Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 43 Records) |
Query Trace: TNFRSF11A[original query] |
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Pathway-based association analyses identified TRAIL pathway for osteoporotic fractures. PloS one 2011 6 (7): e21835. Zhang Yin-Ping, Liu Yao-Zhong, Guo Yan, Liu Xiao-Gang, Xu Xiang-Hong, Guo Yan-Fang, Chen Yuan, Zhang Feng, Pan Feng, Zhu Xue-Zhen, Deng Hong-W |
A nonsynonymous TNFRSF11A variation increases NF?B activity and the severity of Paget's disease. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2012 Feb 27 (2): 443-52. Gianfrancesco Fernando, Rendina Domenico, Di Stefano Marco, Mingione Alessandra, Esposito Teresa, Merlotti Daniela, Gallone Salvatore, Magliocca Sara, Goode Alice, Formicola Daniela, Morello Giovanna, Layfield Robert, Frattini Annalisa, De Filippo Gianpaolo, Nuti Ranuccio, Searle Mark, Strazzullo Pasquale, Isaia Giancarlo, Mossetti Giuseppe, Gennari Lui |
Are bone mineral density loci associated with hip osteoporotic fractures? A validation study on previously reported genome-wide association loci in a Chinese population. Genetics and molecular research : GMR 2012 11 (1): 202-10. Guo Y, Wang J-T, Liu H, Li M, Yang T-L, Zhang X-W, Liu Y-Z, Tian Q, Deng H |
Discovery and fine mapping of serum protein loci through transethnic meta-analysis.
American journal of human genetics 2012 Oct 91 (4): 744-53. Franceschini Nora, van Rooij Frank J A, Prins Bram P, Feitosa Mary F, Karakas Mahir, Eckfeldt John H, Folsom Aaron R, Kopp Jeffrey, Vaez Ahmad, Andrews Jeanette S, Baumert Jens, Boraska Vesna, Broer Linda, Hayward Caroline, Ngwa Julius S, Okada Yukinori, Polasek Ozren, Westra Harm-Jan, Wang Ying A, Del Greco M Fabiola, Glazer Nicole L, Kapur Karen, Kema Ido P, Lopez Lorna M, Schillert Arne, Smith Albert V, Winkler Cheryl A, Zgaga Lina, , Bandinelli Stefania, Bergmann Sven, Boban Mladen, Bochud Murielle, Chen Y D, Davies Gail, Dehghan Abbas, Ding Jingzhong, Doering Angela, Durda J Peter, Ferrucci Luigi, Franco Oscar H, Franke Lude, Gunjaca Grog, Hofman Albert, Hsu Fang-Chi, Kolcic Ivana, Kraja Aldi, Kubo Michiaki, Lackner Karl J, Launer Lenore, Loehr Laura R, Li Guo, Meisinger Christa, Nakamura Yusuke, Schwienbacher Christine, Starr John M, Takahashi Atsushi, Torlak Vesela, Uitterlinden André G, Vitart Veronique, Waldenberger Melanie, Wild Philipp S, Kirin Mirna, Zeller Tanja, Zemunik Tatijana, Zhang Qunyuan, Ziegler Andreas, Blankenberg Stefan, Boerwinkle Eric, Borecki Ingrid B, Campbell Harry, Deary Ian J, Frayling Timothy M, Gieger Christian, Harris Tamara B, Hicks Andrew A, Koenig Wolfgang, O' Donnell Christopher J, Fox Caroline S, Pramstaller Peter P, Psaty Bruce M, Reiner Alex P, Rotter Jerome I, Rudan Igor, Snieder Harold, Tanaka Toshihiro, van Duijn Cornelia M, Vollenweider Peter, Waeber Gerard, Wilson James F, Witteman Jacqueline C M, Wolffenbuttel Bruce H R, Wright Alan F, Wu Qingyu, Liu Yongmei, Jenny Nancy S, North Kari E, Felix Janine F, Alizadeh Behrooz Z, Cupples L Adrienne, Perry John R B, Morris Andrew |
