Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer
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Sebastian M. Armasu | Yurii B. Shvetsov | A. Whittemore | L. Kiemeney | M. Pike | M. Beckmann | P. Fasching | R. Vierkant | T. Sellers | P. Hall | P. Laird | J. Chang-Claude | M. García-Closas | B. Fridley | E. Goode | Robert Brown | B. Karlan | N. Le | A. Berchuck | E. Iversen | G. Giles | G. Severi | T. Dörk | M. Southey | D. Easton | Xifeng Wu | Hui Shen | D. Huntsman | P. Pharoah | D. Lambrechts | D. Stram | M. Köbel | A. Brooks-Wilson | D. Levine | Daniel Vincent | M. Gore | P. Hillemanns | X. Shu | W. Zheng | A. Ziogas | H. Anton-Culver | U. Menon | A. Gentry-Maharaj | E. Benjamin | K. Aben | D. Eccles | G. Chenevix-Trench | L. Brinton | J. Lissowska | H. Nevanlinna | N. Bogdanova | J. Beesley | Xiaoqing Chen | J. Cunningham | M. Goodman | R. Hein | F. Bacot | D. Tessier | S. Nickels | L. Baglietto | A. Ekici | A. Jakubowska | J. Lubiński | N. Antonenkova | K. Matsuo | A. Wu | S. Teo | J. Tyrer | S. Wang-gohrke | C. Bunker | A. Monteiro | S. Gayther | D. Cramer | D. J. Van Den Berg | N. Wentzensen | I. Vergote | R. Ness | A. Vitonis | S. Olson | H. Risch | L. Kelemen | S. Narod | K. Odunsi | I. Campbell | I. Runnebaum | I. Orlow | J. Doherty | J. Schildkraut | K. Moysich | F. Modugno | B. Ji | M. Cicek | H. Kajiyama | K. Lu | J. McLaughlin | G. Keeney | H. Salvesen | L. Massuger | A. V. van Altena | G. Konecny | E. Bandera | M. Hildebrandt | M. K. Halle | J. Flanagan | F. Heitz | P. Harter | A. du Bois | R. Butzow | K. Lawrenson | Hannah P. Yang | C. Cybulski | V. McGuire | W. Sieh | L. Rodriguez-Rodriguez | B. Winterhoff | M. Block | V. Shridhar | Honglin Song | C. Phelan | A. Jensen | L. Cook | J. Gronwald | N. Siddiqui | S. Tworoger | G. Lurie | R. Edwards | E. Høgdall | C. Høgdall | S. Ramus | E. Wik | C. Krakstad | J. Paul | T. Pejović | I. Rzepecka | A. Dansonka-Mieszkowska | J. Kupryjańczyk | E. Despierre | L. Pelttari | S. Armasu | P. Thompson | M. Dürst | S. Hosono | S. Lambrechts | Alice W. Lee | A. Leminen | Dong Liang | L. Lundvall | E. Poole | I. Schwaab | Y. Shvetsov | K. Terry | K. Kalli | E. Wozniak | M. Larson | D. Stram | Yin Ling Woo | Rachel Palmieri Weber | C. Templeman | Mary Anne Rossing | S. Renner | Siti Zawiah Omar | T. Nakanishi | J. Moes-Sosnowska | N. A. Mat Adenan | S. Krüger Kjaer | Rod Karevan | M. Hoatlin | Bridget Charbonneau | D. Brueggmann | Celeste Leigh Pearce | Liisa M. Pelttari | E. Woźniak | T. Pejovic | K. Lu | A. Monteiro | P. Hall | K. Lu | J. Paul | A. van Altena | R. Edwards | M. Larson | A. Wu | J. McLaughlin
[1] M. Pike,et al. Association between endometriosis and risk of histological subtypes of ovarian cancer: a pooled analysis of case–control studies , 2012, The Lancet. Oncology.
[2] A. Berchuck,et al. Role of common genetic variants in ovarian cancer susceptibility and outcome: progress to date from the ovarian cancer association consortium (OCAC) , 2012, Journal of internal medicine.
[3] K. Gunderson,et al. High density DNA methylation array with single CpG site resolution. , 2011, Genomics.
