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.

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.

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.

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.

Sex-Dependent Effects of MAOA Genotypes on the Relations Between Childhood Sexual Abuse, Aggression, and Cannabis Use in Emerging Adults.

Authors: Fite, Paula J Ryder, Annie L Baca, Selena et al.

Source: Journal of Child Sexual Abuse. May2025, Vol. 34 Issue 4, p386-403. 18p.

Subject Terms: *Academic medical centers, *Psychological adaptation, *Retrospective studies, *Child sexual abuse, *Aggression (Psychology), *Comparative studies, Adult child abuse victims, Research funding, Sex distribution, Questionnaires, Research evaluation, Multiple regression analysis, Descriptive statistics, Monoamine oxidase inhibitors, Surveys, Race, Medical records, Acquisition of data, Cannabis (Genus), Data analysis software, Genotypes, Psychosocial factors

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.

Evaluation of Autonomic Nervous System Dysfunction in Childhood Obesity and Prader–Willi Syndrome.

Authors: Richer, Lawrence P. Tan, Qiming Butler, Merlin G. et al.

Source: International Journal of Molecular Sciences. May2023, Vol. 24 Issue 9, p8013. 16p.

The Arduous Path to Drug Approval for the Management of Prader–Willi Syndrome: A Historical Perspective and Call to Action.

Authors: Singh, Deepan Miller, Jennifer L. Wassman, Edward Robert et al.

Source: International Journal of Molecular Sciences. Jul2023, Vol. 24 Issue 14, p11574. 3p.

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

Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader–Willi Syndrome.

Authors: Mahmoud, Ranim Swanson, Heidi D. Butler, Merlin G. et al.

Source: Journal of Clinical Medicine. May2022, Vol. 11 Issue 9, p2572-2572. 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

PHIP gene variants with protein modeling, interactions, and clinical phenotypes.

Authors: Dietrich, Jordan Lovell, Scott Veatch, Olivia J. et al.

Source: American Journal of Medical Genetics. Part A; Feb2022, Vol. 188 Issue 2, p579-589, 11p

A bibliometric analysis of Prader-Willi syndrome from 2002 to 2022.

Authors: Yang CX Jiang XY Li XH

Source: Open medicine (Warsaw, Poland) [Open Med (Wars)] 2024 Nov 28; Vol. 19 (1), pp. 20241058. Date of Electronic Publication: 2024 Nov 28 (Print Publication: 2024).

Publication Type: Journal Article

Journal Info: Publisher: De Gruyter Open Country of Publication: Poland NLM ID: 101672167 Publication Model: eCollection Cited Medium: Print ISSN: 2391-5463 (Print) NLM ISO Abbreviation: Open Med (Wars) Subsets: PubMed not MEDLINE

ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disorders.

Authors: Steinle, Jacob Hossain, Waheeda A. Lovell, Scott et al.

Source: American Journal of Medical Genetics. Part A; Mar2021, Vol. 185 Issue 3, p743-752, 10p

ZEB2 Gene Pathogenic Variants Across Protein-Coding Regions and Impact on Clinical Manifestations: A Review.

Authors: Hossain, Waheeda A. St. Peter, Caroline Lovell, Scott et al.

Source: International Journal of Molecular Sciences. Feb2025, Vol. 26 Issue 3, p1307. 20p.

Critical review of bariatric surgical outcomes in patients with Prader‐Willi syndrome and other hyperphagic disorders.

Authors: Gantz, Marie G. Driscoll, Daniel J. Miller, Jennifer L. et al.

Source: Obesity (19307381). May2022, Vol. 30 Issue 5, p973-981.

Impact of genetic subtypes of Prader–Willi syndrome with growth hormone therapy on intelligence and body mass index.

Authors: Butler, Merlin G. Matthews, Naomi A. Patel, Nidhi et al.

Source: American Journal of Medical Genetics. Part A; Sep2019, Vol. 179 Issue 9, p1826-1835, 10p

Birth seasonality studies in a large Prader–Willi syndrome cohort.

Authors: Butler, Merlin G. Kimonis, Virginia Dykens, Elisabeth et al.

Source: American Journal of Medical Genetics. Part A; Aug2019, Vol. 179 Issue 8, p1531-1534, 4p

Clinical Trials in Prader–Willi Syndrome: A Review.

Authors: Mahmoud, Ranim Kimonis, Virginia Butler, Merlin G.

Source: International Journal of Molecular Sciences. Feb2023, Vol. 24 Issue 3, p2150. 15p.