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Items: 1 to 20 of 136

1.

HGVbaseG2P: a central genetic association database.

Thorisson GA, Lancaster O, Free RC, Hastings RK, Sarmah P, Dash D, Brahmachari SK, Brookes AJ.

Nucleic Acids Res. 2009 Jan;37(Database issue):D797-802. doi: 10.1093/nar/gkn748. Epub 2008 Oct 23.

2.

Gevab: a prototype genome variation analysis browsing server.

Kim WY, Kim SY, Kim TH, Ahn SM, Byun HN, Kim D, Kim DS, Lee YS, Ghang H, Park D, Kim BC, Kim C, Lee S, Kim SJ, Bhak J.

BMC Bioinformatics. 2009 Dec 3;10 Suppl 15:S3. doi: 10.1186/1471-2105-10-S15-S3.

3.

Annotated chromosome maps for renal disease.

McKnight AJ, O'Donoghue D, Peter Maxwell A.

Hum Mutat. 2009 Mar;30(3):314-20. doi: 10.1002/humu.20885.

PMID:
19085929
4.

HGVbase: a curated resource describing human DNA variation and phenotype relationships.

Fredman D, Munns G, Rios D, Sjöholm F, Siegfried M, Lenhard B, Lehväslaiho H, Brookes AJ.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D516-9.

5.

OpenADAM: an open source genome-wide association data management system for Affymetrix SNP arrays.

Yeung JM, Sham PC, Chan AS, Cherny SS.

BMC Genomics. 2008 Dec 31;9:636. doi: 10.1186/1471-2164-9-636.

6.

"GenotypeColour": colour visualisation of SNPs and CNVs.

Barlati S, Chiesa S, Magri C.

BMC Bioinformatics. 2009 Feb 4;10:49. doi: 10.1186/1471-2105-10-49.

7.

Management, presentation and interpretation of genome scans using GSCANDB.

Taylor M, Valdar W, Kumar A, Flint J, Mott R.

Bioinformatics. 2007 Jun 15;23(12):1545-9. Epub 2007 Mar 30.

PMID:
17400728
8.

The PharmGKB: integration, aggregation, and annotation of pharmacogenomic data and knowledge.

Hodge AE, Altman RB, Klein TE.

Clin Pharmacol Ther. 2007 Jan;81(1):21-4.

PMID:
17185992
9.

The Mouse Genome Database genotypes::phenotypes.

Blake JA, Bult CJ, Eppig JT, Kadin JA, Richardson JE; Mouse Genome Database Group.

Nucleic Acids Res. 2009 Jan;37(Database issue):D712-9. doi: 10.1093/nar/gkn886. Epub 2008 Nov 3.

10.

PROPHECY--a database for high-resolution phenomics.

Fernandez-Ricaud L, Warringer J, Ericson E, Pylvänäinen I, Kemp GJ, Nerman O, Blomberg A.

Nucleic Acids Res. 2005 Jan 1;33(Database issue):D369-73.

11.

Genome-wide association database developed in the Japanese Integrated Database Project.

Koike A, Nishida N, Inoue I, Tsuji S, Tokunaga K.

J Hum Genet. 2009 Sep;54(9):543-6. doi: 10.1038/jhg.2009.68. Epub 2009 Jul 24.

PMID:
19629137
12.

SNP@Evolution: a hierarchical database of positive selection on the human genome.

Cheng F, Chen W, Richards E, Deng L, Zeng C.

BMC Evol Biol. 2009 Sep 5;9:221. doi: 10.1186/1471-2148-9-221.

13.

The YH database: the first Asian diploid genome database.

Li G, Ma L, Song C, Yang Z, Wang X, Huang H, Li Y, Li R, Zhang X, Yang H, Wang J, Wang J.

Nucleic Acids Res. 2009 Jan;37(Database issue):D1025-8. doi: 10.1093/nar/gkn966.

14.

GPCR NaVa database: natural variants in human G protein-coupled receptors.

Kazius J, Wurdinger K, van Iterson M, Kok J, Bäck T, Ijzerman AP.

Hum Mutat. 2008 Jan;29(1):39-44.

PMID:
17924574
15.

A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software.

Zaimidou S, van Baal S, Smith TD, Mitropoulos K, Ljujic M, Radojkovic D, Cotton RG, Patrinos GP.

Hum Mutat. 2009 Mar;30(3):308-13. doi: 10.1002/humu.20857.

PMID:
19021233
16.

Genome-wide association studies pipeline (GWASpi): a desktop application for genome-wide SNP analysis and management.

Muñiz-Fernandez F, Carreño-Torres A, Morcillo-Suarez C, Navarro A.

Bioinformatics. 2011 Jul 1;27(13):1871-2. doi: 10.1093/bioinformatics/btr301. Epub 2011 May 17.

PMID:
21586520
17.

PROPHECY--a yeast phenome database, update 2006.

Fernandez-Ricaud L, Warringer J, Ericson E, Glaab K, Davidsson P, Nilsson F, Kemp GJ, Nerman O, Blomberg A.

Nucleic Acids Res. 2007 Jan;35(Database issue):D463-7. Epub 2006 Dec 5.

18.

Profiling of Escherichia coli Chromosome database.

Yamazaki Y, Niki H, Kato J.

Methods Mol Biol. 2008;416:385-9. doi: 10.1007/978-1-59745-321-9_26.

PMID:
18392982
19.

Multiple endocrine neoplasia type 2 RET protooncogene database: repository of MEN2-associated RET sequence variation and reference for genotype/phenotype correlations.

Margraf RL, Crockett DK, Krautscheid PM, Seamons R, Calderon FR, Wittwer CT, Mao R.

Hum Mutat. 2009 Apr;30(4):548-56. doi: 10.1002/humu.20928.

PMID:
19177457
20.

The genetics of bipolar disorder: genome 'hot regions,' genes, new potential candidates and future directions.

Serretti A, Mandelli L.

Mol Psychiatry. 2008 Aug;13(8):742-71. doi: 10.1038/mp.2008.29. Epub 2008 Mar 11. Review.

PMID:
18332878

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