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Citations	Article
6	*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	Calcium Release Deficiency Syndrome (CRDS): Rethinking “Atypical” Catecholaminergic Polymorphic Ventricular Tachycardia by Alessandra P. Porretta, Etienne Pruvot and Zahurul A. Bhuiyan
3	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
3	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
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	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
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	Exosome-Derived microRNAs in Hypertrophic Cardiomyopathy by Brian Xiangzhi Wang

Citations	Article
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	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
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	Calcium Release Deficiency Syndrome (CRDS): Rethinking “Atypical” Catecholaminergic Polymorphic Ventricular Tachycardia by Alessandra P. Porretta, Etienne Pruvot and Zahurul A. Bhuiyan
3	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
3	Exosome-Derived microRNAs in Hypertrophic Cardiomyopathy by Brian Xiangzhi Wang
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	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
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

Citations	Article
3	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
3	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
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	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	From Genetics to Phenotype: Understanding the Diverse Manifestations of Cardiovascular Genetic Diseases in Pediatric Populations by Jule Leonie Gutmann, Alina Spister and Lara Baticic
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
No cited articles available for this period.

Citations	Article
14	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
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
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
10	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
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
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

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13416	Dietary Approach in Familial Hypercholesterolemia by Joanna Popiolek-Kalisz, Klaudia Salamon, Michal Mazur, Klaudia Mikolajczyk and Grzegorz Kalisz
10005	Exploring the Role of Genetics in Sarcoidosis and Its Impact on the Development of Cardiac Sarcoidosis by Sanjay Sivalokanathan
8776	Hypertrophic Cardiomyopathy and Chronic Kidney Disease: An Updated Review by Sheefah Dhuny, Henry H. L. Wu, Manova David and Rajkumar Chinnadurai
8457	Gene Therapy for Inherited Arrhythmia Syndromes by Cameron J. Leong, Sohat Sharma, Jayant Seth, Archan Dave, Abdul Aziz Abdul Ghafoor and Zachary Laksman
7353	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
6794	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
6438	*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
5893	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
5476	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
5108	Exosome-Derived microRNAs in Hypertrophic Cardiomyopathy by Brian Xiangzhi Wang

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13416	Dietary Approach in Familial Hypercholesterolemia by Joanna Popiolek-Kalisz, Klaudia Salamon, Michal Mazur, Klaudia Mikolajczyk and Grzegorz Kalisz
8457	Gene Therapy for Inherited Arrhythmia Syndromes by Cameron J. Leong, Sohat Sharma, Jayant Seth, Archan Dave, Abdul Aziz Abdul Ghafoor and Zachary Laksman
6794	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
5108	Exosome-Derived microRNAs in Hypertrophic Cardiomyopathy by Brian Xiangzhi Wang
5051	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
4917	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
4734	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
4620	*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**
4610	Calcium Release Deficiency Syndrome (CRDS): Rethinking “Atypical” Catecholaminergic Polymorphic Ventricular Tachycardia by Alessandra P. Porretta, Etienne Pruvot and Zahurul A. Bhuiyan
4413	Ballooning and Bursting of Barrels and Pipes: A Rare Case of Suspected Vascular Ehlers–Danlos Disease by Ogechi Agogbuo, Sri Harsha Kanuri, Luis Salinas, Mohamed Goweba, Khashayar Vahdat, Oscar Chastian and Larry Frase

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6794	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
4734	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
3459	From Genetics to Phenotype: Understanding the Diverse Manifestations of Cardiovascular Genetic Diseases in Pediatric Populations by Jule Leonie Gutmann, Alina Spister and Lara Baticic
3329	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
2739	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
2514	Genetic Profile of Pediatric-Onset Cardiac Channelopathies by Sara Giovani, Adelaide Ballerini, Alessia Gozzini, Michele Di Lorenzo, Davide Mei, Silvia Passantino, Mattia Zampieri, Alessia Tomberli, Alberto Marchi, Giovanni Battista Calabri, Gaia Spaziani, Giulio Porcedda, Elena Bennati, Silvia Favilli, Iacopo Olivotto and Francesca Girolami
2364	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
2252	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
2058	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
2045	*Dilated Cardiomyopathy and Sensorimotor Polyneuropathy Associated with a Homozygous ELAC2* Variant: A Case Report and Literature Review by Francesco Ravera, Filippo Angelini, Pier Paolo Bocchino, Gianluca Marcelli, Giulia Gobello, Giuseppe Giannino, Guglielmo Merlino, Benedetta De Guidi, Andrea Destefanis, Giulia Margherita Brach Del Prever, Carla Giustetto, Guglielmo Gallone, Stefano Pidello, Antonella Barreca, Silvia Deaglio, Gaetano Maria De Ferrari, Claudia Raineri and Veronica Dusi**

