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International Journal of Molecular Sciences|February 13, 2025
ZEB2 Gene Pathogenic Variants Across Protein-Coding Regions and Impact on Clinical Manifestations: A ReviewWaheeda A Hossain, Caroline St Peter, Scott Lovell, 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.American Journal of Medical Genetics. Part A|July 29, 2022
Next-generation sequencing and analysis of consecutive patients referred for connective tissue disordersJacob Steinle, Waheeda A Hossain, Olivia J Veatch, 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.International Journal of Molecular Sciences|March 13, 2024
Mowat-Wilson Syndrome: Case Report and Review of <i>ZEB2</i> Gene Variant Types, Protein Defects and Molecular InteractionsCaroline St Peter, Waheeda A Hossain, Scott Lovell, 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 28