MerlinG.ButlerMD

PubMed

• 8 citations
  Clinical Trials in Prader-Willi Syndrome: A Review.
  Ranim Mahmoud, Virginia Kimonis, Merlin G Butler> ;International Journal of Molecular Sciences. 2023 Jan 21
• 8 citations
  Diazoxide Choline Extended-Release Tablet in People With Prader-Willi Syndrome: A Double-Blind, Placebo-Controlled Trial.
  Jennifer L Miller, Evelien Gevers, Nicola Bridges, Jack A Yanovski, Parisa Salehi, Kathryn S Obrynba, Eric I Felner, Lynne M Bird, Ashley H Shoemaker, Moris Angulo, Me...> ;The Journal of Clinical Endocrinology and Metabolism. 2023 Jun 16
• 6 citations
  Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial.
  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, Huss...> ;The Journal of Clinical Endocrinology and Metabolism. 2023 Jun 16
• 1 citations
  Chromosomal Microarray Study in Prader-Willi Syndrome.
  Merlin G Butler, Waheeda A Hossain, Neil Cowen, Anish Bhatnagar> ;International Journal of Molecular Sciences. 2023 Jan 7
• 2 citations
  Autonomic nervous system dysfunction in Prader-Willi syndrome.
  Merlin G Butler, A Kaitlyn Victor, Lawrence T Reiter> ;Clinical Autonomic Research. 2023 Jun 1
• 1 citations
  Prader-Willi syndrome, deletion subtypes, and magnesium: Potential impact on clinical findings.
  Merlin G Butler, Neil Cowen, Anish Bhatnagar> ;American Journal of Medical Genetics. Part A. 2022 Nov 1
• 28 citations
  Genetics of Obesity in Humans: A Clinical Review.
  Ranim Mahmoud, Virginia Kimonis, Merlin G Butler> ;International Journal of Molecular Sciences. 2022 Sep 20
• Connective Tissue Disorders and Fragile X Molecular Status in Females: A Case Series and Review.
  Merlin G Butler, Waheeda A Hossain, Jacob Steinle, Harry Gao, Eleina Cox, Yuxin Niu, May Quach, Olivia J Veatch> ;International Journal of Molecular Sciences. 2022 Aug 13
• Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional study.
  Jacob Steinle, Waheeda A Hossain, Merlin G Butler, Veatch, O.> ;BMC Medical Genomics. 2022 Aug 2
• 1 citations
  Next-generation sequencing and analysis of consecutive patients referred for connective tissue disorders.
  Jacob Steinle, Waheeda A Hossain, Olivia J Veatch, Samuel P Strom, Merlin G Butler> ;American Journal of Medical Genetics. Part A. 2022 Oct 1
• 2 citations
  Central adrenal insufficiency screening with morning plasma cortisol and ACTH levels in Prader-Willi syndrome.
  Moris A Angulo, Merlin G Butler, Waheeda A Hossain, Mariano Castro-Magana, Jorge Corletto> ;Journal of Pediatric Endocrinology & Metabolism. 2022 Jun 27
• 8 citations
  Syndromic and Nonsyndromic Obesity: Underlying Genetic Causes in Humans.
  Jessica Duis, Merlin G Butler> ;Advanced Biology. 2022 Oct 1
• 1 citations
  Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader-Willi Syndrome.
  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,...> ;Journal of Clinical Medicine. 2022 May 4
• 13 citations
  Critical review of bariatric surgical outcomes in patients with Prader-Willi syndrome and other hyperphagic disorders.
  Marie G Gantz, Daniel J Driscoll, Jennifer L Miller, Jessica B Duis, Merlin G Butler, Linda Gourash, Janice Forster, Ann O Scheimann> ;Obesity. 2022 May 1
• 7 citations
  Actionable Genomics in Clinical Practice: Paradigmatic Case Reports of Clinical and Therapeutic Strategies Based upon Genetic Testing.
  Merlin G Butler, Daniel Moreno-De-Luca, Antonio M Persico> ;Genes. 2022 Feb 10
• 8 citations
  Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic Workflow.
  David E Godler, Ling Ling, Dinusha Gamage, Emma K Baker, Minh Bui, Michael J Field, Carolyn Rogers, Merlin G Butler, Alessandra Murgia, Emanuela Leonardi, Roberta Poll...> ;JAMA Network Open. 2022 Jan 4
• 4 citations
  Genetic conditions of short stature: A review of three classic examples.
