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American Journal of Medical Genetics. Part A|June 22, 2019
Birth seasonality studies in a large Prader-Willi syndrome cohortMerlin G Butler, Virginia Kimonis, Elisabeth Dykens, et al.American Journal of Medical Genetics. Part A|April 4, 2017
Oxytocin treatment in children with Prader-Willi syndrome: A double-blind, placebo-controlled, crossover studyJennifer L Miller, Roy Tamura, Merlin G Butler, et al.Journal of Child Sexual Abuse|June 19, 2025
Sex-Dependent Effects of <i>MAOA</i> Genotypes on the Relations Between Childhood Sexual Abuse, Aggression, and Cannabis Use in Emerging AdultsPaula J Fite, Annie L Ryder, Selena Baca, et al.International Journal of Molecular Sciences|July 29, 2023
The Arduous Path to Drug Approval for the Management of Prader-Willi Syndrome: A Historical Perspective and Call to ActionDeepan Singh, Jennifer L Miller, Edward Robert Wassman, et al.International Journal of Molecular Sciences|March 27, 2019
Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) SyndromeKyle W Davis, Moises Serrano, Sara Loddo, et al.Case Reports in Genetics|July 4, 2014
Clinical report of a 17q12 microdeletion with additionally unreported clinical featuresJennifer L Roberts, Stephanie K Gandomi, Melissa Parra, et al.The Journal of Pediatrics|July 16, 2010
Self-injury among a community cohort of young children at risk for intellectual and developmental disabilitiesWilliam E MaClean, Raymond C Tervo, John Hoch, et al.BMC Medical Genomics|January 7, 2011
Gene expression in cardiac tissues from infants with idiopathic conotruncal defectsDouglas C Bittel, Merlin G Butler, Nataliya Kibiryeva, et al.Pediatrics|December 10, 2014
Growth charts for non-growth hormone treated Prader-Willi syndromeMerlin G Butler, Jaehoon Lee, Ann M Manzardo, et al.International Journal of Molecular Sciences|February 10, 2021
Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five FamiliesIsaac Baldwin, Robin L Shafer, Waheeda A Hossain, et al.Pageof 28