{"id":8228,"date":"2025-09-26T15:11:28","date_gmt":"2025-09-26T13:11:28","guid":{"rendered":"https:\/\/ern-ithaca.eu\/?post_type=resources&#038;p=8228"},"modified":"2025-11-24T14:07:04","modified_gmt":"2025-11-24T13:07:04","slug":"ern-ithaca-webinar-non-coding-genome-humain-disease","status":"publish","type":"resources","link":"https:\/\/ern-ithaca.eu\/it\/education\/documentation-for-patients\/ern-ithaca-webinar-non-coding-genome-humain-disease\/","title":{"rendered":"ERN-ITHACA Webinar: Non-coding genome &amp; humain disease"},"content":{"rendered":"<figure class=\"wp-block-embed is-type-video is-provider-youtube wp-block-embed-youtube wp-embed-aspect-16-9 wp-has-aspect-ratio\"><div class=\"wp-block-embed__wrapper\">\n<iframe loading=\"lazy\" title=\"ERN-ITHACA Webinar: NON CODING GENOME AND HUMAN DISEASE\" width=\"640\" height=\"360\" src=\"https:\/\/www.youtube.com\/embed\/Ee23S33DI-c?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture; web-share\" referrerpolicy=\"strict-origin-when-cross-origin\" allowfullscreen><\/iframe>\n<\/div><\/figure>\n\n\n\n<div style=\"height:68px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Welcome and Introduction<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Prof. Florence PETIT, Lille University Hospital, Lille, France<\/li>\n<\/ul>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Interpreting the impact of noncoding structural variants in neurodevelopmental disorders \u2013<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Prof. Sarah VERGULT, Ghent University, Ghent, Belgium<\/li>\n<\/ul>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Finding causes of missing heritability in neurogenetic disorders: exploring the dark matter of the genome<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Dr Stefan BARAKAT, Erasmus MC, Rotterdam, Netherlands<\/li>\n<\/ul>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Enhancer hijacking: A key driver of congenital disorders<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Prof. Malte SPIELMANN, Institut f\u00fcr Humangenetik, L\u00fcbeck, Germany<\/li>\n<\/ul>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Non-coding genome in limb malformations<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Prof. Florence PETIT, Lille University Hospital, Lille, France<\/li>\n<\/ul>\n\n\n\n<p class=\"wp-block-paragraph\"><em>Discussion time<\/em><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Conclusion with speakers and moderator<\/strong>&nbsp;<\/p>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<a class=\"wp-block-ernithaca-documents\" href=\"https:\/\/ern-ithaca.eu\/wp-content\/uploads\/2025\/09\/2025-09-23-NON-CODING-GENOME-Webinar_-ITHACA-Final.pdf\"><div class=\"documents-body\">Download the POWERPOINT of the webinar<\/div><div class=\"icon-circle\"><span class=\"icon-ernithaca-document\"><\/span><\/div><\/a>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>","protected":false},"excerpt":{"rendered":"<p>Welcome and Introduction Interpreting the impact of noncoding structural variants in neurodevelopmental disorders \u2013 Finding causes of missing heritability in neurogenetic disorders: exploring the dark matter of the genome Enhancer hijacking: A key driver of congenital disorders Non-coding genome in limb malformations Discussion time Conclusion with speakers and moderator&nbsp;<\/p>","protected":false},"featured_media":8590,"template":"","tags":[],"resources-type":[17],"class_list":["post-8228","resources","type-resources","status-publish","has-post-thumbnail","hentry","resources-type-webinar"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>ERN-ITHACA Webinar: Non-coding genome &amp; 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