Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: CTBP2[original query] |
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Multiple loci identified in a genome-wide association study of prostate cancer.
Nature genetics 2008 Mar 40 (3): 310-5. Thomas Gilles, Jacobs Kevin B, Yeager Meredith, Kraft Peter, Wacholder Sholom, Orr Nick, Yu Kai, Chatterjee Nilanjan, Welch Robert, Hutchinson Amy, Crenshaw Andrew, Cancel-Tassin Geraldine, Staats Brian J, Wang Zhaoming, Gonzalez-Bosquet Jesus, Fang Jun, Deng Xiang, Berndt Sonja I, Calle Eugenia E, Feigelson Heather Spencer, Thun Michael J, Rodriguez Carmen, Albanes Demetrius, Virtamo Jarmo, Weinstein Stephanie, Schumacher Fredrick R, Giovannucci Edward, Willett Walter C, Cussenot Olivier, Valeri Antoine, Andriole Gerald L, Crawford E David, Tucker Margaret, Gerhard Daniela S, Fraumeni Joseph F, Hoover Robert, Hayes Richard B, Hunter David J, Chanock Stephen |
Generalizability of associations from prostate cancer genome-wide association studies in multiple populations. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009 Mar . Waters KM, Le Marchand L, Kolonel LN, Monroe KR, Stram DO, Henderson BE, Haiman CA |
Interactions between genome-wide significant genetic variants and circulating concentrations of insulin-like growth factor 1, sex hormones, and binding proteins in relation to prostate cancer risk in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium. American journal of epidemiology 2012 Mar . Tsilidis KK, Travis RC, Appleby PN, Allen NE, Lindstrom S, Schumacher FR, Cox D, Hsing AW, Ma J, Severi G, Albanes D, Virtamo J, Boeing H, Bueno-de-Mesquita HB, Johansson M, Quirós JR, Riboli E, Siddiq A, Tjønneland A, Trichopoulos D, Tumino R, Gaziano JM, Giovannucci E, Hunter DJ, Kraft P, Stampfer MJ, Giles GG, Andriole GL, Berndt SI, Chanock SJ, Hayes RB, Key TJ |
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data. Circulation research 2014 Oct 115 (10): 884-96. Glessner Joseph T, Bick Alexander G, Ito Kaoru, Homsy Jason G, Rodriguez-Murillo Laura, Fromer Menachem, Mazaika Erica, Vardarajan Badri, Italia Michael, Leipzig Jeremy, DePalma Steven R, Golhar Ryan, Sanders Stephan J, Yamrom Boris, Ronemus Michael, Iossifov Ivan, Willsey A Jeremy, State Matthew W, Kaltman Jonathan R, White Peter S, Shen Yufeng, Warburton Dorothy, Brueckner Martina, Seidman Christine, Goldmuntz Elizabeth, Gelb Bruce D, Lifton Richard, Seidman Jonathan, Hakonarson Hakon, Chung Wendy |
Identification of genetic variants or genes that are associated with Homoharringtonine (HHT) response through a genome-wide association study in human lymphoblastoid cell lines (LCLs).
Frontiers in genetics 2014 5 465. Tong Yin, Niu Nifang, Jenkins Gregory, Batzler Anthony, Li Liang, Kalari Krishna R, Wang Liew |
PPARGC1? gene DNA methylation variations in human placenta mediate the link between maternal hyperglycemia and leptin levels in newborns. Clinical epigenetics 2016 8 72. Côté Sandra, Gagné-Ouellet Valérie, Guay Simon-Pierre, Allard Catherine, Houde Andrée-Anne, Perron Patrice, Baillargeon Jean-Patrice, Gaudet Daniel, Guérin Renée, Brisson Diane, Hivert Marie-France, Bouchard Lui |
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index. Molecular psychiatry 2016 May . Hinney A, Kesselmeier M, Jall S, Volckmar A-L, Föcker M, Antel J, , , Heid I M, Winkler T W, , Grant S F A, , Guo Y, Bergen A W, Kaye W, Berrettini W, Hakonarson H, , , Herpertz-Dahlmann B, de Zwaan M, Herzog W, Ehrlich S, Zipfel S, Egberts K M, Adan R, Brandys M, van Elburg A, Boraska Perica V, Franklin C S, Tschöp M H, Zeggini E, Bulik C M, Collier D, Scherag A, Müller T D, Hebebrand |
A genome wide association study of fast beta EEG in families of European ancestry.
International journal of psychophysiology : official journal of the International Organization of Psychophysiology 2017 May 115 74-85. Meyers Jacquelyn L, Zhang Jian, Manz Niklas, Rangaswamy Madhavi, Kamarajan Chella, Wetherill Leah, Chorlian David B, Kang Sun J, Bauer Lance, Hesselbrock Victor, Kramer John, Kuperman Samuel, Nurnberger John I, Tischfield Jay, Wang Jen Chyong, Edenberg Howard J, Goate Alison, Foroud Tatiana, Porjesz Berni |
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing. Prenatal diagnosis 2018 Jul . Kammoun Molka, Souche Erika, Brady Paul, Ding Jia, Cosemans Nele, Gratacos Eduard, Devriendt Koen, Eixarch Elisenda, Deprest Jan, Vermeesch Joris Robe |
Single-Nucleotide Polymorphisms Sequencing Identifies Candidate Functional Variants at Prostate Cancer Risk Loci. Genes 2019 7 10 (7): . Zhang Peng, Tillmans Lori S, Thibodeau Stephen N, Wang Lia |
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