Showing Results from 1 to 12 of 158.
10 : 30 AM
22q11 Deletion Syndrome: A Potenitial Risk Factor For Left Pulmonary Artery Hypoplasia and Need For Intervention in Patients With Congeital Heart Disease
Oliver Shannon, Ward Cameron
Final Pr. ID: Sa2020
Authors: Oliver Shannon , Ward Cameron
Keywords: Congenital heart disease, Genetics, Surgical treatment
02 : 00 PM
4-Phenylbutyric Acid Reduces Endoplasmic Reticulum Retention and Partially Restores Function of LDLR p.D622N Mutation In Vitro: A Potential Therapy for Hypercholesterolemia
Wang Yongxiang, Zhang Piyi, Bai Ming, Zhang Zheng
Final Pr. ID: Sa1098
Authors: Wang Yongxiang , Zhang Piyi , Bai Ming , Zhang Zheng
Keywords: Hyperlipoproteinemia, Gene mutations, Family, Cholesterol-lowering drugs, Genetics
Soheili Fariborz, Almontashiri Naif, Heydarikhorneh Niloufar, Vilmundarson Ragnar, Chen Hsiao-huei, Stewart Alexandre
Final Pr. ID: MDP819
Authors: Soheili Fariborz , Almontashiri Naif , Heydarikhorneh Niloufar , Vilmundarson Ragnar , Chen Hsiao-huei , Stewart Alexandre
Keywords: Coronary artery calcification (CAC), Atherosclerosis, Genome-wide association studies (GWAS), Calcification, Genetics
03 : 15 PM
A Case of Hypertrophic Cardimyopathy: Digenic Variants of Uncertain Significance Mutations in MHY7 and RYR2 Genes
Durukan Selina, Uzunoglu Ekin, Farahmandsadr Maryam, Soffer Daniel
Final Pr. ID: Su2177
Authors: Durukan Selina , Uzunoglu Ekin , Farahmandsadr Maryam , Soffer Daniel
Keywords: Hypertrophic cardiomyopathy, Gene mutations, Genetic testing
06 : 00 PM
A Genome-wide CRISPRi Screen Implicates Coronary Artery Disease GWAS Genes as Key Regulators of Adventitial Fibroblast Proliferation
Jackson William, Zhu Ashley, Gu Wenduo, Berezowitz Alexa, Iyer Meghana, Cheng Paul
Final Pr. ID: Tu0067
Authors: Jackson William , Zhu Ashley , Gu Wenduo , Berezowitz Alexa , Iyer Meghana , Cheng Paul
Keywords: Atherosclerosis, Genetic techniques, Aneurysms, Vascular disease
Tran Linh, Everitt Ian, Vaught Arthur, Barth Andreas, Minhas Anum
Final Pr. ID: Mo3065
Authors: Tran Linh , Everitt Ian , Vaught Arthur , Barth Andreas , Minhas Anum
Keywords: Peripartum cardiomyopathy, Arrhythmias, Pregnancy, Genetics
03 : 15 PM
A Multi-Population-First Approach Leveraging UK Biobank (UKBB) and All of Us (AoU) Datasets Reveals Higher Cardiomyopathy Variant Burden in Individuals with Myocarditis
Gurumoorthi Manasa, Khanji Mohammed, Munroe Patricia, Petersen Steffen, Landstrom Andrew, Chahal Anwar, Hesse Kerrick, Asatryan Babken, Shah Ravi, Sharaf Dabbagh Ghaith, Wolfe Rachel, Shyam Sundar Vijay, Mohiddin Saidi, Aung Nay
Final Pr. ID: Su1041
Authors: Gurumoorthi Manasa , Khanji Mohammed , Munroe Patricia , Petersen Steffen , Landstrom Andrew , Chahal Anwar , Hesse Kerrick , Asatryan Babken , Shah Ravi , Sharaf Dabbagh Ghaith , Wolfe Rachel , Shyam Sundar Vijay , Mohiddin Saidi , Aung Nay
