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Office
8500 SW 92nd St
MyGeneticist, Suite 101
Miami, FL 33156Phone+1 786-388-0600Fax+1 305-667-1675
Summary
- Dr. Angelika Erwin is a medical geneticist in Miami, FL and is affiliated with Cleveland Clinic. She received her medical degree from Charité- Universitätsmedizin Berlin and has been in practice 14 years. She also speaks multiple languages, including German, Spanish, and French. She specializes in clinical genetics and is experienced in lysosomal storage diseases, cancer genetics, general medical genetics, lipodystrophy, and porphyrias.
Education & Training
- Icahn School of Medicine at Mount SinaiResidency, Internal Medicine/Medical Genetics and Genomics, 2008 - 2013
- Icahn School of Medicine at Mount Sinai/Mount Sinai HospitalResidency, Internal Medicine, 2011
- Charité - Universitätsmedizin BerlinClass of 2003
Certifications & Licensure
- NY State Medical License 2013 - 2026
- WV State Medical License 2023 - 2026
- CO State Medical License 2021 - 2025
- FL State Medical License 2017 - 2025
- IN State Medical License 2023 - 2025
- OH State Medical License 2013 - 2025
- AL State Medical License 2024 - 2024
- American Board of Internal Medicine Internal Medicine
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- 39 citationsPenetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE NetworkCarlos J. Gallego, Amber A. Burt, Agnes S. Sundaresan, Zi Ye, Christopher G. Shaw
American Journal of Human Genetics. 2015-10-01 - 68 citationsNoninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of ...Jeffrey S Dungan, Susan Klugman, Sandra Darilek, Jennifer Malinowski, Yassmine M N Akkari
Genetics in Medicine. 2023-02-01 - 32 citationsTAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical development.Geeske M. van Woerden, Melanie Bos, Charlotte de Konink, Ben Distel, Rossella Avagliano Trezza
Human Mutation. 2021-02-10
Journal Articles
- De Novo Missense Variants in MEIS2 Recapitulate the Microdeletion Phenotype of Cardiac and Palate Abnormalities, Developmental Delay, Intellectual Disability and Dysmo...Theresa Grebe, Susan Winter, Elaine H Zackai, Angelika L Erwin, Matthew A Deardorff, Margaret Harr, American Journal of Medical Genetics Part A
- Congenital Erythropoietic Porphyria.Erwin A., Balwani M., Desnick R.J., GeneReviews™, 2013
- Thiazolidinedione Response in Familial Lipodystrophy Patients with LMNA Mutations: A Case Series.Luedtke A, Boschmann M, Colpe C, Engeli S, Adams F, Birkenfeld AL, Haufe S, Rahn G, Luft FC, Schmidt HH, Jordan J., Hormone and Metabolic Research, 2012
Press Mentions
- New Drug May Treat Rare Diseases That Make Exposure to Sunlight PainfulApril 13th, 2023
- Alnylam to Present Full 9-Month Results from the HELIOS-A Phase 3 Study of Vutrisiran at the American Academy of Neurology Virtual Annual Meeting 2021March 23rd, 2021
- Treatment and Medication Options for Fabry DiseaseAugust 23rd, 2023
Professional Memberships
- American Society of Human GeneticsMember
- American College of Medical GeneticsMember
Other Languages
- German, Spanish, French
External Links
- MyGeneticisthttp://mygeneticist.com/
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