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Clinical and genetic analysis of children with a dual diagnosis of Tourette syndrome and autism spectrum disorder.
Carias KV, Wevrick R. Carias KV, et al. J Psychiatr Res. 2019 Apr;111:145-153. doi: 10.1016/j.jpsychires.2019.01.023. Epub 2019 Feb 7. J Psychiatr Res. 2019. PMID: 30771620
Preclinical Testing in Translational Animal Models of Prader-Willi Syndrome: Overview and Gap Analysis.
Carias KV, Wevrick R. Carias KV, et al. Mol Ther Methods Clin Dev. 2019 Mar 14;13:344-358. doi: 10.1016/j.omtm.2019.03.001. eCollection 2019 Jun 14. Mol Ther Methods Clin Dev. 2019. PMID: 30989085 Free PMC article. Review.
The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin receptor cell surface abundance through ubiquitination pathways.
Wijesuriya TM, De Ceuninck L, Masschaele D, Sanderson MR, Carias KV, Tavernier J, Wevrick R. Wijesuriya TM, et al. Among authors: carias kv. Hum Mol Genet. 2017 Nov 1;26(21):4215-4230. doi: 10.1093/hmg/ddx311. Hum Mol Genet. 2017. PMID: 28973533 Free PMC article.
A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1.
Carias KV, Zoeteman M, Seewald A, Sanderson MR, Bischof JM, Wevrick R. Carias KV, et al. PLoS One. 2020 Apr 21;15(4):e0230874. doi: 10.1371/journal.pone.0230874. eCollection 2020. PLoS One. 2020. PMID: 32315313 Free PMC article.