Submit to Cardiogenetics Review for Cardiogenetics

Journal Menu

Journal Browser

Most Cited & Viewed

Most Cited & Viewed Papers

Most Cited Papers
Most Viewed Papers
Most Downloaded Papers

Citations	Article
14	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
7	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
5	Exploring the Role of Genetics in Sarcoidosis and Its Impact on the Development of Cardiac Sarcoidosis by Sanjay Sivalokanathan
5	*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
4	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
3	Circulating Cell-Free Nuclear DNA Predicted an Improvement of Systolic Left Ventricular Function in Individuals with Chronic Heart Failure with Reduced Ejection Fraction by Tetiana Berezina, Oleksandr O. Berezin, Michael Lichtenauer and Alexander E. Berezin
3	Beyond the Beat: Understanding Inherited Risk and Therapeutic Opportunities in Cardiovascular Diseases with Emphasis on Inherited Cardiomyopathies and Inherited Arrhythmic Syndromes by Antea Krsek, Lara Baticic and Vlatka Sotosek
3	Gene Therapy for Inherited Arrhythmia Syndromes by Cameron J. Leong, Sohat Sharma, Jayant Seth, Archan Dave, Abdul Aziz Abdul Ghafoor and Zachary Laksman
3	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
2	Integrating Genetic, Clinical, and Histopathological Data for Definitive Diagnosis of PRKAG2-Related Disease by Martina Caiazza, Emanuele Monda, Francesco Loffredo, Rossana Bussani, Vera Fico, Emanuele Bobbio, Chiara Cirillo, Anna Murredda, Immacolata Viscovo, Alessandra Scatteia, Santo Dellegrottaglie, Diego Colonna, Berardo Sarubbi, Maria Giovanna Russo, Paolo Golino, Gianfranco Sinagra and Giuseppe Limongelli

Citations	Article
5	*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
5	Exploring the Role of Genetics in Sarcoidosis and Its Impact on the Development of Cardiac Sarcoidosis by Sanjay Sivalokanathan
3	Gene Therapy for Inherited Arrhythmia Syndromes by Cameron J. Leong, Sohat Sharma, Jayant Seth, Archan Dave, Abdul Aziz Abdul Ghafoor and Zachary Laksman
3	Beyond the Beat: Understanding Inherited Risk and Therapeutic Opportunities in Cardiovascular Diseases with Emphasis on Inherited Cardiomyopathies and Inherited Arrhythmic Syndromes by Antea Krsek, Lara Baticic and Vlatka Sotosek
3	Circulating Cell-Free Nuclear DNA Predicted an Improvement of Systolic Left Ventricular Function in Individuals with Chronic Heart Failure with Reduced Ejection Fraction by Tetiana Berezina, Oleksandr O. Berezin, Michael Lichtenauer and Alexander E. Berezin
2	*Cardiovascular Involvement in SYNE* Variants: A Case Series and Narrative Review by Francesco Ravera, Veronica Dusi, Pier Paolo Bocchino, Giulia Gobello, Giuseppe Giannino, Daniele Melis, Giulia Margherita Brach Del Prever, Filippo Angelini, Andrea Saglietto, Carla Giustetto, Guglielmo Gallone, Stefano Pidello, Margherita Cannillo, Marco Matteo Cingolani, Silvia Deaglio, Walter Grosso Marra, Gaetano Maria De Ferrari and Claudia Raineri**
2	Integrating Genetic, Clinical, and Histopathological Data for Definitive Diagnosis of PRKAG2-Related Disease by Martina Caiazza, Emanuele Monda, Francesco Loffredo, Rossana Bussani, Vera Fico, Emanuele Bobbio, Chiara Cirillo, Anna Murredda, Immacolata Viscovo, Alessandra Scatteia, Santo Dellegrottaglie, Diego Colonna, Berardo Sarubbi, Maria Giovanna Russo, Paolo Golino, Gianfranco Sinagra and Giuseppe Limongelli
2	Desmosomal Versus Non-Desmosomal Arrhythmogenic Cardiomyopathies: A State-of-the-Art Review by Kristian Galanti, Lorena Iezzi, Maria Luana Rizzuto, Daniele Falco, Giada Negri, Hoang Nhat Pham, Davide Mansour, Roberta Giansante, Liborio Stuppia, Lorenzo Mazzocchetti, Sabina Gallina, Cesare Mantini, Mohammed Y. Khanji, C. Anwar A. Chahal and Fabrizio Ricci
2	Cardiomyopathies and Arrythmias in Neuromuscular Diseases by Giuseppe Sgarito, Calogero Volpe, Stefano Bardari, Raimondo Calvanese, Paolo China, Giosuè Mascioli, Martina Nesti, Carlo Pignalberi, Manlio Cipriani and Massimo Zecchin
2	Familial Hypercholesterolemia Screening in a Cardiac Rehabilitation Program After Myocardial Infarction by Carlos Bertolín-Boronat, Víctor Marcos-Garcés, Héctor Merenciano-González, María Luz Martínez Mas, Josefa Inés Climent Alberola, Nerea Perez, Laura López Bueno, María Concepción Esteban Argente, María Valls Reig, Ana Arizón Benito, Alfonso Payá Rubio, César Ríos-Navarro, Elena de Dios, Jose Gavara, Manuel F. Jiménez-Navarro, Francisco Javier Chorro, Juan Sanchis and Vicente Bodi