  Merlin G Butler, Bradley S Miller, Alicia Romano, Judith Ross, M Jennifer Abuzzahab, Philippe Backeljauw, Vaneeta Bamba, Amrit Bhangoo, Nelly Mauras, Mitchell Geffner> ;Frontiers in Endocrinology. 2022 Jan 1
• 7 citations
  Hypogonadism in Women with Prader-Willi Syndrome-Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Dis...
  Karlijn Pellikaan, Yassine Ben Brahim, Anna G W Rosenberg, Kirsten Davidse, Christine Poitou, Muriel Coupaye, Anthony P Goldstone, Charlotte Høybye, Tania P Markovic, ...> ;Journal of Clinical Medicine. 2021 Dec 10
• 4 citations
  PHIP gene variants with protein modeling, interactions, and clinical phenotypes.
  Jordan E. Dietrich, Scott Lovell, Olivia J. Veatch, Merlin G. Butler> ;American Journal of Medical Genetics. Part A. 2021 Nov 13
• 18 citations
  Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental Syndromes.
  , , , , , , , , , , , , , , , , , , , , > ;Pediatric Neurology. 2021 Oct 1
• 10 citations
  Hypogonadism in Adult Males with Prader-Willi Syndrome-Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Pan...
  Karlijn Pellikaan, Yassine Ben Brahim, Anna G W Rosenberg, Kirsten Davidse, Christine Poitou, Muriel Coupaye, Anthony P. Goldstone, Charlotte Höybye, Tania P. Markovic...> ;Journal of Clinical Medicine. 2021 Sep 24
• 2 citations
  Special Issue: Genetics of Prader-Willi Syndrome.
  David E. Godler, Merlin G. Butler> ;Genes. 2021 Sep 16
• 5 citations
  Mosaic de novo SNRPN gene variant associated with Prader-Willi syndrome
  Yue Huang, Katheryn Grand, Virginia Kimonis, Merlin G. Butler, Suparna Jain, Alden Y. Huang, Julian A. Martinez-Agosto, Stanley F. Nelson, Pedro A. Sanchez-Lara> ;Journal of Medical Genetics. 2021 Jun 7
• 11 citations
  A Streamlined Approach to Prader-Willi and Angelman Syndrome Molecular Diagnostics.
  Samuel P. Strom, Waheeda A. Hossain, Melina Grigorian, Mickey Li, Joseph Fierro, William A Scaringe, Hai-Yun Yen, Mirandy Teguh, Joanna Liu, Harry Gao, Merlin G. Butler> ;Frontiers in Genetics. 2021 May 11
• 1 citations
  Prolapsed Rectum and Risk Factors in Prader–Willi Syndrome: A Case-Based Review
  Merlin G. Butler> ;Journal of Pediatric Genetics. 2021 Mar 3
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Journal Articles

• Newborn Screening for Prader–Willi Syndrome Is Feasible: Early Diagnosis for Better Outcomes  
  Virginia Kimonis, Merlin G Butler, American Journal of Medical Genetics Part A
• Preliminary Observations of Mitochondrial Dysfunction in Prader–Willi Syndrome  
  Merlin Butler, MD, American Journal of Medical Genetics Part A
• Rare FMR1 Gene Mutations Causing Fragile X Syndrome: A Review  
  Merlin G Butler, Randi J Hagerman, Adam F Sitzmann, American Journal of Medical Genetics Part A
• Exon microarray analysis of human dorsolateral prefrontal cortex in alcoholism  
  Manzardo, A.M., Gunewardena, S., Wang, K. & Butler, M.G., Alcohol Clin Exp Res, 1/1/2014
• Risk factors for self-injury, aggression, and stereotyped behavior among young children at risk for intellectual and developmental disabilities  
  Schroeder, S. R., Marquis, J., Reese, R.M., Richman, D.M., Mayo-Ortega, L., Oyama-Ganiko, R., LeBlanc, J., Brady, N., Butler, M.G., Peacock, G., Foster, J., Johnson, T..., Am J Intell Dev Disabil, 1/1/2014
• Clinical report of a 17q12 microdeletion with additionally unreported clinical features  
  Roberts, J.L., Gandomi, S.K., Parra, M., Liu, I., Gau, C., Dasouki, M. & Butler, M.G., Case Reports Genet, 1/1/2014
• Congenital arthrogryposis: An extension of the 15q112 BP1-BP2 microdeletion syndrome?  
