A
Andrei Barysenka
Researcher at University of Münster
Publications - 5
Citations - 994
Andrei Barysenka is an academic researcher from University of Münster. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 1, co-authored 1 publications receiving 730 citations. Previous affiliations of Andrei Barysenka include National Institutes of Health.
Papers
More filters
Journal ArticleDOI
Activated STING in a Vascular and Pulmonary Syndrome
Yongmei Liu,A Almeida de Jesus,B Marrero,Dan Yang,Suzanne E. Ramsey,Suzanne E. Ramsey,G.A. Montealegre Sanchez,Klaus Tenbrock,Klaus Tenbrock,Helmut Wittkowski,Helmut Wittkowski,Olcay Y. Jones,Olcay Y. Jones,Hye Sun Kuehn,Chyi-Chia Richard Lee,Michael A. DiMattia,Edward W. Cowen,Benito Gonzalez,Ira Palmer,J.J. DiGiovanna,Angelique Biancotto,H. Kim,Wanxia L. Tsai,Anna M. Trier,Yhu Chering Huang,Deborah L. Stone,S Hill,Hanna Kim,C. St. Hilaire,Shakuntala Gurprasad,Nicole Plass,D. Chapelle,Iren Horkayne-Szakaly,Iren Horkayne-Szakaly,Dirk Foell,Dirk Foell,Andrei Barysenka,Andrei Barysenka,Fabio Candotti,Steven M. Holland,Jason D. Hughes,Jason D. Hughes,Huseyin Mehmet,Huseyin Mehmet,Andrew C. Issekutz,Andrew C. Issekutz,Mark Raffeld,Joshua J McElwee,Joshua J McElwee,Joseph R. Fontana,Caterina P. Minniti,Susan Moir,Daniel L. Kastner,Massimo Gadina,A.C. Steven,Paul T. Wingfield,Stephen R. Brooks,Sofia Rosenzweig,Thomas A. Fleisher,Zuoming Deng,Manfred Boehm,Amy S. Paller,Amy S. Paller,Raphaela Goldbach-Mansky +63 more
TL;DR: STING-associated vasculopathy with onset in infancy (SAVI) is an autoinflammatory disease caused by gain-of-function mutations in TMEM173, the stimulator of interferon genes (STING), andConstitutive up-regulation of phosphorylated STAT1 in patients' lymphocytes was reduced by JAK inhibitors.
Journal ArticleDOI
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
Gyda Bjornsdottir,Gudmar Thorleifsson,Patrick Sulem,Kristjan Norland,Egil Ferkingstad,Asmundur Oddsson,Florian Zink,Sigrun H. Lund,Muhammad Nawaz,G. Bragi Walters,Astros Skuladottir,Sigurjon A. Gudjonsson,G. Einarsson,Gisli H. Halldorsson,Valgerdur Bjarnadottir,Gardar Sveinbjornsson,Anna Helgadottir,Unnur Styrkarsdottir,Larus J. Gudmundsson,Thomas Hansen,Thomas Werge,Karina Banasik,Anders Troelsen,Søren Thorgaard Skou,Lise Wegner Thørner,Christian Erikstrup,Kaspar René Nielsen,Susan Mikkelsen,Steffen Andersen,Søren Brunak,Kristoffer Sølvsten Burgdorf,Henrik Hjalgrim,Gregor B.E. Jemec,Poul Jennum,Pär I. Johansson,Kasper René Nielsen,Mette Nyegaard,Mie Topholm Bruun,O. Pedersen,Khoa Manh Dinh,Erik Sørensen,Daniel F. Gudbjartsson,Unnur Þorsteinsdottir,Margit Hørup Larsen,Maria Didriksen,Susanne Gjørup Sækmose,Eleftheria Zeggini,Konstantinos Hatzikotoulas,Lorraine Southam,Arthur Gilly,Andrei Barysenka,Joyce B. J. van Meurs,Cindy G. Boer,André G. Uitterlinden,Lilja Stefansdottir,Helgi Jonsson,Thorvaldur Ingvarsson,Tõnu Esko,Reedik Mägi,Maris Teder-Laving,Shiro Ikegawa,Chikashi Terao,Hiroshi