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Citations	Article
6	Analysis of ABC Transporter Gene Expression in Atherosclerosis by Stanislav Kotlyarov and Anna Kotlyarova
6	*Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (DSP)* by Nosheen Reza, Alejandro de Feria, Jessica L. Chowns, Lily Hoffman-Andrews, Laura Vann, Jessica Kim, Amy Marzolf and Anjali Tiku Owens
5	*Mutations in MYBPC3* and MYH7 in Association with Brugada Type 1 ECG Pattern: Overlap between Brugada Syndrome and Hypertrophic Cardiomyopathy? by Marianna Farnè, Cristina Balla, Alice Margutti, Rita Selvatici, Martina De Raffele, Assunta Di Domenico, Paola Imbrici, Elia De Maria, Mauro Biffi, Matteo Bertini, Claudio Rapezzi, Alessandra Ferlini and Francesca Gualandi**
5	Biventricular Strain Imaging with Cardiac MRI in Genotyped and Histology Validated Amyloid Cardiomyopathy by Abhinay Reddy, Vasvi Singh, Badri Karthikeyan, Leyi Jiang, Silva Kristo, Sharma Kattel, Ram Amuthan, Saraswati Pokharel and Umesh C. Sharma
4	The Roles of Platelet-Activating Factor and Magnesium in Pathophysiology of Hypertension, Atherogenesis, Cardiovascular Disease, Stroke and Aging by Nilank Shah, Roshni Sethi, Sachin Shah, Komail Jafri, Jonah Duran, Yong Chang, Chirag Soni and Hanna Wollocko
4	Lower Circulating Cell-Free Mitochondrial DNA Is Associated with Heart Failure in Type 2 Diabetes Mellitus Patients by Tetiana A. Berezina, Mykola P. Kopytsya, Olga V. Petyunina, Alexander A. Berezin, Zeljko Obradovic, Lukas Schmidbauer, Michael Lichtenauer and Alexander E. Berezin
4	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
3	Spectrum of Clinical Features and Genetic Profile of Left Ventricular Noncompaction Cardiomyopathy in Children by Agata Paszkowska, Alicja Mirecka-Rola, Dorota Piekutowska-Abramczuk, Elżbieta Ciara, Łukasz Mazurkiewicz, Katarzyna Bieganowska and Lidia Ziółkowska
3	Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort by Elías Cuesta-Llavona, Rebeca Lorca, Beatriz Díaz-Molina, José L. Lambert-Rodríguez, Julián R. Reguero, Sara Iglesias, Belén Alonso, Alejandro Junco-Vicente, Vanesa Alonso, Eliecer Coto and Juan Gómez
3	The Multi-Ethnic New Zealand Study of Acute Coronary Syndromes (MENZACS): Design and Methodology by Malcolm. E. Legget, Vicky. A. Cameron, Katrina. K. Poppe, Sara Aish, Nikki Earle, Yeunhyang Choi, Kathryn. E. Bradbury, Clare Wall, Ralph Stewart, Andrew Kerr, Wil Harrison, Gerry Devlin, Richard Troughton, A. Mark Richards, Graeme Porter, Patrick Gladding, Anna Rolleston and Robert N. Doughty

Citations	Article
4	Lower Circulating Cell-Free Mitochondrial DNA Is Associated with Heart Failure in Type 2 Diabetes Mellitus Patients by Tetiana A. Berezina, Mykola P. Kopytsya, Olga V. Petyunina, Alexander A. Berezin, Zeljko Obradovic, Lukas Schmidbauer, Michael Lichtenauer and Alexander E. Berezin
3	Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort by Elías Cuesta-Llavona, Rebeca Lorca, Beatriz Díaz-Molina, José L. Lambert-Rodríguez, Julián R. Reguero, Sara Iglesias, Belén Alonso, Alejandro Junco-Vicente, Vanesa Alonso, Eliecer Coto and Juan Gómez
2	Diagnosis and Treatment of Obstructive Hypertrophic Cardiomyopathy by Gaetano Todde, Grazia Canciello, Felice Borrelli, Errico Federico Perillo, Giovanni Esposito, Raffaella Lombardi and Maria Angela Losi
2	Prevalence of Polymorphisms of Genes Responsible for Coagulation System and Folate Metabolism and Their Predictive Value for Thrombosis Development in MINOCA Patients: Immediate and Long-Term Prognoses by Sofia Kruchinova, Vladimir Shvartz, Alim Namitokov, Milana Gendugova, Maria Karibova and Elena Kosmacheva
2	Sarcomeric versus Non-Sarcomeric HCM by Felice Borrelli, Maria Angela Losi, Grazia Canciello, Gaetano Todde, Errico Federico Perillo, Leopoldo Ordine, Giulia Frisso, Giovanni Esposito and Raffaella Lombardi
1	*Clinical Exome Sequencing Revealed a De Novo FLNC* Mutation in a Child with Restrictive Cardiomyopathy by Francesca Girolami, Silvia Passantino, Adelaide Ballerini, Alessia Gozzini, Giulio Porcedda, Iacopo Olivotto and Silvia Favilli**
1	*Functional Characterization of the A414G Loss-of-Function Mutation in HCN4* Associated with Sinus Bradycardia by Arie O. Verkerk and Ronald Wilders**
1	Moderately Prolonged QTc in Computer-Assessed ECG, Random Variation or Significant Risk Factor? A Literature Review by Jan Hysing, Charlotte Gibbs, Øystein Lunde Holla, Jacob Thalamus and Kristina H. Haugaa
1	Identification of Single-Nucleotide Polymorphisms in ZNF469 in a Patient with Aortoiliac Aneurysmal Disease by Adam Wolf, Faria Khimani and Mohanakrishnan Sathyamoorthy
1	Recurrent Episodes of Acute Myocardial Infarction Secondary to Paradoxical Coronary Artery Embolism by Mita Singh, Ana Teresa Gomes, Paul Hill and Ansuman Saha

