Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: STAB2[original query] |
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Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.
BMC medical genetics 2011 12 (1): 102. Antoni Guillemette, Oudot-Mellakh Tiphaine, Dimitromanolakis Apostolos, Germain Marine, Cohen William, Wells Philip, Lathrop Mark, Gagnon France, Morange Pierre-Emmanuel, Tregouet David-Alexand |
Genetics of venous thrombosis: insights from a new genome wide association study.
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 |
Pathway analysis of a genome-wide association study in schizophrenia. Gene 2013 Aug 525 (1): 107-15. Lee Young Ho, Kim Jae-Hoon, Song Gwan G |
Identification of aortic arch-specific quantitative trait loci for atherosclerosis by an intercross of DBA/2J and 129S6 apolipoprotein E-deficient mice. PloS one 2015 10 (2): e0117478. Kayashima Yukako, Makhanova Natalia A, Matsuki Kota, Tomita Hirofumi, Bennett Brian J, Maeda Nobu |
Genome-wide association studies identify genetic loci for low von Willebrand factor levels.
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 |
Genetic determinants of VWF clearance and FVIII binding modify FVIII pharmacokinetics in pediatric hemophilia A patients. Blood 2019 Jul . Swystun Laura L, Ogiwara Kenichi, Rawley Orla, Brown Christine, Georgescu Ilinca, Hopman Wilma, Labarque Veerle, Male Christoph, Thom Katharina, Blanchette Victor S, Carcao Manuel, Lillicrap Dav |
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 |
Pan-Cancer Multiomics Analysis of TC2N Gene Suggests its Important Role(s) in Tumourigenesis of Many Cancers. Asian Pacific journal of cancer prevention : APJCP 2020 11 21 (11): 3199-3209. Qureshi Muhammad Asif, Khan Saeed, Tauheed Muhammad Sohaib, Syed Sofia Ali, Ujjan Ikram Din, Lail Amanullah, Sharafat Shahe |
Factor VIII pharmacokinetics associates with genetic modifiers of VWF and FVIII clearance in an adult hemophilia A population. Journal of thrombosis and haemostasis : JTH 2020 Nov . Ogiwara Kenichi, Swystun Laura L, Paine A Simonne, Kepa Sylvia, Choi Seon Jai, Rejtö Judit, Hopman Wilma, Pabinger Ingrid, Lillicrap Dav |
Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus.
Rheumatology (Oxford, England) 2021 Jan . Song Qin, Lei Yao, Shao Li, Li Weiyang, Kong Qingsheng, Lin Zhiming, Qin Xiao, Wei Wei, Hou Fei, Li Jian, Guo Xianghua, Mao Yujing, Cao Yujie, Liu Zhongyi, Zheng Lichuan, Liang Rui, Jiang Yuping, Liu Yan, Zhang Lili, Yang Jing, Lau Yu Lung, Zhang Yan, Ban Bo, Wang Yong-Fei, Yang Wanli |
Modulation of factor VIII pharmacokinetics by genetic components in factor VIII receptors. Haemophilia : the official journal of the World Federation of Hemophilia 2022 12 . Lunghi Barbara, Morfini Massimo, Martinelli Nicola, Branchini Alessio, Linari Silvia, Castaman Giancarlo, Bernardi Frances |
Genome-wide analyses identify novel risk loci for cluster headache in Han Chinese residing in Taiwan. The journal of headache and pain 2022 11 23 (1): 147. Chen Shih-Pin, Hsu Chia-Lin, Wang Yen-Feng, Yang Fu-Chi, Chen Ting-Huei, Huang Jia-Hsin, Pan Li-Ling Hope, Fuh Jong-Ling, Chang Hsueh-Chen, Lee Yi-Lun, Chang Hung-Ching, Lee Ko-Han, Chang Yu-Chuan, Fann Cathy Shen-Jang, Wang Shuu-Ji |
The contribution of the sinusoidal endothelial cell receptors CLEC4M, stabilin-2, and SCARA5 to VWF-FVIII clearance in thrombosis and hemostasis. Journal of thrombosis and haemostasis : JTH 2023 4 . Laura L Swystun, Alison Michels, David Lillicr |
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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