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List of works by Daniel Geschwind

A Multi-network Approach Identifies Protein-Specific Co-expression in Asymptomatic and Symptomatic Alzheimer's Disease

scientific article published on 14 December 2016

A Rare Mutation of β1-Adrenergic Receptor Affects Sleep/Wake Behaviors

scientific article published on 28 August 2019

A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestation

scientific article published on 11 July 2019

A Systems-Level Analysis of the Peripheral Nerve Intrinsic Axonal Growth Program

scientific article

A blood gene expression marker of early Alzheimer's disease

scientific article published on January 2013

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

scientific article

A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders

scientific article published on 06 November 2019

A framework for the investigation of rare genetic disorders in neuropsychiatry

scientific article published on 23 September 2019

A functional genetic link between distinct developmental language disorders

scientific article

A gene expression phenotype in lymphocytes from Friedreich ataxia patients

scientific article published on November 2011

A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

scientific article

A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

scientific article published on 28 January 2019

A genome-wide scan for common alleles affecting risk for autism

scientific journal article

A genomewide screen of 345 families for autism-susceptibility loci

scientific article

A genomic screen for modifiers of tauopathy identifies puromycin-sensitive aminopeptidase as an inhibitor of tau-induced neurodegeneration

scientific article

A gut-derived metabolite alters brain activity and anxiety behaviour in mice

scientific article

A highly conserved program of neuronal microexons is misregulated in autistic brains

scientific article published on December 2014

A human neuron injury model for molecular studies of axonal regeneration

scientific article

A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy

scientific article

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

scientific article published on 14 October 2011

A quantitative framework to evaluate modeling of cortical development by neural stem cells

scientific article

A quantitative trait locus analysis of social responsiveness in multiplex autism families

scientific article published in April 2007

A systems level analysis of transcriptional changes in Alzheimer's disease and normal aging

scientific article

A systems level, functional genomics analysis of chronic epilepsy

scientific article

A unified genetic theory for sporadic and inherited autism

scientific article

A152T tau allele causes neurodegeneration that can be ameliorated in a zebrafish model by autophagy induction

scientific article published on 09 February 2017

ATF4 is an oxidative stress-inducible, prodeath transcription factor in neurons in vitro and in vivo

scientific article published on 5 May 2008

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits

scientific article

Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait

scientific article published on 06 June 2013

Advances in autism

scientific article

Advances in autism genetics: on the threshold of a new neurobiology

scientific article

Advancing the understanding of autism disease mechanisms through genetics

scientific article

Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome.

scientific article

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2

scientific article

Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion

scientific article

Altered proliferation and networks in neural cells derived from idiopathic autistic individuals

scientific article published on 05 July 2016

Alzheimer's disease: From big data to mechanism

scientific article published on 24 July 2013

An age-related sprouting transcriptome provides molecular control of axonal sprouting after stroke.

scientific article

An anatomically comprehensive atlas of the adult human brain transcriptome

scientific article (publication date: 20 September 2012)

An epigenetic signature in peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathy

scientific article

An evaluation of tyramide signal amplification and archived fixed and frozen tissue in microarray gene expression analysis ⬇️

scientific article published on January 15, 2002

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Analysis of the immune response to sciatic nerve injury identifies efferocytosis as a key mechanism of nerve debridement

scientific article published on 02 December 2020

Apolipoprotein E affects both myelin breakdown and cognition: implications for age-related trajectories of decline into dementia

scientific article

Apolipoprotein E genotype and age-related myelin breakdown in healthy individuals: implications for cognitive decline and dementia

scientific article published on 01 January 2006

Apolipoprotein E genotype is associated with temporal and hippocampal atrophy rates in healthy elderly adults: a tensor-based morphometry study

scientific article

Apolipoprotein epsilon4 status is associated with behavioral symptoms in nursing home residents with dementia.

scientific article published on 27 May 2009

Association and mutation analyses of 16p11.2 autism candidate genes

scientific article

Association between human mu-opioid receptor gene polymorphism, pain tolerance, and opioid addiction

scientific article published in August 2003

Association of GSK3B with Alzheimer disease and frontotemporal dementia

scientific article

Association of common variants in the Joubert syndrome gene (AHI1) with autism

scientific article published on 09 September 2008

Association of the serotonin transporter and receptor gene polymorphisms in neuropsychiatric symptoms in Alzheimer disease

scientific article

Astrocyte layers in the mammalian cerebral cortex revealed by a single-cell in situ transcriptomic map

scientific article published on 16 March 2020

Atypical Neurogenesis in Induced Pluripotent Stem Cells From Autistic Individuals

scientific article published on 23 June 2020

Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion

scientific article

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Author Correction: Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism

scientific article published in Nature

Author Correction: Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders

scientific article published on 17 November 2020

Autism genetics: searching for specificity and convergence

scientific article published on 31 July 2012

Autism-associated promoter variant in MET impacts functional and structural brain networks

scientific article

Autism-like phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing

scientific article published in Nature

Autism: Family connections

scientific article

Autism: many genes, common pathways?

scientific article

Autism: searching for coherence.

scientific article published in November 2007

Autism: the ups and downs of neuroligin

scientific article published on November 2009

Biological Psychiatry and Biological Psychiatry: Cognitive Neuroscience and Neuroimaging Adopt Neuroscience-Based Nomenclature

scientific article published in July 2016

Biological Psychiatry and Biological Psychiatry: Cognitive Neuroscience and Neuroimaging Adopt Neuroscience-Based Nomenclature

scientific article published on 22 June 2016

Birdsong decreases protein levels of FoxP2, a molecule required for human speech

scientific article

Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers.

scientific article

Brain calcifications and PCDH12 variants

scientific article published on 26 July 2017

Brain-wide alterations revealed by spatial transcriptomics and proteomics in COVID-19 infection

scientific article published in 2024

Brain-wide neuronal circuit connectome of human glioblastoma

scientific article published on 16 January 2025

Brief report: Under-representation of African americans in autism genetic research: a rationale for inclusion of subjects representing diverse family structures

scientific article published on May 2010

C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia

scientific article published on 18 October 2012

CYFIP1 overexpression increases fear response in mice but does not affect social or repetitive behavioral phenotypes.

scientific article published on 7 June 2019

Cancerous stem cells can arise from pediatric brain tumors

scientific article

Candidate screening of the TRPC3 gene in cerebellar ataxia

scientific article

Cell lineage and regional identity of cultured spinal cord neural stem cells and comparison to brain-derived neural stem cells

scientific article

Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation

scientific article published on 20 May 2021

Cerebellar associative sensory learning defects in five mouse autism models

scientific article published on 9 July 2015

Chromosome conformation elucidates regulatory relationships in developing human brain.

scientific article published on 19 October 2016

Circuit-wide Transcriptional Profiling Reveals Brain Region-Specific Gene Networks Regulating Depression Susceptibility

scientific article published on 11 May 2016

Clinical trials for neurodevelopmental disorders: At a therapeutic frontier.

scientific article

Clinicopathological correlations in behavioural variant frontotemporal dementia.

scientific article published on 6 October 2017

Cloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue

scientific article

Common genetic variants on 5p14.1 associate with autism spectrum disorders

scientific article

Common genetic variants, acting additively, are a major source of risk for autism

scientific article

Common risk variants identified in autism spectrum disorder

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

scientific article published on 26 February 2018

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

scientific article

Comprehensive functional genomic resource and integrative model for the human brain

scientific article published on 01 December 2018

Conference Report: Psychiatric Genomics Consortium Meeting: Pathways to Drugs, London, March 2017.

scientific article published on 8 February 2018

Connecting genes to brain in the autism spectrum disorders

scientific article (publication date: April 2010)

Conservation and divergence of vulnerability and responses to stressors between human and mouse astrocytes

scientific article published on 25 June 2021

Conservation and evolution of gene coexpression networks in human and chimpanzee brains

scholarly article

Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseases

scientific article published on 26 October 2017

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

scientific article

Correction: The Autism Related Protein Contactin-Associated Protein-Like 2 (CNTNAP2) Stabilizes New Spines: An In Vivo Mouse Study

scientific article published on 29 May 2015

Correspondence between Resting-State Activity and Brain Gene Expression

scientific article

Cortical and hippocampal atrophy in patients with autosomal dominant familial Alzheimer's disease

scientific article published on 23 September 2011

Cortical evolution: judge the brain by its cover

scientific article

Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism

scientific article

Cytoplasmic Rbfox1 Regulates the Expression of Synaptic and Autism-Related Genes.

scientific article

DISC1: A Schizophrenia Gene with Multiple Personalities ⬇️

scientific article published on November 17, 2011

DNA microarrays: translation of the genome from laboratory to clinic

scientific article

De novo mutations in regulatory elements cause neurodevelopmental disorders

scholarly article

De novo mutations in regulatory elements in neurodevelopmental disorders.

scientific article

Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders

scientific article published on 01 March 2019

Degradation of tau protein by puromycin-sensitive aminopeptidase in vitro

scientific article

Detecting network modules in fMRI time series: a weighted network analysis approach

scientific article

Developmental disorders

scientific article published in April 2015

Differential transcriptional profiles mediated by exposure to the cannabinoids cannabidiol and Δ9‐tetrahydrocannabinol in BV‐2 microglial cells ⬇️

scientific article published on April 1, 2012

Diffusion tensor imaging in preclinical and presymptomatic carriers of familial Alzheimer's disease mutations

scientific article

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

scholarly article published 3 June 2017

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

scientific article published on 26 November 2018

Disentangling the heterogeneity of autism spectrum disorder through genetic findings

scientific article

Disruption of astrocyte STAT3 signaling decreases mitochondrial function and increases oxidative stress in vitro

scientific article

Distinct Subtypes of Behavioral Variant Frontotemporal Dementia Based on Patterns of Network Degeneration

scientific article published on 18 July 2016

Divergence of human and mouse brain transcriptome highlights Alzheimer disease pathways

scientific article

Early asymmetry of gene transcription in embryonic human left and right cerebral cortex

scientific article

Early-onset Alzheimer's disease versus frontotemporal dementia: resolution with genetic diagnoses?

scientific article

Editorial overview: Neurodevelopment Diseases and Neurogenetics pivot towards mechanisms and therapies

scientific article published on 08 November 2020

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study

scientific article

Effects of risk genes on BOLD activation in presymptomatic carriers of familial Alzheimer's disease mutations during a novelty encoding task.

scientific article

Endocannabinoid signaling mediates oxytocin-driven social reward

scientific article

Endogenous Wnt signaling maintains neural progenitor cell potency

scientific article published on May 2009

Enhancing the Informativeness and Replicability of Imaging Genomics Studies

scientific article published on 20 August 2016

Epidemiology and genetics of frontotemporal dementia/Pick's disease.

scientific article

Evidence for a Language Quantitative Trait Locus on Chromosome 7q in Multiplex Autism Families ⬇️

scientific article published on 06 December 2001

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

scientific article

Evidence for sex-specific risk alleles in autism spectrum disorder

scientific article

Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism

scientific article

Evolutionary genetics: the human brain -- adaptation at many levels

scientific article

Evolving views of human genetic variation and its relationship to neurologic and psychiatric disease

scientific article published in January 2018

Exercise your amyloid

scientific article

Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autism

scientific article published in January 2015

Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus

scientific article published on 19 October 2020

Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia

scientific article

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

scientific article

Explaining human uniqueness: genome interactions with environment, behaviour and culture

scientific article (publication date: October 2008)

Expression patterns of epidermal growth factor receptor and fibroblast growth factor receptor 1 mRNA in fetal human brain

scientific article published in July 2003

FACS-array profiling of striatal projection neuron subtypes in juvenile and adult mouse brains

scientific article published on 19 February 2006

Familial cortical myoclonus with a mutation in NOL3.

scientific article

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain

scientific article

Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

scientific article

Functional cortical neurons and astrocytes from human pluripotent stem cells in 3D culture

scientific article published on 25 May 2015

Functional genomic analyses identify pathways dysregulated by progranulin deficiency, implicating Wnt signaling

scientific article published on 21 September 2011

Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARgamma pathway as a therapeutic target in Friedreich's ataxia

scientific article published on 17 April 2009

Functional genomics and biochemical characterization of the C. elegans orthologue of the Machado-Joseph disease protein ataxin-3.

scientific article published on 18 January 2007

Functional genomics links genetic origins to pathophysiology in neurodegenerative and neuropsychiatric disease

scientific article published on 04 July 2020

Functional impact of global rare copy number variation in autism spectrum disorders

scientific article published on 15 July 2010

Functional neuroimaging provides evidence of anomalous cerebral laterality in adults with Klinefelter's syndrome

scientific article

Functional organization of the transcriptome in human brain

scientific article published on 12 October 2008

Gene expression analysis of neural cells and tissues using DNA microarrays

scientific article

Gene expression in human brain implicates sexually dimorphic pathways in autism spectrum disorders

scientific article published on 19 February 2016

Gene expression profiling in frataxin deficient mice: microarray evidence for significant expression changes without detectable neurodegeneration

scientific article

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 ⬇️

scientific article published on February 18, 2011

Gene expression shifts in yellow-bellied marmots prior to natal dispersal

article

Gene expression study on peripheral blood identifies progranulin mutations

scientific article published on July 2008

Gene hunting in autism spectrum disorder: on the path to precision medicine

scientific article

Genes and pathways underlying regional and cell type changes in Alzheimer's disease

scientific article published on 25 May 2013

Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms

scientific article published on 01 October 2019

Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms

scientific article published on 01 April 2020

Genetic advances in autism: heterogeneity and convergence on shared pathways

scientific article published on 26 May 2009

Genetic analysis of anterior posterior expression gradients in the developing mammalian forebrain

scientific article published on 5 December 2006

Genetic architecture of epigenetic and neuronal ageing rates in human brain regions

scientific article

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 28 February 2019

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

scientific article

Genetics and genomics of psychiatric disease

scientific article

Genetics of autism spectrum disorder

scientific article published in January 2018

Genetics of autism spectrum disorders

scientific article published on 18 August 2011

Genome engineering of isogenic human ES cells to model autism disorders

scientific article published on 11 March 2015

Genome-Wide Analysis of a Wnt1-Regulated Transcriptional Network Implicates Neurodegenerative Pathways ⬇️

scientific article published on October 4, 2011

Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue

scientific article published on 01 July 2019

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

scientific article

Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism

scientific article published on 5 December 2016

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways

scientific article

Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy

scientific article published on 06 May 2019

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

scientific article

Genome-wide, integrative analysis implicates microRNA dysregulation in autism spectrum disorder.

scientific article published on 29 August 2016

Genomic medicine enters the neurology clinic ⬇️

scientific article published on June 6, 2012

Genomic profiles of damage and protection in human intracerebral hemorrhage.

scientific article published on 16 July 2008

Global analysis of gene expression in neural progenitors reveals specific cell-cycle, signaling, and metabolic networks

scientific article published in September 2003

Gyrification abnormalities in presymptomatic c9orf72 expansion carriers

scientific article published on 11 May 2019

HDAC inhibitors correct frataxin deficiency in a Friedreich ataxia mouse model

scientific article (publication date: 2008)

Heritability of lobar brain volumes in twins supports genetic models of cerebral laterality and handedness

scientific article

Heterogeneous dysregulation of microRNAs across the autism spectrum.

scientific article published on 19 June 2008

High density SNP association study of a major autism linkage region on chromosome 17.

scientific article published on 21 March 2007

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders

scientific article

Histone Acetylome-wide Association Study of Autism Spectrum Disorder.

scientific article

Human ARX gene: genomic characterization and expression

scientific article

Human Disease Variation in the Light of Population Genomics

scientific article published on 01 March 2019

Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice

scientific article published on 01 May 2019

Human brain evolution: harnessing the genomics (r)evolution to link genes, cognition, and behavior

scientific article (publication date: 21 October 2010)

Human brain evolution: insights from microarrays

scientific article

Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility

scientific article published on 03 June 2019

Human iPSC-Derived Neuronal Model of Tau-A152T Frontotemporal Dementia Reveals Tau-Mediated Mechanisms of Neuronal Vulnerability

scientific article published on September 2016

Human in vitro models for understanding mechanisms of autism spectrum disorder

scientific article published on 16 April 2020

Human wild-type tau interacts with wingless pathway components and produces neurofibrillary pathology in Drosophila

scientific article published in May 2002

Human-specific transcriptional networks in the brain

scientific article

Human-specific transcriptional regulation of CNS development genes by FOXP2

scientific article

Identification of Conserved Proteomic Networks in Neurodegenerative Dementia

scientific article published on 01 June 2020

Identification of a Hoxd10-regulated transcriptional network and combinatorial interactions with Hoxa10 during spinal cord development

scientific article published on February 2004

Identification of common genetic risk variants for autism spectrum disorder

scientific article published on 25 February 2019

Identification of differentially expressed proteins in murine embryonic and postnatal cortical neural progenitors

scientific article

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

article

Identification of process-localized mRNAs from cultured rodent hippocampal neurons.

scientific article published in December 2006

Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain

scientific article

Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity

scientific article published on 03 March 2020

In vivo cell-autonomous transcriptional abnormalities revealed in mice expressing mutant huntingtin in striatal but not cortical neurons ⬇️

scientific article published on December 20, 2010

Increased fMRI signal with age in familial Alzheimer's disease mutation carriers

scientific article

Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts: Completing the picture

scientific article published on 28 October 2016

Individual common variants exert weak effects on the risk for autism spectrum disorders

scientific journal article

Induced Pluripotent Stem Cell Models of Progranulin-Deficient Frontotemporal Dementia Uncover Specific Reversible Neuronal Defects ⬇️

scientific article published on October 11, 2012

Inducible and reversible phenotypes in a novel mouse model of Friedreich's Ataxia

scientific article published on 19 December 2017

Inflammatory Mediators Alter the Astrocyte Transcriptome and Calcium Signaling Elicited by Multiple G-Protein-Coupled Receptors ⬇️

scientific article published on October 17, 2012

Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks

scientific article published on 01 August 2019

Inhibition of transglutaminase 2 mitigates transcriptional dysregulation in models of Huntington disease.

scientific article

Inosine alters gene expression and axonal projections in neurons contralateral to a cortical infarct and improves skilled use of the impaired limb

scientific article

Inosine augments the effects of a Nogo receptor blocker and of environmental enrichment to restore skilled forelimb use after stroke

scientific article

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

scientific article

Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism

scientific article published on November 2013

Integrative functional genomic analysis of human brain development and neuropsychiatric risks

scientific article published on 01 December 2018

Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism

scientific article published on 25 September 2020

Integrative network analysis reveals biological pathways associated with Williams syndrome

scientific article published on 25 October 2018

Intellectual disability is associated with increased runs of homozygosity in simplex autism

scientific article published on 03 July 2013

Introduction to the year in neurology and psychiatry

scientific article published in March 2015

It is time to take a stand for medical research and against terrorism targeting medical scientists

scientific article

JAKMIP1, a Novel Regulator of Neuronal Translation, Modulates Synaptic Function and Autistic-like Behaviors in Mouse

scientific article

Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases

scholarly article by Jason A Chen published in August 2018

Kinetic profile of the transcriptome changes induced in the choroid plexus by peripheral inflammation

scientific article published on 25 February 2009

Language-related Cntnap2 gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds

scientific article (publication date: June 2010)

Large-scale microarray gene expression analysis in discrete electrophysiologically identified neuronal clusters

scientific article published in February 2004

Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature

scientific article published in December 2005

Leveraging genetics and genomics to define the causes of mental illness

scientific article published in January 2015

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

scientific article

Lipocalin 2 is a Choroid Plexus Acute-Phase Protein

Lipocalin 2 is a choroid plexus acute-phase protein

scientific article

Lipocalin 2 is present in the EAE brain and is modulated by natalizumab

scientific article

Long-term maturation of human cortical organoids matches key early postnatal transitions

scientific article published on 22 February 2021

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

scientific article

Maternal embryonic leucine zipper kinase (MELK) regulates multipotent neural progenitor proliferation

scientific journal article

Maternal embryonic leucine zipper kinase is a key regulator of the proliferation of malignant brain tumors, including brain tumor stem cells

scientific article published in January 2008

Mechanistic Differences in Neuropathic Pain Modalities Revealed by Correlating Behavior with Global Expression Profiling.

scientific article published in January 2018

Memory performance and fMRI signal in presymptomatic familial Alzheimer's disease

scientific article published on 17 July 2012

Microarray and Pathway Analysis Reveal Distinct Mechanisms Underlying Cannabinoid-Mediated Modulation of LPS-Induced Activation of BV-2 Microglial Cells ⬇️

scientific article published on April 24, 2013

Microarray platforms: introduction and application to neurobiology

scientific article published in January 2004

Microarrays and the microscope: balancing throughput with resolution

scientific article published on 29 June 2006

Microglia-organized scar-free spinal cord repair in neonatal mice

scientific article published on 07 October 2020

Middle-aged children of Alzheimer parents, a pilot study: stable neurocognitive performance at 20-year follow-up

scientific article

Mithramycin is a gene-selective Sp1 inhibitor that identifies a biological intersection between cancer and neurodegeneration

scientific article published on May 2011

Mitochondrial dysfunction and immune activation are detectable in early Alzheimer's disease blood

scientific article published on January 2012

Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

scientific article published on 12 May 2014

Molecular Genetics of Neurodegenerative Dementias

scientific article published on 9 December 2016

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

scientific article

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

scientific article (publication date: June 2011)

Multiple chronic pain states are associated with a common amino acid-changing allele in KCNS1

scientific article

Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2

scientific article

Mutations in PDYN are not responsible for multiple system atrophy ⬇️

scientific article published on January 25, 2013

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

scientific article

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

scientific article

Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis

scientific article

Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia ⬇️

scientific article published on January 27, 2012

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

scientific article

Network organization of the huntingtin proteomic interactome in mammalian brain

scientific article

Neural progenitor genes. Germinal zone expression and analysis of genetic overlap in stem cell populations

scientific article published on December 2003

Neural responsivity to social rewards in autistic female youth

scientific article published on 02 June 2020

Neurodegenerative Disease Phenotypes in Carriers of MAPT p.A152T, A Risk Factor for Frontotemporal Dementia Spectrum Disorders and Alzheimer Disease ⬇️

scientific article published on October 1, 2013

Neurodegenerative dementias: connecting psychiatry and neurology through a shared neurobiology

scientific article

Neurodevelopmental disorders: hope for a new beginning ⬇️

scientific article published on April 1, 2011

Neuron-specific signatures in the chromosomal connectome associated with schizophrenia risk

scientific article published on 01 December 2018

Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex

scientific article published on 9 February 2017

Neuronal defects in a human cellular model of 22q11.2 deletion syndrome

scientific article published on 28 September 2020

Neurons selectively targeted in frontotemporal dementia reveal early stage TDP-43 pathobiology

scientific article published on 03 December 2018

Neurons show distinctive DNA methylation profile and higher interindividual variations compared with non-neurons

scientific article

Neuroprotective effects of brain-derived neurotrophic factor in rodent and primate models of Alzheimer's disease

scientific article

Neuroscience in the era of functional genomics and systems biology

scientific article

Neuroscience: Genes and human brain evolution

scientific article

NitroSynapsin therapy for a mouse MEF2C haploinsufficiency model of human autism

scientific article published on 14 November 2017

No Evidence to Suggest that the Use of Acetylcholinesterase Inhibitors Confounds the Results of Two Blood-Based Biomarker Studies in Alzheimer's Disease

scientific article published in August 2015

Novel candidate blood-based transcriptional biomarkers of Machado-Joseph disease

scientific article published on 25 April 2015

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

scientific article

Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis

scientific article

Novel roles for osteopontin and clusterin in peripheral motor and sensory axon regeneration.

scientific article published on January 2014

Novel tau polymorphisms, tau haplotypes, and splicing in familial and sporadic frontotemporal dementia

scientific article

Out FOXing Parkinson disease: where development meets neurodegeneration

scientific article

PTEN negatively regulates neural stem cell self-renewal by modulating G0-G1 cell cycle entry

scholarly article

Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction

scientific article (publication date: 31 March 2004)

Phosphoserine phosphatase is expressed in the neural stem cell niche and regulates neural stem and progenitor cell proliferation

scientific article

Plasma signaling proteins in persons at genetic risk for Alzheimer disease: influence of APOE genotype

scientific article published on June 2012

Postnatal immune activation causes social deficits in a mouse model of tuberous sclerosis: Role of microglia and clinical implications

scientific article published on 17 September 2021

Preface

Preface

Preferential tau aggregation in von Economo neurons and fork cells in frontotemporal lobar degeneration with specific MAPT variants

scientific article published on 22 October 2019

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

scientific article published on 07 June 2018

Prevalence of spinocerebellar ataxia 36 in a US population

scientific article published on 18 July 2017

Prevalent iron metabolism gene variants associated with increased brain ferritin iron in healthy older men.

scientific article

Primary brain calcification: an international study reporting novel variants and associated phenotypes

scientific article published on 28 June 2018

Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health System

scientific article published on 04 July 2020

Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage

scientific article published on 26 August 2019

Progress in realizing the promise of microarrays in systems neurobiology

scientific article

Propositional density and apolipoprotein E genotype among persons at risk for familial Alzheimer's disease

scientific article published on 30 August 2011

Prospective identification, isolation, and profiling of a telomerase-expressing subpopulation of human neural stem cells, using sox2 enhancer-directed fluorescence-activated cell sorting

scientific article

Proteomic Changes in Cerebrospinal Fluid of Presymptomatic and Affected Persons Carrying Familial Alzheimer Disease Mutations ⬇️

scientific article published on January 1, 2012

Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

scientific article published on 01 July 2019

Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

scientific article published on 16 March 2018

RBFOX1 regulates both splicing and transcriptional networks in human neuronal development.

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Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families

scientific article published on 25 August 2016

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

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Rare inherited variation in autism: beginning to see the forest and a few trees

scientific article published in January 2013

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

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Rarity of the Alzheimer disease-protective APP A673T variant in the United States

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Recurrence rates provide evidence for sex-differential, familial genetic liability for autism spectrum disorders in multiplex families and twins

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Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders

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Reduced Prefrontal Synaptic Connectivity and Disturbed Oscillatory Population Dynamics in the CNTNAP2 Model of Autism

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Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk

scientific article published on August 2011

Reliability of human cortical organoid generation

scientific article published on 20 December 2018

Replication of autism linkage: fine-mapping peak at 17q21.

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Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder

scientific article published on 17 February 2014

Retooling spare parts: gene duplication and cognition.

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Robust Axonal Regeneration Occurs in the Injured CAST/Ei Mouse CNS

scientific article published on 21 May 2015

Robust Axonal Regeneration Occurs in the Injured CAST/Ei Mouse CNS

scientific article published on 01 May 2016

Schizophrenia genetics complements its mechanistic understanding

scientific article published on 21 March 2016

Schizophrenia: genome, interrupted

scientific article published in April 2008

Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families

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Selenium Drives a Transcriptional Adaptive Program to Block Ferroptosis and Treat Stroke

scientific article published on 02 May 2019

Self-Organized Cerebral Organoids with Human-Specific Features Predict Effective Drugs to Combat Zika Virus Infection

scientific article published on October 2017

Sex Differences in Functional Connectivity of the Salience, Default Mode, and Central Executive Networks in Youth with ASD

scientific article published on 30 April 2020

Sex differences in autism spectrum disorders

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Sex-chromosome dosage effects on gene expression in humans

scientific article published on 26 June 2018

Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic Overlap

scientific article published on 07 January 2019

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.

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Signaling to transcription networks in the neuronal retrograde injury response.

scientific article published on 13 July 2010

Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language

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Small molecule activation of adaptive gene expression: tilorone or its analogs are novel potent activators of hypoxia inducible factor-1 that provide prophylaxis against stroke and spinal cord injury

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Social responsiveness, an autism endophenotype: genomewide significant linkage to two regions on chromosome 8

scientific article published on 7 November 2014

Spatial fine-mapping for gene-by-environment effects identifies risk hot spots for schizophrenia

scientific article published in Nature Communications

Spatiotemporal dynamics of the postnatal developing primate brain transcriptome

scientific article published on 7 May 2015

Specific functions for ERK/MAPK signaling during PNS development.

scientific article published on January 2011

Strategies for aggregating gene expression data: the collapseRows R function

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Stratification based on language-related endophenotypes in autism: attempt to replicate reported linkage

scientific article published on September 2006

Strong association of de novo copy number mutations with autism

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Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex.

scientific article published in June 2018

Subcellular knockout of importin β1 perturbs axonal retrograde signaling

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Suberoylanilide hydroxamic acid (vorinostat) up-regulates progranulin transcription: rational therapeutic approach to frontotemporal dementia

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Subtraction-coupled custom microarray analysis for gene discovery and gene expression studies in the CNS.

scientific article

Sumoylated MEF2A coordinately eliminates orphan presynaptic sites and promotes maturation of presynaptic boutons.