Citations	Article
2	Diagnosis and Treatment of Obstructive Hypertrophic Cardiomyopathy by Gaetano Todde, Grazia Canciello, Felice Borrelli, Errico Federico Perillo, Giovanni Esposito, Raffaella Lombardi and Maria Angela Losi
2	Sarcomeric versus Non-Sarcomeric HCM by Felice Borrelli, Maria Angela Losi, Grazia Canciello, Gaetano Todde, Errico Federico Perillo, Leopoldo Ordine, Giulia Frisso, Giovanni Esposito and Raffaella Lombardi
1	*Functional Characterization of the A414G Loss-of-Function Mutation in HCN4* Associated with Sinus Bradycardia by Arie O. Verkerk and Ronald Wilders**

Citations	Article
No cited articles available for this period.

Citations	Article
11	Familial Dilated Cardiomyopathy Associated with Congenital Defects in the Setting of a Novel VCL Mutation (Lys815Arg) in Conjunction with a Known MYPBC3 Variant by Quinn S. Wells, Natalie L. Ausborn, Birgit H. Funke, Jean P. Pfotenhauer, Joseph L. Fredi, Samantha Baxter, Thomas G. DiSalvo and Charles C. Hong
11	Combined Use of In Silico and In Vitro Splicing Assays for Interpretation of Genomic Variants of Unknown Significance in Cardiomyopathies and Channelopathies by Hervé Crehalet, Gilles Millat, Juliette Albuisson, Véronique Bonnet, Isabelle Rouvet, Robert Rousson and Dominique Bozon
9	The Interpretation of Genetic Tests in Inherited Cardiovascular Diseases by Lorenzo Monserrat, Andrea Mazzanti, Martín Ortiz-Genga, Roberto Barriales-Villa, Diego Garcia-Giustiniani and Juan Ramon Gimeno-Blanes
7	LQTS-Associated Mutation A257G in α1-Syntrophin Interacts with the Intragenic Variant P74L to Modify Its Biophysical Phenotype by Jianding Cheng, David W. Van Norstrand, Argelia Medeiros-Domingo, David J. Tester, Carmen R. Valdivia, Bi-Hua Tan, Matteo Vatta, Jonathan C. Makielski and Michael J. Ackerman
6	Analysis of ABC Transporter Gene Expression in Atherosclerosis by Stanislav Kotlyarov and Anna Kotlyarova
6	Atrioventricular Canal Defect and Associated Genetic Disorders: New Insights into Polydactyly Syndromes by M. Cristina Digilio, Paolo Versacci, Francesca Lepri, Anwar Baban, Bruno Dallapiccola and Bruno Marino
6	*Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (DSP)* by Nosheen Reza, Alejandro de Feria, Jessica L. Chowns, Lily Hoffman-Andrews, Laura Vann, Jessica Kim, Amy Marzolf and Anjali Tiku Owens
5	*Mutations in Hotspot Region of MYH7* Gene Exon 23 Associated with Restrictive Cardiomyopathy by Mitali Kapoor, Soumi Das, Amitabh Biswas, Sandeep Seth, Balram Bhargava and Vadlamudi Raghavendra Rao**
5	Pompe Disease, a Storage Cardiomyopathy by Tiziana Felice
5	*Mutations in MYBPC3* and MYH7 in Association with Brugada Type 1 ECG Pattern: Overlap between Brugada Syndrome and Hypertrophic Cardiomyopathy? by Marianna Farnè, Cristina Balla, Alice Margutti, Rita Selvatici, Martina De Raffele, Assunta Di Domenico, Paola Imbrici, Elia De Maria, Mauro Biffi, Matteo Bertini, Claudio Rapezzi, Alessandra Ferlini and Francesca Gualandi**

