Clinical Assistant Professor, Department of Pediatric and Adolescent Medicine
Biosketch
Andrea Scheurer, MD, is a board-certified neonatologist employed with Southwest Michigan Neonatology. She practices at Bronson Methodist Hospital in Kalamazoo, Michigan. She is a graduate of the University of Michigan, Ann Arbor, Michigan. She earned her medical degree from Wayne State University School of Medicine. She completed a pediatric residency at Children's Hospital of Michigan in Detroit, Michigan. She completed a fellowship in neonatology at the University of Rochester, Rochester, New York.
Dr. Scheurer's professional, clinical, and research interests include neonatal outcomes for diabetic mothers and patent ductus arteriosus.
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Education and Training
- Fellowship 2010, Neonatal Medicine, University of Rochester
- Residency 2005, Pediatrics, Children's Hospital of Michigan
- MD 2002, School of Medicine, Wayne State University
- BS 1998, Biology, University of Michigan
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Research
- Neonatology
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Publications
Bejma T.A., Beidler W.S., VanSickle E.A., Prokop J.W., Brown W.T., Scheurer-Monaghan A., Rossetti L.Z. Expansion of the phenotypic spectrum of KARS1-related disorders to include arthrogryposis multiplex congenita and summary of experiences with lysine supplementation American Journal of Medical Genetics, Part A. 2024;194
Bupp C.P., Ames E.G., Arenchild M.K., Caylor S., Dimmock D.P., Fakhoury J.D., Karna P., Lehman A., Meghea C.I., Misra V., Nolan D.A., O’Shea J., Sharangpani A., Franck L.S., Scheurer-Monaghan A. Breaking Barriers to Rapid Whole Genome Sequencing in Pediatrics: Michigan’s Project Baby Deer Children. 2023;10
Chung E.H., Frueh J., Lai A., Scheurer-Monaghan A. Whole Genome Sequencing: Early Diagnostic Tool in Newborns with Refractory Seizures NeoReviews. 2022;23:e49-e55.
Franck L.S., Scheurer-Monaghan A., Bupp C.P., Fakhoury J.D., Hoffmann T.J., Deshpandey M., Arenchild M., Dimmock D.P. Healthcare Professionals’ Attitudes toward Rapid Whole Genome Sequencing in Pediatric Acute Care Children. 2022;9
Samuel S., Karpawich P., Scheurer-Monaghan A. A unique case of facial dysmorphism in an infant NeoReviews. 2018;19(2):e127-e129.
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Presentations
- BRAT 1 Mutation: Rapid Whole Genome Sequencing as an Early Diagnostic Tool in a Newborn with Antiepileptic Resistant Seizures. Hee Chung E, Freuh J, Lai A, Scheurer A, 38th Annual Kalamazoo Community Medical and Health Sciences Virtual Research Day, Kalamazoo, Michigan, 04/2021