Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: MAD1L1[original query] |
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Functional evaluation of missense variations in the human MAD1L1 and MAD2L1 genes and their impact on susceptibility to lung cancer. Journal of medical genetics 2010 Sep 47 (9): 616-22. Guo Yongli, Zhang Xuemei, Yang Ming, Miao Xiaoping, Shi Yuankai, Yao Jiarui, Tan Wen, Sun Tong, Zhao Dan, Yu Dianke, Liu Junniao, Lin Dongx |
Meta-analysis identifies four new loci associated with testicular germ cell tumor.
Nature genetics 2013 Jun 45 (6): 680-5. Chung Charles C, Kanetsky Peter A, Wang Zhaoming, Hildebrandt Michelle A T, Koster Roelof, Skotheim Rolf I, Kratz Christian P, Turnbull Clare, Cortessis Victoria K, Bakken Anne C, Bishop D Timothy, Cook Michael B, Erickson R Loren, Fosså Sophie D, Jacobs Kevin B, Korde Larissa A, Kraggerud Sigrid M, Lothe Ragnhild A, Loud Jennifer T, Rahman Nazneen, Skinner Eila C, Thomas Duncan C, Wu Xifeng, Yeager Meredith, Schumacher Fredrick R, Greene Mark H, Schwartz Stephen M, McGlynn Katherine A, Chanock Stephen J, Nathanson Katherine |
Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.
Molecular psychiatry 2013 Nov . Ruderfer DM, Fanous AH, Ripke S, McQuillin A, Amdur RL, Gejman PV, O'Donovan MC, Andreassen OA, Djurovic S, Hultman CM, Kelsoe JR, Jamain S, Landén M, Leboyer M, Nimgaonkar V, Nurnberger J, Smoller JW, Craddock N, Corvin A, Sullivan PF, Holmans P, Sklar P, Kendler KS |
MAD1L1 Arg558His and MAD2L1 Leu84Met interaction with smoking increase the risk of colorectal cancer. Scientific reports 2015 5 12202. Zhong Rong, Chen Xiaohua, Chen Xueqin, Zhu Beibei, Lou Jiao, Li Jiaoyuan, Shen Na, Yang Yang, Gong Yajie, Zhu Ying, Yuan Jing, Xia Xiaoping, Miao Xiaopi |
Genetic association of GWAS-supported MAD1L1 gene polymorphism rs12666575 with schizophrenia susceptibility in a Chinese population. Neuroscience letters 2015 Oct . Su Li, Shen Tingting, Huang Guifeng, Long Jianxiong, Fan Jingyuan, Ling Weijun, Jiang Ju |
Investigating the Impact of a Genome-Wide Supported Bipolar Risk Variant of MAD1L1 on the Human Reward System. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2016 May . Trost Sarah, Diekhof Esther K, Mohr Holger, Vieker Henning, Krämer Bernd, Wolf Claudia, Keil Maria, Dechent Peter, Binder Elisabeth B, Gruber Oliv |
Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activity. Schizophrenia research 2016 Feb . Gadelha Ary, Coleman Jonathan, Breen Gerome, Mazzoti Diego Robles, Yonamine Camila M, Pellegrino Renata, Ota Vanessa Kiyomi, Belangero Sintia Iole, Glessner Joseph, Sleiman Patrick, Hakonarson Hakon, Hayashi Mirian A F, Bressan Rodrigo |
[A search of target regions for association studies between DNA methylation and cognitive impairment in schizophrenia]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2017 117 (8): 72-75. Kondratiev N V, Alfimova M V, Golimbet V |
Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility.
Nature genetics 2017 May 49 (5): 674-679. Wright Daniel J, Day Felix R, Kerrison Nicola D, Zink Florian, Cardona Alexia, Sulem Patrick, Thompson Deborah J, Sigurjonsdottir Svanhvit, Gudbjartsson Daniel F, Helgason Agnar, Chapman J Ross, Jackson Steve P, Langenberg Claudia, Wareham Nicholas J, Scott Robert A, Thorsteindottir Unnur, Ong Ken K, Stefansson Kari, Perry John R |
A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder.
Molecular psychiatry 2017 Jan . Ikeda M, Takahashi A, Kamatani Y, Okahisa Y, Kunugi H, Mori N, Sasaki T, Ohmori T, Okamoto Y, Kawasaki H, Shimodera S, Kato T, Yoneda H, Yoshimura R, Iyo M, Matsuda K, Akiyama M, Ashikawa K, Kashiwase K, Tokunaga K, Kondo K, Saito T, Shimasaki A, Kawase K, Kitajima T, Matsuo K, Itokawa M, Someya T, Inada T, Hashimoto R, Inoue T, Akiyama K, Tanii H, Arai H, Kanba S, Ozaki N, Kusumi I, Yoshikawa T, Kubo M, Iwata |
Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.
