{"id":3749,"date":"2017-04-17T03:55:50","date_gmt":"2017-04-17T03:55:50","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=3749"},"modified":"2017-04-17T16:21:28","modified_gmt":"2017-04-17T16:21:28","slug":"nuevos-estudios-de-asociacion-genetica-2","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2017\/04\/17\/nuevos-estudios-de-asociacion-genetica-2\/","title":{"rendered":"Nuevos estudios de asociaci\u00f3n gen\u00e9tica"},"content":{"rendered":"<p style=\"text-align: justify\">&#8211; <a title=\"Nature Genetics 2017;49:515\u2013526. \" href=\"http:\/\/www.nature.com\/ng\/journal\/v49\/n4\/full\/ng.3792.html\" target=\"_blank\">Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases<\/a><\/p>\n<p style=\"text-align: justify\">&#8211; <a title=\"Nature Genetics 2017;49:559\u2013567. \" href=\"http:\/\/www.nature.com\/ng\/journal\/v49\/n4\/full\/ng.3799.html\" target=\"_blank\">Genome-wide analyses identify common variants associated with macular telangiectasia type 2<\/a><\/p>\n<p style=\"text-align: justify\">&#8211; <a title=\"Nature Genetics 2017;49:568\u2013578. \" href=\"http:\/\/www.nature.com\/ng\/journal\/v49\/n4\/full\/ng.3809.html\" target=\"_blank\">Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites<\/a><\/p>\n<p style=\"text-align: justify\">&#8211; <a title=\"Nature Communications 2017;8:14898. \" href=\"http:\/\/www.nature.com\/articles\/ncomms14898\" target=\"_blank\">Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy<\/a><\/p>\n<p style=\"text-align: justify\">&#8211; <a title=\"OMICS: A Journal of Integrative Biology. March 2017;21(3):123-131.\" href=\"http:\/\/online.liebertpub.com\/doi\/full\/10.1089\/omi.2017.0006\" target=\"_blank\">Genome-Wide Association Studies for Idiosyncratic Drug-Induced Hepatotoxicity: Looking Back\u2013Looking Forward to Next-Generation Innovation<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&#8211; Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases &#8211; Genome-wide analyses identify common variants associated with macular telangiectasia type 2 &#8211; Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites &#8211; Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy &#8211; Genome-Wide Association Studies for Idiosyncratic [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[15,19,29],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3749"}],"collection":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/users\/125"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/comments?post=3749"}],"version-history":[{"count":4,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3749\/revisions"}],"predecessor-version":[{"id":3800,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3749\/revisions\/3800"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=3749"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=3749"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=3749"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}