Citing GeneCards in the Literature
In order to cite the GeneCards Suite databases and tools please note the relevant URL(s) and cite the relevant publication(s). Examples:
-
GeneCards – the human gene database
www.genecards.org
Stelzer G, Rosen R, Plaschkes I, Zimmerman S, Twik M, Fishilevich S, Iny Stein T, Nudel R, Lieder I,
Mazor Y, Kaplan S, Dahary D, Warshawsky D, Guan - Golan Y, Kohn A, Rappaport N, Safran M, and Lancet D.
The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analysis ,
Current Protocols in Bioinformatics(2016),
54:1.30.1 - 1.30.33.doi: 10.1002 / cpbi.5. a >
[PDF]
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MalaCards – the human disease database
www.malacards.org
Rappaport N, Twik M, Plaschkes I, Nudel R, Iny Stein T, Levitt J, Gershoni M, Morrey CP, Safran M, and Lancet D.
MalaCards: an amalgamated human
disease compendium with diverse clinical and genetic annotation and structured search
,
Nucleic Acids Research(2016),
doi: 10.1093 / nar / gkw1012.
[PDF]
-
GeneHancer – the human database of regulatory elements and their target genes
www.genecards.org
Fishilevich S, Nudel R, Rappaport N, Hadar R, Plaschkes I, Iny Stein T, Rosen N, Kohn A, Twik M, Safran M, Lancet D, and Cohen D.
GeneHancer: genome - wide integration of enhancers and target genes in GeneCards
,
Database(Oxford)(2017),
doi: 10.1093 / database / bax028.
[PDF]
-
VarElect – the NGS phenotyper
ve.genecards.org
Stelzer G, Plaschkes I, Oz - Levi D, Alkelai A, Olender T, Zimmerman S, Twik M., Belinky F,
Fishilevich S, Nudel R, Guan - Golan Y, Warshawsky D, Dahary D, Kohn A, Mazor Y, Kaplan S, Iny Stein T, Baris H,
Rappaport N, Safran M, and Lancet D.
VarElect: the phenotype - based variation prioritizer of the GeneCards suite ,
BMC Genomics(2016),
17(Suppl 2):444; DOI: 10.1186 / s12864 - 016 - 2722 - 2.
[PDF]
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TGex - the NGS analysis platform
tgex.genecards.org
Dahary D, Golan Y, Mazor Y, Zelig O, Barshir R, Twik M, Iny Stein T, Rosner G, Kariv R, Chen F, Zhang Q, Shen Y, Safran M, Lancet D and Fishilevich S.
Genome analysis and knowledge-driven variant interpretation with TGex , BMC Med Genomics 12, 200 (2019) doi:10.1186/s12920-019-0647-8
[PDF]
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GeneAnalytics – the gene set analysis tool
ga.genecards.org
Ben-Ari Fuchs S, Lieder I, Stelzer G, Mazor Y, Buzhor E, Kaplan S, Bogoch Y, Plaschkes I,
Shitrit A, Rappaport N, Kohn A, Edgar R, Shenhav L, Safran M, Lancet D, Guan-Golan Y, Warshawsky D,
and Strichman R. GeneAnalytics:An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data,
OMICS(2016) Volume 20, Number 3; DOI: 10.1089/omi.2015.0168.
[PDF]
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PathCards – the pathway unification database
pathcards.genecards.org
Belinky F, Nativ N, Stelzer G, Zimmerman S, Iny Stein T, Safran M, and Lancet, D.
PathCards: multi-source consolidation of human biological pathways,
Database (2015) Vol. 2015: article ID bav006; doi:10.1093/database/bav006.
[PDF]
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HIPED - the database of protein abundance in human tissues
www.genecards.org
Fishilevich S, Zimmerman S, Kohn A, Iny Stein T, Safran M, and Lancet D.
Genic Insights From Integrated Human Proteomics in GeneCards,
Database (2016); doi: 10.1093/database/baw030.
[PDF]
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GeneLoc – the genome locator
genecards.weizmann.ac.il/geneloc
Rosen, N., Chalifa-Caspi, V., Shmueli, O., Adato, A., Lapidot, M., Stampnitzky, J., Safran, M., and Lancet, D.
