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Genes|January 27, 2021
Pharmacogenetic Testing of Cytochrome P450 Drug Metabolizing Enzymes in a Case Series of Patients with Prader-Willi SyndromeJanice Forster, Jessica Duis, Merlin G ButlerAmerican Journal of Medical Genetics. Part A|March 3, 2004
Eye abnormalities in Fryns syndromeDiane M Pierson, Eugenio Taboada, Merlin G ButlerGenes|March 4, 2020
Clinical Observations and Treatment Approaches for Scoliosis in Prader-Willi SyndromeHarold J P van Bosse, Merlin G ButlerCurrent Opinion in Psychiatry|January 13, 2025
Genetics of Prader-Willi and Angelman syndromes: 2024 updateDavid E Godler, Deepan Singh, Merlin G ButlerGenes|January 16, 2020
Age Distribution, Comorbidities and Risk Factors for Thrombosis in Prader-Willi SyndromeMerlin G Butler, Aderonke Oyetunji, Ann M ManzardoGenomics|September 5, 2006
X chromosome gene expression in human tissues: male and female comparisonsZohreh Talebizadeh, Stephen D Simon, Merlin G ButlerPediatrics|September 20, 2006
Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndromeDouglas C Bittel, Nataliya Kibiryeva, Merlin G ButlerCurrent Genomics|February 2, 2012
Genetics and mitochondrial abnormalities in autism spectrum disorders: a reviewSukhbir Dhillon, Jessica A Hellings, Merlin G ButlerGene|October 17, 2017
Functional analysis of schizophrenia genes using GeneAnalytics program and integrated databasesTharani Sundararajan, Ann M Manzardo, Merlin G ButlerAutism Research : Official Journal of the International Society for Autism Research|April 11, 2009
Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autismZohreh Talebizadeh, Merlin G Butler, Mariana F TheodoroPageof 24