{"id":20,"date":"2012-07-23T20:20:59","date_gmt":"2012-07-23T20:20:59","guid":{"rendered":"http:\/\/portfolio-pre.uqac.ca\/gabarit\/?page_id=20"},"modified":"2016-01-20T15:15:27","modified_gmt":"2016-01-20T20:15:27","slug":"publications","status":"publish","type":"page","link":"https:\/\/portfolio.uqac.ca\/simongirard\/publications\/","title":{"rendered":"Publications choisies"},"content":{"rendered":"<h2>Articles choisis<\/h2>\n<ul>\n<li>\n<p id=\"page-title\" class=\"highwire-cite-title\"><span style=\"text-decoration: underline\"><a href=\"https:\/\/biorxiv.org\/content\/early\/2015\/12\/11\/034165\">Human copy number variants are enriched in regions of low-mappability<\/a>.<\/span>\u00a0<span class=\"highwire-citation-author first article-author-popup-processed has-tooltip\" title=\"\"><span class=\"nlm-given-names\">Jean<\/span> <span class=\"nlm-surname\">Monlong<\/span><\/span>, <span class=\"highwire-citation-author article-author-popup-processed has-tooltip\" title=\"\"><span class=\"nlm-given-names\">Caroline<\/span> <span class=\"nlm-surname\">Meloche<\/span><\/span>, <span class=\"highwire-citation-author article-author-popup-processed has-tooltip\"><span class=\"nlm-given-names\">Guy<\/span> <span class=\"nlm-surname\">Rouleau<\/span><\/span>, <span class=\"highwire-citation-author article-author-popup-processed has-tooltip\"><span class=\"nlm-given-names\">Patrick<\/span> <span class=\"nlm-surname\">Cossette<\/span><\/span>, <span class=\"highwire-citation-author article-author-popup-processed has-tooltip\"><span class=\"nlm-given-names\">Simon Louis<\/span> <span class=\"nlm-surname\">Girard<\/span><\/span>, <span class=\"highwire-citation-author article-author-popup-processed has-tooltip\"><span class=\"nlm-given-names\">Guillaume<\/span> <span class=\"nlm-surname\">Bourque.\u00a0https:\/\/biorxiv.org\/content\/early\/2015\/12\/11\/03416<\/span><\/span><\/p>\n<\/li>\n<li>\n<p id=\"page-title\" class=\"highwire-cite-title\"><span style=\"text-decoration: underline\"><a href=\"https:\/\/www.nature.com\/ejhg\/journal\/vaop\/ncurrent\/full\/ejhg2015218a.html\">De novo variants in sporadic cases of childhood onset schizophrenia<\/a>.<\/span>\u00a0Ambalavanan A, <span class=\"highlight\">Girard SL<\/span>, Ahn K, Zhou S, [&#8230;],Rapoport J, Rouleau GA.\u00a0Eur J Hum Genet. 2015<\/p>\n<\/li>\n<li>\n<p id=\"page-title\" class=\"highwire-cite-title\"><a href=\"https:\/\/journals.plos.org\/plosone\/article?id=10.1371\/journal.pone.0128988\"><span style=\"text-decoration: underline\">Mutation burden of rare variants in schizophrenia candidate genes<\/span><\/a>.<span style=\"color: #000000\"><span class=\"highlight\">Girard SL<\/span><sup>1<\/sup>, Dion PA<sup>2<\/sup>, Bourassa CV<sup>3<\/sup>\u00a0[&#8230;]\u00a0Dub\u00e9 MP<sup>8<\/sup>, Rouleau GA<sup>3<\/sup>. PLoS One. 2015\u00a0<\/span><\/p>\n<\/li>\n<li><span style=\"color: #000000\"><span style=\"text-decoration: underline\">Genome-wide association study in FTD: divide to conquer<\/span>.\u00a0<span class=\"highlight\">Girard SL and<\/span>\u00a0Rouleau GA.\u00a0Lancet Neurol. 2014<\/span><\/li>\n<\/ul>\n<ul>\n<li><span style=\"text-decoration: underline\"><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0002929712003576\">Exome sequencing identifies FUS mutations as a cause of essential tremor<\/a><\/span>.\u00a0Merner ND, <span class=\"highlight\">Girard SL<\/span>, Catoire H\u00a0[&#8230;]\u00a0Dion PA, Rouleau GA.\u00a0Am J Hum Genet. 2012<\/li>\n<\/ul>\n<ul>\n<li><span style=\"text-decoration: underline\">Increased exonic de novo mutation rate in individuals with schizophrenia.<\/span>\u00a0<b>Girard SL<\/b>\u00a0[&#8230;]\u00a0Krebs MO, Rouleau GA.\u00a0Nat Genet. 2011 [PDF:\u00a0<a title=\"PDF\" href=\"https:\/\/portfolio.uqac.ca\/simongirard\/files\/2012\/07\/ng.886.pdf\">ng.886<\/a>]<\/li>\n<\/ul>\n<ul>\n<li><span style=\"text-decoration: underline\">Where are the missing pieces of the schizophrenia genetics puzzle?<\/span>\u00a0<span class=\"highlight\">Girard SL<\/span>, Xiong L, Dion PA, Rouleau GA.\u00a0Curr Opin Genet Dev. 2011<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Articles choisis Human copy number variants are enriched in regions of low-mappability.\u00a0Jean Monlong, Caroline Meloche, Guy Rouleau, Patrick Cossette, Simon Louis Girard, Guillaume Bourque.\u00a0https:\/\/biorxiv.org\/content\/early\/2015\/12\/11\/03416 De novo variants in sporadic cases of childhood onset schizophrenia.\u00a0Ambalavanan A, Girard SL, Ahn K, Zhou S, [&#8230;],Rapoport J, Rouleau GA.\u00a0Eur J Hum Genet. 2015 Mutation burden of rare variants in &hellip; <a href=\"https:\/\/portfolio.uqac.ca\/simongirard\/publications\/\" class=\"more-link\">Continuer la lecture de <span class=\"screen-reader-text\">Publications choisies<\/span>  <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":143,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"tags":[],"_links":{"self":[{"href":"https:\/\/portfolio.uqac.ca\/simongirard\/wp-json\/wp\/v2\/pages\/20"}],"collection":[{"href":"https:\/\/portfolio.uqac.ca\/simongirard\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/portfolio.uqac.ca\/simongirard\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/portfolio.uqac.ca\/simongirard\/wp-json\/wp\/v2\/users\/143"}],"replies":[{"embeddable":true,"href":"https:\/\/portfolio.uqac.ca\/simongirard\/wp-json\/wp\/v2\/comments?post=20"}],"version-history":[{"count":15,"href":"https:\/\/portfolio.uqac.ca\/simongirard\/wp-json\/wp\/v2\/pages\/20\/revisions"}],"predecessor-version":[{"id":103,"href":"https:\/\/portfolio.uqac.ca\/simongirard\/wp-json\/wp\/v2\/pages\/20\/revisions\/103"}],"wp:attachment":[{"href":"https:\/\/portfolio.uqac.ca\/simongirard\/wp-json\/wp\/v2\/media?parent=20"}],"wp:term":[{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/portfolio.uqac.ca\/simongirard\/wp-json\/wp\/v2\/tags?post=20"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}