Citations	Article
2	Desmosomal Versus Non-Desmosomal Arrhythmogenic Cardiomyopathies: A State-of-the-Art Review by Kristian Galanti, Lorena Iezzi, Maria Luana Rizzuto, Daniele Falco, Giada Negri, Hoang Nhat Pham, Davide Mansour, Roberta Giansante, Liborio Stuppia, Lorenzo Mazzocchetti, Sabina Gallina, Cesare Mantini, Mohammed Y. Khanji, C. Anwar A. Chahal and Fabrizio Ricci
2	Integrating Genetic, Clinical, and Histopathological Data for Definitive Diagnosis of PRKAG2-Related Disease by Martina Caiazza, Emanuele Monda, Francesco Loffredo, Rossana Bussani, Vera Fico, Emanuele Bobbio, Chiara Cirillo, Anna Murredda, Immacolata Viscovo, Alessandra Scatteia, Santo Dellegrottaglie, Diego Colonna, Berardo Sarubbi, Maria Giovanna Russo, Paolo Golino, Gianfranco Sinagra and Giuseppe Limongelli
1	Genotype–Phenotype Correlation of EVC Variants in Ellis-Van Creveld Syndrome: A Systematic Review and Case Report by Sandra Rodriguez-Cambranis, Addy-Manuela Castillo-Espinola, Claudia-Daniela Fuentelzas-Rosado, Paulina Salazar-Sansores, Claudia-Gabriela Nuñez-Solis, Hugo-Antonio Laviada-Molina, Aurea-Karina Zetina-Solorzano and Felix-Julian Campos-Garcia
1	Cardiac Involvement in Patients with MELAS-Related mtDNA 3243A>G Variant by Aino-Maija Vuorinen, Lauri Lehmonen, Mari Auranen, Sini Weckström, Sari Kivistö, Miia Holmström and Tiina Heliö
1	Systematic Review of Pharmacogenetics of Immunosuppressants in Heart Transplantation by Juan Eduardo Megías-Vericat, Tomás Palanques-Pastor, Mireya Fernández-Sánchez, Eduardo Guerrero-Hurtado, Mayte Gil-Candel, Antonio Solana-Altabella, Octavio Ballesta-López, María Centelles-Oria, Javier García-Pellicer and José Luis Poveda-Andrés
1	Integrated Deep Learning Framework for Cardiac Risk Stratification and Complication Analysis in Leigh’s Disease by Md Aminul Islam, Jayasree Varadarajan, Md Abu Sufian, Bhupesh Kumar Mishra and Md Ruhul Amin Rasel
1	TNNC1 Gene Mutation in Ebstein’s Anomaly and Left Ventricular Hypertrabeculation: A Case Report of a New Causative Mutation? by Irene Raso, Claudia Chillemi, Giorgia Prontera, Arianna Laoreti, Elisa Cattaneo, Valeria Calcaterra, Gian Vincenzo Zuccotti and Savina Mannarino
1	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
1	MicroRNA and DNA Methylation Adaptation Mechanism to Endurance Training in Cardiovascular Disease: A Systematic Review by Jil Delhez, Jeanne Ougier, Francisco Xavier de Araujo, Raphael Martins de Abreu and Camilo Corbellini

