C. Walsh

Yiping Shen, Sandra Friedman, Bai-Lin Wu, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Mechanisms of cerebral cortical patterning in mice and humans

Christopher A. Walsh, Edwin S. Monuki, C. Walsh, 2001, Nature Neuroscience.

Somatic mutation in single human neurons tracks developmental and transcriptional history

Peter J. Park, Eunjung Lee, Thomas W. Chittenden, 2015, Science.

Autism and Brain Development

Eric M. Morrow, John L.R. Rubenstein, Christopher A. Walsh, 2008, Cell.

Reelin is expressed in the accessory olfactory system, but is not a guidance cue for vomeronasal axons.

C. Walsh, Glenn Yiu, Sarah M Teillon, 2003, Brain research. Developmental brain research.

Developmental and Degenerative Features in a Complicated Spastic Paraplegia

C. Walsh, A. LaMantia, T. Maynard, 2009, Annals of neurology.

Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development

I. Scheffer, C. Walsh, P. Huttenlocher, 1996, Neuron.

BothDoublecortinandDoublecortin-LikeKinasePlayaRole inCorticalInterneuronMigration

C. Walsh, Judy S. H. Liu, Judy S. Liu, 2007 .

Parallel RNA and DNA analysis after Deep-sequencing (PRDD-seq) reveals cell type specific lineage patterns in human brain

Trygve E Bakken, C. Walsh, Jeremy A. Miller, 2020, bioRxiv.

Callosal agenesis with cyst: A better understanding and new classification

C. Walsh, A. Barkovich, E. M. Simon, 2001 .

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.

I. Scheffer, D. Ledbetter, C. Walsh, 1997, Human molecular genetics.

Mutations in PNKP cause microcephaly, seizures and defects in DNA repair

C. Walsh, A. Barkovich, M. Topcu, 2010, Nature Genetics.

Evolution and Ontogenetic Development of Cortical Structures

C. Walsh, M. Stryker, T. Hensch, 2019, The Neocortex.

Disease-associated mutations affect GPR56 protein trafficking and cell surface expression.

C. Walsh, L. Bu, I. Tietjen, 2007, Human molecular genetics.

Periventricular heterotopia with complete agenesis of the corpus callosum

C. Walsh, V. Sheen, J. Neal, 2006, Journal of Neurology.

Differences in the gyral pattern distinguish chromosome 17–linked and X-linked lissencephaly

D. Ledbetter, C. Walsh, M. Ross, 1999, Neurology.

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

C. Walsh, P. Grant, Y. Shugart, 2000, Nature Genetics.

Lissencephaly with cerebellar hypoplasia

C. Walsh, E. Olson, 2016, Definitions.

Rare genetic causes of lissencephaly may implicate microtubule‐based transport in the pathogenesis of cortical dysplasias

C. Walsh, Judy S. H. Liu, Judy S. Liu, 2010 .

Cryptic t(1;12)(q44;p13.3) translocation in a previously described syndrome with polymicrogyria, segregating as an apparently X‐linked trait

C. Walsh, G. Neri, O. Zuffardi, 2003, American journal of medical genetics. Part A.

Expanding the Spectrum of Rearrangements Involving Chromosome 19: A Mild Phenotype Associated with a 19p13.12–p13.13 Deletion

C. Walsh, G. Neri, J. Felie, 2012, American journal of medical genetics. Part A.

Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings

I. Scheffer, C. Walsh, P. Huttenlocher, 2000, Pediatric Radiology.

DCAMKL1 Encodes a Protein Kinase with Homology to Doublecortin that Regulates Microtubule Polymerization

C. Walsh, J. Corbo, J. Gleeson, 2000, The Journal of Neuroscience.

LISsen up!

C. Walsh, 1998, Nature Genetics.

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome

Michael E. Coulter, C. Walsh, S. Wiemann, 2017, Genome research.

New innovations: Therapeutic opportunities for intellectual disabilities

C. Walsh, J. Picker, 2013, Annals of neurology.

Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size

C. Walsh, J. Mandeville, X. Papademetris, 2018, Nature.

Doublecortin is expressed in articular chondrocytes.

C. Walsh, Judy S. H. Liu, P. D. Di Cesare, 2007, Biochemical and biophysical research communications.

Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous Trait

Stephan J Sanders, Donna M. Martin, D. Ledbetter, 2013, Biological Psychiatry.

DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome

Timothy J. Edwards, P. Lockhart, C. Walsh, 2018, Human mutation.

Multiple Recurrent De Novo Copy Number Variations , Including Duplications of the 7 q 11 . 23 Williams-Beuren Syndrome Region , Are Associated with Autism

Rebecca, Michael J. DiCola, Stephan J Sanders, 2011 .

Thoracic aortic aneurysm in patients with loss of function Filamin A mutations: Clinical characterization, genetics, and recommendations

C. Walsh, M. Chen, B. Chang, 2018, American journal of medical genetics. Part A.

Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes.

C. Walsh, M. Ross, R. Kuzniecky, 2000, American journal of human genetics.

Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome.

C. Walsh, S. Schneider, K. Bhatia, 2008, American journal of human genetics.

SFI1 promotes centriole duplication by recruiting USP9X to stabilize the microcephaly protein STIL

C. Walsh, J. Reiter, A. Holland, 2019, The Journal of cell biology.

C. Walsh, A. Poduri, M. Salih, 2014 .

Reply: To PMID 24243345.

