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Items: 20

1.

Beyond odds ratios--communicating disease risk based on genetic profiles.

Kraft P, Wacholder S, Cornelis MC, Hu FB, Hayes RB, Thomas G, Hoover R, Hunter DJ, Chanock S.

Nat Rev Genet. 2009 Apr;10(4):264-9. doi: 10.1038/nrg2516. Review.

PMID:
19238176
2.

Genetic causes of myocardial infarction: new insights from genome-wide association studies.

Erdmann J, Linsel-Nitschke P, Schunkert H.

Dtsch Arztebl Int. 2010 Oct;107(40):694-9. doi: 10.3238/arztebl.2010.0694. Epub 2010 Oct 8. Review.

3.

A compendium of genome-wide associations for cancer: critical synopsis and reappraisal.

Ioannidis JP, Castaldi P, Evangelou E.

J Natl Cancer Inst. 2010 Jun 16;102(12):846-58. doi: 10.1093/jnci/djq173. Epub 2010 May 26. Review.

4.

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.

5.

The pursuit of genome-wide association studies: where are we now?

Ku CS, Loy EY, Pawitan Y, Chia KS.

J Hum Genet. 2010 Apr;55(4):195-206. doi: 10.1038/jhg.2010.19. Epub 2010 Mar 19. Review.

PMID:
20300123
6.

Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curse.

Nakaoka H, Inoue I.

J Hum Genet. 2009 Nov;54(11):615-23. doi: 10.1038/jhg.2009.95. Epub 2009 Oct 23. Review.

PMID:
19851339
7.

Predisposition to epilepsy--does the ABCB1 gene play a role?

Nurmohamed L, Garcia-Bournissen F, Buono RJ, Shannon MW, Finkelstein Y.

Epilepsia. 2010 Sep;51(9):1882-5. doi: 10.1111/j.1528-1167.2010.02588.x. Review.

8.

[Is our genome predictive?].

Jordan B.

Med Sci (Paris). 2012 Aug-Sep;28(8-9):785-8. doi: 10.1051/medsci/2012288023. Epub 2012 Aug 22. Review. French. No abstract available.

9.

Schizophrenia genetics: progress, at last.

Mulle JG.

Curr Opin Genet Dev. 2012 Jun;22(3):238-44. doi: 10.1016/j.gde.2012.02.011. Epub 2012 Mar 15. Review.

PMID:
22424801
10.

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
11.

Anti-citrullinated peptide/protein antibody (ACPA)-negative RA shares a large proportion of susceptibility loci with ACPA-positive RA: a meta-analysis of genome-wide association study in a Japanese population.

Terao C, Ohmura K, Kochi Y, Ikari K, Okada Y, Shimizu M, Nishina N, Suzuki A, Myouzen K, Kawaguchi T, Takahashi M, Takasugi K, Murasawa A, Mizuki S, Iwahashi M, Funahashi K, Natsumeda M, Furu M, Hashimoto M, Ito H, Fujii T, Ezawa K, Matsubara T, Takeuchi T, Kubo M, Yamada R, Taniguchi A, Yamanaka H, Momohara S, Yamamoto K, Mimori T, Matsuda F.

Arthritis Res Ther. 2015 Apr 18;17:104. doi: 10.1186/s13075-015-0623-4. Review.

12.

Predictive genetic testing for drug-induced liver injury: considerations of clinical utility.

Alfirevic A, Pirmohamed M.

Clin Pharmacol Ther. 2012 Sep;92(3):376-80. doi: 10.1038/clpt.2012.107. Epub 2012 Aug 1. Review.

PMID:
22850601
13.

Practical issues in building risk-predicting models for complex diseases.

Kang J, Cho J, Zhao H.

J Biopharm Stat. 2010 Mar;20(2):415-40. doi: 10.1080/10543400903572829. Review.

14.

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
15.

Single nucleotide polymorphisms associated with sporadic brain arteriovenous malformations: where do we stand?

Sturiale CL, Puca A, Sebastiani P, Gatto I, Albanese A, Di Rocco C, Maira G, Pola R.

Brain. 2013 Feb;136(Pt 2):665-81. doi: 10.1093/brain/aws180. Epub 2012 Sep 13. Review.

PMID:
22975391
16.

[Genome-wide association study on complex diseases: genetic statistical issues].

Yan WL.

Yi Chuan. 2008 May;30(5):543-9. Review. Chinese.

PMID:
18487142
17.

Prediction of cardiovascular disease outcomes and established cardiovascular risk factors by genome-wide association markers.

Ioannidis JP.

Circ Cardiovasc Genet. 2009 Feb;2(1):7-15. doi: 10.1161/CIRCGENETICS.108.833392. Epub 2009 Jan 23. Review.

18.

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
19.

[Gene mutations; up date].

Nakagawa M.

Rinsho Shinkeigaku. 2013;53(11):903-6. Review. Japanese.

PMID:
24291829
20.

Genome-based prediction of common diseases: advances and prospects.

Janssens AC, van Duijn CM.

Hum Mol Genet. 2008 Oct 15;17(R2):R166-73. doi: 10.1093/hmg/ddn250. Review.

PMID:
18852206

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