  Usrey, K.M., Williams, C.A., Dasouki, M., Fairbrother, L.C. & Butler, M.G., Case Reports Genet, 1/1/2014
• A 5 month old boy with delay in growth and development and decreased muscle tone: A commentary  
  Butler, M.G., Clin Chem, 1/1/2014
• Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology (ART) In Prader-Willi syndrome  
  Gold, J., Ruth, C., Lee, H-S., Butler, M.G., Driscoll, D., Dykens, E., Roof, E., McManus, B., Heinemann, J., Cassidy, S., & Kimonis, V., Genet Med, 1/1/2014
• Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology An erratum  
  Gold, J.A., Ruth, C., Osann, K., Flodman, P., McManus, B., Lee, H.S., Donkervoort, S., Khare, M., Roof, E., Miller, J.L., Driscoll, D.J., Butler, M.G., Heinemann, J., ..., Genet Med, 1/1/2014
• Clinical presentation and microarray analysis of Peruvian children with atypical developmental and/or aberrant behavior  
  Butler, M.G., Usrey, K.M, Roberts, J.L., Schroeder, S.R. & Manzardo, A.M., Genet Res Int, 1/1/2014
• Further phenotypic expansion of 15q112 BP1-BP2 microdeletion (Burnside-Butler) syndrome  
  Jerkovich, A.M. & Butler, M.G., J Ped Genet, 1/1/2014
• Clinically relevant candidate and known genes for autism spectrum disorders with representation on high resolution chromosome ideograms  
  Butler, M.G., Rafi, S.K. & Manzardo, A.M., OA Autism, 1/1/2014
• Hyperphagia-current concepts and future directions: Proceedings of the 2nd International Conference on Hyperphagia  
  Heymsfield, S.B., Avena, N.M., Baier, L., Brantley, P., Bray, G., Burnett, L.C., Butler, M.G., Driscoll, D.J., Elmquist, J., Forster, J.L., Goldstone, T., Gourash, L...., Obesity, 1/1/2014
• Growth charts for non-growth hormone treated Prader-Willi syndrome individuals from 3 to 18 years  
  Butler, M.G., Lee, J., Manzardo, A.M., Gold, J.A., Kimonis, V., Miller, J.L. & Driscoll, D.J., Pediatrics, 1/1/2014
• Plasma cytokine levels in children with autistic disorder and unrelated siblings  
  Manzardo, A.M., Henkhaus, R., Dhillon, S. & Butler, M.G., Psychology Progress, 1/1/2013
• Growth hormone receptor (GHR) gene polymorphism and Prader-Willi syndrome  
  Butler, M.G., J. Roberts, J. Hayes, X. Tan & Manzardo, A.M., Am J Med Genet, 1/1/2013
• Laparoscopic sleeve gastrectomy in 108 obese children and adolescents aged 5 to 21 years  
  Scheimann, A.O., Nadler, E., Driscoll, D.J., Butler, M.G., Miller, J.L., Sheffield, V., Markovic, T.P. & Goldstone, A.P., Ann Surg, 1/1/2013
• Comparison of biological specimens and DNA collection methods for PCR amplification and microarray analysis  
  Rethmeyer, J., Tan, X., Manzardo, A., Schroeder, S.R. & Butler, M.G., Clin Chem Lab Med, 1/1/2013
• Overexpression of the miRNA cluster at chromosome 14q32 in the alcoholic brain correlates with suppression of predicted target mRNA required for oligodendrocyte proli...  