Takuwa,Ingrid Meulenbelt,Rodrigo Coutinho de Almeida,Margreet Kloppenburg,Margo Tuerlings,P. Eline Slagboom,Rob G H H Nelissen,Ana M. Valdes,Massimo Mangino,Aspasia Tsezou,Eleni Zengini,G. Alexiadis,George C. Babis,Kathryn S.E. Cheah,Tian T Wu,Dino Samartzis,Jason Pui Yin Cheung,Pak C. Sham,Peter Kraft,Jae H. Kang,Kristian Hveem,John-Anker Zwart,Almut Luetge,Anne Heidi Skogholt,Marianne Bakke Johnsen,Laurent F. Thomas,Bendik S. Winsvold,Maiken Elvestad Gabrielsen,Ming Ta Michael Lee,Yanfei Zhang,Steven A. Lietman,Manu Shivakumar,George Davey Smith,Joe Tobias,April Hartley,Tom R. Gaunt,Jie Zheng,Jeremy Mark Wilkinson,Julia Steinberg,Andrew P. Morris,Ingileif Jonsdottir,Aron H. Bjornsson,Ingvar Hakon Olafsson,Elfar Ulfarsson,Josep Blondal,Arnor Vikingsson,Sisse R. Ostrowski,Henrik Ullum,Unnur Thorsteinsdottir,Hreinn Stefansson,Thorgeir E. Thorgeirsson,Kari Stefansson +113 more
TL;DR: A genome-wide association study of back pain using diagnoses assigned in clinical practice; dorsalgia (119,100 cases, 909,847 controls) and intervertebral disc disorder (IDD) was conducted in this paper .
Journal ArticleDOI
Gene-based whole genome sequencing meta-analysis of 250 circulating proteins in three isolated European populations
Arthur Gilly,Lucija Klaric,Young-Chan Park,Grace Png,Andrei Barysenka,Joseph A. Marsh,Emmanouil Tsafantakis,Maria Karaleftheri,George Dedoussis,James F. Wilson,Eleftheria Zeggini +10 more
TL;DR: In this paper , a meta-analysis of gene-based rare variant aggregation optimal tests, applied to the human cardiometabolic proteome, was performed across MANOLIS, Pomak and ORCADES.
Journal ArticleDOI
Standing genetic variation affects phenotypic heterogeneity in a SCN5A-mutation founder population with excess sudden cardiac death.
Aaron Isaacs,Andrei Barysenka,Rachel M.A. ter Bekke,Apollonia T. J. M. Helderman-van den Enden,Arthur van den Wijngaard,Paul G.A. Volders,Monika Stoll +6 more
TL;DR: Phe1617del/rs749697698 deletion was associated with isorhythmic dissociation after correction for multiple comparisons (odds ratio 11.23; 95% confidence interval 2.39; P = 1.2 × 10−4) as discussed by the authors .
Journal ArticleDOI
Identifying causal serum protein–cardiometabolic trait relationships using whole genome sequencing
Grace Png,Raffaele Gerlini,Konstantinos Hatzikotoulas,Andrei Barysenka,Nigel W. Rayner,Lucija Klaric,Birgit Rathkolb,Juan Antonio Aguilar-Pimentel,Jan Rozman,Helmut Fuchs,Valerie Gailus-Durner,Emmanouil Tsafantakis,Maria Karaleftheri,George Dedoussis,Claus U. Pietrzik,James F. Wilson,Martin Hrabé de Angelis,Christoph Becker-Pauly,Arthur Gilly,Eleftheria Zeggini +19 more
TL;DR: In this article , the authors performed a protein quantitative trait locus (pQTL) analysis of 248 serum proteins relevant to cardiometabolic processes in 2893 individuals and found 301 independently associated pQTL variants for 170 proteins including 12 rare variants (minor allele frequency < 1%).