# Stephan Ripke

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/stephan-ripke/

## Facts

| Field | Value |
| --- | --- |
| Citations | 113,801 |
| Field | Genetic Associations and Epidemiology |
| h-index | 126 |
| i10-index | 309 |
| Last Known Institution | Broad Institute |
| OpenAlex ID | https://openalex.org/A5043145762 |
| ORCID iD | https://orcid.org/0000-0003-3622-835X |
| Works | 512 |

## Researcher papers

Showing 12 of 29.

- [Biological insights from 108 schizophrenia-associated genetic loci](https://scholariq.org/papers/biological-insights-from-108-schizophrenia-associated-genetic-loci/)
- [Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease](https://scholariq.org/papers/host-microbe-interactions-have-shaped-the-genetic-architecture-of-inflammatory/)
- [Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression](https://scholariq.org/papers/genome-wide-association-analyses-identify-44-risk-variants-and-refine-the/)
- [Partitioning heritability by functional annotation using genome-wide association summary statistics](https://scholariq.org/papers/partitioning-heritability-by-functional-annotation-using-genome-wide-association/)
- [Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations](https://scholariq.org/papers/association-analyses-identify-38-susceptibility-loci-for-inflammatory-bowel/)
- [Identification of common genetic risk variants for autism spectrum disorder](https://scholariq.org/papers/identification-of-common-genetic-risk-variants-for-autism-spectrum-disorder/)
- [Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder](https://scholariq.org/papers/discovery-of-the-first-genome-wide-significant-risk-loci-for-attention-deficit/)
- [Defining the role of common variation in the genomic and biological architecture of adult human height](https://scholariq.org/papers/defining-the-role-of-common-variation-in-the-genomic-and-biological-architecture/)
- [Analysis of shared heritability in common disorders of the brain](https://scholariq.org/papers/analysis-of-shared-heritability-in-common-disorders-of-the-brain/)
- [Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection](https://scholariq.org/papers/common-schizophrenia-alleles-are-enriched-in-mutation-intolerant-genes-and-in/)
- [Genome-wide association study identifies 30 loci associated with bipolar disorder](https://scholariq.org/papers/genome-wide-association-study-identifies-30-loci-associated-with-bipolar/)
- [Genome-wide association analysis identifies 13 new risk loci for schizophrenia](https://scholariq.org/papers/genome-wide-association-analysis-identifies-13-new-risk-loci-for-schizophrenia/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Bipolar Disorder and Treatment](https://scholariq.org/topics/bipolar-disorder-and-treatment/)
- [Schizophrenia research and treatment](https://scholariq.org/topics/schizophrenia-research-and-treatment/)

## Researcher university

- [Broad Institute](https://scholariq.org/institutions/broad-institute/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.