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Journal of Child and Adolescent Psychopharmacology|May 25, 2016
Abnormal Mechanisms of Plasticity and Metaplasticity in Autism Spectrum Disorders and Fragile X SyndromeLindsay M Oberman, Fritz Ifert-Miller, Umer Najib, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 1, 2011
Chromosomal microarray testing influences medical managementMichael E Coulter, David T Miller, David J Harris, et al.
Frontiers in Synaptic Neuroscience|March 23, 2011
Transcranial magnetic stimulation provides means to assess cortical plasticity and excitability in humans with fragile x syndrome and autism spectrum disorderLindsay Oberman, Fritz Ifert-Miller, Umer Najib, et al.
Brain Research|October 16, 2007
Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant miceAmy Lawson-Yuen, Daniel Liu, Liqun Han, et al.
Molecular Genetics & Genomic Medicine|May 5, 2021
Confirming the contribution and genetic spectrum of de novo mutation in infantile spasms: Evidence from a Chinese cohortLiying Liu, Fang Liu, Qiuhong Wang, et al.
The Journal of Biological Chemistry|September 29, 2024
Chemical genetic analysis of enoxolone inhibition of Clostridioides difficile toxin production reveals adenine deaminase and ATP synthase as antivirulence targetsRavi K R Marreddy, Gregory A Phelps, Kelly Churion, et al.
Pediatrics|January 2, 2009
Advances in the treatment of fragile X syndromeRandi J Hagerman, Elizabeth Berry-Kravis, Walter E Kaufmann, et al.
Neurogenetics|September 24, 2015
Clinical heterogeneity associated with KCNA1 mutations include cataplexy and nonataxic presentationsCatherine A Brownstein, Alan H Beggs, Lance Rodan, et al.
The Journal of Clinical Endocrinology and Metabolism|March 18, 2015
Whole exome sequencing identifies RAI1 mutation in a morbidly obese child diagnosed with ROHHAD syndromeVidhu V Thaker, Kristyn M Esteves, Meghan C Towne, et al.
American Journal of Medical Genetics|September 5, 2002
Further delineation of cardiac abnormalities in Costello syndromeAngela E Lin, Paul D Grossfeld, Robert M Hamilton, et al.
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