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Items: 1 to 20 of 89


Commonality of functional annotation: a method for prioritization of candidate genes from genome-wide linkage studies.

Shriner D, Baye TM, Padilla MA, Zhang S, Vaughan LK, Loraine AE.

Nucleic Acids Res. 2008 Mar;36(4):e26. doi: 10.1093/nar/gkn007. Epub 2008 Feb 7.


Integrating genome annotation and QTL position to identify candidate genes for productivity, architecture and water-use efficiency in Populus spp.

Monclus R, Leplé JC, Bastien C, Bert PF, Villar M, Marron N, Brignolas F, Jorge V.

BMC Plant Biol. 2012 Sep 26;12:173. doi: 10.1186/1471-2229-12-173.


Testing groups of genomic locations for enrichment in disease loci using linkage scan data: a method for hypothesis testing.

Avramopoulos D, Zandi P, Gherman A, Fallin MD, Bassett SS.

Hum Genomics. 2006 Jun;2(6):345-52.


Speeding disease gene discovery by sequence based candidate prioritization.

Adie EA, Adams RR, Evans KL, Porteous DJ, Pickard BS.

BMC Bioinformatics. 2005 Mar 14;6:55.


Analysis of disease-associated objects at the Rat Genome Database.

Wang SJ, Laulederkind SJ, Hayman GT, Smith JR, Petri V, Lowry TF, Nigam R, Dwinell MR, Worthey EA, Munzenmaier DH, Shimoyama M, Jacob HJ.

Database (Oxford). 2013 Jun 21;2013:bat046. doi: 10.1093/database/bat046. Print 2013.


Statistical Viewer: a tool to upload and integrate linkage and association data as plots displayed within the Ensembl genome browser.

Stenger JE, Xu H, Haynes C, Hauser ER, Pericak-Vance M, Goldschmidt-Clermont PJ, Vance JM.

BMC Bioinformatics. 2005 Apr 12;6:95.


Integration of text- and data-mining using ontologies successfully selects disease gene candidates.

Tiffin N, Kelso JF, Powell AR, Pan H, Bajic VB, Hide WA.

Nucleic Acids Res. 2005 Mar 14;33(5):1544-52. Print 2005.


Gene Ontology annotation of the rice blast fungus, Magnaporthe oryzae.

Meng S, Brown DE, Ebbole DJ, Torto-Alalibo T, Oh YY, Deng J, Mitchell TK, Dean RA.

BMC Microbiol. 2009 Feb 19;9 Suppl 1:S8. doi: 10.1186/1471-2180-9-S1-S8. Review.


Quantitative genomics: exploring the genetic architecture of complex trait predisposition.

Pomp D, Allan MF, Wesolowski SR.

J Anim Sci. 2004;82 E-Suppl:E300-312. Review.


Prioritization of positional candidate genes using multiple web-based software tools.

Thornblad TA, Elliott KS, Jowett J, Visscher PM.

Twin Res Hum Genet. 2007 Dec;10(6):861-70. doi: 10.1375/twin.10.6.861.


TEAM: a tool for the integration of expression, and linkage and association maps.

Franke L, van Bakel H, Diosdado B, van Belzen M, Wapenaar M, Wijmenga C.

Eur J Hum Genet. 2004 Aug;12(8):633-8.


Improvements to cardiovascular gene ontology.

Lovering RC, Dimmer EC, Talmud PJ.

Atherosclerosis. 2009 Jul;205(1):9-14. doi: 10.1016/j.atherosclerosis.2008.10.014. Epub 2008 Nov 1. Review.


Computational approaches to disease-gene prediction: rationale, classification and successes.

Piro RM, Di Cunto F.

FEBS J. 2012 Mar;279(5):678-96. doi: 10.1111/j.1742-4658.2012.08471.x. Epub 2012 Jan 30. Review.


Genomics of complex traits.

Womack JE, Jang HJ, Lee MO.

Ann N Y Acad Sci. 2012 Oct;1271:33-6. doi: 10.1111/j.1749-6632.2012.06733.x. Review.


A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits.

Ferreira MA, Visscher PM, Martin NG, Duffy DL.

Eur J Hum Genet. 2006 Aug;14(8):953-62. Epub 2006 May 24.


Additional gene ontology structure for improved biological reasoning.

Myhre S, Tveit H, Mollestad T, Laegreid A.

Bioinformatics. 2006 Aug 15;22(16):2020-7. Epub 2006 Jun 20.


Identifying disease-causal genes using Semantic Web-based representation of integrated genomic and phenomic knowledge.

Gudivada RC, Qu XA, Chen J, Jegga AG, Neumann EK, Aronow BJ.

J Biomed Inform. 2008 Oct;41(5):717-29. doi: 10.1016/j.jbi.2008.07.004. Epub 2008 Aug 23.


QTL global meta-analysis: are trait determining genes clustered?

Salih H, Adelson DL.

BMC Genomics. 2009 Apr 24;10:184. doi: 10.1186/1471-2164-10-184.


A domain-centric solution to functional genomics via dcGO Predictor.

Fang H, Gough J.

BMC Bioinformatics. 2013;14 Suppl 3:S9. doi: 10.1186/1471-2105-14-S3-S9. Epub 2013 Feb 28.


A sensitive method for computing GO-based functional similarities among genes with 'shallow annotation'.

Chen X, Yang R, Xu J, Ma H, Chen S, Bian X, Liu L.

Gene. 2012 Nov 1;509(1):131-5. doi: 10.1016/j.gene.2012.07.078. Epub 2012 Aug 10.

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