  Manzardo, A.M., Gunewardena, S. & Butler, M.G., Gene, 1/1/2013
• Effects of growth hormone treatment in adults with Prader-Willi syndrome  
  Butler, M.G., Smith, B., Lee, J., Gibson, C., Schmoll, C., Moore, W. & Donnelly, J.E., Growth Horm, 1/1/2013
• Growth Hormone Research Society workshop summary: Consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome  
  Deal, C., Tony, M., Hoybye, C., Allen, D., Tauber, M., Sandahl- Christiansen, J., Butler, M.G. and the 2011 GH in PWS Clinical Care Guidelines Workshop Participants, J Clin Endo Metab, 1/1/2013
• 20q132-q1333 deletion syndrome: A case report  
  Butler, M.G., Usrey, K.M., Roberts, J.L., Manzardo, A.M. & Schroeder, S.R., J Ped Genet, 1/1/2013
• The neuroanatomy of genetic subtype differences in Prader-Willi syndrome  
  Honea, R.A., Holsen, L.M., Lepping, R.J., Perea, R., Butler, M.G., Brooks, W.M. & Savage, C.R., Am J Med Genet, 1/1/2012
• Development and implementation of electronic growth charts for infants with Prader-Willi syndrome  
  Rosenbloom, S.T. & Butler, M.G., Am J Med Genet, 1/1/2012
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Books/Book Chapters

• The Identification of the Genetic Components of Autism Spectrum Disorders 
  Editors: Butler, M.G. (guest editor).MDPI AG, Basel, Switzerland2015
• 2015 Year Book of Pediatrics (Special Issue “International Journal of Molecular Sciences”) 
  Chapter: Prevalence of Prader-Willi syndrome among infants with hypotonia: A commentary. 
  Butler, M.G.Editors: M. Cabana.Elsevier Publishers, San Francisco, CA2015
• Prader-Willi Syndrome 
  Chapter: Genetic Basis, Genetic Testing and Genetic Counseling for Prader-Willi Syndrome. 
  Butler, M.G. & Cassidy, S.B.Editors: C. Hoybye.Nova Science Publishers, Inc., Hauppauge, NY2013
• Childhood Obesity: Causes, Management and Challenges 
  Chapter: Genomics of Childhood Obesity and Obesity-related Disorders. 
  Butler, M.G.Editors: P. Vinai.Nova Science Publishers, Inc., Hauppauge, NY2013
• Elsevier's First Consult 
  Chapter: Prader-Willi Syndrome. 
  Butler, M.G.Editors: M. Gilliam.Elsevier, Philadelphia, PA2013
• Introduction to Genetics- DNA Methylation, Histone Modification and Gene Regulation 
  Chapter: The Status of Epigenetics and DNA Methylation in Alcoholism. 
  Manzardo, A. M. & Butler, M.G.Editors: J Wan.iConcept Press, Ltd.2013
• Obesity- Epidemiology, Pathophysiology and Prevention 
  Chapter: Ethics Curriculum on the American Academy of Child & Adolescent Pyschiatry website (www.aacap.org). 
  Butler, M.G.Editors: D. Bagchi and H.G. Preuss.CRC Press/Taylor & Francis Group, Boca Raton, FL2012
• Clinical Genomics: Practical Applications in Adult Patient Care 
  Chapter: Prader-Willi and Angelman Syndromes: Examples of Genomic Imprinting. 
  Butler, M.G.Editors: F. Alkuraya, M. Murray, M. Babyatsky, M. Giovanni, and D. Stewart.McGraw Hill Publishers, New York, NY2012
• Handbook of Growth and Growth Monitoring in Health and Disease 
  Chapter: Growth in Prader-Willi syndrome: Anthropometric patterns and analysis. 
  Butler, M.G., & Meaney, F.J.Editors: V.R. Preedy.Springer, New York, NY2012
• Nutritional Care for Infants and Toddlers with Prader-Willi Syndrome 
  Cox, J.H., Doorlag, D., Loker, J., Loker, C., & Butler, M.G.Editors: L. Keder and D. Spencer.Prader-Willi Syndrome Association (USA), Sarasota, FL2012
• Ethics Curriculum on the American Academy of Child & Adolescent Pyschiatry website (www.aacap.org). 
  Chapter: The Ethics of Genetics in Child and Adolescent Psychiatry. 
  Cain, S & Butler, M.G.2012
• Genomics of childhood obesity (Special May Issue “Current Genomics”) 
  Page 153 - 235Butler, M.G.Editors: M.G. Butler.Bentham Science Publishers, Ltd., Oak Park, IL2011
• Obesity: Epidemiology, Pathophysiology, and Prevention 
  Chapter: Genomic imprinting disorders in obesity. 
  Editors: D. Bagchi and H.G. Preuss.CRC Press, London, United KingdomEdition 2nd,2011
• Growth Hormone and Prader-Willi Syndrome: A Reference for Families and Care Providers 
  Angulo, M., Butler, M.G., Clark, K., Hanley, D., Heinemann, J., Miller, J., van Bosse, H.J.P. & Whitman, B.Y.Editors: D.G. Goranson.Prader-Willi Syndrome Association (USA), Sarasota, FLEdition 2nd,2011
• Encyclopedia of Life Sciences 
  Chapter: Imprinting disorders. 
