{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,8,4]],"date-time":"2024-08-04T13:23:19Z","timestamp":1722777799085},"reference-count":28,"publisher":"Public Library of Science (PLoS)","issue":"11","license":[{"start":{"date-parts":[[2010,11,1]],"date-time":"2010-11-01T00:00:00Z","timestamp":1288569600000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["www.plosone.org"],"crossmark-restriction":false},"short-container-title":["PLoS ONE"],"DOI":"10.1371\/journal.pone.0013782","type":"journal-article","created":{"date-parts":[[2010,11,1]],"date-time":"2010-11-01T15:37:51Z","timestamp":1288625871000},"page":"e13782","update-policy":"http:\/\/dx.doi.org\/10.1371\/journal.pone.corrections_policy","source":"Crossref","is-referenced-by-count":23,"title":["Laboratory Mouse Models for the Human Genome-Wide Associations"],"prefix":"10.1371","volume":"5","author":[{"given":"Georgios D.","family":"Kitsios","sequence":"first","affiliation":[]},{"given":"Navdeep","family":"Tangri","sequence":"additional","affiliation":[]},{"given":"Peter J.","family":"Castaldi","sequence":"additional","affiliation":[]},{"given":"John P. A.","family":"Ioannidis","sequence":"additional","affiliation":[]}],"member":"340","published-online":{"date-parts":[[2010,11,1]]},"reference":[{"key":"ref1","doi-asserted-by":"crossref","first-page":"1590","DOI":"10.1172\/JCI34772","article-title":"A HapMap harvest of insights into the genetics of common disease.","volume":"118","author":"TA Manolio","year":"2008","journal-title":"J Clin Invest"},{"key":"ref2","doi-asserted-by":"crossref","first-page":"356","DOI":"10.1038\/nrg2344","article-title":"Genome-wide association studies for complex traits: consensus, uncertainty and challenges.","volume":"9","author":"MI McCarthy","year":"2008","journal-title":"Nat Rev Genet"},{"key":"ref3","doi-asserted-by":"crossref","first-page":"318","DOI":"10.1038\/nrg2544","article-title":"Validating, augmenting and refining genome-wide association signals.","volume":"10","author":"JP Ioannidis","year":"2009","journal-title":"Nat Rev Genet"},{"key":"ref4","doi-asserted-by":"crossref","first-page":"D724","DOI":"10.1093\/nar\/gkm961","article-title":"The Mouse Genome Database (MGD): mouse biology and model systems.","volume":"36","author":"CJ Bult","year":"2008","journal-title":"Nucleic Acids Res"},{"key":"ref5","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1038\/ng.299","article-title":"Variant in the sequence of the LINGO1 gene confers risk of essential tremor.","volume":"41","author":"H Stefansson","year":"2009","journal-title":"Nat Genet"},{"key":"ref6","first-page":"1042","article-title":"Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans.","volume":"119","author":"AC Edmondson","year":"2009","journal-title":"J Clin Invest"},{"key":"ref7","article-title":"A Catalog of Published Genome-Wide Association Studies.","author":"LA Hindorff","year":"2009"},{"key":"ref8","doi-asserted-by":"crossref","first-page":"9362","DOI":"10.1073\/pnas.0903103106","article-title":"Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.","volume":"106","author":"LA Hindorff","year":"2009","journal-title":"Proc Natl Acad Sci U S A"},{"key":"ref9","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1002\/gepi.20292","article-title":"Genome-wide significance for dense SNP and resequencing data.","volume":"32","author":"CJ Hoggart","year":"2008","journal-title":"Genet Epidemiol"},{"key":"ref10","doi-asserted-by":"crossref","first-page":"e1000247-","DOI":"10.1371\/journal.pbio.1000247","article-title":"Linking human diseases to animal models using ontology-based phenotype annotation.","volume":"7","author":"NL Washington","year":"2009","journal-title":"PLoS Biol"},{"key":"ref11","doi-asserted-by":"crossref","first-page":"R2-","DOI":"10.1186\/gb-2010-11-1-r2","article-title":"Integrating phenotype ontologies across multiple species.","volume":"11","author":"CJ Mungall","year":"2010","journal-title":"Genome Biol"},{"key":"ref12","doi-asserted-by":"crossref","first-page":"610","DOI":"10.1016\/j.ajhg.2008.09.017","article-title":"The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease.","volume":"83","author":"PN Robinson","year":"2008","journal-title":"Am J Hum Genet"},{"key":"ref13","doi-asserted-by":"crossref","first-page":"R7-","DOI":"10.1186\/gb-2004-6-1-r7","article-title":"The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information.","volume":"6","author":"CL Smith","year":"2005","journal-title":"Genome Biol"},{"key":"ref14","doi-asserted-by":"crossref","first-page":"390","DOI":"10.1002\/wsbm.44","article-title":"The mammalian phenotype ontology: enabling robust annotation and comparative analysis.","volume":"1","author":"CL Smith","year":"2009","journal-title":"Wiley