Merlin G Butler (M G Butler)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 65

Top Venues

International journal of molecular sciences

American journal of medical genetics. Part A

Genes

Brain sciences

University of Kansas Medical Center

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Kansas Medical Center Jul 25 2008

United States

Professor :: psychiatry

Publications

Caroline St Peter, Waheeda A Hossain, Scott Lovell, Syed K Rafi, Merlin G Butler
Mowat-Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular Interactions. International journal of molecular sciences 25 (5) (2024)
Ann C Genovese, Merlin G Butler
Behavioral and Psychiatric Disorders in Syndromic Autism. Brain sciences 14 (4) (2024)
Ann C Genovese, Merlin G Butler
Behavioral and Psychiatric Disorders in Syndromic Autism. Brain sciences 14 (4) (2024)
Amin J Barakat, Merlin G Butler
Genetics of anomalies of the kidney and urinary tract with congenital heart disease: A review. Clinical genetics (2024)
Caroline St Peter, Waheeda A Hossain, Scott Lovell, Syed K Rafi, Merlin G Butler
Mowat-Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular Interactions. International journal of molecular sciences 25 (5) (2024)
Caroline St Peter, Waheeda A Hossain, Scott Lovell, Syed K Rafi, Merlin G Butler
Mowat-Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular Interactions. International journal of molecular sciences 25 (5) (2024)
Caroline St Peter, Waheeda A Hossain, Scott Lovell, Syed K Rafi, Merlin G Butler
Mowat-Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular Interactions. International journal of molecular sciences 25 (5) (2024)
Merlin G Butler, Waheeda A Hossain, Neil Cowen, Anish Bhatnagar
Chromosomal Microarray Study in Prader-Willi Syndrome. International journal of molecular sciences 24 (2) (2023)
Merlin G Butler
Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review. International journal of molecular sciences 24 (5) (2023)
Ranim Mahmoud, Virginia E Kimonis, Merlin G Butler
Clinical Trials in Prader-Willi Syndrome: A Review. International journal of molecular sciences 24 (3) (2023)
Ranim Mahmoud, Virginia E Kimonis, Merlin G Butler
Clinical Trials in Prader-Willi Syndrome: A Review. International journal of molecular sciences 24 (3) (2023)
Elizabeth Roof, Cheri L Deal, Shawn E McCandless, Ronald L Cowan, Jennifer L Miller, Jill K Hamilton, Elizabeth R Roeder, Shana E McCormack, Tamanna R Roshan Lal, Hussein D Abdul-Latif, Andrea M Haqq, Kathryn S Obrynba, Laura C Torchen, Alaina P Vidmar, David H Viskochil, Jean-Pierre Chanoine, Carol K L Lam, Melinda J Pierce, Laurel L Williams, Lynne M Bird, Merlin G Butler, Diane E Jensen, Susan E Myers, Oliver J Oatman, Charumathi Baskaran, Laura J Chalmers, Cary Fu, Nathalie Alos, Scott D McLean, Ajay Shah, Barbara Y Whitman, Brent A Blumenstein, Sarah F Leonard, Jessica P Ernest, Joseph W Cormier, Sara P Cotter, Davis C Ryman
Intranasal Carbetocin Reduces Hyperphagia, Anxiousness and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial. The Journal of clinical endocrinology and metabolism (2023)
Ann Genovese, Merlin G Butler
The Autism Spectrum: Behavioral, Psychiatric and Genetic Associations. Genes 14 (3) (2023)
Ann Genovese, Merlin G Butler
The Autism Spectrum: Behavioral, Psychiatric and Genetic Associations. Genes 14 (3) (2023)
Merlin G Butler
Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review. International journal of molecular sciences 24 (5) (2023)
Merlin G Butler
Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review. International journal of molecular sciences 24 (5) (2023)
Merlin G Butler
Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review. International journal of molecular sciences 24 (5) (2023)
Merlin G Butler, Waheeda A Hossain, Neil Cowen, Anish Bhatnagar
Chromosomal Microarray Study in Prader-Willi Syndrome. International journal of molecular sciences 24 (2) (2023)
Deepan Singh, Jennifer L Miller, Edward Robert Wassman, Merlin G Butler, Allison Foley Shenk, Monica Converse, Maria Picone
