Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: TCF19[original query] |
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Sequence and haplotype analysis supports HLA-C as the psoriasis susceptibility 1 gene. American journal of human genetics 2006 May 78 (5): 827-51. Nair Rajan P, Stuart Philip E, Nistor Ioana, Hiremagalore Ravi, Chia Nicholas V C, Jenisch Stefan, Weichenthal Michael, Abecasis Gonçalo R, Lim Henry W, Christophers Enno, Voorhees John J, Elder James |
A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.
Human molecular genetics 2013 Oct 22 (20): 4233-8. Kim Yoon Jun, Kim Hwi Young, Lee Jeong-Hoon, Yu Su Jong, Yoon Jung-Hwan, Lee Hyo-Suk, Kim Chung Yong, Cheong Jae Youn, Cho Sung Won, Park Neung Hwa, Park Byung Lae, Namgoong Seok, Kim Lyoung Hyo, Cheong Hyun Sub, Shin Hyoung D |
Genetic association of human leukocyte antigens with chronicity or resolution of hepatitis B infection in thai population. PloS one 2014 9 (1): e86007. Posuwan Nawarat, Payungporn Sunchai, Tangkijvanich Pisit, Ogawa Shintaro, Murakami Shuko, Iijima Sayuki, Matsuura Kentaro, Shinkai Noboru, Watanabe Tsunamasa, Poovorawan Yong, Tanaka Yasuhi |
Host genetic variants influencing the clinical course of hepatitis B virus infection. Journal of medical virology 2015 Aug . Matsuura Kentaro, Isogawa Masanori, Tanaka Yasuhi |
Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B.
Hepatology (Baltimore, Md.) 2015 Jul 62 (1): 118-28. Jiang De-Ke, Ma Xiao-Pin, Yu Hongjie, Cao Guangwen, Ding Dong-Lin, Chen Haitao, Huang Hui-Xing, Gao Yu-Zhen, Wu Xiao-Pan, Long Xi-Dai, Zhang Hongxing, Zhang Youjie, Gao Yong, Chen Tao-Yang, Ren Wei-Hua, Zhang Pengyin, Shi Zhuqing, Jiang Wei, Wan Bo, Saiyin Hexige, Yin Jianhua, Zhou Yuan-Feng, Zhai Yun, Lu Pei-Xin, Zhang Hongwei, Gu Xiaoli, Tan Aihua, Wang Jin-Bing, Zuo Xian-Bo, Sun Liang-Dan, Liu Jun O, Yi Qing, Mo Zengnan, Zhou Gangqiao, Liu Ying, Sun Jielin, Shugart Yin Yao, Zheng S Lilly, Zhang Xue-Jun, Xu Jianfeng, Yu Lo |
The type 2 diabetes risk allele of TMEM154-rs6813195 associates with decreased beta cell function in a study of 6,486 Danes. PloS one 2015 10 (3): e0120890. Harder Marie Neergaard, Appel Emil Vincent Rosenbaum, Grarup Niels, Gjesing Anette Prior, Ahluwalia Tarunveer S, Jørgensen Torben, Christensen Cramer, Brandslund Ivan, Linneberg Allan, Sørensen Thorkild I A, Pedersen Oluf, Hansen Torb |
Identification of novel OCT4 genetic variant associated with the risk of chronic hepatitis B in a Korean population. Liver international : official journal of the International Association for the Study of the Liver 2017 03 37 (3): 354-361. Shin Joong-Gon, Cheong Hyun Sub, Lee Kwanghyun, Ju Bong-Gun, Lee Jeong-Hoon, Yu Su Jong, Yoon Jung-Hwan, Cheong Jae Youn, Cho Sung Won, Park Neung Hwa, Namgoong Suhg, Kim Lyoung Hyo, Kim Yoon Jun, Shin Hyoung D |
Identification of miRSNPs associated with the risk of multiple myeloma. International journal of cancer 2016 Oct . Macauda Angelica, Calvetti Diego, Maccari Giuseppe, Hemminki Kari, Försti Asta, Goldschmidt Hartmut, Weinhold Niels, Houlston Richard, Andersen Vibeke, Vogel Ulla, Buda Gabriele, Varkonyi Judit, Sureda Anna, Lopez Joaquin Martinez, Watek Marzena, Butrym Aleksandra, Sarasquete Maria Eugenia, Dudzi?ski Marek, Jurczyszyn Artur, Druzd-Sitek Agnieszka, Kruszewski Marcin, Subocz Edyta, Petrini Mario, Iskierka-Ja?d?ewska Elzbieta, Ra?ny Malgorzata, Szombath Gergely, Marques Herlander, Zawirska Daria, Chraniuk Dominik, Halka Janusz, Hove Jacobsen Svend Erik, Mazur Grzegorz, Sanz Ramón García, Dumontet Charles, Moreno Victor, St?pie? Anna, Beider Katia, Pelosini Matteo, Reis Rui Manuel, Krawczyk-Kulis Malgorzata, Rymko Marcin, Avet-Loiseau Hervé, Lesueur Fabienne, Grz??ko Norbert, Ostrovsky Olga, Jamroziak Krzysztof, Vangsted Annette J, Jerez Andrés, Tomczak Waldemar, Zaucha Jan Maciej, Kadar Katalin, Pérez Juan Sainz, Nagler Arnon, Landi Stefano, Gemignani Federica, Canzian Federi |
Genetic variants associated with expression of TCF19 contribute to the risk of head and neck cancer in Chinese population. Journal of medical genetics 2021 Mar . Ji Pei, Chang Jiang, Wei Xiaoyu, Song Xueyao, Yuan Hua, Gong Linnan, Li Yuancheng, Ding Dongsheng, Zhang Erbao, Yan Caiwang, Zhu Meng, Miao Xiaoping, Wu Chen, Jin Guangfu, Hu Zhibin, Shen Hongbing, Ma Hongx |
Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran. Clinical genetics 2021 3 100 (1): 59-78. Mohseni Marzieh, Babanejad Mojgan, Booth Kevin T, Jamali Payman, Jalalvand Khadijeh, Davarnia Behzad, Ardalani Fariba, Khoshaeen Atefeh, Arzhangi Sanaz, Ghodratpour Fatemeh, Beheshtian Maryam, Jahanshad Faezeh, Otukesh Hasan, Bahrami Fatemeh, Seifati Seyed Morteza, Bazazzadegan Niloofar, Habibi Farkhonde, Behravan Hanieh, Mirzaei Sepide, Keshavarzi Fatemeh, Nikzat Nooshin, Mehrjoo Zohreh, Thiele Holger, Nothnagel Michael, Azaiez Hela, Smith Richard J, Kahrizi Kimia, Najmabadi Hosse |
Identification of Candidate Genes in Breast Cancer Induced by Estrogen Plus Progestogens Using Bioinformatic Analysis. International journal of molecular sciences 2022 10 23 (19): . Deng Yu, Huang He, Shi Jiangcheng, Jin Hongy |
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