Christopher A. Walsh

Christopher A. Walsh's AcademicInfluence.com Rankings

Medical

#1877

World Rank

#2258

Historical Rank

Neurology

#177

World Rank

#247

Historical Rank

medical Degrees

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Medical

Christopher A. Walsh's Degrees

Bachelors Biochemistry University of California, Berkeley
PhD Biochemistry University of California, Berkeley
Masters Medicine University of California, San Francisco

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Christopher A. Walsh's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Synaptic, transcriptional, and chromatin genes disrupted in autism (2014) (2080)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
Regulation of Cerebral Cortical Size by Control of Cell Cycle Exit in Neural Precursors (2002) (1385)
Association between microdeletion and microduplication at 16p11.2 and autism. (2008) (1338)
Doublecortin Is a Microtubule-Associated Protein and Is Expressed Widely by Migrating Neurons (1999) (1275)
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism (2011) (1218)
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci (2015) (1106)
Directed migration of neural stem cells to sites of CNS injury by the stromal cell-derived factor 1α/CXC chemokine receptor 4 pathway (2004) (1091)
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2018) (1064)
doublecortin , a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein (1998) (1009)
Mutations in filamin 1 Prevent Migration of Cerebral Cortical Neurons in Human Periventricular Heterotopia (1998) (840)
Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry (2008) (738)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. (2002) (665)
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size (2005) (551)
ASPM is a major determinant of cerebral cortical size (2002) (550)
The Cerebrospinal Fluid Provides a Proliferative Niche for Neural Progenitor Cells (2011) (538)
Reelin Binds α3β1 Integrin and Inhibits Neuronal Migration (2000) (537)
Expression of Cux‐1 and Cux‐2 in the subventricular zone and upper layers II–IV of the cerebral cortex (2004) (533)
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations (2000) (528)
Somatic Mutation, Genomic Variation, and Neurological Disease (2013) (495)
G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex (2004) (486)
The many faces of filamin: A versatile molecular scaffold for cell motility and signalling (2004) (481)
Single-Neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain (2012) (480)
PAK3 mutation in nonsyndromic X-linked mental retardation (1998) (465)
Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain (2003) (451)
Aging and neurodegeneration are associated with increased mutations in single human neurons (2017) (425)
Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome (2004) (401)
Using Whole-Exome Sequencing to Identify Inherited Causes of Autism (2013) (397)
Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations (2012) (396)
Sequential phases of cortical specification involve Neurogenin‐dependent and ‐independent pathways (2004) (386)
Common genetic variants, acting additively, are a major source of risk for autism (2012) (372)
POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome (2005) (358)
Early Asymmetry of Gene Transcription in Embryonic Human Left and Right Cerebral Cortex (2005) (356)
Mitotic Spindle Regulation by Nde1 Controls Cerebral Cortical Size (2004) (349)
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. (1998) (345)
Clinical Genetic Testing for Patients With Autism Spectrum Disorders (2010) (337)
Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex (2004) (336)
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations (2001) (333)
Neuronal migration disorders: from genetic diseases to developmental mechanisms (2000) (333)
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations. (2006) (314)
Molecular approaches to brain asymmetry and handedness (2006) (311)
Doublecortin Is Required in Mice for Lamination of the Hippocampus But Not the Neocortex (2002) (303)
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 (2017) (301)
LIS1 Regulates CNS Lamination by Interacting with mNudE, a Central Component of the Centrosome (2000) (298)
