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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
- 10 citationsIon Channels in Gliomas-From Molecular Basis to Treatment.Abdallah F Elias, Bernice C Lin, Beverly J Piggott
International Journal of Molecular Sciences. 2023-01-28 - 7 citationsEnsuring equity: Pharmacogenetic implementation in rural and tribal communities.Tianna M Leitch, Shayna R Killam, Karen E Brown, Kirk C Katseanes, Kathleen M George
Frontiers in Pharmacology. 2022-01-01 - 51 citationsSPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in femalesFrancesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, Michael A. Levy, Andres Hernandez-Garcia
American Journal of Human Genetics. 2021-03-04
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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