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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 6, 2023. (Total: 223792Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Venous Thrombosis and VKORC1[original query]
Single nucleotide polymorphisms in the VKORC1 gene and the risk of stroke in the Southern German population.
Thrombosis and haemostasis 2008 Oct 100 (4): 614-7.
Arnold Marie-Luise, Lichy Christoph, Werner Inge, Radbruch Alexander, Wagner Simone, Grond-Ginsbach Casp
Study of 18 functional hemostatic polymorphisms in mucocutaneous bleeding disorders.
Annals of hematology 2010 Nov 89 (11): 1147-54.
Antón Ana I, González-Conejero Rocio, Roldán Vanessa, Quiroga Teresa, Sánchez-Vega Beatriz, Corral Javier, Vicente Vicente, Mezzano Die
Brief Report: Single-nucleotide polymorphisms in VKORC1 are risk factors for systemic lupus erythematosus in Asians.
Arthritis and rheumatism 2013 Jan 65 (1): 211-5.
Kaiser Rachel, Taylor Kimberly E, Deng Yun, Zhao Jian, Li Yonghong, Nititham Joanne, Chang Monica, Catanese Joseph, Begovich Ann B, Brown Elizabeth E, Edberg Jeffrey C, McGwin Gerald, Alarcón Graciela S, Ramsey-Goldman Rosalind, Reveille John D, Vila Luis M, Petri Michelle, Kimberly Robert P, Feng Xuebing, Sun Lingyun, Shen Nan, Li Wei, Lu Jian-Xin, Wakeland Edward K, Li Quan-Zhen, Yang Wanling, Lau Yu-Lung, Liu Fei-Lan, Chang Deh-Ming, Yu Chack-Yung, Song Yeong W, Tsao Betty P, Criswell Lindsey A,
High prevalence of VKORC1*3 (G9041A) genetic polymorphism in north Indians: A study on patients with cardiac disorders on acenocoumarol.
Drug discoveries & therapeutics 2016 9 (6): 404-10.
Sehgal Tushar, Hira Jasbir Kaur, Ahluwalia Jasmina, Das Reena, Vijayvergiya Rajesh, Rana Sandip Singh, Varma Neel
Prevalence of common hereditary risk factors for thrombophilia in Somalia and identification of a novel Gln544Arg mutation in coagulation factor V.
Journal of thrombosis and thrombolysis 2017 Sep .
Abdi Abshir Ali, Osman Abdimaj
Hyper-responsiveness to warfarin in a young patient with the VKORC1 -1639GA/CYP2C9*1*46 genotype: a case report.
Thrombosis journal 2022 10 20 (1): 65.
Aldiban Weam, Altawil Yara, Hussein Samir, Aljamali Majd, Youssef Lama
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