Filamin A (FLNA) is required for cell–cell contact in vascular development and cardiac morphogenesis (2006) (298)
Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development (1996) (295)
Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes (2007) (295)
Patterning of the Dorsal Telencephalon and Cerebral Cortex by a Roof Plate-Lhx2 Pathway (2001) (287)
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture (2010) (285)
Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders (2010) (282)
Aberrant Splicing of a Mouse disabled Homolog, mdab1, in the scrambler Mouse (1997) (273)
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. (2001) (273)
Reelin binds alpha3beta1 integrin and inhibits neuronal migration. (2000) (271)
Increased neuronal production, enlarged forebrains and cytoarchitectural distortions in beta-catenin overexpressing transgenic mice. (2003) (271)
Genetic Interactions between Doublecortin and Doublecortin-like Kinase in Neuronal Migration and Axon Outgrowth (2006) (265)
Mutations in PNKP cause microcephaly, seizures and defects in DNA repair (2010) (259)
Cux1 and Cux2 Regulate Dendritic Branching, Spine Morphology, and Synapses of the Upper Layer Neurons of the Cortex (2010) (245)
Systematic widespread clonal organization in cerebral cortex (1995) (241)
Single-cell analysis reveals transcriptional heterogeneity of neural progenitors in human cortex (2015) (234)
X-linked malformations of neuronal migration (1996) (232)
Genome-Wide Detection of Single-Nucleotide and Copy-Number Variations of a Single Human Cell (2012) (228)
Human brain malformations and their lessons for neuronal migration. (2001) (228)
Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain (2014) (224)
GPR56 Regulates Pial Basement Membrane Integrity and Cortical Lamination (2008) (220)
Differences in the gyral pattern distinguish chromosome 17–linked and X-linked lissencephaly (1999) (216)
Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex (2016) (214)
Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors (2010) (213)
Cell Lineage Analysis in Human Brain Using Endogenous Retroelements (2015) (210)
Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior (2016) (207)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
Protein–Protein interactions, cytoskeletal regulation and neuronal migration (2001) (204)
A mapping label required for normal scale of body representation in the cortex (2000) (199)
Building a lineage from single cells: genetic techniques for cell lineage tracking (2017) (196)
DCAMKL1 Encodes a Protein Kinase with Homology to Doublecortin that Regulates Microtubule Polymerization (2000) (195)
Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]. (2011) (194)
Autism and Brain Development (2008) (193)
Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias. (2017) (193)
Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network (2017) (190)
Rates, Distribution, and Implications of Post-zygotic Mosaic Mutations in Autism Spectrum Disorder (2017) (187)
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome (2005) (182)
Accelerated Evolution of the ASPM Gene Controlling Brain Size Begins Prior to Human Brain Expansion (2004) (181)
Protein-truncating mutations in ASPM cause variable reduction in brain size. (2003) (180)
Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism (2012) (180)
The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle protein. (2005) (178)
Molecular genetics of human microcephaly (2001) (177)
Evolutionarily Dynamic Alternative Splicing of GPR56 Regulates Regional Cerebral Cortical Patterning (2014) (177)
The exon junction complex component Magoh controls brain size by regulating neural stem cell division (2010) (171)
Somatic mutations in cerebral cortical malformations. (2014) (171)
The Genetics of Primary Microcephaly. (2018) (170)
Neurogenesis at the brain-cerebrospinal fluid interface. (2011) (169)
Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia. (2009) (168)
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome. (2012) (166)
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome (1999) (165)
The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation (2005) (165)
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan. (2013) (164)
What disorders of cortical development tell us about the cortex: one plus one does not always make two. (2011) (163)
