.738, Cited=160, 25159146].
D'Gama AM, Woodworth MB, Hossain AA, ..., Walsh CA (2017) Somatic Mutations Activating the mTOR Pathway in Dorsal
Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias. Cell Reports. [IF=1.738, Cited=147, 29281825].
Coulter ME, Dorobantu CM, Lodewijk GA, ..., Walsh CA (2018) The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic
Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Cell Reports. [IF=1.738, Cited=48, 30044992].
Johnson MB, Walsh CA (2016) Cerebral cortical neuron diversity and development at single-cell resolution. Current
Opinion in Neurobiology. [IF=1.341, Cited=31, 27888678].
Bae BI, Jayaraman D, Walsh CA (2015) Genetic changes shaping the human brain. Developmental Cell. [IF=2.256, Cited=72, 25710529].
Bizzotto S, Walsh CA (2018) Making a Notch in the Evolution of the Human Cortex. Developmental Cell. [IF=2.256,
Cited=4, 29870717].
Qian X, DeGennaro EM, Talukdar M, ..., Walsh CA (2022) Loss of non-motor kinesin KIF26A causes congenital brain
malformations via dysregulated neuronal migration and axonal growth as well as apoptosis. Developmental Cell. [IF=2.256,
Cited=5, 36228617].
Akula SK, Exposito-Alonso D, Walsh CA (2023) Shaping the brain: The emergence of cortical structure and folding.
Developmental Cell. [IF=2.256, Cited=2, 38113850].
Lakhani S, Doan R, Almureikhi M, ..., Ben-Omran T (2017) Identification of a novel CNTNAP1 mutation causing
arthrogryposis multiplex congenita with cerebral and cerebellar atrophy. European Journal of Medical Genetics.
[IF=0.889, Cited=12, 28254648].
Qi C, Feng I, Costa AR, ..., Zhang X (2021) Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis,
and ventriculomegaly in humans. Genetics in Medicine. [IF=2.761, Cited=4, 34906466].
Lai A, Soucy A, El Achkar CM, ..., Poduri A (2022) The ClinGen Brain Malformation Variant Curation Expert Panel: Rules
for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2. Genetics in Medicine. [IF=2.761, Cited=2, 35997716].
Hu WF, Pomp O, Ben-Omran T, ..., Walsh CA (2014) Katanin p80 regulates human cortical development by limiting centriole
and cilia number. Neuron. [IF=3.346, Cited=68, 25521379].
Evrony GD, Lee E, Mehta BK, ..., Walsh CA (2015) Cell lineage analysis in human brain using endogenous retroelements.
Neuron. [IF=3.346, Cited=146, 25569347].
Sanders SJ, He X, Willsey AJ, ..., State MW (2015) Insights into Autism Spectrum Disorder Genomic Architecture and
Biology from 71 Risk Loci. Neuron. [IF=3.346, Cited=739, 26402605].
D'Gama AM, Pochareddy S, Li M, ..., Walsh CA (2015) Targeted DNA Sequencing from Autism Spectrum Disorder Brains
Implicates Multiple Genetic Mechanisms. Neuron. [IF=3.346, Cited=90, 26637798].
Jayaraman D, Kodani A, Gonzalez DM, ..., Walsh CA (2016) Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole
Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate. Neuron. [IF=3.346, Cited=81, 27974163].
Smith RS, Kenny CJ, Ganesh V, ..., Lehtinen MK (2018) Sodium Channel SCN3A (Na_V1.3) Regulation of Human
Cerebral Cortical Folding and Oral Motor Development. Neuron. [IF=3.346, Cited=64, 30146301].
Kodani A, Kenny C, Lai A, ..., Walsh CA (2020) Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L
Identifies Maternal Centriole-Dependent Activation of CDK5. Neuron. [IF=3.346, Cited=7, 32097629].
Girskis KM, Stergachis AB, DeGennaro EM, ..., Walsh CA (2021) Rewiring of human neurodevelopmental gene regulatory
programs by human accelerated regions. Neuron. [IF=3.346, Cited=48, 34478631].
Duy PQ, Rakic P, Alper SL, ..., Kahle KT (2022) Brain ventricles as windows into brain development and disease. Neuron.
[IF=3.346, Cited=22, 34990576].
McClellan JM, Zoghbi AW, Buxbaum JD, ..., King MC (2023) An evolutionary perspective on complex neuropsychiatric
disease. Neuron. [IF=3.346, Cited=0, 38016473].
Jamuar SS, Walsh CA (2015) Genomic variants and variations in malformations of cortical development. Pediatric Clinics
of North America. [IF=1.49, Cited=22, 26022163].
Rodin RE, Walsh CA (2018) Somatic Mutation in Pediatric Neurological Diseases. Pediatric Neurology. [IF=1.152,
Cited=12, 30249355].
Smith RS, Walsh CA (2020) Ion Channel Functions in Early Brain Development. None. [IF=None, Cited=44, 31959360].
Shin T, Song JHT, Kosicki M, ..., Walsh CA (2024) Rare variation in non-coding regions with evolutionary signatures
contributes to autism spectrum disorder risk. Cell Genomics. [IF=2.669, Cited=0, 39019033].
Walsh CA (2001) Neuroscience in the post-genome era: an overview. Trends in Neurosciences. [IF=3.343, Cited=2, 11410254].
Walsh CA (1996) Neural development: identical twins separated at birth? Current Biology. [IF=1.81, Cited=2, 8805214].
Wang P, Shah GL, Landau H, ..., Giese RW (2020) Jettison-MS of Nucleic Acid Species. Journal of the American Society for
Mass Spectrometry. [IF=0.827, Cited=1, 32551641].
Zappaterra MD, Lisgo SN, Lindsay S, ..., Ballif BA (2007) A comparative proteomic analysis of human and rat embryonic
cerebrospinal fluid. Journal of Proteome Research. [IF=0.952, Cited=82, 17696520].
Walsh CA (2013) Peter Huttenlocher (1931-2013). Nature. [IF=11.591, Cited=2, 24108045].
Ataman B, Boulting GL, Harmin DA, ..., Greenberg ME (2016) Evolution of Osteocrin as an activity-regulated factor in the
primate brain. Nature. [IF=11.591, Cited=72, 27830782].
Jamuar SS, Schmitz-Abe K, D'Gama AM, ..., Yu TW (2017) Biallelic mutations in human DCC cause developmental split-brain
syndrome. Nature Genetics. [IF=6.89, Cited=40, 28250456].
Johnson MB, Wang PP, Atabay KD, ..., Walsh CA (2015) Single-cell analysis reveals transcriptional heterogeneity of
neural progenitors in human cortex. Nature Neuroscience. [IF=4.893, Cited=161, 25734491].
Lim ET, Uddin M, De Rubeis S, ..., Walsh CA (2017) Rates, distribution and implications of postzygotic mosaic mutations
in autism spectrum disorder. Nature Neuroscience. [IF=4.893, Cited=151, 28714951].
Woodworth MB, Girskis KM, Walsh CA (2017) Building a lineage from single cells: genetic techniques for cell lineage
tracking. Nature Reviews Genetics. [IF=8.261, Cited=114, 28111472].
Brownstein CA, Smith RS, Rodan LH, ..., Gonzalez-Heydrich J (2021) RCL1 copy number variants are associated with a range
of neuropsychiatric phenotypes. Molecular Psychiatry. [IF=2.603, Cited=6, 33597717].
Haag N, Tan EC, Begemann M, ..., Knopp C (2021) Biallelic loss-of-function variants in WDR11 are associated with
microcephaly and intellectual disability. European Journal of Human Genetics. [IF=1.676, Cited=5, 34413497].
