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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.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 23, 2024
Inhibiting mtDNA transcript translation alters Alzheimer's disease-associated biologyAlexander P Gabrielli, Lesya Novikova, Amol Ranjan, et al.Scientific Reports|December 24, 2025
Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader-Willi syndromeShokouh Shahrokhi, Emma K Baker, Michael See, et al.Human Genetics|March 2, 2011
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delayRachel D Burnside, Romela Pasion, Fady M Mikhail, et al.The Journal of Clinical Endocrinology and Metabolism|January 13, 2023
Diazoxide Choline Extended-Release Tablet in People With Prader-Willi Syndrome: A Double-Blind, Placebo-Controlled TrialJennifer L Miller, Evelien Gevers, Nicola Bridges, et al.JAMA Network Open|January 4, 2022
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic WorkflowDavid E Godler, Ling Ling, Dinusha Gamage, et al.Pageof 26