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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ÌÀÍ·Ìõapp 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
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. 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