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5574	Cardiac Amyloidosis: Diagnostic Tools for a Challenging Disease by Marco Giuseppe Migliaccio, Franco Iodice, Marco Di Mauro, Angela Iannuzzi, Roberta Pacileo, Martina Caiazza and Augusto Esposito
5436	The Multi-Ethnic New Zealand Study of Acute Coronary Syndromes (MENZACS): Design and Methodology by Malcolm. E. Legget, Vicky. A. Cameron, Katrina. K. Poppe, Sara Aish, Nikki Earle, Yeunhyang Choi, Kathryn. E. Bradbury, Clare Wall, Ralph Stewart, Andrew Kerr, Wil Harrison, Gerry Devlin, Richard Troughton, A. Mark Richards, Graeme Porter, Patrick Gladding, Anna Rolleston and Robert N. Doughty
5192	Pancarditis as the Clinical Presentation of Eosinophilic Granulomatosis with Polyangiitis: A Multimodality Approach to Diagnosis by Michele Lioncino, Emanuele Monda, Santo Dellegrottaglie, Annapaola Cirillo, Martina Caiazza, Adelaide Fusco, Francesca Esposito, Federica Verrillo, Giovanni Ciccarelli, Marta Rubino, Massimo Triggiani, Raffaele Scarpa, Alida Linda Patrizia Caforio, Renzo Marcolongo, Stefania Rizzo, Cristina Basso, Gerardo Nigro, Maria Giovanna Russo, Paolo Golino and Giuseppe Limongelli
5179	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
5049	MYH7 Genotype–Phenotype Correlation in a Cohort of Finnish Patients by Teemu Vepsäläinen, Tiina Heliö, Catalina Vasilescu, Laura Martelius, Sini Weckström, Juha Koskenvuo, Anita Hiippala and Tiina Ojala
4847	*Pathogenic Intronic Splice-Affecting Variants in MYBPC3* in Three Patients with Hypertrophic Cardiomyopathy by Katherine A. Wood, Jamie M. Ellingford, James Eden, Huw B. Thomas, Raymond T. O’Keefe, Claire Hopton and William G. Newman**
4746	Clinical and Molecular Characteristics of Patients with PLN R14del Cardiomyopathy: State-of-the-Art Review by Emanuele Monda, Ettore Blasi, Antonio De Pasquale, Alessandro Di Vilio, Federica Amodio, Martina Caiazza, Gaetano Diana, Michele Lioncino, Alessia Perna, Federica Verrillo, Maria Luigia Martucci, Orlando Munciguerra, Andrea Vergara and Giuseppe Limongelli
4417	*Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (DSP)* by Nosheen Reza, Alejandro de Feria, Jessica L. Chowns, Lily Hoffman-Andrews, Laura Vann, Jessica Kim, Amy Marzolf and Anjali Tiku Owens
4411	Constraints in Clinical Cardiology and Personalized Medicine: Interrelated Concepts in Clinical Cardiology by Katerina G. Lourida and George E. Louridas
4390	Diagnosis and Treatment of Obstructive Hypertrophic Cardiomyopathy by Gaetano Todde, Grazia Canciello, Felice Borrelli, Errico Federico Perillo, Giovanni Esposito, Raffaella Lombardi and Maria Angela Losi

Views	Article
4390	Diagnosis and Treatment of Obstructive Hypertrophic Cardiomyopathy by Gaetano Todde, Grazia Canciello, Felice Borrelli, Errico Federico Perillo, Giovanni Esposito, Raffaella Lombardi and Maria Angela Losi
3949	Sarcomeric versus Non-Sarcomeric HCM by Felice Borrelli, Maria Angela Losi, Grazia Canciello, Gaetano Todde, Errico Federico Perillo, Leopoldo Ordine, Giulia Frisso, Giovanni Esposito and Raffaella Lombardi
3813	Studying Epigenetics of Cardiovascular Diseases on Chip Guide by Bandar Ali Alghamdi, Intisar Mahmoud Aljohani, Bandar Ghazi Alotaibi, Muhammad Ahmed, Kholod Abduallah Almazmomi, Salman Aloufi and Jowhra Alshamrani
3283	Lower Circulating Cell-Free Mitochondrial DNA Is Associated with Heart Failure in Type 2 Diabetes Mellitus Patients by Tetiana A. Berezina, Mykola P. Kopytsya, Olga V. Petyunina, Alexander A. Berezin, Zeljko Obradovic, Lukas Schmidbauer, Michael Lichtenauer and Alexander E. Berezin
3124	Moderately Prolonged QTc in Computer-Assessed ECG, Random Variation or Significant Risk Factor? A Literature Review by Jan Hysing, Charlotte Gibbs, Øystein Lunde Holla, Jacob Thalamus and Kristina H. Haugaa
3055	Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort by Elías Cuesta-Llavona, Rebeca Lorca, Beatriz Díaz-Molina, José L. Lambert-Rodríguez, Julián R. Reguero, Sara Iglesias, Belén Alonso, Alejandro Junco-Vicente, Vanesa Alonso, Eliecer Coto and Juan Gómez
3017	Brugada Syndrome within Asian Populations: State-of-the-Art Review by Muzamil Khawaja, Yusuf Kamran Qadeer, Rehma Siddiqui, Mihail G. Chelu, Noppawit Aiumtrakul, June K. Pickett, Ramon Brugada, Josep Brugada, Pedro Brugada and Chayakrit Krittanawong
2997	*Screening Method for 22q11 Deletion Syndrome Involving the Use of TaqMan qPCR for TBX1* in Patients with Conotruncal Congenital Heart Disease by Felix-Julian Campos-Garcia, Addy-Manuela Castillo-Espinola, Carolina-Elizabeth Medina-Escobedo, Juan C. Zenteno, Julio-Cesar Lara-Riegos, Hector Rubio-Zapata, David Cruz-Robles and Ana-Isabel Velazquez-Ibarra**
2944	Sex Differences in Fatty Acid Metabolism and Blood Pressure Response to Dietary Salt in Humans by Jeanne A. Ishimwe, Jane F. Ferguson and Annet Kirabo
2883	Identification of Single-Nucleotide Polymorphisms in ZNF469 in a Patient with Aortoiliac Aneurysmal Disease by Adam Wolf, Faria Khimani and Mohanakrishnan Sathyamoorthy

