Merlin G Butler

59PUBLICATIONS
93CO-AUTHORS
Metabolic medicineNeonatologyEpigenetics (incl. genome methylation and epigenomics)PharmacogenomicsCancer genetics
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Publications (59)

|Sep 09, 2026
Comprehensive functional testing in fibroblasts has strong utility to diagnose mitochondrial disease.

|Aug 31, 2026
Influence of Molecular Genetic Classes on Behavior in Prader-Willi Syndrome.

|Feb 13, 2026
Clinical Presentation, Genetics, and Laboratory Testing with Integrated Genetic Analysis of Molecular Mechanisms in Prader-Willi and Angelman Syndromes: A Review.

Merlin G Butler

|Jan 30, 2026
Integrated Genetic and Protein Mechanisms Underlying Glucagon-like Peptide-1 Receptor Agonists in Treating Diabetes Mellitus and Weight Loss.

Lucas Francis, Merlin G Butler

|Dec 30, 2025
Barriers, Limitations, and Experiences with Clinical Trials-Treatment in Rare Diseases with Prader-Willi Syndrome as an Example.

Merlin G Butler, Spencer Silvey, Harold J P van Bosse

|Sep 27, 2025
RNA Polymerase I Dysfunction Underlying Craniofacial Syndromes: Integrated Genetic Analysis Reveals Parallels to 22q11.2 Deletion Syndrome.

Spencer Silvey, Scott Lovell, Merlin G Butler

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Frequent Collaborators

11 joint publications

Virginia Kimonis

4 joint publications

Ann Manzardo

4 joint publications

Scott Lovell

4 joint publications

Syed K Rafi