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Items: 1 to 20 of 27

1.

Integrating gene expression and epidemiological data for the discovery of genetic interactions associated with cancer risk.

Bonifaci N, Colas E, Serra-Musach J, Karbalai N, Brunet J, Gómez A, Esteller M, Fernández-Taboada E, Berenguer A, Reventós J, Müller-Myhsok B, Amundadottir L, Duell EJ, Pujana MÀ.

Carcinogenesis. 2014 Mar;35(3):578-85. doi: 10.1093/carcin/bgt403. Epub 2013 Dec 2.

PMID:
24296589
2.

Genome-Wide Association Studies (GWAS) breast cancer susceptibility loci in Arabs: susceptibility and prognostic implications in Tunisians.

Shan J, Mahfoudh W, Dsouza SP, Hassen E, Bouaouina N, Abdelhak S, Benhadjayed A, Memmi H, Mathew RA, Aigha II, Gabbouj S, Remadi Y, Chouchane L.

Breast Cancer Res Treat. 2012 Oct;135(3):715-24. doi: 10.1007/s10549-012-2202-6. Epub 2012 Aug 22.

3.

Genome-wide association studies of cancer predisposition.

Stadler ZK, Vijai J, Thom P, Kirchhoff T, Hansen NA, Kauff ND, Robson M, Offit K.

Hematol Oncol Clin North Am. 2010 Oct;24(5):973-96. doi: 10.1016/j.hoc.2010.06.009. Review.

PMID:
20816582
4.

A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study.

Kim HC, Lee JY, Sung H, Choi JY, Park SK, Lee KM, Kim YJ, Go MJ, Li L, Cho YS, Park M, Kim DJ, Oh JH, Kim JW, Jeon JP, Jeon SY, Min H, Kim HM, Park J, Yoo KY, Noh DY, Ahn SH, Lee MH, Kim SW, Lee JW, Park BW, Park WY, Kim EH, Kim MK, Han W, Lee SA, Matsuo K, Shen CY, Wu PE, Hsiung CN, Lee JY, Kim HL, Han BG, Kang D.

Breast Cancer Res. 2012 Mar 27;14(2):R56.

5.

Functional polymorphisms, altered gene expression and genetic association link NRH:quinone oxidoreductase 2 to breast cancer with wild-type p53.

Yu KD, Di GH, Yuan WT, Fan L, Wu J, Hu Z, Shen ZZ, Zheng Y, Huang W, Shao ZM.

Hum Mol Genet. 2009 Jul 1;18(13):2502-17. doi: 10.1093/hmg/ddp171. Epub 2009 Apr 7.

PMID:
19351655
6.

A genetic risk predictor for breast cancer using a combination of low-penetrance polymorphisms in a Japanese population.

Sueta A, Ito H, Kawase T, Hirose K, Hosono S, Yatabe Y, Tajima K, Tanaka H, Iwata H, Iwase H, Matsuo K.

Breast Cancer Res Treat. 2012 Apr;132(2):711-21. doi: 10.1007/s10549-011-1904-5. Epub 2011 Dec 11.

PMID:
22160591
7.

Integrating autoimmune risk loci with gene-expression data identifies specific pathogenic immune cell subsets.

Hu X, Kim H, Stahl E, Plenge R, Daly M, Raychaudhuri S.

Am J Hum Genet. 2011 Oct 7;89(4):496-506. doi: 10.1016/j.ajhg.2011.09.002. Epub 2011 Sep 29. Erratum in: Am J Hum Genet. 2011 Nov 11;89(5):682.

8.

Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.

Liu X, Cheng R, Verbitsky M, Kisselev S, Browne A, Mejia-Sanatana H, Louis ED, Cote LJ, Andrews H, Waters C, Ford B, Frucht S, Fahn S, Marder K, Clark LN, Lee JH.

BMC Med Genet. 2011 Aug 3;12:104. doi: 10.1186/1471-2350-12-104.

9.

A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants.

Tao S, Wang Z, Feng J, Hsu FC, Jin G, Kim ST, Zhang Z, Gronberg H, Zheng LS, Isaacs WB, Xu J, Sun J.

Carcinogenesis. 2012 Mar;33(3):598-603. doi: 10.1093/carcin/bgr316. Epub 2012 Jan 4.

10.

A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation.