  Henkhaus, R., Feinberg, A.P., Niemitz, E.L., & Butler, M.G.Editors: D. Cooper.John Wiley & Sons, Ltd, Chichester, United Kingdom2011
• Neuroscience in the 21st Century 
  Chapter: Prader-Willi and Angelman syndromes: Examples of genomic imprinting. 
  Butler, M.G.Editors: D. Pfaff.Springer, New York, NY2011
• Obesity Before Birth 
  Chapter: Known clinical epigenetic disorders with an obesity phenotype: Prader-Willi syndrome and the GNAS locus. 
  Butler, M.G.Editors: R. Lustig.Springer, New York, NY2011
• Intellectual Disability and Ill Health: A Review of the Evidence 
  Chapter: Congenital causes of intellectual disability. 
  Hellings, J., Grant J.A., Butler, M.G.Editors: J. O'Hara, J. McCarthy, N. Bouras.Cambridge University Press, Cambridge, MA2009
• Encyclopedia of Epidemiology 
  Chapter: Genetic counseling. 
  Page 411 - 413Butler, M.G., Begleiter, M.L., & Lund, M.M.Editors: S. Boslaugh.SAGE Publications, Thousand Oaks, CA2008
• New Encyclopedia of Neuroscience 
  Chapter: Clinical genetics, gene expression and imprinting in Prader-Willi syndrome: Invited review (MS number: 1497). 
  Bittel, D.C. & Butler, M.G.Editors: L. R. Squire.Academic Press, Oxford, England2008
• Management of Prader-Willi Syndrome 
  Chapter: Clinical findings and natural history of Prader-Willi syndrome. 
  Page 3 - 48Butler, M.G., Hanchett, J., & Thompson, T.Editors: M.G. Butler, P.D.K. Lee & B.Y. Whitman.Springer-Verlag Publishers, New York, NYEdition 3rd,2006
• Progress in Medical Genetics Research 
  Chapter: Genetics of autism with emphasis on affected females. 
  Page 149 - 182Butler, M.G., & Talebizadeh, Z.Editors: M.A. Horry.Nova Science Publishers, Hauppauge, NY2006
• Management of Prader-Willi Syndrome 
  Editors: Butler, M.G., Lee, P.D.K. & Whitman, B.Y..Springer-Verlag Publishers, New York, NYEdition 3rd,2006
• Progress in Pediatric Cardiology 
  Chapter: Gene expression in pediatric heart disease with emphasis on conotruncal defects. 
  Page 127 - 141Bittel, D.C., Kibiryeva, N., O’Brien, J.E., Lofland, G.K., & Butler, M.G.Editors: M.G. Butler.Elsevier Science, Amsterdam2005
• Genetics of Pediatric Heart Disease (Special Issue "Progress in Pediatric Cardiology") 
  Editors: Butler, M.G..Elsevier Science, Amsterdam2005
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Abstracts/Posters

• Metabolic profiling in Prader-Willi syndrome and non-syndromic obesity: Sex differences and the role of growth hormone treatment.
  Irizarry, K., Bain, J., Butler, M.G., Ilkayeva, O., Newgard, C., Muehlbauer, M., Haqq, A.M. & Freemark, M., Pediatric Academic Societies (PAS) Meeting, San Diego, CA, 1/25/2015
• Clinically relevant candidate and known genes for alcoholism with representation on high resolution chromosome ideograms.
  Butler, M.G., McGuire, A. & Manzardo, A.M., KUMC Faculty Research Conference, Kansas City, KS, 1/30/2014
• List of clinically relevant candidate and known genes for obesity and their location on high resolution chromosome ideograms.
  Butler, M.G., McGuire, A. & Manzardo, A.M., KUMC Faculty Research Conference, Kansas City, KS, 1/30/2014
• Whole exome sequencing in females with autism implicates novel and candidate genes.
  Butler, M.G., Rafi, S.K., Hossain, W., Wang, H. Stephan, D. & Manzardo, A. M., KUMC Faculty Research Conference, Kansas City, KS, 1/30/2014
• Analysis of phenotype in a large cohort of patients with Prader-Willi syndrome: Differences between gender, molecular type and growth hormone use.
