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Office
555 S 18th St
Columbus, OH 43205Phone+1 614-722-6200Fax+1 614-722-4565
Education & Training
- Washington University/B-JH/SLCH ConsortiumFellowship, Child Neurology, 1987 - 1990
- Washington University/B-JH/SLCH ConsortiumResidency, Pediatrics, 1984 - 1987
- Indiana University School of MedicineClass of 1984
Certifications & Licensure
- MO State Medical License 1986 - 2026
- OH State Medical License 2019 - 2025
- FL State Medical License 2012 - 2014
- American Board of Psychiatry and Neurology Neurology with Special Qualification in Child Neurology
Clinical Trials
- Longitudinal Study of the Natural History of Duchenne Muscular Dystrophy (DMD) Start of enrollment: 2005 Dec 01
- This is a Study to Get More Information About Non Ambulatory Boys & Men With Duchenne Muscular Dystrophy Start of enrollment: 2010 Mar 01
- Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping Start of enrollment: 2012 Apr 01
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Publications & Presentations
PubMed
- Transitioning From Nusinersen to Risdiplam for Spinal Muscular Atrophy in Clinical Practice: A Single-Center Experience.Can Ebru Bekircan-Kurt, Sharmada Subramanian, Shannon Chagat, Samuel J Mackenzie, Megan Iammarino
Muscle & Nerve. 2025-03-01 - Gross motor delays in infants and young boys with Duchenne muscular dystrophy.Linda P Lowes, Natalie F Reash, Megan A Iammarino, Anne M Connolly, Lindsay Pietruszewski
Journal of Neuromuscular Diseases. 2024-11-01 - 2 citationsTaldefgrobep Alfa and the Phase 3 RESILIENT Trial in Spinal Muscular Atrophy.Laurent Servais, Lindsey Lee Lair, Anne M Connolly, Barry J Byrne, Karen S Chen
International Journal of Molecular Sciences. 2024-09-24
Press Mentions
- Parent Project Muscular Dystrophy Awards $450,000 to Collaborative Duchenne Muscular Dystrophy Care ProjectsApril 6th, 2021
- Local Family with Little One Battling Spinal Muscular Atrophy Says “Miracle Drug” Is Changing Their Daughter’s LifeNovember 13th, 2017
- Public Health Cuts Mean over One in Three Councils Close Services Delivering Contraceptive CareNovember 2nd, 2017
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Grant Support
- Clinical Trial Readiness for Children 0-5 years with Congenital Muscular Dystrophy Secondary to LAMA2 MutationsRESEARCH INST NATIONWIDE CHILDREN'S HOSP2023–2028
- Clinical Trial Readiness for Children 0-5 years with Congenital Muscular Dystrophy Secondary to LAMA2 MutationsRESEARCH INST NATIONWIDE CHILDREN'S HOSP2023–2028
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