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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.

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Genetic comorbidity between major depression and cardio-metabolic disease, stratified by age at onset of major depression

Saskia P. Hagenaars, +56 more
- 24 May 2019 - 
TL;DR: The phenotypic associations between major depression and cardio-metabolic traits may partly reflect their overlapping genetic aetiology irrespective of the age depression first presents.
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A recessive genetic model and runs of homozygosity in major depressive disorder

TL;DR: The analysis of ROH suggested that there was significant heterogeneity of effect across studies in effect, and it was associated with genotyping platform and country of origin, and the results of the ROH analysis show that differences across studies can lead to conflicting systematic genome‐wide differences between cases and controls that are unaccounted for by traditional covariates.
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A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies.

TL;DR: This work calls this concept the Universal Control Repository Network (UNICORN), a means to perform association analyses without necessitating direct access to individual-level control data, and demonstrates how it controls false positives, provides power similar to that achieved when all control data are directly accessible, and enhances power when controlData are limiting or even imperfectly matched ancestrally.
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Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

Simone de Jong, +376 more
TL;DR: Studying patterns of assortative mating and anticipation, it appears increased polygenic risk is contributed by affected individuals who married into the family, resulting in an increasing genetic risk over generations, which may explain the observation of anticipation in mood disorders.
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Genetic Variation in the Lymphotoxin-Alpha Pathway and the Risk of Ischemic Stroke in European Populations

TL;DR: Genetic variation in the lymphotoxin-α cascade (LTA, LGALS2, and PSMA6) is not a major risk factor for ischemic stroke, and none of these associations could be replicated in the UK population.