Literature Based Discovery Support System and Its Application to Disease Gene Identification

2007 ◽  
pp. 307-326 ◽  
Author(s):  
Dimitar Hristovski ◽  
Borut Peterlin ◽  
Sašo Džeroski ◽  
Janez Stare
Keyword(s):  
Support System ◽  
Disease Gene ◽  
Gene Identification ◽  
Literature Based Discovery

Human Gene Mapping and Disease Gene Identification

2007 ◽  
pp. 207-230
Author(s):  
Robert L. Nussbaum ◽  
Roderick R. McInnes ◽  
Huntington F. Willard ◽  
Ada Hamosh
Keyword(s):  
Gene Mapping ◽  
Disease Gene ◽  
Human Gene ◽  
Gene Identification ◽  
Human Gene Mapping

scholarly journals Disease gene identification by using graph kernels and Markov random fields

2014 ◽  
Vol 57 (11) ◽  
pp. 1054-1063 ◽  
Author(s):  
BoLin Chen ◽  
Min Li ◽  
JianXin Wang ◽  
Fang-Xiang Wu
Keyword(s):  
Random Fields ◽  
Markov Random Fields ◽  
Disease Gene ◽  
Gene Identification ◽  
Graph Kernels ◽  
Markov Random

scholarly journals New Tools for Mendelian Disease Gene Identification: PhenoDB Variant Analysis Module; and GeneMatcher, a Web-Based Tool for Linking Investigators with an Interest in the Same Gene

2015 ◽  
Vol 36 (4) ◽  
pp. 425-431 ◽  
Author(s):  
Nara Sobreira ◽  
François Schiettecatte ◽  
Corinne Boehm ◽  
David Valle ◽  
Ada Hamosh
Keyword(s):  
Disease Gene ◽  
Gene Identification ◽  
Mendelian Disease ◽  
Web Based ◽  
Variant Analysis

scholarly journals Symptom-driven idiopathic disease gene identification

2015 ◽  
Vol 17 (11) ◽  
pp. 859-865 ◽  
Author(s):  
Bhuvan Molparia ◽  
Phillip H. Pham ◽  
Ali Torkamani
Keyword(s):  
Disease Gene ◽  
Gene Identification ◽  
Idiopathic Disease

SCO-ping Out the Mechanisms Underlying the Etiology of Hydrocephalus

Physiology ◽  
2009 ◽  
Vol 24 (2) ◽  
pp. 117-126 ◽  
Author(s):  
Michael S. Huh ◽  
Matthew A. M. Todd ◽  
David J. Picketts
Keyword(s):  
Disease Gene ◽  
Subcommissural Organ ◽  
Clinical Problem ◽  
Gene Identification ◽  
Transgenic Mouse Models ◽  
Heterogeneous Nature ◽  
And Function ◽  
Identification And Characterization ◽  
Common Clinical Problem

The heterogeneous nature of congenital hydrocephalus has hampered our understanding of the molecular basis of this common clinical problem. However, disease gene identification and characterization of multiple transgenic mouse models has highlighted the importance of the subcommissural organ (SCO) and the ventricular ependymal (vel) cells. Here, we review how altered development and function of the SCO and vel cells contributes to hydrocephalus.

scholarly journals Prediction of osteoporosis candidate genes by computational disease-gene identification strategy

2008 ◽  
Vol 53 (7) ◽  
pp. 644-655 ◽  
Author(s):  
Qing-Yang Huang ◽  
Gloria H. Y. Li ◽  
William M. W. Cheung ◽  
You-Qiang Song ◽  
Annie W. C. Kung
Keyword(s):  
Candidate Genes ◽  
Disease Gene ◽  
Gene Identification ◽  
Identification Strategy
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