|
Michael J. Ackerman, M.D., Ph.D.
![]() Michael J. Ackerman, M.D., Ph.D.
Location:
Minnesota
SummaryGenomics and Genotype-Phenotype Relationships in Heritable Cardiovascular Diseases Predisposing to Sudden Death
In our Sudden Death Genomics Laboratory, research interests include genomics, mutational analysis, and novel gene discovery related to the cardiac channelopathies like long QT syndrome, catecholaminergic polymorphic ventricular tachycardia, and sudden unexplained death including sudden infant death syndrome and inherited sarcomere diseases like hypertrophic cardiomyopathy. In addition, as Director of the Long QT Syndrome Clinic, there are active clinical translational research efforts devoted to identifying individuals at greatest risk for sudden death. These projects include autonomic nervous system studies and overnight sleep studies.
Current studies include:
Recent publicationsEducation
Fellowship
–
Pediatric Cardiology
Post-Doc
–
Postdoctoral Research - Molecular and Functional Basis of the Inherited Long QT Syndrome. Mentor: Stephen N. Thibodeau, PhD.
Residency
–
Pediatric And Adolescent Medicine
Ph.D.
–
Thesis: Molecular and Electrophysical Characterization of the Swelling-Induced Chloride Conductance Pathway in Xenopus Oocytes.
Mentor: David E. Clapham, M.D., Ph.D.
M.D.
B.A.
–
Chemistry and Mathematics
|
Legal restrictions and terms of use applicable to this site
Use of this site signifies your agreement to the terms of use
Copyright © 2008 Mayo Foundation for Medical Education and Research.