Interdiscip Rev Syst Biol Med"},{"key":"ref15","doi-asserted-by":"crossref","first-page":"832","DOI":"10.1038\/ejhg.2010.26","article-title":"Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies.","volume":"18","author":"KC Siontis","year":"2010","journal-title":"Eur J Hum Genet"},{"key":"ref16","doi-asserted-by":"crossref","first-page":"1510","DOI":"10.1038\/sj.onc.1208229","article-title":"Knockin of SV40 Tag oncogene in a mouse adenocarcinoma of the prostate model demonstrates advantageous features over the transgenic model.","volume":"24","author":"W Duan","year":"2005","journal-title":"Oncogene"},{"key":"ref17","doi-asserted-by":"crossref","first-page":"7435","DOI":"10.1128\/MCB.24.17.7435-7443.2004","article-title":"Disruption of the SH2-B gene causes age-dependent insulin resistance and glucose intolerance.","volume":"24","author":"C Duan","year":"2004","journal-title":"Mol Cell Biol"},{"key":"ref18","doi-asserted-by":"crossref","first-page":"3066","DOI":"10.1128\/MCB.22.9.3066-3077.2002","article-title":"SH2-B is required for both male and female reproduction.","volume":"22","author":"S Ohtsuka","year":"2002","journal-title":"Mol Cell Biol"},{"key":"ref19","doi-asserted-by":"crossref","first-page":"1175","DOI":"10.1172\/JCI1744","article-title":"Biological effects of targeted inactivation of hepatocyte growth factor-like protein in mice.","volume":"101","author":"JA Bezerra","year":"1998","journal-title":"J Clin Invest"},{"key":"ref20","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1152\/physrev.00040.2007","article-title":"Interpreting neonatal lethal phenotypes in mouse mutants: insights into gene function and human diseases.","volume":"89","author":"B Turgeon","year":"2009","journal-title":"Physiol Rev"},{"key":"ref21","doi-asserted-by":"crossref","first-page":"1-","DOI":"10.1186\/1755-8794-3-1","article-title":"Systematic analysis, comparison, and integration of disease based human genetic association data and mouse genetic phenotypic information.","volume":"3","author":"Y Zhang","year":"2010","journal-title":"BMC Med Genomics"},{"key":"ref22","doi-asserted-by":"crossref","first-page":"6544","DOI":"10.1073\/pnas.0910200107","article-title":"Systematic discovery of nonobvious human disease models through orthologous phenotypes.","volume":"107","author":"KL McGary","year":"2010","journal-title":"Proc Natl Acad Sci U S A"},{"key":"ref23","article-title":"Genome-wide Significant Associations for Variants With Minor Allele Frequency of 5% or Less\u2014An Overview: A HuGE Review.","author":"OA Panagiotou","year":"2010","journal-title":"Am J Epidemiol"},{"key":"ref24","doi-asserted-by":"crossref","first-page":"707","DOI":"10.1038\/nature09270","article-title":"Biological, clinical and population relevance of 95 loci for blood lipids.","volume":"466","author":"TM Teslovich","year":"2010","journal-title":"Nature"},{"key":"ref25","doi-asserted-by":"crossref","first-page":"265","DOI":"10.1016\/j.ygeno.2008.07.011","article-title":"Pathway analysis of seven common diseases assessed by genome-wide association.","volume":"92","author":"A Torkamani","year":"2008","journal-title":"Genomics"},{"key":"ref26","doi-asserted-by":"crossref","first-page":"415","DOI":"10.1038\/nrg2779","article-title":"Uncovering the roles of rare variants in common disease through whole-genome sequencing.","volume":"11","author":"ET Cirulli","year":"2010","journal-title":"Nat Rev Genet"},{"key":"ref27","doi-asserted-by":"crossref","first-page":"921","DOI":"10.1038\/ng0904-921","article-title":"The knockout mouse project.","volume":"36","author":"CP Austin","year":"2004","journal-title":"Nat Genet"},{"key":"ref28","doi-asserted-by":"crossref","first-page":"514","DOI":"10.1111\/j.1469-1809.2009.00533.x","article-title":"Genomic convergence of genome-wide investigations for complex traits.","volume":"73","author":"GD Kitsios","year":"2009","journal-title":"Ann Hum Genet"}],"container-title":["PLoS ONE"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/dx.plos.org\/10.1371\/journal.pone.0013782","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2018,10,22]],"date-time":"2018-10-22T08:56:13Z","timestamp":1540198573000},"score":1,"resource":{"primary":{"URL":"https:\/\/dx.plos.org\/10.1371\/journal.pone.0013782"}},"subtitle":[],"editor":[{"given":"Amanda Ewart","family":"Toland","sequence":"first","affiliation":[]}],"short-title":[],"issued":{"date-parts":[[2010,11,1]]},"references-count":28,"journal-issue":{"issue":"11","published-online":{"date-parts":[[2010,11,1]]}},"URL":"https:\/\/doi.org\/10.1371\/journal.pone.0013782","relation":{},"ISSN":["1932-6203"],"issn-type":[{"value":"1932-6203","type":"electronic"}],"subject":[],"published":{"date-parts":[[2010,11,1]]}}}