{"id":3822,"date":"2017-06-26T05:55:54","date_gmt":"2017-06-26T05:55:54","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=3822"},"modified":"2017-07-23T04:53:56","modified_gmt":"2017-07-23T04:53:56","slug":"nuevas-variantes-mutaciones-y-asociaciones","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2017\/06\/26\/nuevas-variantes-mutaciones-y-asociaciones\/","title":{"rendered":"Nuevas variantes, mutaciones y asociaciones"},"content":{"rendered":"<p>&#8211; <a title=\"Nature Genetics 2017; doi:10.1038\/ng.3895 \" href=\"https:\/\/www.nature.com\/ng\/journal\/vaop\/ncurrent\/full\/ng.3895.html\" target=\"_blank\">Variants in the fetal genome near FLT1 are associated with risk of preeclampsia<\/a><br \/>\n&#8211; <a title=\"PLoS Genet 2017;13(6):e1006328. \" href=\"http:\/\/journals.plos.org\/plosgenetics\/article?id=10.1371\/journal.pgen.1006328\" target=\"_blank\">Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy<\/a>.<br \/>\n&#8211; <a title=\"Nature Genetics 2017; doi:10.1038\/?ng.3894 \" href=\"https:\/\/www.nature.com\/ng\/journal\/vaop\/ncurrent\/full\/ng.3894.html\" target=\"_blank\">Truncating mutations in RBM12 are associated with psychosis<\/a><br \/>\n&#8211; <a title=\"Nature Genetics 2017; doi:10.1038\/ng.3898 \" href=\"https:\/\/www.nature.com\/ng\/journal\/vaop\/ncurrent\/full\/ng.3898.html\" target=\"_blank\">Germline hypomorphic CARD11 mutations in severe atopic disease<\/a><br \/>\n&#8211; <a title=\"Nature Neuroscience 2017;20:602\u2013611. \" href=\"http:\/\/www.nature.com\/neuro\/journal\/v20\/n4\/full\/nn.4524.html\" target=\"_blank\">Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder<\/a><br \/>\n&#8211; <a title=\"Human Genome Variation 2017;4:7019 \" href=\"http:\/\/www.nature.com\/articles\/hgv201719\" target=\"_blank\">A novel UBE2A mutation causes X-linked intellectual disability type Nascimento<\/a><br \/>\n&#8211; <a title=\"Nature Genetics 2017;49:946\u2013952 \" href=\"http:\/\/www.nature.com\/ng\/journal\/v49\/n6\/full\/ng.3843.html\" target=\"_blank\">Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation<\/a><br \/>\n&#8211; <a title=\"Nature Genetics 2017 \" href=\"https:\/\/www.nature.com\/ng\/journal\/vaop\/ncurrent\/full\/ng.3869.htmlNature%20Genetics 2017 https:\/\/www.nature.com\/ng\/journal\/vaop\/ncurrent\/full\/ng.3869.html\" target=\"_blank\">Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence<\/a><br \/>\n&#8211; <a title=\"Neuron 2017;94(6):1101\u20131111.e7 \" href=\"http:\/\/www.cell.com\/neuron\/fulltext\/S0896-6273(17)30508-1\" target=\"_blank\">Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&#8211; Variants in the fetal genome near FLT1 are associated with risk of preeclampsia &#8211; Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy. &#8211; Truncating mutations in RBM12 are associated with psychosis &#8211; Germline hypomorphic CARD11 mutations in severe atopic disease &#8211; Whole genome sequencing resource identifies 18 new [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[23,26,28,29],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3822"}],"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=3822"}],"version-history":[{"count":2,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3822\/revisions"}],"predecessor-version":[{"id":3913,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3822\/revisions\/3913"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=3822"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=3822"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=3822"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}