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Office
Department of Medical Genetics, Shodair Children's Hospital
2755 Colonial Drive
Helena, MT 59601Phone+1 406-444-7500Fax+1 406-444-1022
Summary
- Dr. Abdallah (Abe) Elias is a medical geneticist in Helena, MT and is affiliated with multiple hospitals in the Rocky Mountain Region. He serves as Medical Director of the Genetics Department at Shodair Children's Hospital and is Adjunct Associated Professor in Pediatrics at the University of Utah. He received his medical degree from Albert-Ludwigs University in Freiburg, Germany and completed residencies in Pediatrics (University of Freiburg), Family Medicine (University of South Dakota), and Medical Genetics (Johns Hopkins University). He has been in practice 22 years. He specializes in clinical genetics and is experienced in pediatric genetics, connective tissue diseases, genomics, and infection control.
Education & Training
- Johns Hopkins University School of MedicineFellowship, Clinical Biochemical Genetics, 2011 - 2012
- Johns Hopkins UniversityResidency, Medical Genetics and Genomics, 2009 - 2011
- Center for Family Medicine (Sioux Falls)Residency, Family Medicine, 2005 - 2008
- Albert Ludwigs University Faculty of MedicineClass of 1995
Certifications & Licensure
- MT State Medical License 2010 - 2026
- UT State Medical License 2020 - 2026
- ID State Medical License 2022 - 2025
- WY State Medical License 2022 - 2025
- NV State Medical License 2022 - 2023
- American Board of Family Medicine Family Medicine
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Awards, Honors, & Recognition
- CMS Meaningful Use Stage 1 Certification EpicCare Ambulatory EMR, Epic Systems Corporation, 2013
Publications & Presentations
PubMed
- 337 citationsOuter-surface protein C of the Lyme disease spirochete: A protein induced in ticks for infection of mammalsDorothee Grimm, Kit Tilly, Rebecca Byram, Philip E. Stewart, Jonathan G. Krum
Proceedings of the National Academy of Sciences of the United States of America. 2004-03-02 - 320 citationsLoss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysmMark E. Lindsay, Dorien Schepers, Nikhita Ajit Bolar, Jefferson J. Doyle, Elena M. Gallo
Nature Genetics. 2012-08-01 - 19 citationsTruncating de novo mutations in the Kruppel-type zinc-finger gene ZNF148 in patients with corpus callosum defects, developmental delay, short stature, and dysmorphismsServi J. C. Stevens, Anthonie J. van Essen, Conny M. A. van Ravenswaaij, Abdallah F. Elias, Jaclyn Haven
Genome Medicine. 2016-12-13
Professional Memberships
- American College of Medical GeneticsFellow
- American Society of Human GeneticsMember
- Fellow
- European Society for Paediatric Infectious DiseasesMember
- Fellow
Other Languages
- German, French
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