{"id":2581,"date":"2016-07-26T15:20:00","date_gmt":"2016-07-26T19:20:00","guid":{"rendered":"https:\/\/www.med.unc.edu\/genetics\/berg-published-in-clinical-cancer-research\/"},"modified":"2018-02-07T12:20:55","modified_gmt":"2018-02-07T17:20:55","slug":"berg-published-in-clinical-cancer-research","status":"publish","type":"post","link":"https:\/\/www.med.unc.edu\/genetics\/berg-published-in-clinical-cancer-research\/","title":{"rendered":"Berg published in Clinical Cancer Research"},"content":{"rendered":"<p><!-- description --><\/p>\n<p class=\"lead\">Jonathan Berg, MD, PhD, a UNC Lineberger member and an assistant professor in the UNC School of Medicine Department of Genetics, was corresponding author of a study that investigated the frequency of pathogenic germline variants in hereditary cancer susceptibility genes in cancer patients undergoing tumor-germline sequencing.<\/p>\n<div class=\"newsitem\">\n<figure id=\"attachment_2582\" class=\"thumbnail wp-caption alignnone\" style=\"width: 310px\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2582\" src=\"https:\/\/www.med.unc.edu\/genetics\/wp-content\/uploads\/sites\/481\/2017\/10\/berg-published-in-clinical-cancer-research-image-206x300.jpeg\" alt=\"Jonathan Berg, MD, PhD\" width=\"300\" height=\"436\" srcset=\"https:\/\/www.med.unc.edu\/genetics\/wp-content\/uploads\/sites\/481\/2017\/10\/berg-published-in-clinical-cancer-research-image-206x300.jpeg 206w, https:\/\/www.med.unc.edu\/genetics\/wp-content\/uploads\/sites\/481\/2017\/10\/berg-published-in-clinical-cancer-research-image.jpeg 440w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><figcaption class=\"caption wp-caption-text\">Jonathan Berg, MD, PhD<\/figcaption><\/figure>\n<\/div>\n<div class=\"newsitem\"><\/div>\n<p>~From the <a class=\"external-link\" title=\"\" href=\"http:\/\/unclineberger.org\/newsletters\/lineup\/honors-and-awards\/2016\/unc-lineberger-researchers-publish-in-clinical-cancer-research?utm_source=lineup&amp;utm_medium=email&amp;utm_campaign=20\" target=\"_blank\" rel=\"noopener noreferrer\">UNC LIneberger Newsroom<\/a><\/p>\n<p class=\" \"><span class=\"btn btn-primary btn-large\"><a class=\"external-link\" title=\"\" href=\"http:\/\/clincancerres.aacrjournals.org\/content\/early\/2016\/04\/15\/1078-0432.CCR-16-0015.full.pdf+html?sid=c57ada3f-1273-4dce-8f4d-63e05d389164\" target=\"_blank\" rel=\"noopener noreferrer\">Full Article<\/a><\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Jonathan Berg, MD, PhD, a UNC Lineberger member and an assistant professor in the UNC School of Medicine Department of Genetics, was corresponding author of a study that investigated the frequency of pathogenic germline variants in hereditary cancer susceptibility genes in cancer patients undergoing tumor-germline sequencing. ~From the UNC LIneberger Newsroom Full Article<\/p>\n","protected":false},"author":22429,"featured_media":2582,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":"","_links_to":"","_links_to_target":""},"categories":[2],"tags":[],"class_list":["post-2581","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news","odd"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Berg published in Clinical Cancer Research | Department of Genetics<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.med.unc.edu\/genetics\/berg-published-in-clinical-cancer-research\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Berg published in Clinical Cancer Research | Department of Genetics\" \/>\n<meta property=\"og:description\" content=\"Jonathan Berg, MD, PhD, a UNC Lineberger member and an assistant professor in the UNC School of Medicine Department of Genetics, was corresponding author of a study that investigated the frequency of pathogenic germline variants in hereditary cancer susceptibility genes in cancer patients undergoing tumor-germline sequencing. ~From the UNC LIneberger Newsroom Full Article\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.med.unc.edu\/genetics\/berg-published-in-clinical-cancer-research\/\" \/>\n<meta property=\"og:site_name\" content=\"Department of Genetics\" \/>\n<meta property=\"article:published_time\" content=\"2016-07-26T19:20:00+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2018-02-07T17:20:55+00:00\" \/>\n<meta property=\"og:image\" 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