Genetic factors influencing bone mineral content in a black South African population. Journal of bone and mineral metabolism 2013 Nov 31 (6): 708-16. May Andrew, Pettifor John M, Norris Shane A, Ramsay Michèle, Lombard Za |
Human cardiovascular disease IBC chip-wide association with weight loss and weight regain in the look AHEAD trial. Human heredity 2013 75 (2-4): 160-74. McCaffery Jeanne M, Papandonatos George D, Huggins Gordon S, Peter Inga, Erar Bahar, Kahn Steven E, Knowler William C, Lipkin Edward W, Kitabchi Abbas E, Wagenknecht Lynne E, Wing Rena R, , |
Raloxifene pharmacodynamics is influenced by genetic variants in the RANKL/RANK/OPG system and in the Wnt signaling pathway. Drug metabolism and drug interactions 2014 29 (2): 111-4. Mencej-Bedra? Simona, Zupan Janja, Mlakar Simona Jurkovi?, Zavratnik Andrej, Preželj Janez, Marc Jan |
Association study of genetic variants in PLA2G4A, PLCG1, LAT, SYK, and TNFRS11A genes in NSAIDs-induced urticaria and/or angioedema patients. Pharmacogenetics and genomics 2015 Sep . Ayuso Pedro, Plaza-Serón María Del Carmen, Doña Inmaculada, Blanca-López Natalia, Campo Paloma, Cornejo-García José A, Perkins James R, Torres Maria J, Blanca Miguel, Canto Gabrie |
Gene polymorphisms in RANKL/RANK/OPG pathway are associated with ages at menarche and natural menopause in Chinese women. BMC women's health 2015 15 32. Duan Peng, Wang Zhi-Ming, Liu Jiang, Wang Li-Na, Yang Zhi, Tu Pi |
Association of gene polymorphisms in RANKL/RANK/OPG system with hypertension and blood pressure in Chinese women. Journal of human hypertension 2015 Mar . Duan P, Wang Z-M, Liu J, Wang L-N, Yang Z, Tu |
A genome-wide association study of myasthenia gravis.
JAMA neurology 2015 Apr 72 (4): 396-404. Renton Alan E, Pliner Hannah A, Provenzano Carlo, Evoli Amelia, Ricciardi Roberta, Nalls Michael A, Marangi Giuseppe, Abramzon Yevgeniya, Arepalli Sampath, Chong Sean, Hernandez Dena G, Johnson Janel O, Bartoccioni Emanuela, Scuderi Flavia, Maestri Michelangelo, Gibbs J Raphael, Errichiello Edoardo, Chiò Adriano, Restagno Gabriella, Sabatelli Mario, Macek Mark, Scholz Sonja W, Corse Andrea, Chaudhry Vinay, Benatar Michael, Barohn Richard J, McVey April, Pasnoor Mamatha, Dimachkie Mazen M, Rowin Julie, Kissel John, Freimer Miriam, Kaminski Henry J, Sanders Donald B, Lipscomb Bernadette, Massey Janice M, Chopra Manisha, Howard James F, Koopman Wilma J, Nicolle Michael W, Pascuzzi Robert M, Pestronk Alan, Wulf Charlie, Florence Julaine, Blackmore Derrick, Soloway Aimee, Siddiqi Zaeem, Muppidi Srikanth, Wolfe Gil, Richman David, Mezei Michelle M, Jiwa Theresa, Oger Joel, Drachman Daniel B, Traynor Bryan |
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations.
