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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. Among authors: wevrick r. 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
Genome-wide analysis of gene transcription in the hypothalamus.
Bischof JM, Wevrick R. Bischof JM, et al. Among authors: wevrick r. Physiol Genomics. 2005 Jul 14;22(2):191-6. doi: 10.1152/physiolgenomics.00071.2005. Epub 2005 May 3. Physiol Genomics. 2005. PMID: 15870395
Evaluation of Prader-Willi Syndrome gene MAGEL2 in severe childhood-onset obesity.
O'Neill MA, Farooqi IS, Wevrick R. O'Neill MA, et al. Among authors: wevrick r. Obes Res. 2005 Oct;13(10):1841-2. doi: 10.1038/oby.2005.224. Obes Res. 2005. PMID: 16286533
Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2.
Mercer RE, Kwolek EM, Bischof JM, van Eede M, Henkelman RM, Wevrick R. Mercer RE, et al. Among authors: wevrick r. Am J Med Genet B Neuropsychiatr Genet. 2009 Dec 5;150B(8):1085-99. doi: 10.1002/ajmg.b.30934. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19199291
Leptin signaling defects in a mouse model of Prader-Willi syndrome: An orphan genetic obesity syndrome no more?
Colmers WF, Wevrick R. Colmers WF, et al. Among authors: wevrick r. Rare Dis. 2013 Mar 27;1:e24421. doi: 10.4161/rdis.24421. eCollection 2013. Rare Dis. 2013. PMID: 25002992 Free PMC article.
Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the Magel2-null mouse model of Prader-Willi syndrome.
Pravdivyi I, Ballanyi K, Colmers WF, Wevrick R. Pravdivyi I, et al. Among authors: wevrick r. Hum Mol Genet. 2015 Aug 1;24(15):4276-83. doi: 10.1093/hmg/ddv159. Epub 2015 Apr 29. Hum Mol Genet. 2015. PMID: 25926624
Genetic analysis of very obese children with autism spectrum disorder.
Cortes HD, Wevrick R. Cortes HD, et al. Among authors: wevrick r. Mol Genet Genomics. 2018 Jun;293(3):725-736. doi: 10.1007/s00438-018-1418-5. Epub 2018 Jan 11. Mol Genet Genomics. 2018. PMID: 29327328
Chronic diazoxide treatment decreases fat mass and improves endurance capacity in an obese mouse model of Prader-Willi syndrome.
Bischof JM, Wevrick R. Bischof JM, et al. Among authors: wevrick r. Mol Genet Metab. 2018 Apr;123(4):511-517. doi: 10.1016/j.ymgme.2018.02.018. Epub 2018 Feb 27. Mol Genet Metab. 2018. PMID: 29506955
ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison.
Barclay SF, Rand CM, Nguyen L, Wilson RJA, Wevrick R, Gibson WT, Bech-Hansen NT, Weese-Mayer DE. Barclay SF, et al. Among authors: wevrick r. Orphanet J Rare Dis. 2018 Jul 20;13(1):124. doi: 10.1186/s13023-018-0860-0. Orphanet J Rare Dis. 2018. PMID: 30029683 Free PMC article.
Preclinical Testing in Translational Animal Models of Prader-Willi Syndrome: Overview and Gap Analysis.
Carias KV, Wevrick R. Carias KV, et al. Among authors: wevrick r. 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.
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