GeneLoc: Exon-based integration of human genome maps.
Bioinformatics:
19,S1: 222-224 (2003)
.
[PDF]
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GeneALaCart – the GeneCards batch-query processor
genealacart.genecards.org
Stelzer G, Rosen R, Plaschkes I, Zimmerman S, Twik M, Fishilevich S, Iny Stein T, Nudel R, Lieder I,
Mazor Y, Kaplan S, Dahary D, Warshawsky D, Guan - Golan Y, Kohn A, Rappaport N, Safran M, and Lancet D.
The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analysis ,
Current Protocols in Bioinformatics(2016),
54:1.30.1 - 1.30.33.doi: 10.1002 / cpbi.5. a >
[PDF]
-
GenesLikeMe – the partner hunter
glm.genecards.org
Stelzer G, Inger A, Olender T, Iny Stein T, Dalah I, Harel A, Safran M and Lancet D.
GeneDecks: paralog hunting and gene-set distillation with GeneCards annotation
OMICS, 2009, 13(6): 477-487
[PDF]
Complete list of our publications and presentations
-
Dahary D, Golan Y, Mazor Y, Zelig O, Barshir R, Twik M, Iny Stein T, Rosner G, Kariv R, Chen F, Zhang Q, Shen Y, Safran M, Lancet D and Fishilevich S.
Genome analysis and knowledge-driven variant interpretation with TGex, BMC Med Genomics 12, 200 (2019) doi:10.1186/s12920-019-0647-8 [PDF]
-
Safran M, Rosen N, Twik M, BarShir R, Iny Stein T, Dahary D, Fishilevich S, and Lancet D.
The GeneCards Suite Chapter, Practical Guide to Life Science Databases, Spring Nature Reference MRW, in press
-
Rappaport S, Fishilevich S, Nudel R, Twik M, Belinky F, Plaschkes I, Iny Stein T, Cohen D, Oz-Levi D, Safran M, and Lancet D.
Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElect,
BioMed Eng OnLine 2017, 16(Suppl 1):72, DOI: 10.1186/s12938-017-0359-2
[PDF]
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Fishilevich S, Nudel R, Rappaport N, Hadar R, Plaschkes I, Iny Stein T, Rosen N, Kohn A, Twik M, Safran M, Lancet D, and Cohen D.
GeneHancer: genome - wide integration of enhancers and target genes in GeneCards
,
Database(Oxford)(2017),
doi: 10.1093 / database / bax028.
[PDF]
-
Rappaport N, Twik M, Plaschkes I, Nudel R, Iny Stein T, Levitt J, Gershoni M, Morrey CP, Safran M, and Lancet D.
MalaCards: an amalgamated human
disease compendium with diverse clinical and genetic annotation and structured search
,
Nucleic Acids Research(2016),
doi: 10.1093 / nar / gkw1012.
[PDF]
-
Stelzer G, Plaschkes I, Oz - Levi D, Alkelai A, Olender T, Zimmerman S, Twik M., Belinky F,
Fishilevich S, Nudel R, Guan - Golan Y, Warshawsky D, Dahary D, Kohn A, Mazor Y, Kaplan S, Iny Stein T, Baris H,
Rappaport N, Safran M, and Lancet D.
VarElect: the phenotype - based variation prioritizer of the GeneCards suite ,
BMC Genomics(2016),
17(Suppl 2):444; DOI: 10.1186 / s12864 - 016 - 2722 - 2.
[PDF]
-
Stelzer G, Rosen R, Plaschkes I, Zimmerman S, Twik M, Fishilevich S, Iny Stein T, Nudel R, Lieder I,
Mazor Y, Kaplan S, Dahary, D, Warshawsky D, Guan - Golan Y, Kohn A, Rappaport N, Safran M, and Lancet D.
The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analysis ,
Current Protocols in Bioinformatics(2016),
54:1.30.1 - 1.30.33.doi: 10.1002 / cpbi.5. a >
[PDF]
-
Fishilevich S, Zimmerman S, Kohn A, Iny Stein T, Safran M, and Lancet D.