Citations	Article
2	Integrating Genetic, Clinical, and Histopathological Data for Definitive Diagnosis of PRKAG2-Related Disease by Martina Caiazza, Emanuele Monda, Francesco Loffredo, Rossana Bussani, Vera Fico, Emanuele Bobbio, Chiara Cirillo, Anna Murredda, Immacolata Viscovo, Alessandra Scatteia, Santo Dellegrottaglie, Diego Colonna, Berardo Sarubbi, Maria Giovanna Russo, Paolo Golino, Gianfranco Sinagra and Giuseppe Limongelli
1	MicroRNA and DNA Methylation Adaptation Mechanism to Endurance Training in Cardiovascular Disease: A Systematic Review by Jil Delhez, Jeanne Ougier, Francisco Xavier de Araujo, Raphael Martins de Abreu and Camilo Corbellini

Citations

Article

Integrating Genetic, Clinical, and Histopathological Data for Definitive Diagnosis of PRKAG2-Related Disease

by Martina Caiazza, Emanuele Monda, Francesco Loffredo, Rossana Bussani, Vera Fico, Emanuele Bobbio, Chiara Cirillo, Anna Murredda, Immacolata Viscovo, Alessandra Scatteia, Santo Dellegrottaglie, Diego Colonna, Berardo Sarubbi, Maria Giovanna Russo, Paolo Golino, Gianfranco Sinagra and Giuseppe Limongelli

MicroRNA and DNA Methylation Adaptation Mechanism to Endurance Training in Cardiovascular Disease: A Systematic Review

by Jil Delhez, Jeanne Ougier, Francisco Xavier de Araujo, Raphael Martins de Abreu and Camilo Corbellini

Citations	Article
14	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
13	*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
12	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
12	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
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
10	Analysis of ABC Transporter Gene Expression in Atherosclerosis by Stanislav Kotlyarov and Anna Kotlyarova
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
9	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
9	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
8	Mosaic Fabry Disease in a Male Presenting as Hypertrophic Cardiomyopathy by Maria Xu, Christopher Orsborne, James Eden, Andrew Wallace, Heather J. Church, Karen Tylee, Sasalu Deepak, Christopher Cassidy, Peter Woolfson, Christopher Miller, Matthias Schmitt, Ana Jovanovic and William G. Newman

More Articles...

Views	Article
14350	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
14235	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
11179	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
10806	Dietary Approach in Familial Hypercholesterolemia by Joanna Popiolek-Kalisz, Klaudia Salamon, Michal Mazur, Klaudia Mikolajczyk and Grzegorz Kalisz
9071	Exploring the Role of Genetics in Sarcoidosis and Its Impact on the Development of Cardiac Sarcoidosis by Sanjay Sivalokanathan
8061	Hypertrophic Cardiomyopathy and Chronic Kidney Disease: An Updated Review by Sheefah Dhuny, Henry H. L. Wu, Manova David and Rajkumar Chinnadurai
7831	Gene Therapy for Inherited Arrhythmia Syndromes by Cameron J. Leong, Sohat Sharma, Jayant Seth, Archan Dave, Abdul Aziz Abdul Ghafoor and Zachary Laksman
6753	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
5809	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
5703	*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