  Swanson-Fellows, H., Gold, J., Osann, K., Flodman, P., Clark, S., Roof, E., Dykens, E., Butler, M.G., Miller, J., Driscoll, D. & Kimonis, V., American College of Medical Genetics and Genomics (ACMG) Annual Clinical Genetics Meeting, Nashville, TN, 1/25/2014
• Autism spectrum disorder: 629 clinically relevant candidate and known genes.
  Butler, M.G., Rafi, S.K. & Manzardo, A.M., Beyond the Diagnosis: Conference on Autism Across the Life Span, Overland Park, KS, 1/24/2014
• Clinically relevant candidate and known genes for alcoholism with representation on high resolution chromosome ideograms.
  Butler, M.G., Marshall, J.D., Rethmeyer, K., Wang, K. & Manzardo, A. M., 64th Annual Meeting of American Society of Human Genetics, San Diego, CA, 1/19/2014
• Whole exome sequencing in females with autism implicates novel and candidate genes.
  Butler, M.G., Rafi, S.K., Hossain, W., Wang, H. Stephan, D. & Manzardo, A. M., 64th Annual Meeting of American Society of Human Genetics, San Diego, CA, 1/19/2014
• Influence of CAG repeat polymorphism of the androgen receptor (AR) gene on impulsive phenotype and psychiatric symptomology in alcohol dependent men.
  Aedma, K., Butler, M.G., Poje, A.B., Penick, E.C., & Manzardo, A.M., American Psychiatric Association, San Francisco, CA, 1/18/2014
• Relationship between cytokine levels and psychiatric measures in men with alcoholism.
  Negi, R., Butler, M.G., Poje, A.B., Penick, E.C. & Manzardo, A.M., American Psychiatric Association, San Francisco, CA, 1/18/2014
• Alcoholism severity influences psychiatric symptomatology and treatment response to benfotiamine in males.
  Pendleton, T., Poje, A.B., Penick, E.C., Butler, M.G. & Manzardo, A.M., American Psychiatric Association, San Francisco, CA, 1/18/2014
• List of clinically relevant candidate and known genes for obesity and their location on high resolution chromosome ideograms.
  Butler, M.G., McGuire, A. & Manzardo, A.M., Obesity Society/ Prader-Willli Syndrome Conference, Boston, MA, 1/4/2014
• Metabolic correlates of hyperphagia and insulin sensitivity in Prader-Willi syndrome and non-syndromic obesity.
  Irizarry, K., Bain, J., Butler, M.G., Ilkayeva, O., Newgard, C., Muehlbauer, M., Broadhurst, D., Haqq, A. & Freemark, M., Pediatric Academic Societies (PAS) and Asian Society for Pediatric Research (ASPR) Joint Meeting, Vancouver, British Columbia, Canada, 1/3/2014
• LAASDAI: Loxapine add-on for adolescents and adults with autism spectrum disorders, aggression and irritability.
  Hellings, J.A., Palaguachi, G., Reed, G., Barth, F., Cain, S., Logan, M., Dunham, J., Butler, M.G., Zhou, X., Andridge, R., Aman, M. & Han, J., National Clinical Drug Evaluation Unit (NCDEU), Hollywood, FL, 1/28/2013
• Androgen receptor gene polymorphism is associated with impulsivity and alcoholism severity in women with alcoholism. (Abstract #12)
  Manzardo, A.M., Mettman, D.J., Penick, E.C., Poje, A.B. & Butler, M.G., 61st Nebraska Pyschology Symposium on Motivation: Genes and the Motivation to Use Substances, Lincoln, NE, 1/26/2013
• Androgen receptor gene polymorphism is associated with impulsivity and alcoholism severity in women with alcoholism.
  Manzardo, A.M., Mettman, D.J., Penick, E.C., Poje, A.B. & Butler, M.G., 61st Nebraska Symposium on Motivation: Genes and the Motivation to Use Substances, Lincoln, NE, 1/26/2013
• Probing genes for hyperphagia in rare obesity-related disorders.
  Butler, M.G., Marshall, J.D., Rethmeyer, K., Wang, K. & Manzardo, A. M., 63rd Annual Meeting of American Society of Human Genetics, Boston, MA, 1/25/2013
• Probing genes for hyperphagia in rare obesity-related disorders. (Abstract #589)
  Butler, M.G., Marshall, J.D., Rethmeyer, K., Wang, K. & Manzardo, A. M., 63rd Annual Meeting of American Society of Human Genetics, Boston, MA, 1/25/2013
• Androgen receptor gene polymorphism is associated with impulsivity and alcoholism severity in women with alcoholism.
