Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and PRRC2A[original query] |
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| Genetic variations in MOV10 and CACNB2 are associated with hypertension in a Chinese Han population. Genetics and molecular research : GMR 2013 12 (4): 6220-7. Hong G L, Chen X Z, Liu Y, Liu Y H, Fu X, Lin S B, Zhu |
| Interactions within the MHC contribute to the genetic architecture of celiac disease. PloS one 2017 12 (3): e0172826. Goudey Benjamin, Abraham Gad, Kikianty Eder, Wang Qiao, Rawlinson Dave, Shi Fan, Haviv Izhak, Stern Linda, Kowalczyk Adam, Inouye Micha |
| Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population. Journal of neurology 2020 Aug . Zhang Juan, Chen Mei-Jiao, Zhao Gui-Xian, Li Hong-Fu, Wu Lei, Xu Yong-Feng, Liao Yajin, Yuan Zengqiang, Wu Zhi-Yi |
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length.
American journal of human genetics 2020 Feb . Li Chen, Stoma Svetlana, Lotta Luca A, Warner Sophie, Albrecht Eva, Allione Alessandra, Arp Pascal P, Broer Linda, Buxton Jessica L, Da Silva Couto Alves Alexessander, Deelen Joris, Fedko Iryna O, Gordon Scott D, Jiang Tao, Karlsson Robert, Kerrison Nicola, Loe Taylor K, Mangino Massimo, Milaneschi Yuri, Miraglio Benjamin, Pervjakova Natalia, Russo Alessia, Surakka Ida, van der Spek Ashley, Verhoeven Josine E, Amin Najaf, Beekman Marian, Blakemore Alexandra I, Canzian Federico, Hamby Stephen E, Hottenga Jouke-Jan, Jones Peter D, Jousilahti Pekka, Mägi Reedik, Medland Sarah E, Montgomery Grant W, Nyholt Dale R, Perola Markus, Pietiläinen Kirsi H, Salomaa Veikko, Sillanpää Elina, Suchiman H Eka, van Heemst Diana, Willemsen Gonneke, Agudo Antonio, Boeing Heiner, Boomsma Dorret I, Chirlaque Maria-Dolores, Fagherazzi Guy, Ferrari Pietro, Franks Paul, Gieger Christian, Eriksson Johan Gunnar, Gunter Marc, Hägg Sara, Hovatta Iiris, Imaz Liher, Kaprio Jaakko, Kaaks Rudolf, Key Timothy, Krogh Vittorio, Martin Nicholas G, Melander Olle, Metspalu Andres, Moreno Concha, Onland-Moret N Charlotte, Nilsson Peter, Ong Ken K, Overvad Kim, Palli Domenico, Panico Salvatore, Pedersen Nancy L, Penninx Brenda W J H, Quirós J Ramón, Jarvelin Marjo Riitta, Rodríguez-Barranco Miguel, Scott Robert A, Severi Gianluca, Slagboom P Eline, Spector Tim D, Tjonneland Anne, Trichopoulou Antonia, Tumino Rosario, Uitterlinden André G, van der Schouw Yvonne T, van Duijn Cornelia M, Weiderpass Elisabete, Denchi Eros Lazzerini, Matullo Giuseppe, Butterworth Adam S, Danesh John, Samani Nilesh J, Wareham Nicholas J, Nelson Christopher P, Langenberg Claudia, Codd Very |
| Unraveling the Genetic Susceptibility of Irritable Bowel Syndrome: integrative genome-wide analyses in 845,492 individuals: a diagnostic study. International journal of surgery (London, England) 2024 8 . Wentao Huang, Lijun Zhang, Yuying Ma, Shiyi Yu, Yanlin Lyu, Shuangshuang Tong, Jiaxuan Wang, Rui Jiang, Meijun Meng, Yanjun Wu, Ruibang Luo, Xinqi Qiu, Weihong Sha, Hao Ch |
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