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Items: 17

1.

The continued need to synthesize the results of genetic associations across multiple studies.

Yesupriya A, Yu W, Clyne M, Gwinn M, Khoury MJ.

Genet Med. 2008 Aug;10(8):633-5. doi: 10.1097GIM.0b013e3181815360. No abstract available.

PMID:
18641511
2.

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database.

Allen NC, Bagade S, McQueen MB, Ioannidis JP, Kavvoura FK, Khoury MJ, Tanzi RE, Bertram L.

Nat Genet. 2008 Jul;40(7):827-34. doi: 10.1038/ng.171.

PMID:
18583979
3.

Genetic susceptibility to cancer: the role of polymorphisms in candidate genes.

Dong LM, Potter JD, White E, Ulrich CM, Cardon LR, Peters U.

JAMA. 2008 May 28;299(20):2423-36. doi: 10.1001/jama.299.20.2423. Review.

4.

A HapMap harvest of insights into the genetics of common disease.

Manolio TA, Brooks LD, Collins FS.

J Clin Invest. 2008 May;118(5):1590-605. doi: 10.1172/JCI34772. Review.

5.

GAPscreener: an automatic tool for screening human genetic association literature in PubMed using the support vector machine technique.

Yu W, Clyne M, Dolan SM, Yesupriya A, Wulf A, Liu T, Khoury MJ, Gwinn M.

BMC Bioinformatics. 2008 Apr 22;9:205. doi: 10.1186/1471-2105-9-205.

6.

Genome-wide association studies for complex traits: consensus, uncertainty and challenges.

McCarthy MI, Abecasis GR, Cardon LR, Goldstein DB, Little J, Ioannidis JP, Hirschhorn JN.

Nat Rev Genet. 2008 May;9(5):356-69. doi: 10.1038/nrg2344. Review.

PMID:
18398418
7.

A navigator for human genome epidemiology.

Yu W, Gwinn M, Clyne M, Yesupriya A, Khoury MJ.

Nat Genet. 2008 Feb;40(2):124-5. doi: 10.1038/ng0208-124. No abstract available.

PMID:
18227866
8.
10.

SNP genotyping: technologies and biomedical applications.

Kim S, Misra A.

Annu Rev Biomed Eng. 2007;9:289-320. Review.

PMID:
17391067
11.

PolyDoms: a whole genome database for the identification of non-synonymous coding SNPs with the potential to impact disease.

Jegga AG, Gowrisankar S, Chen J, Aronow BJ.

Nucleic Acids Res. 2007 Jan;35(Database issue):D700-6. Epub 2006 Nov 16.

12.

Tracking the epidemiology of human genes in the literature: the HuGE Published Literature database.

Lin BK, Clyne M, Walsh M, Gomez O, Yu W, Gwinn M, Khoury MJ.

Am J Epidemiol. 2006 Jul 1;164(1):1-4. Epub 2006 Apr 26. Review.

13.

SNPs3D: candidate gene and SNP selection for association studies.

Yue P, Melamud E, Moult J.

BMC Bioinformatics. 2006 Mar 22;7:166.

14.

Realizing the promise of genomics in biomedical research.

Guttmacher AE, Collins FS.

JAMA. 2005 Sep 21;294(11):1399-402. No abstract available.

PMID:
16174701
15.

G2D: a tool for mining genes associated with disease.

Perez-Iratxeta C, Wjst M, Bork P, Andrade MA.

BMC Genet. 2005 Aug 22;6:45.

16.

Assessing the function of genetic variants in candidate gene association studies.

Rebbeck TR, Spitz M, Wu X.

Nat Rev Genet. 2004 Aug;5(8):589-97. Review. No abstract available.

PMID:
15266341
17.

GeneCards: a novel functional genomics compendium with automated data mining and query reformulation support.

Rebhan M, Chalifa-Caspi V, Prilusky J, Lancet D.

Bioinformatics. 1998;14(8):656-64.

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