Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Disease and MAD1L1[original query] |
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| Coding mutations in NUS1 contribute to Parkinson's disease. Proceedings of the National Academy of Sciences of the United States of America 2018 10 115 (45): 11567-11572. Guo Ji-Feng, Zhang Lu, Li Kai, Mei Jun-Pu, Xue Jin, Chen Jia, Tang Xia, Shen Lu, Jiang Hong, Chen Chao, Guo Hui, Wu Xue-Li, Sun Si-Long, Xu Qian, Sun Qi-Ying, Chan Piu, Shang Hui-Fang, Wang Tao, Zhao Guo-Hua, Liu Jing-Yu, Xie Xue-Feng, Jiang Yi-Qi, Liu Zhen-Hua, Zhao Yu-Wen, Zhu Zuo-Bin, Li Jia-da, Hu Zheng-Mao, Yan Xin-Xiang, Fang Xiao-Dong, Wang Guang-Hui, Zhang Feng-Yu, Xia Kun, Liu Chun-Yu, Zhu Xiong-Wei, Yue Zhen-Yu, Li Shuai Cheng, Cai Huai-Bin, Zhang Zhuo-Hua, Duan Ran-Hui, Tang Bei-S |
Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis.
American journal of respiratory and critical care medicine 2020 03 201 (5): 564-574. Allen Richard J, Guillen-Guio Beatriz, Oldham Justin M, Ma Shwu-Fan, Dressen Amy, Paynton Megan L, Kraven Luke M, Obeidat Ma'en, Li Xuan, Ng Michael, Braybrooke Rebecca, Molina-Molina Maria, Hobbs Brian D, Putman Rachel K, Sakornsakolpat Phuwanat, Booth Helen L, Fahy William A, Hart Simon P, Hill Mike R, Hirani Nik, Hubbard Richard B, McAnulty Robin J, Millar Ann B, Navaratnam Vidyia, Oballa Eunice, Parfrey Helen, Saini Gauri, Whyte Moira K B, Zhang Yingze, Kaminski Naftali, Adegunsoye Ayodeji, Strek Mary E, Neighbors Margaret, Sheng Xuting R, Gudmundsson Gunnar, Gudnason Vilmundur, Hatabu Hiroto, Lederer David J, Manichaikul Ani, Newell John D, O'Connor George T, Ortega Victor E, Xu Hanfei, Fingerlin Tasha E, Bossé Yohan, Hao Ke, Joubert Philippe, Nickle David C, Sin Don D, Timens Wim, Furniss Dominic, Morris Andrew P, Zondervan Krina T, Hall Ian P, Sayers Ian, Tobin Martin D, Maher Toby M, Cho Michael H, Hunninghake Gary M, Schwartz David A, Yaspan Brian L, Molyneaux Philip L, Flores Carlos, Noth Imre, Jenkins R Gisli, Wain Louise |
| Prognostic Significance of the MAD1L1 1673 G: A Polymorphism in Ovarian Adenocarcinomas. Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion 2020 May 73 (3): . Bandala-Jacques Antonio, Hernández-Cruz Irwin A, Castro-Hernández Clementina, Díaz-Chávez José, Arriaga-Canon Cristian, Barquet-Muñoz Salim A, Prada-Ortega Diddier G, Cantú-de León David, Herrera Luis |
| Revisiting Schizophrenia from an Evolutionary Perspective: An Association Study of Recent Evolutionary Markers and Schizophrenia. Schizophrenia bulletin 2020 Dec . Bhattacharyya Upasana, Deshpande Smita N, Bhatia Triptish, Thelma B |
| Prognostic Significance of the MAD1L1 1673 G: A Polymorphism in Ovarian Adenocarcinomas. Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion 2020 May 73 (5): . Bandala-Jacques Antonio, Hernández-Cruz Irwin A, Castro-Hernández Clementina, Díaz-Chávez José, Arriaga-Canon Cristian, Barquet-Muñoz Salim A, Prada-Ortega Diddier G, Cantú-de León David, Herrera Luis |
| Causal influences of neuroticism on mental health and cardiovascular disease. Human genetics 2021 May . Zhang Fuquan, Baranova Ancha, Zhou Chao, Cao Hongbao, Chen Jiu, Zhang Xiangrong, Xu Mingqi |
| Association of rare single nucleotide variant MUC5B rs35705950 with interstitial lung disease in Japanese rheumatoid arthritis. Rheumatology (Oxford, England) 2024 8 . Takashi Higuchi, Shomi Oka, Kota Shimada, Shinichiro Tsunoda, Satoshi Ito, Akira Okamoto, Misuzu Fujimori, Tadashi Nakamura, Masao Katayama, Michita Suzuki, Koichiro Saisho, Satoshi Shinohara, Toshihiro Matsui, Kiyoshi Migita, Shouhei Nagaoka, Shigeto Tohma, Hiroshi Furuka |
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