{"id":2290,"date":"2013-09-26T19:55:00","date_gmt":"2013-09-26T23:55:00","guid":{"rendered":"https:\/\/med.sites.unc.edu\/genetics\/berglab\/publications\/"},"modified":"2022-09-28T16:28:47","modified_gmt":"2022-09-28T20:28:47","slug":"publications","status":"publish","type":"page","link":"https:\/\/www.med.unc.edu\/genetics\/berglab\/publications\/","title":{"rendered":"Recent publications"},"content":{"rendered":"<div id='PubMed_Publications' class='widgets_on_page wop_tiny1  wop_small1  wop_medium1  wop_large1  wop_wide1'>\n\t\t\t<ul><li id=\"rss-2\" class=\"widget widget_rss\"><h2 class=\"widgettitle\"><a class=\"rsswidget rss-widget-feed\" href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/rss\/search\/1H_ca59kJO-Kxb-jxilwtkgyX49GtDXIH6g_Dj57iNIUORbgO9\/?limit=15&#038;utm_campaign=pubmed-2&#038;fc=20220928144844\"><img decoding=\"async\" class=\"rss-widget-icon\" style=\"border:0\" width=\"14\" height=\"14\" src=\"https:\/\/www.med.unc.edu\/genetics\/berglab\/wp-includes\/images\/rss.png\" alt=\"RSS\" loading=\"lazy\" \/><\/a> <a class=\"rsswidget rss-widget-title\" href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/rss-feed\/?feed_id=1H_ca59kJO-Kxb-jxilwtkgyX49GtDXIH6g_Dj57iNIUORbgO9&#038;utm_medium=rss&#038;utm_content=1H_ca59kJO-Kxb-jxilwtkgyX49GtDXIH6g_Dj57iNIUORbgO9&#038;utm_campaign=pubmed-2&#038;v=2.18.0.post9+e462414&#038;ff=20250604121133&#038;fc=20220928144844&#038;utm_source=WordPress\">PubMed Publications<\/a><\/h2><ul><li><a class='rsswidget' href="https:\/\/pubmed.ncbi.nlm.nih.gov\/40463576\/?utm_source=WordPress&#038;utm_medium=rss&#038;utm_campaign=pubmed-2&#038;utm_content=1H_ca59kJO-Kxb-jxilwtkgyX49GtDXIH6g_Dj57iNIUORbgO9&#038;fc=20220928144844&#038;ff=20250604121133&#038;v=2.18.0.post9+e462414">Medical Multimorbidity in Patients with Treatment-Resistant Psychosis and Rare Copy Number Variants: A Retrospective Case Series of 24 Patients<\/a> <span class=\"rss-date\">June 4, 2025<\/span><\/li><li><a class='rsswidget' href="https:\/\/pubmed.ncbi.nlm.nih.gov\/40258355\/?utm_source=WordPress&#038;utm_medium=rss&#038;utm_campaign=pubmed-2&#038;utm_content=1H_ca59kJO-Kxb-jxilwtkgyX49GtDXIH6g_Dj57iNIUORbgO9&#038;fc=20220928144844&#038;ff=20250604121133&#038;v=2.18.0.post9+e462414">Age-Based Genomic Screening: Pediatric Providers&#039; Perspectives on Implementation<\/a> <span class=\"rss-date\">April 21, 2025<\/span><\/li><li><a class='rsswidget' href="https:\/\/pubmed.ncbi.nlm.nih.gov\/40227346\/?utm_source=WordPress&#038;utm_medium=rss&#038;utm_campaign=pubmed-2&#038;utm_content=1H_ca59kJO-Kxb-jxilwtkgyX49GtDXIH6g_Dj57iNIUORbgO9&#038;fc=20220928144844&#038;ff=20250604121133&#038;v=2.18.0.post9+e462414">Automated collateral assessment restricted to the hypoperfused area for distal vessel occlusions in ischemic stroke<\/a> <span class=\"rss-date\">April 14, 2025<\/span><\/li><\/ul><\/li><\/ul><\/div><!