Uwe Völker - Genetic Mutations

Author Information

Uwe Völker is a prominent researcher affiliated with the Department of Functional Genomics at the Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Germany. He is also associated with the German Center for Cardiovascular Research, Partner Site Greifswald, Germany. His extensive research contributions span various aspects of genetics and functional genomics.

Research Contributions

In 2022 alone, Uwe Völker has made significant contributions to the scientific community with a variety of publications. His research covers diverse topics such as the pathogenesis of vaccine-induced immune thrombotic thrombocytopenia (VITT), the genetic determinants of human height, the genetic architecture of mood and psychotic disorders, and multi-omics analysis of atrial fibrillation. His work also includes studies on the proteome analysis of Schistosoma mansoni, genome-wide association studies on abdominal aortic diameter, and comparative analyses of SARS-CoV-2 vector vaccines. Additionally, he has explored the metabolic health connections revealed by NMR metabolomics and developed a hybrid federated tool as an alternative to meta-analysis in genome-wide association studies.

Aliases

Uwe Völker is also known by several aliases including U Völker, U. Völker, and Uwe Völker.

Publication and Citation Metrics

Metric	Value
Citation Count	41,050
h-index	98
Paper Count	622

Publications:

Pathogenesis of vaccine-induced immune thrombotic thrombocytopenia (VITT)

DOI: 10.1053/j.seminhematol.2022.02.004

Year: 2022

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

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

DOI: 10.1016/j.biopsych.2021.02.972

Year: 2022

Tissue-specific multi-omics analysis of atrial fibrillation

DOI: 10.1038/s41467-022-27953-1

Year: 2022

Cohort Profile Update: The Study of Health in Pomerania (SHIP).

DOI: 10.1093/ije/dyac034

Year: 2022

Comparative proteome analysis of the tegument of male and female adult Schistosoma mansoni

DOI: 10.21203/rs.3.rs-1291198/v1

Year: 2022

Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study.

DOI: 10.1093/hmg/ddac051

Year: 2022

Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines

DOI: 10.3324/haematol.2021.280154

Year: 2022

NMR Metabolomics Reveal Urine Markers of Microbiome Diversity and Identify Benzoate Metabolism as a Mediator between High Microbial Alpha Diversity and Metabolic Health

DOI: 10.3390/metabo12040308

Year: 2022

sPLINK: a hybrid federated tool as a robust alternative to meta-analysis in genome-wide association studies

DOI: 10.1186/s13059-021-02562-1

Year: 2022

How Common are BRCA1 and BRCA2 Mutations?

How Are Synonymous Mutations Detected?

How Does Genetics Influence Occupational Therapy?

How is Data Collected in Populace Genomics?

What Are the Types of Phylogenetic Trees?

What Evidence Supports the Neutral Theory?

What is the Prognosis for Individuals with Cystic Fibrosis?

Can Immunotherapy Cause Genetic Mutations?

How Does Genetic Testing Help in Managing Cystic Fibrosis?

What Types of Prenatal Tests Are Available?

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