scispace - formally typeset
S

Stephan Ripke

Researcher at Broad Institute

Publications -  311
Citations -  80990

Stephan Ripke is an academic researcher from Broad Institute. The author has contributed to research in topics: Genome-wide association study & Population. The author has an hindex of 97, co-authored 278 publications receiving 63650 citations. Previous affiliations of Stephan Ripke include Icahn School of Medicine at Mount Sinai & University of Texas Southwestern Medical Center.

Papers
More filters
Journal ArticleDOI

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Daniel J. Weiner, +108 more
- 24 Oct 2022 - 
TL;DR: In this article , the authors identify the 33-Mb p-arm of chromosome 16 (16p) as harboring the greatest excess of autism's common polygenic influences, including the mechanistically cryptic and autism-associated 16p11.2 copy number variant.
Posted ContentDOI

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium

Christian R. Marshall, +343 more
- 23 Feb 2016 - 
TL;DR: In this article, a centralized analysis pipeline was applied to a SCZ cohort of 21,094 cases and 20,227 controls and the authors observed a global enrichment of CNV burden in cases (OR=1.11, P=5.7e −15 ), which persisted after excluding loci implicated in previous studies.
Journal ArticleDOI

Common Genetic Variation And Age at Onset Of Anorexia Nervosa

Hunna J. Watson, +211 more
TL;DR: Early- and typical-onset AN showed distinct genetic correlation patterns with putative risk factors for AN, which provide evidence consistent with a common variant genetic basis for age at onset and implicate biological pathways regulating menarche and reproduction.