Views	Article
10806	Dietary Approach in Familial Hypercholesterolemia by Joanna Popiolek-Kalisz, Klaudia Salamon, Michal Mazur, Klaudia Mikolajczyk and Grzegorz Kalisz
9071	Exploring the Role of Genetics in Sarcoidosis and Its Impact on the Development of Cardiac Sarcoidosis by Sanjay Sivalokanathan
7831	Gene Therapy for Inherited Arrhythmia Syndromes by Cameron J. Leong, Sohat Sharma, Jayant Seth, Archan Dave, Abdul Aziz Abdul Ghafoor and Zachary Laksman
5809	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
5703	*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
4984	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
4537	Beyond the Beat: Understanding Inherited Risk and Therapeutic Opportunities in Cardiovascular Diseases with Emphasis on Inherited Cardiomyopathies and Inherited Arrhythmic Syndromes by Antea Krsek, Lara Baticic and Vlatka Sotosek
4523	Exosome-Derived microRNAs in Hypertrophic Cardiomyopathy by Brian Xiangzhi Wang
4446	Cardiomyopathies and Arrythmias in Neuromuscular Diseases by Giuseppe Sgarito, Calogero Volpe, Stefano Bardari, Raimondo Calvanese, Paolo China, Giosuè Mascioli, Martina Nesti, Carlo Pignalberi, Manlio Cipriani and Massimo Zecchin
4034	Desmosomal Versus Non-Desmosomal Arrhythmogenic Cardiomyopathies: A State-of-the-Art Review by Kristian Galanti, Lorena Iezzi, Maria Luana Rizzuto, Daniele Falco, Giada Negri, Hoang Nhat Pham, Davide Mansour, Roberta Giansante, Liborio Stuppia, Lorenzo Mazzocchetti, Sabina Gallina, Cesare Mantini, Mohammed Y. Khanji, C. Anwar A. Chahal and Fabrizio Ricci

Views	Article
5809	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
4034	Desmosomal Versus Non-Desmosomal Arrhythmogenic Cardiomyopathies: A State-of-the-Art Review by Kristian Galanti, Lorena Iezzi, Maria Luana Rizzuto, Daniele Falco, Giada Negri, Hoang Nhat Pham, Davide Mansour, Roberta Giansante, Liborio Stuppia, Lorenzo Mazzocchetti, Sabina Gallina, Cesare Mantini, Mohammed Y. Khanji, C. Anwar A. Chahal and Fabrizio Ricci
3547	*Cardiac Phenotype Associated with Two Heterozygous LMNA* Variants by Aura Siikjärvi, Krista Heliö, Tiina Heliö and Miia Holmström**
3435	Genotype–Phenotype Correlation of EVC Variants in Ellis-Van Creveld Syndrome: A Systematic Review and Case Report by Sandra Rodriguez-Cambranis, Addy-Manuela Castillo-Espinola, Claudia-Daniela Fuentelzas-Rosado, Paulina Salazar-Sansores, Claudia-Gabriela Nuñez-Solis, Hugo-Antonio Laviada-Molina, Aurea-Karina Zetina-Solorzano and Felix-Julian Campos-Garcia
2907	TNNC1 Gene Mutation in Ebstein’s Anomaly and Left Ventricular Hypertrabeculation: A Case Report of a New Causative Mutation? by Irene Raso, Claudia Chillemi, Giorgia Prontera, Arianna Laoreti, Elisa Cattaneo, Valeria Calcaterra, Gian Vincenzo Zuccotti and Savina Mannarino
2859	From Genetics to Phenotype: Understanding the Diverse Manifestations of Cardiovascular Genetic Diseases in Pediatric Populations by Jule Leonie Gutmann, Alina Spister and Lara Baticic
2799	Novel Perspectives on Genetic Evaluation in Early-Onset Atrial Fibrillation: Clinical Implications and Future Directions by Angelo Laconi, Tatiana Fancello, Giuliana Solinas and Gavino Casu
2794	Medical Therapy Versus Percutaneous Coronary Intervention in Patients with Myocardial Bridging from a National Population-Based Cohort Study: The Use of Big Data Analytics by Chayakrit Krittanawong, Song Peng Ang, Fernando Alexis Padilla, Yusuf Kamran Qadeer, Zhen Wang, Nicola Gaibazzi, Samin K. Sharma, Carl J. Lavie, Hartzell V. Schaff and Ernst R. Schwarz
2733	Brugada Syndrome: Channelopathy and/or Cardiomyopathy by Michele Ciabatti, Pasquale Notarstefano, Chiara Zocchi, Giacomo Virgili, Fulvio Bellocci, Iacopo Olivotto and Maurizio Pieroni
2326	How to Enhance Diagnosis in Fabry Disease: The Power of Information by Maria Chiara Meucci, Rosa Lillo, Margherita Calcagnino, Giampaolo Tocci, Eustachio Agricola, Federico Biondi, Claudio Di Brango, Vincenzo Guido, Valentina Parisi, Francesca Giordana, Veronica Melita, Mariaelena Lombardi, Angela Beatrice Scardovi, Li Van Stella Truong, Francesca Musella, Francesco di Spigno, Benedetta Matrone, Ivana Pariggiano, Paolo Calabrò, Roberto Spoladore, Stefania Luceri, Stefano Carugo, Francesca Graziani and Francesco Burzotta Show full author list Hide full author list

