DimitriMaamariMD

PubMed

• 23 citations
  Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank.
  Kiran J Biddinger, Sean J Jurgens, Dimitri Maamari, Liam Gaziano, Seung Hoan Choi
  JAMA Cardiology. 2022-07-01
• 1 citations
  Genotyping in Anticoagulated Patients After Percutaneous Coronary Intervention: Should It Be Routine?
  Dimitri J Maamari, Farouc A Jaffer, Amit V Khera, Akl C Fahed
  Circulation. 2022-03-08
• 20 citations
  Association of the Interaction Between Familial Hypercholesterolemia Variants and Adherence to a Healthy Lifestyle With Risk of Coronary Artery Disease.
  Akl C Fahed, Minxian Wang, Aniruddh P Patel, Ezimamaka Ajufo, Dimitri J Maamari
  JAMA Network Open. 2022-03-01

Journal Articles

• Clinical implementation of combined monogenic and polygenic risk disclosure for coronary artery disease  
  Maamari, D.J., Brockman, D.G., Aragam, K.G., Pelletier, R.C., Folkerts, E., Neben, C.L., Okumura, S., Hull, L.E., Philippakis, A.A., Natarajan, P., Ellinor, P.T., Ng, ..., JACC: Advances, 8/1/2022

Books/Book Chapters

• Cardio-Oncology Practice Manual: A Companion to Braunwald's Heart Disease 
  Chapter: Structural Heart Disease Management 
  Nkomo, V.T., Maamari, D.J., Oh, J.2022
• Cardio-Oncology Practice Manual: A Companion to Braunwald's Heart Disease 
  Chapter: Structural Heart Disease 
  Nkomo, V.T., Maamari, D.J., Oh, J.2022