The Arduous Path to Drug Approval for the Management of Prader-Willi Syndrome: A Historical Perspective and Call to Action. International journal of molecular sciences 24 (14) (2023)
Lawrence P Richer, Qiming Tan, Merlin G Butler, Hayford M Avedzi, Darren S DeLorey, Ye Peng, Hein M Tun, Arya M Sharma, Steven Ainsley, Camila E Orsso, Lucila Triador, Michael Freemark, Andrea M Haqq
Evaluation of Autonomic Nervous System Dysfunction in Childhood Obesity and Prader-Willi Syndrome. International journal of molecular sciences 24 (9) (2023)
Ann Genovese, Merlin G Butler
The Autism Spectrum: Behavioral, Psychiatric and Genetic Associations. Genes 14 (3) (2023)
Elizabeth Roof, Cheri L Deal, Shawn E McCandless, Ronald L Cowan, Jennifer L Miller, Jill K Hamilton, Elizabeth R Roeder, Shana E McCormack, Tamanna R Roshan Lal, Hussein D Abdul-Latif, Andrea M Haqq, Kathryn S Obrynba, Laura C Torchen, Alaina P Vidmar, David H Viskochil, Jean-Pierre Chanoine, Carol K L Lam, Melinda J Pierce, Laurel L Williams, Lynne M Bird, Merlin G Butler, Diane E Jensen, Susan E Myers, Oliver J Oatman, Charumathi Baskaran, Laura J Chalmers, Cary Fu, Nathalie Alos, Scott D McLean, Ajay Shah, Barbara Y Whitman, Brent A Blumenstein, Sarah F Leonard, Jessica P Ernest, Joseph W Cormier, Sara P Cotter, Davis C Ryman
Intranasal Carbetocin Reduces Hyperphagia, Anxiousness and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial. The Journal of clinical endocrinology and metabolism (2023)
Merlin G Butler, Waheeda A Hossain, Neil Cowen, Anish Bhatnagar
Chromosomal Microarray Study in Prader-Willi Syndrome. International journal of molecular sciences 24 (2) (2023)
Ranim Mahmoud, Virginia E Kimonis, Merlin G Butler
Clinical Trials in Prader-Willi Syndrome: A Review. International journal of molecular sciences 24 (3) (2023)
Merlin G Butler, Waheeda A Hossain, Neil Cowen, Anish Bhatnagar
Chromosomal Microarray Study in Prader-Willi Syndrome. International journal of molecular sciences 24 (2) (2023)
Lawrence P Richer, Qiming Tan, Merlin G Butler, Hayford M Avedzi, Darren S DeLorey, Ye Peng, Hein M Tun, Arya M Sharma, Steven Ainsley, Camila E Orsso, Lucila Triador, Michael Freemark, Andrea M Haqq
Evaluation of Autonomic Nervous System Dysfunction in Childhood Obesity and Prader-Willi Syndrome. International journal of molecular sciences 24 (9) (2023)
Moris A Angulo, Merlin G Butler, Waheeda A Hossain, Mariano Castro-Magana, Jorge Corletto
Central adrenal insufficiency screening with morning plasma cortisol and ACTH levels in Prader-Willi syndrome. Journal of pediatric endocrinology & metabolism : JPEM 35 (6) (2022)
Merlin G Butler, Daniel Moreno-De-Luca, Antonio M Persico
Actionable Genomics in Clinical Practice: Paradigmatic Case Reports of Clinical and Therapeutic Strategies Based upon Genetic Testing. Genes 13 (2) (2022)
Merlin G Butler, Waheeda A Hossain, Jacob Steinle, Harry Gao, Eleina Cox, Yuxin Niu, May Quach, Olivia J Veatch
Connective Tissue Disorders and Fragile X Molecular Status in Females: A Case Series and Review. International journal of molecular sciences 23 (16) (2022)
Ranim Mahmoud, Heidi D Swanson, Merlin G Butler, Pamela Flodman, June-Anne Gold, Jennifer L Miller, Elizabeth Roof, Kathryn Osann, Elisabeth Dykens, Daniel J Driscoll, Virginia E Kimonis
Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader-Willi Syndrome. Journal of clinical medicine 11 (9) (2022)
Merlin G Butler, A Kaitlyn Victor, Lawrence T Reiter
Autonomic nervous system dysfunction in Prader-Willi syndrome. Clinical autonomic research : official journal of the Clinical Autonomic Research Society (2022)
Jacob Steinle, Waheeda A Hossain, Olivia J Veatch, Samuel P Strom, Merlin G Butler
Next-generation sequencing and analysis of consecutive patients referred for connective tissue disorders. American journal of medical genetics. Part A 188 (10) (2022)
Merlin G Butler, Neil Cowen, Anish Bhatnagar
Prader-Willi syndrome, deletion subtypes, and magnesium: Potential impact on clinical findings. American journal of medical genetics. Part A 188 (11) (2022)
Ranim Mahmoud, Virginia E Kimonis, Merlin G Butler
