Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: SLC44A2[original query] |
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Characterization of the human neutrophil alloantigen-3a. Nature medicine 2009 12 16 (1): 45-8. Greinacher Andreas, Wesche Jan, Hammer Elke, Fürll Birgitt, Völker Uwe, Reil Angelika, Bux Jürg |
Frequencies of SLC44A2 alleles encoding human neutrophil antigen-3 variants in the African American population. Transfusion 2012 May 52 (5): 1106-11. Huvard Michael J, Schmid Pirmin, Stroncek David F, Flegel Willy |
Genotyping of human neutrophil antigens by polymerase chain reaction sequence-based typing. Blood transfusion = Trasfusione del sangue 2014 Jan 12 Suppl 1 s292-8. He Junjun, Zhang Wei, Wang Wei, Chen Nanying, Han Zhedong, He Ji, Zhu Faming, Lv Hangj |
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 |
Genotype frequency of human neutrophil antigen-3 polymorphisms in the Yi, Han, and Tibetan populations of China. Transfusion 2015 Nov . Chen Qing, Srivastava Kshitij, Liu Zhong, Xiao Jianyu, Huang Chengyin, Sun Jun, Li Min, Flegel Willy Albe |
Genetic risk factors for venous thrombosis in women using combined oral contraceptives: update of the PILGRIM study. Clinical genetics 2016 Jul . Suchon Pierre, Frouh Fadi Al, Ibrahim Manal, Sarlon Gabrielle, Venton Geoffroy, Alessi Marie-Christine, Trégouët David-Alexandre, 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 |
HNA-1, -3, -4, and -5 genotyping using multiplex PCR among southern Thais: Developing continual HNA-1 null detection. Journal of clinical laboratory analysis 2018 8 33 (1): e22651. Intharanut Kamphon, Sasikarn Wiradee, Mitundee Supattra, Nathalang Oyt |
HNA-3a and HNA-3b antigens among 9 ethnic populations and the Han population in Southwest China. Journal of translational medicine 2018 Mar 16 (1): 67. Ou Guo-Jin, Su Pin-Can, Yu Hao, Ji Xin, Liu Fan, Wang Sheng-Lan, Kong Yu-Jie, Li Ling, Wang Jue, Liu Zhong, Flegel Willy Albe |
Association between SLC44A2 rs2288904 polymorphism and risk of recurrent venous thromboembolism among Thai patients. Thrombosis research 2019 Jan 174 163-165. Apipongrat Dollapak, Numbenjapon Tontanai, Prayoonwiwat Wichai, Arnutti Pasra, Nathalang Oyt |
The Effect of Common Variants in SLC44A2 on the Contribution to the Risk of Deep Cein Thrombosis after Orthopedic Surgery. Journal of atherosclerosis and thrombosis 2020 6 28 (3): 293-303. Zhi Liqiang, Feng Weilou, Liang Jingqi, Zhong Qing, Ren Liaoyuan, Ma Jianbing, Yao Shuxin, |
Rare Variants of Putative Candidate Genes Associated With Sporadic Meniere's Disease in East Asian Population. Frontiers in neurology 2019 10 1424. Oh Eun Hye, Shin Jin-Hong, Kim Hyang-Sook, Cho Jae Wook, Choi Seo Young, Choi Kwang-Dong, Rhee Je-Keun, Lee Seowhang, Lee Changwook, Choi Jae-Hw |
Human neutrophil antigen 3 genotype impacts neutrophil-mediated endothelial cell cytotoxicity in a two-event model of TRALI. Blood transfusion = Trasfusione del sangue 2022 7 20 (6): 465-474. Chiaretti Sara, Burton Mark, Hassel Penny, Radenkovic Filip, Devikashri Nilam, Sultana Annette J, Temple Fergal T, Dean Melinda M, Tung John-Pa |
SLC44A2 Frequency, a New TaqMan Real-Time Polymerase Chain Reaction Method for HNA-3A/3B Genotyping, and a New Application of Droplet Digital PCR. Frontiers in genetics 2022 6 13 794285. Wang Yufeng, Chen Xihui, Chen Qi, Chen Tangdong, Chen Kun, Wu Yuanming, Wang |
A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study.
American journal of medical genetics. Part A 2022 4 188 (8): 2303-2314. Rashkin Sara R, Cleves Mario, Shaw Gary M, Nembhard Wendy N, Nestoridi Eirini, Jenkins Mary M, Romitti Paul A, Lou Xiang-Yang, Browne Marilyn L, Mitchell Laura E, Olshan Andrew F, Lomangino Kevin, Bhattacharyya Sudeepa, Witte John S, Hobbs Charlotte A, |
Human Neutrophil Antigen Genotype and Allele Frequencies in Iranian Blood Donors. Journal of immunology research 2022 2022 4387555. Esmaeili Behnaz, Bayat Behnaz, Alirezaee Atefe, Delkhah Mona, Mehdizadeh Mohammad Reza, Pourpak Zah |
Genetic landscape of human neutrophil antigen variants in India from population-scale genomes. HLA 2022 12 101 (3): 262-269. Rophina Mercy, Bhoyar Rahul C, Imran Mohamed, Senthivel Vigneshwar, Divakar Mohit Kumar, Mishra Anushree, Jolly Bani, Sivasubbu Sridhar, Scaria Vin |
Human neutrophil antigen-1, -3, -4, and -5 allele and genotype frequencies in the Croatian blood donor population and their clinical significance. Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine 2022 Oct . Stimac R, Tomicic M, Bingulac-Popovic J, Kundid R, Babic I, Hecimovic A, Vuk T, Jukic |
Phenotyping and Genotyping of HNA: Prevalence, Risk of Alloimmunization, and HNA Incompatibilities in Indians. Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie 2023 2 50 (1): 30-38. Gogri Harita, Parihar Meghana, Kulkarni Swati, Madkaikar Manisha, Sharma Jayashree, Gorakshakar Aj |
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- Page last updated:Apr 22, 2024
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