  Manzardo, A.M., Mettman, D.J., Penick, E.C., Poje, A.B. & Butler, M.G., 63rd Annual Meeting of American Society of Human Genetics, Boston, MA, 1/24/2013
• Androgen receptor gene polymorphism is associated with impulsivity and alcoholism severity in women with alcoholism. (Abstract #1398)
  Manzardo, A.M., Mettman, D.J., Penick, E.C., Poje, A.B. & Butler, M.G., 63rd Annual Meeting of American Society of Human Genetics, Boston, MA, 1/24/2013
• Resources to advance research in Prader-Willi syndrome.
  Strong, T.V., Bohonowych, J., Butler, M.G. & Miller, J., International Prader-Willi Syndrome Organization (IPWSO), 8th International PWS Conference, Cambridge, United Kingdom, 1/17/2013
• LAASDAI: Loxapine add-on for adolescents and adults with autism spectrum disorders, aggression and irritability.
  Hellings, J.A., Han, J., Reed, G., Cain, S., Barth, F., Logan, M., Hayes, J. & Butler, M.G., International Meeting For Autism Research (IMFAR), Barcelona, Spain, 1/15/2013
• Genetics of obesity and obesity-related disorders.
  Butler, M.G. & Marshall, J., 7th Alstrom Syndrome International Family Conference, Research Clinic, and Scientific Symposium, Plymouth, MA, 1/11/2013
• Probing the genes for hyperphagia in obesity-related disorders.
  Butler, M.G. & Marshall, J., 7th Alstrom Syndrome International Family Conference, Research Clinic, and Scientific Symposium, Plymouth, MA, 1/9/2013
• Clinical report of a 17q12 microdeletion with additional unreported clinical features: Expansion on the phenotype.
  Gandomi, S., Roberts, J., Parra, M., Gau, C.L., & Butler, M.G., National Society of Genetic Counselors, 32nd Annual Education Conference-The Future is Now: Leading the Way in Genomic Health, Anaheim, CA, 1/9/2013
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Lectures

• RNA Sequencing in Adult Males with Obesity, Leanness or Alstrom Syndrome 
  University of Kansas Medical Center, Kansas City, KS - 1/29/2014
• Genetics of Autism and Candidate Gene Approach 
  Overland Park, KS - 1/24/2014
• Behavioral Genetics 
  Kansas University Medical Center, Kansas City, KS - 1/17/2014
• Prader-Willi Syndrome:Genetic Lessons Learned 
  Indianapolis, IN - 1/14/2014
• Psychiatry Department Annual Research Report 
  Kansas University Medical Center, Kansas City, KS - 1/12/2014
• Pitfalls and Opportunities of Conducting Clinical Trials with the Prader-Willi Syndrome Population 
  Boston, MA - 1/4/2014
• Genetics of Autism: An Update 
  Kansas University Medical Center, Kansas City, KS - 1/25/2013
• Genetics I and II 
  Kansas University Medical Center, Kansas City, KS - 1/18/2013
• Dysmorphology and Genetics 
  Kansas University Medical Center, Kansas City, KS - 1/16/2013
• Genetics of Obesity and Obesity-related Disorders 
  Plymouth, MA - 1/11/2013
• Probing the Genes for Hyperphagia in Obesity-related Disorders 
  Plymouth, MA - 1/9/2013
• Overview of Scientific Conference- Parent Session 
  Orlando, FL - 1/7/2013
• Principles and Applications of Medical Genetics and Genetic Testing 
  Kansas City, MO - 1/3/2013
• Principles and applications of medical genetics and genetic testing. 
  Kansas City, MO - 1/3/2013
• Research Activities in the KUMC Department of Psychiatry and Behavioral Sciences 
  Kansas University Medical Center, Kansas City, KS - 1/21/2012
• Medical Genetics, Behavior and Autism 
  Kansas University Medical Center, Kansas City, KS - 1/19/2012
• Probing the genes for hyperphagia in rare obesity-related syndromes. 
