<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Imamura M</submitter><funding>British Heart Foundation</funding><funding>European Research Council</funding><funding>NIDDK NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>FIC NIH HHS</funding><funding>Medical Research Council</funding><funding>NCI NIH HHS</funding><funding>NNF Center for Basic Metabolic Research</funding><funding>Wellcome Trust</funding><pagination>10531</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4738362</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7</volume><pubmed_abstract>Genome-wide association studies (GWAS) have identified more than 80 susceptibility loci for type 2 diabetes (T2D), but most of its heritability still remains to be elucidated. In this study, we conducted a meta-analysis of GWAS for T2D in the Japanese population. Combined data from discovery and subsequent validation analyses (23,399 T2D cases and 31,722 controls) identify 7 new loci with genome-wide significance (P&lt;5 × 10(-8)), rs1116357 near CCDC85A, rs147538848 in FAM60A, rs1575972 near DMRTA1, rs9309245 near ASB3, rs67156297 near ATP8B2, rs7107784 near MIR4686 and rs67839313 near INAFM2. Of these, the association of 4 loci with T2D is replicated in multi-ethnic populations other than Japanese (up to 65,936 T2Ds and 158,030 controls, P&lt;0.007). These results indicate that expansion of single ethnic GWAS is still useful to identify novel susceptibility loci to complex traits not only for ethnicity-specific loci but also for common loci across different ethnicities.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes.</pubmed_title><pmcid>PMC4738362</pmcid><funding_grant_id>K01 TW006087</funding_grant_id><funding_grant_id>268834</funding_grant_id><funding_grant_id>UM1 CA182910</funding_grant_id><funding_grant_id>KO1TW006087</funding_grant_id><funding_grant_id>R37CA070867</funding_grant_id><funding_grant_id>279233</funding_grant_id><funding_grant_id>SP/09/002</funding_grant_id><funding_grant_id>R37 CA070867</funding_grant_id><funding_grant_id>R01 CA064277</funding_grant_id><funding_grant_id>R01CA124558</funding_grant_id><funding_grant_id>R01 CA124558</funding_grant_id><funding_grant_id>Grarup Group</funding_grant_id><funding_grant_id>R01CA64277</funding_grant_id><funding_grant_id>G0800270</funding_grant_id><funding_grant_id>UL1 RR024975</funding_grant_id><funding_grant_id>BC050791</funding_grant_id><funding_grant_id>R01 DK082766</funding_grant_id><funding_grant_id>R01DK082766</funding_grant_id><pubmed_authors>Florez JC</pubmed_authors><pubmed_authors>Burtt NP</pubmed_authors><pubmed_authors>Hirose H</pubmed_authors><pubmed_authors>Watada H</pubmed_authors><pubmed_authors>Tai ES</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Kaku K</pubmed_authors><pubmed_authors>Yasuda K</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Jorgensen ME</pubmed_authors><pubmed_authors>Ito C</pubmed_authors><pubmed_authors>Hosoe J</pubmed_authors><pubmed_authors>Moon S</pubmed_authors><pubmed_authors>Maeda S</pubmed_authors><pubmed_authors>Takahashi A</pubmed_authors><pubmed_authors>Kawamori R</pubmed_authors><pubmed_authors>Huerta-Chagoya A</pubmed_authors><pubmed_authors>Sanghera D</pubmed_authors><pubmed_authors>Zheng W</pubmed_authors><pubmed_authors>Kim BJ</pubmed_authors><pubmed_authors>Singh JR</pubmed_authors><pubmed_authors>Cho YS</pubmed_authors><pubmed_authors>Hu C</pubmed_authors><pubmed_authors>Maegawa H</pubmed_authors><pubmed_authors>Christensen C</pubmed_authors><pubmed_authors>Mercader JM</pubmed_authors><pubmed_authors>Shojima N</pubmed_authors><pubmed_authors>Long J</pubmed_authors><pubmed_authors>Saxena R</pubmed_authors><pubmed_authors>Zhao W</pubmed_authors><pubmed_authors>Kadowaki T</pubmed_authors><pubmed_authors>Suzuki K</pubmed_authors><pubmed_authors>Park KS</pubmed_authors><pubmed_authors>Tanaka Y</pubmed_authors><pubmed_authors>Danesh J</pubmed_authors><pubmed_authors>Kim YJ</pubmed_authors><pubmed_authors>Hara K</pubmed_authors><pubmed_authors>Jia W</pubmed_authors><pubmed_authors>Iwasaki M</pubmed_authors><pubmed_authors>Kubo M</pubmed_authors><pubmed_authors>Rasheed A</pubmed_authors><pubmed_authors>Yamauchi T</pubmed_authors><pubmed_authors>Brandslund I</pubmed_authors><pubmed_authors>Tam CH</pubmed_authors><pubmed_authors>Chan JC</pubmed_authors><pubmed_authors>Pedersen O</pubmed_authors><pubmed_authors>Frossard P</pubmed_authors><pubmed_authors>Shu XO</pubmed_authors><pubmed_authors>Imamura M</pubmed_authors><pubmed_authors>Tobe K</pubmed_authors><pubmed_authors>Iwata M</pubmed_authors><pubmed_authors>Fujita H</pubmed_authors><pubmed_authors>Witte DR</pubmed_authors><pubmed_authors>Tusie-Luna T</pubmed_authors><pubmed_authors>Hansen T</pubmed_authors><pubmed_authors>Moreno-Macias H</pubmed_authors><pubmed_authors>Kwak SH</pubmed_authors><pubmed_authors>Okada Y</pubmed_authors><pubmed_authors>Ma RC</pubmed_authors><pubmed_authors>Grarup N</pubmed_authors><pubmed_authors>Jorgensen T</pubmed_authors><pubmed_authors>Saleheen D</pubmed_authors><pubmed_authors>Flannick J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes.</name><description>Genome-wide association studies (GWAS) have identified more than 80 susceptibility loci for type 2 diabetes (T2D), but most of its heritability still remains to be elucidated. In this study, we conducted a meta-analysis of GWAS for T2D in the Japanese population. Combined data from discovery and subsequent validation analyses (23,399 T2D cases and 31,722 controls) identify 7 new loci with genome-wide significance (P&lt;5 × 10(-8)), rs1116357 near CCDC85A, rs147538848 in FAM60A, rs1575972 near DMRTA1, rs9309245 near ASB3, rs67156297 near ATP8B2, rs7107784 near MIR4686 and rs67839313 near INAFM2. Of these, the association of 4 loci with T2D is replicated in multi-ethnic populations other than Japanese (up to 65,936 T2Ds and 158,030 controls, P&lt;0.007). These results indicate that expansion of single ethnic GWAS is still useful to identify novel susceptibility loci to complex traits not only for ethnicity-specific loci but also for common loci across different ethnicities.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jan</publication><modification>2024-11-08T14:59:48.167Z</modification><creation>2019-03-27T02:08:14Z</creation></dates><accession>S-EPMC4738362</accession><cross_references><pubmed>26818947</pubmed><doi>10.1038/ncomms10531</doi></cross_references></HashMap>