Views	Article
2859	From Genetics to Phenotype: Understanding the Diverse Manifestations of Cardiovascular Genetic Diseases in Pediatric Populations by Jule Leonie Gutmann, Alina Spister and Lara Baticic
1972	MicroRNA and DNA Methylation Adaptation Mechanism to Endurance Training in Cardiovascular Disease: A Systematic Review by Jil Delhez, Jeanne Ougier, Francisco Xavier de Araujo, Raphael Martins de Abreu and Camilo Corbellini
1812	Integrating Genetic, Clinical, and Histopathological Data for Definitive Diagnosis of PRKAG2-Related Disease by Martina Caiazza, Emanuele Monda, Francesco Loffredo, Rossana Bussani, Vera Fico, Emanuele Bobbio, Chiara Cirillo, Anna Murredda, Immacolata Viscovo, Alessandra Scatteia, Santo Dellegrottaglie, Diego Colonna, Berardo Sarubbi, Maria Giovanna Russo, Paolo Golino, Gianfranco Sinagra and Giuseppe Limongelli
1450	The Hidden Face of Danon Disease: Unique Challenges for Female Patients by Laura Torlai Triglia, Federico Barocelli, Enrico Ambrosini, Alberto Bettella, Filippo Luca Gurgoglione, Michele Bianconcini, Angela Guidorossi, Francesca Russo, Antonio Percesepe and Giampaolo Niccoli
1296	Sinus Bradycardia and Long QT Syndrome: Double Heterozygosity for Variants in KCNH2 and HCN4 by Jaël S. Copier, Fenna Tuijnenburg, Karolina Andrzejczyk, Alex V. Postma, Saskia N. van der Crabben, Oussama Najih, Caroline Pham, Leander Beekman, Arie O. Verkerk, Ahmad S. Amin and Elisabeth M. Lodder
634	*Digenic Contribution of Heterozygous ALPK3* and TRIM63 Variants to End-Stage Hypertrophic Cardiomyopathy in a Young Adult by Olga S. Chumakova, Natalia V. Milovanova, Elena A. Mershina, Sergey I. Kutsev and Ekaterina Y. Zakharova**
514	Non-Lysosomal Glycogen Storage Cardiomyopathy with Hypertrophic Phenotype Due to PRKAG2 c.905G>A (p.Arg302Gln): Case Report and Narrative Review by Pasquale Crea, Alice Moncada, Francesco Catanzariti, Graziella Agnelli, Michela Navarra, Claudia Rubino, Irene Scimè, Lucio Teresi, Maurizio Cusmà Piccione, Luigi Colarusso, Roberto Licordari, Giuseppe Dattilo and Gianluca Di Bella
451	Exploring the Genetic Architecture of Myocarditis and Inherited Cardiomyopathies by Sukruth Pradeep Kundur, Ali Malik, Rasi Mizori and Sanjay Sivalokanathan
442	The Genetic Architecture of Sudden Cardiac Death: A State-of-the-Art Review by Sabrina Montuoro, Emanuele Monda, Gaetano Diana, Emanuele Bobbio, Vera Fico, Marta Rubino, Martina Caiazza, Adelaide Fusco, Annapaola Cirillo, Federica Verrillo, Francesca Dongiglio, Giuseppe Palmiero, Federica Barra, Giulia Frisso, Maria Giovanna Russo, Paolo Calabrò and Giuseppe Limongelli
405	Genetic Variants as a Potentially Arrhythmogenic Substrate in Mitral Annular Disjunction: Case Report and a Systematic Review of the Literature by Lorenzo Bianchi, Marialaura Buscemi, Domenico Coviello, Massimiliano Cecconi, Andrea Minghini, Stefano Cornara, Matteo Astuti, Francesco Pentimalli, Pietro Bellone, Emmanuel Androulakis and Alberto Somaschini

