Citation Impact
Citing Papers
The maternal interleukin-17a pathway in mice promotes autism-like phenotypes in offspring
2016 StandoutScience
A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice
2007 StandoutScienceNobel
adegenet 1.3-1 : new tools for the analysis of genome-wide SNP data
2011 Standout
A Meta-Analysis of Cytokines in Major Depression
2009 Standout
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
2013 Standout
Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2
2010
Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe
2018 StandoutNobel
Human ITCH E3 Ubiquitin Ligase Deficiency Causes Syndromic Multisystem Autoimmune Disease
2010
Recent developments in the genetics of autism spectrum disorders
2013
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex
2010
A 12 Mb deletion at 7q33–q35 associated with autism spectrum disorders and primary amenorrhea
2008
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31‐q14.3
2010 StandoutNobel
CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy
2007
Advances in autism genetics: on the threshold of a new neurobiology
2008
Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c
2016 StandoutNobel
Genetic Advances in the Study of Speech and Language Disorders
2010
Decoding the genetics of speech and language
2012
Genetics of autism spectrum disorders
2011
FOXP2 as a molecular window into speech and language
2009
Current Developments in the Genetics of Autism: From Phenome to Genome
2008
Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5
2007
The Human Transcription Factors
2018 Standout
Disruption of an Evolutionarily Novel Synaptic Expression Pattern in Autism
2016 StandoutNobel
The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders
2009
mTOR at the nexus of nutrition, growth, ageing and disease
2020 Standout
Database resources of the National Center for Biotechnology Information: update
2003 Standout
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
2007 Standout
The immunoglobulin superfamily of neuronal cell adhesion molecules: Lessons from animal models and correlation with human disease
2008
Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
2008
DNA methylation landscapes: provocative insights from epigenomics
2008 Standout
Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acquired neuromyotonia
2010 Standout
High Affinity Neurexin Binding to Cell Adhesion G-protein-coupled Receptor CIRL1/Latrophilin-1 Produces an Intercellular Adhesion Complex
2012 StandoutNobel
Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series
2010 Standout
Serum markers support disease-specific glial pathology in major depression
2008
Next-generation DNA sequencing
2008 Standout
Common SNPs explain a large proportion of the heritability for human height
2010 Standout
Humanized Foxp2 specifically affects cortico-basal ganglia circuits
2010 StandoutNobel
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance
2009 StandoutNature
Functional mapping and annotation of genetic associations with FUMA
2017 Standout
What does CNTNAP2 reveal about autism spectrum disorder?
2012
Neuronal autoantigens—pathogenesis, associated disorders and antibody testing
2012
Autism
2013 Standout
A Functional Genetic Link between Distinct Developmental Language Disorders
2008
The conundrums of understanding genetic risks for autism spectrum disorders
2011
Coming of age: ten years of next-generation sequencing technologies
2016 Standout
Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders
2013 Standout
GCTA: A Tool for Genome-wide Complex Trait Analysis
2010 Standout
Genetics and pathogenesis of inflammatory bowel disease
2011 StandoutNature
Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows
2010 Standout
Autism spectrum disorders: developmental disconnection syndromes
2007
Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study
2013 Standout
A Recent Evolutionary Change Affects a Regulatory Element in the Human FOXP2 Gene
2012 StandoutNobel
Cardiac Ion Channel Gene Mutations in Sudden Infant Death Syndrome
2008
Spatiotemporal Dynamics of Intratumoral Immune Cells Reveal the Immune Landscape in Human Cancer
2013 Standout
NCBI GEO: mining millions of expression profiles--database and tools
2004
Research Domain Criteria (RDoC): Toward a New Classification Framework for Research on Mental Disorders
2010 Standout
CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
2012
Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits
2011
A Robust, Simple Genotyping-by-Sequencing (GBS) Approach for High Diversity Species
2011 Standout
[1] The Affymetrix GeneChip® Platform: An Overview
2006
A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism
2008
A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export
2009 StandoutNobel
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila
2009
Single-cell transcriptomic analysis of Alzheimer’s disease
2019 StandoutNature
Clinical experience and laboratory investigations in patients with anti-NMDAR encephalitis
2010 Standout
BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies
2006
Sequencing technologies — the next generation
2009 Standout
Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome
2007
MDGAs interact selectively with neuroligin-2 but not other neuroligins to regulate inhibitory synapse development
2012 StandoutNobel
Genetic structure and domestication history of the grape
2011 Standout
A high-performance computing toolset for relatedness and principal component analysis of SNP data
2012 Standout
Loss ofCntnap2Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior
2017
Ancient Ethiopian genome reveals extensive Eurasian admixture in Eastern Africa
2015 StandoutScience
Altered Functional Connectivity in Frontal Lobe Circuits Is Associated with Variation in the Autism Risk Gene CNTNAP2
2010
GAPIT: genome association and prediction integrated tool
2012 Standout
Second-generation PLINK: rising to the challenge of larger and richer datasets
2015 Standout
Excavating Neandertal and Denisovan DNA from the genomes of Melanesian individuals
2016 StandoutScienceNobel
GEOquery: a bridge between the Gene Expression Omnibus (GEO) and BioConductor
2007 Standout
Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function
2011 StandoutNobel
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
2012 StandoutNobel
The Emerging Link Between Autoimmune Disorders and Neuropsychiatric Disease
2011
Robust relationship inference in genome-wide association studies
2010 Standout
Part 14: Pediatric Advanced Life Support
2010 Standout
Works of Seth Dobrin being referenced
Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function
2004
Candidate gene analysis of 21q22: Support for S100B as a susceptibility gene for bipolar affective disorder with psychosis
2007
Recessive Symptomatic Focal Epilepsy and Mutant Contactin-Associated Protein-like 2
2006
Integrating microarrays into disease-gene identification strategies
2003