Views	Article
4390	Diagnosis and Treatment of Obstructive Hypertrophic Cardiomyopathy by Gaetano Todde, Grazia Canciello, Felice Borrelli, Errico Federico Perillo, Giovanni Esposito, Raffaella Lombardi and Maria Angela Losi
3949	Sarcomeric versus Non-Sarcomeric HCM by Felice Borrelli, Maria Angela Losi, Grazia Canciello, Gaetano Todde, Errico Federico Perillo, Leopoldo Ordine, Giulia Frisso, Giovanni Esposito and Raffaella Lombardi
1911	*Functional Characterization of the A414G Loss-of-Function Mutation in HCN4* Associated with Sinus Bradycardia by Arie O. Verkerk and Ronald Wilders**
1716	GMDS Intragenic Deletions Associate with Congenital Heart Disease including Ebstein Anomaly by Shirley M. Lo-A-Njoe, Eline A. Verberne, Lars T. van der Veken, Eric Arends, J. Peter van Tintelen, Alex V. Postma and Mieke M. van Haelst
1545	From Natural History to Contemporary Management of Aortic Diseases: A State-of-the-Art Review of Thoracic Aortic Aneurysm by Yuliya Paulenka, Christopher Lee, Mays Tawayha, Sam Dow, Kajal Shah, Stanislav Henkin and Wassim Mosleh
1519	Hypertrophic Cardiomyopathy and Chronic Kidney Disease: An Updated Review by Sheefah Dhuny, Henry H. L. Wu, Manova David and Rajkumar Chinnadurai
1484	Unraveling the Genetic and Epigenetic Complexities of Hereditary Aortic Diseases and the Breakthroughs of Precision Medicine: An Editorial by Fares Awa, Mays Tawayha and Wassim Mosleh
1197	*A Family with a Single LMNA* Mutation Illustrates Diversity in Cardiac Phenotypes Associated with Laminopathic Progeroid Syndromes by Anna-Gaëlle Giguet-Valard, Astrid Monfort, Hugues Lucron, Helena Mosbah, Franck Boccara, Camille Vatier, Corinne Vigouroux, Pascale Richard, Karim Wahbi, Remi Bellance, Elisabeth Sarrazin and Jocelyn Inamo**
1126	*Sudden Cardiac Death in Biventricular Arrhythmogenic Cardiomyopathy: A New Undescribed Variant of the MYH6* Gene by Pedro Garcia Brás, Isabel Cardoso, José Viegas, Diana Antunes and Sílvia Aguiar Rosa**
962	Gene-Specific Discriminative Echocardiogram Findings in Hypertrophic Cardiomyopathy Determined Using Artificial Intelligence: A Pilot Study by Mila Glavaški, Aleksandra Ilić and Lazar Velicki