Coulter ME, Musaev D, DeGennaro EM, ..., Walsh CA (2020) Regulation of human cerebral cortical development by EXOC7 and
EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival. Genetics in
Medicine. [IF=2.761, Cited=13, 32103185].
Sundberg M, Pinson H, Smith RS, ..., Sahin M (2021) 16p11.2 deletion is associated with hyperactivation of human iPSC-
derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro. Nature Communications. [IF=3.268,
Cited=24, 34006844].
Lim ET, Chan Y, Dawes P, ..., Church GM (2022) Orgo-Seq integrates single-cell and bulk transcriptomic data to identify
cell type specific-driver genes associated with autism spectrum disorder. Nature Communications. [IF=3.268, Cited=11, 35688811].
Kim J, Huang AY, Johnson SL, ..., Lee EA (2022) Prevalence and mechanisms of somatic deletions in single human neurons
during normal aging and in DNA repair disorders. Nature Communications. [IF=3.268, Cited=4, 36207339].
Bizzotto S, Walsh CA (2022) Genetic mosaicism in the human brain: from lineage tracing to neuropsychiatric disorders.
Nature Reviews Neuroscience. [IF=4.332, Cited=20, 35322263].
Johnson MB, Sun X, Kodani A, ..., Bae BI (2018) Aspm knockout ferret reveals an evolutionary mechanism governing
cerebral cortical size. Nature. [IF=11.591, Cited=82, 29643508].
Kim J, Zhao B, Huang AY, ..., Lee EA (2020) APP gene copy number changes reflect exogenous contamination. Nature.
[IF=11.591, Cited=10, 32814883].
Miller MB, Huang AY, Kim J, ..., Walsh CA (2022) Somatic genomic changes in single Alzheimer's disease neurons. Nature.
[IF=11.591, Cited=57, 35444284].
Dou Y, Kwon M, Rodin RE, ..., Park PJ (2020) Accurate detection of mosaic variants in sequencing data without matched
controls. Nature Biotechnology. [IF=8.861, Cited=35, 31907404].
Bohrson CL, Barton AR, Lodato MA, ..., Park PJ (2019) Linked-read analysis identifies mutations in single-cell DNA-
sequencing data. Nature Genetics. [IF=6.89, Cited=52, 30886424].
Doan RN, Lim ET, De Rubeis S, ..., Yu TW (2019) Recessive gene disruptions in autism spectrum disorder. Nature Genetics.
[IF=6.89, Cited=75, 31209396].
D'Gama AM, Walsh CA (2018) Somatic mosaicism and neurodevelopmental disease. Nature Neuroscience. [IF=4.893, Cited=116, 30349109].
Rodin RE, Dou Y, Kwon M, ..., Walsh CA (2021) The landscape of somatic mutation in cerebral cortex of autistic and
neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nature Neuroscience. [IF=4.893, Cited=49, 33432195].
Lim ET, Uddin M, De Rubeis S, ..., Walsh CA (2020) Publisher Correction: Rates, distribution and implications of
postzygotic mosaic mutations in autism spectrum disorder. Nature Neuroscience. [IF=4.893, Cited=0, 32665711].
Rodin RE, Dou Y, Kwon M, ..., Walsh CA (2021) Author Correction: The landscape of somatic mutation in cerebral cortex of
autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nature Neuroscience. [IF=4.893,
Cited=4, 33753946].
Duy PQ, Weise SC, Marini C, ..., Kahle KT (2022) Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-
based genetic subtype of congenital hydrocephalus. Nature Neuroscience. [IF=4.893, Cited=31, 35379995].
Rodin RE, Dou Y, Kwon M, ..., Walsh CA (2023) Author Correction: The landscape of somatic mutation in cerebral cortex of
autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nature Neuroscience. [IF=4.893,
Cited=0, 37644260].
Garrison MA, Jang Y, Bae T, ..., Abyzov A (2023) Genomic data resources of the Brain Somatic Mosaicism Network for
neuropsychiatric diseases. Scientific data. [IF=2.887, Cited=0, 37985666].
Schmitz-Abe K, Sanchez-Schmitz G, Doan RN, ..., Markianos K (2020) Homozygous deletions implicate non-coding epigenetic
marks in Autism spectrum disorder. Scientific Reports. [IF=1.312, Cited=9, 32820185].
Murayama AY, Kuwako KI, Okahara J, ..., Okano H (2020) The polymicrogyria-associated GPR56 promoter preferentially
drives gene expression in developing GABAergic neurons in common marmosets. Scientific Reports. [IF=1.312, Cited=5, 33299078].
Choudhury S, Huang AY, Kim J, ..., Walsh CA (2022) Somatic mutations in single human cardiomyocytes reveal age-
associated DNA damage and widespread oxidative genotoxicity. Nature Aging. [IF=2.12, Cited=14, 36051457].
Imitola J, Raddassi K, Park KI, ..., Khoury SJ (2004) Directed migration of neural stem cells to sites of CNS injury by
the stromal cell-derived factor 1alpha/CXC chemokine receptor 4 pathway. Proceedings of the National Academy of Sciences
of the United States of America. [IF=2.765, Cited=709, 15608062].
Soukoulis V, Reddy S, Pooley RD, ..., Bader DM (2005) Cytoplasmic LEK1 is a regulator of microtubule function through
its interaction with the LIS1 pathway. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=24, 15939891].
Huang AY, Li P, Rodin RE, ..., Walsh CA (2020) Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals
cell type-specific lineage patterns in human brain. Proceedings of the National Academy of Sciences of the United States
of America. [IF=2.765, Cited=21, 32522880].
Smith RS, Florio M, Akula SK, ..., Walsh CA (2021) Early role for a Na⁺,K⁺-ATPase (ATP1A3)
in brain development. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765,
Cited=18, 34161264].
Akula SK, Marciano JH, Lim Y, ..., Walsh CA (2023) TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog
signaling, and ciliary structure in the developing central nervous system. Proceedings of the National Academy of
Sciences of the United States of America. [IF=2.765, Cited=9, 36669111].
Dias CM, Issac B, Sun L, ..., Walsh CA (2023) Glial dysregulation in the human brain in fragile X-associated
tremor/ataxia syndrome. Proceedings of the National Academy of Sciences of the United States of America. [IF=2.765,
Cited=4, 37252957].
Duy PQ, Rakic P, Alper SL, ..., Kahle KT (2023) A neural stem cell paradigm of pediatric hydrocephalus. Cerebral Cortex.
[IF=1.159, Cited=8, 36097331].
Oaks AW, Zamarbide M, Tambunan DE, ..., Manzini MC (2017) Cc2d1a Loss of Function Disrupts Functional and Morphological
Development in Forebrain Neurons Leading to Cognitive and Social Deficits. Cerebral Cortex. [IF=1.159, Cited=23, 26826102].
Reiff RE, Ali BR, Baron B, ..., Mochida GH (2014) METTL23, a transcriptional partner of GABPA, is essential for human
cognition. Human Molecular Genetics. [IF=1.158, Cited=27, 24501276].
Lodato MA, Walsh CA (2019) Genome aging: somatic mutation in the brain links age-related decline with disease and
nominates pathogenic mechanisms. Human Molecular Genetics. [IF=1.158, Cited=28, 31578549].
Lodato MA, Walsh CA (2020) Corrigendum: Genome aging: somatic mutation in the brain links age-related decline with
disease and nominates pathogenic mechanisms. Human Molecular Genetics. [IF=1.158, Cited=0, 31778186].
