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Journal of Molecular Evolution|July 30, 2009
Acyl-CoA dehydrogenases: Dynamic history of protein family evolutionZuzana Swigonová, Al-Walid Mohsen, Jerry VockleyMolecular Genetics and Metabolism|November 4, 2008
Short-chain acyl-coenzyme A dehydrogenase deficiencyReena Jethva, Michael J Bennett, Jerry VockleyThe Journal of Biological Chemistry|July 12, 2003
A novel approach to the characterization of substrate specificity in short/branched chain Acyl-CoA dehydrogenaseMiao He, Thomas P Burghardt, Jerry VockleyPediatric Reports|December 30, 2017
Medium chain acyl-CoA dehydrogenase deficiency in a premature infantSteven F Dobrowolski, Lina Ghaloul-Gonzalez, Jerry VockleyAmerican Journal of Medical Genetics. Part A|October 1, 2024
Examining Roles, Challenges, and Opportunities Within the Metabolic Genetics WorkforceKara Simpson, Stephanie Offord, Chanel Suares, et al.Molecular Genetics and Metabolism|February 23, 2013
Development of clinical guidelines for inborn errors of metabolism: commentaryJerry Vockley, Kimberly A Chapman, Georgianne L ArnoldJournal of Inherited Metabolic Disease|January 17, 2022
Biomarkers for drug development in propionic and methylmalonic acidemiasNicola Longo, Jörn Oliver Sass, Agnieszka Jurecka, et al.Current Opinion in Clinical Nutrition and Metabolic Care|October 24, 2002
Diagnosis and management of defects of mitochondrial beta-oxidationJerry Vockley, Rani H Singh, David A H WhitemanJCEM Case Reports|May 7, 2026
MEN4 variant of unknown significance in two generations of patients presenting with Cushing diseaseStephanie Gambino, Akanksha Aggarwal, Jerry Vockley, et al.Journal of Inherited Metabolic Disease|February 4, 2011
Advances and challenges in the treatment of branched-chain amino/keto acid metabolic defectsIna Knerr, Natalie Weinhold, Jerry Vockley, et al.Pageof 28