Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 37 Records) |
Query Trace: PROS1[original query] |
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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 |
Genetic determinants of tissue factor pathway inhibitor plasma levels. Thrombosis and haemostasis 2015 Jul 114 (2): 245-57. Dennis J, Kassam I, Morange P-E, Trégouët D-A, Gagnon |
PROS1 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency. Thrombosis and haemostasis 2015 Oct 115 (3): . Alhenc-Gelas M, Plu-Bureau G, Horellou M H, Rauch A, Suchon P, |
Population-specific single-nucleotide polymorphism confers increased risk of venous thromboembolism in African Americans. Molecular genetics & genomic medicine 2016 Sep 4 (5): 513-20. Daneshjou Roxana, Cavallari Larisa H, Weeke Peter E, Karczewski Konrad J, Drozda Katarzyna, Perera Minoli A, Johnson Julie A, Klein Teri E, Bustamante Carlos D, Roden Dan M, Shaffer Christian, Denny Joshua C, Zehnder James L, Altman Russ |
Analysis of receptor tyrosine kinase genetics identifies two novel risk loci in GAS6 and PROS1 in Behçet's disease. Scientific reports 2016 6 26662. Qin Jieying, Li Lin, Zhang Donglei, Yu Hongsong, Tan Handan, Zhang Jun, Deng Bolin, Kijlstra Aize, Yang Peize |
Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis. PloS one 2016 11 (3): e0151347. Gorski Marcin M, Lotta Luca A, Pappalardo Emanuela, de Haan Hugoline G, Passamonti Serena M, van Hylckama Vlieg Astrid, Martinelli Ida, Peyvandi Flo |
Prevalence and in silico analysis of missense mutations in the PROS1 gene in the Swedish population: The SweGen dataset. Thrombosis research 2018 Jun 168 28-30. Zöller Ben |
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 |
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 |
Analysis of PROC and PROS1 single nucleotide polymorphisms in a thrombophilia family. The clinical respiratory journal 2019 Jul . Wu Dawen, Zhong Zhanghua, Chen Yunfei, Ding Haibo, Yang Minxia, Lian Ningfang, Huang Zhigui, Zhang Qiaoxian, Zhao Jianming, Deng Chaoshe |
[Exhaustive analysis of genetic mutations associated with protein S deficiency utilizing next-generation sequencing analysis]. [Rinsho ketsueki] The Japanese journal of clinical hematology 2019 5 60 (3): 171-183. Ichiki Akito, Inaba Hiroshi, Shinozawa Keiko, Amano Kagehiro, Fukutake Katsuyu |
Natural anticoagulant deficiencies in Thais: A population-based study. Thrombosis research 2019 Mar 178 7-11. Rojnuckarin Ponlapat, Settapiboon Rung, Akkawat Benjaporn, Teocharoen Sudawadee, Suksusut Amornchai, Uaprasert Noppacha |
Recurrent PROC and novel PROS1 mutations in Vietnamese patients diagnosed with idiopathic deep venous thrombosis. International journal of laboratory hematology 2020 9 43 (2): 266-272. Do Minh Duc, Pham Dung Van, Le Long Phi, Gia Le Linh Hoang, Minh Tran Luan Bao, Dang Huynh Minh Duc, Do Quang Minh, Vu Hoang Anh, Nguyen Nam Hoai, Mai Thao Phuo |
Two Novel Variants in the Protein S Gene PROS1 Are Associated with Protein S Deficiency and Thrombophilia. Acta haematologica 2020 7 144 (2): 222-226. Juhl David, Kuta Piotr, Shneyder Maria, Wünsche Falko, Nowak-Göttl Ulri |
Identification of PROS1 as a Novel Candidate Gene for Juvenile Retinitis Pigmentosa. International journal of molecular and cellular medicine 2020 6 8 (3): 179-190. Bushehri Ata, Zare-Abdollahi Davood, Alavi Afagh, Dehghani Alireza, Mousavimikala Mohammadreza, Khorram Khorshid Hamid Re |
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 |
A Case of a Pediatric Patient With Protein S Heerlen Polymorphism and Deep Venous Thrombosis. Journal of pediatric hematology/oncology 2021 9 44 (2): e442-e443. Kacar Marija, Bhatt Mih |
Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism. Clinica chimica acta; international journal of clinical chemistry 2021 5 519 247-254. Athar Mohammad, Ghita Ibrahim S, Albagenny Amani A, Abduljaleel Zainularifeen, Shadab Ghulam, Elsendiony Ahmed, Halawani Saeed H, Alkazmi Mohammad M, Alquthami Khalid, Alkhuzae Mohammad M, Althebyani Abdulaziz A, Bogari Neda M, Dannoun Anas, Al-Allaf Faisal |
[Genetic and Clinical Characteristics of A Family with Combined PROC and PROS1 Genetic Variants]. Zhongguo shi yan xue ye xue za zhi 2021 4 29 (2): 591-595. Wang Xing, Sheng Guang-Ying, Zhang Wei, Zhao Yun-Xiao, Xia Li-Jun, Jiang Mi |
Genetic Variants in the Protein S ( PROS1 ) Gene and Protein S Deficiency in a Danish Population. TH open : companion journal to thrombosis and haemostasis 2021 11 5 (4): e479-e488. Larsen Ole Halfdan, Kjaergaard Alisa D, Hvas Anne-Mette, Nissen Peter |
Protein S Deficiency and the Risk of Venous Thromboembolism in the Han Chinese Population. Frontiers in cardiovascular medicine 2021 8 796755. Wu Yingying, Liu Jingdi, Zeng Wei, Hu Bei, Hu Yu, Tang Liang |
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 |
The effects of pathogenic variants for inherited hemostasis disorders in 140,214 UK Biobank participants. Blood 2023 8 . Luca Stefanucci, Janine H Collins, Matthew Christopher Sims, Iñigo Barrio-Hernandez, Luanluan Sun, Oliver Burren, Livia Perfetto, Isobel Bender, Tiffany J Callahan, Kathryn Fleming, Jose Antonio Guerrero, Henning Hermjakob, Maria J Martin, James David Stephenson, Kalpana Paneerselvam, Slavé Petrovski, Pablo Porras, Peter N Robinson, Quanli Wang, Xavier Watkins, Mattia Frontini, Roman A Laskowski, Pedro Beltrao, Emanuele Di Angelantonio, Keith Gomez, Michael Laffan, Willem H Ouwehand, Andrew D Mumford, Kathleen Freson, Keren Jacqueline Carss, Kate Downes, Nicholas S Gleadall, Karyn Megy, Elspeth Bruford, Dragana Vuckov |
The impact of PROS1 mutation position on thrombotic risk in protein S-deficient patients. Research and practice in thrombosis and haemostasis 2023 6 7 (4): 100194. Tereza Fenclova, Miloslava Matyskova, Dana Provaznikova, Frantisek Marecek, Vera Geierova, Zuzana Kovarova-Kudrnova, Ingrid Hrachovino |
Replication Study of the Association of GAS6 and PROS1 Polymorphisms with Behçet's Disease in a Japanese Population. Ocular immunology and inflammation 2023 5 1-7. Takeshi Teshigawara, Akira Meguro, Masaki Takeuchi, Mizuho Ishido, Yutaro Soejima, Lisa Hirahara, Yohei Kirino, Shigeaki Ohno, Nobuhisa Mizu |
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 |
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- Page last updated:Apr 22, 2024
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