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1564	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
1512	Exploring the Genetic Architecture of Myocarditis and Inherited Cardiomyopathies by Sukruth Pradeep Kundur, Ali Malik, Rasi Mizori and Sanjay Sivalokanathan
1226	*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**
1145	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
1007	Noonan Syndrome: A Comprehensive Review from Clinical Delineation to the Molecular Era of RASopathies and Lifelong Cardiologic Management by Giuseppe Calcaterra, Maria Giulia Gagliardi, Carlo Bassano, Rosalinda Palmieri, Giuseppe Vadalà, Pier Paolo Bassareo and Marco Cappa
906	Whole-Genome Sequencing in Premature Coronary Artery Disease in South Asians: A Pilot Case–Control Study by Iftikhar Ali Ch, Azhar Chaudhry, Fazal Jalil, Yasir Ali, Waseem Iqbal, Yusra Javed, Salman Khalid, Azeen Razzaq, Muhammad Azhar, Amna Nadeem, Tayyab Afzal, Naeem Tahirkheli, Ankur Kalra and Khurram Nasir
877	Report on the Post-Translational Modifications (PTMs) Prediction in Hypertrophic Cardiomyopathy-Associated Proteins MYH7, MYBPC3, TNNT2, and TNNI3, and Five Unknown PTMs in MYH7 (K129, K1451) and MYBPC3 (K14, R44, T705) by Natasha Trajkovska, Lenche Jovova and Done Stojanov
874	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
767	Genetic Basis of Cardiomyopathies Associated with Endocrinopathies: A Comprehensive Review by Antonio Concistrè, Claudia Caramazza, Marco D’Abbondanza, Rachele Santori and Giuseppe Imperoli
747	Influence of Genetic and Epigenetic Factors in Takotsubo Syndrome: Insights and Gaps of an Incompletely Understood Disease by Giulio La Rosa, Gemma Pelargonio, Francesco Santoro, Sergio Conti, Francesco Campo and Giuseppe Sgarito

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15683	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
15274	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
14015	Cardiac Involvement in Autosomal Dominant Polycystic Kidney Disease by Letizia Spinelli, Giuseppe Giugliano and Giovanni Esposito
13416	Dietary Approach in Familial Hypercholesterolemia by Joanna Popiolek-Kalisz, Klaudia Salamon, Michal Mazur, Klaudia Mikolajczyk and Grzegorz Kalisz
12131	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
10005	Exploring the Role of Genetics in Sarcoidosis and Its Impact on the Development of Cardiac Sarcoidosis by Sanjay Sivalokanathan
10003	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
9564	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
8915	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
8776	Hypertrophic Cardiomyopathy and Chronic Kidney Disease: An Updated Review by Sheefah Dhuny, Henry H. L. Wu, Manova David and Rajkumar Chinnadurai

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1845	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
1295	Gene-Specific Discriminative Echocardiogram Findings in Hypertrophic Cardiomyopathy Determined Using Artificial Intelligence: A Pilot Study by Mila Glavaški, Aleksandra Ilić and Lazar Velicki
1107	*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
1093	*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**
1089	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
1074	Hypertrophic Cardiomyopathy and Chronic Kidney Disease: An Updated Review by Sheefah Dhuny, Henry H. L. Wu, Manova David and Rajkumar Chinnadurai
1071	Gene Therapy for Inherited Arrhythmia Syndromes by Cameron J. Leong, Sohat Sharma, Jayant Seth, Archan Dave, Abdul Aziz Abdul Ghafoor and Zachary Laksman
1049	*Functional Characterization of the A414G Loss-of-Function Mutation in HCN4* Associated with Sinus Bradycardia by Arie O. Verkerk and Ronald Wilders**
1049	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
1020	Exploring the Role of Genetics in Sarcoidosis and Its Impact on the Development of Cardiac Sarcoidosis by Sanjay Sivalokanathan

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1845	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
1071	Gene Therapy for Inherited Arrhythmia Syndromes by Cameron J. Leong, Sohat Sharma, Jayant Seth, Archan Dave, Abdul Aziz Abdul Ghafoor and Zachary Laksman
920	Dietary Approach in Familial Hypercholesterolemia by Joanna Popiolek-Kalisz, Klaudia Salamon, Michal Mazur, Klaudia Mikolajczyk and Grzegorz Kalisz
886	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
881	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
799	Exosome-Derived microRNAs in Hypertrophic Cardiomyopathy by Brian Xiangzhi Wang
774	*Review of p.(Val429Met), a Variant of LDLR* That Is Associated with Familial Hypercholesterolemia by Eric F. Jotch and Mark S. Kindy**
760	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
746	*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**
740	Calcium Release Deficiency Syndrome (CRDS): Rethinking “Atypical” Catecholaminergic Polymorphic Ventricular Tachycardia by Alessandra P. Porretta, Etienne Pruvot and Zahurul A. Bhuiyan