Sherman MA, Barton AR, Lodato MA, ..., Park PJ (2018) PaSD-qc: quality control for single cell whole-genome sequencing
data using power spectral density estimation. Nucleic Acids Research. [IF=4.663, Cited=8, 29186545].
Ganz J, Luquette LJ, Bizzotto S, ..., Walsh CA (2023) Contrasting patterns of somatic mutations in neurons and glia
reveal differential predisposition to disease in the aging human brain. None. [IF=None, Cited=0, 36711756].
Shin T, Song JHT, Kosicki M, ..., Walsh CA (2023) Rare variation in noncoding regions with evolutionary signatures
contributes to autism spectrum disorder risk. None. [IF=None, Cited=0, 37790480].
Lemire G, Sanchis-Juan A, Russell K, ..., O'Donnell-Luria A (2023) Exome copy number variant detection, analysis and
classification in a large cohort of families with undiagnosed rare genetic disease. None. [IF=None, Cited=0, 37873196].
Kim SN, Viswanadham VV, Doan RN, ..., Walsh CA (2023) Cell lineage analysis with somatic mutations reveals late
divergence of neuronal cell types and cortical areas in human cerebral cortex. None. [IF=None, Cited=0, 37986891].
Zhou Z, Kim J, Huang AY, ..., Walsh CA (2023) Somatic Mosaicism in Amyotrophic Lateral Sclerosis and Frontotemporal
Dementia Reveals Widespread Degeneration from Focal Mutations. None. [IF=None, Cited=0, 38077003].
Huang AY, Zhou Z, Talukdar M, ..., Walsh CA (2024) Somatic cancer driver mutations are enriched and associated with
inflammatory states in Alzheimer's disease microglia. None. [IF=None, Cited=0, 38260600].
Dias C, Mo A, Cai C, ..., Walsh CA (2024) Cell-type-specific effects of autism-associated chromosome 15q11.2-13.1
duplications in human brain. None. [IF=None, Cited=0, 38826276].
Qian X, Coleman K, Jiang S, ..., Walsh CA (2024) Spatial Single-cell Analysis Decodes Cortical Layer and Area
Specification. None. [IF=None, Cited=0, 38915567].
Andersen RE, Alkuraya IF, Ajeesh A, ..., Morton CC (2024) Rare germline disorders implicate long non-coding RNAs
disrupted by chromosomal structural rearrangements. None. [IF=None, Cited=0, 38946951].
McDonough GA, Cheng Y, Morillo K, ..., Miller MB (2024) Neuropathologically-directed profiling of PRNP somatic
and germline variants in sporadic human prion disease. None. [IF=None, Cited=0, 38979287].
Murn J, Zarnack K, Yang YJ, ..., Shi Y (2015) Control of a neuronal morphology program by an RNA-binding zinc finger
protein, Unkempt. Genes and Development. [IF=1.985, Cited=23, 25737280].
Evrony GD, Cordero DR, Shen J, ..., Walsh CA (2017) Integrated genome and transcriptome sequencing identifies a
noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome.
Genome Research. [IF=1.745, Cited=30, 28630177].
Khoshkhoo S, Lal D, Walsh CA (2021) Application of single cell genomics to focal epilepsies: A call to action. Brain
Pathology. [IF=1.576, Cited=4, 34196990].
Stouffs K, Stergachis AB, Vanderhasselt T, ..., Jansen AC (2018) Expanding the clinical spectrum of biallelic ZNF335
variants. Clinical Genetics. [IF=1.39, Cited=6, 29652087].
Khan A, Alaamery M, Massadeh S, ..., Eyaid W (2020) PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in
microcephaly. Clinical Genetics. [IF=1.39, Cited=8, 32286682].
Walsh CA (2018) Rainer W. Guillery and the genetic analysis of brain development. European Journal of Neuroscience.
[IF=0.891, Cited=1, 30152010].
Blümcke I, Coras R, Busch RM, ..., Najm I (2021) Toward a better definition of focal cortical dysplasia: An iterative
histopathological and genetic agreement trial. Epilepsia. [IF=1.893, Cited=33, 33949696].
Najm I, Lal D, Alonso Vanegas M, ..., Blümcke I (2022) The ILAE consensus classification of focal cortical dysplasia: An
update proposed by an ad hoc task force of the ILAE diagnostic methods commission. Epilepsia. [IF=1.893, Cited=54, 35706131].
Piao X, Hill RS, Bodell A, ..., Walsh CA (2004) G protein-coupled receptor-dependent development of human frontal
cortex. Science. [IF=7.729, Cited=317, 15044805].
Sun T, Patoine C, Abu-Khalil A, ..., Walsh CA (2005) Early asymmetry of gene transcription in embryonic human left and
right cerebral cortex. Science. [IF=7.729, Cited=216, 15894532].
Morrow EM, Yoo SY, Flavell SW, ..., Walsh CA (2008) Identifying autism loci and genes by tracing recent shared ancestry.
Science. [IF=7.729, Cited=460, 18621663].
Poduri A, Evrony GD, Cai X, Walsh CA (2013) Somatic mutation, genomic variation, and neurological disease. Science.
[IF=7.729, Cited=332, 23828942].
Bae BI, Tietjen I, Atabay KD, ..., Walsh CA (2014) Evolutionarily dynamic alternative splicing of GPR56 regulates
regional cerebral cortical patterning. Science. [IF=7.729, Cited=120, 24531968].
Bae Bi, Walsh CA (2013) Neuroscience. What are mini-brains? Science. [IF=7.729, Cited=6, 24115427].
Lodato MA, Woodworth MB, Lee S, ..., Walsh CA (2015) Somatic mutation in single human neurons tracks developmental and
transcriptional history. Science. [IF=7.729, Cited=312, 26430121].
McConnell MJ, Moran JV, Abyzov A, ..., Vaccarino FM (2017) Intersection of diverse neuronal genomes and neuropsychiatric
disease: The Brain Somatic Mosaicism Network. Science. [IF=7.729, Cited=125, 28450582].
Lodato MA, Rodin RE, Bohrson CL, ..., Walsh CA (2017) Aging and neurodegeneration are associated with increased
mutations in single human neurons. Science. [IF=7.729, Cited=280, 29217584].
Bizzotto S, Dou Y, Ganz J, ..., Walsh CA (2021) Landmarks of human embryonic development inscribed in somatic mutations.
Science. [IF=7.729, Cited=37, 33737485].
Bae T, Fasching L, Wang Y, ..., Abyzov A (2022) Analysis of somatic mutations in 131 human brains reveals aging-
associated hypermutability. Science. [IF=7.729, Cited=17, 35901164].
Jorstad NL, Song JHT, Exposito-Alonso D, ..., Bakken TE (2023) Comparative transcriptomics reveals human-specific
cortical features. Science. [IF=7.729, Cited=13, 37824638].
Lehtinen MK, Walsh CA (2011) Neurogenesis at the brain-cerebrospinal fluid interface. Annual Review of Cell and
Developmental Biology. [IF=2.757, Cited=120, 21801012].
Jayaraman D, Bae BI, Walsh CA (2018) The Genetics of Primary Microcephaly. Annual Review of Genomics and Human Genetics.
[IF=2.394, Cited=131, 29799801].
Hu WF, Chahrour MH, Walsh CA (2014) The diverse genetic landscape of neurodevelopmental disorders. Annual Review of
Genomics and Human Genetics. [IF=2.394, Cited=99, 25184530].
Dias CM, Walsh CA (2020) Recent Advances in Understanding the Genetic Architecture of Autism. Annual Review of Genomics
and Human Genetics. [IF=2.394, Cited=24, 32396753].
Miller MB, Reed HC, Walsh CA (2021) Brain Somatic Mutation in Aging and Alzheimer's Disease. Annual Review of Genomics
and Human Genetics. [IF=2.394, Cited=22, 33979534].
