Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: PRDM2[original query] |
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Genetic variants in epigenetic genes and breast cancer risk. Carcinogenesis 2006 Aug 27 (8): 1661-9. Cebrian Arancha, Pharoah Paul D, Ahmed Shahana, Ropero Santiago, Fraga Mario F, Smith Paula L, Conroy Don, Luben Robert, Perkins Barbara, Easton Douglas F, Dunning Alison M, Esteller Manel, Ponder Bruce A |
Genetic polymorphisms in the Rb-binding zinc finger gene RIZ and the risk of lung cancer. Carcinogenesis 2007 Sep 28 (9): 1971-7. Yoon Kyong-Ah, Park Sohee, Hwangbo Bin, Shin Hyoung Doo, Cheong Hyun Sub, Shin Hai-Rim, Lee Jin S |
Genetic variants of methyl metabolizing enzymes and epigenetic regulators: associations with promoter CpG island hypermethylation in colorectal cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009 Nov 18 (11): 3086-96. de Vogel Stefan, Wouters Kim A D, Gottschalk Ralph W H, van Schooten Frederik J, de Goeij Anton F P M, de Bruïne Adriaan P, Goldbohm Royle A, van den Brandt Piet A, Weijenberg Matty P, van Engeland Man |
Variants in estrogen-related genes and risk of Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2011 Jun 26 (7): 1234-42. Chung Sun Ju, Armasu Sebastian M, Biernacka Joanna M, Lesnick Timothy G, Rider David N, Cunningham Julie M, Maraganore Demetrius |
CCDC62 variant rs12817488 is associated with the risk of Parkinson's disease in a Han Chinese population. European neurology 2014 71 (1-2): 77-83. Liu Rong-Rong, Zhou Li-Li, Cheng Xing, Sun Miao-Xuan, Hu Yan-Bing, Chen Song-Fang, Zhang Xiong, Zhu Jian-Ho |
A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson's Disease in the Han Population of Chinese Mainland.
Molecular neurobiology 2015 Jul . Hu Yakun, Deng Libing, Zhang Jie, Fang Xin, Mei Puming, Cao Xuebing, Lin Jiari, Wei Yi, Zhang Xiong, Xu Rens |
Folate-mediated one-carbon metabolism genes and interactions with nutritional factors on colorectal cancer risk: Women's Health Initiative Observational Study. Cancer 2015 Jun . Cheng Ting-Yuan David, Makar Karen W, Neuhouser Marian L, Miller Joshua W, Song Xiaoling, Brown Elissa C, Beresford Shirley A A, Zheng Yingye, Poole Elizabeth M, Galbraith Rachel L, Duggan David J, Habermann Nina, Bailey Lynn B, Maneval David R, Caudill Marie A, Toriola Adetunji T, Green Ralph, Ulrich Cornelia |
Genomic Copy Number Variations Characterize the Prognosis of Both P16-Positive and P16-Negative Oropharyngeal Squamous Cell Carcinoma After Curative Resection. Medicine 2015 Dec 94 (50): e2187. Rhie Arang, Park Weon Seo, Choi Moon Kyung, Kim Ji-Hyun, Ryu Junsun, Ryu Chang Hwan, Kim Jong-Il, Jung Yuh-Se |
Analysis of somatic microsatellite indels identifies driver events in human tumors. Nature biotechnology 2017 9 35 (10): 951-959. Maruvka Yosef E, Mouw Kent W, Karlic Rosa, Parasuraman Prasanna, Kamburov Atanas, Polak Paz, Haradhvala Nicholas J, Hess Julian M, Rheinbay Esther, Brody Yehuda, Koren Amnon, Braunstein Lior Z, D'Andrea Alan, Lawrence Michael S, Bass Adam, Bernards Andre, Michor Franziska, Getz G |
Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults.
Pharmacogenetics and genomics 2017 Jul 27 (7): 247-254. Wells Quinn S, Veatch Olivia J, Fessel Joshua P, Joon Aron Y, Levinson Rebecca T, Mosley Jonathan D, Held Elizabeth P, Lindsay Chase S, Shaffer Christian M, Weeke Peter E, Glazer Andrew M, Bersell Kevin R, Van Driest Sara L, Karnes Jason H, Blair Marcia A, Lagrone Lore W, Su Yan R, Bowton Erica A, Feng Ziding, Ky Bonnie, Lenihan Daniel J, Fisch Michael J, Denny Joshua C, Roden Dan |
Detection of Molecular Alterations in Taiwanese Patients with Medullary Thyroid Cancer Using Whole-Exome Sequencing. Endocrine pathology 2018 Aug . Chang Ya-Sian, Chang Chun-Chi, Huang Hsi-Yuan, Lin Chien-Yu, Yeh Kun-Tu, Chang Jan-Gow |
Distinct subtypes of polycystic ovary syndrome with novel genetic associations: An unsupervised, phenotypic clustering analysis.
PLoS medicine 2020 06 17 (6): e1003132. Dapas Matthew, Lin Frederick T J, Nadkarni Girish N, Sisk Ryan, Legro Richard S, Urbanek Margrit, Hayes M Geoffrey, Dunaif Andr |
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- Page last updated:Apr 29, 2024
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