Views	Article
1545	From Natural History to Contemporary Management of Aortic Diseases: A State-of-the-Art Review of Thoracic Aortic Aneurysm by Yuliya Paulenka, Christopher Lee, Mays Tawayha, Sam Dow, Kajal Shah, Stanislav Henkin and Wassim Mosleh
1519	Hypertrophic Cardiomyopathy and Chronic Kidney Disease: An Updated Review by Sheefah Dhuny, Henry H. L. Wu, Manova David and Rajkumar Chinnadurai
962	Gene-Specific Discriminative Echocardiogram Findings in Hypertrophic Cardiomyopathy Determined Using Artificial Intelligence: A Pilot Study by Mila Glavaški, Aleksandra Ilić and Lazar Velicki
903	Inherited Arrhythmogenic Syndromes by Georgia Sarquella-Brugada and Oscar Campuzano
868	Risk of Cardiac Arrhythmias in Patients with Late-Onset Pompe Disease—Results from a Long Follow-Up in a Group of 12 Patients and Review of Literature by Alberto Palladino, Luigia Passamano, Marianna Scutifero, Salvatore Morra, Esther Picillo, Andrea Antonio Papa, Gerardo Nigro and Luisa Politano
825	*Consideration of the Medical Economics of Cardiac Genetics, Focusing on the Cost-Effectiveness of P2Y12 Inhibitor Selection Based on the CYP2C19* Loss-of-Function Allele: A Semi-Systematic Review by Tomoyuki Takura**
812	COVID-19 and the Heart: Lessons Learned and Future Research Directions by Tetz Cheng-Che Lee, Alaa Mabrouk Salem Omar and Jonathan N. Bella
689	Anderson–Fabry Disease Homozygosity: Rare Case of Late-Onset Variant by Gabriela Dostalova, Jaroslav Januska, Michaela Veselá, Petra Reková, Anna Taborska, Martin Pleva, David Zemanek and Aleš Linhart
516	A Single Nucleotide Variant in Ankyrin-2 Influencing Ventricular Tachycardia in COVID-19 Associated Myocarditis by Erin Haase, Chandana Kulkarni, Peyton Moore, Akash Ramanathan and Mohanakrishnan Sathyamoorthy
289	*Gene Polymorphisms LEP, LEPR, 5HT2A, GHRL, NPY, and FTO-Obesity Biomarkers in Metabolic Risk Assessment: A Retrospective Pilot Study in Overweight and Obese Population in Romania* by Ovidiu Nicolae Penes, Bernard Weber, Anca Lucia Pop, Mihaela Bodnarescu-Cobanoglu, Valentin Nicolae Varlas, Aleksandru Serkan Kucukberksun, Dragos Cretoiu, Roxana Georgiana Varlas and Cornelia Zetu

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9085	Cardiac Involvement in Autosomal Dominant Polycystic Kidney Disease by Letizia Spinelli, Giuseppe Giugliano and Giovanni Esposito
5574	Cardiac Amyloidosis: Diagnostic Tools for a Challenging Disease by Marco Giuseppe Migliaccio, Franco Iodice, Marco Di Mauro, Angela Iannuzzi, Roberta Pacileo, Martina Caiazza and Augusto Esposito
5436	The Multi-Ethnic New Zealand Study of Acute Coronary Syndromes (MENZACS): Design and Methodology by Malcolm. E. Legget, Vicky. A. Cameron, Katrina. K. Poppe, Sara Aish, Nikki Earle, Yeunhyang Choi, Kathryn. E. Bradbury, Clare Wall, Ralph Stewart, Andrew Kerr, Wil Harrison, Gerry Devlin, Richard Troughton, A. Mark Richards, Graeme Porter, Patrick Gladding, Anna Rolleston and Robert N. Doughty
5192	Pancarditis as the Clinical Presentation of Eosinophilic Granulomatosis with Polyangiitis: A Multimodality Approach to Diagnosis by Michele Lioncino, Emanuele Monda, Santo Dellegrottaglie, Annapaola Cirillo, Martina Caiazza, Adelaide Fusco, Francesca Esposito, Federica Verrillo, Giovanni Ciccarelli, Marta Rubino, Massimo Triggiani, Raffaele Scarpa, Alida Linda Patrizia Caforio, Renzo Marcolongo, Stefania Rizzo, Cristina Basso, Gerardo Nigro, Maria Giovanna Russo, Paolo Golino and Giuseppe Limongelli
5179	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
5049	MYH7 Genotype–Phenotype Correlation in a Cohort of Finnish Patients by Teemu Vepsäläinen, Tiina Heliö, Catalina Vasilescu, Laura Martelius, Sini Weckström, Juha Koskenvuo, Anita Hiippala and Tiina Ojala
4961	Cardiac Amyloidosis Therapy: A Systematic Review by Franco Iodice, Marco Di Mauro, Marco Giuseppe Migliaccio, Angela Iannuzzi, Roberta Pacileo, Martina Caiazza and Augusto Esposito
4847	*Pathogenic Intronic Splice-Affecting Variants in MYBPC3* in Three Patients with Hypertrophic Cardiomyopathy by Katherine A. Wood, Jamie M. Ellingford, James Eden, Huw B. Thomas, Raymond T. O’Keefe, Claire Hopton and William G. Newman**
4746	Clinical and Molecular Characteristics of Patients with PLN R14del Cardiomyopathy: State-of-the-Art Review by Emanuele Monda, Ettore Blasi, Antonio De Pasquale, Alessandro Di Vilio, Federica Amodio, Martina Caiazza, Gaetano Diana, Michele Lioncino, Alessia Perna, Federica Verrillo, Maria Luigia Martucci, Orlando Munciguerra, Andrea Vergara and Giuseppe Limongelli
4417	*Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (DSP)* by Nosheen Reza, Alejandro de Feria, Jessica L. Chowns, Lily Hoffman-Andrews, Laura Vann, Jessica Kim, Amy Marzolf and Anjali Tiku Owens