Doan RN, Shin T, Walsh CA (2018) Evolutionary Changes in Transcriptional Regulation: Insights into Human Behavior and
Neurological Conditions. Annual Review of Neuroscience. [IF=3.679, Cited=13, 29986162].
Ross ME, Walsh CA (2001) Human brain malformations and their lessons for neuronal migration. Annual Review of
Neuroscience. [IF=3.679, Cited=148, 11520927].
Ganz J, Maury EA, Becerra B, ..., Walsh CA (2021) Rates and Patterns of Clonal Oncogenic Mutations in the Normal Human
Brain. Cancer Discovery. [IF=3.608, Cited=16, 34389641].
Chen MH, Deng ES, Yamada JM, ..., Doan RN (2024) Contributions of Germline and Somatic Mosaic Genetics to Thoracic
Aortic Aneurysms in Nonsyndromic Individuals. Journal of the American Heart Association. [IF=1.737, Cited=0, 38958128].
Dies KA, Bodell A, Hisama FM, ..., Walsh CA (2012) Schizencephaly: association with young maternal age, alcohol use, and
lack of prenatal care. Journal of Child Neurology. [IF=1.025, Cited=11, 23266945].
Doan RN, Miller MB, Kim SN, ..., Walsh CA (2021) MIPP-Seq: ultra-sensitive rapid detection and validation of low-
frequency mosaic mutations. BMC Medical Genomics. [IF=0.73, Cited=12, 33579278].
Wang Y, Bae T, Thorpe J, ..., Abyzov A (2021) Comprehensive identification of somatic nucleotide variants in human brain
tissue. None. [IF=None, Cited=21, 33781308].
Borges-Monroy R, Chu C, Dias C, ..., Lee EA (2021) Whole-genome analysis reveals the contribution of non-coding de novo
transposon insertions to autism spectrum disorder. Mobile DNA. [IF=1.3, Cited=14, 34838103].
Chang BS, Ly J, Appignani B, ..., Walsh CA (2005) Reading impairment in the neuronal migration disorder of
periventricular nodular heterotopia. Neurology. [IF=2.47, Cited=74, 15753412].
Sheen VL, Wheless JW, Bodell A, ..., Sherr EH (2003) Periventricular heterotopia associated with chromosome 5p
anomalies. Neurology. [IF=2.47, Cited=60, 12654978].
Sheen VL, Topçu M, Berkovic S, ..., Walsh CA (2003) Autosomal recessive form of periventricular heterotopia. Neurology.
[IF=2.47, Cited=41, 12682315].
Chang BS, Piao X, Giannini C, ..., Walsh CA (2004) Bilateral generalized polymicrogyria (BGP): a distinct syndrome of
cortical malformation. Neurology. [IF=2.47, Cited=36, 15159468].
Chang BS, Apse KA, Caraballo R, ..., Walsh CA (2006) A familial syndrome of unilateral polymicrogyria affecting the
right hemisphere. Neurology. [IF=2.47, Cited=27, 16401865].
Chang BS, Katzir T, Liu T, ..., Walsh CA (2007) A structural basis for reading fluency: white matter defects in a
genetic brain malformation. Neurology. [IF=2.47, Cited=47, 18056578].
Phillips HW, D'Gama AM, Wang Y, ..., Walsh CA (2023) Somatic Mosaicism in PIK3CA Variant Correlates With
Stereoelectroencephalography-Derived Electrophysiology. Neurology: Genetics. [IF=1.05, Cited=0, 38149038].
Ahmed MY, Chioza BA, Rajab A, ..., Mochida GH (2015) Loss of PCLO function underlies pontocerebellar hypoplasia type
III. Neurology. [IF=2.47, Cited=27, 25832664].
Poduri A, Wang Y, Gordon D, ..., Ottman R (2009) Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with
GEFS+. Neurology. [IF=2.47, Cited=12, 19841378].
Clapham KR, Yu TW, Ganesh VS, ..., Walsh CA (2012) FLNA genomic rearrangements cause periventricular nodular
heterotopia. Neurology. [IF=2.47, Cited=14, 22238415].
Berg MJ, Schifitto G, Powers JM, ..., Walsh CA (1998) X-linked female band heterotopia-male lissencephaly syndrome.
Neurology. [IF=2.47, Cited=30, 9566411].
Barkovich AJ, Simon EM, Walsh CA (2001) Callosal agenesis with cyst: a better understanding and new classification.
Neurology. [IF=2.47, Cited=69, 11160959].
Lizarraga SB, Margossian SP, Harris MH, ..., Fleming MD (2010) Cdk5rap2 regulates centrosome function and chromosome
segregation in neuronal progenitors. Development (Cambridge). [IF=1.291, Cited=171, 20460369].
Reid CB, Tavazoie SF, Walsh CA (1997) Clonal dispersion and evidence for asymmetric cell division in ferret cortex.
Development (Cambridge). [IF=1.291, Cited=57, 9199370].
Heinzen EL, O'Neill AC, Zhu X, ..., Zhang M (2018) De novo and inherited private variants in MAP1B in periventricular
nodular heterotopia. PLoS Genetics. [IF=1.236, Cited=27, 29738522].
Shen Y, Miller DT, Cheung SW, ..., Wu BL (2007) Development of a focused oligonucleotide-array comparative genomic
hybridization chip for clinical diagnosis of genomic imbalance. Clinical Chemistry. [IF=1.432, Cited=39, 17901113].
Shen Y, Dies KA, Holm IA, ..., Miller DT (2010) Clinical genetic testing for patients with autism spectrum disorders.
Pediatrics. [IF=2.905, Cited=209, 20231187].
Mutch CA, Poduri A, Sahin M, ..., Barkovich AJ (2015) Disorders of Microtubule Function in Neurons: Imaging Correlates.
None. [IF=None, Cited=32, 26564436].
Alaamery M, Massadeh S, Aldarwish M, ..., Eyaid W (2024) Case report: A founder UGDH variant associated with
developmental epileptic encephalopathy in Saudi Arabia. Frontiers in Genetics. [IF=0.935, Cited=0, 38292436].
Evrony GD, Lee E, Park PJ, Walsh CA (2016) Resolving rates of mutation in the brain using single-neuron genomics. eLife.
[IF=1.743, Cited=88, 26901440].
Mathew RS, Tatarakis A, Rudenko A, ..., Moazed D (2016) A microRNA negative feedback loop downregulates vesicle
transport and inhibits fear memory. eLife. [IF=1.743, Cited=10, 28001126].

Publication with MISMATCHING institution:

Walsh CA (2000) Genetics of neuronal migration in the cerebral cortex. None. [IF=None, Cited=15, 10899795].
Picker JD, Walsh CA (2013) New innovations: therapeutic opportunities for intellectual disabilities. Annals of
Neurology. [IF=2.769, Cited=21, 24038210].
Akawi NA, Canpolat FE, White SM, ..., Al-Gazali L (2013) Delineation of the clinical, molecular and cellular aspects of
novel JAM3 mutations underlying the autosomal recessive hemorrhagic destruction of the brain, subependymal
calcification, and congenital cataracts. Human Mutation. [IF=1.507, Cited=20, 23255084].
Walsh CA, Dawson WE, Birch MA, Gallagher JA (1990) The effects of extracellular pH on bone resorption by avian
osteoclasts in vitro. Journal of Bone and Mineral Research. [IF=1.839, Cited=11, 2075837].
