Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Thromboembolism and PROCR[original query] |
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Lack of association of soluble endothelial protein C receptor and PROCR 6936A/G polymorphism with the risk of venous thromboembolism in a prospective study. British journal of haematology 2009 Apr 145 (2): 221-6. Yamagishi Kazumasa, Cushman Mary, Heckbert Susan R, Tsai Michael Y, Folsom Aaron |
Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.
Blood 2010 Dec 116 (23): 5032-6. Tang Weihong, Basu Saonli, Kong Xiaoxiao, Pankow James S, Aleksic Nena, Tan Adrian, Cushman Mary, Boerwinkle Eric, Folsom Aaron |
Paternal endothelial protein C receptor 219Gly variant as a mild and limited risk factor for deep vein thrombosis during pregnancy. Journal of thrombosis and haemostasis : JTH 2010 Apr 8 (4): 707-13. Galanaud J P, Cochery-Nouvellon E, Alonso S, Chauleur C, Mercier E, Lissalde-Lavigne G, Fabbro-Peray P, Reny J L, Mares P, Dauzat M, Quere I, Gris J |
A genome-wide association study of the Protein C anticoagulant pathway.
PloS one 2011 6 (12): e29168. Athanasiadis Georgios, Buil Alfonso, Souto Juan Carlos, Borrell Montserrat, López Sonia, Martinez-Perez Angel, Lathrop Mark, Fontcuberta Jordi, Almasy Laura, Soria José Manu |
Effects of oral anticoagulant therapy and haplotype 1 of the endothelial protein C receptor gene on activated protein C levels. Thrombosis and haemostasis 2012 Mar 107 (3): 448-57. Medina Pilar, Bonet Elena, Navarro Silvia, Martos Laura, Estellés Amparo, Ferrando Fernando, Vicente Vicente, Bertina Rogier M, España Francis |
The endothelial protein C receptor (PROCR) Ser219Gly variant and risk of common thrombotic disorders: a HuGE review and meta-analysis of evidence from observational studies. Blood 2012 Mar 119 (10): 2392-400. Dennis Jessica, Johnson Candice Y, Adediran Adeniyi Samuel, de Andrade Mariza, Heit John A, Morange Pierre-Emmanuel, Trégouët David-Alexandre, Gagnon Fran |
Targeted gene sequencing identifies variants in the protein C and endothelial protein C receptor genes in patients with unprovoked venous thromboembolism. Arteriosclerosis, thrombosis, and vascular biology 2013 Nov 33 (11): 2674-81. Wu Cynthia, Dwivedi Dhruva J, Pepler Laura, Lysov Zakhar, Waye John, Julian Jim, Desch Karl, Ginsburg David, Weitz Jeffrey I, Kearon Clive, Liaw Patricia |
Functional analysis of two haplotypes of the human endothelial protein C receptor gene. Arteriosclerosis, thrombosis, and vascular biology 2014 Mar 34 (3): 684-90. Medina P, Navarro S, Bonet E, Martos L, Estellés A, Bertina R M, Vos H L, España |
Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism.
American journal of human genetics 2015 Apr 96 (4): 532-42. Germain Marine, Chasman Daniel I, de Haan Hugoline, Tang Weihong, Lindström Sara, Weng Lu-Chen, de Andrade Mariza, de Visser Marieke C H, Wiggins Kerri L, Suchon Pierre, Saut Noémie, Smadja David M, Le Gal Grégoire, van Hylckama Vlieg Astrid, Di Narzo Antonio, Hao Ke, Nelson Christopher P, Rocanin-Arjo Ares, Folkersen Lasse, Monajemi Ramin, Rose Lynda M, Brody Jennifer A, Slagboom Eline, Aïssi Dylan, Gagnon France, Deleuze Jean-Francois, Deloukas Panos, Tzourio Christophe, Dartigues Jean-Francois, Berr Claudine, Taylor Kent D, Civelek Mete, Eriksson Per, , Psaty Bruce M, Houwing-Duitermaat Jeanine, Goodall Alison H, Cambien François, Kraft Peter, Amouyel Philippe, Samani Nilesh J, Basu Saonli, Ridker Paul M, Rosendaal Frits R, Kabrhel Christopher, Folsom Aaron R, Heit John, Reitsma Pieter H, Trégouët David-Alexandre, Smith Nicholas L, Morange Pierre-Emmanu |
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
Human molecular genetics 2016 May 25 (9): 1867-74. Hinds David A, Buil Alfonso, Ziemek Daniel, Martinez-Perez Angel, Malik Rainer, Folkersen Lasse, Germain Marine, Mälarstig Anders, Brown Andrew, Soria Jose Manuel, Dichgans Martin, Bing Nan, Franco-Cereceda Anders, Souto Juan Carlos, Dermitzakis Emmanouil T, Hamsten Anders, Worrall Bradford B, Tung Joyce Y, , Sabater-Lleal Mar |
Implications of venous thromboembolism GWAS reported genetic makeup in the clinical outcome of ovarian cancer patients. The pharmacogenomics journal 2020 Nov . Tavares Valéria, Pinto Ricardo, Assis Joana, Coelho Sara, Brandão Mariana, Alves Sara, Pereira Deolinda, Medeiros R |
Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus. Nature communications 2022 3 13 (1): 1222. Stacey David, Chen Lingyan, Stanczyk Paulina J, Howson Joanna M M, Mason Amy M, Burgess Stephen, MacDonald Stephen, Langdown Jonathan, McKinney Harriett, Downes Kate, Farahi Neda, Peters James E, Basu Saonli, Pankow James S, Tang Weihong, Pankratz Nathan, Sabater-Lleal Maria, de Vries Paul S, Smith Nicholas L, , Gelinas Amy D, Schneider Daniel J, Janjic Nebojsa, Samani Nilesh J, Ye Shu, Summers Charlotte, Chilvers Edwin R, Danesh John, Paul Dirk |
Thrombotic Risk Determined by Protein C Receptor (PROCR) Variants among Middle-Aged and Older Adults: A Population-Based Cohort Study. Thrombosis and haemostasis 2022 1 122 (8): 1326-1332. Manderstedt Eric, Halldén Christer, Lind-Halldén Christina, Elf Johan, Svensson Peter J, Engström Gunnar, Melander Olle, Baras Aris, Lotta Luca A, Zöller Bengt, |
Thrombogenesis-associated genetic determinants as predictors of thromboembolism and prognosis in cervical cancer. Scientific reports 2023 6 13 (1): 9519. Beatriz Vieira Neto, Valéria Tavares, José Brito da Silva, Joana Liz-Pimenta, Inês Soares Marques, Luísa Carvalho, Lurdes Salgado, Deolinda Pereira, Rui Medeir |
The association between EPCR gene p.Ser219Gly polymorphism and venous thromboembolism risk: a case-control study, meta-analysis, and a reproducibility study. Frontiers in cardiovascular medicine 2023 12 10 1270093. Dóra Pituk, Tünde Miklós, Ágota Schlammadinger, Katalin Rázsó, Zsuzsanna Berecz |
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