# Michael Preuß

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/michael-preu/

## Facts

| Field | Value |
| --- | --- |
| Citations | 33,222 |
| Field | Genetic Associations and Epidemiology |
| h-index | 67 |
| i10-index | 137 |
| Last Known Institution | Beth Israel Deaconess Medical Center |
| OpenAlex ID | https://openalex.org/A5076419751 |
| ORCID iD | https://orcid.org/0000-0001-5266-8465 |
| Works | 233 |

## Researcher papers

- [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/)
- [Genetic analyses of diverse populations improves discovery for complex traits](https://scholariq.org/papers/genetic-analyses-of-diverse-populations-improves-discovery-for-complex-traits/)
- [Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants](https://scholariq.org/papers/genome-wide-association-of-early-onset-myocardial-infarction-with-single/)
- [The trans-ancestral genomic architecture of glycemic traits](https://scholariq.org/papers/the-trans-ancestral-genomic-architecture-of-glycemic-traits/)
- [The Polygenic and Monogenic Basis of Blood Traits and Diseases](https://scholariq.org/papers/the-polygenic-and-monogenic-basis-of-blood-traits-and-diseases/)
- [Genetic drivers of heterogeneity in type 2 diabetes pathophysiology](https://scholariq.org/papers/genetic-drivers-of-heterogeneity-in-type-2-diabetes-pathophysiology/)
- [Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease](https://scholariq.org/papers/genome-wide-haplotype-association-study-identifies-the-slc22a3-lpal2-lpa-gene/)
- [Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes](https://scholariq.org/papers/refining-the-accuracy-of-validated-target-identification-through-coding-variant/)
- [Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease](https://scholariq.org/papers/global-biobank-meta-analysis-initiative-powering-genetic-discovery-across-human/)
- [Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data](https://scholariq.org/papers/assessing-the-contribution-of-rare-variants-to-complex-trait-heritability-from/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Metabolomics and Mass Spectrometry Studies](https://scholariq.org/topics/metabolomics-and-mass-spectrometry-studies/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)
- [Genetic Mapping and Diversity in Plants and Animals](https://scholariq.org/topics/genetic-mapping-and-diversity-in-plants-and-animals/)

## Researcher university

- [Beth Israel Deaconess Medical Center](https://scholariq.org/institutions/beth-israel-deaconess-medical-center/)

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