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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and STAB2[original query]
Genetics of venous thrombosis: insights from a new genome wide association study. GWAS Catalog
PloS one 2011 6 (9): e25581.
Germain Marine, Saut Noémie, Greliche Nicolas, Dina Christian, Lambert Jean-Charles, Perret Claire, Cohen William, Oudot-Mellakh Tiphaine, Antoni Guillemette, Alessi Marie-Christine, Zelenika Diana, Cambien François, Tiret Laurence, Bertrand Marion, Dupuy Anne-Marie, Letenneur Luc, Lathrop Mark, Emmerich Joseph, Amouyel Philippe, Trégouët David-Alexandre, Morange Pierre-Emmanu
Genome-wide association studies identify genetic loci for low von Willebrand factor levels. GWAS Catalog
European journal of human genetics : EJHG 2015 Oct .
van Loon Janine, Dehghan Abbas, Weihong Tang, Trompet Stella, McArdle Wendy L, Asselbergs Folkert F W, Chen Ming-Huei, Lopez Lorna M, Huffman Jennifer E, Leebeek Frank W G, Basu Saonli, Stott David J, Rumley Ann, Gansevoort Ron T, Davies Gail, Wilson James J F, Witteman Jacqueline C M, Cao Xiting, de Craen Anton J M, Bakker Stephan J L, Psaty Bruce M, Starr John M, Hofman Albert, Wouter Jukema J, Deary Ian J, Hayward Caroline, van der Harst Pim, Lowe Gordon D O, Folsom Aaron R, Strachan David P, Smith Nicolas, de Maat Moniek P M, O'Donnell Christoph
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease.
Blood 2020 May .
Desch Karl C, Ozel Ayse B, Halvorsen Matt, Jacobi Paula M, Golden Krista, Underwood Mary, Germain Marine, Tregouet David-Alexandre, Reitsma Pieter H, Kearon Clive, Mokry Lauren, Richards J Brent, Williams Frances, Li Jun Z, Goldstein David, Ginsburg Dav
Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients.
TH open : companion journal to thrombosis and haemostasis 2020 11 4 (4): e322-e331.
Manderstedt Eric, Lind-Halldén Christina, Lethagen Stefan, Halldén Christ
Rare variant associations with plasma protein levels in the UK Biobank.
Nature 2023 10 622 (7982): 339-347.
Ryan S Dhindsa, Oliver S Burren, Benjamin B Sun, Bram P Prins, Dorota Matelska, Eleanor Wheeler, Jonathan Mitchell, Erin Oerton, Ventzislava A Hristova, Katherine R Smith, Keren Carss, Sebastian Wasilewski, Andrew R Harper, Dirk S Paul, Margarete A Fabre, Heiko Runz, Coralie Viollet, Benjamin Challis, Adam Platt, , Dimitrios Vitsios, Euan A Ashley, Christopher D Whelan, Menelas N Pangalos, Quanli Wang, Slavé Petrovs
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