Daniel Geschwind
#37,369
Most Influential Person Now
American geneticist
Daniel Geschwind's AcademicInfluence.com Rankings
Daniel Geschwindbiology Degrees
Biology
#2846
World Rank
#4448
Historical Rank
#1225
USA Rank
Genetics
#219
World Rank
#265
Historical Rank
#113
USA Rank
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Biology
Daniel Geschwind's Degrees
- Bachelors Biochemistry University of California, Berkeley
Why Is Daniel Geschwind Influential?
(Suggest an Edit or Addition)According to Wikipedia, Daniel H. Geschwind is the Gordon and Virginia MacDonald Distinguished Professor of Human Genetics, Neurology and Psychiatry at the David Geffen School of Medicine at the University of California, Los Angeles . He also directs the UCLA Neurogenetics Program and the UCLA Center for Autism Research and Treatment , and holds the Gordon and Virginia MacDonald Distinguished Chair of Human Genetics there. Since March 1, 2016, he has served as the Senior Associate Dean and Associate Vice Chancellor for Precision Medicine at UCLA. His brother, Michael Geschwind, is also a professor of neurology, and behavioral neurology pioneer Norman Geschwind is his father's first cousin.
Daniel Geschwind'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
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS (2011) (4089)
- Strong Association of De Novo Copy Number Mutations with Autism (2007) (2746)
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
- An anatomically comprehensive atlas of the adult human brain transcriptome (2012) (2002)
- Dentate Granule Cell Neurogenesis Is Increased by Seizures and Contributes to Aberrant Network Reorganization in the Adult Rat Hippocampus (1997) (1918)
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism (2012) (1893)
- Functional impact of global rare copy number variation in autism spectrum disorders (2010) (1891)
- Cancerous stem cells can arise from pediatric brain tumors (2003) (1830)
- Advances in autism genetics: on the threshold of a new neurobiology (2008) (1798)
- Common variants in MS4A4/MS4A6E, CD2uAP, CD33, and EPHA1 are associated with late-onset Alzheimer’s disease (2011) (1656)
- Transcriptomic Analysis of Autistic Brain Reveals Convergent Molecular Pathology (2011) (1601)
- Analysis of shared heritability in common disorders of the brain (2016) (1385)
- Mapping autism risk loci using genetic linkage and chromosomal rearrangements (2007) (1382)
- Autism spectrum disorders: developmental disconnection syndromes (2007) (1321)
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) (1248)
- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism (2011) (1218)
- Identification of common genetic risk variants for autism spectrum disorder (2019) (1140)
- Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (1124)
- Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci (2015) (1106)
- Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (1073)
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2018) (1064)
- Transcriptional Landscape of the Prenatal Human Brain (2014) (1059)
- Functional cortical neurons and astrocytes from human pluripotent stem cells in 3D culture (2015) (1038)
- Common genetic variants on 5p14.1 associate with autism spectrum disorders (2009) (970)
- Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. (1998) (951)
- The UK10K project identifies rare variants in health and disease (2015) (926)
- Neuroprotective effects of brain-derived neurotrophic factor in rodent and primate models of Alzheimer's disease (2009) (882)
- Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism (2013) (862)
- Sex differences in autism spectrum disorders. (2013) (855)
- Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits (2011) (829)
- The Central Nervous System and the Gut Microbiome (2016) (822)
- Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders (2014) (814)
- Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. (2008) (807)
- Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap (2016) (742)
- Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
- Functional organization of the transcriptome in human brain (2008) (718)
- Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease (2017) (693)
- Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder (2018) (687)
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
- A functional genetic link between distinct developmental language disorders. (2008) (662)
- Advancing the understanding of autism disease mechanisms through genetics (2016) (607)
- Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism (2015) (580)
- Comprehensive functional genomic resource and integrative model for the human brain (2018) (575)
- Conservation and evolution of gene coexpression networks in human and chimpanzee brains (2006) (570)
- A genome-wide scan for common alleles affecting risk for autism (2010) (567)
- Functional and Evolutionary Insights into Human Brain Development through Global Transcriptome Analysis (2009) (562)
- Disentangling the heterogeneity of autism spectrum disorder through genetic findings (2014) (554)
- Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice (2019) (545)
- Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. (2008) (516)
- Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism (2016) (490)
- Elevated gene expression levels distinguish human from non-human primate brains (2003) (487)
- A Highly Conserved Program of Neuronal Microexons Is Misregulated in Autistic Brains (2014) (483)
- Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. (1998) (478)
- Human Wild-Type Tau Interacts with wingless Pathway Components and Produces Neurofibrillary Pathology in Drosophila (2002) (477)
- Integrative functional genomic analysis of human brain development and neuropsychiatric risks (2018) (464)
- Mapping the human genetic architecture of COVID-19 (2021) (455)
- Mapping the human genetic architecture of COVID-19 (2021) (455)
- Chromosome conformation elucidates regulatory relationships in developing human brain (2016) (445)
- Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis (2008) (433)
- Cortical Evolution: Judge the Brain by Its Cover (2013) (427)
- Divergence of human and mouse brain transcriptome highlights Alzheimer disease pathways (2010) (422)
- FACS-array profiling of striatal projection neuron subtypes in juvenile and adult mouse brains (2006) (409)
- Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes (2009) (400)
- Genetics of autism spectrum disorders (2011) (387)
- X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment (2008) (386)
- Common genetic variants, acting additively, are a major source of risk for autism (2012) (372)
- Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders (2016) (363)
- Human-Specific Transcriptional Regulation of CNS Development Genes by FOXP2 (2009) (362)
- Gene hunting in autism spectrum disorder: on the path to precision medicine (2015) (362)
- The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery (2016) (360)
- Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis (2004) (359)
- Analysis of oncogenic signaling networks in glioblastoma identifies ASPM as a molecular target (2006) (357)
- Early Asymmetry of Gene Transcription in Embryonic Human Left and Right Cerebral Cortex (2005) (356)
- A Systems Level Analysis of Transcriptional Changes in Alzheimer's Disease and Normal Aging (2008) (350)
- Individual common variants exert weak effects on the risk for autism spectrum disorders (2012) (346)
- Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders (2015) (338)
- A genomewide screen for autism susceptibility loci. (2001) (336)
- A unified genetic theory for sporadic and inherited autism (2007) (335)
- Parallel FoxP1 and FoxP2 Expression in Songbird and Human Brain Predicts Functional Interaction (2004) (334)
- LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia (2007) (334)
- Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights (2016) (327)
- Genetics and genomics of psychiatric disease (2015) (325)
- Autism: Many Genes, Common Pathways? (2008) (325)
- The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions. (2001) (317)
- Altered proliferation and networks in neural cells derived from idiopathic autistic individuals (2016) (313)
- PTEN negatively regulates neural stem cell self-renewal by modulating G0-G1 cell cycle entry. (2006) (309)
- Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis (2012) (308)
- From hematopoiesis to neuropoiesis: Evidence of overlapping genetic programs (2001) (307)
- The PsychENCODE project (2015) (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)
- Using iPS cell-derived neurons to uncover cellular phenotypes associated with Timothy Syndrome (2011) (299)
- Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) (296)
- Strategies for aggregating gene expression data: The collapseRows R function (2011) (294)
- An age-related sprouting transcriptome provides molecular control of axonal sprouting after stroke (2010) (290)
- A Multi-network Approach Identifies Protein-Specific Co-expression in Asymptomatic and Symptomatic Alzheimer's Disease. (2017) (286)
- A genomewide screen of 345 families for autism-susceptibility loci. (2003) (285)
- Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autism (2015) (282)
- Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. (2007) (280)
- Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. (2002) (277)
- Common variants at MS 4 A 4 / MS 4 A 6 E , CD 2 AP , CD 33 and EPHA 1 are associated with late-onset Alzheimer ’ s disease (2011) (274)
- The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic mice (2008) (272)
- Heritability of lobar brain volumes in twins supports genetic models of cerebral laterality and handedness (2002) (270)
- Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain (2011) (270)
- A Systems-Level Analysis of the Peripheral Nerve Intrinsic Axonal Growth Program (2016) (267)
- The Human Brain in a Dish: The Promise of iPSC-Derived Neurons (2011) (267)
- Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways. (2007) (266)
- Network Organization of the Huntingtin Proteomic Interactome in Mammalian Brain (2012) (266)
- Advances in autism. (2009) (260)
- A Genetic Analysis of Neural Progenitor Differentiation (2001) (258)
