UCSF Medical Center
50 papers found
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation
Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority
The female protective effect in autism spectrum disorder is not mediated by a single genetic locus
Loss of δ-catenin function in severe autism
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
A Markov random field-based approach to characterizing human brain development using spatial–temporal transcriptome data
No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins
Genotype to phenotype relationships in autism spectrum disorders
The contribution of de novo coding mutations to autism spectrum disorder
Synaptic, transcriptional and chromatin genes disrupted in autism.
De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder
A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?
Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data
A framework for the interpretation of de novo mutation in human disease
Most genetic risk for autism resides with common variation
Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism
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