-- widgets_on_page -->\n<h3 style=\"text-align: right;\"><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=Berg+JS&amp;cauthor_id=21558861\"><strong>More&#8230;<\/strong><\/a><\/h3>\n<p>&nbsp;<\/p>\n<h2 class=\"title\">Clinical Genomics<\/h2>\n<p>&nbsp;<\/p>\n<table id=\"sortable\" class=\"table table-hover listing\" border=\"0\">\n<thead>\n<tr>\n<th><strong>Title<\/strong><\/th>\n<th><strong>Authors<\/strong><\/th>\n<th><strong>Year<\/strong><\/th>\n<th><strong><span style=\"color: #000000;\">Journal<\/span><\/strong><\/th>\n<th><strong><span style=\"color: #000000;\">Volume: Pages<\/span><\/strong><\/th>\n<th><strong><span style=\"color: #000000;\">PMID<\/span><\/strong><\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time<\/td>\n<td><strong>Berg JS<\/strong>, Khoury MJ, <strong>Evans JP<\/strong><\/td>\n<td>2011<\/td>\n<td>Genet Med<\/td>\n<td>13(6): 499-504<\/td>\n<td>21558861<\/td>\n<\/tr>\n<tr>\n<td>An informatics approach to analyzing the incidentalome<\/td>\n<td><strong>Berg JS<\/strong>, <strong>Adams M<\/strong>, Nassar N, Bizon C, <strong>Lee K<\/strong>, Schmitt CP, Wilhelmsen KC, <strong>Evans JP<\/strong><\/td>\n<td>2013<\/td>\n<td>Genet Med<\/td>\n<td>15(1): 36-44<\/td>\n<td>22995991<\/td>\n<\/tr>\n<tr>\n<td>Comprehensive molecular portraits of human breast tumours<\/td>\n<td>Cancer Genome Atlas Network<\/td>\n<td>2012<\/td>\n<td>Nature<\/td>\n<td>490(7418): 61-70<\/td>\n<td>23000897<\/td>\n<\/tr>\n<tr>\n<td>Next-generation DNA sequencing, regulation, and the limits of paternalism: the next challenge<\/td>\n<td><strong>Evans JP<\/strong>,<strong> Berg JS<\/strong><\/td>\n<td>2011<\/td>\n<td>JAMA<\/td>\n<td>306(21): 2376-7<\/td>\n<td>22147382<\/td>\n<\/tr>\n<tr>\n<td>A Genetic Counselor\u2019s Guide to Using Next-Generation<br \/>\nSequencing in Clinical Practice<\/td>\n<td>Facio FM, <strong>Lee K<\/strong>, <strong>O&#8217;Daniel JM<\/strong><\/td>\n<td>2014<\/td>\n<td>J Genet Counsel<\/td>\n<td>23(4): 455-62<\/td>\n<td>24151055<\/td>\n<\/tr>\n<tr>\n<td>The NCGENES Project:<br \/>\nExploring the New World of Genome Sequencing<\/td>\n<td><strong>Foreman AKM<\/strong>, <strong>Lee K<\/strong>, <strong>Evans JP<\/strong><\/td>\n<td>2013<\/td>\n<td>NC Med J<\/td>\n<td>74(6): 500-4<\/td>\n<td>24316776<\/td>\n<\/tr>\n<tr>\n<td>Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies<\/td>\n<td>Goddard KA, Whitlock EP, <strong>Berg JS<\/strong>, Williams MS, Webber EM, Webster JA, Lin JS, Schrader KA, Campos-Outcalt D, Offit K, Feigelson HS, Hollombe C<\/td>\n<td>2013<\/td>\n<td>Genet Med<\/td>\n<td>15(9): 721-8<\/td>\n<td>23558254<\/td>\n<\/tr>\n<tr>\n<td>Exploring concordance and discordance for return of incidental findings from clinical sequencing<\/td>\n<td>Green RC, <strong>Berg JS<\/strong>, Berry GT, Biesecker LG, Dimmock DP, <strong>Evans JP<\/strong>, Grody WW, Hegde MR, Kalia S, Korf BR, Krantz I, McGuire AL, Miller DT, Murray MF, Nussbaum RL, Plon SE, Rehm HL, Jacob HJ<\/td>\n<td>2012<\/td>\n<td>Genet Med<\/td>\n<td>14(4): 405-10<\/td>\n<td>22422049<\/td>\n<\/tr>\n<tr>\n<td>ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing<\/td>\n<td>Green RC, <strong>Berg JS<\/strong>, Grody WW, Kalia SS, Korf BR, Martin CL, McGuire AL, Nussbaum RL, <strong>O&#8217;Daniel JM<\/strong>, Ormond KE, Rehm HL, Watson MS, Williams MS, Biesecker LG<\/td>\n<td>2013<\/td>\n<td>Genet Med<\/td>\n<td>15(7): 565-74<\/td>\n<td>23788249<\/td>\n<\/tr>\n<tr>\n<td>Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia<\/td>\n<td>Knowles MR, Leigh MW, Ostrowski LE, Huang L, Carson JL, Hazucha MJ, Yin W<strong>, Berg JS<\/strong>, Davis SD, Dell SD, Ferkol TW, Rosenfeld M, Sagel SD, Milla CE, Olivier KN, Turner EH, Lewis AP, Bamshad MJ, Nickerson DA, Shendure J, Zariwala MA; Genetic Disorders of Mucociliary Clearance Consortium<\/td>\n<td>2013<\/td>\n<td>Am J Hum Genet<\/td>\n<td>92(1): 99-106<\/td>\n<td>23261302<\/td>\n<\/tr>\n<tr>\n<td>\n<p class=\" \">High Diagnostic Yield of Whole Exome Sequencing in Participants with Retinal Dystrophies in a Clinical Ophthalmology Setting.