  Baton Rouge, LA - 1/17/2012
• Genetics of Autism: An Update and Clinical Experience 
  Kansas University Medical Center, Kansas City, KS - 1/14/2012
• Dysmorphology and Genetic Disorders 
  Kansas University Medical Center, Kansas City, KS - 1/10/2012
• Medical Genetics 
  Kansas University Medical Center, Kansas City, KS - 1/10/2012
• Psychiatry Resident Research Activities and Forum 
  Kansas University Medical Center, Kansas City, KS - 1/4/2012
• Principles of Medical Genetics and Application to Autism Spectrum Disorders 
  Kansas City, KS - 1/25/2011
• Genetics for the General Public 
  North Cross Methodist Church, Kansas City, MO - 1/22/2011
• Principles and Practice of Medical Genetics 
  Kansas City, KS - 1/21/2011
• Practice and Application of Medical Genetics in Clinical Care 
  Stormont-Vail Hospital, Topeka, KS - 1/21/2011
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Other

• Prader-Willi Syndrome Website Module: An Update 
  Butler, M.G., Welch, J., Riske, M., Vogel, R., Troxell, R., & Rope, A.
  www.medicalhomeportal.org:9090/diagnoses-and-conditions/prader-willi-syndrome/
  1/1/2011
• Is gestation in Prader-Willi syndrome affected by the genetic subtype: A commentary. 
  Butler, M.G.
  www.mdlinx.com/art_author_comment.cfm/Abbeb6ab15aeeab04
  1/1/2009
• Prader-Willi Syndrome Website Module 
  Butler, M.G., Welch, J., Riske, M., Vogel, R., Troxell, R., Rope, A.
  www.medicalhomeportal.org:9090/diagnoses-and-conditions/prader-willi-syndrome/
  1/1/2009
• Chromosome 15. In: Genetics Home Reference- Your Guide to Understanding Genetic Conditions 
  Butler, M.G.
  http://ghr.nlm.nih.gov/chromosome=15
  1/1/2006
• Angelman Syndrome. In: Genetics Home Reference- Your Guide to Understanding Genetic Conditions 
  Butler, M.G.
  http://ghr.nlm.nih.gov/condition=angelmansyndrome
  1/1/2006
• Prader-Willi Syndrome. Genetics Home Reference- Your Guide to Understanding Genetic Conditions 
  Butler, M.G.
  http://ghr.nlm.nih.gov/condition=praderwillisyndrome
  1/1/2006
• OCA2. Genetics Home Reference- Your Guide to Understanding Genetic Conditions 
  Butler, M.G.
  http://ghr.nlm.nih.gov/gene=oca2
  1/1/2006
• UBE3A. In: Genetics Home Reference- Your Guide to Understanding Genetic Conditions 
  Butler, M.G.
  http://ghr.nlm.nih.gov/gene=ube3a
  1/1/2006
• Current Therapy of Prader-Willi Syndrome; A CME Interactive Symposium. 
  Lee, P.D.K., Angulo, M., Butler, M.G., Carrel, A.L., Cassidy, S.B., Heinemann, J., Mogul, H.R., Scheimann, A. & Whitman, B.Y.
  Genetics Center, Orange, CA - 1/1/2002
• The Biology of Appetite 
  Butler MG, Discover Magazine
  1/1/2002
• Prader-Willi Syndrome: An Overview for Health Professionals. 
  Butler, M.G., Cassidy, S.B., Heinemann, J., Lee, P.D.K. & Whitman, B.Y., Titus Production Videos
  Brentwood, TN - 1/1/2001
• Prader-Willi Syndrome: The Early Years. 
  Butler, M.G., Cassidy, S.B., Heinemann, J., Lee, P.D.K., Smith, K. & Whitman, B.Y., Titus Production Videos
  Brentwood, TN - 1/1/2001
• Dissertation: Clinical and Cytogenetics Survey of the Prader-Willi Syndrome 
  Butler MG
  Indiana University, Bloomington, NE - 1/1/1984
• Clinical and Cytogenetic Survey of the Prader-Willi Syndrome. Ph.D. Thesis 
  Butler, M.G.
  Indiana University, Indianapolis, IN - 1/1/1984
• Thesis: Sister Chromatid Exchange Frequencies in Alcoholics and Recovering Alcoholics 
  Butler MG
  University of Nebraska, Lincoln, NE - 1/1/1980
• Sister chromatid exchange frequencies in alcoholics and recovering alcoholics. M.S. Thesis 
  Butler, M.G.
  University of Nebraska, Lincoln, NE - 1/1/1980
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