- A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestation (2019) (255)
- Heterogeneous dysregulation of microRNAs across the autism spectrum (2008) (254)
- Reliability of human 3D cortical organoid generation (2018) (254)
- Altered Functional Connectivity in Frontal Lobe Circuits Is Associated with Variation in the Autism Risk Gene CNTNAP2 (2010) (250)
- Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders (2019) (250)
- Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice (2013) (248)
- Self-Organized Cerebral Organoids with Human-Specific Features Predict Effective Drugs to Combat Zika Virus Infection. (2017) (247)
- High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. (2007) (242)
- Human-Specific Transcriptional Networks in the Brain (2012) (239)
- The Dynamic Landscape of Open Chromatin during Human Cortical Neurogenesis (2018) (238)
- The emerging picture of autism spectrum disorder: genetics and pathology. (2015) (233)
- The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia. (1997) (233)
- Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity (2014) (233)
- Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). (1999) (230)
- Discovery of the first genome-wide significant risk loci for ADHD (2017) (229)
- Multiple chronic pain states are associated with a common amino acid-changing allele in KCNS1. (2010) (229)
- Genome-Wide Detection of Single-Nucleotide and Copy-Number Variations of a Single Human Cell (2012) (228)
- Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks (2019) (227)
- Circuit-wide Transcriptional Profiling Reveals Brain Region-Specific Gene Networks Regulating Depression Susceptibility (2016) (227)
- Diffusion tensor imaging in preclinical and presymptomatic carriers of familial Alzheimer's disease mutations. (2007) (226)
- Identification of Process-Localized mRNAs from Cultured Rodent Hippocampal Neurons (2006) (224)
- HDAC Inhibitors Correct Frataxin Deficiency in a Friedreich Ataxia Mouse Model (2008) (221)
- Astrocyte layers in the mammalian cerebral cortex revealed by a single-cell in situ transcriptomic map (2020) (220)
- Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative (2007) (218)
- Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia. (2014) (216)
- Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export (2015) (214)
- ATF4 is an oxidative stress–inducible, prodeath transcription factor in neurons in vitro and in vivo (2008) (213)
- Human brain evolution: insights from microarrays (2004) (210)
- Histone Acetylome-wide Association Study of Autism Spectrum Disorder (2016) (209)
- Genes and pathways underlying regional and cell type changes in Alzheimer's disease (2013) (208)
- Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases. (2012) (208)
- Inheritance of frontotemporal dementia. (1999) (207)
- Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
- Biochemical markers in persons with preclinical familial Alzheimer disease (2008) (204)
- Neuroscience in the era of functional genomics and systems biology (2009) (203)
- Accelerating axonal growth promotes motor recovery after peripheral nerve injury in mice. (2011) (203)
- Transcriptional Architecture of the Primate Neocortex (2012) (203)
- Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism (2007) (202)
- Specific Functions for ERK/MAPK Signaling during PNS Development (2011) (200)
- Combined Intrinsic and Extrinsic Neuronal Mechanisms Facilitate Bridging Axonal Regeneration One Year after Spinal Cord Injury (2009) (200)
- Lithium regulates adult hippocampal progenitor development through canonical Wnt pathway activation (2008) (200)
- The BRAIN Initiative Cell Census Consortium: Lessons Learned toward Generating a Comprehensive Brain Cell Atlas (2017) (196)
- Gene expression in human brain implicates sexually dimorphic pathways in autism spectrum disorders (2016) (195)
- Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study (2019) (194)
- Clinicopathological correlations in behavioural variant frontotemporal dementia (2017) (193)
- De novo mutations in regulatory elements in neurodevelopmental disorders (2018) (193)
- Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion (2012) (193)
- Genome-wide analyses of human perisylvian cerebral cortical patterning (2007) (189)
- Evidence for sex-specific risk alleles in autism spectrum disorder. (2004) (189)
- Connecting genes to brain in the autism spectrum disorders. (2010) (187)
- A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder (2011) (186)
- Autism genetics: searching for specificity and convergence (2012) (184)
- The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability (2017) (182)
- RBFOX1 regulates both splicing and transcriptional networks in human neuronal development. (2012) (181)
- Neurons show distinctive DNA methylation profile and higher interindividual variations compared with non-neurons. (2011) (181)
- Cytoplasmic Rbfox1 Regulates the Expression of Synaptic and Autism-Related Genes (2016) (178)
- Klinefelter syndrome: Expanding the phenotype and identifying new research directions (2003) (177)
- Inflammatory Mediators Alter the Astrocyte Transcriptome and Calcium Signaling Elicited by Multiple G-Protein-Coupled Receptors (2012) (175)
- Frontotemporal dementia due to C9ORF72 mutations (2012) (173)
- A Quantitative Framework to Evaluate Modeling of Cortical Development by Neural Stem Cells (2014) (171)
- The road to precision psychiatry: translating genetics into disease mechanisms (2016) (171)
- Genetic advances in autism: heterogeneity and convergence on shared pathways. (2009) (170)
- Endogenous Wnt Signaling Maintains Neural Progenitor Cell Potency (2009) (169)
- Subcellular Knockout of Importin β1 Perturbs Axonal Retrograde Signaling (2012) (167)
- Human uniqueness: genome interactions with environment, behaviour and culture (2008) (164)
- Neurobehavioral phenotype of Klinefelter syndrome. (2000) (164)
- Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families. (2016) (164)
- Signaling to Transcription Networks in the Neuronal Retrograde Injury Response (2010) (164)
- Maternal embryonic leucine zipper kinase is a key regulator of the proliferation of malignant brain tumors, including brain tumor stem cells (2008) (160)
- Divergent whole-genome methylation maps of human and chimpanzee brains reveal epigenetic basis of human regulatory evolution. (2012) (160)
- Replication of autism linkage: fine-mapping peak at 17q21. (2005) (158)
- Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders. (2012) (155)
- An evaluation of tyramide signal amplification and archived fixed and frozen tissue in microarray gene expression analysis. (2002) (152)
- Oculomotor phenotypes in autosomal dominant ataxias. (1998) (149)
- Disruption of Astrocyte STAT3 Signaling Decreases Mitochondrial Function and Increases Oxidative Stress In Vitro (2010) (149)
- Maternal embryonic leucine zipper kinase (MELK) regulates multipotent neural progenitor proliferation (2005) (149)
- Endocannabinoid signaling mediates oxytocin-driven social reward (2015) (148)
- Tet3 regulates synaptic transmission and homeostatic plasticity via DNA oxidation and repair (2015) (147)
- A quantitative trait locus analysis of social responsiveness in multiplex autism families. (2007) (147)
- Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts (2012) (147)
- Transcriptional Reprogramming of Distinct Peripheral Sensory Neuron Subtypes after Axonal Injury (2019) (145)
- Neuron-specific signatures in the chromosomal connectome associated with schizophrenia risk (2018) (145)
- Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. (2014) (140)
- Autism recurrence in half siblings: strong support for genetic mechanisms of transmission in ASD (2013) (140)
- A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment (2019) (138)
- Association of the serotonin transporter and receptor gene polymorphisms in neuropsychiatric symptoms in Alzheimer disease. (2004) (137)
- Genome-wide, integrative analysis implicates microRNA dysregulation in autism spectrum disorder (2016) (137)
- Tauopathy with paired helical filaments in an aged chimpanzee (2008) (137)
- From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP‐17) caused by the P301L tau mutation (1999) (136)
- Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families (2006) (136)
- Autism-Associated Promoter Variant in MET Impacts Functional and Structural Brain Networks (2012) (135)
- A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity? (2015) (134)
- TDP-43 frontotemporal lobar degeneration and autoimmune disease (2013) (133)
- Inhibition of transglutaminase 2 mitigates transcriptional dysregulation in models of Huntington disease (2010) (132)
- Mitochondrial dysfunction and immune activation are detectable in early Alzheimer's disease blood. (2012) (132)
- Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion. (2014) (132)
- Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport (2016) (131)
- Tau Phosphorylation, Tangles, and Neurodegeneration The Chicken or the Egg? (2003) (131)
- Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs (2005) (130)
- A Genomic Screen for Modifiers of Tauopathy Identifies Puromycin-Sensitive Aminopeptidase as an Inhibitor of Tau-Induced Neurodegeneration (2006) (130)
- Functional Genomic Analyses Identify Pathways Dysregulated by Progranulin Deficiency, Implicating Wnt Signaling (2011) (128)
- What does CNTNAP2 reveal about autism spectrum disorder? (2012) (126)
- Widespread RNA editing dysregulation in brains from autistic individuals (2018) (126)
- Epidemiology and genetics of frontotemporal dementia/Pick's disease (2003) (125)
- Apolipoprotein E genotype and age-related myelin breakdown in healthy individuals: implications for cognitive decline and dementia. (2006) (125)
- Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification (2013) (124)
- Spinocerebellar ataxia type 6 (1997) (124)
- Neuropsychological profiles of adults with Klinefelter syndrome (2000) (121)
- Dementia and neurodevelopmental predisposition: Cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia (2001) (121)
- Timing and significance of pathological features in C9orf72 expansion-associated frontotemporal dementia. (2016) (120)
