Michael J. Ackerman MD, PhD
Windland Smith Rice Cardiovascular Genomics Research Professor; Professor of Medicine, Pediatrics, and Pharmacology; Director of the Windland Smith Rice Genetic Heart Rhythm Clinic and Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MinnesotaMichael J. Ackerman is the Windland Smith Rice Cardiovascular Genomics Research Professor and Professor of Medicine, Pediatrics, and Pharmacology at the Mayo Clinic in Rochester, Minnesota.
Dr. Ackerman received his MD and PhD from the Mayo Clinic Alix School of Medicine and the Mayo Clinic Graduate School of Biomedical Sciences and residency and fellowship training in Pediatric and Pediatric Cardiology in the Mayo Clinic School of Graduate Medical Education.
Currently, he serves as director of Mayo Clinic’s Windland Smith Rice Genetic Heart Rhythm Clinic and the Windland Smith Rice Sudden Death Genomics Laboratory. He has published over 650 peer-reviewed articles. Dr. Ackerman has also served as the president of the Sudden Arrhythmia Death Syndromes (SADS) Foundation since 2006.
In 2015, he received Mayo Clinic’s Distinguished Clinician Award. In 2018, he received the Mayo Clinic Distinguished Pediatric Investigator Award and the Distinguished Scientist Award from the Heart Rhythm Society. In 2021, he was inducted into the prestigious Association of American Physicians and received the Mayo Clinic Distinguished Investigator Award.
Disclosures
Dr. Ackerman reports the following:- Consultant: Abbot, BioMarin Pharmaceuticals, Boston Scientific, Bristol Myers Squibb, Daiichi Sankyo, Illumina, Invitae, Medtronic, Tenaya Therapeutics, and UpToDate
- IP/Royalties: AliveCor, Anumana, ARMGO Pharma, Pfizer, and Thryv Therapeutics.
Recent Contributions to PracticeUpdate:
- Type of Syncope Trigger and Risk of Subsequent Life-Threatening Events in Patients With Long QT Syndrome
- Arrhythmia Variants in a Multi-Center Cohort
- Effectiveness of ICDs to Reduce Mortality in Patients With Long QT Syndrome
- Interplay Among Genetic Substrate, QTc Duration, and Arrhythmia Risk in Patients With Long QT Syndrome
- The Molecular Autopsy From Down Under
- Sudden Cardiac Death Among Children and Young Adults
- Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in EMR
- MY APPROACH to Treatment of the Congenital Long QT Syndromes