Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and GP6[original query] |
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| Effect of genetic variations in platelet glycoproteins Ibalpha and VI on the risk for coronary heart disease events in postmenopausal women taking hormone therapy. Blood 2007 Mar 109 (5): 1862-9. Bray Paul F, Howard Timothy D, Vittinghoff Eric, Sane David C, Herrington David |
| An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigrees. Journal of thrombosis and haemostasis : JTH 2006 1 4 (1): 137-47. Kunicki T J, Baronciani L, Canciani M T, Gianniello F, Head S R, Mondala T S, Salomon D R, Federici A |
Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach.
Blood 2009 May 113 (21): 5298-303. Trégouët David-Alexandre, Heath Simon, Saut Noémie, Biron-Andreani Christine, Schved Jean-François, Pernod Gilles, Galan Pilar, Drouet Ludovic, Zelenika Diana, Juhan-Vague Irène, Alessi Marie-Christine, Tiret Laurence, Lathrop Mark, Emmerich Joseph, Morange Pierre-Emmanu |
| Lack of association between aspirin responsiveness and seven candidate gene haplotypes in patients with symptomatic vascular disease. Thrombosis and haemostasis 2009 Jan 101 (1): 123-33. Kunicki Thomas J, Williams Shirley A, Nugent Diane J, Harrison Paul, Segal Helen C, Syed Anila, Rothwell Peter |
| The minor allele of GP6 T13254C is associated with decreased platelet activation and a reduced risk of recurrent cardiovascular events and mortality: results from the SMILE-Platelets project. Journal of thrombosis and haemostasis : JTH 2010 Nov 8 (11): 2377-84. Snoep J D, Gaussem P, Eikenboom J C J, Emmerich J, Zwaginga J J, Holmes C E, Vos H L, de Groot Ph G, Herrington D M, Bray P F, Rosendaal F R, van der Bom J |
| Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population. PLoS genetics 2013 Mar 9 (3): e1003419. Haiman Christopher A, Han Ying, Feng Ye, Xia Lucy, Hsu Chris, Sheng Xin, Pooler Loreall C, Patel Yesha, Kolonel Laurence N, Carter Erin, Park Karen, Le Marchand Loic, Van Den Berg David, Henderson Brian E, Stram Daniel |
| High-throughput elucidation of thrombus formation reveals sources of platelet function variability. Haematologica 2018 12 104 (6): 1256-1267. van Geffen Johanna P, Brouns Sanne L N, Batista Joana, McKinney Harriet, Kempster Carly, Nagy Magdolna, Sivapalaratnam Suthesh, Baaten Constance C F M J, Bourry Nikki, Frontini Mattia, Jurk Kerstin, Krause Manuela, Pillitteri Daniele, Swieringa Frauke, Verdoold Remco, Cavill Rachel, Kuijpers Marijke J E, Ouwehand Willem H, Downes Kate, Heemskerk Johan W |
| Delineation of the Germline and Somatic Mutation Interaction Landscape in Triple-Negative and Non-Triple-Negative Breast Cancer. International journal of genomics 2020 2020 2641370. Wu Jiande, Mamidi Tarun K K, Zhang Lu, Hicks Chin |
| Polymorphisms in GP6, PEAR1A, MRVI1, PIK3CG, JMJD1C, and SHH Genes in Patients with Unstable Angina. International journal of environmental research and public health 2020 Oct 17 (20): . Rudzik Rafa?, Dziedziejko Violetta, Ra? Monika Ewa, Sawczuk Marek, Maciejewska-Skrendo Agnieszka, Safranow Krzysztof, Pawlik Andrz |
| The associations of candidate gene polymorphisms with aspirin resistance in patients with ischemic disease: a meta-analysis. Human genomics 2024 12 18 (1): 135. Chun-Xing Li, Li-Chaoyue Sun, Yu-Qiao Wang, Tian-Tian Liu, Jin-Rui Cai, Hua Liu, Zhao Ren, Zhanmiao |
- Page last reviewed:Feb 1, 2024
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