Genic Insights From Integrated Human Proteomics in GeneCards,
Database (2016); doi: 10.1093/database/baw030.
[PDF]
-
Ben-Ari Fuchs S, Lieder I, Stelzer G, Mazor Y, Buzhor E, Kaplan S, Bogoch Y, Plaschkes I,
Shitrit A, Rappaport N, Kohn A, Edgar R, Shenhav L, Safran M, Lancet D, Guan-Golan Y, Warshawsky D,
and Strichman R. GeneAnalytics:An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data,
OMICS(2016) Volume 20, Number 3; DOI: 10.1089/omi.2015.0168.
[PDF]
-
Belinky F, Nativ N, Stelzer G, Zimmerman S, Iny Stein T, Safran M, and Lancet, D.
PathCards: multi-source consolidation of human biological pathways,
Database (2015) Vol. 2015: article ID bav006; doi:10.1093/database/bav006.
[PDF]
-
Rappaport N, Twik M, Nativ N, Stelzer G, Bahir I, Iny Stein T, Safran M and Lancet D.
MalaCards: A Comprehensive Automatically-Mined Database of Human Diseases,
Curr. Protoc. Bioinform. 47:1.24:1.24.11.24.19. (Sept 2014)
[PDF]
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Lancet D, Stelzer G, Golan Y, and Rinon A.
Gene Trends: On Muscle, Fat, and Brain
Genetic Engineering & Biotechnology News, Dec 16, 2013.
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Lancet D, Golan Y, Leshansky L, and Stelzer G.
Gene Trends: Eye-Openers for Unusual Gene Variations
Genetic Engineering & Biotechnology News, Oct 24, 2013.
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Lancet D, Golan Y, and Stelzer G.
Gene Trends: Which Ones Should You Be Studying Now?
Genetic Engineering & Biotechnology News, Oct 3, 2013.
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Olender T, Safran M, Edgar R, Stelzer G, Nativ N, Rosen N, Shtrichman R, Mazor Y, West M D, Keydar I, Rappaport N, Belinky F, Warshawsky D, and Lancet D.
An Overview of Synergistic Data Tools for Biological Scrutiny
Israel Journal of Chemistry, Volume 53, Issue 3-4, pages 185–198, April 2013.
[PDF]
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Rappaport N, Nativ N, Stelzer G, Twik M, Guan-Golan Y, Iny Stein T, Bahir I, Belinky F, Morrey CP, Safran M and
Lancet D.
MalaCards: an integrated compendium for diseases and their annotation,
Database 2013; doi: 10.1093/database/bat018.
[PDF]
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Belinky F, Bahir I, Stelzer G, Zimmerman S, Rosen N, Nativ N, Dalah I, Iny Stein T, Rappaport N, Mituyama M, Safran M and Lancet D.
Non-redundant compendium of human ncRNA genes in GeneCards,
Bioinformatics 29, 2: 255-61 (2013).
[PDF]
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Safran M, Nativ N, Golan Y, Dalah I, Iny Stein T, Stelzer G, and Lancet D.
MalaCards – the integrated Human Malady Compendium,
ISMB 2012.
[PDF]
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Stelzer G, Dalah I, Iny Stein T, Satanower Y, Rosen N, Nativ N, Oz-Levi D, Olender T, Belinky F,
Bahir I, Krug H, Perco P, Mayer B, Kolker E, Safran M and Lancet, D.
In-silico Human Genomics with GeneCards,
Human Genomics, 2011 Oct;5(6):709-17.
[PDF]
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Harel A, Dalah I, Pietrokovski M, Safran M and Lancet D.
Omics Data Management and Annotation, Chapter 3
Bioinformatics for Omics Data: Methods and Protocols
Series: Methods in Molecular Biology, Vol. 719, ISBN: 978-1-61779-026-3,
Mayer, Bernd (Ed.), Humana Press, March, 2011
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Safran M, Dalah I, Alexander J, Rosen N, Iny Stein T, Shmoish M, Nativ N, Bahir I, Doniger T, Krug H, Sirota-Madi A,
Olender T, Golan Y, Stelzer G, Harel A and Lancet D.