- Induced pluripotent stem cell models of progranulin-deficient frontotemporal dementia uncover specific reversible neuronal defects. (2012) (120)
- Proteomic changes in cerebrospinal fluid of presymptomatic and affected persons carrying familial Alzheimer disease mutations. (2012) (120)
- Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms (2019) (120)
- Long Term Maturation of Human Cortical Organoids Matches Key Early Postnatal Transitions (2021) (120)
- Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers (2016) (119)
- The organization of the transcriptional network in specific neuronal classes (2009) (119)
- Early postmitotic neurons transiently express TOAD‐64, a neural specific protein (1995) (119)
- Global analysis of gene expression in neural progenitors reveals specific cell-cycle, signaling, and metabolic networks. (2003) (118)
- Mithramycin Is a Gene-Selective Sp1 Inhibitor That Identifies a Biological Intersection between Cancer and Neurodegeneration (2011) (117)
- Understanding sex bias in autism spectrum disorder (2013) (117)
- Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2017) (115)
- A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism (2012) (114)
- Apolipoprotein E Affects Both Myelin Breakdown and Cognition: Implications for Age-Related Trajectories of Decline Into Dementia (2007) (111)
- Mice, microarrays, and the genetic diversity of the brain. (2000) (108)
- Progranulin mutations as risk factors for Alzheimer disease. (2013) (106)
- Common risk variants identified in autism spectrum disorder (2017) (106)
- Molecular approaches to cerebral laterality: development and neurodegeneration. (2001) (105)
- Cerebellar associative sensory learning defects in five mouse autism models (2015) (104)
- Suberoylanilide Hydroxamic Acid (Vorinostat) Up-regulates Progranulin Transcription (2011) (104)
- Sex-chromosome dosage effects on gene expression in humans (2017) (103)
- Mechanistic Differences in Neuropathic Pain Modalities Revealed by Correlating Behavior with Global Expression Profiling (2018) (101)
- Association and Mutation Analyses of 16p11.2 Autism Candidate Genes (2009) (101)
- Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARγ pathway as a therapeutic target in Friedreich’s ataxia (2009) (100)
- Kinetic Profile of the Transcriptome Changes Induced in the Choroid Plexus by Peripheral Inflammation (2009) (100)
- Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders (2020) (100)
- Regulation of MET by FOXP2, Genes Implicated in Higher Cognitive Dysfunction and Autism Risk (2011) (100)
- Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease) (2004) (99)
- Distinct Subtypes of Behavioral Variant Frontotemporal Dementia Based on Patterns of Network Degeneration. (2016) (99)
- Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature. (2005) (99)
- Microarray Applications in Neuroscience (2001) (99)
- The Disruption of Celf6, a Gene Identified by Translational Profiling of Serotonergic Neurons, Results in Autism-Related Behaviors (2013) (98)
- Conditioning lesions before or after spinal cord injury recruit broad genetic mechanisms that sustain axonal regeneration: Superiority to camp-mediated effects (2012) (98)
- Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR (2014) (98)
- Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseases (2018) (96)
- Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray. (1998) (96)
- Inosine Alters Gene Expression and Axonal Projections in Neurons Contralateral to a Cortical Infarct and Improves Skilled Use of the Impaired Limb (2009) (96)
- Association of GSK3B with Alzheimer disease and frontotemporal dementia. (2008) (96)
- Birdsong decreases protein levels of FoxP2, a molecule required for human speech. (2008) (95)
- Correspondence between Resting-State Activity and Brain Gene Expression (2015) (95)
- Transcriptome signature of the adult mouse choroid plexus (2011) (93)
- Gene expression study on peripheral blood identifies progranulin mutations (2008) (92)
- Microglia-organized scar-free spinal cord repair in neonatal mice (2020) (90)
- Recurrence rates provide evidence for sex-differential, familial genetic liability for autism spectrum disorders in multiplex families and twins (2015) (90)
- The apolipoprotein E ε4 allele is not a significant risk factor for frontotemporal dementia (1998) (89)
- Autism-like phenotype and risk gene-RNA deadenylation by CPEB4 mis-splicing (2018) (88)
- Singing Mice, Songbirds, and More: Models for FOXP2 Function and Dysfunction in Human Speech and Language (2006) (88)
- A blood gene expression marker of early Alzheimer's disease. (2013) (87)
- Microarray and Pathway Analysis Reveal Distinct Mechanisms Underlying Cannabinoid-Mediated Modulation of LPS-Induced Activation of BV-2 Microglial Cells (2013) (86)
- PBK/TOPK, a Proliferating Neural Progenitor-Specific Mitogen-Activated Protein Kinase Kinase (2005) (86)
- C9ORF72 repeat expansions in cases with previously identified pathogenic mutations (2013) (85)
- Timing of the Diagnosis of Autism in African American Children (2020) (85)
- Mapping and characterization of structural variation in 17,795 human genomes (2020) (84)
- Association of common variants in the Joubert syndrome gene (AHI1) with autism. (2008) (82)
- Robust Axonal Regeneration Occurs in the Injured CAST/Ei Mouse CNS (2015) (81)
- Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia. (2018) (81)
- Human iPSC-Derived Neuronal Model of Tau-A152T Frontotemporal Dementia Reveals Tau-Mediated Mechanisms of Neuronal Vulnerability (2016) (81)
- Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice (2012) (81)
- Inosine Augments the Effects of a Nogo Receptor Blocker and of Environmental Enrichment to Restore Skilled Forelimb Use after Stroke (2011) (80)
- INHERITED AND DE NOVO GENETIC RISK FOR AUTISM IMPACTS SHARED BIOLOGICAL NETWORKS (2019) (80)
- A gut-derived metabolite alters brain activity and anxiety behaviour in mice (2022) (79)
- Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome (2014) (79)
- Neuronal defects in a human cellular model of 22q11.2 deletion syndrome (2020) (78)
- Genetics of autism spectrum disorder. (2018) (78)
- Lipocalin 2 is a Choroid Plexus Acute-Phase Protein (2008) (77)
- A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (2019) (77)
- Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous Trait (2013) (76)
- Brief Report: Under-Representation of African Americans in Autism Genetic Research: A Rationale for Inclusion of Subjects Representing Diverse Family Structures (2010) (76)
- Differential transcriptional profiles mediated by exposure to the cannabinoids cannabidiol and Δ9‐tetrahydrocannabinol in BV‐2 microglial cells (2012) (75)
- Prevalent iron metabolism gene variants associated with increased brain ferritin iron in healthy older men. (2010) (74)
- Modeling the functional genomics of autism using human neurons (2010) (74)
- Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers (2015) (74)
- Lipocalin 2 is present in the EAE brain and is modulated by natalizumab (2012) (73)
- A152T tau allele causes neurodegeneration that can be ameliorated in a zebrafish model by autophagy induction (2017) (73)
- A framework for the investigation of rare genetic disorders in neuropsychiatry (2019) (73)
- Detecting network modules in fMRI time series: A weighted network analysis approach (2010) (73)
- Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility (2019) (73)
- Apolipoprotein E genotype is associated with temporal and hippocampal atrophy rates in healthy elderly adults: a tensor-based morphometry study. (2011) (72)
- Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study. (2018) (71)
- Alien hand syndrome (1995) (71)
- A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans (2014) (69)
- “High Density SNP Association Study of the 17q21 Chromosomal Region Linked to Autism Identifies CACNA1G as a Novel Candidate Gene” (2009) (69)
- Functional genomics and biochemical characterization of the C. elegans orthologue of the Machado‐Joseph disease protein ataxin‐3 (2007) (69)
- Genetic architecture of epigenetic and neuronal ageing rates in human brain regions (2017) (68)
- A Systems Level, Functional Genomics Analysis of Chronic Epilepsy (2011) (68)
- Wnt genes define distinct boundaries in the developing human brain: Implications for human forebrain patterning (2004) (68)
- p53 is a central regulator driving neurodegeneration caused by C9orf72 poly(PR) (2021) (68)
- Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts (2016) (67)
- Human Disease Variation in the Light of Population Genomics (2019) (67)
- Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes (2019) (66)
- An Epigenetic Signature in Peripheral Blood Associated with the Haplotype on 17q21.31, a Risk Factor for Neurodegenerative Tauopathy (2014) (66)
- Association between human μ‐opioid receptor gene polymorphism, pain tolerance, and opioid addiction (2003) (65)
- Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex (2017) (64)
- Degradation of tau protein by puromycin-sensitive aminopeptidase in vitro. (2006) (64)
- Distribution of major neurotransmitter receptors in the motor and somatosensory cortex of the rhesus monkey (1989) (63)
- Working memory and relational reasoning in Klinefelter syndrome (2003) (63)
- NitroSynapsin therapy for a mouse MEF2C haploinsufficiency model of human autism (2017) (63)
- Genes for endosomal NHE6 and NHE9 are misregulated in autism brains (2013) (62)
- In vivo cell-autonomous transcriptional abnormalities revealed in mice expressing mutant huntingtin in striatal but not cortical neurons. (2011) (62)
- DNA microarrays: translation of the genome from laboratory to clinic (2003) (62)
- Human ARX gene: genomic characterization and expression. (2002) (62)
- Neural progenitor genes. Germinal zone expression and analysis of genetic overlap in stem cell populations. (2003) (62)
- Methyl‐CpG‐binding protein 2 polymorphisms and vulnerability to autism (2008) (62)
- The choroid plexus response to a repeated peripheral inflammatory stimulus (2009) (61)
- Genomic Profiles of Damage and Protection in Human Intracerebral Hemorrhage (2008) (61)
- Neurons selectively targeted in frontotemporal dementia reveal early stage TDP-43 pathobiology (2018) (61)