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1462	The Multi-Ethnic New Zealand Study of Acute Coronary Syndromes (MENZACS): Design and Methodology by Malcolm. E. Legget, Vicky. A. Cameron, Katrina. K. Poppe, Sara Aish, Nikki Earle, Yeunhyang Choi, Kathryn. E. Bradbury, Clare Wall, Ralph Stewart, Andrew Kerr, Wil Harrison, Gerry Devlin, Richard Troughton, A. Mark Richards, Graeme Porter, Patrick Gladding, Anna Rolleston and Robert N. Doughty
1429	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
1293	*Pathogenic Intronic Splice-Affecting Variants in MYBPC3* in Three Patients with Hypertrophic Cardiomyopathy by Katherine A. Wood, Jamie M. Ellingford, James Eden, Huw B. Thomas, Raymond T. O’Keefe, Claire Hopton and William G. Newman**
1210	Left Ventricular Non-Compaction Spectrum in Adults and Children: From a Morphological Trait to a Structural Muscular Disease by Flavia Fusco, Nunzia Borrelli, Rosaria Barracano, Giovanni Domenico Ciriello, Federica Verrillo, Giancarlo Scognamiglio and Berardo Sarubbi
1191	The Roles of Platelet-Activating Factor and Magnesium in Pathophysiology of Hypertension, Atherogenesis, Cardiovascular Disease, Stroke and Aging by Nilank Shah, Roshni Sethi, Sachin Shah, Komail Jafri, Jonah Duran, Yong Chang, Chirag Soni and Hanna Wollocko
1143	*Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (DSP)* by Nosheen Reza, Alejandro de Feria, Jessica L. Chowns, Lily Hoffman-Andrews, Laura Vann, Jessica Kim, Amy Marzolf and Anjali Tiku Owens
968	Constraints in Clinical Cardiology and Personalized Medicine: Interrelated Concepts in Clinical Cardiology by Katerina G. Lourida and George E. Louridas
959	Modified Body Mass Index as a Novel Nutritional and Prognostic Marker in Patients with Cardiac Amyloidosis by Francesca Dongiglio, Giuseppe Palmiero, Emanuele Monda, Marta Rubino, Federica Verrillo, Martina Caiazza, Annapaola Cirillo, Adelaide Fusco, Erica Vetrano, Michele Lioncino, Gaetano Diana, Francesco Di Fraia, Giuseppe Cerciello, Fiore Manganelli, Olga Vriz and Giuseppe Limongelli
955	Biventricular Strain Imaging with Cardiac MRI in Genotyped and Histology Validated Amyloid Cardiomyopathy by Abhinay Reddy, Vasvi Singh, Badri Karthikeyan, Leyi Jiang, Silva Kristo, Sharma Kattel, Ram Amuthan, Saraswati Pokharel and Umesh C. Sharma
937	*Mutations in MYBPC3* and MYH7 in Association with Brugada Type 1 ECG Pattern: Overlap between Brugada Syndrome and Hypertrophic Cardiomyopathy? by Marianna Farnè, Cristina Balla, Alice Margutti, Rita Selvatici, Martina De Raffele, Assunta Di Domenico, Paola Imbrici, Elia De Maria, Mauro Biffi, Matteo Bertini, Claudio Rapezzi, Alessandra Ferlini and Francesca Gualandi**