Genetics of Obesity in Humans: A Clinical Review. International journal of molecular sciences 23 (19) (2022)
David E Godler, Merlin G Butler
Special Issue: Genetics of Prader-Willi Syndrome. Genes 12 (9) (2021)
Albert B Poje, Merlin G Butler, Kathleen M Gustafson, Ke Liao, Laura E Martin, Merlin G Butler
Effects of Transcranial Direct Current Stimulation (tDCS) on Go/NoGo Performance Using Food and Non-Food Stimuli in Patients with Prader-Willi Syndrome. Brain sciences 11 (2) (2021)
Yue Huang, Katheryn Grand, Virginia Kimonis, Merlin G Butler, Suparna Jain, Alden Yen-Wen Huang, Julian A Martinez, Stanley F Nelson, Pedro A Sanchez-Lara
Mosaic de novo SNRPN gene variant associated with Prader-Willi syndrome. Journal of medical genetics (2021)
Janice Forster, Jessica Duis, Merlin G Butler
Pharmacogenetic Testing of Cytochrome P450 Drug Metabolizing Enzymes in a Case Series of Patients with Prader-Willi Syndrome. Genes 12 (2) (2021)
Karlijn Pellikaan, Yassine Ben Brahim, Anna G W Rosenberg, Kirsten Davidse, Christine Poitou, Muriel Coupaye, Anthony Peter Goldstone, Charlotte Höybye, Tania P Markovic, Graziano Grugni, Antonino Crinò, Assumpta Caixàs, Talia Eldar-Geva, Harry J Hirsch, Varda Gross-Tsur, Merlin G Butler, Jennifer L Miller, Paul-Hugo M van der Kuy, Sjoerd A A van den Berg, Jenny A Visser, Aart J van der Lely, Laura C G de Graaff
Hypogonadism in Women with Prader-Willi Syndrome-Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion. Journal of clinical medicine 10 (24) (2021)
Karlijn Pellikaan, Yassine Ben Brahim, Anna G W Rosenberg, Kirsten Davidse, Christine Poitou, Muriel Coupaye, Anthony Peter Goldstone, Charlotte Höybye, Tania P Markovic, Graziano Grugni, Antonino Crinò, Assumpta Caixàs, Talia Eldar-Geva, Harry J Hirsch, Varda Gross-Tsur, Merlin G Butler, Jennifer L Miller, Sjoerd A A van den Berg, Aart J van der Lely, Laura C G de Graaff
Hypogonadism in Adult Males with Prader-Willi Syndrome-Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion. Journal of clinical medicine 10 (19) (2021)
Jordan Dietrich, Scott Lovell, Olivia J Veatch, Merlin G Butler
PHIP gene variants with protein modeling, interactions, and clinical phenotypes. American journal of medical genetics. Part A (2021)
Ranim Mahmoud, Anna Leonenko, Merlin G Butler, Pamela Flodman, June-Anne Gold, Jennifer L Miller, Elizabeth Roof, Elisabeth Dykens, Daniel J Driscoll, Virginia E Kimonis
Influence of molecular classes and growth hormone treatment on growth and dysmorphology in Prader-Willi syndrome: A multicenter study. Clinical genetics 100 (1) (2021)
Isaac Baldwin, Robin L Shafer, Waheeda A Hossain, Sumedha Gunewardena, Olivia J Veatch, Matthew W Mosconi, Merlin G Butler
Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families. International journal of molecular sciences 22 (4) (2021)
Syed K Rafi, Merlin G Butler
The 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes. International journal of molecular sciences 21 (9) (2020)
Ann Genovese, Merlin G Butler
Clinical Assessment, Genetics, and Treatment Approaches in Autism Spectrum Disorder (ASD). International journal of molecular sciences 21 (13) (2020)
Andrea S Montes, Kathryn E Osann, June Anne Gold, Roy N Tamura, Daniel J Driscoll, Merlin G Butler, Virginia E Kimonis
Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome. Genes 11 (11) (2020)
Jacob Steinle, Waheeda A Hossain, Scott Lovell, Olivia J Veatch, Merlin G Butler
ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disorders. American journal of medical genetics. Part A 185 (3) (2020)
Olivia J Veatch, Merlin G Butler, Sarah H Elsea, Beth A Malow, James S Sutcliffe, Jason H Moore
An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder. International journal of molecular sciences 21 (23) (2020)
Syed K Rafi, Alberto Fernández Jaén, Sara Álvarez, Owen W Nadeau, Merlin G Butler
High Functioning Autism with Missense Mutations in Synaptotagmin-Like Protein 4 (SYTL4) and Transmembrane Protein 187 (TMEM187) Genes: SYTL4- Protein Modeling, Protein-Protein Interaction, Expression Profiling and MicroRNA Studies. International journal of molecular sciences 20 (13) (2019)