- Rare Inherited Variation in Autism: Beginning to See the Forest and a Few Trees (2013) (60)
- Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2 (2014) (60)
- Intellectual disability is associated with increased runs of homozygosity in simplex autism. (2013) (59)
- Language‐related Cntnap2 gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds (2010) (59)
- A gene expression phenotype in lymphocytes from friedreich ataxia patients (2011) (59)
- Patient-Tailored, Connectivity-Based Forecasts of Spreading Brain Atrophy (2019) (59)
- Gene expression profiling of R6/2 transgenic mice with different CAG repeat lengths reveals genes associated with disease onset and progression in Huntington's disease (2011) (59)
- High density SNP association study of a major autism linkage region on chromosome 17. (2007) (59)
- Sharing gene expression data: an array of options (2001) (58)
- Reduced prefrontal synaptic connectivity and disturbed oscillatory population dynamics in the CNTNAP2 model of autism (2018) (58)
- Conservation and divergence of vulnerability and responses to stressors between human and mouse astrocytes (2020) (57)
- Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder (2006) (56)
- Novel Roles for Osteopontin and Clusterin in Peripheral Motor and Sensory Axon Regeneration (2014) (55)
- Genome-Wide Analysis of a Wnt1-Regulated Transcriptional Network Implicates Neurodegenerative Pathways (2011) (55)
- Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk (2018) (55)
- SCA8 repeat expansions in ataxia: A controversial association (2001) (55)
- The choroid plexus transcriptome reveals changes in type I and II interferon responses in a mouse model of Alzheimer’s disease (2015) (54)
- The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism (2014) (54)
- Small Molecule Activation of Adaptive Gene Expression (2008) (54)
- VoICE: A semi-automated pipeline for standardizing vocal analysis across models (2015) (54)
- Tau interactome maps synaptic and mitochondrial processes associated with neurodegeneration (2022) (53)
- Novel tau polymorphisms, tau haplotypes, and splicing in familial and sporadic frontotemporal dementia. (2003) (53)
- Cell Lineage and Regional Identity of Cultured Spinal Cord Neural Stem Cells and Comparison to Brain-Derived Neural Stem Cells (2009) (53)
- Gene expression profiling in frataxin deficient mice: Microarray evidence for significant expression changes without detectable neurodegeneration (2006) (52)
- Social responsiveness, an autism endophenotype: genomewide significant linkage to two regions on chromosome 8. (2015) (52)
- Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases (2018) (52)
- Neurobehavioral and Psychosocial Issues in Klinefelter Syndrome (2004) (51)
- CCDC22: a novel candidate gene for syndromic X-linked intellectual disability (2012) (50)
- Stratification based on language‐related endophenotypes in autism: Attempt to replicate reported linkage (2006) (50)
- Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus (2020) (50)
- Thresholding rules for recovering a sparse signal from microarray experiments. (2002) (50)
- Plasma signaling proteins in persons at genetic risk for Alzheimer disease: influence of APOE genotype. (2012) (49)
- Inducible and reversible phenotypes in a novel mouse model of Friedreich’s Ataxia (2017) (49)
- Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health System (2020) (48)
- Analysis of the immune response to sciatic nerve injury identifies efferocytosis as a key mechanism of nerve debridement (2020) (48)
- Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue (2019) (48)
- Functional neuroimaging provides evidence of anomalous cerebral laterality in adults with Klinefelter's syndrome (2003) (46)
- Molecular markers in CNS stem cell research: hitting a moving target (2001) (46)
- C9orf72 deficiency promotes microglial-mediated synaptic loss in aging and amyloid accumulation (2021) (46)
- Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2. (2014) (45)
- 3D visualization of the regional differences (2015) (45)
- Possible association of the tau H1/H1 genotype with primary progressive aphasia (2003) (44)
- Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism (2019) (44)
- Human Brain Evolution: Harnessing the Genomics (R)evolution to Link Genes, Cognition, and Behavior (2010) (44)
- Clinical trials for neurodevelopmental disorders: At a therapeutic frontier (2016) (44)
- Enhancing the Informativeness and Replicability of Imaging Genomics Studies (2017) (43)
- Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (43)
- The apolipoprotein E epsilon4 allele is not a significant risk factor for frontotemporal dementia. (1998) (42)
- A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders (2020) (42)
- A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy. (2015) (41)
- Molecular Genetics of Neurodegenerative Dementias. (2017) (41)
- Neurodegenerative Disease Phenotypes in Carriers of MAPT p.A152T, A Risk Factor for Frontotemporal Dementia Spectrum Disorders and Alzheimer Disease (2013) (41)
- Neonatal microglia-organized scar-free spinal cord repair (2020) (40)
- Poly(GP), neurofilament and grey matter deficits in C9orf72 expansion carriers (2018) (40)
- Primary brain calcification: an international study reporting novel variants and associated phenotypes (2018) (39)
- Rarity of the Alzheimer disease-protective APP A673T variant in the United States. (2015) (39)
- A Rare Mutation of β1-Adrenergic Receptor Affects Sleep/Wake Behaviors (2019) (39)
- Cell-type specific effects of genetic variation on chromatin accessibility during human neuronal differentiation (2020) (38)
- Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant–Mediated Risk for Neuropsychiatric Disorders (2020) (38)
- Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and Immunosuppression (2020) (37)
- Revealing the brain's molecular architecture. (2018) (37)
- Sneddon's Syndrome Is a Thrombotic Vasculopathy (1995) (37)
- Longitudinal system-based analysis of transcriptional responses to type I interferons. (2009) (36)
- Transcriptome Profiling of Peripheral Blood in 22q11.2 Deletion Syndrome Reveals Functional Pathways Related to Psychosis and Autism Spectrum Disorder (2015) (36)
- Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms (2020) (36)
- Prospective Identification, Isolation, and Profiling of a Telomerase-Expressing Subpopulation of Human Neural Stem Cells, using sox2 Enhancer-Directed Fluorescence-Activated Cell Sorting (2010) (36)
- Molecular stages of rapid and uniform neuralization of human embryonic stem cells (2009) (36)
- Identification of a Hoxd10‐regulated transcriptional network and combinatorial interactions with Hoxa10 during spinal cord development (2004) (36)
- Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex (2018) (36)
- Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxia (1997) (35)
- Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study (2009) (34)
- Additive effects of oxytocin receptor gene polymorphisms on reward circuitry in youth with autism (2017) (34)
- Sumoylated MEF2A Coordinately Eliminates Orphan Presynaptic Sites and Promotes Maturation of Presynaptic Boutons (2013) (34)
- Phosphoserine Phosphatase Is Expressed in the Neural Stem Cell Niche and Regulates Neural Stem and Progenitor Cell Proliferation (2007) (34)
- Cortical and Hippocampal Atrophy in Patients with Autosomal Dominant Familial Alzheimer’s Disease (2011) (33)
- Spatiotemporal dynamics of the postnatal developing primate brain transcriptome (2015) (33)
- Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder (2014) (33)
- Identification of Conserved Proteomic Networks in Neurodegenerative Dementia (2019) (33)
- Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia (2012) (33)
- The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses (2014) (33)
- Sex Differences in Functional Connectivity of the Salience, Default Mode, and Central Executive Networks in Youth with ASD. (2020) (32)
- GENSAT: a genomic resource for neuroscience research (2004) (32)
- Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis (2019) (31)
- Dissecting the molecular basis of human interneuron migration in forebrain assembloids from Timothy syndrome. (2021) (31)
- Effects of risk genes on BOLD activation in presymptomatic carriers of familial Alzheimer's disease mutations during a novelty encoding task. (2011) (30)
- JAKMIP1, a Novel Regulator of Neuronal Translation, Modulates Synaptic Function and Autistic-like Behaviors in Mouse (2015) (29)
- Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders (2021) (28)
- Genetic analysis of anterior posterior expression gradients in the developing mammalian forebrain. (2007) (27)
- Transcriptomic networks implicate neuronal energetic abnormalities in three mouse models harboring autism and schizophrenia-associated mutations (2019) (27)
- QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders (2013) (27)
- Tau Mutations in Frontotemporal Dementia (1999) (27)
- Genetic correlates of phenotypic heterogeneity in autism (2020) (26)
- Atypical Neurogenesis in Induced Pluripotent Stem Cells From Autistic Individuals (2020) (26)
- Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (26)
- Schizophrenia: Genome, Interrupted (2008) (26)
- Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (25)
- Autism: Searching for Coherence (2007) (25)
- Cloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue. (2004) (25)
- Candidate Screening of the TRPC3 Gene in Cerebellar Ataxia (2011) (25)
- Profiling allele specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage (2019) (24)
- Microarrays for the neurosciences : an essential guide (2002) (24)
- Novel candidate blood‐based transcriptional biomarkers of machado‐joseph disease (2015) (24)
- Transcriptomic and Cellular Decoding of Regional Brain Vulnerability to Neurodevelopmental Disorders (2019) (24)
- The SCA12 mutation as a rare cause of spinocerebellar ataxia. (2001) (24)
- Progress in Realizing the Promise of Microarrays in Systems Neurobiology (2005) (24)
- Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia. (2001) (23)
- Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers (2019) (23)
- Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders (2016) (23)
