Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: KERA[original query] |
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A cross-sectional study of polycyclic aromatic hydrocarbon-DNA adducts and polymorphism of glutathione S-transferases among heavy smokers by race/ethnicity. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 0 8 (2): 142-55. Weiserbs Kera F, Jacobson Judith S, Begg Melissa D, Wang Lian Wen, Wang Qiao, Agrawal Meenaksh, Norkus Edward P, Young Tie-Lan, Santella Regina |
Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci.
Nature genetics 2010 Aug 42 (8): 703-6. Mizuki Nobuhisa, Meguro Akira, Ota Masao, Ohno Shigeaki, Shiota Tomoko, Kawagoe Tatsukata, Ito Norihiko, Kera Jiro, Okada Eiichi, Yatsu Keisuke, Song Yeong-Wook, Lee Eun-Bong, Kitaichi Nobuyoshi, Namba Kenichi, Horie Yukihiro, Takeno Mitsuhiro, Sugita Sunao, Mochizuki Manabu, Bahram Seiamak, Ishigatsubo Yoshiaki, Inoko Hidetos |
Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness. Molecular vision 2010 16 562-9. Dimasi David P, Burdon Kathryn P, Hewitt Alex W, Savarirayan Ravi, Healey Paul R, Mitchell Paul, Mackey David A, Craig Jamie |
Evaluation of proteoglycan gene polymorphisms as risk factors in the genetic susceptibility to high myopia. Investigative ophthalmology & visual science 2011 Aug 52 (9): 6396-403. Yip Shea Ping, Leung Kim Hung, Ng Po Wah, Fung Wai Yan, Sham Pak Chung, Yap Maurice K |
Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9.
Frontiers in genetics 2013 4 277. Simino Jeannette, Sung Yun Ju, Kume Rezart, Schwander Karen, Rao D |
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
Nature communications 2018 May 9 (1): 1864. Iglesias Adriana I, Mishra Aniket, Vitart Veronique, Bykhovskaya Yelena, Höhn René, Springelkamp Henriët, Cuellar-Partida Gabriel, Gharahkhani Puya, Bailey Jessica N Cooke, Willoughby Colin E, Li Xiaohui, Yazar Seyhan, Nag Abhishek, Khawaja Anthony P, Polašek Ozren, Siscovick David, Mitchell Paul, Tham Yih Chung, Haines Jonathan L, Kearns Lisa S, Hayward Caroline, Shi Yuan, van Leeuwen Elisabeth M, Taylor Kent D, , Bonnemaijer Pieter, Rotter Jerome I, Martin Nicholas G, Zeller Tanja, Mills Richard A, Staffieri Sandra E, Jonas Jost B, Schmidtmann Irene, Boutin Thibaud, Kang Jae H, Lucas Sionne E M, Wong Tien Yin, Beutel Manfred E, Wilson James F, , , Uitterlinden André G, Vithana Eranga N, Foster Paul J, Hysi Pirro G, Hewitt Alex W, Khor Chiea Chuen, Pasquale Louis R, Montgomery Grant W, Klaver Caroline C W, Aung Tin, Pfeiffer Norbert, Mackey David A, Hammond Christopher J, Cheng Ching-Yu, Craig Jamie E, Rabinowitz Yaron S, Wiggs Janey L, Burdon Kathryn P, van Duijn Cornelia M, MacGregor Stua |
Congenital glaucoma and CYP1B1: an old story revisited. Human genetics 2018 3 138 (8-9): 1043-1049. Alsaif Hessa S, Khan Arif O, Patel Nisha, Alkuraya Hisham, Hashem Mais, Abdulwahab Firdous, Ibrahim Niema, Aldahmesh Mohammed A, Alkuraya Fowzan |
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