Christopher A. Walsh
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Christopher A. Walshmedical Degrees
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Neurology
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Christopher A. Walsh's Degrees
- Bachelors Biochemistry University of California, Berkeley
- PhD Biochemistry University of California, Berkeley
- Masters Medicine University of California, San Francisco
Why Is Christopher A. Walsh Influential?
(Suggest an Edit or Addition)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?
Christopher A. Walsh is affiliated with the following schools: