Disease similarity network analysis of Autism Spectrum Disorder and comorbid brain disorders

Clinical Study of 8 Cases of CHD2 Gene Mutation–Related Neurological Diseases and Their Mechanisms

(2022) Xiaona Luo et al.   Frontiers in Cell and Developmental Biology

Gene variations in autism spectrum disorder are associated with alteration of gut microbiota, metabolites and cytokines

(2021) Zhi Liu et al.   Gut Microbes

Transcriptome Profiling of Dysregulated GPCRs Reveals Overlapping Patterns across Psychiatric Disorders and Age-Disease Interactions

(2021) Roudabeh Vakil Monfared et al.   Cells

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

(2020) F. Kyle Satterstrom et al.   CELL

Clinical Assessment, Genetics, and Treatment Approaches in Autism Spectrum Disorder (ASD)

(2020) Ann Genovese et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Role of Ash1l in Tourette syndrome and other neurodevelopmental disorders

(2020) Cheng Zhang et al.   Developmental Neurobiology

g:Profiler: a web server for functional enrichment analysis and conversions of gene lists (2019 update)

(2019) Uku Raudvere et al.   NUCLEIC ACIDS RESEARCH

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

(2019) F. Kyle Satterstrom et al.   NATURE NEUROSCIENCE

The DisGeNET knowledge platform for disease genomics: 2019 update

(2019) Janet Piñero et al.   NUCLEIC ACIDS RESEARCH

The reactome pathway knowledgebase

(2019) Bijay Jassal et al.   NUCLEIC ACIDS RESEARCH

Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

(2019) Phil H. Lee et al.   CELL

Genetic and clinical evidence of mitochondrial dysfunction in autism spectrum disorder and intellectual disability

(2018) Alba Valiente-Pallejà et al.   HUMAN MOLECULAR GENETICS

SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research

(2018) Pamela Feliciano et al.   NEURON

Analysis of shared heritability in common disorders of the brain

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De novo Mutations (DNMs) in Autism Spectrum Disorder (ASD): Pathway and Network Analysis

(2018) Aitana Alonso-Gonzalez et al.   Frontiers in Genetics

Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD

(2017) W. Guo et al.   EUROPEAN NEUROPSYCHOPHARMACOLOGY

ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

(2017) B St Pourcain et al.   MOLECULAR PSYCHIATRY

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

(2017) Ryan K C Yuen et al.   NATURE NEUROSCIENCE

SHANK proteins: roles at the synapse and in autism spectrum disorder

(2017) Patricia Monteiro et al.   NATURE REVIEWS NEUROSCIENCE

Widespread signatures of positive selection in common risk alleles associated to autism spectrum disorder

(2017) Renato Polimanti et al.   PLoS Genetics

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)   Molecular Autism

Risk of epilepsy and autism in full and half siblings-A population-based cohort study

(2016) Jakob Christensen et al.   EPILEPSIA

Association Between Polymorphisms of DNA Repair Genes and Risk of Schizophrenia

(2016) Sibel Odemis et al.   Genetic Testing and Molecular Biomarkers

The Role of the Immune System in Autism Spectrum Disorder

(2016) Amory Meltzer et al.   NEUROPSYCHOPHARMACOLOGY

DNA Damage in Major Psychiatric Diseases

(2016) Muhammad Ummear Raza et al.   NEUROTOXICITY RESEARCH

DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants

(2016) Janet Piñero et al.   NUCLEIC ACIDS RESEARCH

Histone methyltransferase Ash1L mediates activity-dependent repression of neurexin-1α

(2016) Τao Zhu et al.   Scientific Reports

Exome Sequencing of Familial Bipolar Disorder

(2016) Fernando S. Goes et al.   JAMA Psychiatry

DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes

(2015) J. Pinero et al.   Database-The Journal of Biological Databases and Curation

Obsessive-Compulsive Disorder and Autism Spectrum Disorders: Longitudinal and Offspring Risk

(2015) Sandra M Meier et al.   PLoS One

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

(2014) S E McCarthy et al.   MOLECULAR PSYCHIATRY

Most genetic risk for autism resides with common variation

(2014) Trent Gaugler et al.   NATURE GENETICS

Epilepsy associated with autism and attention deficit hyperactivity disorder: Is there a genetic link?

(2013) Adriana Lo-Castro et al.   BRAIN & DEVELOPMENT

Activity-dependent neuronal signalling and autism spectrum disorder

(2013) Daniel H. Ebert et al.   NATURE

The Sacred Disease: The Puzzling Genetics of Epileptic Disorders

(2013) Gaia Novarino et al.   NEURON

Catatonia in DSM-5

(2013) Rajiv Tandon et al.   SCHIZOPHRENIA RESEARCH

Patterns and rates of exonic de novo mutations in autism spectrum disorders

(2012) Benjamin M. Neale et al.   NATURE

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

(2012) Stephan J. Sanders et al.   NATURE

De novo mutations in human genetic disease

(2012) Joris A. Veltman et al.   NATURE REVIEWS GENETICS

De Novo Gene Disruptions in Children on the Autistic Spectrum

(2012) Ivan Iossifov et al.   NEURON

DSM-5 Status of Psychotic Disorders: 1 Year Prepublication

(2012) R. Tandon et al.   SCHIZOPHRENIA BULLETIN

Mitochondrial complex I deficiency of nuclear origin

(2011) Hélène Pagniez-Mammeri et al.   MOLECULAR GENETICS AND METABOLISM

SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism

(2011) C M Durand et al.   MOLECULAR PSYCHIATRY

Cell Signaling Underlying Epileptic Behavior

(2011) Yuri Bozzi et al.   Frontiers in Behavioral Neuroscience

Mitochondrial complex I deficiency: from organelle dysfunction to clinical disease

(2009) F. Distelmaier et al.   BRAIN

AmiGO: online access to ontology and annotation data

(2008) Seth Carbon et al.   BIOINFORMATICS