Patient Mutations in Doublecortin Define a Repeated Tubulin-binding Domain* (2000) (159)
Somatic mutations in cerebral cortical malformations. (2014) (158)
The diverse genetic landscape of neurodevelopmental disorders. (2014) (153)
Somatic mosaicism and neurodevelopmental disease (2018) (151)
Genetic Malformations of the Human Cerebral Cortex (1999) (150)
Microcephaly Gene Links Trithorax and REST/NRSF to Control Neural Stem Cell Proliferation and Differentiation (2012) (149)
Both Doublecortin and Doublecortin-Like Kinase Play a Role in Cortical Interneuron Migration (2007) (146)
A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly. (2009) (142)
Innovations present in the primate interneuron repertoire (2020) (140)
Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact. (2002) (140)
Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation. (2000) (140)
Mechanisms of cerebral cortical patterning in mice and humans (2001) (139)
A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity? (2015) (134)
Resolving rates of mutation in the brain using single-neuron genomics (2016) (132)
Smooth, rough and upside-down neocortical development. (2002) (132)
The DCX-domain tandems of doublecortin and doublecortin-like kinase (2003) (128)
The hyh mutation uncovers roles for αSnap in apical protein localization and control of neural cell fate (2004) (124)
COL4A1 Mutations Cause Ocular Dysgenesis, Neuronal Localization Defects, and Myopathy in Mice and Walker-Warburg Syndrome in Humans (2011) (122)
A comparative proteomic analysis of human and rat embryonic cerebrospinal fluid. (2007) (122)
Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes. (2000) (120)
Bilateral frontoparietal polymicrogyria: Clinical and radiological features in 10 families with linkage to chromosome 16 (2003) (120)
Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome. (2008) (120)
Impaired Neuronal Positioning and Dendritogenesis in the Neocortex after Cell-Autonomous Dab1 Suppression (2006) (119)
Disease-associated mutations affect GPR56 protein trafficking and cell surface expression. (2007) (118)
Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy (2012) (117)
Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype (1997) (116)
Cux-2 controls the proliferation of neuronal intermediate precursors of the cortical subventricular zone. (2008) (115)
An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21. (2002) (115)
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis (2006) (114)
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms (2015) (114)
Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia (2005) (112)
Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication (2015) (112)
SLC25A22 is a novel gene for migrating partial seizures in infancy (2013) (112)
Molecular Basis for Specific Regulation of Neuronal Kinesin-3 Motors by Doublecortin Family Proteins (2012) (111)
The Apical Complex Couples Cell Fate and Cell Survival to Cerebral Cortical Development (2010) (110)
Genetic Changes Shaping the Human Brain (2015) (110)
Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures. (2014) (107)
Cortical malformations and epilepsy. (2000) (105)
Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size (2018) (102)
Identification of Neural Outgrowth Genes using Genome-Wide RNAi (2008) (101)
Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate (2016) (100)
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain. (1997) (99)
Callosal agenesis with cyst (2001) (99)
NFIA Haploinsufficiency Is Associated with a CNS Malformation Syndrome and Urinary Tract Defects (2007) (98)
Potential mechanisms of mutations that affect neuronal migration in man and mouse. (2000) (98)
Clonal dispersion and evidence for asymmetric cell division in ferret cortex. (1997) (94)
Evolution of Osteocrin as an activity-regulated factor in the primate brain (2016) (91)
Molecular insights into human brain evolution (2005) (88)
Genetic and neuroradiological heterogeneity of double cortex syndrome (2000) (88)
Insights into the gyrification of developing ferret brain by magnetic resonance imaging (2007) (88)
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts. (2010) (86)
Recessive gene disruptions in autism spectrum disorder (2019) (85)