[4] J. Brenton,et al. Ovarian clear cell carcinoma—bad endometriosis or bad endometrium? , 2011, The Journal of pathology.
[5] R. Ward,et al. Dominantly inherited constitutional epigenetic silencing of MLH1 in a cancer-affected family is linked to a single nucleotide variant within the 5'UTR. , 2011, Cancer cell.
[6] M. Thun,et al. Large-scale fine mapping of the HNF1B locus and prostate cancer risk. , 2011, Human molecular genetics.
[7] Benjamin J. Raphael,et al. Integrated Genomic Analyses of Ovarian Carcinoma , 2011, Nature.
[8] M. Beckmann,et al. Genome-wide association study identifies a common variant associated with risk of endometrial cancer , 2011, Nature Genetics.
[9] Timothy J. Durham,et al. Systematic analysis of chromatin state dynamics in nine human cell types , 2011, Nature.
[10] Joseph K. Pickrell,et al. DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines , 2011, Genome Biology.
[11] A. Whittemore,et al. A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24 , 2010, Nature Genetics.
[12] A. Whittemore,et al. Common variants at 19p13 are associated with susceptibility to ovarian cancer , 2010, Nature Genetics.
[13] Ie-Ming Shih,et al. The Origin and Pathogenesis of Epithelial Ovarian Cancer: A Proposed Unifying Theory , 2010, The American journal of surgical pathology.
[14] C. Gilks. Molecular Abnormalities in Ovarian Cancer Subtypes Other than High-Grade Serous Carcinoma , 2009, Journal of oncology.
[15] A. Whittemore,et al. A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2 , 2009, Nature Genetics.
[16] S. Leung,et al. Ovarian Carcinoma Subtypes Are Different Diseases: Implications for Biomarker Studies , 2008, PLoS medicine.
[17] Simon Kasif,et al. Genomewide Analysis of PRC1 and PRC2 Occupancy Identifies Two Classes of Bivalent Domains , 2008, PLoS genetics.
[18] J. Carpten,et al. Evidence for two independent prostate cancer risk–associated loci in the HNF1B gene at 17q12 , 2008, Nature Genetics.
[19] W. Willett,et al. Multiple loci identified in a genome-wide association study of prostate cancer , 2008, Nature Genetics.
[20] E. Halperin,et al. Estimating Local Ancestry in Admixed Populations , 2022 .
[21] D. Gudbjartsson,et al. Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes , 2007, Nature Genetics.
[22] Kristin G Ardlie,et al. Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes , 2007, Diabetes.
[23] R. Drapkin,et al. The distal fallopian tube: a new model for pelvic serous carcinogenesis , 2007, Current opinion in obstetrics & gynecology.
[24] P. Laird,et al. Epigenetic stem cell signature in cancer , 2007, Nature Genetics.
[25] D. Easton,et al. Risk prediction models for familial breast cancer. , 2006, Future oncology.
[26] T. Seidal,et al. Clinical and biological characteristics of clear cell carcinomas of the ovary in FIGO stages I-II. , 2005, International journal of oncology.
[27] E. Negri,et al. A pooled analysis of case-control studies of thyroid cancer¶ III. Oral contraceptives, menopausal replacement therapy and other female hormones , 1999, Cancer Causes & Control.
[28] Tsutomu Ohta,et al. Expression profiling in ovarian clear cell carcinoma: identification of hepatocyte nuclear factor-1 beta as a molecular marker and a possible molecular target for therapy of ovarian clear cell carcinoma. , 2003, The American journal of pathology.
[29] Daniel O. Stram,et al. Modeling and E-M Estimation of Haplotype-Specific Relative Risks from Genotype Data for a Case-Control Study of Unrelated Individuals , 2003, Human Heredity.
[30] J. Kaprio,et al. Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland. , 2000, The New England journal of medicine.
[31] G. Bell,et al. Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY. , 1997, Nature genetics.
[32] H. Risch,et al. Differences in risk factors for epithelial ovarian cancer by histologic type. Results of a case-control study. , 1996, American journal of epidemiology.
[33] R. Sankila,et al. Cancer incidence in the first-degree relatives of ovarian cancer patients. , 1996, British Journal of Cancer.