Keywords: Myocarditis, Genetics, Cardiomyopathy, Genomics
Chang Stephen, Albertelli Megan, Quertermous Thomas, Wright Patricia, Terrien Jeremy, Aujard Fabienne, Wu Joseph, Krasnow Mark, Karanewsky Caitlin, Pendleton Jozeph, Ren Lu, Anzeraey Aude, Froelicher Victor, Liang David, Razafindrakoto Andriamahery, Ravelonjanahary Noeline
Final Pr. ID: LBP24
Authors: Chang Stephen , Albertelli Megan , Quertermous Thomas , Wright Patricia , Terrien Jeremy , Aujard Fabienne , Wu Joseph , Krasnow Mark , Karanewsky Caitlin , Pendleton Jozeph , Ren Lu , Anzeraey Aude , Froelicher Victor , Liang David , Razafindrakoto Andriamahery , Ravelonjanahary Noeline
Keywords: Arrhythmias, Genomics, Genetics, Atrial arrhythmias, Sinoatrial node
10 : 30 AM
A Novel Missense Mutation in TNNT2 Gene in a Lebanese Pedigree With Ebstein Anomaly And Wolf-Parkinson-White Syndrome: A Case Report
Atasi Montaser, Dankar Razan, Barakat Salim, Wehbi Jad, Refaat Marwan
Final Pr. ID: Sa1070
Authors: Atasi Montaser , Dankar Razan , Barakat Salim , Wehbi Jad , Refaat Marwan
Keywords: Wolff-Parkinson-White syndrome, Genetic testing, Congenital Cardiology
04 : 00 PM
A Polygenic Score to Identify Risk of Incident Stroke and Benefit from Primary Prevention Statin Therapy
Mcclintick Daniel, Kamanu Frederick, Melloni Giorgio, Sabatine Marc, Ruff Christian, Ridker Paul, Chasman Daniel, Marston Nicholas
Final Pr. ID: MDP64
Authors: Mcclintick Daniel , Kamanu Frederick , Melloni Giorgio , Sabatine Marc , Ruff Christian , Ridker Paul , Chasman Daniel , Marston Nicholas
Keywords: Stroke, Genetics, Polygenic Risk, Statins, Prevention
04 : 30 PM
Adipocyte Enhancer Binding Protein 1 (AEBP1) Inhibition as a Potential Anti-Fibrotic Therapy in Heart Failure
Shankar Thirupura S, Calder Dallen, Sachse Frank, Kyriakopoulos Christos, Maneta Eleni, Srinivasan Harini, Tseliou Eleni, Navankasattusas Sutip, Selzman Craig, Boudina Sihem, Seidel Thomas, Visker Joseph, Lavine Kory, Drakos Stavros, Amrute Junedh, Polishchuk Georgiy, Lunde J Ty, Ling Jing, Ferrin Peter, Hamouche Rana, Feigle Dominik
Final Pr. ID: We108
Authors: Shankar Thirupura S , Calder Dallen , Sachse Frank , Kyriakopoulos Christos , Maneta Eleni , Srinivasan Harini , Tseliou Eleni , Navankasattusas Sutip , Selzman Craig , Boudina Sihem , Seidel Thomas , Visker Joseph , Lavine Kory , Drakos Stavros , Amrute Junedh , Polishchuk Georgiy , Lunde J Ty , Ling Jing , Ferrin Peter , Hamouche Rana , Feigle Dominik
Keywords: Fibrosis, Heart failure, Tissue engineering, Genetics, Genomics
12 : 10 PM
Advanced Machine Learning Models for Classifying Transthyretin Amyloidosis in Clinical Settings
Verma Anurag, Hsu Po-ya, Kripke Colleen, Howard William, Sirugo Giorgio, Myes Kelly
Final Pr. ID: MDP1346
Authors: Verma Anurag , Hsu Po-ya , Kripke Colleen , Howard William , Sirugo Giorgio , Myes Kelly
Keywords: Cardiomyopathy, Genetic testing, Amyloidosis