{"id":5147,"date":"2021-12-01T05:18:34","date_gmt":"2021-12-01T05:18:34","guid":{"rendered":"https:\/\/blogs.sld.cu\/oserranob\/?p=5147"},"modified":"2021-12-01T05:18:34","modified_gmt":"2021-12-01T05:18:34","slug":"variantes-y-asociaciones-enfermedad-renal-leucemia-cancer-de-pulmon-alzheimer-hepatitis-c","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2021\/12\/01\/variantes-y-asociaciones-enfermedad-renal-leucemia-cancer-de-pulmon-alzheimer-hepatitis-c\/","title":{"rendered":"Variantes y asociaciones: enfermedad renal, leucemia, c\u00e1ncer de pulm\u00f3n, Alzheimer, hepatitis C"},"content":{"rendered":"<p>&#8211; <a href=\"https:\/\/www.science.org\/doi\/10.1126\/sciadv.abi8051\">Genome-wide association studies identify the role of caspase-9 in kidney disease<\/a><br \/>\n&#8211; <a href=\"https:\/\/www.nature.com\/articles\/s41467-021-26551-x\">Genome-wide association study identifies susceptibility loci for acute myeloid leukemia<\/a><br \/>\n&#8211; <a href=\"https:\/\/academic.oup.com\/bib\/article\/22\/6\/bbab187\/6278152\">Identification of genetic variations associated with drug resistance in non-small cell lung cancer patients undergoing systemic treatment<\/a><br \/>\n&#8211; <a href=\"https:\/\/www.cell.com\/ajhg\/fulltext\/S0002-9297(21)00386-4\">Genome-wide analysis of common and rare variants via multiple knockoffs at biobank scale, with an application to Alzheimer disease genetics<\/a><br \/>\n&#8211; <a href=\"https:\/\/www.pnas.org\/content\/118\/47\/e2107830118\">Genome-wide association study reveals genetic variants associated with HIV-1C infection in a Botswana study population<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&#8211; Genome-wide association studies identify the role of caspase-9 in kidney disease &#8211; Genome-wide association study identifies susceptibility loci for acute myeloid leukemia &#8211; Identification of genetic variations associated with drug resistance in non-small cell lung cancer patients undergoing systemic treatment &#8211; Genome-wide analysis of common and rare variants via multiple knockoffs at biobank scale, [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[11,28,29],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/5147"}],"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=5147"}],"version-history":[{"count":1,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/5147\/revisions"}],"predecessor-version":[{"id":5148,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/5147\/revisions\/5148"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=5147"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=5147"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=5147"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}