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Human Molecular Genetics|July 4, 2002
Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32Kazuhiko Nakabayashi, Louise Bentley, Megan P Hitchins, et al.
Frontiers in Neurology|May 3, 2021
An Epigenetically Distinct Subset of Children With Autism Spectrum Disorder Resulting From Differences in Blood Cell CompositionMaryam Jangjoo, Sarah J Goodman, Sanaa Choufani, et al.
NPJ Genomic Medicine|January 13, 2022
Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delayYi Liu, Yuqiang Lv, Mehdi Zarrei, et al.
NPJ Genomic Medicine|June 27, 2017
Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genesMarc Woodbury-Smith, Rob Nicolson, Mehdi Zarrei, et al.
NPJ Genomic Medicine|February 22, 2022
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variantsIslam Oguz Tuncay, Nancy L Parmalee, Raida Khalil, et al.
European Journal of Human Genetics : EJHG|July 29, 2026
Characterizing ARID1B-related disorders and variants of uncertain significance using DNA methylationAnthony Chen, Manav Jain, Danielle Baribeau, et al.
NPJ Genomic Medicine|December 22, 2017
Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosageBreanne Dale, Bonnie MacKinnon Modi, Sanne Jilderda, et al.
Genomics|September 1, 1996
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsL R Osborne, D Martindale, S W Scherer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 1, 2014
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literatureChelsea Lowther, Gregory Costain, Dimitri J Stavropoulos, et al.
Clinical Genetics|March 30, 2010
Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from PakistanM A Rafiq, M Ansar, C R Marshall, et al.
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