C. Walsh, A. Poduri, M. Salih, 2014, Annals of neurology.

ASPM mutations identified in patients with primary microcephaly and seizures

C. Walsh, C. Woods, G. Mochida, 2005, Journal of Medical Genetics.

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome

C. Walsh, Y. Shugart, M. Ruvolo, 2004, Nature Genetics.

Cc2d1a Loss of Function Disrupts Functional and Morphological Development in Forebrain Neurons Leading to Cognitive and Social Deficits

Guangying K. Wu, C. Walsh, E. Klann, 2017, Cerebral cortex.

Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation.

C. Walsh, H. Bokhoven, J. Fryns, 2000, American journal of medical genetics.

Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females.

N W Wood, F Andermann, S M Sisodiya, 2001, Human molecular genetics.

C. Walsh, Ming-Hui Chen, 2015 .

Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia

C. Walsh, M. Sahin, V. Sheen, 2006, American journal of medical genetics. Part A.

Periventricular heterotopia associated with chromosome 5p anomalies

C. Walsh, S. Packman, O. Glenn, 2003, Neurology.

PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly

C. Walsh, Manal A. Alaamery, Salam Massadeh, 2020, Clinical genetics.

Loss of PCLO function underlies pontocerebellar hypoplasia type III

M. Hurles, C. Walsh, M. Patton, 2015, Neurology.

Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number

C. Walsh, F. Alkuraya, T. Yu, 2014, Neuron.

A 2‐Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome

C. Walsh, W. Sellers, L. Garraway, 2007, American journal of medical genetics. Part A.

Callosal agenesis with cyst

C. Walsh, A. Barkovich, E. M. Simon, 2001, Neurology.

A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasia

C. Walsh, M. Ross, G. Mochida, 2007, American journal of medical genetics. Part A.

Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+

C. Walsh, N. Risch, W. Hauser, 2009, Neurology.

PAK3 mutation in nonsyndromic X-linked mental retardation

C. Walsh, J. Mulley, M. Partington, 1998, Nature Genetics.

Molecular genetics of human developmental brain disorders of the arabian gulf region

C. Walsh, 2009, Hamdan Medical Journal.

Studies of the candidate genes in X-linked congenital cerebellar hypoplasia

C. Walsh, S. Tsuji, J. Gleeson, 1999, Journal of Neurology.

Gene Associated with Juvenile Myoclonic Epilepsy

C. Walsh, 2002 .

Making a Notch in the Evolution of the Human Cortex.

C. Walsh, Sara Bizzotto, S. Bizzotto, 2018, Developmental cell.

microcephaly and seizures mutations identified in patients with primary ASPM

C. Walsh, C. Woods, G. Mochida, 2005 .

APP gene copy number changes reflect exogenous contamination

C. Walsh, E. Lee, Michael A. Lodato, 2020, Nature.

Somatic Mutation in Pediatric Neurological Diseases.

C. Walsh, Rachel E. Rodin, 2018, Pediatric neurology.

Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans.

Marni J. Falk, H. Hakonarson, C. Walsh, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

Genomic and phenotypic delineation of congenital microcephaly

C. Walsh, F. Alkuraya, S. Arold, 2018, Genetics in Medicine.

What Are Mini-Brains?

C. Walsh, B. Bae, 2013, Science.

COL4A1 Mutations Cause Ocular Dysgenesis, Neuronal Localization Defects, and Myopathy in Mice and Walker-Warburg Syndrome in Humans

C. Walsh, D. Dilworth, W. Dobyns, 2011, PLoS genetics.

[18] Polymerase chain reaction-based techniques for utilizing retroviruses as cell lineage markers

C. Walsh, 1995 .

Mutations in POMT1 are found in a minority of patients with Walker–Warburg syndrome

C. Walsh, L. Lagae, G. Enns, 2005, American journal of medical genetics. Part A.

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

C. Walsh, G. Mochida, L. Al-Gazali, 2013, Human mutation.

Schizencephaly: association with young maternal age, alcohol use, and lack of prenatal care.

C. Walsh, A. Barkovich, F. Hisama, 2013, Journal of child neurology.

Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network

Ryan E. Mills, J. V. Moran, Jennifer A. Erwin, 2017, Science.

Molecular contributions to cerebral cortical specification - Discussion

Jack Price, Tobias Bonhoeffer, Leah Krubitzer, 1995 .

Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene.

C. Walsh, M. Tekin, M. Kafali, 2008, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Duplication 2p16 is associated with perisylvian polymicrogyria

C. Walsh, B. Dan, F. Andermann, 2019, American journal of medical genetics. Part A.

Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortex

Renzo Guerrini, Hitoshi Takahashi, Christopher A. Walsh, 2002, Acta Neuropathologica.

Acute Slices by In Vivo Injection of Sindbis Virus Abundant GFP Expression and LTP in Hippocampal

Eugenia G. Giannopoulou, Seonhee Kim, C. Walsh, 2015 .

Targeted Disruption of Tgif, the Mouse Ortholog of a Human Holoprosencephaly Gene, Does Not Result in Holoprosencephaly in Mice

Christopher A. Walsh, C. Walsh, Jun Shen, 2005, Molecular and Cellular Biology.

Cortical malformations and epilepsy.

C. Walsh, P. Schwartzkroin, 2000, Mental retardation and developmental disabilities research reviews.

LIS1 Regulates CNS Lamination by Interacting with mNudE, a Central Component of the Centrosome

C. Walsh, M. Kirschner, E. Olson, 2000, Neuron.

G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex

William B. Dobyns, A. James Barkovich, Bernard S. Chang, 2004, Science.

Genetic Disorders of Cerebral Cortical Development

C. Walsh, G. Mochida, A. Poduri, 2013 .

MIPP-Seq: ultra-sensitive rapid detection and validation of low-frequency mosaic mutations

C. Walsh, Ryan N. Doan, A. Huang, 2021, BMC medical genomics.

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

Hussain Jafri, Emma Roberts, Sheila Scott, 2005, Nature Genetics.

