List of works - Merlin Butler

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

scientific article published on 27 December 2020

Age Distribution, Comorbidities and Risk Factors for Thrombosis in Prader-Willi Syndrome

scientific article published on 07 January 2020

An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder

scientific article published on 27 November 2020

Analysis of the Prader-Willi syndrome imprinting center using droplet digital PCR and next-generation whole-exome sequencing

scientific article published on 21 February 2019

Birth seasonality studies in a large Prader-Willi syndrome cohort

scientific article published on 21 June 2019

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders

scientific article

Clinical Assessment, Genetics, and Treatment Approaches in Autism Spectrum Disorder (ASD) ⬇️

scientific article published on 02 July 2020

Clinical Observations and Treatment Approaches for Scoliosis in Prader-Willi Syndrome

scientific article published on 28 February 2020

Contributing factors of mortality in Prader-Willi syndrome

scientific article published on 19 December 2018

Early Diagnosis in Prader-Willi Syndrome Reduces Obesity and Associated Co-Morbidities

scientific article published on 06 November 2019

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

scientific article published on 28 February 2017

GeneAnalytics Pathways and Profiling of Shared Autism and Cancer Genes ⬇️

article

Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome

scientific article published on 23 October 2020

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

scientific article published on 09 July 2019

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

scientific article published on 16 July 2019

Newborn screening for Prader-Willi syndrome is feasible: Early diagnosis for better outcomes

scientific article published on 17 December 2018

Obestatin and adropin in Prader-Willi syndrome and nonsyndromic obesity: Associations with weight, BMI-z, and HOMA-IR

scientific article published on 27 December 2018

Oxytocin treatment in children with Prader-Willi syndrome: A double-blind, placebo-controlled, crossover study.

scientific article published on 30 March 2017

Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome ⬇️

scientific article published on 22 March 2019

Prader-Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study.

scientific article published on 22 December 2017

Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.

scientific article published on 6 October 2017

Rare FMR1 gene mutations causing fragile X syndrome: A review.

scientific article published on 27 November 2017

The 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes

scientific article published on 06 May 2020

Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.

scientific article published on 13 February 2018

Venous Thromboembolism in Prader-Willi Syndrome: A Questionnaire Survey

scientific article published on 19 July 2019

List of works by Merlin Butler