Views	Article
14350	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
14235	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
13528	Cardiac Involvement in Autosomal Dominant Polycystic Kidney Disease by Letizia Spinelli, Giuseppe Giugliano and Giovanni Esposito
11179	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
10806	Dietary Approach in Familial Hypercholesterolemia by Joanna Popiolek-Kalisz, Klaudia Salamon, Michal Mazur, Klaudia Mikolajczyk and Grzegorz Kalisz
9540	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
9071	Exploring the Role of Genetics in Sarcoidosis and Its Impact on the Development of Cardiac Sarcoidosis by Sanjay Sivalokanathan
9018	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
8322	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
8105	*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

More Articles...

Downloads	Article
1700	Cardiomyopathies and Arrythmias in Neuromuscular Diseases by Giuseppe Sgarito, Calogero Volpe, Stefano Bardari, Raimondo Calvanese, Paolo China, Giosuè Mascioli, Martina Nesti, Carlo Pignalberi, Manlio Cipriani and Massimo Zecchin
1683	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
1288	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
1137	Gene-Specific Discriminative Echocardiogram Findings in Hypertrophic Cardiomyopathy Determined Using Artificial Intelligence: A Pilot Study by Mila Glavaški, Aleksandra Ilić and Lazar Velicki
1117	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
1048	*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**
1028	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
1020	*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
1010	Gene Therapy for Inherited Arrhythmia Syndromes by Cameron J. Leong, Sohat Sharma, Jayant Seth, Archan Dave, Abdul Aziz Abdul Ghafoor and Zachary Laksman
990	*Functional Characterization of the A414G Loss-of-Function Mutation in HCN4* Associated with Sinus Bradycardia by Arie O. Verkerk and Ronald Wilders**

Downloads	Article
1700	Cardiomyopathies and Arrythmias in Neuromuscular Diseases by Giuseppe Sgarito, Calogero Volpe, Stefano Bardari, Raimondo Calvanese, Paolo China, Giosuè Mascioli, Martina Nesti, Carlo Pignalberi, Manlio Cipriani and Massimo Zecchin
1020	*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
1010	Gene Therapy for Inherited Arrhythmia Syndromes by Cameron J. Leong, Sohat Sharma, Jayant Seth, Archan Dave, Abdul Aziz Abdul Ghafoor and Zachary Laksman
942	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
940	Exploring the Role of Genetics in Sarcoidosis and Its Impact on the Development of Cardiac Sarcoidosis by Sanjay Sivalokanathan
865	*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**
820	Circulating Cell-Free Nuclear DNA Predicted an Improvement of Systolic Left Ventricular Function in Individuals with Chronic Heart Failure with Reduced Ejection Fraction by Tetiana Berezina, Oleksandr O. Berezin, Michael Lichtenauer and Alexander E. Berezin
802	Dietary Approach in Familial Hypercholesterolemia by Joanna Popiolek-Kalisz, Klaudia Salamon, Michal Mazur, Klaudia Mikolajczyk and Grzegorz Kalisz
796	Genetic Testing for Patients with Cardiomyopathies: The INDACO Study—Towards a Cardiogenetic Clinic by Matteo Bianco, Noemi Giordano, Valentina Gazzola, Carloalberto Biolè, Giulia Nangeroni, Maurizio Lazzero, Giulia Margherita Brach del Prever, Fiorenza Mioli, Giulia Gobello, Amir Hassan Mousavi, Monica Guidante, Silvia Deaglio, Daniela Francesca Giachino and Alessandra Chinaglia
730	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

