AngelikaLudtke(Ludtke)ErwinMDPhD

Clinical Genetics

Interim Medical Director, Center for Personalized Genetic Healthcare, Cleveland Clinic; Founder and director, MyGeneticist, Miami

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Office
8500 SW 92nd St
MyGeneticist, Suite 101
Miami, FL 33156
Phone+1 786-388-0600

Fax+1 305-667-1675

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.

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

PubMed

67 citations
Noninvasive 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
110 citations
PNPLA3 Gene Polymorphism Is Associated With Predisposition to and Severity of Alcoholic Liver Disease
Habeeb Salameh, Evan Raff, Angelika Erwin, Devanshi Seth, Hans Dieter Nischalke
The American Journal of Gastroenterology. 2015-05-12
41 citations
Liver Transplantation for Acute Intermittent Porphyria: Biochemical and Pathologic Studies of the Explanted Liver
Makiko Yasuda, Angelika Erwin, Lawrence U Liu, Manisha Balwani, Brenden Chen
Molecular Medicine. 2015-06-05

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

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