Department of Genetics faculty, postdocs, students and collaborators published four manuscripts during April 5-18, 2020.

 

Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.
Halvorsen M, Huh R, Oskolkov N, Wen J, Netotea S, Giusti-Rodriguez P, Karlsson R, Bryois J, Nystedt B, Ameur A, Kähler AK, Ancalade N, Farrell M, Crowley JJ, Li Y, Magnusson PKE, Gyllensten U, Hultman CM, Sullivan PF, Szatkiewicz JP.
Nat Commun. 2020 Apr 15;11(1):1842. doi: 10.1038/s41467-020-15707-w.
PMID: 32296054

 

Lymphatic Function and Dysfunction in the Context of Sex Differences.
Trincot CE, Caron KM.
ACS Pharmacol Transl Sci. 2019 Sep 9;2(5):311-324. doi: 10.1021/acsptsci.9b00051. eCollection 2019 Oct 11. Review.
PMID: 32259065

 

Innovation and Discovery in Cardiovascular Biology.
Caron KM.
ACS Pharmacol Transl Sci. 2019 Sep 27;2(5):291-292. doi: 10.1021/acsptsci.9b00077. eCollection 2019 Oct 11. No abstract available.
PMID: 32259063

 

Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities.
Wagner M, Skorobogatko Y, Pode-Shakked B, Powell CM, 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.
Am J Hum Genet. 2020 Feb 6;106(2):246-255. doi: 10.1016/j.ajhg.2020.01.002. Epub 2020 Jan 30.
PMID: 32004447