Walsh CA, Beresford JN, Birch MA, ..., Gallagher JA (1991) Application of reflected light microscopy to identify and
quantitate resorption by isolated osteoclasts. Journal of Bone and Mineral Research. [IF=1.839, Cited=26, 1950671].
Schöfl C, Cuthbertson KS, Walsh CA, ..., Gallagher JA (1992) Evidence for P2-purinoceptors on human osteoblast-like
cells. Journal of Bone and Mineral Research. [IF=1.839, Cited=38, 1615757].
Birch MA, Ginty AF, Walsh CA, ..., Bilbe G (1993) PCR detection of cytokines in normal human and pagetic osteoblast-like
cells. Journal of Bone and Mineral Research. [IF=1.839, Cited=32, 8256652].
Walsh CA, Birch MA, Fraser WD, ..., Gallagher JA (1995) Expression and secretion of parathyroid hormone-related protein
by human bone-derived cells in vitro: effects of glucocorticoids. Journal of Bone and Mineral Research. [IF=1.839,
Cited=25, 7747625].
Walsh CA, McAuliffe FM (2012) Recurrent twin-twin transfusion syndrome after selective fetoscopic laser
photocoagulation: a systematic review of the literature. Ultrasound in Obstetrics and Gynecology. [IF=2.976, Cited=10, 22378622].
Walsh CA, Doyle B, Quigley J, ..., McParland P (2014) Reassessing critical maternal antibody threshold in RhD
alloimmunization: a 16-year retrospective cohort study. Ultrasound in Obstetrics and Gynecology. [IF=2.976, Cited=3, 24706487].
Walsh CA, Wilkinson M, Downey P, ..., Carroll S (2015) 'False' lambda sign in monochorionic twin pregnancy. Ultrasound
in Obstetrics and Gynecology. [IF=2.976, Cited=1, 25708185].
Walsh CA, Bowler WB, Bilbe G, ..., Gallagher JA (1997) Effects of PTH on PTHrP gene expression in human osteoblasts: up-
regulation with the kinetics of an immediate early gene. Biochemical and Biophysical Research Communications. [IF=0.643,
Cited=10, 9345287].
Walsh CA, Morrow EM, Rubenstein JLR (2008) Autism and brain development. Cell. [IF=8.479, Cited=124, 18984148].
Maury EA, Walsh CA (2021) Somatic copy number variants in neuropsychiatric disorders. Current Opinion in Genetics and
Development. [IF=0.801, Cited=6, 33444936].
van Jaarsveld RH, Reilly J, Cornips MC, ..., Oegema R (2022) Delineation of a KDM2B-related neurodevelopmental disorder
and its associated DNA methylation signature. Genetics in Medicine. [IF=2.761, Cited=4, 36322151].
Walsh CA, Engle EC (2010) Allelic diversity in human developmental neurogenetics: insights into biology and disease.
Neuron. [IF=3.346, Cited=32, 20955932].
Baizabal JM, Mistry M, García MT, ..., Harwell CC (2018) The Epigenetic State of PRDM16-Regulated Enhancers in Radial
Glia Controls Cortical Neuron Position. Neuron. [IF=3.346, Cited=29, 29779941].
Maury EA, Sherman MA, Genovese G, ..., Walsh CA (2023) Schizophrenia-associated somatic copy-number variants from 12,834
cases reveal recurrent NRXN1 and ABCB11 disruptions. Cell Genomics. [IF=2.669, Cited=4, 37601975].
Walsh CA, Birch MA, Fraser WD, ..., Gallagher JA (1994) Primary cultures of human bone-derived cells produce parathyroid
hormone-related protein: a study of 40 patients of varying age and pathology. None. [IF=None, Cited=11, 7849545].
Walsh CA (1999) Genetic malformations of the human cerebral cortex. Neuron. [IF=3.346, Cited=92, 10402190].
Walsh CA, Goffinet AM (2000) Potential mechanisms of mutations that affect neuronal migration in man and mouse. Current
Opinion in Genetics and Development. [IF=0.801, Cited=58, 10826984].
Walsh CA, MacTiernan A, Farrell S, ..., McAuliffe FM (2014) Mode of delivery in pregnancies complicated by major fetal
congenital heart disease: a retrospective cohort study. Journal of Perinatology. [IF=1.323, Cited=7, 24875409].
Shao DD, Straussberg R, Ahmed H, ..., Walsh CA (2021) A recurrent, homozygous EMC10 frameshift variant is associated
with a syndrome of developmental delay with variable seizures and dysmorphic features. Genetics in Medicine. [IF=2.761,
Cited=11, 33531666].
Krienen FM, Goldman M, Zhang Q, ..., McCarroll SA (2020) Innovations present in the primate interneuron repertoire.
Nature. [IF=11.591, Cited=120, 32999462].
Krienen FM, Goldman M, Zhang Q, ..., McCarroll SA (2020) Author Correction: Innovations present in the primate
interneuron repertoire. Nature. [IF=11.591, Cited=1, 33230336].
Luquette LJ, Miller MB, Zhou Z, ..., Park PJ (2022) Single-cell genome sequencing of human neurons identifies somatic
point mutation and indel enrichment in regulatory elements. Nature Genetics. [IF=6.89, Cited=18, 36163278].
Sherman MA, Rodin RE, Genovese G, ..., Loh PR (2021) Large mosaic copy number variations confer autism risk. Nature
Neuroscience. [IF=4.893, Cited=26, 33432194].
Walsh CA, Birch MA, Fraser WD, ..., Gallagher JA (2000) Cytokine expression by cultured osteoblasts from patients with
osteoporotic fractures. International Journal of Experimental Pathology. [IF=0.937, Cited=9, 10762443].
Sio H, Moody JD, Ho DD, ..., Appelbe B (2021) Diagnosing plasma magnetization in inertial confinement fusion implosions
using secondary deuterium-tritium reactions. Review of Scientific Instruments. [IF=0.917, Cited=0, 34243465].
Pérez-Callejo G, Bailly-Grandvaux M, Florido R, ..., Santos JJ (2022) X-ray imaging and radiation transport effects on
cylindrical implosions. Review of Scientific Instruments. [IF=0.917, Cited=0, 36461474].
Heuer PV, Haberberger D, Ivancic ST, ..., Davies JR (2024) Improved filters for angular filter refractometry. Review of
Scientific Instruments. [IF=0.917, Cited=0, 38341714].
Feng Y, Chen MH, Moskowitz IP, ..., Walsh CA (2006) Filamin A (FLNA) is required for cell-cell contact in vascular
development and cardiac morphogenesis. Proceedings of the National Academy of Sciences of the United States of America.
[IF=2.765, Cited=205, 17172441].
Walsh CA, Mahony RT, Foley ME, ..., O'Herlihy C (2007) Recurrence of fetal macrosomia in non-diabetic pregnancies.
Journal of Obstetrics and Gynaecology. [IF=0.776, Cited=16, 17654189].
Walsh CA, Rausch ME, Baxi LV (2007) Intrauterine cystocentesis to facilitate vaginal delivery in a fetus with trisomy
13. Journal of Obstetrics and Gynaecology. [IF=0.776, Cited=0, 17999310].
Kodani A, Moyer T, Chen A, ..., Reiter JF (2019) SFI1 promotes centriole duplication by recruiting USP9X to stabilize
the microcephaly protein STIL. Journal of Cell Biology. [IF=1.509, Cited=10, 31197030].
Di Costanzo S, Balasubramanian A, Pond HL, ..., Manzini MC (2014) POMK mutations disrupt muscle development leading to a
spectrum of neuromuscular presentations. Human Molecular Genetics. [IF=1.158, Cited=39, 24925318].
