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Items: 1 to 20 of 698


Gene Prospector: an evidence gateway for evaluating potential susceptibility genes and interacting risk factors for human diseases.

Yu W, Wulf A, Liu T, Khoury MJ, Gwinn M.

BMC Bioinformatics. 2008 Dec 8;9:528. doi: 10.1186/1471-2105-9-528.


Syndrome to gene (S2G): in-silico identification of candidate genes for human diseases.

Gefen A, Cohen R, Birk OS.

Hum Mutat. 2010 Mar;31(3):229-36. doi: 10.1002/humu.21171.


An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases.

Yang JO, Hwang S, Oh J, Bhak J, Sohn TK.

BMC Bioinformatics. 2008 Dec 12;9 Suppl 12:S19. doi: 10.1186/1471-2105-9-S12-S19.


A new web-based data mining tool for the identification of candidate genes for human genetic disorders.

van Driel MA, Cuelenaere K, Kemmeren PP, Leunissen JA, Brunner HG.

Eur J Hum Genet. 2003 Jan;11(1):57-63.


GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies.

Yu W, Yesupriya A, Wulf A, Hindorff LA, Dowling N, Khoury MJ, Gwinn M.

Eur J Hum Genet. 2011 Oct;19(10):1095-9. doi: 10.1038/ejhg.2011.91. Epub 2011 May 25.


Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes.

Franke L, van Bakel H, Fokkens L, de Jong ED, Egmont-Petersen M, Wijmenga C.

Am J Hum Genet. 2006 Jun;78(6):1011-25. Epub 2006 Apr 25.


GeneSeeker: extraction and integration of human disease-related information from web-based genetic databases.

van Driel MA, Cuelenaere K, Kemmeren PP, Leunissen JA, Brunner HG, Vriend G.

Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W758-61.


Satellog: a database for the identification and prioritization of satellite repeats in disease association studies.

Missirlis PI, Mead CL, Butland SL, Ouellette BF, Devon RS, Leavitt BR, Holt RA.

BMC Bioinformatics. 2005 Jun 10;6:145.


SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes.

Packer BR, Yeager M, Staats B, Welch R, Crenshaw A, Kiley M, Eckert A, Beerman M, Miller E, Bergen A, Rothman N, Strausberg R, Chanock SJ.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D528-32.


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.


Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.

Patrinos GP, van Baal S, Petersen MB, Papadakis MN.

Hum Mutat. 2005 Apr;25(4):327-33.


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.


SNPRanker: a tool for identification and scoring of SNPs associated to target genes.

Calabria A, Mosca E, Viti F, Merelli I, Milanesi L.

J Integr Bioinform. 2010 Mar 25;7(3). doi: 10.2390/biecoll-jib-2010-138.


VSD: a database for schizophrenia candidate genes focusing on variations.

Zhou M, Zhuang YL, Xu Q, Li YD, Shen Y.

Hum Mutat. 2004 Jan;23(1):1-7.


GenoWatch: a disease gene mining browser for association study.

Chen YH, Liu CK, Chang SC, Lin YJ, Tsai MF, Chen YT, Yao A.

Nucleic Acids Res. 2008 Jul 1;36(Web Server issue):W336-40. doi: 10.1093/nar/gkn214. Epub 2008 Apr 25.


EICO (Expression-based Imprint Candidate Organizer): finding disease-related imprinted genes.

Nikaido I, Saito C, Wakamoto A, Tomaru Y, Arakawa T, Hayashizaki Y, Okazaki Y.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D548-51.


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.


Comparison of automated candidate gene prediction systems using genes implicated in type 2 diabetes by genome-wide association studies.

Teber ET, Liu JY, Ballouz S, Fatkin D, Wouters MA.

BMC Bioinformatics. 2009 Jan 30;10 Suppl 1:S69. doi: 10.1186/1471-2105-10-S1-S69.

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