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome.

C. Walsh, H. Brunner, B. van der Zwaag, 2002, American journal of human genetics.

POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome

M. Huynen, C. Walsh, F. Muntoni, 2005, Journal of Medical Genetics.

Somatic copy number variants in neuropsychiatric disorders.

C. Walsh, Eduardo A. Maury, 2021, Current opinion in genetics & development.

Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate

C. Walsh, N. Krogan, Jeffrey R. Johnson, 2016, Neuron.

Reelin/Dab1 Signaling in the Developing Cerebral Cortex

C. Walsh, E. Olson, 2008 .

Impaired Neuronal Positioning and Dendritogenesis in the Neocortex after Cell-Autonomous Dab1 Suppression

Seonhee Kim, Christopher A Walsh, Seonhee Kim, 2006, The Journal of Neuroscience.

Smooth, rough and upside-down neocortical development.

C. Walsh, E. Olson, 2002, Current opinion in genetics & development.

Protein–Protein interactions, cytoskeletal regulation and neuronal migration

C. Walsh, Yuanyi Feng, 2001, Nature Reviews Neuroscience.

Human brain malformations and their lessons for neuronal migration.

C. Walsh, M. Ross, M. Ross, 2001, Annual review of neuroscience.

Neuronal migration disorders: from genetic diseases to developmental mechanisms

C. Walsh, J. Gleeson, 2000, Trends in Neurosciences.

Reelin Binds α3β1 Integrin and Inhibits Neuronal Migration

C. Walsh, E. Anton, E. Olson, 2000, Neuron.

Potential mechanisms of mutations that affect neuronal migration in man and mouse.

C. Walsh, A. Goffinet, Christopher A. Walsh, 2000, Current opinion in genetics & development.

Genetics of neuronal migration in the cerebral cortex.

C. Walsh, 2000, Mental retardation and developmental disabilities research reviews.

Genes that regulate neuronal migration in the cerebral cortex

Christopher A. Walsh, C. Walsh, K. Allen, 1999, Epilepsy Research.

Coexistence of widespread clones and large radial clones in early embryonic ferret cortex.

C. Walsh, S. Tavazoie, M. Ware, 1999, Cerebral cortex.

Periventricular heterotopia and the genetics of neuronal migration in the cerebral cortex.

C. Walsh, J. W. Fox, C A Walsh, 1999, American journal of human genetics.

Genetic Malformations of the Human Cerebral Cortex

C. Walsh, C A Walsh, 1999, Neuron.

Cell Fate and Cell Migration in the Developing Cerebral Cortex

C. Walsh, M. Ware, 1999 .

Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype

C. Walsh, D. Goldowitz, M. Davisson, 1997, The Journal of Neuroscience.

A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21

C. Walsh, P. Grant, Y. Shugart, 2003, Neurology.

Identifying cell type specific driver genes in autism-associated copy number loci from cerebral organoids

G. Church, C. Walsh, J. Hirschhorn, 2020, bioRxiv.

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Christopher S. Poultney, Stephan J Sanders, Stephen J. Guter, 2017, Molecular Autism.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Rates, Distribution, and Implications of Post-zygotic Mosaic Mutations in Autism Spectrum Disorder

Christopher S. Poultney, A. P. Goldberg, S. Scherer, 2017, Nature Neuroscience.

The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle protein.

Vladimir Larionov, Greg Solomon, Christopher A Walsh, 2005, Human molecular genetics.

Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry

Eric M. Morrow, Soher Balkhy, Christopher A. Walsh, 2008, Science.

Single-cell analysis reveals transcriptional heterogeneity of neural progenitors in human cortex

Kutay D Atabay, Christopher A Walsh, C. Walsh, 2015, Nature Neuroscience.

Cux-2 controls the proliferation of neuronal intermediate precursors of the cortical subventricular zone.

B. Cubelos, Álvaro Sebastián‐Serrano, Seonhee Kim, 2008, Cerebral cortex.

Aberrant Splicing of a Mouse disabled Homolog, mdab1, in the scrambler Mouse

C. Walsh, S. Chua, A. Goffinet, 1997, Neuron.

Neuroscience in the post-genome era: an overview

C. Walsh, 2001, Trends in Neurosciences.

Recent Advances in Understanding the Genetic Architecture of Autism.

C. Walsh, Caroline Dias, 2020, Annual review of genomics and human genetics.

The Landscape of Mutational Mosaicism in Autistic and Normal Human Cerebral Cortex

Lovelace J. Luquette, C. Walsh, P. Park, 2020, bioRxiv.

PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features

S. Gabriel, C. Walsh, J. Ellison, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The diverse genetic landscape of neurodevelopmental disorders.

C. Walsh, M. Chahrour, Maria H. Chahrour, 2014, Annual review of genomics and human genetics.

Chapter 90 – Autism Spectrum Disorders

Michael E. Coulter, C. Walsh, T. Yu, 2013 .

OUTLINE “ Obligatory ” Somatic Mosaic Disorders ? How Do Somatic Mutations Manifest as Neurological Disease ? “ Second Hit ”

C. Walsh, A. Poduri, G. Evrony, 2013 .

Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus

I. Scheffer, C. Walsh, Y. Shugart, 2004, Brain and Development.

CC2D1A Regulates Human Intellectual and Social Function as well as NF-κB Signaling Homeostasis

C. Walsh, F. Alkuraya, R. Hill, 2014, Cell reports.

Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism

Timothy W. Yu, Christopher A. Walsh, Michael E. Coulter, 2012, PLoS genetics.

