# Thomas Meitinger

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/thomas-meitinger/

## Facts

| Field | Value |
| --- | --- |
| Citations | 135,102 |
| Field | Genetic Associations and Epidemiology |
| h-index | 171 |
| i10-index | 616 |
| Last Known Institution | Institute of Human Genetics |
| OpenAlex ID | https://openalex.org/A5006468847 |
| ORCID iD | 0000-0002-8838-8403 |
| Works | 967 |

## Researcher papers

Showing 12 of 38.

- [Biological, clinical and population relevance of 95 loci for blood lipids](https://scholariq.org/papers/biological-clinical-and-population-relevance-of-95-loci-for-blood-lipids/)
- [A reference panel of 64,976 haplotypes for genotype imputation](https://scholariq.org/papers/a-reference-panel-of-64-976-haplotypes-for-genotype-imputation/)
- [Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology](https://scholariq.org/papers/mutations-in-lrrk2-cause-autosomal-dominant-parkinsonism-with-pleomorphic/)
- [A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease](https://scholariq.org/papers/a-comprehensive-1000-genomes-based-genome-wide-association-meta-analysis-of/)
- [Transcriptome and genome sequencing uncovers functional variation in humans](https://scholariq.org/papers/transcriptome-and-genome-sequencing-uncovers-functional-variation-in-humans/)
- [Genomewide Association Analysis of Coronary Artery Disease](https://scholariq.org/papers/genomewide-association-analysis-of-coronary-artery-disease/)
- [Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps](https://scholariq.org/papers/fine-mapping-type-2-diabetes-loci-to-single-variant-resolution-using-high/)
- [Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease](https://scholariq.org/papers/large-scale-association-analysis-identifies-13-new-susceptibility-loci-for/)
- [Systematic identification of trans eQTLs as putative drivers of known disease associations](https://scholariq.org/papers/systematic-identification-of-trans-eqtls-as-putative-drivers-of-known-disease/)
- [Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23](https://scholariq.org/papers/autosomal-dominant-hypophosphataemic-rickets-is-associated-with-mutations-in/)
- [Genome-wide association study identifies eight loci associated with blood pressure](https://scholariq.org/papers/genome-wide-association-study-identifies-eight-loci-associated-with-blood/)
- [A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets](https://scholariq.org/papers/a-gene-pex-with-homologies-to-endopeptidases-is-mutated-in-patients-with-x/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-disorders/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)

## Researcher university

- [Institute of Human Genetics](https://scholariq.org/institutions/institute-of-human-genetics/)

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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.