Autosomal recessive form of periventricular heterotopia (2003) (84)
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development (2012) (83)
Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortex (2002) (82)
Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number (2014) (81)
Lis1–Nde1-dependent neuronal fate control determines cerebral cortical size and lamination (2008) (78)
ASPM mutations identified in patients with primary microcephaly and seizures (2005) (77)
Targeted Disruption of Tgif, the Mouse Ortholog of a Human Holoprosencephaly Gene, Does Not Result in Holoprosencephaly in Mice (2005) (77)
Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous Trait (2013) (76)
Genetic basis of developmental malformations of the cerebral cortex. (2004) (74)
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain. (2015) (73)
Comment on "Ongoing Adaptive Evolution of ASPM, a Brain Size Determinant in Homo sapiens" (2007) (72)
Genomic and phenotypic delineation of congenital microcephaly (2018) (71)
Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance. (2007) (68)
Ethnically diverse causes of Walker‐Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East (2008) (67)
A structural basis for reading fluency: White matter defects in a genetic brain malformation (2007) (66)
CC2D1A Regulates Human Intellectual and Social Function as well as NF-κB Signaling Homeostasis (2014) (65)
The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles (2018) (65)
Linked-read analysis identifies mutations in single-cell DNA-sequencing data (2019) (64)
Mutations in POMT1 are found in a minority of patients with Walker–Warburg syndrome (2005) (63)
Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings (2000) (63)
POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations. (2014) (63)
Developmental basis for filamin-A-associated myxomatous mitral valve disease. (2012) (63)
Impact of PNKP mutations associated with microcephaly, seizures and developmental delay on enzyme activity and DNA strand break repair (2012) (61)
A 2‐Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome (2007) (60)
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21 (2003) (60)
Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2 (2014) (60)
Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation (2010) (59)
Genomic and evolutionary analyses of asymmetrically expressed genes in human fetal left and right cerebral cortex. (2006) (59)
Allelic Diversity in Human Developmental Neurogenetics: Insights into Biology and Disease (2010) (57)
Biallelic Mutations In Human DCC Cause Developmental Split Brain Syndrome (2017) (57)
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk (2018) (55)
Coexistence of widespread clones and large radial clones in early embryonic ferret cortex. (1999) (54)
Periventricular heterotopia and the genetics of neuronal migration in the cerebral cortex. (1999) (53)
Cux‐1 and Cux‐2 control the development of Reelin expressing cortical interneurons (2008) (52)
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus (2004) (51)
Ion Channel Functions in Early Brain Development (2020) (51)
Callosal agenesis with cyst: A better understanding and new classification (2001) (49)
Disorders of Microtubule Function in Neurons: Imaging Correlates (2016) (48)
Cerebral cortical neuron diversity and development at single-cell resolution (2017) (48)
Genes that regulate neuronal migration in the cerebral cortex (1999) (47)
X-linked female band heterotopia-male lissencephaly syndrome (1998) (45)
Transcription factor Lmo4 defines the shape of functional areas in developing cortices and regulates sensorimotor control. (2009) (44)
Loss of PCLO function underlies pontocerebellar hypoplasia type III (2015) (44)
A familial syndrome of unilateral polymicrogyria affecting the right hemisphere (2006) (43)
Periventricular heterotopia: new insights into Ehlers-Danlos syndrome. (2005) (43)
Broader geographical spectrum of Cohen syndrome due to COH1 mutations (2004) (42)
METTL23, a transcriptional partner of GABPA, is essential for human cognition. (2014) (42)
De novo and inherited private variants in MAP1B in periventricular nodular heterotopia (2018) (41)
Innovations in Primate Interneuron Repertoire (2019) (40)