- Subtraction-coupled custom microarray analysis for gene discovery and gene expression studies in the CNS. (2002) (23)
- Preferential tau aggregation in von Economo neurons and fork cells in frontotemporal lobar degeneration with specific MAPT variants (2019) (23)
- Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes (2021) (23)
- Gyrification abnormalities in presymptomatic c9orf72 expansion carriers (2019) (22)
- Genome engineering of isogenic human ES cells to model autism disorders (2015) (22)
- Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity (2020) (22)
- C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia (2012) (22)
- Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2018) (22)
- Functional regulatory variants implicate distinct transcriptional networks in dementia (2021) (22)
- Increased fMRI signal with age in familial Alzheimer's disease mutation carriers (2012) (22)
- DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya Disease. (2021) (21)
- Wnt-pathway activation during the early stage of neurodegeneration in FTDP-17 mice (2009) (21)
- Familial cortical myoclonus with a mutation in NOL3 (2012) (21)
- GENETICS OF AUTISM (2001) (21)
- Alzheimer's disease: From big data to mechanism (2013) (20)
- Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes (2019) (20)
- Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice (2012) (20)
- Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease"). (2007) (20)
- DISC1: A Schizophrenia Gene with Multiple Personalities (2011) (20)
- Evolutionary conservation and divergence of the human brain transcriptome (2021) (19)
- Brain-trait-associated variants impact cell-type-specific gene regulation during neurogenesis. (2021) (19)
- Coexpression network architecture reveals the brain-wide and multiregional basis of disease susceptibility (2021) (19)
- ASD Restricted and Repetitive Behaviors Associated at 17q21.33: Genes Prioritized by Expression in Fetal Brains (2017) (19)
- A biotinylated MutS fusion protein and its use in a rapid mutation screening technique. (1996) (19)
- Genome‐wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy (2019) (19)
- Human in vitro models for understanding mechanisms of autism spectrum disorder (2020) (19)
- Neural responsivity to social rewards in autistic female youth (2020) (18)
- Three decades of ASD genetics: Building a foundation for neurobiological understanding and treatment. (2021) (18)
- Neural responsivity to social rewards in autistic female youth (2020) (18)
- Focusing attention on cognitive impairment in spinocerebellar ataxia. (1999) (18)
- Identification and characterization of novel developmentally regulated proteins in rat spinal cord. (1996) (17)
- Meta-analysis fine-mapping is often miscalibrated at single-variant resolution (2022) (17)
- Genomic medicine enters the neurology clinic (2012) (17)
- Expression patterns of epidermal growth factor receptor and fibroblast growth factor receptor 1 mRNA in fetal human brain (2003) (16)
- Neuroscience: Genes and human brain evolution (2012) (16)
- The Neurogenetics of Atypical Parkinsonian Disorders (2014) (16)
- Apolipoprotein ϵ4 status is associated with behavioral symptoms in nursing home residents with dementia (2009) (16)
- Integrative network analysis reveals biological pathways associated with Williams syndrome (2018) (16)
- Prevalence of spinocerebellar ataxia 36 in a US population (2017) (16)
- Alterations in Retrotransposition, Synaptic Connectivity, and Myelination Implicated by Transcriptomic Changes Following Maternal Immune Activation in Nonhuman Primates (2020) (16)
- Memory performance and fMRI signal in presymptomatic familial Alzheimer's disease (2013) (16)
- Schizophrenia genetics complements its mechanistic understanding (2016) (15)
- Population structure confounds autism genetic classifier (2014) (15)
- Brain calcifications and PCDH12 variants (2017) (15)
- Core transcription programs controlling injury-induced neurodegeneration of retinal ganglion cells (2022) (15)
- Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative (2022) (15)
- A human neuron injury model for molecular studies of axonal regeneration (2010) (14)
- Reliability of human cortical organoid generation (2018) (14)
- Validation of two parent-reported autism spectrum disorders screening tools M-CHAT-R and SCQ in Bamako, Mali (2019) (14)
- Middle-Aged Children of Alzheimer Parents, A Pilot Study: Stable Neurocognitive Performance at 20-Year Follow-up (2005) (14)
- Pick's disease and frontotemporal dementias: Emerging clinical and molecular concepts (1999) (14)
- Spatial fine-mapping for gene-by-environment effects identifies risk hot spots for schizophrenia (2018) (14)
- Association of GSK 3 B With Alzheimer Disease and Frontotemporal Dementia (2008) (14)
- Analysis of Candidate Genes at the IBGC1 Locus Associated with Idiopathic Basal Ganglia Calcification (“Fahr” Disease’) (2007) (13)
- A genome-wide association study for shared risk across major psychiatric disorders in a nation-wide birth cohort implicates fetal neurodevelopment as a key mediator (2017) (13)
- A neurogenetic analysis of female autism (2021) (13)
- Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders (2014) (13)
- Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. (2021) (13)
- Oxytocin normalizes altered circuit connectivity for social rescue of the Cntnap2 knockout mouse (2021) (13)
- Autism Screening and Diagnostic Evaluation: CAN Consensus Statement (1998) (13)
- A neurogenetic analysis of female autism (2021) (13)
- Maternal immune activation during pregnancy alters postnatal brain growth and cognitive development in nonhuman primate offspring. (2021) (13)
- Brain ventricles as windows into brain development and disease (2022) (13)
- Genomic organization, 5' flanking enhancer region, and chromosomal assignment of the cell cycle gene, p55Cdc. (1998) (13)
- Single-cell in situ transcriptomic map of astrocyte cortical layer diversity (2018) (13)
- Brain volumetric deficits in MAPT mutation carriers: a multisite study (2020) (12)
- Molecular alterations in areas generating fast ripples in an animal model of temporal lobe epilepsy (2015) (12)
- Correction: The Autism Related Protein Contactin-Associated Protein-Like 2 (CNTNAP2) Stabilizes New Spines: An In Vivo Mouse Study (2015) (12)
- Identification of Differentially Expressed Proteins in Murine Embryonic and Postnatal Cortical Neural Progenitors (2010) (12)
- Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD (2022) (12)
- Exercise Your Amyloid (2005) (12)
- Transcription factor network analysis identifies REST/NRSF as an intrinsic regulator of CNS regeneration in mice (2020) (12)
- CYFIP1 overexpression increases fear response in mice but does not affect social or repetitive behavioral phenotypes (2019) (12)
- Autism: Family connections (2008) (11)
- Whole genome sequencing in multiplex families reveals novel inherited and de novo genetic risk in autism (2018) (11)
- Ageing-associated myelin dysfunction drives amyloid deposition in mouse models of Alzheimer’s disease (2021) (11)
- Oxytocin for Autism Spectrum Disorder - Down, but Not Out. (2021) (10)
- Retooling spare parts: gene duplication and cognition (2012) (10)
- Microarrays and the microscope: balancing throughput with resolution (2006) (10)
- Gene Expression Analysis of Neural Cells and Tissues Using DNA Microarrays (2008) (10)
- Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (10)
- Technology Insight: querying the genome with microarrays—progress and hope for neurological disease (2006) (10)
- The use of representational difference analysis and cDNA microarrays in neural repair research. (2001) (10)
- Lipocalin 2 is a Choroid Plexus Acute-Phase Protein (2013) (10)
- Correspondence between resting state activity and brain gene expression (2015) (10)
- Commentary: Autism Genetics and Genomics: A Brief Overview and Synthesis (2011) (10)
- Gene co-expression network analysis in human spinal cord highlights mechanisms underlying amyotrophic lateral sclerosis susceptibility (2020) (10)
- Deconstructing language by comparative gene expression: from neurobiology to microarray (2006) (10)
- Dissecting the molecular basis of human interneuron migration in forebrain assembloids from Timothy syndrome (2021) (9)
- Leveraging genomic diversity for discovery in an EHR-linked biobank: the UCLA ATLAS Community Health Initiative (2021) (9)
- Beliefs in vaccine as causes of autism among SPARK cohort caregivers. (2020) (9)
- It Is Time to Take a Stand for Medical Research and Against Terrorism Targeting Medical Scientists (2008) (9)
- Propositional Density and Apolipoprotein E Genotype among Persons at Risk for Familial Alzheimer’s Disease (2011) (8)
- Genome-wide changes in lncRNA, alternative splicing, and cortical patterning in autism (2016) (8)
- Ataxia and calcium channels: what a headache! (2001) (8)
- Out FOXing Parkinson Disease: Where Development Meets Neurodegeneration (2007) (8)
- Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms (2020) (8)
- Right temporal lobe and socioemotional semantics: semantic behavioural variant frontotemporal dementia. (2022) (7)
- Author Correction: Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism (2018) (7)
- Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factors (2021) (7)
- Young‐onset frontotemporal dementia in a homozygous tau R406W mutation carrier (2015) (7)
- A single cell transcriptomic analysis of human neocortical development (2018) (7)
- Atypical neurogenesis and excitatory-inhibitory progenitor generation in induced pluripotent stem cell (iPSC) from autistic individuals (2019) (7)
- Polygenicity in Psychiatry—Like It or Not, We Have to Understand It (2021) (7)
- Associations between patterns in comorbid diagnostic trajectories of individuals with schizophrenia and etiological factors (2021) (7)
- Broad transcriptomic dysregulation across the cerebral cortex in ASD (2020) (7)
- Autism-like phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing (2018) (7)
- Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders (2016) (7)
- De novo mutations in regulatory elements cause neurodevelopmental disorders (2017) (7)
- LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells (2007) (7)
