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American Journal of Medical Genetics. Part A|November 28, 2017
Rare FMR1 gene mutations causing fragile X syndrome: A reviewAdam F Sitzmann, Robert T Hagelstrom, Flora Tassone, et al.International Journal of Molecular Sciences|July 21, 2019
High Functioning Autism with Missense Mutations in Synaptotagmin-Like Protein 4 (SYTL4) and Transmembrane Protein 187 (TMEM187) Genes: SYTL4- Protein Modeling, Protein-Protein Interaction, Expression Profiling and MicroRNA StudiesSyed K Rafi, Alberto Fernández-Jaén, Sara Álvarez, et al.American Journal of Medical Genetics. Part A|May 24, 2016
Higher plasma orexin A levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controlsAnn M Manzardo, Lisa Johnson, Jennifer L Miller, et al.CNS Neuroscience & Therapeutics|June 29, 2018
Tobacco and cannabis use in college students are predicted by sex-dimorphic interactions between MAOA genotype and child abusePaula J Fite, Shaquanna Brown, Waheeda Hossain, et al.American Journal of Medical Genetics. Part A|December 1, 2015
Elevated plasma oxytocin levels in children with Prader-Willi syndrome compared with healthy unrelated siblingsLisa Johnson, Ann M Manzardo, Jennifer L Miller, et al.American Journal of Medical Genetics. Part A|August 13, 2016
Higher plasma orexin a levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controlsAnn M Manzardo, Lisa Johnson, Jennifer L Miller, et al.Journal of Mental Health Research in Intellectual Disabilities|February 7, 2017
Long-Term Aripiprazole in Youth With Developmental Disabilities Including AutismJessica A Hellings, Danna Boehm, Hung Wen Yeh, et al.Genetics Research International|November 18, 2014
Clinical Presentation and Microarray Analysis of Peruvian Children with Atypical Development and/or Aberrant BehaviorMerlin G Butler, Kelly Usrey, Jennifer L Roberts, et al.American Journal of Medical Genetics. Part A|January 20, 2007
Whole genome microarray analysis of gene expression in Prader-Willi syndromeDouglas C Bittel, Nataliya Kibiryeva, Susan M Sell, et al.International Journal of Molecular Sciences|January 10, 2015
Whole exome sequencing in females with autism implicates novel and candidate genesMerlin G Butler, Syed K Rafi, Waheeda Hossain, et al.Pageof 24