A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype (2011) (40)
Cytoplasmic LEK1 is a regulator of microtubule function through its interaction with the LIS1 pathway. (2005) (40)
Mutations in ARFGEF 2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex (39)
Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia (2006) (38)
Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors (2010) (38)
Cc2d1a Loss of Function Disrupts Functional and Morphological Development in Forebrain Neurons Leading to Cognitive and Social Deficits (2017) (37)
Accurate detection of mosaic variants in sequencing data without matched controls (2019) (37)
Landmarks of human embryonic development inscribed in somatic mutations (2021) (37)
Thoracic aortic aneurysm in patients with loss of function Filamin A mutations: Clinical characterization, genetics, and recommendations (2018) (36)
Evidence of Common Progenitors and Patterns of Dispersion in Rat Striatum and Cerebral Cortex (2002) (35)
New innovations: Therapeutic opportunities for intellectual disabilities (2013) (34)
Developmental and Degenerative Features in a Complicated Spastic Paraplegia (2009) (34)
An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation (2006) (30)
Genome aging: somatic mutation in the brain links age-related decline with disease and nominates pathogenic mechanisms. (2019) (30)
Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome (2017) (30)
Control of a neuronal morphology program by an RNA-binding zinc finger protein, Unkempt (2015) (29)
Large mosaic copy number variations confer autism risk (2020) (29)
Bilateral generalized polymicrogyria (BGP) (2004) (29)
Genetics of neuronal migration in the cerebral cortex. (2000) (29)
Developmental genetic malformations of the cerebral cortex (2003) (29)
Detecting natural selection by empirical comparison to random regions of the genome (2009) (28)
Genomic variants and variations in malformations of cortical development. (2015) (28)
Cryptic t(1;12)(q44;p13.3) translocation in a previously described syndrome with polymicrogyria, segregating as an apparently X‐linked trait (2003) (27)
Genetics of disorders of cortical development. (2004) (27)
Location of Periventricular Nodular Heterotopia Is Related to the Malformation Phenotype on MRI (2013) (26)
SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic system. (2010) (25)
Doublecortin is expressed in articular chondrocytes. (2007) (25)
Clonal mixing, clonal restriction, and specification of cell types in the developing rat olfactory bulb (1999) (24)
Schizencephaly: association with young maternal age, alcohol use, and lack of prenatal care. (2013) (24)
Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene. (2008) (24)
Candidate Gene Sequencing of LHX2, HESX1, and SOX2 in a Large Schizencephaly Cohort (2010) (24)
Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder (2019) (23)
Brain Evolution and Uniqueness in the Human Genome (2006) (23)
FLNA-Related Periventricular Nodular Heterotopia (2015) (22)
Reelin is expressed in the accessory olfactory system, but is not a guidance cue for vomeronasal axons. (2003) (21)
Comprehensive identification of somatic nucleotide variants in human brain tissue (2020) (21)
Recent Advances in Understanding the Genetic Architecture of Autism. (2020) (20)
Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+ (2009) (20)
Neocortical neuronal arrangement in Miller Dieker syndrome (2006) (19)
Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy. (2017) (18)
The syndrome of perisylvian polymicrogyria with congenital arthrogryposis (2010) (18)
EMX2‐independent familial schizencephaly: Clinical and genetic analyses (2005) (18)
A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasia (2007) (18)
Genes that control the size of the cerebral cortex. (2007) (17)
The Epigenetic State of PRDM16-Regulated Enhancers in Radial Glia Controls Cortical Neuron Position (2018) (16)
What Are Mini-Brains? (2013) (16)
PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features (2018) (16)
Somatic Mutation in Pediatric Neurological Diseases. (2018) (16)
SFI1 promotes centriole duplication by recruiting USP9X to stabilize the microcephaly protein STIL (2019) (15)
Numb, neurogenesis and epithelial polarity (2007) (15)
