Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Thromboembolism and SERPINC1[original query] |
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Single nucleotide polymorphisms and the risk of venous thrombosis: results from a Danish case-cohort study. British journal of haematology 2012 Nov . El-Galaly TC, Severinsen MT, Overvad K, Steffensen R, Vistisen AK, Tjønneland A, Kristensen SR |
The association of idiopathic recurrent pregnancy loss with polymorphisms in hemostasis-related genes. Gene 2013 Nov 530 (2): 248-52. Cao Yunlei, Zhang Zhaofeng, Xu Jianhua, Yuan Wei, Wang Jian, Huang Xianliang, Shen Yueping, Du Ji |
Prevalence of hereditary antithrombin mutations is higher than estimated in patients with thrombotic events. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2013 Jun 24 (4): 444-8. Fischer Ronald, Sachs Ulrich J, Heidinger Kathrin S, Eisenburger Dominik, Kemkes-Matthes Betti |
Influence of single nucleotide polymorphisms on thrombin generation in factor V Leiden heterozygotes. Thrombosis and haemostasis 2014 Mar 111 (3): 438-46. Segers O, Simioni P, Tormene D, Castoldi |
Distinct frequencies and mutation spectrums of genetic thrombophilia in Korea in comparison with other Asian countries both in patients with thromboembolism and in the general population. Haematologica 2014 Mar 99 (3): 561-9. Kim Hee-Jin, Seo Ja-Young, Lee Ki-O, Bang Sung-Hwan, Lee Seung-Tae, Ki Chang-Seok, Kim Jong-Won, Jung Chul Won, Kim Duk-Kyung, Kim Sun-H |
Multilocus genetic risk scores for venous thromboembolism risk assessment. Journal of the American Heart Association 2014 Oct 3 (5): e001060. Soria José Manuel, Morange Pierre-Emmanuel, Vila Joan, Souto Juan Carlos, Moyano Manel, Trégouët David-Alexandre, Mateo José, Saut Noémi, Salas Eduardo, Elosua Rober |
Antithrombin deficiency and decreased protein C activity in a young man with venous thromboembolism: a case report. Frontiers of medicine 2017 9 12 (3): 319-323. Wang Dong, Tian Min, Cui Guanglin, Wang Dao W |
Associations between polymorphisms in coagulation-related genes and venous thromboembolism: A meta-analysis with trial sequential analysis. Medicine 2017 Mar 96 (13): e6537. Jiang Jun, Liu Kang, Zou Junjie, Ma Hao, Yang Hongyu, Zhang Xiwei, Jiao Yuanyo |
Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency. Thrombosis and haemostasis 2017 Mar . Alhenc-Gelas Martine, Plu-Bureau Genevieve, Hugon-Rodin Justine, Picard Véronique, Horellou Marie-Helene, |
Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency. Oncotarget 2017 11 8 (48): 84417-84425. Zeng Wei, Hu Bei, Tang Liang, You Yan-Yan, Toderici Mara, de la Morena-Barrio Maria Eugenia, Corral Javier, Hu |
Next-Generation Sequencing of 17 Genes Associated with Venous Thromboembolism Reveals a Deficit of Non-Synonymous Variants in Procoagulant Genes. Thrombosis and haemostasis 2019 7 119 (9): 1441-1450. Manderstedt Eric, Lind-Halldén Christina, Svensson Peter, Zöller Bengt, Halldén Christ |
Association of SERPINC1 Gene Polymorphism (rs2227589) With Pulmonary Embolism Risk in a Chinese Population. Frontiers in genetics 2019 10 10 844. Yue Yongjian, Sun Qing, Xiao Lu, Liu Shengguo, Huang Qijun, Wang Minlian, Huo Mei, Yang Mo, Fu Yingy |
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease. Blood 2020 May . Desch Karl C, Ozel Ayse B, Halvorsen Matt, Jacobi Paula M, Golden Krista, Underwood Mary, Germain Marine, Tregouet David-Alexandre, Reitsma Pieter H, Kearon Clive, Mokry Lauren, Richards J Brent, Williams Frances, Li Jun Z, Goldstein David, Ginsburg Dav |
The Higher Prevalence of Venous Thromboembolism in the Hungarian Roma Population Could Be Due to Elevated Genetic Risk and Stronger Gene-Environmental Interactions. Frontiers in cardiovascular medicine 2021 11 8 647416. Natae Shewaye Fituma, Kósa Zsigmond, Sándor János, Merzah Mohammed Abdulridha, Bereczky Zsuzsanna, Pikó Péter, Ádány Róza, Fiatal Szilv |
Classic Thrombophilias and Thrombotic Risk Among Middle-Aged and Older Adults: A Population-Based Cohort Study. Journal of the American Heart Association 2022 2 11 (4): e023018. Manderstedt Eric, Lind-Halldén Christina, Halldén Christer, Elf Johan, Svensson Peter J, Dahlbäck Björn, Engström Gunnar, Melander Olle, Baras Aris, Lotta Luca A, Zöller Bengt, |
Patients with SERPINC1 rs2227589 polymorphism found to have multiple cerebral venous sinus thromboses despite a normal antithrombin level: A case report. World journal of clinical cases 2022 1 10 (2): 618-624. Liao Feng, Zeng Jun-Ling, Pan Jian-Gang, Ma Jing, Zhang Zhi-Jian, Lin Zhi-Jun, Lin Li-Feng, Chen Yu-Sen, Ma Xiao-Ta |
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program. Circulation. Genomic and precision medicine 2023 3 e003532. Seyerle Amanda A, Laurie Cecelia A, Coombes Brandon J, Jain Deepti, Conomos Matthew P, Brody Jennifer, Chen Ming-Huei, Gogarten Stephanie M, Beutel Kathleen M, Gupta Namrata, Heckbert Susan R, Jackson Rebecca D, Johnson Andrew D, Ko Darae, Manson JoAnn E, McKnight Barbara, Metcalf Ginger A, Morrison Alanna C, Reiner Alexander P, Sofer Tamar, Tang Weihong, Wiggins Kerri L, , Boerwinkle Eric, Andrade Mariza de, Gabriel Stacey B, Gibbs Richard A, Laurie Cathy C, Psaty Bruce M, Vasan Ramachandran S, Rice Ken, Kooperberg Charles, Pankow James S, Smith Nicholas L, Pankratz Nath |
Impact of SERPINC1 mutation on thrombotic phenotype in children with congenital antithrombin deficiency-first analysis of the International Society on Thrombosis and Haemostasis pediatric antithrombin deficiency database and biorepository. Journal of thrombosis and haemostasis : JTH 2023 2 . Kumar Riten, Bakeer Nihal, Dawson Jennifer, Al-Mughairy Alyaa, Stanek Joseph, Dunn Amy, Male Christoph, Chan Anthony, Williams Suz |
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