Molecular medicine (Cambridge, Mass.) 2015 Oct . Seldin Michael F, Alkhairy Omar K, Lee Annette T, Lamb Janine A, Sussman Jon, Pirskanen-Matell Ritva, Piehl Fredrik, Verschuuren J J G M, Kostera-Pruszczyk Anna, Szczudlik Piotr, Mckee David, Maniaol Angelina H, Harbo Hanne F, Lie Benedicte A, Melms Arthur, Garchon Henri-Jean, Willcox Nicholas, Gregersen Peter K, Hammarstrom Lenna |
Polymorphisms in Inflammatory Mediator Genes and Risk of Preeclampsia in Taiyuan, China. Reproductive sciences (Thousand Oaks, Calif.) 2016 Aug . Wu Weiwei, Yang Hailan, Feng Yongliang, Zhang Ping, Li Shuzhen, Wang Xin, Peng Tingting, Wang Fang, Xie Bingjie, Guo Pengge, Li Mei, Wang Ying, Zhao Nan, Wang Suping, Zhang Yaw |
Gene Polymorphisms in the RANKL/RANK/OPG Pathway Are Associated with Type 2 Diabetes Mellitus in Southern Han Chinese Women. Genetic testing and molecular biomarkers 2016 May . Duan Peng, Tu Ping, Si Lian, Hu Wan, Liu Meng, Liu Jia, Xue Yaomi |
Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese families. Acta pharmacologica Sinica 2017 8 38 (11): 1456-1465. Zhang Xiao-Ya, He Jin-Wei, Fu Wen-Zhen, Wang Chun, Zhang Zhen-L |
Interaction between LRP5 and periostin gene polymorphisms on serum periostin levels and cortical bone microstructure. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2018 02 29 (2): 339-346. Pepe J, Bonnet N, Herrmann F R, Biver E, Rizzoli R, Chevalley T, Ferrari S |
Six novel susceptibility loci for coronary artery disease and cerebral infarction identified by longitudinal exome-wide association studies in a Japanese population. Biomedical reports 2018 Aug 9 (2): 123-134. Yasukochi Yoshiki, Sakuma Jun, Takeuchi Ichiro, Kato Kimihiko, Oguri Mitsutoshi, Fujimaki Tetsuo, Horibe Hideki, Yamada Yoshi |
Targeted sequencing of DCSTAMP in familial Paget's disease of bone. Bone reports 2019 3 10 100198. Sultana M A, Pavlos N J, Ward Lynley, Walsh J P, Rea S |
[Association between TNFRSF11A and TNFRSF11B gene polymorphisms and the outcome of hepatitis C virus infection]. Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi 2019 Oct 40 (10): 1291-1295. Wu J J, Huang P, Yue M, Wang C H, Wu C, Shao J G, Xue H, Fu Z Q, Zhuo L Y, Yu R B, Zhang |
A Meta-Analysis of the Transferability of Bone Mineral Density Genetic Loci Associations From European to African Ancestry Populations. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2020 Nov . Yau Michelle S, Kuipers Allison L, Price Ryan, Nicolas Aude, Tajuddin Salman M, Handelman Samuel K, Arbeeva Liubov, Chesi Alessandra, Hsu Yi-Hsiang, Liu Ching-Ti, Karasik David, Zemel Babette S, Grant Struan Fa, Jordan Joanne M, Jackson Rebecca D, Evans Michele K, Harris Tamara B, Zmuda Joseph M, Kiel Douglas |
The third case of TNFRSF11A-associated dysosteosclerosis with a mutation producing elongating proteins. Journal of human genetics 2020 10 66 (4): 371-377. Xue Jing-Yi, Wang Zheng, Smithson Sarah F, Burren Christine P, Matsumoto Naomichi, Nishimura Gen, Ikegawa Shiro, Guo Lo |
Protective Effect of TNFRSF11A rs7239667 G > C Gene Polymorphism on Coronary Outcome of Kawasaki Disease in Southern Chinese Population. Frontiers in genetics 2021 9 12 691282. Zhang Linyuan, Lin Kun, Wang Yishuai, Yu Hongyan, Li Jinqing, Fu Lanyan, Xu Yufen, Wei Bing, Mai Hanran, Jiang Zhiyong, Che Di, Pi Lei, Gu Xiaoqio |
The effect of genetic polymorphisms on treatment duration following premolar extraction. Scientific reports 2021 Aug 11 (1): 15942. Yu Jiyon, Choi Yoon Jeong, Choi Sung-Hwan, Jung Han-Sung, Lee Ji Hyun, Cha Jung-Y |
