Showing Results from 1 to 12 of 289.
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
01 : 00 PM
A-band titin-truncating variant promotes the development of arrhythmia-induced cardiomyopathy in a novel genetically-engineered porcine model
Lee Kwonjae, Bhatnagar Ashita, Glinton Kristofor, Burrell Amy, Ober Rebecca, Mcluckie Alicia, Bishop Brian, Rogers Christopher, Geist Gail, Del Rio Carlos, Mcnally Elizabeth, Pfenniger Anna
Final Pr. ID: Mo4050
Authors: Lee Kwonjae, Bhatnagar Ashita, Glinton Kristofor, Burrell Amy, Ober Rebecca, Mcluckie Alicia, Bishop Brian, Rogers Christopher, Geist Gail, Del Rio Carlos, Mcnally Elizabeth, Pfenniger Anna
Keywords: Cardiomyopathy, Genetics, Atrial fibrillation, Ventricular remodeling, Ventricular arrhythmia
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, Hesse Kerrick, Asatryan Babken, Shah Ravi, Sharaf Dabbagh Ghaith, Wolfe Rachel, Shyam Sundar Vijay, Mohiddin Saidi, Aung Nay, Khanji Mohammed, Munroe Patricia, Petersen Steffen, Landstrom Andrew, Chahal Anwar
Final Pr. ID: Su1041
Authors: Gurumoorthi Manasa, Hesse Kerrick, Asatryan Babken, Shah Ravi, Sharaf Dabbagh Ghaith, Wolfe Rachel, Shyam Sundar Vijay, Mohiddin Saidi, Aung Nay, Khanji Mohammed, Munroe Patricia, Petersen Steffen, Landstrom Andrew, Chahal Anwar
Keywords: Myocarditis, Genetics, Cardiomyopathy, Genomics
12 : 53 PM
A Nationwide Italian Network for the Clinical and Genetic Diagnosis of Familial Dyslipidemias: The LIPIGEN registry
Casula Manuela, Galimberti Federica, Olmastroni Elena, Arca Marcello, Averna Maurizio, Catapano Alberico
Final Pr. ID: MP1502
Authors: Casula Manuela, Galimberti Federica, Olmastroni Elena, Arca Marcello, Averna Maurizio, Catapano Alberico
Keywords: Dyslipidemia, Hypercholesterolemia, Genetic testing, Cardiovascular health, Epidemiology
Chang Stephen, Karanewsky Caitlin, Pendleton Jozeph, Ren Lu, Anzeraey Aude, Froelicher Victor, Liang David, Razafindrakoto Andriamahery, Ravelonjanahary Noeline, Albertelli Megan, Quertermous Thomas, Wright Patricia, Terrien Jeremy, Aujard Fabienne, Wu Joseph, Krasnow Mark
Final Pr. ID: LBP24
Authors: Chang Stephen, Karanewsky Caitlin, Pendleton Jozeph, Ren Lu, Anzeraey Aude, Froelicher Victor, Liang David, Razafindrakoto Andriamahery, Ravelonjanahary Noeline, Albertelli Megan, Quertermous Thomas, Wright Patricia, Terrien Jeremy, Aujard Fabienne, Wu Joseph, Krasnow Mark
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
Bulut Aybike, Saygili E. Alper, Pirli Dogukan, Aydin Eylul, Ozdemir Ozkan, Balci Nermin, Alanay Yasemin, Bilguvar Kaya, Akgun Dogan Ozlem, Karacan Mehmet
Final Pr. ID: Wed103
Authors: Bulut Aybike, Saygili E. Alper, Pirli Dogukan, Aydin Eylul, Ozdemir Ozkan, Balci Nermin, Alanay Yasemin, Bilguvar Kaya, Akgun Dogan Ozlem, Karacan Mehmet
Keywords: Genetic testing, Genomics, Atrial fibrillation, Potassium channel, Arrhythmias