Search Results - "Butler, Merlin G."

Clinical Presentation, Genetics, and Laboratory Testing with Integrated Genetic Analysis of Molecular Mechanisms in Prader–Willi and Angelman Syndromes: A Review.

Authors: Butler, Merlin G.¹ (AUTHOR)

Source: International Journal of Molecular Sciences. Feb2026, Vol. 27 Issue 3, p1270. 32p.

Barriers, Limitations, and Experiences with Clinical Trials—Treatment in Rare Diseases with Prader–Willi Syndrome as an Example.

Authors: Butler, Merlin G. Silvey, Spencer van Bosse, Harold J. P.

Source: Genes. Dec2025, Vol. 16 Issue 12, p1436. 19p.

Behavioral and Psychiatric Disorders in Syndromic Autism.

Authors: Genovese, Ann C. Butler, Merlin G.

Source: Brain Sciences (2076-3425). Apr2024, Vol. 14 Issue 4, p343. 33p.

PTEN Gene and Autism: Genetic Underpinnings and Neurodevelopmental Impacts.

Authors: Genovese, Ann C. Butler, Merlin G.

Source: Genes. Sep2025, Vol. 16 Issue 9, p1061. 15p.

Prader–Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review.

Authors: Butler, Merlin G.¹ (AUTHOR) mbutler4@kumc.edu

Source: International Journal of Molecular Sciences. Mar2023, Vol. 24 Issue 5, p4271. 13p.

Chromosomal Microarray Study in Prader-Willi Syndrome.

Authors: Butler, Merlin G. Hossain, Waheeda A. Cowen, Neil et al.

Source: International Journal of Molecular Sciences. Jan2023, Vol. 24 Issue 2, p1220. 15p.

Connective Tissue Disorders and Fragile X Molecular Status in Females: A Case Series and Review.

Authors: Butler, Merlin G. Hossain, Waheeda A. Steinle, Jacob et al.

Source: International Journal of Molecular Sciences. Aug2022, Vol. 23 Issue 16, p9090-N.PAG. 10p.

Systematic Review: Fragile X Syndrome Across the Lifespan with a Focus on Genetics, Neurodevelopmental, Behavioral and Psychiatric Associations.

Authors: Genovese, Ann C. Butler, Merlin G.

Source: Genes. Feb2025, Vol. 16 Issue 2, p149. 19p.

Mass Screening for Severe Problem Behavior among Infants and Toddlers in Peru

Authors: Mayo-Ortega, Liliana Oyama-Ganiko, Rosa Leblanc, Judith et al.

Source: Journal of Mental Health Research in Intellectual Disabilities. 2012 5(3-4):246-259.

Peer Reviewed: Y

Page Count: 14

Descriptors: Behavior Problems, Early Intervention, Mental Retardation, Developmental Disabilities, Toddlers, Identification, Infants, Risk, Foreign Countries, Longitudinal Studies, Questionnaires, Evaluation, Satisfaction, Parent Attitudes, Prevention, Check Lists, Behavior Rating Scales, At Risk Persons, Screening Tests

Geographic Terms: Peru

Assessment and Survey Identifiers: Aberrant Behavior Checklist

Genetics of anomalies of the kidney and urinary tract with congenital heart disease: A review.

Authors: Barakat, Amin J. Butler, Merlin G.

Source: Clinical Genetics. Dec2024, Vol. 106 Issue 6, p667-678. 12p.

Prader-Willi Syndrome: Genetics and Behavior.

Authors: Thompson, Travis Butler, Merlin G. MacLean, William E. et al.

Source: Peabody Journal of Education. 1996 71(4):187-212.

Peer Reviewed: Y

Page Count: 26

Descriptors: Academic Achievement, Adolescents, Adults, Behavior Disorders, Child Development, Children, Cognitive Development, Developmental Disabilities, Eating Disorders, Genetics, Higher Education, Obesity, Research and Development Centers

Autonomic nervous system dysfunction in Prader–Willi syndrome.

Authors: Butler, Merlin G. Victor, A. Kaitlyn Reiter, Lawrence T.

Source: Clinical Autonomic Research. Jun2023, Vol. 33 Issue 3, p281-286. 6p.

GeneAnalytics Pathway Analysis and Genetic Overlap among Autism Spectrum Disorder, Bipolar Disorder and Schizophrenia.

Authors: Khanzada, Naveen S. Butler, Merlin G. Manzardo, Ann M.

Source: International Journal of Molecular Sciences. Mar2017, Vol. 18 Issue 3, p527. 11p. 1 Diagram, 5 Charts.

The Autism Spectrum: Behavioral, Psychiatric and Genetic Associations.

Authors: Genovese, Ann Butler, Merlin G.

Source: Genes. Mar2023, Vol. 14 Issue 3, p677. 21p.

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

Authors: Miller, Jennifer L. Gevers, Evelien Bridges, Nicola et al.

Source: Obesity (19307381). Feb2024, Vol. 32 Issue 2, p252-261.

Prader–Willi syndrome, deletion subtypes, and magnesium: Potential impact on clinical findings.

Authors: Butler, Merlin G. Cowen, Neil Bhatnagar, Anish

Source: American Journal of Medical Genetics. Part A; Nov2022, Vol. 188 Issue 11, p3278-3286, 9p

Next‐generation sequencing and analysis of consecutive patients referred for connective tissue disorders.

Authors: Steinle, Jacob Hossain, Waheeda A. Veatch, Olivia J. et al.

Source: American Journal of Medical Genetics. Part A; Oct2022, Vol. 188 Issue 10, p3016-3023, 8p

High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorders.

Authors: Butler, Merlin G. Rafi, Syed K. Manzardo, Ann M.

Source: International Journal of Molecular Sciences. 2015, Vol. 16 Issue 3, p6464-6495. 32p. 1 Diagram, 1 Chart.

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

Authors: Cox, Devin M. Butler, Merlin G.

Source: International Journal of Molecular Sciences. 2015, Vol. 16 Issue 2, p4068-4082. 15p. 1 Diagram, 5 Charts.

Whole Exome Sequencing in Females with Autism Implicates Novel and Candidate Genes.

Authors: Butler, Merlin G. Rafi, Syed K. Hossain, Waheeda et al.

Source: International Journal of Molecular Sciences. 2015, Vol. 16 Issue 1, p1312-1335. 24p. 2 Charts.