Michael L. Boehnke - Public Health

Author Information

Michael L. Boehnke is a prominent researcher affiliated with the School of Public Health at the University of Michigan, Ann Arbor. His work primarily focuses on genetic epidemiology and public health, contributing significantly to understanding the genetic basis of various human traits and diseases. His affiliation with a leading institution underscores his position and influence within the field of public health and genetic research.

Research Contributions

Michael L. Boehnke has made substantial contributions to the field of genetic epidemiology, with a particular focus on the genetic architecture of complex traits and diseases. In 2022 alone, he co-authored numerous impactful papers exploring topics such as genetic variants associated with human height, type 2 diabetes in diverse populations, and schizophrenia risk. His research also delves into the genetic interplay of cardiometabolic traits and psychiatric disorders. Additionally, he has contributed to the development of tools like the FIVEx eQTL browser, which enhances the accessibility of genetic data for researchers worldwide.

Aliases

Michael L. Boehnke is also known by several aliases, including M Boehnke, Michael Boehnke, M. Boehnke, and Mike Boehnke. These variations are commonly used in academic and scientific publications.

Publication and Citation Metrics

Metric	Value
Citation Count	116,599
H-index	141
Paper Count	587

Publications:

A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries

DOI: 10.1101/2022.01.07.475305

Year: 2022

Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

DOI: 10.1038/s41467-022-29143-5

Year: 2022

Identification of genetic effects underlying type 2 diabetes in South Asian and European populations

DOI: 10.1038/s42003-022-03248-5

Year: 2022

Subcutaneous adipose tissue splice quantitative trait loci reveal differences in isoform usage associated with cardiometabolic traits.

DOI: 10.1016/j.ajhg.2021.11.019

Year: 2022

Rare coding variants in ten genes confer substantial risk for schizophrenia.

DOI: 10.1038/s41586-022-04556-w

Year: 2022

FIVEx: an interactive eQTL browser across public datasets

DOI: 10.1093/bioinformatics/btab614

Year: 2022

Digenic Inheritance of Dominant TRAF6 and Recessive OSMR Pathogenic Variants Associated with Short Stature, Atopy, and Eosinophilic Inflammation

DOI: 10.1016/j.jaci.2021.12.514

Year: 2022

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

DOI: 10.1016/j.biopsych.2021.05.029

Year: 2022

Physical activity and sedentary behavior; mechanistic insights and role in disease prevention

DOI: 10.21203/rs.3.rs-1129252/v1

Year: 2021

Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer

DOI: 10.1038/s41467-021-27675-w

Year: 2021

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