GeneCards Version 3: the human gene integrator
Database
2010; doi: 10.1093/database/baq020
[PDF]
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Stelzer G, Inger A, Olender T, Iny Stein T, Dalah I, Harel A, Safran M and Lancet D.
GeneDecks: paralog hunting and gene-set distillation with GeneCards annotation
OMICS, 2009, 13(6): 477-487
[PDF]
-
Harel A, Inger A, Stelzer G, Strichman-Almashanu L, Dalah I, Safran M and Lancet D.
GIFtS: annotation landscape analysis with GeneCards
BMC Bioinformatics 2009, 10:348
[PDF]
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Stelzer G, Harel A, Inger A, Olender T, Dalah I, Shmoish M, Ron S, Safran M and Lancet D.
GeneDecks: GeneCards-based paralog hunting and gene set distillation.
CSB2008 Aug, 2008
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Lancet D, Safran M, Olender T, Dalah I, Iny-Stein T, Inger A, Harel A and Stelzer G.
GeneCards tools for combinatorial annotation and dissemination of human genome
information
GIACS Conference on Data in Complex Systems
April, 2008
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Stelzer G, Harel A, Dalah A, Rosen N, Shmoish M, Iny Stein T, Sirota A, Madi A,
Safran M and Lancet D.
GeneCards: One stop site for human gene research
FISEB (ILANIT)
, Jan, 2008
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Ferrari F, Bortoluzzi S, Coppe A, Sirota A, Safran M, Shmoish M, Ferrari S, Lancet D, Danieli G A,
and Bicciato S. Novel definition files for human GeneChips based on GeneAnnot.
BMC Bioinformatics 2007, 8:446 (15 NOV 2007).
[PDF]
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Safran M, Dalah I, Ron S, Shmoish M, Iny-Stein T, Rosen N, Madi A, Sirota A, Stelzer G
and Lancet D. GeneDecks annotation combinatorics and unification for human genes.
ISMB ECCB 2007
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Ron S, Strichman-Almashanu L, Shmoish M, Greenshpan O, Sirota A, Madi A, Iny-Stein T, Rosen N,
Dalah I, Shmueli O, Safran M, Aumann Y, and Lancet D.
GeneDecks: Gene-Set Analyses of GeneCards
Annotations.
ECCB
2006
.
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Lancet D, Ron S, Shmoish M, Madi A, Sirota A, Noy K, Rosen N, Greenshpan O, Shmueli O, Safran M,
Aumann Y, and Strichman-Almashanu L.
GeneDecks: A Systems Biology Facilitator with Combinatorial
GeneCards Display.
Transcriptome 2005.
[PDF]
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Ron S, Strichman-Almashanu L, Shmoish M, Madi A, Sirota A, Noy K, Rosen N, Shmueli O, Safran M,
and Lancet D. GeneDecks: A Systems Biology Facilitator With Combinatorial GeneCards Outlook.
Poster and abstract at ISMB 2005.
[PDF]
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Shklar M, Strichman-Almashanu L, Shmueli O, Shmoish M, Safran M, and Lancet D.
GeneTide--Terra Incognita Discovery Endeavor: a new transcriptome focused member of the
GeneCards/GeneNote suite of databases.
Nucleic Acids Res.
33: D556 - D561 (2005)
.
[PDF]
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Yanai I, Benjamin H, Shmoish M, Chalifa-Caspi V, Shklar M, Ophir R, Bar-Even A,
Horn-Saban S, Safran M, Domany E, Lancet D, Shmueli O.
Genome-wide midrange transcription profiles
reveal expression level relationships in human tissue specification.
Bioinformatics 21, 5: 650-659 (2005).
[PDF]
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Shklar, M., Shmueli, O., Strichman-Almashanu, L., Shmoish, M.,
Iny-Stein, T., Safran, M. and Lancet, D.
TIDE--Terra Incognita Discovery Endeavor: Comprehensive EST assignment to GeneCards genes.