- A comprehensive map of genetic relationships among diagnostic categories based on 48.6 million relative pairs from the Danish genealogy (2022) (6)
- Finding Genes in Spite of Heterogeneity: Endophenotypes, QTL Mapping, and Expression Profiling in Autism (2006) (6)
- Evolutionary Genetics: The human brain – adaptation at many levels (2005) (6)
- Leveraging Genetics and Genomics to Define the Causes of Mental Illness (2015) (6)
- Genetics of Familial Idiopathic Basal Ganglia Calcification (FIBGC) (2003) (6)
- Transcriptional Cartography Integrates Multiscale Biology of the Human Cortex (2023) (6)
- The genetics of cortical organisation and development: a study of 2,347 neuroimaging phenotypes (2022) (6)
- Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder (2021) (5)
- Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism (2016) (5)
- Comprehensive cross-sectional and longitudinal analyses of plasma neurofilament light across FTD spectrum disorders (2022) (5)
- Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts (2023) (5)
- Autism: The Ups and Downs of Neuroligin (2009) (5)
- Microarray platforms: introduction and application to neurobiology. (2004) (5)
- Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer (2022) (5)
- Genetic overlap between educational attainment, schizophrenia and autism (2016) (5)
- Neuronal and glial 3D chromatin architecture illustrates cellular etiology of brain disorders (2020) (5)
- Neurodevelopmental disorders: hope for a new beginning. (2011) (5)
- Shared gene co-expression networks in autism from induced pluripotent stem cell (iPSC) neurons (2018) (5)
- Postnatal immune activation causes social deficits in a mouse model of tuberous sclerosis: Role of microglia and clinical implications (2021) (5)
- The UCLA ATLAS Community Health Initiative: Promoting precision health research in a diverse biobank (2022) (5)
- Understanding the biological basis of psychiatric disease: What’s next? (2022) (5)
- Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree (2021) (5)
- An Integrated, Scalable, Electronic Video Consent Process to Power Precision Health Research: Large, Population-Based, Cohort Implementation and Scalability Study. (2021) (5)
- Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification (2013) (4)
- A neural stem cell paradigm of pediatric hydrocephalus. (2022) (4)
- Genetic control of gene expression and splicing in the developing human brain (2018) (4)
- Abstract 24: Multi-feature ensemble learning on cell-free dna for accurately detecting and locating cancer (2021) (4)
- Mutations in PDYN are not responsible for multiple system atrophy (2013) (4)
- Manifestations of Alzheimer’s disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90 (2022) (4)
- Abnormal sleep physiology in children with 15q11.2-13.1 duplication (Dup15q) syndrome (2021) (4)
- Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative (2022) (4)
- ASLPrep: a platform for processing of arterial spin labeled MRI and quantification of regional brain perfusion (2022) (4)
- Dementia risk genes engage gene networks poised to tune the immune response towards chronic inflammatory states (2019) (4)
- Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic forms of autism in post-mortem human brain tissue (2018) (4)
- Evolving views of human genetic variation and its relationship to neurologic and psychiatric disease. (2018) (4)
- Defining the nature of human pluripotent stem cell-derived interneurons via single-cell analysis (2021) (4)
- Temporal order of clinical and biomarker changes in familial frontotemporal dementia (2022) (4)
- Advances in autism genetics: on the threshold of a new neurobiology (2008) (3)
- Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic Overlap. (2019) (3)
- Genetic influences on cell type specific gene expression and splicing during neurogenesis elucidate regulatory mechanisms of brain traits (2020) (3)
- Corrections to "Robust Axonal Regeneration Occurs in the Injured CAST/Ei Mouse CNS"[Neuron 86, 1215-1227; June 3, 2015] (2016) (3)
- Clinically relevant small-molecule promotes nerve repair and visual function recovery (2022) (3)
- Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARg pathway as a therapeutic target in Friedreich’s ataxia (2009) (3)
- Functional genomics links genetic origins to pathophysiology in neurodegenerative and neuropsychiatric disease. (2020) (3)
- Selective Neuronal Vulnerability in Alzheimer’s Disease: A Modern Holy Grail (2020) (3)
- Large-scale microarray gene expression analysis in discrete electrophysiologically identified neuronal clusters (2004) (3)
- Atypical neurogenesis in induced pluripotent stem cell (iPSC) from autistic individuals (2018) (3)
- Comparative genomics: Grasping human transcriptome evolution: what does it all mean? (2006) (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)
- Quantitative linkage analysis to the autism endophenotype social responsiveness identifies genome-wide significant linkage to two regions on chromosome 8 (2015) (3)
- Polygenic profiles define aspects of clinical heterogeneity in ADHD (2021) (3)
- Early-onset Alzheimer’s disease versus frontotemporal dementia: resolution with genetic diagnoses? (2016) (3)
- Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2018) (3)
- Whole Genome Linkage and Association Analyses (2011) (3)
- Gene expression shifts in yellow-bellied marmots prior to natal dispersal. (2018) (3)
- Author Correction: Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders (2020) (3)
- Robust Axonal Regeneration Occurs in the Injured CAST/Ei Mouse CNS (2016) (3)
- Genes and the long and winding road to cortical construction and cognition (2010) (2)
- Elk-1 regulates retinal ganglion cell axon regeneration after injury (2022) (2)
- M11 ASSESSING THE ROLE OF LONG NONCODING RNAS (LNCRNAS) IN AUTISM SPECTRUM DISORDERS (2019) (2)
- Neurodegenerative Dementias: Connecting Psychiatry and Neurology Through a Shared Neurobiology (2014) (2)
- Sequence and characterization of a developmentally regulated protein during early corticogenesis in the rat (1992) (2)
- P300 promotes tumor recurrence by regulating radiation-induced conversion of glioma stem cells to vascular-like cells (2022) (2)
- SA75LARGE-SCALE TRANSCRIPTOME-WIDE CHARACTERIZATION OF ASD, SCHIZOPHRENIA, AND BIPOLAR DISORDER (2019) (2)
- Erratum: Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice (Molecular Psychiatry (2012) 17, (62-70) DOI:10.1038/mp.2010.115) (2012) (2)
- Changes in protein expression during neural development analyzed by two‐dimensional gel electrophoresis (1996) (2)
- Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (2)
- The Genetics-Driven Revival in Neuropsychiatric Drug Development (2016) (2)
- Voting-based segmentation of overlapping nuclei in clarity images (2018) (2)
- Biological Psychiatry and Biological Psychiatry: Cognitive Neuroscience and Neuroimaging Adopt Neuroscience-Based Nomenclature (2016) (2)
- Alterations in retrotransposition, synaptic connectivity, and myelination implicated by transcriptomic changes following maternal immune activation in non-human primates (2020) (2)
- Transcriptional Changes in Alzheimer's Disease (2010) (2)
- Neuronal subpopulations and genetic background in tauopathies: A catch 22 story? Commentary (2001) (2)
- Rearrangements in the 22q11.2 Region: Prevalence and Population-Based Risk for Neuropsychiatric and Developmental Disorders (2019) (2)
- Founders and CAG repeats (1999) (2)
- Phenotypic Analysis, Magnetic Resonance Imaging Findings, and Review of the Literature (2016) (2)
- Health facility-based prevalence and potential risk factors of autism spectrum disorders in Mali (2019) (2)
- The vaccine-autism controversy (2009) (2)
- Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 CNV Mediated Risk for Neuropsychiatric Disorders (2019) (2)
- Conference Report: Psychiatric Genomics Consortium Meeting: Pathways to Drugs, London, March 2017 (2018) (2)
- Biological Psychiatry and Biological Psychiatry: Cognitive Neuroscience and Neuroimaging Adopt Neuroscience-Based Nomenclature. (2016) (2)
- Title Inhibition of transglutaminase 2 mitigates transcriptional dysregulation in models of Huntington ' s disease (2010) (1)
- Beyond The Gene List : Using Bioinformatics To Make Sense Out Of Array Data (2001) (1)
- Primary brain calcification: an international study reporting novel variants and associated phenotypes (2018) (1)
- Expression and network analysis of Illumina microarray data (2009) (1)
- Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative (2022) (1)
- Challenges and Opportunities for Precision Medicine in Neurodevelopmental Disorders. (2022) (1)
- Tau interactome mapping reveals dynamic processes in synapses and mitochondria associated with neurodegenerative disease (2021) (1)
- The injured sciatic nerve atlas (iSNAT), insights into the cellular and molecular basis of neural tissue degeneration and regeneration (2022) (1)
- Spatial gene-by-environment mapping for schizophrenia reveals locale of upbringing effects beyond urban-rural differences (2018) (1)
- From genes to neurons to brain (2006) (1)
- Pathway-based Approach Reveals Differential Sensitivity to E2F1 Inhibition in Glioblastoma (2022) (1)
- Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2019) (1)
- Widespread RNA editing dysregulation in Autism Spectrum Disorders (2018) (1)
- Methods for culturing adult CNS neurons reveal a CNS conditioning effect (2022) (1)
- Impact of autism genetic risk on brain connectivity: a mechanism for the female protective effect. (2021) (1)
- 238. Transcriptome-Wide Isoform-Level Dysregulation in Schizophrenia, Autism, and Bipolar Disorder (2019) (1)
- M52 CONVERGENT METHYLOMIC SIGNATURES BETWEEN AUTISM ASSOCIATED WITH DUPLICATIONS OF CHROMOSOME 15Q AND IDIOPATHIC AUTISM (2019) (1)
- AMultiancestral Genome-Wide Exome Array Study of Alzheimer Disease , Frontotemporal Dementia , and Progressive Supranuclear Palsy (2015) (1)
- O3-06-06 [18F]FDDNP-PET imaging in persons at-risk for familial AD (2006) (1)
- Gene Networks in Neuropsychiatric Disease (2016) (1)
- MicroRNA-eQTLs in the developing human neocortex link miR-4707-3p expression to brain size (2023) (1)
- Autism genetics: searching for specificity and convergence (2012) (1)
