{"id":8403,"date":"2020-04-20T09:03:12","date_gmt":"2020-04-20T13:03:12","guid":{"rendered":"https:\/\/www.med.unc.edu\/genetics\/?p=8403"},"modified":"2020-04-20T09:03:50","modified_gmt":"2020-04-20T13:03:50","slug":"department-of-genetics-publications-for-april-5-18-2020","status":"publish","type":"post","link":"https:\/\/www.med.unc.edu\/genetics\/department-of-genetics-publications-for-april-5-18-2020\/","title":{"rendered":"Department of Genetics Publications for April 5-18, 2020"},"content":{"rendered":"

\"\"<\/p>\n

Department of Genetics faculty, postdocs, students and collaborators published four manuscripts during April 5-18, 2020.<\/p>\n

 <\/p>\n\n\n\n\n\n\n
<\/td>\nIncreased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.<\/a><\/td>\n<\/tr>\n
<\/td>\nHalvorsen M<\/strong>, Huh R, Oskolkov N, Wen J, Netotea S, Giusti-Rodriguez P<\/strong>, Karlsson R, Bryois J, Nystedt B, Ameur A, K\u00e4hler AK, Ancalade N, Farrell M, Crowley JJ, Li Y<\/strong>, Magnusson PKE, Gyllensten U, Hultman CM, Sullivan PF, Szatkiewicz JP<\/strong>.<\/td>\n<\/tr>\n
<\/td>\nNat Commun. 2020 Apr 15;11(1):1842. doi: 10.1038\/s41467-020-15707-w.<\/td>\n<\/tr>\n
<\/td>\nPMID: 32296054<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

 <\/p>\n\n\n\n\n\n\n
<\/td>\nLymphatic Function and Dysfunction in the Context of Sex Differences.<\/a><\/td>\n<\/tr>\n
<\/td>\nTrincot CE, Caron KM<\/strong>.<\/td>\n<\/tr>\n
<\/td>\nACS Pharmacol Transl Sci. 2019 Sep 9;2(5):311-324. doi: 10.1021\/acsptsci.9b00051. eCollection 2019 Oct 11. Review.<\/td>\n<\/tr>\n
<\/td>\nPMID: 32259065<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

 <\/p>\n\n\n\n\n\n\n
<\/td>\nInnovation and Discovery in Cardiovascular Biology.<\/a><\/td>\n<\/tr>\n
<\/td>\nCaron KM<\/strong>.<\/td>\n<\/tr>\n
<\/td>\nACS Pharmacol Transl Sci. 2019 Sep 27;2(5):291-292. doi: 10.1021\/acsptsci.9b00077. eCollection 2019 Oct 11. No abstract available.<\/td>\n<\/tr>\n
<\/td>\nPMID: 32259063<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

 <\/p>\n\n\n\n\n\n\n
<\/td>\nBi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities.<\/a><\/td>\n<\/tr>\n
<\/td>\nWagner M, Skorobogatko Y, Pode-Shakked B, Powell CM<\/strong>, Alhaddad B, Seibt A, Barel O, Heimer G, Hoffmann C, Demmer LA, Perilla-Young Y, Remke M, Wieczorek D, Navaratnarajah T, Lichtner P, Klee D, Shamseldin HE, Al Mutairi F, Mayatepek E, Strom T, Meitinger T, Alkuraya FS, Anikster Y, Saltiel AR, Distelmaier F.<\/td>\n<\/tr>\n
<\/td>\nAm J Hum Genet. 2020 Feb 6;106(2):246-255. doi: 10.1016\/j.ajhg.2020.01.002. Epub 2020 Jan 30.<\/td>\n<\/tr>\n
<\/td>\nPMID: 32004447<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

 <\/p>\n","protected":false},"excerpt":{"rendered":"

Department of Genetics faculty, postdocs, students and collaborators published four manuscripts during April 5-18, 2020.<\/p>\n","protected":false},"author":28418,"featured_media":6539,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":"","_links_to":"","_links_to_target":""},"categories":[2],"tags":[139,78,57,165,80,58,76,55,74,28],"class_list":["post-8403","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news","tag-ancalade","tag-caron","tag-crowley","tag-farrell","tag-giusti-rodriguez","tag-halvorsen","tag-powell","tag-sullivan","tag-szatkiewicz","tag-unc-genetics","odd"],"acf":[],"yoast_head":"\nDepartment of Genetics Publications for April 5-18, 2020 | 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\" 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