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Items: 1 to 20 of 27

1.

The emerging landscape of breast cancer susceptibility.

Stratton MR, Rahman N.

Nat Genet. 2008 Jan;40(1):17-22.

PMID:
18163131
2.

Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?

Lovelock PK, Spurdle AB, Mok MT, Farrugia DJ, Lakhani SR, Healey S, Arnold S, Buchanan D; kConFab Investigators., Couch FJ, Henderson BR, Goldgar DE, Tavtigian SV, Chenevix-Trench G, Brown MA.

Breast Cancer Res. 2007;9(6):R82.

3.
4.

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.

Tomlinson I, Webb E, Carvajal-Carmona L, Broderick P, Kemp Z, Spain S, Penegar S, Chandler I, Gorman M, Wood W, Barclay E, Lubbe S, Martin L, Sellick G, Jaeger E, Hubner R, Wild R, Rowan A, Fielding S, Howarth K; CORGI Consortium., Silver A, Atkin W, Muir K, Logan R, Kerr D, Johnstone E, Sieber O, Gray R, Thomas H, Peto J, Cazier JB, Houlston R.

Nat Genet. 2007 Aug;39(8):984-8. Epub 2007 Jul 8.

PMID:
17618284
5.

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Wellcome Trust Case Control Consortium..

Nature. 2007 Jun 7;447(7145):661-78.

6.

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.

Todd JA, Walker NM, Cooper JD, Smyth DJ, Downes K, Plagnol V, Bailey R, Nejentsev S, Field SF, Payne F, Lowe CE, Szeszko JS, Hafler JP, Zeitels L, Yang JH, Vella A, Nutland S, Stevens HE, Schuilenburg H, Coleman G, Maisuria M, Meadows W, Smink LJ, Healy B, Burren OS, Lam AA, Ovington NR, Allen J, Adlem E, Leung HT, Wallace C, Howson JM, Guja C, Ionescu-Tîrgovişte C; Genetics of Type 1 Diabetes in Finland., Simmonds MJ, Heward JM, Gough SC; Wellcome Trust Case Control Consortium., Dunger DB, Wicker LS, Clayton DG.

Nat Genet. 2007 Jul;39(7):857-64. Epub 2007 Jun 6.

7.

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.

Yeager M, Orr N, Hayes RB, Jacobs KB, Kraft P, Wacholder S, Minichiello MJ, Fearnhead P, Yu K, Chatterjee N, Wang Z, Welch R, Staats BJ, Calle EE, Feigelson HS, Thun MJ, Rodriguez C, Albanes D, Virtamo J, Weinstein S, Schumacher FR, Giovannucci E, Willett WC, Cancel-Tassin G, Cussenot O, Valeri A, Andriole GL, Gelmann EP, Tucker M, Gerhard DS, Fraumeni JF Jr, Hoover R, Hunter DJ, Chanock SJ, Thomas G.

Nat Genet. 2007 May;39(5):645-9. Epub 2007 Apr 1.

PMID:
17401363
8.

The Genetical Interpretation of Statistics of the Third Degree in the Study of Quantitative Inheritance.

Fisher RA, Immer FR, Tedin O.

Genetics. 1932 Mar;17(2):107-24. No abstract available.

9.
10.

Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men.

Freedman ML, Haiman CA, Patterson N, McDonald GJ, Tandon A, Waliszewska A, Penney K, Steen RG, Ardlie K, John EM, Oakley-Girvan I, Whittemore AS, Cooney KA, Ingles SA, Altshuler D, Henderson BE, Reich D.

Proc Natl Acad Sci U S A. 2006 Sep 19;103(38):14068-73. Epub 2006 Aug 31.

11.

Cancer genetics: colorectal cancer as a model.

Bodmer WF.

J Hum Genet. 2006;51(5):391-6. Epub 2006 Apr 5. Review.

12.

Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model.

Fearnhead NS, Winney B, Bodmer WF.

Cell Cycle. 2005 Apr;4(4):521-5. Epub 2005 Apr 7. Review.

PMID:
15753653
13.

Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas.

Fearnhead NS, Wilding JL, Winney B, Tonks S, Bartlett S, Bicknell DC, Tomlinson IP, Mortensen NJ, Bodmer WF.

Proc Natl Acad Sci U S A. 2004 Nov 9;101(45):15992-7. Epub 2004 Nov 1.

14.

Multiple rare alleles contribute to low plasma levels of HDL cholesterol.

Cohen JC, Kiss RS, Pertsemlidis A, Marcel YL, McPherson R, Hobbs HH.

Science. 2004 Aug 6;305(5685):869-72.

15.

GENETIC BASIS OF SUSCEPTIBILITY TO VIRAL LEUKAEMOGENESIS.

LILLY F, BOYSE EA, OLD LJ.

Lancet. 1964 Dec 5;2(7371):1207-9. No abstract available.

PMID:
14215561
16.

A relationship between cancer of stomach and the ABO blood groups.

AIRD I, BENTALL HH, ROBERTS JA.

Br Med J. 1953 Apr 11;1(4814):799-801. No abstract available.

17.

Familial adenomatous polyposis (FAP) and its gene, APC.

Bodmer W.

Cytogenet Cell Genet. 1999;86(2):99-104. Review. No abstract available.

PMID:
10545698
18.

The APC variants I1307K and E1317Q are associated with colorectal tumors, but not always with a family history.

Frayling IM, Beck NE, Ilyas M, Dove-Edwin I, Goodman P, Pack K, Bell JA, Williams CB, Hodgson SV, Thomas HJ, Talbot IC, Bodmer WF, Tomlinson IP.

Proc Natl Acad Sci U S A. 1998 Sep 1;95(18):10722-7.

19.

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

Laken SJ, Petersen GM, Gruber SB, Oddoux C, Ostrer H, Giardiello FM, Hamilton SR, Hampel H, Markowitz A, Klimstra D, Jhanwar S, Winawer S, Offit K, Luce MC, Kinzler KW, Vogelstein B.

Nat Genet. 1997 Sep;17(1):79-83.

PMID:
9288102
20.

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.

Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R Jr, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Prass CE, Quintana L, Starnes SM, Schatzman RC, Brunke KJ, Drayna DT, Risch NJ, Bacon BR, Wolff RK.

Nat Genet. 1996 Aug;13(4):399-408.

PMID:
8696333

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