# Stefan Herms

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/stefan-herms/

## Facts

| Field | Value |
| --- | --- |
| Citations | 35,915 |
| Field | Genetic Associations and Epidemiology |
| h-index | 72 |
| i10-index | 178 |
| Last Known Institution | University of Basel |
| OpenAlex ID | https://openalex.org/A5034534740 |
| ORCID iD | https://orcid.org/0000-0002-2786-8200 |
| Works | 275 |

## Researcher papers

Showing 12 of 13.

- [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/)
- [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 study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology](https://scholariq.org/papers/genome-wide-association-study-of-more-than-40-000-bipolar-disorder-cases/)
- [Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa](https://scholariq.org/papers/genome-wide-association-study-identifies-eight-risk-loci-and-implicates-metabo/)
- [A mega-analysis of genome-wide association studies for major depressive disorder](https://scholariq.org/papers/a-mega-analysis-of-genome-wide-association-studies-for-major-depressive-disorder/)
- [Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects](https://scholariq.org/papers/contribution-of-copy-number-variants-to-schizophrenia-from-a-genome-wide-study/)
- [Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease](https://scholariq.org/papers/rare-coding-variants-in-plcg2-abi3-and-trem2-implicate-microglial-mediated/)
- [The genetic architecture of the human cerebral cortex](https://scholariq.org/papers/the-genetic-architecture-of-the-human-cerebral-cortex/)
- [Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders](https://scholariq.org/papers/transancestral-gwas-of-alcohol-dependence-reveals-common-genetic-underpinnings/)
- [Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa](https://scholariq.org/papers/significant-locus-and-metabolic-genetic-correlations-revealed-in-genome-wide/)
- [Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes](https://scholariq.org/papers/mutations-in-grin2a-cause-idiopathic-focal-epilepsy-with-rolandic-spikes/)
- [Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease](https://scholariq.org/papers/genetic-identification-of-cell-types-underlying-brain-complex-traits-yields/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Bipolar Disorder and Treatment](https://scholariq.org/topics/bipolar-disorder-and-treatment/)
- [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/)
- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)

## Researcher university

- [University of Basel](https://scholariq.org/institutions/university-of-basel/)

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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.