Walsh CA, Minnock P, Slattery C, ..., FitzGerald O (2007) Quality of life and economic impact of switching from
established infliximab therapy to adalimumab in patients with rheumatoid arthritis. Rheumatology. [IF=1.686, Cited=16, 17478471].
Walsh CA (2022) Magnetized ablative Rayleigh-Taylor instability in three dimensions. Physical Review E. [IF=0.912,
Cited=0, 35291065].
Pérez-Callejo G, Vlachos C, Walsh CA, ..., Santos JJ (2022) Cylindrical implosion platform for the study of highly
magnetized plasmas at Laser MegaJoule. Physical Review E. [IF=0.912, Cited=0, 36266806].
Walsh CA, Clark DS (2023) Nonlinear ablative Rayleigh-Taylor instability: Increased growth due to self-generated
magnetic fields. Physical Review E. [IF=0.912, Cited=0, 36797872].
Walsh CA, Chittenden JP, McGlinchey K, ..., Appelbe BD (2017) Self-Generated Magnetic Fields in the Stagnation Phase of
Indirect-Drive Implosions on the National Ignition Facility. Physical Review Letters. [IF=2.288, Cited=1, 28452551].
Campbell PT, Walsh CA, Russell BK, ..., Willingale L (2020) Magnetic Signatures of Radiation-Driven Double Ablation
Fronts. Physical Review Letters. [IF=2.288, Cited=3, 33064539].
Sadler JD, Walsh CA, Li H (2021) Symmetric Set of Transport Coefficients for Collisional Magnetized Plasma. Physical
Review Letters. [IF=2.288, Cited=1, 33666444].
Bose A, Peebles J, Walsh CA, ..., Petrasso RD (2022) Effect of Strongly Magnetized Electrons and Ions on Heat Flow and
Symmetry of Inertial Fusion Implosions. Physical Review Letters. [IF=2.288, Cited=0, 35622051].
Abu-Shawareb H, Acree R, Adams P, ..., Zylstra AB (2022) Lawson Criterion for Ignition Exceeded in an Inertial Fusion
Experiment. Physical Review Letters. [IF=2.288, Cited=8, 36018710].
Moody JD, Pollock BB, Sio H, ..., Fujioka S (2022) Increased Ion Temperature and Neutron Yield Observed in Magnetized
Indirectly Driven D_{2}-Filled Capsule Implosions on the National Ignition Facility. Physical Review Letters. [IF=2.288,
Cited=0, 36399755].
Arran C, Bradford P, Dearling A, ..., Woolsey NC (2023) Measurement of Magnetic Cavitation Driven by Heat Flow in a
Plasma. Physical Review Letters. [IF=2.288, Cited=0, 37478421].
Abu-Shawareb H, Acree R, Adams P, ..., Zylstra AB (2024) Achievement of Target Gain Larger than Unity in an Inertial
Fusion Experiment. Physical Review Letters. [IF=2.288, Cited=1, 38394591].
Walsh CA (2015) What the gynaecologist fears most in the pelvis? BJOG: An International Journal of Obstetrics and
Gynaecology. [IF=2.577, Cited=0, 26411295].
Mo A, Paz-Ebstein E, Yanovsky-Dagan S, ..., Harel T (2023) A recurrent de novo variant in NUSAP1 escapes nonsense-
mediated decay and leads to microcephaly, epilepsy, and developmental delay. Clinical Genetics. [IF=1.39, Cited=3, 37005340].
Wu MP, Doyle JR, Barry B, ..., Gussoni E (2013) G-protein coupled receptor 56 promotes myoblast fusion through serum
response factor- and nuclear factor of activated T-cell-mediated signalling but is not essential for muscle development
in vivo. None. [IF=None, Cited=29, 24102982].
Walsh CA, Mulvin D (2003) Collateral urethral duplication in the frontal plane. BJU International. [IF=1.809, Cited=0, 19127644].
Walsh CA, Singer LP, Mercando AD, Furman S (1988) Differentiation of arrhythmias in the dog by measurement of activation
sequence using an atrial and two ventricular electrodes. PACE - Pacing and Clinical Electrophysiology. [IF=0.715,
Cited=6, 2463541].
Walsh CA, McAlister HF, Andrews CA, ..., Furman S (1988) Pacemaker implantation in children: a 21-year experience. PACE
- Pacing and Clinical Electrophysiology. [IF=0.715, Cited=19, 2463570].
Walsh CA, Singer LP, Mercando AD, Furman S (1990) Differentiation of sinus rhythms from supraventricular
tachydysrhythmias by activation sequence and timing. PACE - Pacing and Clinical Electrophysiology. [IF=0.715, Cited=2, 1704577].
Chenn A, Walsh CA (2002) Regulation of cerebral cortical size by control of cell cycle exit in neural precursors.
Science. [IF=7.729, Cited=938, 12130776].
Chenn A, Walsh CA (1999) Perspectives: neurobiology. Cranking it up a notch. Science. [IF=7.729, Cited=3, 10577225].
Maury EA, Walsh CA, Kahle KT (2023) Neurosurgery elucidates somatic mutations. Science. [IF=7.729, Cited=0, 38127765].
Shen J, Walsh CA (2005) Targeted disruption of Tgif, the mouse ortholog of a human holoprosencephaly gene, does not
result in holoprosencephaly in mice. Molecular and Cellular Biology. [IF=1.026, Cited=59, 15831469].
Dobyns WB, Truwit CL, Ross ME, ..., Barkovich AJ (1999) Differences in the gyral pattern distinguish chromosome
17-linked and X-linked lissencephaly. Neurology. [IF=2.47, Cited=111, 10430413].
Powers SE, Taniguchi K, Yen W, ..., Wotton D (2010) Tgif1 and Tgif2 regulate Nodal signaling and are required for
gastrulation. Development (Cambridge). [IF=1.291, Cited=44, 20040491].
Walsh CA, Carron JA, Gallagher JA (1996) The isolation of osteoclasts from human giant cell tumors and long-term marrow
cultures. None. [IF=None, Cited=1, 21359748].
Walsh CA, Allen W, Moore KH (2010) 'Urinary incontinence' post-radiotherapy: a diagnostic conundrum. Journal of
Obstetrics and Gynaecology. [IF=0.776, Cited=0, 20455740].
Walsh CA, Pistilli M, Karantanis E (2010) Cardiac arrhythmias and gynaecological laparoscopy: a reminder. Journal of
Obstetrics and Gynaecology. [IF=0.776, Cited=1, 21126142].
Kodani A, Yu TW, Johnson JR, ..., Reiter JF (2015) Centriolar satellites assemble centrosomal microcephaly proteins to
recruit CDK2 and promote centriole duplication. eLife. [IF=1.743, Cited=75, 26297806].
Walsh CA (2001) Syncope and sudden death in the adolescent. None. [IF=None, Cited=0, 11224026].
Walsh CA, Fearon U, FitzGerald O, ..., Bresnihan B (2008) Decreased CD20 expression in rheumatoid arthritis synovium
following 8 weeks of rituximab therapy. Clinical and Experimental Rheumatology. [IF=1.039, Cited=0, 18799100].
Walsh CA, McAuliffe F, Kinsella V, McParland P (2013) Routine obstetric ultrasound services. Irish Medical Journal.
[IF=0.182, Cited=0, 24579412].

Publication with MISSING institution:

Mochida GH, Walsh CA (2004) Genetic basis of developmental malformations of the cerebral cortex. None. [IF=None,
Cited=45, 15148137].
Tsao JW, Neal J, Apse K, ..., Sheen VL (2006) Cerebellar ataxia with progressive improvement. None. [IF=None, Cited=4, 16606775].
