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Items: 12


Applying Systems Biology Methodology To Identify Genetic Factors Possibly Associated with Recovery after Traumatic Brain Injury.

Kurowski BG, Treble-Barna A, Pitzer AJ, Wade SL, Martin LJ, Chima RS, Jegga A.

J Neurotrauma. 2017 Jul 15;34(14):2280-2290. doi: 10.1089/neu.2016.4856. Epub 2017 May 3.


Candidate gene discovery and prioritization in rare diseases.

Jegga AG.

Methods Mol Biol. 2014;1168:295-312. doi: 10.1007/978-1-4939-0847-9_17. Review.


A vertex similarity-based framework to discover and rank orphan disease-related genes.

Zhu C, Kushwaha A, Berman K, Jegga AG.

BMC Syst Biol. 2012;6 Suppl 3:S8. doi: 10.1186/1752-0509-6-S3-S8. Epub 2012 Dec 17.


The orphan disease networks.

Zhang M, Zhu C, Jacomy A, Lu LJ, Jegga AG.

Am J Hum Genet. 2011 Jun 10;88(6):755-766. doi: 10.1016/j.ajhg.2011.05.006.


Systems biology of the autophagy-lysosomal pathway.

Jegga AG, Schneider L, Ouyang X, Zhang J.

Autophagy. 2011 May;7(5):477-89. Epub 2011 May 1.


Integrative systems biology approaches to identify and prioritize disease and drug candidate genes.

Kaimal V, Sardana D, Bardes EE, Gudivada RC, Chen J, Jegga AG.

Methods Mol Biol. 2011;700:241-59. doi: 10.1007/978-1-61737-954-3_16.


PhenoHM: human-mouse comparative phenome-genome server.

Sardana D, Vasa S, Vepachedu N, Chen J, Gudivada RC, Aronow BJ, Jegga AG.

Nucleic Acids Res. 2010 Jul;38(Web Server issue):W165-74. doi: 10.1093/nar/gkq472. Epub 2010 May 27.


ToppGene Suite for gene list enrichment analysis and candidate gene prioritization.

Chen J, Bardes EE, Aronow BJ, Jegga AG.

Nucleic Acids Res. 2009 Jul;37(Web Server issue):W305-11. doi: 10.1093/nar/gkp427. Epub 2009 May 22.


Disease candidate gene identification and prioritization using protein interaction networks.

Chen J, Aronow BJ, Jegga AG.

BMC Bioinformatics. 2009 Feb 27;10:73. doi: 10.1186/1471-2105-10-73. Erratum in: BMC Bioinformatics. 2009;10:406.


Improved human disease candidate gene prioritization using mouse phenotype.

Chen J, Xu H, Aronow BJ, Jegga AG.

BMC Bioinformatics. 2007 Oct 16;8:392.


PolyDoms: a whole genome database for the identification of non-synonymous coding SNPs with the potential to impact disease.

Jegga AG, Gowrisankar S, Chen J, Aronow BJ.

Nucleic Acids Res. 2007 Jan;35(Database issue):D700-6. Epub 2006 Nov 16.

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