AmandaBaronePritchardMD
Medical Genetics • Ann Arbor, MIClinical Genetics, Medical Biochemical Genetics, Pediatric Medical Genetics
Assistant Professor of Pediatrics Division of Pediatric Genetics, Metabolism, and Genomic Medicine
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Office
1500 E Medical Center Dr
Ann Arbor, MI 48109- Is this information wrong?
Summary
- Dr. Amanda Barone is a medical geneticist in Ann Arbor, MI and is affiliated with multiple hospitals in the area, including Children's Hospital of Philadelphia and Michigan Medicine. She received her medical degree from University of Pittsburgh School of Medicine and has been in practice 5 years. She specializes in clinical genetics, medical biochemical genetics, and pediatric medical genetics. She has 1 publication and over 50 citings.
Education & Training
Children's Hospital of PhiladelphiaFellowship, Medical Biochemical Genetics, 2017 - 2018
McGaw Medical Center of Northwestern UniversityResidency, Pediatrics, 2013 - 2016
University of Pittsburgh School of MedicineClass of 2013
Certifications & Licensure
MI State Medical License 2019 - 2026
PA State Medical License 2016 - 2021
IL State Medical License 2013 - 2016- American Board of Medical Genetics and Genomics Medical Biochemical Genetics
- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- 4 citationsTELO2-related syndrome (You-Hoover-Fong syndrome): Description of 14 new affected individuals and review of the literature.Daniah Albokhari, Amanda Barone Pritchard, Adelyn Beil, Candace Muss, Caleb Bupp, Dorothy K Grange, Geoffroy Delplancq, Jennifer Heeley, Melissa Zuteck, Michelle M Mor...> ;American Journal of Medical Genetics. Part A. 2023 May 1
- Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphism.Dong Li, Alanna Strong, Cuiping Hou, Helen Downes, Amanda Barone Pritchard, Pamela Mazzeo, Elaine H Zackai, Laura K Conlin, Hakon Hakonarson> ;Molecular Cytogenetics. 2022 Aug 5
- 7 citationsFurther description of two patients with biallelic variants in NADSYN1 in association with cardiac and vertebral anomalies.Hannah Kortbawi, Elizabeth Ames, Amanda Pritchard, Patrick Devine, Jessica van Ziffle, Anne Slavotinek> ;American Journal of Medical Genetics. Part A. 2022 Aug 1
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Press Mentions
Sponge on a String Reduces Long Waits for Diagnostic Test for Cancer | CancerFebruary 26th, 2024
Hospital Affiliations
Children's Hospital of PhiladelphiaPhiladelphia, Pennsylvania
University of Michigan Medical CenterAnn Arbor, Michigan
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