Mapping form and function in the human brain: the emerging field of functional neuroimaging in cortical malformations (2003) (14)
APP gene copy number changes reflect exogenous contamination (2020) (14)
Evolution and Ontogenetic Development of Cortical Structures (2019) (14)
Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals cell type-specific lineage patterns in human brain (2020) (14)
Early role for a Na+,K+-ATPase (ATP1A3) in brain development (2021) (14)
Evolutionary Changes in Transcriptional Regulation: Insights into Human Behavior and Neurological Conditions. (2018) (13)
Brain ventricles as windows into brain development and disease (2022) (13)
A YAC contig in Xq22.3-q23, from DXS287 to DXS8088, spanning the brain-specific genes doublecortin (DCX) and PAK3. (1998) (13)
Ultraspecific somatic SNV and indel detection in single neurons using primary template-directed amplification (2021) (12)
Sequence analysis of P21-activated kinase 3 (PAK3) in chronic schizophrenia with cognitive impairment (2008) (12)
Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5 (2020) (11)
The Landscape of Mutational Mosaicism in Autistic and Normal Human Cerebral Cortex (2020) (11)
Cranking It Up a Notch (1999) (11)
Expanding the clinical spectrum of biallelic ZNF335 variants (2018) (11)
Peter Huttenlocher (1931–2013) (2013) (10)
Isolation of cerebrospinal fluid from rodent embryos for use with dissected cerebral cortical explants. (2013) (10)
Early development of the cerebral cortex. (1996) (10)
PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation (2017) (10)
A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features (2021) (10)
Parallel RNA and DNA analysis after Deep-sequencing (PRDD-seq) reveals cell type specific lineage patterns in human brain (2020) (9)
Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2 (2011) (9)
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 (2005) (9)
MIPP-Seq: ultra-sensitive rapid detection and validation of low-frequency mosaic mutations (2021) (9)
Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival (2020) (9)
Rare variant association test in family-based sequencing studies (2016) (8)
Corrigendum: Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome (2004) (8)
Chapter 2 Early development of the cerebral cortex (1996) (8)
Expanding the Spectrum of Rearrangements Involving Chromosome 19: A Mild Phenotype Associated with a 19p13.12–p13.13 Deletion (2012) (8)
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. (2005) (7)
Cerebellar ataxia with progressive improvement. (2006) (7)
Polymicrogyria is Associated With Pathogenic Variants in PTEN (2020) (7)
Rare genetic causes of lissencephaly may implicate microtubule‐based transport in the pathogenesis of cortical dysplasias (2010) (6)
A Novel Signaling Mechanism in Brain Development (2004) (6)
Proto-mapping the areas of cerebral cortex: transcription factors make the grade (2000) (6)
LISsen up! (1998) (6)
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder (2020) (6)
PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly (2020) (5)
The Genetics of Brain Malformations (2015) (5)
Reelin/Dab1 Signaling in the Developing Cerebral Cortex (2008) (5)
New Genetic Insights into Cerebral Cortical Development (1997) (5)
The polymicrogyria-associated GPR56 promoter preferentially drives gene expression in developing GABAergic neurons in common marmosets (2020) (5)
Growth and Plasticity of Neural Connections (1989) (5)
Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7 (2002) (5)
Genetic Disorders of Cerebral Cortical Development (2013) (4)
Evidence that APP gene copy number changes reflect recombinant vector contamination (2019) (4)
Faculty Opinions recommendation of The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases. (2007) (4)
Reading and Interpretation (1999) (4)
Whole-genome analysis of de novo and polymorphic retrotransposon insertions in Autism Spectrum Disorder (2021) (4)
Somatic copy number variants in neuropsychiatric disorders. (2021) (4)
Somatic Mosaicism and Neurological Diseases (2016) (4)
Making a Notch in the Evolution of the Human Cortex. (2018) (4)
Corrigendum: The hyh mutation uncovers roles for αSnap in apical protein localization and control of neural cell fate (2004) (4)
Abstract P6-04-01: Global analysis of breast cancer metastasis suggests cellular reprogramming is central to the endocrine resistant phenotype. (2012) (4)
