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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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Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex

Cell reports (Cambridge), 2020-04, Vol.31 (1), p.107489-107489, Article 107489

2020

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Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

Translational psychiatry, 2021-03, Vol.11 (1), p.171-171, Article 171

2021

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

Biological psychiatry (1969), 2015-05, Vol.77 (9), p.775-784

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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Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk

Translational psychiatry, 2022-08, Vol.12 (1), p.340-340, Article 340

2022

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Discovering genetic ancestry using spectral graph theory

Genetic epidemiology, 2010-01, Vol.34 (1), p.51-59

2010

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How rare and common risk variation jointly affect liability for autism spectrum disorder

Molecular autism, 2021-10, Vol.12 (1), p.66-66, Article 66

2021

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Evaluating and improving health equity and fairness of polygenic scores

HGG advances, 2024-04, Vol.5 (2), p.100280, Article 100280

2024

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Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder

Molecular autism, 2021-10, Vol.12 (1), p.65-12, Article 65

2021

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African ancestry and lung function in Puerto Rican children

Journal of allergy and clinical immunology, 2012-06, Vol.129 (6), p.1484-1490.e6

2012

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DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

Molecular autism, 2014-03, Vol.5 (1), p.22-22, Article 22

2014

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On the Use of General Control Samples for Genome-wide Association Studies: Genetic Matching Highlights Causal Variants

American journal of human genetics, 2008-02, Vol.82 (2), p.453-463

2008

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Genetic associations with psychosis and affective disturbance in Alzheimer's disease

Alzheimer's & dementia : translational research & clinical interventions, 2024-04, Vol.10 (2), p.e12472-n/a

2024

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Semisoft clustering of single-cell data

Proceedings of the National Academy of Sciences - PNAS, 2019-01, Vol.116 (2), p.466-471

2019

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Consanguinity and increased risk for schizophrenia in Egypt

Schizophrenia research, 2010-07, Vol.120 (1), p.108-112

2010

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Candidate gene analysis of femoral neck trabecular and cortical volumetric bone mineral density in older men

Journal of bone and mineral research, 2010-02, Vol.25 (2), p.330-338

2010

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An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders

Nature genetics, 2018-07, Vol.50 (7), p.1032-1040

2018

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T20. POLYGENIC RISK FOR SCHIZOPHRENIA IS ASSOCIATED WITH HIPPOCAMPAL VOLUME IN TYPICALLY DEVELOPING YOUTH

Schizophrenia bulletin, 2019-04, Vol.45 (Supplement_2), p.S211-S211

2019

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Most genetic risk for autism resides with common variation

Nature genetics, 2014-08, Vol.46 (8), p.881-885

2014

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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Nature genetics, 2022-09, Vol.54 (9), p.1320-1331

2022

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Synaptic, transcriptional and chromatin genes disrupted in autism

Nature (London), 2014-11, Vol.515 (7526), p.209-215

2014

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Testing for association based on excess allele sharing in a sample of related cases and controls

Human genetics, 2007-06, Vol.121 (5), p.549-557

2007

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

Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex

Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

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

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

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk

Discovering genetic ancestry using spectral graph theory

How rare and common risk variation jointly affect liability for autism spectrum disorder

Evaluating and improving health equity and fairness of polygenic scores

Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder

African ancestry and lung function in Puerto Rican children

DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

On the Use of General Control Samples for Genome-wide Association Studies: Genetic Matching Highlights Causal Variants

Genetic associations with psychosis and affective disturbance in Alzheimer's disease

Semisoft clustering of single-cell data

Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2

Consanguinity and increased risk for schizophrenia in Egypt

Candidate gene analysis of femoral neck trabecular and cortical volumetric bone mineral density in older men

An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders

T20. POLYGENIC RISK FOR SCHIZOPHRENIA IS ASSOCIATED WITH HIPPOCAMPAL VOLUME IN TYPICALLY DEVELOPING YOUTH

Most genetic risk for autism resides with common variation

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Synaptic, transcriptional and chromatin genes disrupted in autism

Testing for association based on excess allele sharing in a sample of related cases and controls

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