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Gene ontology: tool for the unification of biology. The Gene Ontology Consortium.
Ashburner M,
Ball CA,
Blake JA,
Botstein D,
Butler H,
Cherry JM,
Davis AP,
Dolinski K,
Dwight SS,
Eppig JT,
Harris MA,
Hill DP,
Issel-Tarver L,
Kasarskis A,
Lewis S,
Matese JC,
Richardson JE,
Ringwald M,
Rubin GM,
Sherlock G.
Department of Genetics, Stanford University School of Medicine, California, USA. cherry@stanford.edu
PMID: 10802651 [PubMed - indexed for MEDLINE]
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Cited by over 100 PubMed Central articles
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Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.
Raychaudhuri S, Plenge RM, Rossin EJ, Ng AC, International Schizophrenia Consortium, Purcell SM, Sklar P, Scolnick EM, Xavier RJ, Altshuler D, et al.
PLoS Genet. 2009 Jun; 5(6):e1000534. Epub 2009 Jun 26.
[PLoS Genet. 2009]
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Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
Webber C, Hehir-Kwa JY, Nguyen DQ, de Vries BB, Veltman JA, Ponting CP.
PLoS Genet. 2009 Jun; 5(6):e1000531. Epub 2009 Jun 26.
[PLoS Genet. 2009]
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Functional assessment of time course microarray data.
Nueda MJ, Sebastián P, Tarazona S, García-García F, Dopazo J, Ferrer A, Conesa A.
BMC Bioinformatics. 2009 Jun 16; 10 Suppl 6:S9. Epub 2009 Jun 16.
[BMC Bioinformatics. 2009]
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