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621	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
482	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
479	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
451	Polygenic Risk Scores and Coronary Artery Disease by Salman Ansari, Suvasini Lakshmanan and Matthew J. Budoff
426	Association Between Angiotensinogen Gene M235T and Renin–Angiotensin System Insertion/Deletion Variants and Risk of Cardiovascular Disease in North African and Middle Eastern Populations: A Systematic Review and Meta-Analysis by Rajaa El Mansouri, Hind Dehbi and Rachida Habbal
409	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
402	*Dilated Cardiomyopathy and Sensorimotor Polyneuropathy Associated with a Homozygous ELAC2* Variant: A Case Report and Literature Review by Francesco Ravera, Filippo Angelini, Pier Paolo Bocchino, Gianluca Marcelli, Giulia Gobello, Giuseppe Giannino, Guglielmo Merlino, Benedetta De Guidi, Andrea Destefanis, Giulia Margherita Brach Del Prever, Carla Giustetto, Guglielmo Gallone, Stefano Pidello, Antonella Barreca, Silvia Deaglio, Gaetano Maria De Ferrari, Claudia Raineri and Veronica Dusi**
398	From Genetics to Phenotype: Understanding the Diverse Manifestations of Cardiovascular Genetic Diseases in Pediatric Populations by Jule Leonie Gutmann, Alina Spister and Lara Baticic
396	Genetic Profile of Pediatric-Onset Cardiac Channelopathies by Sara Giovani, Adelaide Ballerini, Alessia Gozzini, Michele Di Lorenzo, Davide Mei, Silvia Passantino, Mattia Zampieri, Alessia Tomberli, Alberto Marchi, Giovanni Battista Calabri, Gaia Spaziani, Giulio Porcedda, Elena Bennati, Silvia Favilli, Iacopo Olivotto and Francesca Girolami
385	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

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270	*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**
265	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
263	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
224	Exploring the Genetic Architecture of Myocarditis and Inherited Cardiomyopathies by Sukruth Pradeep Kundur, Ali Malik, Rasi Mizori and Sanjay Sivalokanathan
196	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
175	Genetic Basis of Cardiomyopathies Associated with Endocrinopathies: A Comprehensive Review by Antonio Concistrè, Claudia Caramazza, Marco D’Abbondanza, Rachele Santori and Giuseppe Imperoli
172	Influence of Genetic and Epigenetic Factors in Takotsubo Syndrome: Insights and Gaps of an Incompletely Understood Disease by Giulio La Rosa, Gemma Pelargonio, Francesco Santoro, Sergio Conti, Francesco Campo and Giuseppe Sgarito
172	Report on the Post-Translational Modifications (PTMs) Prediction in Hypertrophic Cardiomyopathy-Associated Proteins MYH7, MYBPC3, TNNT2, and TNNI3, and Five Unknown PTMs in MYH7 (K129, K1451) and MYBPC3 (K14, R44, T705) by Natasha Trajkovska, Lenche Jovova and Done Stojanov
168	Whole-Genome Sequencing in Premature Coronary Artery Disease in South Asians: A Pilot Case–Control Study by Iftikhar Ali Ch, Azhar Chaudhry, Fazal Jalil, Yasir Ali, Waseem Iqbal, Yusra Javed, Salman Khalid, Azeen Razzaq, Muhammad Azhar, Amna Nadeem, Tayyab Afzal, Naeem Tahirkheli, Ankur Kalra and Khurram Nasir
151	Beyond Wall Thickness: Clinical Predictors of Genotype Positivity in Hypertrophic Cardiomyopathy by Filippo Angelini, Veronica Dusi, Amedeo Maria Feneziani, Rossella Manai, Matteo Bianco, Enrica Lonni, Giulia Margherita Brach Del Prever, Pier Paolo Bocchino, Giuseppe Giannino, Daniele Melis, Giulia Gobello, Francesco Ravera, Lucia Elena Laiso, Federico Juvenal, Guglielmo Gallone, Stefano Pidello, Barbara Mabritto, Daniela Giachino, Giuseppe Musumeci, Alessandra Chinaglia, Walter Grosso Marra, Silvia Deaglio, Gaetano Maria De Ferrari and Claudia Raineri Show full author list Hide full author list

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2145	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
1971	Cardiac Amyloidosis Therapy: A Systematic Review by Franco Iodice, Marco Di Mauro, Marco Giuseppe Migliaccio, Angela Iannuzzi, Roberta Pacileo, Martina Caiazza and Augusto Esposito
1968	Genetics of Heritable Thoracic Aortic Disease by Efstathios Papatheodorou, Dimitrios Degiannis and Aris Anastasakis
1855	*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
1845	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
1796	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
1731	*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**
1717	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
1637	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
1523	Cardiac Involvement in Autosomal Dominant Polycystic Kidney Disease by Letizia Spinelli, Giuseppe Giugliano and Giovanni Esposito

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