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Results: 1 to 20 of 47

1.

Genome-wide association studies for detecting cancer susceptibility.

Hosking FJ, Dobbins SE, Houlston RS.

Br Med Bull. 2011;97:27-46. doi: 10.1093/bmb/ldq038. Epub 2011 Jan 18. Review.

PMID:
21247937
[PubMed - indexed for MEDLINE]
2.

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
[PubMed - indexed for MEDLINE]
3.

General lessons from large-scale studies to identify human cancer predisposition genes.

Cazier JB, Tomlinson I.

J Pathol. 2010 Jan;220(2):255-62. doi: 10.1002/path.2650. Review. Erratum in: J Pathol. 2010 Apr;220(5):618.

PMID:
19927315
[PubMed - indexed for MEDLINE]
4.

The search for low-penetrance cancer susceptibility alleles.

Houlston RS, Peto J.

Oncogene. 2004 Aug 23;23(38):6471-6. Review.

PMID:
15322517
[PubMed - indexed for MEDLINE]
5.

Genome-wide association studies of cancer: principles and potential utility.

Stadler ZK, Gallagher DJ, Thom P, Offit K.

Oncology (Williston Park). 2010 Jun;24(7):629-37. Review. Erratum in: Oncology (Williston Park). 2010 Jul;24(8):667.

PMID:
20669800
[PubMed - indexed for MEDLINE]
6.

Genetic basis for susceptibility to lung cancer: Recent progress and future directions.

Yokota J, Shiraishi K, Kohno T.

Adv Cancer Res. 2010;109:51-72. doi: 10.1016/B978-0-12-380890-5.00002-8. Review.

PMID:
21070914
[PubMed - indexed for MEDLINE]
7.

New insights into susceptibility to glioma.

Liu Y, Shete S, Hosking FJ, Robertson LB, Bondy ML, Houlston RS.

Arch Neurol. 2010 Mar;67(3):275-8. doi: 10.1001/archneurol.2010.4. Review.

PMID:
20212223
[PubMed - indexed for MEDLINE]
8.

Role of common genetic variants in ovarian cancer susceptibility and outcome: progress to date from the Ovarian Cancer Association Consortium (OCAC).

Bolton KL, Ganda C, Berchuck A, Pharaoh PD, Gayther SA.

J Intern Med. 2012 Apr;271(4):366-78. doi: 10.1111/j.1365-2796.2011.02509.x. Review.

PMID:
22443200
[PubMed - indexed for MEDLINE]
9.

Uncovering the roles of rare variants in common disease through whole-genome sequencing.

Cirulli ET, Goldstein DB.

Nat Rev Genet. 2010 Jun;11(6):415-25. doi: 10.1038/nrg2779. Review.

PMID:
20479773
[PubMed - indexed for MEDLINE]
10.

Architecture of inherited susceptibility to common cancer.

Fletcher O, Houlston RS.

Nat Rev Cancer. 2010 May;10(5):353-61. doi: 10.1038/nrc2840. Review.

PMID:
20414203
[PubMed - indexed for MEDLINE]
11.

New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.

Rudan I.

Psychiatr Danub. 2010 Jun;22(2):190-2. Review.

PMID:
20562745
[PubMed - indexed for MEDLINE]
Free Article
12.

Genetic variants in association studies--review of strengths and weaknesses in study design and current knowledge of impact on cancer risk.

Andersson U, McKean-Cowdin R, Hjalmars U, Malmer B.

Acta Oncol. 2009;48(7):948-54. Review.

PMID:
19863254
[PubMed - indexed for MEDLINE]
13.

Association studies for finding cancer-susceptibility genetic variants.

Pharoah PD, Dunning AM, Ponder BA, Easton DF.

Nat Rev Cancer. 2004 Nov;4(11):850-60. Review.

PMID:
15516958
[PubMed - indexed for MEDLINE]
14.

Identification of causal sequence variants of disease in the next generation sequencing era.

Kingsley CB.

Methods Mol Biol. 2011;700:37-46. doi: 10.1007/978-1-61737-954-3_3. Review.

PMID:
21204025
[PubMed - indexed for MEDLINE]
15.

[Cancer genetic predisposition: current events and perspectives in 2010].

Stoppa-Lyonnet D, Stern MH, Soufir N, Lenoir G.

Pathol Biol (Paris). 2010 Oct;58(5):324-30. doi: 10.1016/j.patbio.2010.02.004. Epub 2010 Aug 5. Review. French.

PMID:
20691548
[PubMed - indexed for MEDLINE]
16.

Search for cancer risk factors with microarray-based genome-wide association studies.

Zhang L, Zhang W, Chen K.

Technol Cancer Res Treat. 2010 Apr;9(2):107-21. Review.

PMID:
20218734
[PubMed - indexed for MEDLINE]
17.

What will whole genome searches for susceptibility genes for common complex disease offer to clinical practice?

Lango H, Weedon MN.

J Intern Med. 2008 Jan;263(1):16-27. Review.

PMID:
18088250
[PubMed - indexed for MEDLINE]
18.

Genetic dissection of intermediate phenotypes as a way to discover novel cancer susceptibility alleles.

Carvajal-Carmona LG.

Curr Opin Genet Dev. 2010 Jun;20(3):308-14. doi: 10.1016/j.gde.2010.03.013. Epub 2010 Apr 24. Review.

PMID:
20456939
[PubMed - indexed for MEDLINE]
19.

Genome-wide association studies in the genetics of asthma.

Willis-Owen SA, Cookson WO, Moffatt MF.

Curr Allergy Asthma Rep. 2009 Jan;9(1):3-9. Review.

PMID:
19063818
[PubMed - indexed for MEDLINE]
20.

Genome-wide association studies and genetic risk assessment of liver diseases.

Krawczyk M, M├╝llenbach R, Weber SN, Zimmer V, Lammert F.

Nat Rev Gastroenterol Hepatol. 2010 Dec;7(12):669-81. doi: 10.1038/nrgastro.2010.170. Epub 2010 Nov 2. Review.

PMID:
21045792
[PubMed - indexed for MEDLINE]

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