B. Sheppard

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Genome-wide association study of obsessive-compulsive disorder

Y Wang, Dan J Stein, D V Conti, 2013, Molecular Psychiatry.

Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture

Benjamin D. Greenberg, Ying Wang, Naomi R. Wray, 2013, PLoS genetics.

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

Stephan J Sanders, Michael C. Gilson, K. Roeder, 2020, Cell reports.

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

Matthew W. Mosconi, Ryan L. Collins, Stephan J Sanders, 2019, Cell.

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

Stephan J Sanders, Michael C. Gilson, K. Roeder, 2019, bioRxiv.

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

Stephan J Sanders, Alicia R. Martin, K. Roeder, 2018, Cell.

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

Matthew W. Mosconi, Ryan L. Collins, Stephan J Sanders, 2018, bioRxiv.

Case-control meta-analysis of blood DNA methylation and autism spectrum disorder

Shan V Andrews, A. Feinberg, S. Warren, 2018, Molecular Autism.

Cross-tissue integration of genetic and epigenetic data offers insight into autism spectrum disorder

Shannon E. Ellis, Shan V Andrews, A. Feinberg, 2016, Nature Communications.

Genome-wide association study of obsessive-compulsive disorder

Dan J Stein, R. Delorme, M. Leboyer, 2013, Molecular Psychiatry.

Medical Comorbidity of Attention-Deficit/Hyperactivity Disorder in US Adolescents

K. Merikangas, Jian-ping He, J. V. Vande Voort, 2016, Journal of child neurology.

Peripheral blood DNA methylation and autism spectrum disorder

Shan V Andrews, A. Feinberg, S. Warren, 2018, bioRxiv.

Genome-Wide Linkage Analysis of Obsessive-Compulsive Disorder Implicates Chromosome 1p36

E. Cook, J. Grant, J. Badner, 2012, Biological Psychiatry.

Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD

S. Murray, Jessica Ross, J. Badner, 2011, Human Genetics.

Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders

Michael J. Purcaro, Emily E. Burke, Annie W Shieh, 2021, Nature Communications.

ADHD prevalence and association with hoarding behaviors in childhood‐onset OCD

M. Grados, C. Mathews, A. Azzam, 2010, Depression and anxiety.

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.

Dan J Stein, F. A. Schroeder, S. E. Stewart, 2014, Journal of the American Academy of Child and Adolescent Psychiatry.

Coordinated Interaction: A model and test for globally signed epistasis in complex traits

Stephan J Sanders, N. Zaitlen, N. Rappoport, 2020, bioRxiv.

A model and test for coordinated polygenic epistasis in complex traits

Stephan J Sanders, N. Zaitlen, N. Rappoport, 2021, Proceedings of the National Academy of Sciences.

Revealing the brain's molecular architecture.

Michael J. Purcaro, Emily E. Burke, Annie W Shieh, 2018, Science.

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

Stephan J Sanders, Michael C. Gilson, J. Rubenstein, 2021, Genome Medicine.

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

Stephan J Sanders, Michael C. Gilson, J. Rubenstein, 2020, bioRxiv.

Comorbidity and patterns of familial aggregation in attention-deficit/hyperactivity disorder and bipolar disorder in a family study of affective and anxiety spectrum disorders.

K. Merikangas, B. Sheppard, A. V. Van Meter, 2020, Journal of psychiatric research.

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

S. E. Stewart, C. Sabatti, N. Freimer, 2015, The American journal of psychiatry.

Characteristics and comorbidity of ADHD sib pairs in the Central Valley of Costa Rica.

J. McGough, C. Mathews, D. Chavira, 2012, Comprehensive psychiatry.

29 BRAINVAR DATA SET: WHOLE-GENOME AND RNA SEQUENCING REVEAL VARIATION AND TRANSCRIPTOMIC COORDINATION IN THE DEVELOPING HUMAN PREFRONTAL CORTEX

Stephan J Sanders, K. Roeder, B. Devlin, 2019, European Neuropsychopharmacology.

Cross-tissue integration of genetic and epigenetic data offers insight into autism spectrum disorder

A. Feinberg, I. Hertz-Picciotto, D. Arking, 2016, bioRxiv.

Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia

Melissa J. Green, R. Ophoff, E. Gamazon, 2013, Molecular Psychiatry.

Neuronal and glial 3D chromatin architecture informs the cellular Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders etiology of brain disorders Let us know how access to this document benefits you.

Michael J. Purcaro, Luis de la Torre Ubieta, Emily E. Burke, 2021 .