Literature DB >> 15211356

From syndrome families to functional genomics.

Han G Brunner1, Marc A van Driel.   

Abstract

Mesh：

Year:  2004        PMID： 15211356     DOI： 10.1038/nrg1383

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN： 1471-0056            Impact factor:   53.242


× No keyword cloud information.
  69 in total

1.  Genomic patterns of pleiotropy and the evolution of complexity.

Authors:  Zhi Wang; Ben-Yang Liao; Jianzhi Zhang
Journal:  Proc Natl Acad Sci U S A       Date:  2010-09-27       Impact factor: 11.205

2.  Predicting disease genes using protein-protein interactions.

Authors:  M Oti; B Snel; M A Huynen; H G Brunner
Journal:  J Med Genet       Date:  2006-04-12       Impact factor: 6.318

3.  Towards building a disease-phenotype knowledge base: extracting disease-manifestation relationship from literature.

Authors:  Rong Xu; Li Li; Quanqiu Wang
Journal:  Bioinformatics       Date:  2013-07-04       Impact factor: 6.937

4.  The common biological basis for common complex diseases: evidence from lipoprotein lipase gene.

Authors:  Cui Xie; Zeng Chan Wang; Xiao Feng Liu; Mao Sheng Yang
Journal:  Eur J Hum Genet       Date:  2010-01       Impact factor: 4.246

5.  Walking the interactome for prioritization of candidate disease genes.

Authors:  Sebastian Köhler; Sebastian Bauer; Denise Horn; Peter N Robinson
Journal:  Am J Hum Genet       Date:  2008-03-27       Impact factor: 11.025

Review 6.  The pleiotropic structure of the genotype-phenotype map: the evolvability of complex organisms.

Authors:  Günter P Wagner; Jianzhi Zhang
Journal:  Nat Rev Genet       Date:  2011-03       Impact factor: 53.242

7.  Discovery of protein interaction networks shared by diseases.

Authors:  Lee Sam; Yang Liu; Jianrong Li; Carol Friedman; Yves A Lussier
Journal:  Pac Symp Biocomput       Date:  2007

8.  The biological coherence of human phenome databases.

Authors:  Martin Oti; Martijn A Huynen; Han G Brunner
Journal:  Am J Hum Genet       Date:  2009-12       Impact factor: 11.025

9.  The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease.

Authors:  Peter N Robinson; Sebastian Köhler; Sebastian Bauer; Dominik Seelow; Denise Horn; Stefan Mundlos
Journal:  Am J Hum Genet       Date:  2008-10-23       Impact factor: 11.025

Review 10.  Joubert syndrome: insights into brain development, cilium biology, and complex disease.

Authors:  Dan Doherty
Journal:  Semin Pediatr Neurol       Date:  2009-09       Impact factor: 1.636
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.