- IC-P-090 Elevated hippocampal myo-inositol in subjects with or at-risk for familial AD (2006) (1)
- Molecular Genetics and Inherited Ataxias: Redefining Phenotypes and Pathogenesis (2000) (1)
- Microenvironment Impacts the Molecular Architecture and Interactivity of Resident Cells in Marmoset Brain (2021) (1)
- Neurogenetic Profiles of Risk and Resilience in Female Autism (2020) (1)
- Comment on: What genes are differentially expressed in individuals with schizophrenia? A systematic review (2022) (1)
- Aberrant gliogenesis and excitation in MEF2C autism patient hiPSC-neurons and cerebral organoids (2020) (1)
- Neuroscience and the Genomic Revolution: An Overview (2013) (1)
- Gene Expression in the Evolution of the Human Brain (2009) (1)
- Genes and pathways underlying regional and cell type changes in Alzheimer's disease (2013) (1)
- Author response: Inducible and reversible phenotypes in a novel mouse model of Friedreich’s Ataxia (2017) (1)
- Sex Chromosome Aneuploidies are Underdiagnosed and Associated with Increased Risk of Mental Disorders (2022) (1)
- Psychiatric and Medical Profiles of Autistic Adults in the SPARK Cohort (2020) (1)
- Erratum: What does CNTNAP2 reveal about autism spectrum disorder?: [Trends in Molecular Medicine 18 (2012), 156–163] (2012) (1)
- - Van Zeeland CNTNAP 2 with Variation in the Autism Risk Gene Altered Functional Connectivity in Frontal Lobe Circuits Is Associated (2010) (1)
- Maternal immune activation during pregnancy alters early neurobehavioral development in nonhuman primate offspring (2020) (1)
- Integrin-driven Axon Regeneration in the Spinal Cord Activates a Distinctive CNS Regeneration Program (2021) (1)
- The Contributions of Rare Inherited and Polygenic Risk to ASD in Multiplex Families (2022) (1)
- Screening for axon regeneration promoting compounds with human iPSC-derived motor neurons (2021) (1)
- Widespread RNA editing dysregulation in brains from autistic individuals (2018) (1)
- Multiplexed functional genomic assays to decipher the noncoding genome. (2022) (1)
- 374. Circuit-Wide Transcriptional Profiling Reveals Region Specific Gene Co-Expression Networks Regulating Depression Susceptibility (2017) (1)
- Developmental disorders. (2015) (1)
- Corrigendum (1990) (0)
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- Radiation-reprogrammed glioma stem cells generate vascular-like cells to build a trophic niche driving tumor recurrence (2021) (0)
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- Correction (2002) (0)
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- A framework for the investigation of rare genetic disorders in neuropsychiatry (2019) (0)
- Editorial Board (2010) (0)
- Editorial Board (2014) (0)
- Evolutionary conservation and divergence of the human brain transcriptome (2021) (0)
- Table 3. [PDGFRB Pathogenic Allelic Variants Discussed in This GeneReview]. (2014) (0)
- IC-P3-197: Apolipoprotein genotype predicts rate of brain atrophy in healthy elderly adults: A tensor-based morphometry study (2008) (0)
- FOXP2 gene and human language (2011) (0)
- Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus (2020) (0)
- Editorial Board (2011) (0)
- Editorial Board (2011) (0)
- Extraordinary Variations of the Human Mind: Lessons for Anthropogeny Glossary (2017) (0)
- Handedness and Cerebral Laterality (2014) (0)
- Editorial Board (2010) (0)
- Editorial Board (2014) (0)
- IC-P-069 Decreased fractional anisotropy in the fornix of presymptomatic carriers of FAD mutations (2006) (0)
- Increased fMRI Activity with Age in Left Temporal Lobe of Familial Alzheimer's Disease Mutation Carriers (2010) (0)
- 1451 GENOME-WIDE EXPRESSION PROFILING OF CASTRATION-RESISTANT PROSTATE CANCER XENOGRAFTS IN THE BONE-NICHE REVEALED UP-REGULATION OF THE ANTI-APOPTOSIS GENE, YWHAZ, A NETWORK MODULE HUB GENE (2011) (0)
- Presymptomatic and symptomatic MAPT mutation carriers feature functional connectivity alterations (2021) (0)
- Multiple sclerosis and iron homeostasis (2012) (0)
- Gyrification abnormalities in presymptomatic expansion carriers. (2019) (0)
- A genome-wide association study for shared risk across major psychiatric disorders in a nation- wide birth cohort implicates fetal neurodevelopment as a key mediator Authors (2017) (0)
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- Single Cell Sequencing and Integrative Analysis of Epigenetic and Transcriptomic Profiling in ASD (2019) (0)
- Functional genomic investigation of human brain evolution (2010) (0)
- S2-03-04: Role of aminopeptidase NPPS in tauopathy (2008) (0)
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- Commentary (2001) (0)
- and pathway analysis reveal distinct mechanisms underlying cannabinoid-mediated modulation of LPS-induced activation of BV-2 microglial cells. (2013) (0)
- Gearing up for the future: Exploring facilitators and barriers to inform clinical trial design in frontotemporal lobar degeneration (2021) (0)
- Editorial Board (2010) (0)
- Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease (2018) (0)
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- ASPM Analysis of oncogenic signaling networks in glioblastoma identifies (2006) (0)
- WARFARIN IN SNEDDON'S SYNDROME. AUTHORS' REPLY (1996) (0)
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- 38. COMMON AND RARE GENETIC RISK FACTORS FOR SCHIZOPHRENIA AT CHROMOSOME 22Q INDUCE CONVERGENT, DISPERSED CHANGES IN GENE EXPRESSION (2022) (0)
- Editorial Board (2014) (0)
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- Editorial overview: Neurodevelopment Diseases and Neurogenetics pivot towards mechanisms and therapies. (2020) (0)
- Faculty Opinions recommendation of Early frontotemporal dementia targets neurons unique to apes and humans. (2007) (0)
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- Autism: from gene to brain to behavior (2008) (0)
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- 2 REGIONAL VARIATION IN TRANSCRIPTIONAL DYSREGULATION AND PATTERNING IN POSTMORTEM CEREBRAL CORTEX IN ASD (2019) (0)
- Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights (2018) (0)
- Increased Striatal Presynaptic Dopamine in a Nonhuman Primate Model of Maternal Immune Activation: A Longitudinal Neurodevelopmental Positron Emission Tomography Study With Implications for Schizophrenia. (2022) (0)
- Associations of psychiatric disorders with sex chromosome aneuploidies in the Danish iPSYCH2015 dataset: a case-cohort study. (2023) (0)
- Correction: Sleiman et al., Mithramycin Is a Gene-Selective Sp1 Inhibitor That Identifies a Biological Intersection between Cancer and Neurodegeneration (2012) (0)
- P2-164 Biochemical markers in blood and cerebrospinal fluid of persons with or at-risk for familial AD (2006) (0)
- Prevalence, Timing, and Network Localization of Emergent Visual Creativity in Frontotemporal Dementia (2023) (0)
- Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome (2014) (0)
- Tuberous sclerosis complex is associated with a novel human tauopathy (2022) (0)
- Genetics of cognitive disorders (2005) (0)
- UNDERSTANDING SINGLE CELL FUNCTIONAL GENOMICS FOR NEUROPSYCHIATRIC DISORDERS (2019) (0)
- Title Integrative network analysis reveals biological pathwaysassociated with Williams syndrome (2019) (0)
- alterations in areas generating fast ripples in an animal model of temporal lobe epilepsy (2015) (0)
- UK 10 K Consortium (2019) (0)
- is an oxidative stress-inducible, prodeath transcription factor in neurons in vitro and in vivo. (2008) (0)
- Rare Genetic Risk in Progressive Supranuclear Palsy (2022) (0)
- Title Human iPSC-Derived Neuronal Model of TauA 152 T Frontotemporal Dementia Reveals Tau-Mediated Mechanisms of Neuronal Vulnerability Permalink (0)
- The OMICs: Applications in Neuroscience (2013) (0)
- NEURODEVELOPMENTAL DIFFERENCES AND ENVIRONMENTAL INSULTS INVERSELY CORRELATE WITH AGE OF ONSET IN ALZHEIMER’S DISEASE (2019) (0)
- Left-handedness, learning disability, autoimmune disease, and seizure history influence age at onset and phenotypical targeting of Alzheimer's disease (2022) (0)
- Editorial Board (2010) (0)
- Diagnostic value of plasma P‐tau217 in frontotemporal dementia spectrum disorders (2021) (0)
- Neuron Reviewers (2002) (0)
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- Principles of Psychiatric Genetics: Autism and autism spectrum disorders (2012) (0)
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- Role of tau in non-familial dementia (2000) (0)
- Right Anterior Temporal Degeneration, Emotions, and Loss of Nonverbal Semantics: Guidelines for Diagnosis of the Emotional Semantic Variant Frontotemporal Dementia (2021) (0)
- Editorial Board (2009) (0)
- Growth factor gene delivery for Alzheimer's disease: from animal models to clinical trials (2009) (0)
- Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex (2018) (0)
- Transcriptional networks predating cognition-associated pyramidal lineages are restructured by erythropoietin (2023) (0)
- Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility (2019) (0)
- Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study (2020) (0)
- available empirical evidence and give specific recommendations for the identification of children with autism Target Population Infants and children Interventions and Practices Considered Developmental Surveillance and Screening : 1 . Developmental surveillance at all well-child visits from infancy (0)
- Inflammation Altered Iron Metabolism Is Part of the Choroid Plexus Response to Peripheral (2009) (0)
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- , Daniel Required for Human Speech Birdsong Decreases Protein Levels of FoxP 2 , a Molecule (2008) (0)
- 25. Neurogenetics of FTD—recent developments (2000) (0)
- Reply from the Authors (1996) (0)
- Core transcription programs controlling injury-induced neurodegeneration of retinal ganglion cells (2023) (0)
- T55SYNAPTIC AND GENE REGULATORY MECHANISMS IN SCHIZOPHRENIA, AUTISM, AND 22Q11.2 CNV MEDIATED RISK FOR NEUROPSYCHIATRIC DISORDERS (2019) (0)
- Editorial Board (2012) (0)
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- Neural Correlates of Reward Processing are Modulated by CNTNAP-2 Genotype in Children with and without Autism (2009) (0)
