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Items: 1 to 20 of 133

1.

Database tools in genetic diseases research.

Bianco AM, Marcuzzi A, Zanin V, Girardelli M, Vuch J, Crovella S.

Genomics. 2013 Feb;101(2):75-85. doi: 10.1016/j.ygeno.2012.11.001. Epub 2012 Nov 10. Review.

2.

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.

3.

Disease gene discovery through integrative genomics.

Giallourakis C, Henson C, Reich M, Xie X, Mootha VK.

Annu Rev Genomics Hum Genet. 2005;6:381-406. Review.

PMID:
16124867
4.

Bioinformatics tools to understand human diseases.

Debes JD, Urrutia R.

Surgery. 2004 Jun;135(6):579-85. Review. No abstract available.

PMID:
15179363
5.

Managing core resources for genomics and proteomics.

Apweiler R, Martin MJ, O'Donovan C, Pruess M.

Pharmacogenomics. 2003 May;4(3):343-50. Review.

PMID:
12718724
6.

Current bioinformatics tools in genomic biomedical research (Review).

Teufel A, Krupp M, Weinmann A, Galle PR.

Int J Mol Med. 2006 Jun;17(6):967-73. Review.

PMID:
16685403
7.

Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics.

Burren OS, Healy BC, Lam AC, Schuilenburg H, Dolman GE, Everett VH, Laneri D, Nutland S, Rance HE, Payne F, Smyth D, Lowe C, Barratt BJ, Twells RC, Rainbow DB, Wicker LS, Todd JA, Walker NM, Smink LJ.

Hum Genomics. 2004 Jan;1(2):98-109.

8.

Genome-wide identification of genes likely to be involved in human genetic disease.

López-Bigas N, Ouzounis CA.

Nucleic Acids Res. 2004 Jun 4;32(10):3108-14. Print 2004.

9.

Rat Genome Database (RGD): mapping disease onto the genome.

Twigger S, Lu J, Shimoyama M, Chen D, Pasko D, Long H, Ginster J, Chen CF, Nigam R, Kwitek A, Eppig J, Maltais L, Maglott D, Schuler G, Jacob H, Tonellato PJ.

Nucleic Acids Res. 2002 Jan 1;30(1):125-8.

10.

2005 Human Genome Variation Society Scientific Meeting.

Oetting WS.

Hum Mutat. 2006 Mar;27(3):286-9.

PMID:
16419082
11.

Atlas - a data warehouse for integrative bioinformatics.

Shah SP, Huang Y, Xu T, Yuen MM, Ling J, Ouellette BF.

BMC Bioinformatics. 2005 Feb 21;6:34.

12.

Databases for neurogenetics: introduction, overview, and challenges.

Sobrido MJ, Cacheiro P, Carracedo A, Bertram L.

Hum Mutat. 2012 Sep;33(9):1311-4. doi: 10.1002/humu.22164.

PMID:
22890789
13.

Genome resources and comparative analysis tools for cardiovascular research.

Liu GE, Adams MD.

Methods Mol Med. 2006;128:101-23.

PMID:
17071992
14.

EYE on bioinformatics: dissecting complex disease traits in silico.

Leung YF, Pang CP.

Appl Bioinformatics. 2002;1(2):69-80. Review.

PMID:
15130846
15.

Targetability of human disease genes.

Sakharkar MK, Sakharkar KR.

Curr Drug Discov Technol. 2007 Jun;4(1):48-58. Review.

PMID:
17630928
16.

Inherited disorder phenotypes: controlled annotation and statistical analysis for knowledge mining from gene lists.

Masseroli M, Galati O, Manzotti M, Gibert K, Pinciroli F.

BMC Bioinformatics. 2005 Dec 1;6 Suppl 4:S18.

17.

F-SNP: computationally predicted functional SNPs for disease association studies.

Lee PH, Shatkay H.

Nucleic Acids Res. 2008 Jan;36(Database issue):D820-4. Epub 2007 Nov 5.

18.

BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge.

Moore CB, Wallace JR, Frase AT, Pendergrass SA, Ritchie MD.

BMC Med Genomics. 2013;6 Suppl 2:S6. doi: 10.1186/1755-8794-6-S2-S6. Epub 2013 May 7.

19.

Comparative genomics for detecting human disease genes.

Moreno C, Lazar J, Jacob HJ, Kwitek AE.

Adv Genet. 2008;60:655-97. doi: 10.1016/S0065-2660(07)00423-3. Review.

PMID:
18358336
20.

[Systematic genome-wide approach to positional candidate cloning for identification of novel human disease genes].

Hasegawa Y.

Tanpakushitsu Kakusan Koso. 2004 Dec;49(17 Suppl):2894-901. Review. Japanese. No abstract available.

PMID:
15669273

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