Bienvenu T, des Portes V, McDonell N, ..., Beldjord C (2000) Missense mutation in PAK3, R67C, causes X-linked
nonspecific mental retardation. None. [IF=None, Cited=94, 10946356].
Schwartzkroin PA, Walsh CA (2000) Cortical malformations and epilepsy. None. [IF=None, Cited=59, 11107192].
Gleeson JG, Minnerath SR, Fox JW, ..., Walsh CA (1999) Characterization of mutations in the gene doublecortin in
patients with double cortex syndrome. Annals of Neurology. [IF=2.769, Cited=87, 9989615].
Chae TH, Walsh CA (2007) Genes that control the size of the cerebral cortex. None. [IF=None, Cited=9, 18494253].
Zollino M, Colosimo C, Zuffardi O, ..., Neri G (2003) Cryptic t(1;12)(q44;p13.3) translocation in a previously described
syndrome with polymicrogyria, segregating as an apparently X-linked trait. American Journal of Medical Genetics, Part A.
[IF=1.165, Cited=17, 12548742].
Currier SC, Lee CK, Chang BS, ..., Walsh CA (2005) Mutations in POMT1 are found in a minority of patients with Walker-
Warburg syndrome. American Journal of Medical Genetics, Part A. [IF=1.165, Cited=33, 15637732].
Tietjen I, Erdogan F, Currier S, ..., Walsh CA (2005) EMX2-independent familial schizencephaly: clinical and genetic
analyses. American Journal of Medical Genetics, Part A. [IF=1.165, Cited=8, 15887302].
Ferland RJ, Gaitanis JN, Apse K, ..., Sheen VL (2006) Periventricular nodular heterotopia and Williams syndrome.
American Journal of Medical Genetics, Part A. [IF=1.165, Cited=37, 16691586].
Rajab A, Yoo SY, Abdulgalil A, ..., Walsh CA (2006) An autosomal recessive form of spastic cerebral palsy (CP) with
microcephaly and mental retardation. American Journal of Medical Genetics, Part A. [IF=1.165, Cited=16, 16761294].
Neal J, Apse K, Sahin M, ..., Sheen VL (2006) Deletion of chromosome 1p36 is associated with periventricular nodular
heterotopia. American Journal of Medical Genetics, Part A. [IF=1.165, Cited=26, 16835933].
Tietjen I, Bodell A, Apse K, ..., Walsh CA (2007) Comprehensive EMX2 genotyping of a large schizencephaly case series.
American Journal of Medical Genetics, Part A. [IF=1.165, Cited=23, 17506092].
Hill AD, Chang BS, Hill RS, ..., Walsh CA (2007) A 2-Mb critical region implicated in the microcephaly associated with
terminal 1q deletion syndrome. American Journal of Medical Genetics, Part A. [IF=1.165, Cited=39, 17603806].
Rajab A, Manzini MC, Mochida GH, ..., Ross ME (2007) A novel form of lethal microcephaly with simplified gyral pattern
and brain stem hypoplasia. American Journal of Medical Genetics, Part A. [IF=1.165, Cited=7, 17975804].
Dobyns WB, Mirzaa G, Christian SL, ..., Shaffer LG (2008) Consistent chromosome abnormalities identify novel
polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2. American Journal of Medical Genetics,
Part A. [IF=1.165, Cited=57, 18536050].
Kantarci S, Ragge NK, Thomas NS, ..., Pober BR (2008) Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous
LRP2 mutation due to complete chromosome 2 paternal isodisomy. American Journal of Medical Genetics, Part A. [IF=1.165,
Cited=38, 18553518].
Travaglini L, Brancati F, Attie-Bitach T, ..., Viskochil D (2009) Expanding CEP290 mutational spectrum in ciliopathies.
American Journal of Medical Genetics, Part A. [IF=1.165, Cited=23, 19764032].
Sheen VL, Torres AR, Du X, ..., Kimonis VE (2010) Mutation in PQBP1 is associated with periventricular heterotopia.
American Journal of Medical Genetics, Part A. [IF=1.165, Cited=12, 20886605].
Mellado C, Poduri A, Gleason D, ..., Walsh CA (2010) Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large
schizencephaly cohort. American Journal of Medical Genetics, Part A. [IF=1.165, Cited=8, 20949537].
Ben-Omran T, Ali R, Almureikhi M, ..., Teebi A (2011) Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new
families with a mutation in the C2orf37 gene. American Journal of Medical Genetics, Part A. [IF=1.165, Cited=17, 21964978].
Marangi G, Orteschi D, Vigevano F, ..., Neri G (2012) Expanding the spectrum of rearrangements involving chromosome 19:
a mild phenotype associated with a 19p13.12-p13.13 deletion. American Journal of Medical Genetics, Part A. [IF=1.165,
Cited=6, 22419660].
Chang BS, Duzcan F, Kim S, ..., Walsh CA (2007) The role of RELN in lissencephaly and neuropsychiatric disease. American
Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. [IF=0.858, Cited=38, 16958033].
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Sheen VL, Ganesh VS, Topcu M, ..., Walsh CA (2003) Mutations in ARFGEF2 implicate vesicle trafficking in neural
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Ferland RJ, Eyaid W, Collura RV, ..., Walsh CA (2004) Abnormal cerebellar development and axonal decussation due to
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mosaic epilepsy-related variants. None. [IF=None, Cited=0, 39108522].
Neal J, Takahashi M, Silva M, ..., Sheen VL (2007) Insights into the gyrification of developing ferret brain by magnetic
resonance imaging. Journal of Anatomy. [IF=1.098, Cited=60, 17229284].
Walsh CA, Manias T, Brockelsby J (2007) Relationship between haemoglobin change and estimated blood loss after delivery.
BJOG: An International Journal of Obstetrics and Gynaecology. [IF=2.577, Cited=3, 17949386].
Parrini E, Ferrari AR, Dorn T, ..., Guerrini R (2008) Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome,
and GPR56 gene mutations. Epilepsia. [IF=1.893, Cited=26, 19016831].
Amrom D, Walsh CA (2010) Genetic malformations of the human frontal lobe. Epilepsia. [IF=1.893, Cited=2, 20331705].
Poduri A, Chopra SS, Neilan EG, ..., Kothare SV (2012) Homozygous PLCB1 deletion associated with malignant migrating
partial seizures in infancy. Epilepsia. [IF=1.893, Cited=49, 22690784].
Yu F, Hill RS, Schaffner SF, ..., Reich D (2007) Comment on "Ongoing adaptive evolution of ASPM, a brain size
determinant in Homo sapiens". Science. [IF=7.729, Cited=22, 17446375].
Walsh CA, Mullan RH, Minnock PB, ..., Bresnihan B (2008) Consistency in assessing the Disease Activity Score-28 in
routine clinical practice. Annals of the Rheumatic Diseases. [IF=5.147, Cited=9, 18077544].
Mochida GH, Rajab A, Eyaid W, ..., Walsh CA (2004) Broader geographical spectrum of Cohen syndrome due to COH1
mutations. Journal of Medical Genetics. [IF=1.598, Cited=21, 15173253].
Shen J, Eyaid W, Mochida GH, ..., Walsh CA (2005) ASPM mutations identified in patients with primary microcephaly and
seizures. Journal of Medical Genetics. [IF=1.598, Cited=48, 16141009].
van Reeuwijk J, Janssen M, van den Elzen C, ..., van Bokhoven H (2005) POMT2 mutations cause alpha-dystroglycan
hypoglycosylation and Walker-Warburg syndrome. Journal of Medical Genetics. [IF=1.598, Cited=251, 15894594].
