# Markus M. Nöthen

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/markus-m-nothen/

## Facts

| Field | Value |
| --- | --- |
| Citations | 138,699 |
| Field | Genetic Associations and Epidemiology |
| h-index | 159 |
| i10-index | 895 |
| Last Known Institution | University of Bonn |
| OpenAlex ID | https://openalex.org/A5091235988 |
| ORCID iD | https://orcid.org/0000-0002-8770-2464 |
| Works | 1,971 |

## Researcher papers

Showing 12 of 18.

- [Large recurrent microdeletions associated with schizophrenia](https://scholariq.org/papers/large-recurrent-microdeletions-associated-with-schizophrenia/)
- [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/)
- [Genetic Associations with Valvular Calcification and Aortic Stenosis](https://scholariq.org/papers/genetic-associations-with-valvular-calcification-and-aortic-stenosis/)
- [Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants](https://scholariq.org/papers/discovery-and-systematic-characterization-of-risk-variants-and-genes-for/)
- [Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis](https://scholariq.org/papers/genome-wide-association-analyses-identify-new-risk-variants-and-the-genetic/)
- [Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations](https://scholariq.org/papers/loss-of-function-variations-within-the-filaggrin-gene-predispose-for-atopic/)
- [A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis](https://scholariq.org/papers/a-genome-wide-association-study-confirms-pnpla3-and-identifies-tm6sf2-and-mboat7/)
- [A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer](https://scholariq.org/papers/a-common-bim-deletion-polymorphism-mediates-intrinsic-resistance-and-inferior/)
- [Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies](https://scholariq.org/papers/genome-wide-mega-analysis-identifies-16-loci-and-highlights-diverse-biological/)
- [Disruption of the neurexin 1 gene is associated with schizophrenia](https://scholariq.org/papers/disruption-of-the-neurexin-1-gene-is-associated-with-schizophrenia/)
- [Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies](https://scholariq.org/papers/interrogating-the-genetic-determinants-of-tourette-s-syndrome-and-other-tic/)
- [Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo](https://scholariq.org/papers/genome-wide-association-for-major-depressive-disorder-a-possible-role-for-the/)

## 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/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)

## Researcher university

- [University of Bonn](https://scholariq.org/institutions/university-of-bonn/)

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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.