Butler, Merlin G.

Prader-Willi Syndrome: Consensus Diagnostic Criteria

Holm, V. A., Cassidy, S. B., Butler, M. G., Hanchett, J. M., Greenswag, L. R., Whitman, B. Y., & Greenberg, F. (1993) · Pediatrics

Genetic Syndromes and ImprintingGenomic variations and chromosomal abnormalities

Cited by 1,278

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

Butler, M. G., Dasouki, M. J., Zhou, X.-P., Talebizadeh, Z., Brown, M., Takahashi, T. N., Miles, J. H., Wang, C. H., Stratton, R., Pilarski, R., et al. (2005) · Journal of Medical Genetics

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 778

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy

Butler, M. G., Bittel, D. C., Kibiryeva, N., Talebizadeh, Z., & Thompson, T. (2004) · Pediatrics

Genetic Syndromes and ImprintingGenomic variations and chromosomal abnormalities

Cited by 298

Obese children show hyperactivation to food pictures in brain networks linked to motivation, reward and cognitive control

Bruce, A. S., Holsen, L. M., Chambers, R. J., Martin, L. E., Brooks, W. M., Zarcone, J. R., Butler, M. G., & Savage, C. R. (2010) · International Journal of Obesity

Eating Disorders and BehaviorsRegulation of Appetite and Obesity

Cited by 282

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: A susceptibility region for neurological dysfunction including developmental and language delay

Burnside, R. D., Pasion, R., Mikhail, F. M., Carroll, A. J., Robin, N. H., Youngs, E. L., Gadi, I. K., Keitges, E., Jaswaney, V. L., Papenhausen, P. R., et al. (2011) · Human Genetics

Genomic variations and chromosomal abnormalitiesGenetic Syndromes and Imprinting

Cited by 257

The 15q11.2 BP1–BP2 Microdeletion Syndrome: A Review

Cox, D., & Butler, M. (2015) · International Journal of Molecular Sciences

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 243

Neural Mechanisms Underlying Hyperphagia in Prader‐Willi Syndrome

Holsen, L. M., Zarcone, J. R., Brooks, W. M., Butler, M. G., Thompson, T. I., Ahluwalia, J. S., Nollen, N. L., & Savage, C. R. (2006) · Obesity

Regulation of Appetite and ObesityEating Disorders and Behaviors

Cited by 189

Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome

Bittel, D. C., Kibiryeva, N., & Butler, M. G. (2006) · Pediatrics

Genetic Syndromes and ImprintingGenomic variations and chromosomal abnormalities

Cited by 188

Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism

Talebizadeh, Z., Butler, M. G., & Theodoro, M. F. (2008) · Autism Research

Autism Spectrum Disorder ResearchMicroRNA in disease regulation

Cited by 157

Importance of reward and prefrontal circuitry in hunger and satiety: Prader–Willi syndrome vs simple obesity

Holsen, L. M., Savage, C. R., Martin, L. E., Bruce, A. S., Lepping, R. J., Ko, E., Brooks, W. M., Butler, M. G., Zarcone, J. R., & Goldstein, J. M. (2012) · International Journal of Obesity

Regulation of Appetite and ObesityEating Disorders and Behaviors

Cited by 128

Maladaptive behaviors and risk factors among the genetic subtypes of Prader-Willi syndrome

Hartley, S. L., MacLean, W. E., Butler, M. G., Zarcone, J., & Thompson, T. (2005) · American Journal of Medical Genetics Part A

Genetic Syndromes and ImprintingWilliams Syndrome Research

Cited by 112

Clinical and genetic aspects of the 15q11.2 BP1–BP2 microdeletion disorder

Butler, M. G. (2017) · Journal of Intellectual Disability Research

Genomic variations and chromosomal abnormalitiesGenetic Syndromes and Imprinting

Cited by 102

Diazoxide choline extended-release tablet in people with Prader-Willi syndrome: a double-blind, placebo-controlled trial

Miller, J. L., Gevers, E., Bridges, N., Yanovski, J. A., Salehi, P., Obrynba, K. S., Felner, E. I., Bird, L. M., Shoemaker, A. H., Angulo, M., et al. (2023) · The Journal of Clinical Endocrinology & Metabolism

Genetic Syndromes and ImprintingRegulation of Appetite and Obesity

Cited by 55

Diazoxide choline extended‐release tablet in people with Prader‐Willi syndrome: results from long‐term open‐label study

Miller, J. L., Gevers, E., Bridges, N., Yanovski, J. A., Salehi, P., Obrynba, K. S., Felner, E. I., Bird, L. M., Shoemaker, A. H., Angulo, M., et al. (2024) · Obesity

Genetic Syndromes and ImprintingRegulation of Appetite and Obesity

Cited by 26

Further phenotypic expansion of 15q11.2 BP1–BP2 microdeletion (Burnside-Butler) syndrome

Jerkovich, A., & Butler, M. (2015) · Journal of Pediatric Genetics

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 20

Congenital Arthrogryposis: An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?

Usrey, K. M., Williams, C. A., Dasouki, M., Fairbrother, L. C., & Butler, M. G. (2014) · Case Reports in Genetics

Genomic variations and chromosomal abnormalitiesCongenital limb and hand anomalies

Cited by 16