scientific article published on March 2013

Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders

scientific article published on 11 July 2019

Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders

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TDP-43 frontotemporal lobar degeneration and autoimmune disease

scientific article published on 30 March 2013

Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and Immunosuppression

scientific article published on 01 November 2020

Tau phosphorylation, tangles, and neurodegeneration: the chicken or the egg?

scientific article published on October 2003

Tauopathy with paired helical filaments in an aged chimpanzee

scientific article published on July 2008

Technology Insight: querying the genome with microarrays--progress and hope for neurological disease

scientific article published on March 2006

Tet3 regulates synaptic transmission and homeostatic plasticity via DNA oxidation and repair

scientific article published on 27 April 2015

Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers

The Autism Related Protein Contactin-Associated Protein-Like 2 (CNTNAP2) Stabilizes New Spines: An In Vivo Mouse Study

scientific article published on 7 May 2015

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

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The BRAIN Initiative Cell Census Consortium: Lessons Learned toward Generating a Comprehensive Brain Cell Atlas

scientific article published on November 2017

The Central Nervous System and the Gut Microbiome.

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The Dynamic Landscape of Open Chromatin during Human Cortical Neurogenesis

scientific article published on 2 January 2018

The Genetics-Driven Revival in Neuropsychiatric Drug Development.

scientific article published on April 2016

The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic mice

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The Human Brain in a Dish: The Promise of iPSC-Derived Neurons ⬇️

scientific article published on June 10, 2011

The PsychENCODE project

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The choroid plexus response to a repeated peripheral inflammatory stimulus

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The choroid plexus transcriptome reveals changes in type I and II interferon responses in a mouse model of Alzheimer's disease

scientific article published on 16 June 2015

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.

scientific article published on 26 June 2017

The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors

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The emerging picture of autism spectrum disorder: genetics and pathology

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The neurogenetics of atypical parkinsonian disorders

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The organization of the transcriptional network in specific neuronal classes.

scientific article published on 28 July 2009

The road to precision psychiatry: translating genetics into disease mechanisms.

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Thresholding rules for recovering a sparse signal from microarray experiments

scientific article published in March 2002

Timing and significance of pathological features in C9orf72 expansion-associated frontotemporal dementia

scientific article published on 22 October 2016

Timing of the Diagnosis of Autism in African American Children

scientific article published on 24 August 2020

Transcriptional Reprogramming of Distinct Peripheral Sensory Neuron Subtypes after Axonal Injury

scientific article published on 14 August 2020

Transcriptional architecture of the primate neocortex

scientific article published on 21 March 2012

Transcriptional landscape of the prenatal human brain

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Transcriptome Profiling of Peripheral Blood in 22q11.2 Deletion Syndrome Reveals Functional Pathways Related to Psychosis and Autism Spectrum Disorder

scientific article published on 22 July 2015

Transcriptome signature of the adult mouse choroid plexus

scientific article published on 18 January 2011

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

article

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder

scientific article

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

scientific article (publication date: 25 May 2011)

Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders

scientific article published on 03 July 2020

Transcriptomic networks implicate neuronal energetic abnormalities in three mouse models harboring autism and schizophrenia-associated mutations

scientific article published on 08 November 2019

Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study.

scientific article published on 12 April 2009

Understanding sex bias in autism spectrum disorder

scientific article published on 8 March 2013

Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome ⬇️

scientific article published on November 27, 2011

VOTING-BASED SEGMENTATION OF OVERLAPPING NUCLEI IN CLARITY IMAGES

scientific article published on 01 April 2018

Validation of two parent-reported autism spectrum disorders screening tools M-CHAT-R and SCQ in Bamako, Mali

research work

VoICE: A semi-automated pipeline for standardizing vocal analysis across models

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What does CNTNAP2 reveal about autism spectrum disorder?

scientific article (publication date: March 2012)

Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

scientific article published in December 2017

Widespread RNA editing dysregulation in brains from autistic individuals

scientific article published on 17 December 2018

Wnt genes define distinct boundaries in the developing human brain: implications for human forebrain patterning

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Wnt-pathway activation during the early stage of neurodegeneration in FTDP-17 mice

scientific article published on 02 July 2007

Working memory and relational reasoning in Klinefelter syndrome.

scientific article published on September 2003

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

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Young-onset frontotemporal dementia in a homozygous tau R406W mutation carrier

scientific article

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