Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Thrombosis and MAF[original query] |
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Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data. PloS one 2013 8 (12): e81503. Mosley Jonathan D, Van Driest Sara L, Larkin Emma K, Weeke Peter E, Witte John S, Wells Quinn S, Karnes Jason H, Guo Yan, Bastarache Lisa, Olson Lana M, McCarty Catherine A, Pacheco Jennifer A, Jarvik Gail P, Carrell David S, Larson Eric B, Crosslin David R, Kullo Iftikhar J, Tromp Gerard, Kuivaniemi Helena, Carey David J, Ritchie Marylyn D, Denny Josh C, Roden Dan |
Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency. PloS one 2016 11 (3): e0152159. Toderici Mara, de la Morena-Barrio María Eugenia, Padilla José, Miñano Antonia, Antón Ana Isabel, Iniesta Juan Antonio, Herranz María Teresa, Fernández Nuria, Vicente Vicente, Corral Javi |
Identification of Genetic Aberrations in Thrombomodulin Gene in Patients With Recurrent Venous Thromboembolism. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2017 Jan 1076029616686716. Ahmad Abrar, Sundquist Kristina, Zöller Bengt, Svensson Peter J, Sundquist Jan, Memon Ashfaque |
Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes. Journal of thrombosis and haemostasis : JTH 2018 Aug . de Haan H G, van Hylckama Vlieg A, Lotta L A, Gorski M M, Bucciarelli P, Martinelli I, Baglin T P, Peyvandi F, Rosendaal F R, |
Next-generation DNA sequencing to identify novel genetic risk factors for cerebral vein thrombosis. Thrombosis research 2018 7 169 76-81. Gorski Marcin M, de Haan Hugoline G, Mancini Ilaria, Lotta Luca A, Bucciarelli Paolo, Passamonti Serena M, Cairo Andrea, Pappalardo Emanuela, van Hylckama Vlieg Astrid, Martinelli Ida, Rosendaal Frits R, Peyvandi Flo |
Clinical, laboratory, and genetic risk factors for thrombosis in sickle cell disease. Blood advances 2020 May 4 (9): 1978-1986. Srisuwananukorn Andrew, Raslan Rasha, Zhang Xu, Shah Binal N, Han Jin, Gowhari Michel, Molokie Robert E, Gordeuk Victor R, Saraf Santosh |
Genetics of osteopontin in patients with chronic kidney disease: The German Chronic Kidney Disease study. PLoS genetics 2022 4 18 (4): e1010139. Cheng Yurong, Li Yong, Scherer Nora, Grundner-Culemann Franziska, Lehtimäki Terho, Mishra Binisha H, Raitakari Olli T, Nauck Matthias, Eckardt Kai-Uwe, Sekula Peggy, Schultheiss Ulla T, |
Thrombotic risk determined by rare and common SERPINA1 variants in a population-based cohort study. Journal of thrombosis and haemostasis : JTH 2022 3 20 (6): 1421-1427. Manderstedt Eric, Halldén Christer, Lind-Halldén Christina, Elf Johan, Svensson Peter J, Engström Gunnar, Melander Olle, Baras Aris, Lotta Luca A, Zöller Bengt, |
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