Myasthenia gravis genome-wide association study implicates AGRN as a risk locus. Journal of medical genetics 2021 Aug . Topaloudi Apostolia, Zagoriti Zoi, Flint Alyssa Camille, Martinez Melanie Belle, Yang Zhiyu, Tsetsos Fotis, Christou Yiolanda-Panayiota, Lagoumintzis George, Yannaki Evangelia, Zamba-Papanicolaou Eleni, Tzartos John, Tsekmekidou Xanthippi, Kotsa Kalliopi, Maltezos Efstratios, Papanas Nikolaos, Papazoglou Dimitrios, Passadakis Ploumis, Roumeliotis Athanasios, Roumeliotis Stefanos, Theodoridis Marios, Thodis Elias, Panagoutsos Stylianos, Yovos John, Stamatoyannopoulos John, Poulas Konstantinos, Kleopa Kleopas, Tzartos Socrates, Georgitsi Marianthi, Paschou Periste |
A Panel-Based Sequencing Analysis of Patients with Paget's Disease of Bone Suggests Enrichment of Rare Genetic Variation in regulators of NF-?B Signaling and Supports the Importance of the 7q33 Locus. Calcified tissue international 2021 Jun . De Ridder Raphaël, Vandeweyer Geert, Boudin Eveline, Hendrickx Gretl, Huybrechts Yentl, Cremers Tycho Canter, Devogelaer Jean-Pierre, Mortier Geert, Fransen Erik, Van Hul W |
Investigation of The Relationship of TNFRSF11A Gene Polymorphisms with Breast Cancer Development and Metastasis Risk in Patients with BRCA1 Or BRCA2 Pathogenic Variants Living in The Trakya Region of Turkey. Balkan journal of medical genetics : BJMG 2021 4 23 (2): 49-58. Özdemir K, Gürkan H, Demir S, Atli E, Özen Y, Sezer A, Tunçbilek N, Çicin |
Genetic Mutations in TNFSF11 Were Associated With the Chronicity of Hepatitis C Among Chinese Han Population. Frontiers in medicine 2021 10 8 743406. Huang Peng, Hou Yu-Qing, Wu Jing-Jing, Wang Yi-Di, Ye Xiang-Yu, Zang Feng, Yu Rong-Bin, Yang She |
Identification by whole-exome sequencing of new single-nucleotide polymorphisms associated with molar-incisor hypomineralisation among the Lebanese population. European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry 2022 Aug . Elzein R, Abdel-Sater F, Mehawej C, Jalkh N, Ayoub F, Chouery |
Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study.
Proceedings of the National Academy of Sciences of the United States of America 2022 02 119 (5): . Chia Ruth, Saez-Atienzar Sara, Murphy Natalie, Chiò Adriano, Blauwendraat Cornelis, , Roda Ricardo H, Tienari Pentti J, Kaminski Henry J, Ricciardi Roberta, Guida Melania, De Rosa Anna, Petrucci Loredana, Evoli Amelia, Provenzano Carlo, Drachman Daniel B, Traynor Bryan |
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis.
Nature genetics 2022 11 54 (11): 1640-1651. Ishigaki Kazuyoshi, Sakaue Saori, Terao Chikashi, Luo Yang, Sonehara Kyuto, Yamaguchi Kensuke, Amariuta Tiffany, Too Chun Lai, Laufer Vincent A, Scott Ian C, Viatte Sebastien, Takahashi Meiko, Ohmura Koichiro, Murasawa Akira, Hashimoto Motomu, Ito Hiromu, Hammoudeh Mohammed, Emadi Samar Al, Masri Basel K, Halabi Hussein, Badsha Humeira, Uthman Imad W, Wu Xin, Lin Li, Li Ting, Plant Darren, Barton Anne, Orozco Gisela, Verstappen Suzanne M M, Bowes John, MacGregor Alexander J, Honda Suguru, Koido Masaru, Tomizuka Kohei, Kamatani Yoichiro, Tanaka Hiroaki, Tanaka Eiichi, Suzuki Akari, Maeda Yuichi, Yamamoto Kenichi, Miyawaki Satoru, Xie Gang, Zhang Jinyi, Amos Christopher I, Keystone Edward, Wolbink Gertjan, van der Horst-Bruinsma Irene, Cui Jing, Liao Katherine P, Carroll Robert J, Lee Hye-Soon, Bang So-Young, Siminovitch Katherine A, de Vries Niek, Alfredsson Lars, Rantapää-Dahlqvist Solbritt, Karlson Elizabeth W, Bae Sang-Cheol, Kimberly Robert P, Edberg Jeffrey C, Mariette Xavier, Huizinga Tom, Dieudé Philippe, Schneider Matthias, Kerick Martin, Denny Joshua C, , Matsuda Koichi, Matsuo Keitaro, Mimori Tsuneyo, Matsuda Fumihiko, Fujio Keishi, Tanaka Yoshiya, Kumanogoh Atsushi, Traylor Matthew, Lewis Cathryn M, Eyre Stephen, Xu Huji, Saxena Richa, Arayssi Thurayya, Kochi Yuta, Ikari Katsunori, Harigai Masayoshi, Gregersen Peter K, Yamamoto Kazuhiko, Louis Bridges S, Padyukov Leonid, Martin Javier, Klareskog Lars, Okada Yukinori, Raychaudhuri Soum |
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