Isolate Populations and Rare Variation in Autism Spectrum Disorders

C. Walsh, E. Morrow, 2011 .

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation

C. Walsh, D. Bercovich, T. Olender, 2005, Journal of Medical Genetics.

A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?

Eric M. Morrow, Shrikant M. Mane, Edwin H. Cook, 2015, Biological Psychiatry.

Clinical Genetic Testing for Patients With Autism Spectrum Disorders

Sharyn A. Lincoln, C. Walsh, K. Miller, 2010, Pediatrics.

Filamin A (FLNA) is required for cell–cell contact in vascular development and cardiac morphogenesis

Luis Vidali, Christopher A Walsh, Fumihiko Nakamura, 2006, Proceedings of the National Academy of Sciences.

Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior

Soher Balkhy, Christopher A. Walsh, Byoung-Il Bae, 2016, Cell.

Somatic mutations in cerebral cortical malformations.

C. Walsh, S. Jamuar, 2014, The New England journal of medicine.

SLC25A22 is a novel gene for migrating partial seizures in infancy

I. Scheffer, C. Walsh, A. Barkovich, 2013, Annals of neurology.

Whole-genome analysis of de novo and polymorphic retrotransposon insertions in Autism Spectrum Disorder

C. Walsh, P. Park, E. Lee, 2021, bioRxiv.

Genome aging: somatic mutation in the brain links age-related decline with disease and nominates pathogenic mechanisms.

C. Walsh, Michael A. Lodato, 2019, Human molecular genetics.

Exome Analyses Reveal New Autism Genes in Synaptic, Transcriptional, and Chromatin Networks Supplementary Methods

Christopher S. Poultney, Stephan J Sanders, Evan T. Geller, 2022 .

Large mosaic copy number variations confer autism risk

Ronen E. Mukamel, B. Berger, C. Walsh, 2020, Nature Neuroscience.

Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder

C. Walsh, M. Greenberg, T. Yu, 2020, Scientific Reports.

Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder

J. Lupski, C. Walsh, S. Jhangiani, 2019, American journal of human genetics.

Resolving rates of mutation in the brain using single-neuron genomics

C. Walsh, P. Park, E. Lee, 2016, eLife.

Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain.

Annapurna Poduri, Christopher A Walsh, C. Walsh, 2015, Cell reports.

Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations

Maria K. Lehtinen, C. Walsh, R. Beroukhim, 2012, Neuron.

Cranking It Up a Notch

Christopher A. Walsh, Anjen Chenn, C. Walsh, 1999, Science.

Ion Channel Functions in Early Brain Development

C. Walsh, Richard S. Smith, 2020, Trends in Neurosciences.

Doublecortin Is Required in Mice for Lamination of the Hippocampus But Not the Neocortex

C. Walsh, J. Corbo, A. Wynshaw-Boris, 2002, The Journal of Neuroscience.

Innovations present in the primate interneuron repertoire

David Kulp, Bernardo Rudy, Qiangge Zhang, 2020, Nature.

Evolution of Osteocrin as an activity-regulated factor in the primate brain

Athar N. Malik, Eric C. Griffith, C. Walsh, 2016, Nature.

Genetics of disorders of cortical development.

Christopher A Walsh, C. Walsh, J. Gaitanis, 2004, Neuroimaging clinics of North America.

Linked-read analysis identifies mutations in single-cell DNA-sequencing data

Lovelace J. Luquette, Michael E. Coulter, C. Walsh, 2019, Nature Genetics.

A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts.

C. Walsh, A. Barkovich, S. Tinschert, 2010, American journal of human genetics.

Broader geographical spectrum of Cohen syndrome due to COH1 mutations

C. Walsh, K. Kosaki, G. Mochida, 2004, Journal of Medical Genetics.

Numb, neurogenesis and epithelial polarity

Seonhee Kim, C. Walsh, 2007, Nature Neuroscience.

Aging and neurodegeneration are associated with increased mutations in single human neurons

Peter J. Park, Minseok Kwon, Thomas W. Chittenden, 2017, Science.

Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation

C. Walsh, D. Wotton, Kenichiro Taniguchi, 2010, Development.

Genomic and phenotypic delineation of congenital microcephaly

C. Walsh, F. Alkuraya, S. Arold, 2018, Genetics in Medicine.

Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2

Stephan J Sanders, Donna M. Martin, D. Ledbetter, 2014, Autism research : official journal of the International Society for Autism Research.

Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms

C. Walsh, N. Šestan, S. Jamuar, 2015, Neuron.

Title: Rates and patterns of clonal oncogenic mutations in the normal human brain

C. Walsh, E. Lee, Junho Kim, 2021 .

Recessive gene disruptions in autism spectrum disorder

M. Daly, C. Freitag, J. Buxbaum, 2019, Nature Genetics.

Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis

C. Walsh, G. Rechavi, A. Simon, 2006, Annals of neurology.

Allelic Diversity in Human Developmental Neurogenetics: Insights into Biology and Disease

C. Walsh, E. Engle, 2010, Neuron.

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.

Josemir W Sander, C. Walsh, P. Striano, 2006, Brain : a journal of neurology.

Genomic variants and variations in malformations of cortical development.

C. Walsh, S. Jamuar, 2015, Pediatric clinics of North America.

Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.

S. Cheung, C. Walsh, Yiping Shen, 2007, Clinical chemistry.

NFIA Haploinsufficiency Is Associated with a CNS Malformation Syndrome and Urinary Tract Defects

C. Walsh, K. Devriendt, J. Gusella, 2007, PLoS genetics.

Sequential phases of cortical specification involve Neurogenin‐dependent and ‐independent pathways

C. Walsh, M. Nieto, C. Schuurmans, 2004, The EMBO journal.

Evolutionary Changes in Transcriptional Regulation: Insights into Human Behavior and Neurological Conditions.

