Rebhan M, Chalifa-Caspi V, Prilusky J, Lancet D (abril de 1997). «GeneCards: integrating information about genes, proteins and diseases». Trends Genet. 13 (4). 163 páginas. PMID9097728. doi:10.1016/S0168-9525(97)01103-7
Rebhan M, Chalifa-Caspi V, Prilusky J, Lancet D (1998). «GeneCards: a novel functional genomics compendium with automated data mining and query reformulation support». Bioinformatics. 14 (8): 656–64. PMID9789091. doi:10.1093/bioinformatics/14.8.656
Safran M, Solomon I, Shmueli O, Lapidot M, Shen-Orr S, Adato A, Ben-Dor U, Esterman N, Rosen N, Peter I, Olender T, Chalifa-Caspi V, Lancet D (novembro de 2002). «GeneCards 2002: towards a complete, object-oriented, human gene compendium». Bioinformatics. 18 (11): 1542–3. PMID12424129. doi:10.1093/bioinformatics/18.11.1542
Shah, S. H.; et al. (2006). «Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5q». Annals of Human Genetics. 70 (6): 738–748. PMID17044848. doi:10.1111/j.1469-1809.2006.00288.x
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ncbi.nlm.nih.gov
Rebhan M, Chalifa-Caspi V, Prilusky J, Lancet D (abril de 1997). «GeneCards: integrating information about genes, proteins and diseases». Trends Genet. 13 (4). 163 páginas. PMID9097728. doi:10.1016/S0168-9525(97)01103-7
Rebhan M, Chalifa-Caspi V, Prilusky J, Lancet D (1998). «GeneCards: a novel functional genomics compendium with automated data mining and query reformulation support». Bioinformatics. 14 (8): 656–64. PMID9789091. doi:10.1093/bioinformatics/14.8.656
Safran M, Solomon I, Shmueli O, Lapidot M, Shen-Orr S, Adato A, Ben-Dor U, Esterman N, Rosen N, Peter I, Olender T, Chalifa-Caspi V, Lancet D (novembro de 2002). «GeneCards 2002: towards a complete, object-oriented, human gene compendium». Bioinformatics. 18 (11): 1542–3. PMID12424129. doi:10.1093/bioinformatics/18.11.1542
Shah, S. H.; et al. (2006). «Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5q». Annals of Human Genetics. 70 (6): 738–748. PMID17044848. doi:10.1111/j.1469-1809.2006.00288.x