<\/p>\n<\/td>\n<td><strong>Lee K<\/strong>, <strong>Berg JS<\/strong>, <strong>Milko L<\/strong>, Crooks K, Lu M, Bizon C, Owen P, Wilhelmsen KC, Weck KE, <strong>Evans JP<\/strong>, Garg S<\/td>\n<td>2015<\/td>\n<td>Am J Opthalmol<\/td>\n<td>Epub ahead of print<\/td>\n<td>25910913<\/td>\n<\/tr>\n<tr>\n<td>\n<p class=\" \">Navigating the current landscape of clinical genetic testing<br \/>\nfor inherited retinal dystrophies<\/p>\n<\/td>\n<td><strong>Lee K<\/strong>, Garg S<\/td>\n<td>2015<\/td>\n<td>Genet Med<\/td>\n<td>17(4): 245-252<\/td>\n<td>25790163<\/td>\n<\/tr>\n<tr>\n<td>\n<p class=\" \">Whole-Genome and Whole-Exome Sequencing in Hereditary Cancer: Impact on Genetic Testing and Counseling<\/p>\n<\/td>\n<td><strong>O&#8217;Daniel JM<\/strong>, <strong>Lee K<\/strong><\/td>\n<td>2012<\/td>\n<td>Cancer J<\/td>\n<td>18(4): 287-292<\/td>\n<td>22846728<\/td>\n<\/tr>\n<tr>\n<td>ACMG clinical laboratory standards for next-generation sequencing<\/td>\n<td>Rehm HL, Bale SJ, Bayrak-Toydemir P, <strong>Berg JS<\/strong>, Brown KK, Deignan JL, Friez MJ, Funke BH, Hegde MR, Lyon E<\/td>\n<td>2013<\/td>\n<td>Genet Med<\/td>\n<td>15(9): 733-47<\/td>\n<td>23887774<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<div class=\"rprt\">\n<div class=\"rslt\">\n<p class=\"title\">\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>More&#8230; &nbsp; Clinical Genomics &nbsp; Title Authors Year Journal Volume: Pages PMID Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time Berg JS, Khoury MJ, Evans JP 2011 Genet Med 13(6): 499-504 21558861 An informatics approach to analyzing the incidentalome Berg JS, Adams M, Nassar N, &hellip; <a href=\"https:\/\/www.med.unc.edu\/genetics\/berglab\/publications\/\" aria-label=\"Read more about Recent publications\">Read more<\/a><\/p>\n","protected":false},"author":14331,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":"","_links_to":"","_links_to_target":""},"class_list":["post-2290","page","type-page","status-publish","hentry","odd"],"acf":[],"_links_to":[],"_links_to_target":[],"_links":{"self":[{"href":"https:\/\/www.med.unc.edu\/genetics\/berglab\/wp-json\/wp\/v2\/pages\/2290","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.med.unc.edu\/genetics\/berglab\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.med.unc.edu\/genetics\/berglab\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.med.unc.edu\/genetics\/berglab\/wp-json\/wp\/v2\/users\/14331"}],"replies":[{"embeddable":true,"href":"https:\/\/www.med.unc.edu\/genetics\/berglab\/wp-json\/wp\/v2\/comments?post=2290"}],"version-history":[{"count":1,"href":"https:\/\/www.med.unc.edu\/genetics\/berglab\/wp-json\/wp\/v2\/pages\/2290\/revisions"}],"predecessor-version":[{"id":3878,"href":"https:\/\/www.med.unc.edu\/genetics\/berglab\/wp-json\/wp\/v2\/pages\/2290\/revisions\/3878"}],"wp:attachment":[{"href":"https:\/\/www.med.unc.edu\/genetics\/berglab\/wp-json\/wp\/v2\/media?parent=2290"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}