C. Walsh, Ryan N. Doan, Taehwan Shin, 2018, Annual review of neuroscience.

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture

C. Walsh, R. Folkerth, A. Barkovich, 2010, Nature Genetics.

Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy

I. Scheffer, C. Walsh, Bai-Lin Wu, 2012, Epilepsia.

The many faces of filamin: A versatile molecular scaffold for cell motility and signalling

C. Walsh, Yuanyi Feng, 2004, Nature Cell Biology.

METTL23, a transcriptional partner of GABPA, is essential for human cognition.

Michael E. Coulter, C. Walsh, C. Schubert, 2014, Human molecular genetics.

The exon junction complex component Magoh controls brain size by regulating neural stem cell division

C. Walsh, D. Watkins-Chow, W. Pavan, 2010, Nature Neuroscience.

SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic system.

C. Walsh, C. Manzini, G. Rechavi, 2010, American journal of human genetics.

Clonal dispersion and evidence for asymmetric cell division in ferret cortex.

C. Walsh, S. Tavazoie, Christopher A. Walsh, 1997, Development.

De novo and inherited private variants in MAP1B in periventricular nodular heterotopia

C. Walsh, A. Allen, S. Robertson, 2018, PLoS genetics.

ASPM is a major determinant of cerebral cortical size

Alexander F. Markham, Emma Roberts, Christopher A. Walsh, 2002, Nature Genetics.

The Cerebrospinal Fluid Provides a Proliferative Niche for Neural Progenitor Cells

Maria K. Lehtinen, X. Chen, Seonhee Kim, 2011, Neuron.

Microcephaly Gene Links Trithorax and REST/NRSF to Control Neural Stem Cell Proliferation and Differentiation

C. Walsh, J. Golden, H. Samuels, 2012, Cell.

CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development

Athar N. Malik, C. Walsh, L. Zon, 2012, Nature Genetics.

Lis1–Nde1-dependent neuronal fate control determines cerebral cortical size and lamination

C. Walsh, A. Chenn, A. Wynshaw-Boris, 2008, Human molecular genetics.

Genetic Interactions between Doublecortin and Doublecortin-like Kinase in Neuronal Migration and Axon Outgrowth

C. Walsh, J. Corbo, Judy S. H. Liu, 2006, Neuron.

The Apical Complex Couples Cell Fate and Cell Survival to Cerebral Cortical Development

Jarema Malicki, Maria K. Lehtinen, Seonhee Kim, 2010, Neuron.

Focal cortical dysplasia

C. Walsh, A. D’Gama, 2020, Neurodevelopmental Disorders.

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain

Christopher A Walsh, C. Walsh, E. Morrisey, 2003, The Journal of comparative neurology.

Comprehensive identification of somatic nucleotide variants in human brain tissue

Peter J. Park, Jonathan Pevsner, Eduardo Soriano, 2020, bioRxiv.

Somatic mutations in cerebral cortical malformations.

J. Shendure, I. Scheffer, C. Walsh, 2014, The New England journal of medicine.

Neurogenesis at the brain-cerebrospinal fluid interface.

Maria K. Lehtinen, C. Walsh, 2011, Annual review of cell and developmental biology.

Cytoplasmic LEK1 is a regulator of microtubule function through its interaction with the LIS1 pathway.

C. Walsh, D. Bader, Yuanyi Feng, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia.

C. Walsh, R. Folkerth, A. Banham, 2009, Human molecular genetics.

Evidence that APP gene copy number changes reflect recombinant vector contamination

C. Walsh, E. Lee, Michael A. Lodato, 2019, bioRxiv.

Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias.

C. Walsh, G. Mathern, J. Madsen, 2017, Cell reports.

Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex

Peter V. Kharchenko, Phillip A. Sharp, Nobuaki Yoshida, 2016, Cell.

Directed migration of neural stem cells to sites of CNS injury by the stromal cell-derived factor 1α/CXC chemokine receptor 4 pathway

Samia J. Khoury, Yang D. Teng, Richard L. Sidman, 2004, Proceedings of the National Academy of Sciences of the United States of America.

The practice of reading

C. Walsh, D. Alsop, 1999 .

insights into repair mechanisms in multiple sclerosis stem/progenitor cells during demyelination: potential Genetic programs and responses of neural

C. Walsh, M. Nieto, R. Sidman, 2015 .

Comment on "Ongoing Adaptive Evolution of ASPM, a Brain Size Determinant in Homo sapiens"

David Reich, Christopher A Walsh, Pardis C Sabeti, 2007, Science.

Ultraspecific somatic SNV and indel detection in single neurons using primary template-directed amplification

Lovelace J. Luquette, C. Walsh, P. Park, 2021, bioRxiv.

Cerebral cortical neuron diversity and development at single-cell resolution

Christopher A Walsh, C. Walsh, Matthew B. Johnson, 2017, Current Opinion in Neurobiology.

The Genetics of Brain Malformations

C. Walsh, M. C. Manzini, Christopher A. Walsh, 2015 .

Expression of Cux‐1 and Cux‐2 in the subventricular zone and upper layers II–IV of the cerebral cortex

C. Walsh, M. Nieto, S. Khoury, 2004, The Journal of comparative neurology.

Developmental basis for filamin-A-associated myxomatous mitral valve disease.

C. Walsh, R. Levine, R. Markwald, 2012, Cardiovascular research.

Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5

C. Walsh, E. Yang, A. Barkovich, 2020, Neuron.

Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes

Dian Donnai, Graeme C.M. Black, Nicolas Chassaing, 2007, Nature Genetics.

Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome.

