Center-Authored Papers

Filters: Author is Pharoah, Paul  [Clear All Filters]
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Al Olama AA, Kote-Jarai Z, Berndt SI, Conti DV, Schumacher F, Han Y, Benlloch S, Hazelett DJ, Wang Z, Saunders E et al..  2014.  A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer.. Nature genetics. 46(10):1103-9. Abstract
Al Olama AA, Dadaev T, Hazelett DJ, Li Q, Leongamornlert D, Saunders EJ, Stephens S, Cieza-Borrella C, Whitmore I, Benlloch Garcia S et al..  2015.  Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans.. Human molecular genetics. 24(19):5589-5602. Abstract
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Brisbin AG, Asmann YW, Song H, Tsai Y-Y, Aakre JA, Yang P, Jenkins RB, Pharoah P, Schumacher F, Conti DV et al..  2011.  Meta-analysis of 8q24 for seven cancers reveals a locus between NOV and ENPP2 associated with cancer development.. BMC medical genetics. 12(1):156. Abstract
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Cheng TH, Thompson D, Painter J, O'Mara T, Gorman M, Martin L, Palles C, Jones A, Buchanan DD, Win AK et al..  2015.  Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.. Scientific reports. 5:17369. Abstract
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Dunlop MG, Tenesa A, Farrington SM, Ballereau S, Brewster DH, Koessler T, Pharoah P, Schafmayer C, Hampe J, Völzke H et al..  2012.  Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42 103 individuals.. Gut. Abstract
Dunlop MG, Dobbins SE, Farrington SM, Jones AM, Palles C, Whiffin N, Tenesa A, Spain S, Broderick P, Ooi L-Y et al..  2012.  Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.. Nature genetics. 44(7):770-6. Abstract
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Figueroa JD, Garcia-Closas M, Humphreys M, Platte R, Hopper JL, Southey MC, Apicella C, Hammet F, Schmidt MK, Broeks A et al..  2011.  Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: Findings from the Breast Cancer Association Consortium.. Human molecular genetics. 20(23):4693-4706. Abstract
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Gharahkhani P, Fitzgerald RC, Vaughan TL, Palles C, Gockel I, Tomlinson I, Buas MF, May A, Gerges C, Anders M et al..  2016.  Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.. The Lancet. Oncology. Abstract
Guo Y, Warren Andersen S, Shu X-O, Michailidou K, Bolla MK, Wang Q, Garcia-Closas M, Milne RL, Schmidt MK, Chang-Claude J et al..  2016.  Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent.. PLoS medicine. 13(8):e1002105. Abstract
Gusev A, Shi H, Kichaev G, Pomerantz M, Li F, Long HW, Ingles SA, Kittles RA, Strom SS, Rybicki BA et al..  2016.  Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation.. Nature communications. 7:10979. Abstract
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Johnatty S, Tyrer JP, Kar SP, Beesley J, Lu Y, Gao B, Fasching PA, Hein A, Ekici AB, Beckmann MW et al..  2015.  Genome-wide analysis identifies novel loci associated with ovarian cancer outcomes: findings from the Ovarian Cancer Association Consortium.. Clinical cancer research : an official journal of the American Association for Cancer Research. 21(23):5264-5276. Abstract
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Karami S, Han Y, Pande M, Cheng I, Rudd J, Pierce BL, Nutter EL, Schumacher FR, Kote-Jarai Z, Lindstrom S et al..  2016.  Telomere structure and maintenance gene variants and risk of five cancer types.. International journal of cancer. 139(12):2655-2670. Abstract
Kote-Jarai Z, Saunders EJ, Leongamornlert DA, Tymrakiewicz M, Dadaev T, Jugurnauth-Little S, Ross-Adams H, Al Olama AA, Benlloch S, Halim S et al..  2013.  Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.. Human molecular genetics. Abstract
Kote-Jarai Z, Al Olama AA, Giles GG, Severi G, Schleutker J, Weischer M, Campa D, Riboli E, Key T, Gronberg H et al..  2011.  Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.. Nature genetics. 43(8):785-791. Abstract
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Lagergren K, Ek WE, Levine D, Chow W-H, Bernstein L, Casson AG, Risch HA, Shaheen NJ, Bird NC, Reid BJ et al..  2015.  Polymorphisms in Genes of Relevance for Oestrogen and Oxytocin Pathways and Risk of Barrett's Oesophagus and Oesophageal Adenocarcinoma: A Pooled Analysis from the BEACON Consortium.. PloS one. 10(9):e0138738. Abstract
Lophatananon A, Stewart-Brown S, Kote-Jarai Z, Al Olama AA, Benlloch Garcia S, Neal DE, Hamdy FC, Donovan JL, Giles GG, Fitzgerald LM et al..  2017.  Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium.. British journal of cancer. Abstract
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Machiela MJ, Hofmann JN, Carreras-Torres R, Brown KM, Johansson M, Wang Z, Foll M, Li P, Rothman N, Savage SA et al..  2017.  Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma.. European urology. Abstract
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Praestegaard C, Jensen A, Jensen SM, Nielsen TSS, Webb PM, Nagle CM, Defazio A, Høgdall E, Rossing MA, Doherty JA et al..  2017.  Cigarette smoking is associated with adverse survival among women with ovarian cancer: results from a pooled analysis of 19 studies.. International journal of cancer. Abstract
Præstegaard C, Kjaer SK, Nielsen TSS, Jensen SM, Webb PM, Nagle CM, Høgdall E, Risch HA, Rossing MA, Doherty JA et al..  2016.  The association between socioeconomic status and tumour stage at diagnosis of ovarian cancer: A pooled analysis of 18 case-control studies.. Cancer epidemiology. 41:71-79. Abstract
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Saunders EJ, Dadaev T, Leongamornlert DA, Jugurnauth-Little S, Tymrakiewicz M, Wiklund F, Al Olama AA, Benlloch S, Neal DE, Hamdy FC et al..  2014.  Fine-Mapping the HOXB Region Detects Common Variants Tagging a Rare Coding Allele: Evidence for Synthetic Association in Prostate Cancer.. PLoS genetics. 10(2):e1004129. Abstract
Scelo G, Purdue MP, Brown KM, Johansson M, Wang Z, Eckel-Passow JE, Ye Y, Hofmann JN, Choi J, Foll M et al..  2017.  Genome-wide association study identifies multiple risk loci for renal cell carcinoma.. Nature communications. 8:15724. Abstract
Stegeman S, Amankwah E, Klein K, O'Mara TA, Kim D, Lin H-Y, Permuth-Wey J, Sellers TA, Srinivasan S, Eeles R et al..  2015.  A Large-Scale Analysis of Genetic Variants within Putative miRNA Binding Sites in Prostate Cancer.. Cancer discovery. 5(4):368-79. Abstract
Sucheston-Campbell LE, Cannioto R, Clay AI, Etter JL, Eng KH, Liu S, Battaglia S, Hu Q, Szender BJ, Minlikeeva A et al..  2016.  No evidence that genetic variation in the myeloid-derived suppressor cell pathway influences ovarian cancer survival.. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. Abstract
Szulkin R, Whitington T, Eklund M, Aly M, Eeles RA, Easton D, Kote-Jarai Z, Al Olama AA, Benlloch S, Muir K et al..  2015.  Prediction of individual genetic risk to prostate cancer using a polygenic score.. The Prostate. Abstract
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Tomlinson IPM, Carvajal-Carmona LG, Dobbins SE, Tenesa A, Jones AM, Howarth K, Palles C, Broderick P, Jaeger EEM, Farrington S et al..  2011.  Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.. PLoS genetics. 7(6):e1002105. Abstract