Neuroscience in the post-genome era: an overview (2001) (4)
Studies of the candidate genes in X-linked congenital cerebellar hypoplasia (1999) (3)
Multiple Recurrent De Novo Copy Number Variations , Including Duplications of the 7 q 11 . 23 Williams-Beuren Syndrome Region , Are Associated with Autism (2011) (3)
Perspectives: neurobiology. Cranking it up a notch. (1999) (3)
Periventricular heterotopia with complete agenesis of the corpus callosum (2006) (3)
Linked-read analysis identifies mutations in single-cell DNA-sequencing data (2017) (3)
Rainer W. Guillery and the genetic analysis of brain development (2018) (3)
Identifying cell type specific driver genes in autism-associated copy number loci from cerebral organoids (2020) (3)
Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans. (2021) (3)
The practice of reading (1999) (3)
Author response: Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication (2015) (2)
The next generation of teachers: A phenomenological study of brain-based professional development for the new middle school teacher (2010) (2)
The Genetic Basis of Human Cerebral Cortical Malformations (2006) (2)
Cell Fate and Cell Migration in the Developing Cerebral Cortex (1999) (2)
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing (2021) (2)
The Practice of Reading: Interpreting the Novel (1999) (2)
Reply: To PMID 24243345. (2014) (1)
Reading the Self: Beckett’s Trilogy — Molloy; Malone Dies; The Unnamable (1999) (1)
Duplication 2p16 is associated with perisylvian polymicrogyria (2019) (1)
Development of Cerebral Cortex (1943) (1)
Response: Filamin A, Periventricular Nodular Heterotopia, and West Syndrome (2006) (1)
[18] Polymerase chain reaction-based techniques for utilizing retroviruses as cell lineage markers (1995) (1)
Congenital Muscular Dystrophy and Hypoglycosylation of a-Dystroglycan (2013) (1)
Lissencephaly with cerebellar hypoplasia (2016) (1)
Chapter 90 – Autism Spectrum Disorders (2013) (1)
Author Correction: Innovations present in the primate interneuron repertoire (2020) (1)
Erratum: Human mutations in NDE1 cause extreme microcephaly with lissencephaly (The American Journal of Human Genetics (2011) 88 (536-547)) (2011) (1)
The Role of the Reader: Tristram Shandy (1999) (1)
Isolate Populations and Rare Variation in Autism Spectrum Disorders (2011) (1)
Faculty Opinions recommendation of Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex. (2003) (1)
Corrigendum: A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size (2005) (0)
Acute Slices by In Vivo Injection of Sindbis Virus Abundant GFP Expression and LTP in Hippocampal (2015) (0)
Faculty Opinions recommendation of Slit proteins prevent midline crossing and determine the dorsoventral position of major axonal pathways in the mammalian forebrain. (2002) (0)
insights into repair mechanisms in multiple sclerosis stem/progenitor cells during demyelination: potential Genetic programs and responses of neural (2015) (0)
Congenital disorders of cerebral cortical development (2002) (0)
Faculty Opinions recommendation of Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy. (2002) (0)
Homo sapiensa Brain Size Determinant in , ASPMComment on " Ongoing Adaptive Evolution (2008) (0)
microcephaly and seizures mutations identified in patients with primary ASPM (2005) (0)
Table 2. [Nonsyndromic Mendelian Disorders with Polymicrogyria: Radiologic Findings]. (2007) (0)
The Process of Reading: Pride and Prejudice (1999) (0)
BothDoublecortinandDoublecortin-LikeKinasePlayaRole inCorticalInterneuronMigration (2007) (0)
OUTLINE “ Obligatory ” Somatic Mosaic Disorders ? How Do Somatic Mutations Manifest as Neurological Disease ? “ Second Hit ” (2013) (0)
Microcephalies and DNA Repair (2008) (0)
G protein-coupled receptor transcript variants modulate human cerebral cortex patterning (2006) (0)
Figure 3, Neuronal migration signaling pathways (2012) (0)
Refining a locus for pontocerebellar hypoplasia 3; a human genetics linkage inquiry (2007) (0)
Clinical, Radiological and Genetic Results in a Cohort of 50 Patients with Nonsyndromic and Syndromic Polymicrogyria (S25.005) (2013) (0)
Principles of Neural Development by Dale Purves and Jeff W. Lichtman (review) (2015) (0)