S. Gabriel, K. Shianna, C. Walsh, 2012, American journal of human genetics.

Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors

C. Walsh, M. Fleming, M. Harris, 2010, Journal of Cell Science.

Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors

C. Walsh, M. Fleming, M. Harris, 2010, Development.

Patterning of the Dorsal Telencephalon and Cerebral Cortex by a Roof Plate-Lhx2 Pathway

C. Walsh, E. Monuki, F. Porter, 2001, Neuron.

Biallelic Mutations In Human DCC Cause Developmental Split Brain Syndrome

C. Walsh, E. Lein, P. Grant, 2017, Nature Genetics.

Cux‐1 and Cux‐2 control the development of Reelin expressing cortical interneurons

B. Cubelos, Álvaro Sebastián‐Serrano, Seonhee Kim, 2008, Developmental neurobiology.

EMX2‐independent familial schizencephaly: Clinical and genetic analyses

C. Walsh, I. Tietjen, B. Chang, 2005, American journal of medical genetics. Part A.

Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures.

C. Walsh, L. Zon, A. Munnich, 2014, American journal of human genetics.

Disorders of Microtubule Function in Neurons: Imaging Correlates

C. Walsh, A. Barkovich, M. Sahin, 2016, American Journal of Neuroradiology.

Systematic widespread clonal organization in cerebral cortex

C. Walsh, Christopher B. Reid, Ivan Llang, 1995, Neuron.

Molecular genetics of human microcephaly

Christopher A. Walsh, C. Walsh, G. Mochida, 2001, Current opinion in neurology.

Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan.

M. Hurles, C. Walsh, F. Muntoni, 2013, American journal of human genetics.

Congenital Muscular Dystrophy and Hypoglycosylation of a-Dystroglycan

M. Hurles, C. Walsh, F. Muntoni, 2013 .

Accurate detection of mosaic variants in sequencing data without matched controls

Peter J. Park, Minseok Kwon, Isidro Cortés-Ciriano, 2019, Nature Biotechnology.

Ethnically diverse causes of Walker‐Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East

C. Walsh, W. Dobyns, Karen R Schmidt, 2008, Human mutation.

Candidate Gene Sequencing of LHX2, HESX1, and SOX2 in a Large Schizencephaly Cohort

C. Walsh, G. Shaw, A. Barkovich, 2010, American journal of medical genetics. Part A.

POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations.

C. Walsh, T. Yu, A. Rozkalne, 2014, Human molecular genetics.

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex

C. Walsh, P. Grant, Y. Shugart, 2004, Nature Genetics.

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

C. Walsh, P. Grant, Y. Shugart, 2001, Nature Genetics.

A comparative proteomic analysis of human and rat embryonic cerebrospinal fluid.

C. Walsh, S. Gygi, S. Lindsay, 2007, Journal of proteome research.

Control of a neuronal morphology program by an RNA-binding zinc finger protein, Unkempt

C. Walsh, J. Ule, L. Tsai, 2015, Genes & development.

Molecular insights into human brain evolution

C. Walsh, R. Hill, 2005, Nature.

Brain Evolution and Uniqueness in the Human Genome

C. Walsh, J. Amadio, 2006, Cell.

Early role for a Na+,K+-ATPase (ATP1A3) in brain development

C. Walsh, S. Mccarroll, Melissa Goldman, 2021, Proceedings of the National Academy of Sciences.

Mitotic Spindle Regulation by Nde1 Controls Cerebral Cortical Size

C. Walsh, Yuanyi Feng, 2004, Neuron.

Evolutionarily Dynamic Alternative Splicing of GPR56 Regulates Regional Cerebral Cortical Patterning

P. Ellen Grant, Hideyuki Okano, Kiho Im, 2014, Science.

Neocortical neuronal arrangement in Miller Dieker syndrome

C. Walsh, J. Corbo, R. Folkerth, 2006, Acta Neuropathologica.

Reelin binds alpha3beta1 integrin and inhibits neuronal migration.

C. Walsh, E. Anton, E. Olson, 2000, Neuron.

Landmarks of human embryonic development inscribed in somatic mutations

C. Walsh, P. Park, A. Abyzov, 2021, Science.

Genetic and neuroradiological heterogeneity of double cortex syndrome

I. Scheffer, C. Walsh, P. Huttenlocher, 2000, Annals of neurology.

The DCX-domain tandems of doublecortin and doublecortin-like kinase

C. Walsh, J. Otlewski, Z. Dauter, 2003, Nature Structural Biology.

A structural basis for reading fluency: White matter defects in a genetic brain malformation

D Alsop, C. Walsh, Tianming Liu, 2007, Neurology.

Mapping form and function in the human brain: the emerging field of functional neuroimaging in cortical malformations

C. Walsh, B. Chang, 2003, Epilepsy & Behavior.

Sequence analysis of P21-activated kinase 3 (PAK3) in chronic schizophrenia with cognitive impairment

C. Walsh, D. Goff, E. Morrow, 2008, Schizophrenia Research.

Impact of PNKP mutations associated with microcephaly, seizures and developmental delay on enzyme activity and DNA strand break repair

Keith W. Caldecott, Christopher A. Walsh, C. Walsh, 2012, Nucleic acids research.

Brain ventricles as windows into brain development and disease

D. Geschwind, C. Walsh, P. Rakic, 2022, Neuron.

Polymicrogyria is Associated With Pathogenic Variants in PTEN

C. Walsh, S. Srivastava, Ryan N. Doan, 2020, Annals of neurology.

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.

D. Ledbetter, C. Walsh, M. Ross, 1998, Human molecular genetics.

Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7

C. Walsh, M. Davisson, K. Allen, 2002, Mammalian Genome.

The hyh mutation uncovers roles for αSnap in apical protein localization and control of neural cell fate

Seonhee Kim, Christopher A Walsh, Seonhee Kim, 2004, Nature Genetics.