Short paper and talk at ISMB/ECCB 2004.
[PDF]
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Chalifa-Caspi, V., Yanai, I., Ophir, R., Rosen, N.,
Shmoish, M., Benjamin-Rodrig, H., Iny Stein, T.,
Shmueli, O., Safran, M. and Lancet, D.
GeneAnnot: comprehensive two-way linking between oligonucleotide array
probesets and GeneCards genes.
Bioinformatics 20, 9: 1457-1458 (2004).
[PDF]
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Chalifa-Caspi, V., Shmueli, O., Benjamin-Rodrig, H., Rosen, N., Shmoish, M., Yanai, I., Ophir, R., Kats, P., Safran, M. and Lancet, D.
GeneAnnot: Interfacing GeneCards with high throughput gene expression compendia.
Briefings in Bioinformatics 4, 4: 349-360 (2003)
.
[PDF]
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Safran, M., Chalifa-Caspi, V., Shmueli, O., Rosen, N., Benjamin-Rodrig,
H., Ophir, R., Yanai, I., Shmoish, M., and Lancet, D.
The GeneCards Family of Databases: GeneCards, GeneLoc, GeneNote and
GeneAnnot.
Proceedings of the IEEE Computer Science Bioinformatics Conference CSB2003,(2003)
(Poster Abstract at CSB2003).
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Shmueli, O., Horn-Saban, S., Chalifa-Caspi, V., Shmoish, M.,
Ophir, R., Benjamin-Rodrig, H., Safran, M., Domany, E., and Lancet, D.
GeneNote: whole genome expression profiles in normal human tissues.
Comptes Rendus Biologies: 326, 10-11:1067-1072 (2003)
.
[PDF]
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Chalifa-Caspi, V., Yanai, I., Ophir, R., Shmoish,M.,
Benjamin-Rodrig, H., Rosen, N.,
Kats, P., Safran, M., Shmueli, O., and Lancet, D.
GeneAnnot: Annotation of high-density oligunocleotide arrays and their
linking with GeneCards.
Poster Abstract at ISMB 2003
-
Rosen, N., Chalifa-Caspi, V., Shmueli, O., Adato, A., Lapidot, M., Stampnitzky, J., Safran, M., and Lancet, D.
GeneLoc: Exon-based integration of human genome maps.
Bioinformatics:
19,S1: 222-224 (2003)
.
[PDF]
-
Safran, M., Chalifa-Caspi, V., Shmueli, O., Olender, T., Lapidot, M.,
Rosen, N., Shmoish, M., Peter, Y., Glusman, G., Feldmesser, E., Adato, A.,
Peter, I., Khen, M., Atarot, T., Groner, Y., and Lancet, D.
Human Gene-Centric Databases at the Weizmann Institute of Science: GeneCards,
UDB, CroW 21 and HORDE
.
Nucleic Acids Research 31,1:142-146 (2003).
[PDF]
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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., and Lancet, D.
GeneCards 2002: towards a complete, object-oriented, human gene
compendium
.
Bioinformatics: 18,11: 1542-1543 (2002).
[PDF]
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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., and Lancet, D.
GeneCards 2002: An Evolving Human Gene Compendium.
Proceedings of the IEEE Computer Science Bioinformatics Conference CSB2002, p. 339
(2002)
.
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Rebhan, M., Chalifa-Caspi, V., Prilusky, J., and Lancet, D.
GeneCards: A
novel functional genomics compendium with
automated data mining and query reformulation support.
Bioinformatics: 14: 656-664 (1998)
.
[PDF]
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Rebhan, M., Prilusky, J.
Rapid access to biomedical knowledge with
GeneCards and HotMolecBase: Implications for the electrophoretic analysis
of large sets of gene products.
Electrophoresis, special issue on
'Biomedicine and Biocomputing' , vol. 18: 2774-80 (1997)
.
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Rebhan, M., Chalifa-Caspi, V., Prilusky, J., Lancet, D.
GeneCards:
integrating information about genes,
proteins and diseases.
Trends in Genetics 13: 163 (1997)
.
[PDF]