Dalgaard MD, Weinhold N, Edsgärd D, Silver JD, Pers TH, Nielsen JE, Jørgensen N, Juul A, Gerds TA, Giwercman A, Giwercman YL, Cohn-Cedermark G, Virtanen HE, Toppari J, Daugaard G, Jensen TS, Brunak S, Rajpert-De Meyts E, Skakkebæk NE, Leffers H, Gupta R.

J Med Genet. 2012 Jan;49(1):58-65. doi: 10.1136/jmedgenet-2011-100174. Epub 2011 Dec 3.

11.

Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies.

Peng S, Lü B, Ruan W, Zhu Y, Sheng H, Lai M.

Breast Cancer Res Treat. 2011 Jun;127(2):309-24. doi: 10.1007/s10549-011-1459-5. Epub 2011 Mar 29. Review.

PMID:
21445572
12.

Breast cancer risk associated with genotypic polymorphism of the genes involved in the estrogen-receptor-signaling pathway: a multigenic study on cancer susceptibility.

Yu JC, Hsu HM, Chen ST, Hsu GC, Huang CS, Hou MF, Fu YP, Cheng TC, Wu PE, Shen CY.

J Biomed Sci. 2006 May;13(3):419-32. Epub 2006 Feb 25.

PMID:
16502042
13.

A systematic review of replication studies of prostate cancer susceptibility genetic variants in high-risk men originally identified from genome-wide association studies.

Ishak MB, Giri VN.

Cancer Epidemiol Biomarkers Prev. 2011 Aug;20(8):1599-610. doi: 10.1158/1055-9965.EPI-11-0312. Epub 2011 Jun 29. Review.

14.

Elements of 'missing heritability'.

Marian AJ.

Curr Opin Cardiol. 2012 May;27(3):197-201. doi: 10.1097/HCO.0b013e328352707d. Review.

PMID:
22450721
15.

Genome-wide germline analyses on cancer susceptibility and GeMDBJ database: Gastric cancer as an example.

Yoshida T, Ono H, Kuchiba A, Saeki N, Sakamoto H.

Cancer Sci. 2010 Jul;101(7):1582-9. doi: 10.1111/j.1349-7006.2010.01590.x. Epub 2010 Apr 9. Review.

16.

Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese.

Jin G, Ma H, Wu C, Dai J, Zhang R, Shi Y, Lu J, Miao X, Wang M, Zhou Y, Chen J, Li H, Pan S, Chu M, Lu F, Yu D, Jiang Y, Dong J, Hu L, Chen Y, Xu L, Shu Y, Pan S, Tan W, Zhou B, Lu D, Wu T, Zhang Z, Chen F, Wang X, Hu Z, Lin D, Shen H.

Am J Hum Genet. 2012 Nov 2;91(5):928-34. doi: 10.1016/j.ajhg.2012.09.009. Epub 2012 Oct 25.

17.

Genome-wide meta-analysis of genetic susceptible genes for Type 2 Diabetes.

Hale PJ, López-Yunez AM, Chen JY.

BMC Syst Biol. 2012;6 Suppl 3:S16. doi: 10.1186/1752-0509-6-S3-S16. Epub 2012 Dec 17.

18.

The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression.

Pittman AM, Naranjo S, Webb E, Broderick P, Lips EH, van Wezel T, Morreau H, Sullivan K, Fielding S, Twiss P, Vijayakrishnan J, Casares F, Qureshi M, Gómez-Skarmeta JL, Houlston RS.

Genome Res. 2009 Jun;19(6):987-93. doi: 10.1101/gr.092668.109. Epub 2009 Apr 24.

19.

Mapping of numerous disease-associated expression polymorphisms in primary peripheral blood CD4+ lymphocytes.

Murphy A, Chu JH, Xu M, Carey VJ, Lazarus R, Liu A, Szefler SJ, Strunk R, Demuth K, Castro M, Hansel NN, Diette GB, Vonakis BM, Adkinson NF Jr, Klanderman BJ, Senter-Sylvia J, Ziniti J, Lange C, Pastinen T, Raby BA.

Hum Mol Genet. 2010 Dec 1;19(23):4745-57. doi: 10.1093/hmg/ddq392. Epub 2010 Sep 10.

20.

A genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North Indians.

Negi S, Juyal G, Senapati S, Prasad P, Gupta A, Singh S, Kashyap S, Kumar A, Kumar U, Gupta R, Kaur S, Agrawal S, Aggarwal A, Ott J, Jain S, Juyal RC, Thelma BK.

Arthritis Rheum. 2013 Dec;65(12):3026-35. doi: 10.1002/art.38110.

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