Genetic basis of developmental malformations of the cerebral cortex.

Christopher A Walsh, C. Walsh, G. Mochida, 2004, Archives of neurology.

Clinical Report Periventricular Nodular Heterotopia and Williams Syndrome

C. Walsh, R. J. Ferland, V. Sheen, 2006 .

The Genetics of Primary Microcephaly.

C. Walsh, B. Bae, D. Jayaraman, 2018, Annual review of genomics and human genetics.

Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].

C. Walsh, G. Gascon, F. Alkuraya, 2011, American journal of human genetics.

Bilateral generalized polymicrogyria (BGP)

A J Barkovich, I. Scheffer, C. Walsh, 2004, Neurology.

A mapping label required for normal scale of body representation in the cortex

Ron D. Frostig, John G. Flanagan, Jonas Frisén, 2000, Nature Neuroscience.

X-linked malformations of neuronal migration

D. Ledbetter, C. Walsh, M. Ross, 1996, Neurology.

Patient Mutations in Doublecortin Define a Repeated Tubulin-binding Domain*

C. Walsh, J. Gleeson, J. Bazan, 2000, The Journal of Biological Chemistry.

Microcephalies and DNA Repair

C. Walsh, Edward C. Gilmore, 2008 .

Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication

C. Walsh, N. Krogan, Jeffrey R. Johnson, 2015, eLife.

Protein-truncating mutations in ASPM cause variable reduction in brain size.

C. Walsh, R. Hennekam, C. Woods, 2003, American journal of human genetics.

Periventricular heterotopia: new insights into Ehlers-Danlos syndrome.

C. Walsh, V. Sheen, 2005, Clinical medicine & research.

GPR56 Regulates Pial Basement Membrane Integrity and Cortical Lamination

C. Walsh, R. Hynes, L. Bu, 2008, The Journal of Neuroscience.

Characterization of mutations in the gene doublecortin in patients with double cortex syndrome

I. Scheffer, C. Walsh, G. Holmes, 1999, Annals of neurology.

Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival

E. M. DeGennaro, Kiely N. James, Michael E. Coulter, 2020, Genetics in Medicine.

Bilateral frontoparietal polymicrogyria: Clinical and radiological features in 10 families with linkage to chromosome 16

P Ellen Grant, Thomas Voit, William B Dobyns, 2003, Annals of neurology.

A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features

C. Walsh, P. Bauer, A. Barkovich, 2021, Genetics in Medicine.

What disorders of cortical development tell us about the cortex: one plus one does not always make two.

Christopher A Walsh, C. Walsh, M. C. Manzini, 2011, Current opinion in genetics & development.

Characterization of Rho-GDIγ and Rho-GDIα mRNA in the developing and mature brain with an analysis of mice with targeted deletions of Rho-GDIγ

C. Walsh, B. Lim, R. J. Ferland, 2005, Brain Research.

Characterization of Rho-GDIgamma and Rho-GDIalpha mRNA in the developing and mature brain with an analysis of mice with targeted deletions of Rho-GDIgamma.

C. Walsh, B. Lim, R. J. Ferland, 2005, Brain research.

Reviews-X-linked malformations migration of neuronal

D. Ledbetter, C. Walsh, C. Truwit, 2007 .

Reading and Interpretation

C. Walsh, D. Alsop, 1999 .

Autosomal recessive form of periventricular heterotopia

C. Walsh, Y. Shugart, S. Berkovic, 2003, Neurology.

PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation

Michael E. Coulter, C. Walsh, P. Park, 2017, bioRxiv.

Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing

Lovelace J. Luquette, C. Walsh, P. Park, 2021, Nature neuroscience.

Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals cell type-specific lineage patterns in human brain

Trygve E Bakken, C. Walsh, Jeremy A. Miller, 2020, Proceedings of the National Academy of Sciences.

The polymicrogyria-associated GPR56 promoter preferentially drives gene expression in developing GABAergic neurons in common marmosets

C. Walsh, H. Okano, E. Sasaki, 2020, Scientific Reports.

A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype

Danielle K. Manning, C. Walsh, D. O'Leary, 2011, Neural Development.

A familial syndrome of unilateral polymicrogyria affecting the right hemisphere

C. Walsh, J. Cross, K. Valente, 2006, Neurology.

X-linked female band heterotopia-male lissencephaly syndrome

C. Walsh, G. Schifitto, L. Epstein, 1998, Neurology.

The Epigenetic State of PRDM16-Regulated Enhancers in Radial Glia Controls Cortical Neuron Position

C. Walsh, Matthew B. Johnson, M. Mistry, 2018, Neuron.

Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2

C. Walsh, K. Campbell, L. Morandi, 2011, BMC Research Notes.

The Genetic Basis of Human Cerebral Cortical Malformations

C. Walsh, B. Chang, 2006 .

Evidence of Common Progenitors and Patterns of Dispersion in Rat Striatum and Cerebral Cortex

C. Walsh, C. Reid, 2002, The Journal of Neuroscience.

Local Hosts and Organizing Committee

Lovelace J. Luquette, C. Walsh, P. Park, 2015 .

Role for the Na+/K+ ATPase pump alpha 3 (ATP1A3) subunit in folding and lamination of the human neocortex

C. Walsh, S. Mccarroll, Melissa Goldman, 2020 .

Cerebellar ataxia with progressive improvement.