- No Evidence to Suggest that the Use of Acetylcholinesterase Inhibitors Confounds the Results of Two Blood-Based Biomarker Studies in Alzheimer's Disease. (2015) (0)
- Editorial Board (2010) (0)
- Editorial Board (2014) (0)
- Table 2. [SLC20A2 Pathogenic Allelic Variants Discussed in This GeneReview]. (2014) (0)
- Complement and NfL associations with brain structure and functional connectivity alterations in presymptomatic and symptomatic GRN mutation carriers (2021) (0)
- Editorial Board (2009) (0)
- 196 Multi-omic Convergence of Human Craniosynostosis Genes Within a Developmental Bone-Dura-Brain Nexus (2022) (0)
- Genetic effects on brain traits impact cell-type specific gene regulation during neurogenesis (2021) (0)
- Editorial Board (2011) (0)
- Single-cell analysis characterizes non-enhancing region of recurrent high-grade glioma (2022) (0)
- Editorial Board (2012) (0)
- A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment (2019) (0)
- Editorial Board (2013) (0)
- 96. Genetic and Functional Genomic Investigation of Neuropsychiatric Disorders (2018) (0)
- Title Human-Specific Transcriptional Networks in the Brain Permalink (0)
- Cross-ancestry, cell-type-informed atlas of gene, isoform, and splicing regulation in the developing human brain (2023) (0)
- New Clues to Autism (2006) (0)
- Editorial Board (2016) (0)
- Linear discriminant analysis of phenotypic data for classifying autism spectrum disorder by diagnosis and sex (2022) (0)
- analyses of exonic number variants in a family-based study point to novel autism susceptibility genes. (2009) (0)
- Editorial Board (2011) (0)
- STEM-05. SINGLE CELL SEQUENCING CHARACTERIZES SPATIAL AND TEMPORAL RELATIONSHIPS OF ENHANCING AND NON-ENHANCING REGIONS IN HIGH-GRADE GLIOMA (2020) (0)
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- Protein co-expression network analysis in Alzheimer’s disease (2015) (0)
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- Astrocyte layers in the mammalian cerebral cortex revealed by a single-cell in situ transcriptomic map (2020) (0)
- Global changes in patterning, splicing and primate specific lncRNAs in autism brain (2016) (0)
- Editorial Board (2010) (0)
- The impact of ApoE alleles on age-related myelin breakdown (2005) (0)
- Genomics, Proteomics, and Neurology (2005) (0)
- Title Inducible and reversible phenotypes in a novel mouse model of Friedreich ' s Ataxia (2018) (0)
- Table 1. [Summary of Molecular Genetic Testing Used in PFBC]. (2014) (0)
- Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia (2018) (0)
- Senescent Schwann cells induced by aging and chronic denervation impair axonal regeneration after peripheral nerve injury (2023) (0)
- Spatial fine-mapping for gene-by-environment effects identifies risk hot spots for schizophrenia (2018) (0)
- Mapping and characterization of structural variation in 17,795 human genomes (2020) (0)
- Editorial Board (2016) (0)
- An Intermittent Fasting Mimetic Drives Plasticity Via an Adaptive ER Stress-ATF4 Pathwayand Elicits Stroke Recovery and Alzheimer's Resilience (2022) (0)
- Profiling of Peripheral Blood in Deletion Syndrome Reveals Functional Pathways Related to Psychosis and Autism Spectrum Disorder. (2015) (0)
- PL.01.01 Functional genomic and transcriptional networks in autism spectrum disorder (ASD) (2016) (0)
- 28 GENETIC VARIANTS AFFECTING CHROMATIN ACCESSIBILITY DURING HUMAN NEURONAL DIFFERENTIATION (2019) (0)
- APOE genotype differences in plasma protein levels in young and elderly cohorts (2011) (0)
- Editorial Board (2013) (0)
- Knockdown of CNTNAP2A causes morphological and behavioural changes in zebrafish (2010) (0)
- 804: WEIGHTED GENE COEXPRESSION NETWORK ANALYSIS OF THE GUT-BRAIN AXIS TRANSCRIPTOME SUPPORTS THE PRESENCE OF INDEPENDENT PATHOPHYSIOLOGY IN THE GUT AND THE BRAIN OF A MOUSE MODEL OF PARKINSON DISEASE. (2022) (0)
- Editorial Board (2015) (0)
- An Integrated, Scalable, Electronic Video Consent Process to Power Precision Health Research: Large, Population-Based, Cohort Implementation and Scalability Study (Preprint) (2021) (0)
- Presentation Title: Neural stem cells, brain tumors, and brain tumor stem cells (2008) (0)
- Use Of Weighted Gene Coexpression Network Analysis To Identify Connectivity Between Gut And Brain Gene Expression (2022) (0)
- Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2017) (0)
- Microglia-organized scar-free spinal cord repair in neonatal mice (2020) (0)
- Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2018) (0)
- Editorial Board (2016) (0)
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) (0)
- Identification of common genetic risk variants for autism spectrum disorder (2019) (0)
- Methylation risk scores are associated with a collection of phenotypes within electronic health record systems (2022) (0)
- Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) (0)
- 3D Genome Structure and Epigenetic Transcription Regulation in Pediatric High-Grade Glioma (2022) (0)
- Editorial Board (2016) (0)
- Clinical Issues: Migraine Biomarkers, BP and Recurrent ICH, and Autism Genetics (2015) (0)
- Editorial Board (2008) (0)
- Effects of HDAC inhibitor 106 on frataxin mRNA and protein levels and on histone acetylation in KIKI mice. (2008) (0)
- Editorial Board (2011) (0)
- Preferential tau aggregation in von Economo neurons and fork cells in frontotemporal lobar degeneration with specific MAPT variants (2019) (0)
- Preface: Lars Gustafson, Lund; Arne Brun, Lund (1999) (0)
- Restorative effects of BDNF gene delivery into entorhinal cortex in APP transgenic mice (2009) (0)
- Editorial Board (2015) (0)
- Cannabidiol effects on mRNA levels and signaling pathways in MOG-35–55 activated encephalitogenic T cells (2014) (0)
- A Rare Mutation of bAdr 1 energic Receptor Affects Sleep / Wake Behaviors Highlights (2019) (0)
- Editorial Board (2016) (0)
- Exome Sequencing Improves Clinical Diagnosis of Sporadic or Familial Cerebellar Ataxia (S32.003) (2015) (0)
- Radiation-induced reprogramming drives glioma vascular transdifferentiation and tumor recurrence (2021) (0)
- Neuronal protein interaction networks in autism spectrum disorder (2023) (0)
- Editorial Board (2014) (0)
- Editorial Board (2014) (0)
- Case Report: Novel CSF1R Variant in a Patient With Behavioral Variant Frontotemporal Dementia Syndrome With Prodromal Repetitive Scratching Behavior (2022) (0)
- Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative (2022) (0)
- Editorial Board (2012) (0)
- Editorial Board (2009) (0)
- Editorial Board (2008) (0)
- Transcriptomic architecture of nuclei in the marmoset CNS (2022) (0)
- Author Correction: Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders (2020) (0)
- Studying the natural history of frontotemporal lobar degeneration (FTLD): The ARTFL LEFFTDS longitudinal FTLD (ALLFTD) protocol (2020) (0)
- Emergent visual creativity in frontotemporal dementia is associated with dorsomedial visual cortex enhancement (2022) (0)
- High-resolution analysis of genome copy number variation in autism (2006) (0)
- Editorial Board (2013) (0)
- Differences in Motor Features of C9orf72, MAPT, or GRN Variant Carriers With Familial Frontotemporal Lobar Degeneration (2022) (0)
- Editorial Board (2011) (0)
- Editorial Board (2011) (0)
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- Editorial Board (2016) (0)
- ATYPICAL ALZHEIMER’S GREAT EXPECTATIONS FROM THE UNEXPECTED NEURODEVELOPMENTAL DIFFERENCES AND ENVIRONMENTAL INSULTS INVERSELY CORRELATE WITH AGE OF ONSET IN ALZHEIMER’S DISEASE (2019) (0)
- Editorial Board (2013) (0)
- Editorial Board (2014) (0)
- Author and Subject Index (1998) (0)
- Introduction to The Year in Neurology and Psychiatry (2015) (0)
- Deciphering complexity in autism genetics: Endophenotypes and pathway analysis (2006) (0)
- Editorial Board (2012) (0)
- Editorial Board (2008) (0)
- F.24. Longitudinal System-based Analysis Uncovers Both General and Specific Transcriptional Responses to Type I Interferons (2009) (0)
- Editorial Board (2012) (0)
- The Contribution of Autism-Related Common Variants to the Familial Aggregation of Quantitative Autistic Traits (2021) (0)
- Editorial Board (2013) (0)
- Universitet Low-frequency variation in TP 53 has large effects on head circumference and intracranial (2019) (0)
- Title Histone Acetylome-wide Association Study of Autism Spectrum Disorder (2016) (0)
- Editorial Board (2012) (0)
- Editorial Board (2009) (0)
- A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder (2011) (0)
- Editorial Board (2011) (0)
- The Genetics of Frontotemporal Dementia and Related Disorders (2000) (0)
- Cell-Type Specific Genetic Influences on Gene Regulation During Human Neocortical Differentiation (2021) (0)
- Nav1.7 gain-of-function mutation I228M triggers age-dependent nociceptive insensitivity and C-LTMR dysregulation (2023) (0)
- Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases (2018) (0)
- Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (2020) (0)
- Editorial Board (2010) (0)
- Neuronal defects in a human cellular model of 22q11.2 deletion syndrome (2020) (0)
- Identification of shared molecular pathways involved in autism by brain transcriptome profiling (2010) (0)
- Editorial Board (2015) (0)
- Editorial Board (2010) (0)
- NitroSynapsin therapy for a mouse MEF2C haploinsufficiency model of human autism (2017) (0)
- Demographic and psychosocial factors associated with the decision to learn mutation status in familial frontotemporal dementia and the impact of disclosure on mood (2021) (0)
- Editorial Board (2015) (0)
- Clinical value of CSF tau, p‐tau181, neurogranin and neurofilaments in familial frontotemporal lobar degeneration (2021) (0)
- Table 4. [Pathogenic Allelic Variants Discussed in This GeneReview]. (2014) (0)
- Autism Sequencing Consortium (ASC) iPSYCH-BROAD Consortium Broad Institute Center for Common Disease Genomics (Broad-CCDG) (2021) (0)
- Editorial Board (2015) (0)
- Editorial Board (2016) (0)
- Editorial Board (2015) (0)
- Microarrays in Systems Neurobiology and Translational Neuroscience – From Genome Research to Clinical Applications (2008) (0)
- Editorial Board (2010) (0)
- Molecular cascades and cell-type specific signatures in ASD revealed by single cell genomics (2023) (0)
- Editorial Board (2013) (0)
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