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American Journal on Intellectual and Developmental Disabilities|July 10, 2014
Risk factors for self-injury, aggression, and stereotyped behavior among young children at risk for intellectual and developmental disabilitiesStephen R Schroeder, Janet G Marquis, R Matthew Reese, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 23, 2015
Transcranial direct current stimulation reduces food-craving and measures of hyperphagia behavior in participants with Prader-Willi syndromeGabriela L Bravo, Albert B Poje, Iago Perissinotti, et al.Translational Psychiatry|October 29, 2020
Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disordersEmma K Baker, Merlin G Butler, Samantha N Hartin, et al.Archives of Otolaryngology--Head & Neck Surgery|December 21, 2005
Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafnessAbram P Vore, Eugene H Chang, Jane E Hoppe, et al.Journal of Child and Adolescent Psychopharmacology|March 18, 2015
Loxapine add-on for adolescents and adults with autism spectrum disorders and irritabilityJessica A Hellings, Gregory Reed, Sharon E Cain, et al.International Journal of Molecular Sciences|May 13, 2023
Evaluation of Autonomic Nervous System Dysfunction in Childhood Obesity and Prader-Willi SyndromeLawrence P Richer, Qiming Tan, Merlin G Butler, et al.Archives of Pathology & Laboratory Medicine|July 13, 2006
Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for yearsArthur R Brothman, Nancy R Schneider, Irene Saikevych, et al.Scientific Reports|February 17, 2017
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosisJennifer Zieba, Wenjuan Zhang, Jessica X Chong, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 10, 2013
Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technologyJune-Anne Gold, Chelsey Ruth, Kathryn Osann, et al.Journal of Medical Genetics|April 14, 2012
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleUppala Radhakrishna, Swapan K Nath, Ken McElreavey, et al.Pageof 24