C. Walsh, J. Tsao, W. Dobyns, 2006, Archives of neurology.

Proto-mapping the areas of cerebral cortex: transcription factors make the grade

C. Walsh, E. Monuki, 2000, Nature Neuroscience.

Somatic mosaicism and neurodevelopmental disease

C. Walsh, A. D’Gama, 2018, Nature Neuroscience.

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21.

C. Walsh, P. Grant, K. Doheny, 2002, American journal of human genetics.

Mutations in ARFGEF 2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex

C. Walsh, P. Grant, Y. Shugart, 2022 .

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact.

Christopher A. Walsh, C. Walsh, S. Shapiro, 2002, Human molecular genetics.

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome

C. Walsh, Ming-Hui Chen, S. Robertson, 2005, Neurology.

Transcription factor Lmo4 defines the shape of functional areas in developing cortices and regulates sensorimotor control.

C. Walsh, J. Visvader, T. Sun, 2009, Developmental biology.

Location of Periventricular Nodular Heterotopia Is Related to the Malformation Phenotype on MRI

C. Walsh, A. Barkovich, A. Poduri, 2013, American Journal of Neuroradiology.

New Genetic Insights into Cerebral Cortical Development

C. Walsh, J. Gleeson, 1997 .

Clonal mixing, clonal restriction, and specification of cell types in the developing rat olfactory bulb

C. Walsh, C. Reid, Ivan Liang,†, 1999, The Journal of comparative neurology.

Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy.

C. Walsh, Ryan N. Doan, J. Partlow, 2017, European journal of medical genetics.

Isolation of cerebrospinal fluid from rodent embryos for use with dissected cerebral cortical explants.

Maria K. Lehtinen, C. Walsh, A. LaMantia, 2013, Journal of visualized experiments : JoVE.

A YAC contig in Xq22.3-q23, from DXS287 to DXS8088, spanning the brain-specific genes doublecortin (DCX) and PAK3.

C. Walsh, J. Gleeson, K. Allen, 1998, Genomics.

Rainer W. Guillery and the genetic analysis of brain development

C. Walsh, 2018, The European journal of neuroscience.

Expanding the clinical spectrum of biallelic ZNF335 variants

C. Walsh, S. Seneca, A. Stergachis, 2018, Clinical genetics.

Response: Filamin A, Periventricular Nodular Heterotopia, and West Syndrome

C. Walsh, A. Sakamoto, R. Hill, 2006 .

Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia

C. Walsh, A. Galaburda, D. Hackney, 2005, Neurology.

Developmental genetic malformations of the cerebral cortex

C. Walsh, V. Sheen, 2003, Current neurology and neuroscience reports.

Corrigendum: Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome

C. Walsh, Y. Shugart, M. Ruvolo, 2004, Nature Genetics.

nonsyndromic mental retardation C2 domains, is involved in autosomal recessive The CC2D1A, a member of a new gene family with

C. Walsh, D. Bercovich, T. Olender, 2005 .

Insights into the gyrification of developing ferret brain by magnetic resonance imaging

Grace Tiao, Jason Neal, Christopher A Walsh, 2007, Journal of anatomy.

Chapter 2 Early development of the cerebral cortex

C. Walsh, C. Reid, 1996 .

A Novel Signaling Mechanism in Brain Development

C. Walsh, X. Piao, 2004, Pediatric Research.

The syndrome of perisylvian polymicrogyria with congenital arthrogryposis

C. Walsh, A. Barkovich, D. Riva, 2010, Brain and Development.

Genetic Changes Shaping the Human Brain

C. Walsh, B. Bae, D. Jayaraman, 2015, Developmental cell.

Recessive gene disruptions in autism spectrum disorder

M. Daly, C. Freitag, J. Buxbaum, 2019, Nature Genetics.

Recent Advances in Understanding the Genetic Architecture of Autism

C. Walsh, Caroline Dias, 2020, Annual Review of Genomics and Human Genetics.

The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles

Maria K. Lehtinen, Michael E. Coulter, D. Haussler, 2018, Cell reports.

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Christopher S. Poultney, Stephan J Sanders, Stephen J. Guter, 2017, Molecular Autism.

Early development of the cerebral cortex.

C. Walsh, C. Reid, 1996, Progress in brain research.

Corrigendum: The hyh mutation uncovers roles for αSnap in apical protein localization and control of neural cell fate

C. Walsh, P. Hanson, K. Marz, 2004, Nature Genetics.

Genes that control the size of the cerebral cortex.

Christopher A Walsh, C. Walsh, Teresa H Chae, 2007, Novartis Foundation symposium.

Rare variant association test in family-based sequencing studies

Seunggeun Lee, Xuefeng Wang, Tianxi Cai, 2016, Briefings Bioinform..

Genomic variants and variations in malformations of cortical development.

C. Walsh, S. Jamuar, 2015, Pediatric clinics of North America.

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21.

C. Walsh, K. Doheny, E. Pugh, 2002, American journal of human genetics.

Rainer W. Guillery and the genetic analysis of brain development

C. Walsh, 2018, The European journal of neuroscience.

Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome.

S. Gabriel, K. Shianna, C. Walsh, 2012, American journal of human genetics.

APP gene copy number changes reflect exogenous contamination

C. Walsh, E. Lee, Gwendolyn E. Kaeser, 2020, Nature.

Linked-read analysis identifies mutations in single-cell DNA-sequencing data

Minseok Kwon, Lovelace J Luquette, Isidro Cortés-Ciriano, 2019, Nature Genetics.

Linked-read analysis identifies mutations in single cell DNA sequencing data

Lovelace J. Luquette, Michael E. Coulter, C. Walsh, 2017, bioRxiv.

Faculty Opinions recommendation of Slit1 and Slit2 cooperate to prevent premature midline crossing of retinal axons in the mouse visual system.

C. Walsh, 2002 .