Melanie B Gillingham (Melanie Gillingham)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 8

Top Venues

Journal of inherited metabolic disease

Obesity (Silver Spring, Md.)

Communications biology

Oregon Health and Science University

University of Wisconsin Madison (PHD)

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

Affiliation History

Oregon Health and Science University

United States

Associate Professor :: Molecular and Medical Genetics

Education History

University of Wisconsin Madison

United States

PHD :: Nutritional Sciences

University Of Oklahoma College of Public Health

United States

MSC :: Nutritional Sciences

Publications

Melanie B Gillingham, Dongseok Choi, Ashley Gregor, Nida Wongchaisuwat, Danielle Black, Hannah L Scanga, Ken K Nischal, Jose-Alain Sahel, Georgianne Arnold, Jerry Vockley, Cary O Harding, Mark E Pennesi
Early diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long-chain 3-hydroxyacylCoA dehydrogenase deficiency (LCHADD) chorioretinopathy. Journal of inherited metabolic disease 47 (4) (2024)
Melanie B Gillingham, Dongseok Choi, Ashley Gregor, Nida Wongchaisuwat, Danielle Black, Hannah L Scanga, Ken K Nischal, Jose-Alain Sahel, Georgianne Arnold, Jerry Vockley, Cary O Harding, Mark E Pennesi
Early diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long-chain 3-hydroxyacylCoA dehydrogenase deficiency (LCHADD) chorioretinopathy. Journal of inherited metabolic disease 47 (4) (2024)
Melanie B Gillingham, Dongseok Choi, Ashley Gregor, Nida Wongchaisuwat, Danielle Black, Hannah L Scanga, Ken K Nischal, Jose-Alain Sahel, Georgianne Arnold, Jerry Vockley, Cary O Harding, Mark E Pennesi
Early diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long-chain 3-hydroxyacylCoA dehydrogenase deficiency (LCHADD) chorioretinopathy. Journal of inherited metabolic disease (2024)
Melanie B Gillingham, Dongseok Choi, Ashley Gregor, Nida Wongchaisuwat, Danielle Black, Hannah L Scanga, Ken K Nischal, Jose-Alain Sahel, Georgianne Arnold, Jerry Vockley, Cary O Harding, Mark E Pennesi
Early diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long-chain 3-hydroxyacylCoA dehydrogenase deficiency (LCHADD) chorioretinopathy. Journal of inherited metabolic disease 47 (4) (2024)
Andrew W McHill, Saurabh Suhas Thosar, Nicole P Bowles, Matthew P Butler, Omar H Ordaz, Jonathan S Emens, Jonathan Q Purnell, Melanie B Gillingham, Steven A Shea
Obesity alters the circadian profiles of energy metabolism and glucose regulation in humans. Obesity (Silver Spring, Md.) (2023)
Garen Gaston, Shannon Babcock, Renee Ryals, Gabriela Elizondo, Tiffany DeVine, Dahlia Wafai, William Packwood, Sarah Holden, Jacob Raber, Jonathan R Lindner, Mark E Pennesi, Cary O Harding, Melanie B Gillingham
A G1528C Hadha knock-in mouse model recapitulates aspects of human clinical phenotypes for long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Communications biology 6 (1) (2023)
Garen Gaston, Jon A Gangoiti, Shelley Winn, Benjamin Chan, Bruce A Barshop, Cary O Harding, Melanie B Gillingham
Cardiac tissue citric acid cycle intermediates in exercised very long-chain acyl-CoA dehydrogenase-deficient mice fed triheptanoin or medium-chain triglyceride. Journal of inherited metabolic disease 43 (6) (2020)
Melanie B Gillingham, Gabriela Elizondo, Annie Behrend, Dietrich Matern, Dale A Schoeller, Cary O Harding, Jonathan Q Purnell
Higher dietary protein intake preserves lean body mass, lowers liver lipid deposition, and maintains metabolic control in participants with long-chain fatty acid oxidation disorders. Journal of inherited metabolic disease 42 (5) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Melanie B Gillingham (Melanie Gillingham)