Downloads	Article
541	*Cardiac Phenotype Associated with Two Heterozygous LMNA* Variants by Aura Siikjärvi, Krista Heliö, Tiina Heliö and Miia Holmström**
494	Desmosomal Versus Non-Desmosomal Arrhythmogenic Cardiomyopathies: A State-of-the-Art Review by Kristian Galanti, Lorena Iezzi, Maria Luana Rizzuto, Daniele Falco, Giada Negri, Hoang Nhat Pham, Davide Mansour, Roberta Giansante, Liborio Stuppia, Lorenzo Mazzocchetti, Sabina Gallina, Cesare Mantini, Mohammed Y. Khanji, C. Anwar A. Chahal and Fabrizio Ricci
447	Genotype–Phenotype Correlation of EVC Variants in Ellis-Van Creveld Syndrome: A Systematic Review and Case Report by Sandra Rodriguez-Cambranis, Addy-Manuela Castillo-Espinola, Claudia-Daniela Fuentelzas-Rosado, Paulina Salazar-Sansores, Claudia-Gabriela Nuñez-Solis, Hugo-Antonio Laviada-Molina, Aurea-Karina Zetina-Solorzano and Felix-Julian Campos-Garcia
424	Systematic Review of Pharmacogenetics of Immunosuppressants in Heart Transplantation by Juan Eduardo Megías-Vericat, Tomás Palanques-Pastor, Mireya Fernández-Sánchez, Eduardo Guerrero-Hurtado, Mayte Gil-Candel, Antonio Solana-Altabella, Octavio Ballesta-López, María Centelles-Oria, Javier García-Pellicer and José Luis Poveda-Andrés
407	Brugada Syndrome: Channelopathy and/or Cardiomyopathy by Michele Ciabatti, Pasquale Notarstefano, Chiara Zocchi, Giacomo Virgili, Fulvio Bellocci, Iacopo Olivotto and Maurizio Pieroni
402	How to Enhance Diagnosis in Fabry Disease: The Power of Information by Maria Chiara Meucci, Rosa Lillo, Margherita Calcagnino, Giampaolo Tocci, Eustachio Agricola, Federico Biondi, Claudio Di Brango, Vincenzo Guido, Valentina Parisi, Francesca Giordana, Veronica Melita, Mariaelena Lombardi, Angela Beatrice Scardovi, Li Van Stella Truong, Francesca Musella, Francesco di Spigno, Benedetta Matrone, Ivana Pariggiano, Paolo Calabrò, Roberto Spoladore, Stefania Luceri, Stefano Carugo, Francesca Graziani and Francesco Burzotta Show full author list Hide full author list
397	Novel Perspectives on Genetic Evaluation in Early-Onset Atrial Fibrillation: Clinical Implications and Future Directions by Angelo Laconi, Tatiana Fancello, Giuliana Solinas and Gavino Casu
372	TNNC1 Gene Mutation in Ebstein’s Anomaly and Left Ventricular Hypertrabeculation: A Case Report of a New Causative Mutation? by Irene Raso, Claudia Chillemi, Giorgia Prontera, Arianna Laoreti, Elisa Cattaneo, Valeria Calcaterra, Gian Vincenzo Zuccotti and Savina Mannarino
358	The Influence of Genotype on the Cardiopulmonary Test Response in Patients Affected by Hypertrophic Cardiomyopathy by Maria Felicia Gagliardi, Gabriella Malfatto, Claudia Baratto, Alessia Giglio, Valeria Rella, Paolo Cerea, Davide Mariani, Sabrina Salerno, Silvia Ravaro, Silvia Castelletti, Gerardina Fratianni, Chiara Alberio, Matteo Pedrazzini, Mariam Khujadze, Luigi P. Badano, Denisa Muraru, Gianfranco Parati, Franco Cecchi, Sergio Caravita and Lia Crotti
343	Integrated Deep Learning Framework for Cardiac Risk Stratification and Complication Analysis in Leigh’s Disease by Md Aminul Islam, Jayasree Varadarajan, Md Abu Sufian, Bhupesh Kumar Mishra and Md Ruhul Amin Rasel