EM.P.2.04 Unraveling the genetic complexity of alpha-dystroglycanopathies: Ethnically diverse pathogenic mutations (2009) (0)
Postmodernist Readings: Possession (1999) (0)
Rigor kinesin motor domain with an ordered neck-linker, docked on tubulin dimer, modelled into the 8A cryo-EM map of doublecortin- microtubules decorated with kinesin (2012) (0)
Faculty Opinions recommendation of Conserved and divergent patterns of Reelin expression in the zebrafish central nervous system. (2002) (0)
Table 1. [Molecular Genetic Testing Used in FLNA-Related Periventricular Nodular Heterotopia]. (2015) (0)
Essential roles of a novel zinc finger protein in human cerebral cortical development (2010) (0)
Faculty Opinions recommendation of Area identity shifts in the early cerebral cortex of Emx2-/- mutant mice. (2001) (0)
Faculty Opinions recommendation of Short- and long-range attraction of cortical GABAergic interneurons by neuregulin-1. (2004) (0)
Reply (2014) (0)
Molecular Genetics of Human Developmental Brain Disorders of the Arabian Gulf Region (2009) (0)
Table 3. [Nonsyndromic Mendelian Disorders with Polymicrogyria: Molecular Genetics]. (2007) (0)
Corrigendum: Genome aging: somatic mutation in the brain links age-related decline with disease and nominates pathogenic mechanisms. (2019) (0)
Faculty Opinions recommendation of Par6alpha signaling controls glial-guided neuronal migration. (2004) (0)
Table 1, Lissencephaly genetics (2012) (0)
Bilateral periventricular nodular heterotopiaの1剖検例 (2002) (0)
Cortical development and neuropathology in schizophrenia - Discussion (1995) (0)
Faculty Opinions recommendation of Slit1 and Slit2 cooperate to prevent premature midline crossing of retinal axons in the mouse visual system. (2002) (0)
Focal cortical dysplasia (2020) (0)
Figure 4, Microtubule regulation in neurons (2012) (0)
The handshake hypothesis - General discussion III (1995) (0)
Title: Rates and patterns of clonal oncogenic mutations in the normal human brain (2021) (0)
Figure 1, MRI of lissencephaly caused by microtubule pathway genes (2012) (0)
Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder (2020) (0)
nonsyndromic mental retardation C2 domains, is involved in autosomal recessive The CC2D1A, a member of a new gene family with (2005) (0)
Deconstruction and Reading: Daniel Deronda (1999) (0)
Molecular contributions to cerebral cortical specification - Discussion (1995) (0)
Impaired Viability, Platelet Survival, Morphology and Function in Mice Lacking Filamin A. (2006) (0)
Cover Image, Volume 176A, Number 2, February 2018. (2018) (0)
STRUCTURE OF N-TERMINAL DOUBLECORTIN DOMAIN FROM DCLK: SELENOMETHIONINE LABELED PROTEIN (2003) (0)
Reviews-X-linked malformations migration of neuronal (2007) (0)
Table 1. [Nonsyndromic Mendelian Disorders with Polymicrogyria: Clinical Findings]. (2007) (0)
Local Hosts and Organizing Committee (2015) (0)
Identification of genes for autosomal recessive microcephaly by whole-exome sequencing (2014) (0)
STRUCTURE OF N-TERMINAL DOUBLECORTIN DOMAIN FROM DCLK: WILD TYPE PROTEIN (2003) (0)
Clinical Report Periventricular Nodular Heterotopia and Williams Syndrome (2006) (0)
The Experience of Reading: Great Expectations (1999) (0)
Molecular Biology of the Human Brain (Proceedings of an Upjohn‐UCLA Symposium Held in Keystone, Colorado, April 19‐26, 1987) (1988) (0)
Figure 1. [Anatomic phenotype of PVNH in...]. (2015) (0)
Role for the Na+/K+ ATPase pump alpha 3 (ATP1A3) subunit in folding and lamination of the human neocortex (2020) (0)
Figure 2, Neuronal migration (2012) (0)
Gene Associated with Juvenile Myoclonic Epilepsy (2002) (0)
PATHOGENESIS OF HUMAN CEREBRAL DYSGENESIS: S105 (1997) (0)
Structure of N-terminal domain of human doublecortin (2003) (0)
Human doublecortin N-DC repeat plus linker, and tubulin (2XRP) docked into an 8A cryo-EM map of doublecortin-stabilised microtubules reconstructed in absence of kinesin (2012) (0)
Teleology for tangential migration - General discussion II (1995) (0)
Development (2004) (0)
Reading as Revelation: A Portrait of the Artist as a Young Man (1999) (0)
Promoter-mediated dysregulation of gene expression in autism spectrum disorder (2021) (0)

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What Schools Are Affiliated With Christopher A. Walsh?

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