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Artificial Organs|November 12, 2020
Novel use of cangrelor in pediatrics: A pilot cohort study demonstrating use in ventricular assist devicesSarah E Fahnhorst, Gary Beasley, Jason F Goldberg, et al.
Genes|January 23, 2024
Exploring the Regulation and Function of Rpl3l in the Development of Early-Onset Dilated Cardiomyopathy and Congestive Heart Failure Using Systems Genetics ApproachAkhilesh K Bajpai, Qingqing Gu, Buyan-Ochir Orgil, et al.
Cardio-Oncology (London, England)|June 3, 2025
Unraveling the genetic blueprint of doxorubicin-induced cardiotoxicity through systems genetics approachesBuyan-Ochir Orgil, Akhilesh K Bajpai, Neely Alberson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2012
Cardiovascular findings in duplication 17p11.2 syndromeJohn L Jefferies, Ricardo H Pignatelli, Hugo R Martinez, et al.
Research Square|May 5, 2025
Unraveling the Genetic Blueprint of Doxorubicin-Induced Cardiotoxicity Through Systems Genetics ApproachesBuyan-Ochir Orgil, Akhilesh K Bajpai, Neely Alberson, et al.
The Annals of Thoracic Surgery|May 30, 2025
The Fate of the Truncal Valve: Multiinstitutional Insights Into Reintervention After Truncus Arteriosus RepairMario O'Connor, Maria E Hoyos, Catherine E Stauber, et al.
Circulation|May 29, 2024
Evaluation and Management of Chronic Heart Failure in Children and Adolescents With Congenital Heart Disease: A Scientific Statement From the American Heart AssociationShahnawaz Amdani, Jennifer Conway, Kristen George, et al.
Pediatric Reports|November 25, 2024
Elevation of NT-proBNP Levels in Pediatric and Young Adult Hematopoietic Stem Cell Transplant Patients with EndotheliopathyKimberly Uchida, Xiaomeng Yuan, Jennifer McArthur, et al.
Cardio-Oncology (London, England)|February 10, 2022
Bridging the gap to advance the care of individuals with cancer: collaboration and partnership in the Cardiology Oncology Innovation Network (COIN)Sherry-Ann Brown, Craig Beavers, Hugo R Martinez, et al.
American Journal of Medical Genetics. Part A|July 31, 2013
Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndromeAlana Cecchi, Naomi Ogawa, Hugo R Martinez, et al.
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