Journal of medical genetics 2018 Aug . Galván-Femenía Iván, Obón-Santacana Mireia, Piñeyro David, Guindo-Martinez Marta, Duran Xavier, Carreras Anna, Pluvinet Raquel, Velasco Juan, Ramos Laia, Aussó Susanna, Puig Lluis, Perucho Manuel, Torrents David, Moreno Victor, Sumoy Lauro, de Cid Rafa |
Genome-wide association study and in silico functional analysis of the number of embryos produced by Holstein donors. Journal of dairy science 2018 5 101 (8): 7248-7257. Jaton C, Schenkel F S, Sargolzaei M, Cánova A, Malchiodi F, Price C A, Baes C, Miglior |
Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population. Translational psychiatry 2018 12 8 (1): 270. Zhao Lijuan, Chang Hong, Zhou Dong-Sheng, Cai Jun, Fan Weixing, Tang Wei, Tang Wenxin, Li Xingxing, Liu Weiqing, Liu Fang, He Yuanfang, Bai Yan, Sun Yan, Dai Jiapei, Li Lingyi, Xiao Xiao, Zhang Chen, Li Mi |
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 |
Association of MAD1L1 polymorphism (rs871925) with prenatal famine exposure and schizophrenia in a Chinese population: A case-control study. IUBMB life 2019 Sep . Sun Yaoyao, Kang Guojun, Zhu Xiaojing, Li Rixin, Kang Qi, Zhang Mingyuan, Wang Yueying, Chen Xin, Yu Yaqin, Yu Qio |
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 |
Reproducible Genetic Risk Loci for Anxiety: Results From ~200,000 Participants in the Million Veteran Program.
The American journal of psychiatry 2020 03 177 (3): 223-232. Levey Daniel F, Gelernter Joel, Polimanti Renato, Zhou Hang, Cheng Zhongshan, Aslan Mihaela, Quaden Rachel, Concato John, Radhakrishnan Krishnan, Bryois Julien, Sullivan Patrick F, , Stein Murray |
Longitudinal epigenome-wide association studies of three male military cohorts reveal multiple CpG sites associated with post-traumatic stress disorder. Clinical epigenetics 2020 1 12 (1): 11. Snijders Clara, Maihofer Adam X, Ratanatharathorn Andrew, Baker Dewleen G, Boks Marco P, Geuze Elbert, Jain Sonia, Kessler Ronald C, Pishva Ehsan, Risbrough Victoria B, Stein Murray B, Ursano Robert J, Vermetten Eric, Vinkers Christiaan H, , Smith Alicia K, Uddin Monica, Rutten Bart P F, Nievergelt Caroline |
MAD1L1 and TSNARE gene polymorphisms are associated with schizophrenia susceptibility in the Han Chinese population. BMC medical genomics 2021 9 14 (1): 218. Liu Xianglai, Xie Hailing, Fu Zejuan, Yao Qiankun, Han Tianming, Zhan Dafei, Lin Zhan, Zhu Ho |
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 |
Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk. Translational psychiatry 2022 8 12 (1): 340. McKinney Brandon C, McClain Lora L, Hensler Christopher M, Wei Yue, Klei Lambertus, Lewis David A, Devlin Bernie, Wang Jiebiao, Ding Ying, Sweet Robert |
Risk Allele Frequency Analysis and Risk Prediction of Single-Nucleotide Polymorphisms for Prostate Cancer. Genes 2022 11 13 (11): . Yoon Byung Woo, Shin Hyun-Tae, Seo Je Hy |
Identification of a Risk Locus at 7p22.3 for Schizophrenia and Bipolar Disorder in East Asian Populations.
Frontiers in genetics 2022 1 12 789512. Li Wenqiang, Zhang Chu-Yi, Liu Jiewei, Guan Fanglin, Shao Minglong, Zhang Luwen, Liu Qing, Yang Yongfeng, Su Xi, Zhang Yan, Xiao Xiao, Luo Xiong-Jian, Li Ming, Lv Luxi |
Maternal genetic polymorphisms in the major mitotic checkpoint genes MAD1L1 and MAD2L1 associated with the risk of survival in abnormal chromosomal fetuses. Frontiers in genetics 2023 4 14 1105184. Chan Ying, Liu Yize, Kong Yamin, Xu Weiming, Zeng Xiaohong, Li Haichun, Guo Yan, Tang Xinhua, Zhang Jinman, Zhu Baoshe |
Methylation in MAD1L1 is associated with the severity of suicide attempt and phenotypes of depression. Clinical epigenetics 2023 1 15 (1): 1. Sokolov Aleksandr V, Manu Diana-Maria, Nordberg Didi O T, Boström Adrian D E, Jokinen Jussi, Schiöth Helgi |
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- Page last updated:Apr 16, 2024
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