Staff Details

Andrei Barysenka

Phone: +49 89 3187 43713
Building/Room: 3533/215




  • Statistical genetics of complex traits
  • RNA and DNA Seq' analysis
  • Population genetics
  • Genetic epidemiology
  • Developing bioinformatics software

Selected publications:

Witten, A. ;... Barysenka, A. ; Stoll, M.
Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study.
J Mol Med (Berl). 765-775 (2018)

Ter Bekke, RMA. ; ... Barysenka, A. ; Volders, PGA. 
Heritability in a SCN5A-mutation founder population with increased female susceptibility to non-nocturnal ventricular tachyarrhythmia and sudden cardiac death.
Heart Rhythm. 1873-1881 (2017)

Rühle, F. ; ... Barysenka, A. ; Stoll, M. 
Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism.
Blood. 783-790 (2017)

Stoll, M. ; ... Barysenka, A. ; Nowak-Göttl, U. 
Rare variants in the ADAMTS13 Von Willebrand Factor-Binding Domain Contribute to Pediatric Stroke.
Circ' Cardiovasc Genet. 357-67 (2016)

Liu, Y. ; ... Barysenka, A. ; Goldbach-Mansky, R. 
Activated STING in a vascular and pulmonary syndrome.
New Engl J Med. 507-518. (2014)