Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and TCF19[original query] |
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| 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 |
| 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 |
| 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 |
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