Downloads	Article
259	Integrating Genetic, Clinical, and Histopathological Data for Definitive Diagnosis of PRKAG2-Related Disease by Martina Caiazza, Emanuele Monda, Francesco Loffredo, Rossana Bussani, Vera Fico, Emanuele Bobbio, Chiara Cirillo, Anna Murredda, Immacolata Viscovo, Alessandra Scatteia, Santo Dellegrottaglie, Diego Colonna, Berardo Sarubbi, Maria Giovanna Russo, Paolo Golino, Gianfranco Sinagra and Giuseppe Limongelli
253	From Genetics to Phenotype: Understanding the Diverse Manifestations of Cardiovascular Genetic Diseases in Pediatric Populations by Jule Leonie Gutmann, Alina Spister and Lara Baticic
236	MicroRNA and DNA Methylation Adaptation Mechanism to Endurance Training in Cardiovascular Disease: A Systematic Review by Jil Delhez, Jeanne Ougier, Francisco Xavier de Araujo, Raphael Martins de Abreu and Camilo Corbellini
209	Sinus Bradycardia and Long QT Syndrome: Double Heterozygosity for Variants in KCNH2 and HCN4 by Jaël S. Copier, Fenna Tuijnenburg, Karolina Andrzejczyk, Alex V. Postma, Saskia N. van der Crabben, Oussama Najih, Caroline Pham, Leander Beekman, Arie O. Verkerk, Ahmad S. Amin and Elisabeth M. Lodder
201	The Hidden Face of Danon Disease: Unique Challenges for Female Patients by Laura Torlai Triglia, Federico Barocelli, Enrico Ambrosini, Alberto Bettella, Filippo Luca Gurgoglione, Michele Bianconcini, Angela Guidorossi, Francesca Russo, Antonio Percesepe and Giampaolo Niccoli
165	*Digenic Contribution of Heterozygous ALPK3* and TRIM63 Variants to End-Stage Hypertrophic Cardiomyopathy in a Young Adult by Olga S. Chumakova, Natalia V. Milovanova, Elena A. Mershina, Sergey I. Kutsev and Ekaterina Y. Zakharova**
156	Non-Lysosomal Glycogen Storage Cardiomyopathy with Hypertrophic Phenotype Due to PRKAG2 c.905G>A (p.Arg302Gln): Case Report and Narrative Review by Pasquale Crea, Alice Moncada, Francesco Catanzariti, Graziella Agnelli, Michela Navarra, Claudia Rubino, Irene Scimè, Lucio Teresi, Maurizio Cusmà Piccione, Luigi Colarusso, Roberto Licordari, Giuseppe Dattilo and Gianluca Di Bella
98	Genetic Variants as a Potentially Arrhythmogenic Substrate in Mitral Annular Disjunction: Case Report and a Systematic Review of the Literature by Lorenzo Bianchi, Marialaura Buscemi, Domenico Coviello, Massimiliano Cecconi, Andrea Minghini, Stefano Cornara, Matteo Astuti, Francesco Pentimalli, Pietro Bellone, Emmanuel Androulakis and Alberto Somaschini
97	The Genetic Architecture of Sudden Cardiac Death: A State-of-the-Art Review by Sabrina Montuoro, Emanuele Monda, Gaetano Diana, Emanuele Bobbio, Vera Fico, Marta Rubino, Martina Caiazza, Adelaide Fusco, Annapaola Cirillo, Federica Verrillo, Francesca Dongiglio, Giuseppe Palmiero, Federica Barra, Giulia Frisso, Maria Giovanna Russo, Paolo Calabrò and Giuseppe Limongelli
76	Exploring the Genetic Architecture of Myocarditis and Inherited Cardiomyopathies by Sukruth Pradeep Kundur, Ali Malik, Rasi Mizori and Sanjay Sivalokanathan

Downloads	Article
2064	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
1925	Cardiac Amyloidosis Therapy: A Systematic Review by Franco Iodice, Marco Di Mauro, Marco Giuseppe Migliaccio, Angela Iannuzzi, Roberta Pacileo, Martina Caiazza and Augusto Esposito
1903	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
1784	*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
1700	Cardiomyopathies and Arrythmias in Neuromuscular Diseases by Giuseppe Sgarito, Calogero Volpe, Stefano Bardari, Raimondo Calvanese, Paolo China, Giosuè Mascioli, Martina Nesti, Carlo Pignalberi, Manlio Cipriani and Massimo Zecchin
1683	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
1660	*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**
1643	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
1579	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
1470	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

Journal Menu

Journal Browser

Most Cited & Viewed

Most Cited & Viewed Papers

Further Information

Guidelines

MDPI Initiatives

Follow MDPI