Samantha N Hartin, Waheeda A Hossain, David Francis, David E Godler, Sangjucta Barkataki, Merlin G Butler
Analysis of the Prader-Willi syndrome imprinting center using droplet digital PCR and next-generation whole-exome sequencing. Molecular genetics & genomic medicine 7 (4) (2019)
Alexander P Gabrielli, Merlin G Butler, Merlin G Butler
GeneAnalytics Pathways and Profiling of Shared Autism and Cancer Genes. International journal of molecular sciences 20 (5) (2019)
Merlin G Butler, Virginia E Kimonis, Elisabeth Dykens, June Anne Gold, Roy Tamura, Jennifer L Miller, Daniel J Driscoll
Birth seasonality studies in a large Prader-Willi syndrome cohort. American journal of medical genetics. Part A 179 (8) (2019)
Virginia E Kimonis, Roy Tamura, June-Anne Gold, Nidhi Patel, Abhilasha Surampalli, Javeria Manazir, Jennifer L Miller, Elizabeth Roof, Elisabeth Dykens, Merlin G Butler, Daniel J Driscoll
Early Diagnosis in Prader-Willi Syndrome Reduces Obesity and Associated Co-Morbidities. Genes 10 (11) (2019)
Merlin G Butler, Janalee Heinemann, Barbara McManus, Carolyn Loker, James Loker, Merlin G Butler
Venous Thromboembolism in Prader-Willi Syndrome: A Questionnaire Survey. Genes 10 (7) (2019)
Kyle Walter Davis, Moises Serrano, Sara Loddo, Catherine Robinson, Viola Alesi, Bruno Dallapiccola, Antonio Novelli, Merlin G Butler
Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome. International journal of molecular sciences 20 (6) (2019)
Merlin G Butler, Naomi A Matthews, Nidhi Patel, Abhilasha Surampalli, June-Anne Gold, Manaswitha Khare, Travis Thompson, Suzanne B Cassidy, Virginia E Kimonis
Impact of genetic subtypes of Prader-Willi syndrome with growth hormone therapy on intelligence and body mass index. American journal of medical genetics. Part A 179 (9) (2019)
Jennifer Proffitt, Kathryn Osann, Barbara McManus, Virginia E Kimonis, Janalee Heinemann, Merlin G Butler, David A Stevenson, June-Anne Gold
Contributing factors of mortality in Prader-Willi syndrome. American journal of medical genetics. Part A 179 (2) (2018)
Samantha N Hartin, Waheeda A Hossain, Nicolette Weisensel, Merlin G Butler
Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review. American journal of medical genetics. Part A 176 (4) (2018)
Merlin G Butler, Waheeda A Hossain, Robert Tessman, Partha C Krishnamurthy
Preliminary observations of mitochondrial dysfunction in Prader-Willi syndrome. American journal of medical genetics. Part A 176 (12) (2018)
Merlin G Butler, N Weisensel, S Ayala, W Hossain, Merlin G Butler
Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults. Clinical genetics 93 (3) (2018)
Ranim Mahmoud, Preeti Singh, Lan Weiss, Anita Lakatos, Melanie Oakes, Waheeda Hossain, Merlin G Butler, Virginia E Kimonis
Newborn screening for Prader-Willi syndrome is feasible: Early diagnosis for better outcomes. American journal of medical genetics. Part A 179 (1) (2018)
Camila E Orsso, Andrew A Butler, Michael Muehlbauer, H N Cui, Daniela A Rubin, Mohammadreza Pakseresht, Merlin G Butler, C M Prado, Michael Freemark, Andrea M Haqq
Obestatin and adropin in Prader-Willi syndrome and nonsyndromic obesity: Associations with weight, BMI-z, and HOMA-IR. Pediatric obesity 14 (5) (2018)
Adam F Sitzmann, Robert T Hagelstrom, Flora Tassone, Randi J Hagerman, Merlin G Butler
Rare FMR1 gene mutations causing fragile X syndrome: A review. American journal of medical genetics. Part A 176 (1) (2017)
Jennifer L Miller, Roy Tamura, Merlin G Butler, Virginia Kimonis, Carlos Sulsona, June-Anne Gold, Daniel J Driscoll
Oxytocin treatment in children with Prader-Willi syndrome: A double-blind, placebo-controlled, crossover study. American journal of medical genetics. Part A 173 (5) (2017)
Merlin G Butler, Virginia Kimonis, Elisabeth Dykens, June A Gold, Jennifer Miller, Roy Tamura, Daniel J Driscoll
Prader-Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study. American journal of medical genetics. Part A 176 (2) (2017)

Merlin G Butler.css-eqlu8i{font-size:small;padding-left:4px;} (M G Butler)

Publication Activity (10 Years)

Top Topics

Top Venues

Merlin G Butler (M G Butler)