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First glimpses of the neurobiology of autism spectrum disorder

Current opinion in genetics & development, 2015-08, Vol.33, p.80-92

Sanders, Stephan J

2015

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

American journal of human genetics, 2016-09, Vol.99 (3), p.540-554

2016

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The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex

Neuron (Cambridge, Mass.), 2019-08, Vol.103 (4), p.673-685.e5

2019

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Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

Nature genetics, 2017-04, Vol.49 (4), p.504-510

2017

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

Nature genetics, 2016-05, Vol.48 (5), p.552-555

2016

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The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

Nature communications, 2015-03, Vol.6 (1), p.6404-6404, Article 6404

2015

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A Chromatin Accessibility Atlas of the Developing Human Telencephalon

Cell, 2020-08, Vol.182 (3), p.754-769.e18

2020

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Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes

PLoS genetics, 2013-08, Vol.9 (8), p.e1003671-e1003671

2013

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Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority

Molecular autism, 2015-06, Vol.6 (1), p.36-36, Article 36

2015

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Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders

American journal of human genetics, 2012-07, Vol.91 (1), p.38-55

2012

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Characterization of De Novo Promoter Variants in Autism Spectrum Disorder with Massively Parallel Reporter Assays

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3509

2023

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Building a Precision Medicine Delivery Platform for Clinics: The University of California, San Francisco, BRIDGE Experience

Journal of medical Internet research, 2022-02, Vol.24 (2), p.e34560-e34560

2022

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Clinical impact of splicing in neurodevelopmental disorders

Genome medicine, 2020-04, Vol.12 (1), p.36-36, Article 36

2020

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Detection of subtle white matter lesions in MRI through texture feature extraction and boundary delineation using an embedded clustering strategy

Scientific reports, 2022-03, Vol.12 (1), p.4433-4433, Article 4433

2022

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Intergenerational Neuroimaging of Human Brain Circuitry

Trends in neurosciences (Regular ed.), 2016-10, Vol.39 (10), p.644-648

2016

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Homeostatic plasticity fails at the intersection of autism-gene mutations and a novel class of common genetic modifiers

eLife, 2020-07, Vol.9

2020

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Intellectual Disability Is Associated with Increased Runs of Homozygosity in Simplex Autism

American journal of human genetics, 2013-07, Vol.93 (1), p.103-109

2013

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Neuropsychiatric biomarker discovery: go big or go home

Trends in molecular medicine, 2023-11, Vol.29 (11), p.878-879

2023

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Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse brain

Genome medicine, 2021-08, Vol.13 (1), p.135-135, Article 135

2021

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First glimpses of the neurobiology of autism spectrum disorder

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

The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

A framework for the interpretation of de novo mutation in human disease

The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism

A Chromatin Accessibility Atlas of the Developing Human Telencephalon

Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes

Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority

Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome

Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders

Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data

Characterization of De Novo Promoter Variants in Autism Spectrum Disorder with Massively Parallel Reporter Assays

A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?

Building a Precision Medicine Delivery Platform for Clinics: The University of California, San Francisco, BRIDGE Experience

Clinical impact of splicing in neurodevelopmental disorders

Detection of subtle white matter lesions in MRI through texture feature extraction and boundary delineation using an embedded clustering strategy

Intergenerational Neuroimaging of Human Brain Circuitry

Homeostatic plasticity fails at the intersection of autism-gene mutations and a novel class of common genetic modifiers

Intellectual Disability Is Associated with Increased Runs of Homozygosity in Simplex Autism

Neuropsychiatric biomarker discovery: go big or go home

Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse brain

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

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