The influence of disease categories on gene candidate predictions from model organism phenotypes

[1]  Damian Smedley,et al.  Improved exome prioritization of disease genes through cross-species phenotype comparison , 2014, Genome research.

[2]  E. Liu,et al.  The Cinderella effect: searching for the best fit between mouse models and human diseases. , 2013, The Journal of investigative dermatology.

[3]  Katherine Smith Liver disease: Quest to find new mouse models for liver diseases , 2013, Nature Reviews Gastroenterology &Hepatology.

[4]  Damian Smedley,et al.  PhenoDigm: analyzing curated annotations to associate animal models with human diseases , 2013, Database J. Biol. Databases Curation.

[5]  T. Miyakawa,et al.  Genomic responses in mouse models poorly mimic human inflammatory diseases , 2013 .

[6]  R. Gamelli,et al.  Genomic responses in mouse models poorly mimic human inflammatory diseases , 2013, Proceedings of the National Academy of Sciences.

[7]  Bart De Moor,et al.  An unbiased evaluation of gene prioritization tools , 2012, Bioinform..

[8]  Jacqueline K. White,et al.  Generation of the Sotos syndrome deletion in mice , 2012, Mammalian Genome.

[9]  Jing Chen,et al.  The Role of Sphingosine-1-Phosphate Transporter Spns2 in Immune System Function , 2012, The Journal of Immunology.

[10]  Damian Smedley,et al.  MouseFinder: Candidate disease genes from mouse phenotype data , 2012, Human mutation.

[11]  Mark W. Moore,et al.  Towards an encyclopaedia of mammalian gene function: the International Mouse Phenotyping Consortium , 2012, Disease Models & Mechanisms.

[12]  N. Trede,et al.  A model 450 million years in the making: zebrafish and vertebrate immunity , 2012, Disease Models & Mechanisms.

[13]  Paul N. Schofield,et al.  PhenomeNET: a whole-phenome approach to disease gene discovery , 2011, Nucleic acids research.

[14]  Carol A. Bocchini,et al.  A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®) , 2011, Human mutation.

[15]  Wolfgang Meissner,et al.  Reverse crosstalk of TGFβ and PPARβ/δ signaling identified by transcriptional profiling , 2010, Nucleic Acids Res..

[16]  S. Schulte-Merker,et al.  Zebrafish as a unique model system in bone research: the power of genetics and in vivo imaging , 2010 .

[17]  Cynthia L. Smith,et al.  Integrating phenotype ontologies across multiple species , 2010, Genome Biology.

[18]  Matthew Mort,et al.  The Human Gene Mutation Database: providing a comprehensive central mutation database for molecular diagnostics and personalised genomics , 2009, Human Genomics.

[19]  Monte Westerfield,et al.  Linking Human Diseases to Animal Models Using Ontology-Based Phenotype Annotation , 2009, PLoS biology.

[20]  P. Robinson,et al.  Walking the interactome for prioritization of candidate disease genes. , 2008, American journal of human genetics.

[21]  D. Gifford,et al.  Tissue-specific transcriptional regulation has diverged significantly between human and mouse , 2007, Nature Genetics.

[22]  J. Gogos,et al.  Modeling Madness in Mice: One Piece at a Time , 2006, Neuron.

[23]  L. Tecott The genes and brains of mice and men. , 2003, The American journal of psychiatry.

[24]  Ségolène Aymé,et al.  [Orphanet, an information site on rare diseases]. , 2003, Soins; la revue de reference infirmiere.

[25]  M. DeRuiter,et al.  Comparative anatomy and ontogeny of the ductus arteriosus, a vascular outsider , 1999, Anatomy and Embryology.