Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: SCARA5[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 |
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.
Blood 2019 Aug . Lindstrom Sara, Wang Lu, Smith Erin N, Gordon William, van Hylckama Vlieg Astrid, de Andrade Mariza, Brody Jennifer A, Pattee Jack W, Haessler Jeffrey, Brumpton Ben M, Chasman Daniel I, Suchon Pierre, Chen Ming-Huei, Turman Constance, Germain Marine, Wiggins Kerri L, MacDonald James, Braekkan Sigrid K, Armasu Sebastian M, Pankratz Nathan, Jackson Rebecca D, Nielsen Jonas B, Giulianini Franco, Puurunen Marja K, Ibrahim Manal, Heckbert Susan R, Damrauer Scott M, Natarajan Pradeep, Klarin Derek, de Vries Paul S, Sabater-Lleal Maria, Huffman Jennifer E, Bammler Theo K, Frazer Kelly A, McCauley Bryan M, Taylor Kent, Pankow James S, Reiner Alexander P, Gabrielsen Maiken E, Deleuze Jean-François, O'Donnell Chris J, Kim Jihye, McKnight Barbara, Kraft Peter, Hansen John-Bjarne, Rosendaal Frits R, Heit John A, Psaty Bruce M, Tang Weihong, Kooperberg Charles, Hveem Kristian, Ridker Paul M, Morange Pierre-Emmanuel, Johnson Andrew D, Kabrhel Christopher, Trégouët David-Alexandre, Smith Nicholas |
Gene-level genome-wide association analysis of suicide attempt, a preliminary study in a psychiatric Mexican population. Molecular genetics & genomic medicine 2019 Oct e983. González-Castro Thelma Beatriz, Martínez-Magaña José Jaime, Tovilla-Zárate Carlos Alfonso, Juárez-Rojop Isela Esther, Sarmiento Emmanuel, Genis-Mendoza Alma Delia, Nicolini Humber |
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 |
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 |
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