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926	Studying Epigenetics of Cardiovascular Diseases on Chip Guide by Bandar Ali Alghamdi, Intisar Mahmoud Aljohani, Bandar Ghazi Alotaibi, Muhammad Ahmed, Kholod Abduallah Almazmomi, Salman Aloufi and Jowhra Alshamrani
794	*Association of GSTT1, GSTM1* and GSTP1 (Ile105Val) mRNA Expression with Cardiometabolic Risk Parameters in Women with Breast Cancer and Comorbidities by Yizel Becerril Alarcón, Fernando Bastida González, Isidro Roberto Camacho Beiza, Eduardo Dávila González, José Alfonso Cruz Ramos, Alejandra Donají Benítez Arciniega, Roxana Valdés Ramos and Alexandra Estela Soto Piña**
775	Moderately Prolonged QTc in Computer-Assessed ECG, Random Variation or Significant Risk Factor? A Literature Review by Jan Hysing, Charlotte Gibbs, Øystein Lunde Holla, Jacob Thalamus and Kristina H. Haugaa
771	Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort by Elías Cuesta-Llavona, Rebeca Lorca, Beatriz Díaz-Molina, José L. Lambert-Rodríguez, Julián R. Reguero, Sara Iglesias, Belén Alonso, Alejandro Junco-Vicente, Vanesa Alonso, Eliecer Coto and Juan Gómez
750	*Screening Method for 22q11 Deletion Syndrome Involving the Use of TaqMan qPCR for TBX1* in Patients with Conotruncal Congenital Heart Disease by Felix-Julian Campos-Garcia, Addy-Manuela Castillo-Espinola, Carolina-Elizabeth Medina-Escobedo, Juan C. Zenteno, Julio-Cesar Lara-Riegos, Hector Rubio-Zapata, David Cruz-Robles and Ana-Isabel Velazquez-Ibarra**
702	*Clinical Exome Sequencing Revealed a De Novo FLNC* Mutation in a Child with Restrictive Cardiomyopathy by Francesca Girolami, Silvia Passantino, Adelaide Ballerini, Alessia Gozzini, Giulio Porcedda, Iacopo Olivotto and Silvia Favilli**
695	Recurrent Episodes of Acute Myocardial Infarction Secondary to Paradoxical Coronary Artery Embolism by Mita Singh, Ana Teresa Gomes, Paul Hill and Ansuman Saha
626	Could the BGN Gene Be Pathogenic with Spontaneous Coronary Artery Dissection (SCAD) and Fibromuscular Dysplasia (FMD)? by Lexie Kolton, Charlie Robin, Jianfeng Xu, Jun Wei, Rupa Patil and Jason Robin
621	Sex Differences in Fatty Acid Metabolism and Blood Pressure Response to Dietary Salt in Humans by Jeanne A. Ishimwe, Jane F. Ferguson and Annet Kirabo
603	Identification of Single-Nucleotide Polymorphisms in ZNF469 in a Patient with Aortoiliac Aneurysmal Disease by Adam Wolf, Faria Khimani and Mohanakrishnan Sathyamoorthy

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582	Sarcomeric versus Non-Sarcomeric HCM by Felice Borrelli, Maria Angela Losi, Grazia Canciello, Gaetano Todde, Errico Federico Perillo, Leopoldo Ordine, Giulia Frisso, Giovanni Esposito and Raffaella Lombardi
538	Diagnosis and Treatment of Obstructive Hypertrophic Cardiomyopathy by Gaetano Todde, Grazia Canciello, Felice Borrelli, Errico Federico Perillo, Giovanni Esposito, Raffaella Lombardi and Maria Angela Losi
459	*Functional Characterization of the A414G Loss-of-Function Mutation in HCN4* Associated with Sinus Bradycardia by Arie O. Verkerk and Ronald Wilders**
427	*Sudden Cardiac Death in Biventricular Arrhythmogenic Cardiomyopathy: A New Undescribed Variant of the MYH6* Gene by Pedro Garcia Brás, Isabel Cardoso, José Viegas, Diana Antunes and Sílvia Aguiar Rosa**
348	GMDS Intragenic Deletions Associate with Congenital Heart Disease including Ebstein Anomaly by Shirley M. Lo-A-Njoe, Eline A. Verberne, Lars T. van der Veken, Eric Arends, J. Peter van Tintelen, Alex V. Postma and Mieke M. van Haelst
330	Unraveling the Genetic and Epigenetic Complexities of Hereditary Aortic Diseases and the Breakthroughs of Precision Medicine: An Editorial by Fares Awa, Mays Tawayha and Wassim Mosleh
321	Inherited Arrhythmogenic Syndromes by Georgia Sarquella-Brugada and Oscar Campuzano
320	From Natural History to Contemporary Management of Aortic Diseases: A State-of-the-Art Review of Thoracic Aortic Aneurysm by Yuliya Paulenka, Christopher Lee, Mays Tawayha, Sam Dow, Kajal Shah, Stanislav Henkin and Wassim Mosleh
281	Gene-Specific Discriminative Echocardiogram Findings in Hypertrophic Cardiomyopathy Determined Using Artificial Intelligence: A Pilot Study by Mila Glavaški, Aleksandra Ilić and Lazar Velicki
279	*A Family with a Single LMNA* Mutation Illustrates Diversity in Cardiac Phenotypes Associated with Laminopathic Progeroid Syndromes by Anna-Gaëlle Giguet-Valard, Astrid Monfort, Hugues Lucron, Helena Mosbah, Franck Boccara, Camille Vatier, Corinne Vigouroux, Pascale Richard, Karim Wahbi, Remi Bellance, Elisabeth Sarrazin and Jocelyn Inamo**