Basel-Vanagaite L, Attia R, Yahav M, ..., Shohat M (2005) The CC2D1A, a member of a new gene family with C2 domains, is
involved in autosomal recessive non-syndromic mental retardation. Journal of Medical Genetics. [IF=1.598, Cited=100, 16033914].
MacMillan HL, Fleming JE, Streiner DL, ..., Beardslee WR (2001) Childhood abuse and lifetime psychopathology in a
community sample. American Journal of Psychiatry. [IF=3.582, Cited=485, 11691695].
Dwyer ND, Manning DK, Moran JL, ..., Beier DR (2011) A forward genetic screen with a thalamocortical axon reporter mouse
yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype. Neural Development. [IF=0.89, Cited=29, 21214893].
Di Blasi C, Bellafiore E, Salih MA, ..., Mora M (2011) Variable disease severity in Saudi Arabian and Sudanese families
with c.3924 + 2 T > C mutation of LAMA2. BMC Research Notes. [IF=0.869, Cited=8, 22166137].
Klei L, Sanders SJ, Murtha MT, ..., Devlin B (2012) Common genetic variants, acting additively, are a major source of
risk for autism. Molecular Autism. [IF=1.69, Cited=240, 23067556].
Piao X, Walsh CA (2004) A novel signaling mechanism in brain development. Pediatric Research. [IF=1.273, Cited=2, 15269343].
Sheen VL, Jansen A, Chen MH, ..., Walsh CA (2005) Filamin A mutations cause periventricular heterotopia with Ehlers-
Danlos syndrome. Neurology. [IF=2.47, Cited=119, 15668422].
Rajab A, Mochida GH, Hill A, ..., Walsh CA (2003) A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21.
Neurology. [IF=2.47, Cited=41, 12771259].
Dobyns WB, Andermann E, Andermann F, ..., Truwit CL (1996) X-linked malformations of neuronal migration. Neurology.
[IF=2.47, Cited=115, 8757001].
Silence SM, Donckers MC, Walsh CA, ..., Moerner WE (1994) Optical properties of poly(N-vinylcarbazole)-based guest-host
photorefractive polymer systems. Applied Optics. [IF=0.885, Cited=1, 20885569].
Silence SM, Walsh CA, Walsh CA, ..., Moerner WE (1992) Subsecond grating growth in a photorefractive polymer. Optics
Letters. [IF=1.297, Cited=8, 19794733].
Donckers MC, Silence SM, Walsh CA, ..., Twieg RJ (1993) Net two-beam-coupling gain in a polymeric photorefractive
material. Optics Letters. [IF=1.297, Cited=5, 19823284].
Kouprina N, Pavlicek A, Mochida GH, ..., Larionov V (2004) Accelerated evolution of the ASPM gene controlling brain size
begins prior to human brain expansion. PLoS Biology. [IF=2.285, Cited=104, 15045028].
Lu W, Quintero-Rivera F, Fan Y, ..., Maas RL (2007) NFIA haploinsufficiency is associated with a CNS malformation
syndrome and urinary tract defects. PLoS Genetics. [IF=1.236, Cited=75, 17530927].
Sepp KJ, Hong P, Lizarraga SB, ..., Perrimon N (2008) Identification of neural outgrowth genes using genome-wide RNAi.
PLoS Genetics. [IF=1.236, Cited=66, 18604272].
Labelle-Dumais C, Dilworth DJ, Harrington EP, ..., Gould DB (2011) COL4A1 mutations cause ocular dysgenesis, neuronal
localization defects, and myopathy in mice and Walker-Warburg syndrome in humans. PLoS Genetics. [IF=1.236, Cited=82, 21625620].
Chahrour MH, Yu TW, Lim ET, ..., Walsh CA (2012) Whole-exome sequencing and homozygosity analysis implicate
depolarization-regulated neuronal genes in autism. PLoS Genetics. [IF=1.236, Cited=122, 22511880].
Li S, Jin Z, Koirala S, ..., Piao X (2008) GPR56 regulates pial basement membrane integrity and cortical lamination.
Journal of Neuroscience. [IF=1.471, Cited=142, 18509043].
González JL, Russo CJ, Goldowitz D, ..., Walsh CA (1997) Birthdate and cell marker analysis of scrambler: a novel
mutation affecting cortical development with a reeler-like phenotype. Journal of Neuroscience. [IF=1.471, Cited=63, 9364067].
Lin PT, Gleeson JG, Corbo JC, ..., Walsh CA (2000) DCAMKL1 encodes a protein kinase with homology to doublecortin that
regulates microtubule polymerization. Journal of Neuroscience. [IF=1.471, Cited=136, 11124993].
McCarthy M, Turnbull DH, Walsh CA, Fishell G (2001) Telencephalic neural progenitors appear to be restricted to regional
and glial fates before the onset of neurogenesis. Journal of Neuroscience. [IF=1.471, Cited=75, 11517265].
Reid CB, Walsh CA (2002) Evidence of common progenitors and patterns of dispersion in rat striatum and cerebral cortex.
Journal of Neuroscience. [IF=1.471, Cited=22, 12019320].
Corbo JC, Deuel TA, Long JM, ..., Walsh CA (2002) Doublecortin is required in mice for lamination of the hippocampus but
not the neocortex. Journal of Neuroscience. [IF=1.471, Cited=210, 12196578].
Olson E, Kim S, Walsh CA (2006) Impaired neuronal positioning and dendritogenesis in the neocortex after cell-autonomous
Dab1 suppression. Journal of Neuroscience. [IF=1.471, Cited=93, 16467525].
Friocourt G, Liu JS, Antypa M, ..., Parnavelas JG (2007) Both doublecortin and doublecortin-like kinase play a role in
cortical interneuron migration. Journal of Neuroscience. [IF=1.471, Cited=101, 17409252].
Sheen VL, Walsh CA (2005) Periventricular heterotopia: new insights into Ehlers-Danlos syndrome. Clinical Medicine and
Research. [IF=0.651, Cited=26, 16303888].
Adachi Y, Poduri A, Kawaguch A, ..., Barkovich AJ (2011) Congenital microcephaly with a simplified gyral pattern:
associated findings and their significance. None. [IF=None, Cited=28, 21454410].
Zappaterra MW, LaMantia AS, Walsh CA, Lehtinen MK (2013) Isolation of cerebrospinal fluid from rodent embryos for use
with dissected cerebral cortical explants. Journal of Visualized Experiments. [IF=0.398, Cited=9, 23524481].
Reid CB, Liang I, Walsh CA (1999) Clonal mixing, clonal restriction, and specification of cell types in the developing
rat olfactory bulb. Journal of Comparative Neurology. [IF=0.928, Cited=0, 10075446].
MacMillan HL, Boyle MH, Wong MY, ..., Walsh CA (1999) Slapping and spanking in childhood and its association with
lifetime prevalence of psychiatric disorders in a general population sample. CMAJ. [IF=1.802, Cited=0, 10530296].
Gleeson JG, Luo RF, Grant PE, ..., Walsh CA (2000) Genetic and neuroradiological heterogeneity of double cortex
syndrome. Annals of Neurology. [IF=2.769, Cited=0, 10665503].
Walsh CA, Ahmed S (2010) RE: Pregnant until proven otherwise. Irish Medical Journal. [IF=0.182, Cited=0, 20845607].
Goëb V, Walsh CA, Reece RJ, ..., Ponchel F (2012) Potential role of arthroscopy in the management of inflammatory
arthritis. Clinical and Experimental Rheumatology. [IF=1.039, Cited=0, 22734971].
Walsh CA, Graham TE (1986) Male-female responses in various body temperatures during and following exercise in cold air.
None. [IF=None, Cited=0, 3778395].