Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 52 Records) |
Query Trace: SERPINC1[original query] |
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Identification of 2 Novel Polymorphisms and rs3138521 in 5' Untranslated Region of SERPINC1 Gene in North Indian Population With Deep Vein Thrombosis. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2016 Jun . Bhakuni Teena, Sharma Amit, Ali Mohammad Farhan, Mahapatra Manoranjan, Saxena Renu, Jairajpuri Mohamad Am |
A common missense variant in exon 5 of antithrombin gene (SERPINC1) in Indian patients with thrombosis. Thrombosis research 2016 Apr 143 1-2. Deshpande Rutuja, Kulkarni Bipin, Ghosh Kanjaksha, Shetty Shrima |
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 |
Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study.
Molecular psychiatry 2017 May . Jorgenson E, Thai K K, Hoffmann T J, Sakoda L C, Kvale M N, Banda Y, Schaefer C, Risch N, Mertens J, Weisner C, Choquet |
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, |
Clinical and laboratory characteristics of antithrombin deficiencies: A large cohort study from a single diagnostic center. Thrombosis research 2017 11 160 119-128. Gindele Réka, Selmeczi Anna, Oláh Zsolt, Ilonczai Péter, Pfliegler György, Marján Erzsébet, Nemes László, Nagy Ágnes, Losonczy Hajna, Mitic Gorana, Kovac Mirjana, Balogh Gábor, Komáromi István, Schlammadinger Ágota, Rázsó Katalin, Boda Zoltán, Muszbek László, Bereczky Zsuzsan |
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 |
The influence of specific mutations in the AT gene (SERPINC1) on the type of pregnancy related complications. Thrombosis research 2019 01 173 12-19. Kovac Mirjana, Mitic Gorana, Mikovic Zeljko, Mandic Vesna, Miljic Predrag, Mitrovic Mirjana, Tomic Branko, Bereczky Zsuzsan |
Polymorphisms of F2, PROC, PROZ, and F13A1 Genes are Associated With Recurrent Spontaneous Abortion in Chinese Han Women. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2018 Jan 1076029617750487. Xu Zuying, Zhang Ying, Liu Wei, Liu Yunyun, Su Yezhou, Xing Qiong, He Xiaojin, Wei Zhaolian, Cao Yunxia, Xiang Huif |
Genotype phenotype correlation in a pediatric population with antithrombin deficiency. European journal of pediatrics 2019 7 178 (10): 1471-1478. Kovac Mirjana, Mitic Gorana, Djilas Iva, Kuzmanovic Milos, Serbic Olivera, Lekovic Danijela, Tomic Branko, Bereczky Zsuzsan |
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 |
SERPINC1 variants causing hereditary antithrombin deficiency in a Danish population. Thrombosis research 2019 Jan 175 68-75. Kjaergaard Alisa D, Larsen Ole Halfdan, Hvas Anne-Mette, Nissen Peter |
Congenital antithrombin deficiency in patients with splanchnic vein thrombosis. Liver international : official journal of the International Association for the Study of the Liver 2019 12 40 (5): 1168-1177. Baiges Anna, de la Morena-Barrio María Eugenia, Turon Fanny, Miñano Antonia, Alberto Ferrusquía Jose, Magaz Marta, Reverter Juan Carlos, Vicente Vicente, Hernández-Gea Virginia, Corral Javier, García-Pagán Juan Carl |
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 |
Genes and variants in hematopoiesis-related pathways are associated with gemcitabine/carboplatin-induced thrombocytopenia. The pharmacogenomics journal 2019 10 20 (2): 179-191. Björn Niclas, Sigurgeirsson Benjamín, Svedberg Anna, Pradhananga Sailendra, Brandén Eva, Koyi Hirsh, Lewensohn Rolf, de Petris Luigi, Apellániz-Ruiz Maria, Rodríguez-Antona Cristina, Lundeberg Joakim, Gréen Henr |
Genetic modifiers of long-term survival in sickle cell anemia. Clinical and translational medicine 2020 Aug 10 (4): e152. Wonkam Ambroise, Chimusa Emile R, Mnika Khuthala, Pule Gift Dineo, Ngo Bitoungui Valentina Josiane, Mulder Nicola, Shriner Daniel, Rotimi Charles N, Adeyemo Adebowa |
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 |
Molecular Profiling for Predictors of Radiosensitivity in Patients with Breast or Head-and-Neck Cancer. Cancers 2020 4 12 (3): . Drobin Kimi, Marczyk Michal, Halle Martin, Danielsson Daniel, Papiez Anna, Sangsuwan Traimate, Bendes Annika, Hong Mun-Gwan, Qundos Ulrika, Harms-Ringdahl Mats, Wersäll Peter, Polanska Joanna, Schwenk Jochen M, Haghdoost Siam |
Age and Origin of the Founder Antithrombin Budapest 3 (p.Leu131Phe) Mutation; Its High Prevalence in the Roma Population and Its Association With Cardiovascular Diseases. Frontiers in cardiovascular medicine 2021 2 7 617711. Bereczky Zsuzsanna, Gindele Réka, Fiatal Szilvia, Speker Marianna, Miklós Tünde, Balogh László, Mezei Zoltán, Szabó Zsuzsanna, Ádány Ró |
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 |
Utility of the SERPINC1 Gene Test in Ischemic Stroke Patients With Antithrombin Deficiency. Frontiers in neurology 2022 6 13 841934. Kim Seondeuk, Lee Woo-Jin, Moon Jangsup, Jung Keun-H |
Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing. Diagnostics (Basel, Switzerland) 2022 5 12 (5): . Vrtel Petr, Slavik Ludek, Vodicka Radek, Stellmachova Julia, Prochazka Martin, Prochazkova Jana, Ulehlova Jana, Rohon Peter, Simurda Tomas, Stasko Jan, Martinkova Ivana, Vrtel Rad |
PROS1 variant in sudden death case of pulmonary embolism caused by calcification in the inferior vena cava: The importance of postmortem genetic analysis. Legal medicine (Tokyo, Japan) 2022 2 55 102029. Miura Aya, Funayama Kazuhisa, Nyuzuki Hiromi, Takahashi Naoya, Yamamoto Takuma, Koyama Akihide, Ikeuchi Takeshi, Takatsuka Hisakazu, Nishio Haji |
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, |
Prevalence, Genetic Background, and Clinical Phenotype of Congenital Thrombophilia in Chronic Thromboembolic Pulmonary Hypertension. JACC. Asia 2022 11 2 (3): 247-255. Lian Tian-Yu, Liu Jian-Zhou, Guo Fan, Zhou Yu-Ping, Wu Tao, Wang Hui, Li Jing-Yi, Yan Xin-Xin, Peng Fu-Hua, Sun Kai, Xu Xi-Qi, Han Zhi-Yan, Jiang Xin, Wang Duo-Lao, Miao Qi, Jing Zhi-Che |
Cryptogenic Stroke in the Young: Role of Candidate Gene Polymorphisms in Indian Patients with Ischemic Etiology. Neurology India 2022 1 69 (6): 1655-1662. Salomi Bodda S B, Solomon Raja, Turaka Vijay Prakash, Aaron Sanjith, Christudass Christhunesa |
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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- Page last updated:Apr 22, 2024
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