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321	Inherited Arrhythmogenic Syndromes by Georgia Sarquella-Brugada and Oscar Campuzano
320	From Natural History to Contemporary Management of Aortic Diseases: A State-of-the-Art Review of Thoracic Aortic Aneurysm by Yuliya Paulenka, Christopher Lee, Mays Tawayha, Sam Dow, Kajal Shah, Stanislav Henkin and Wassim Mosleh
281	Gene-Specific Discriminative Echocardiogram Findings in Hypertrophic Cardiomyopathy Determined Using Artificial Intelligence: A Pilot Study by Mila Glavaški, Aleksandra Ilić and Lazar Velicki
270	Hypertrophic Cardiomyopathy and Chronic Kidney Disease: An Updated Review by Sheefah Dhuny, Henry H. L. Wu, Manova David and Rajkumar Chinnadurai
241	Risk of Cardiac Arrhythmias in Patients with Late-Onset Pompe Disease—Results from a Long Follow-Up in a Group of 12 Patients and Review of Literature by Alberto Palladino, Luigia Passamano, Marianna Scutifero, Salvatore Morra, Esther Picillo, Andrea Antonio Papa, Gerardo Nigro and Luisa Politano
233	*Consideration of the Medical Economics of Cardiac Genetics, Focusing on the Cost-Effectiveness of P2Y12 Inhibitor Selection Based on the CYP2C19* Loss-of-Function Allele: A Semi-Systematic Review by Tomoyuki Takura**
203	COVID-19 and the Heart: Lessons Learned and Future Research Directions by Tetz Cheng-Che Lee, Alaa Mabrouk Salem Omar and Jonathan N. Bella
194	Anderson–Fabry Disease Homozygosity: Rare Case of Late-Onset Variant by Gabriela Dostalova, Jaroslav Januska, Michaela Veselá, Petra Reková, Anna Taborska, Martin Pleva, David Zemanek and Aleš Linhart
135	A Single Nucleotide Variant in Ankyrin-2 Influencing Ventricular Tachycardia in COVID-19 Associated Myocarditis by Erin Haase, Chandana Kulkarni, Peyton Moore, Akash Ramanathan and Mohanakrishnan Sathyamoorthy
79	*Gene Polymorphisms LEP, LEPR, 5HT2A, GHRL, NPY, and FTO-Obesity Biomarkers in Metabolic Risk Assessment: A Retrospective Pilot Study in Overweight and Obese Population in Romania* by Ovidiu Nicolae Penes, Bernard Weber, Anca Lucia Pop, Mihaela Bodnarescu-Cobanoglu, Valentin Nicolae Varlas, Aleksandru Serkan Kucukberksun, Dragos Cretoiu, Roxana Georgiana Varlas and Cornelia Zetu

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1581	Cardiac Amyloidosis Therapy: A Systematic Review by Franco Iodice, Marco Di Mauro, Marco Giuseppe Migliaccio, Angela Iannuzzi, Roberta Pacileo, Martina Caiazza and Augusto Esposito
1462	The Multi-Ethnic New Zealand Study of Acute Coronary Syndromes (MENZACS): Design and Methodology by Malcolm. E. Legget, Vicky. A. Cameron, Katrina. K. Poppe, Sara Aish, Nikki Earle, Yeunhyang Choi, Kathryn. E. Bradbury, Clare Wall, Ralph Stewart, Andrew Kerr, Wil Harrison, Gerry Devlin, Richard Troughton, A. Mark Richards, Graeme Porter, Patrick Gladding, Anna Rolleston and Robert N. Doughty
1429	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
1293	*Pathogenic Intronic Splice-Affecting Variants in MYBPC3* in Three Patients with Hypertrophic Cardiomyopathy by Katherine A. Wood, Jamie M. Ellingford, James Eden, Huw B. Thomas, Raymond T. O’Keefe, Claire Hopton and William G. Newman**
1210	Left Ventricular Non-Compaction Spectrum in Adults and Children: From a Morphological Trait to a Structural Muscular Disease by Flavia Fusco, Nunzia Borrelli, Rosaria Barracano, Giovanni Domenico Ciriello, Federica Verrillo, Giancarlo Scognamiglio and Berardo Sarubbi
1191	The Roles of Platelet-Activating Factor and Magnesium in Pathophysiology of Hypertension, Atherogenesis, Cardiovascular Disease, Stroke and Aging by Nilank Shah, Roshni Sethi, Sachin Shah, Komail Jafri, Jonah Duran, Yong Chang, Chirag Soni and Hanna Wollocko
1156	Three Myocardial Diseases in One Heart: Arrhythmogenic Right Ventricular Cardiomyopathy, Left Ventricular Noncompaction and Myocarditis by Yulia Lutokhina, Olga Blagova, Nadezhda Varionchik, Svetlana Alexandrova, Nina Gagarina, Eugenia Kogan, Vsevolod Sedov, Anna Shestak, Elena Zaklyazminskaya and Alexander Nedostup
1143	*Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (DSP)* by Nosheen Reza, Alejandro de Feria, Jessica L. Chowns, Lily Hoffman-Andrews, Laura Vann, Jessica Kim, Amy Marzolf and Anjali Tiku Owens
1101	Cardiac Involvement in Autosomal Dominant Polycystic Kidney Disease by Letizia Spinelli, Giuseppe Giugliano and Giovanni Esposito
1053	Genetic Susceptibility to SARS-CoV-2: From the Nehandertal Age to 2020 by Federica Amodio, Martina Caiazza, Paolo Calabrò and Giuseppe Limongelli

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