Connie R. Bezzina

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 22 papers. Top paper: “52 Genetic Loci Influencing Myocardial Mass”.

52 Genetic Loci Influencing Myocardial Mass

Journal of the American College of Cardiology(2016)10.1016/j.jacc.2016.07.729

N/A

2.4DataRank · unranked

135 citations

Jessica van Setten, Niek Verweij, Georg Vogler, Matthew T. Maurano, Xinchen Wang +172 more

Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy

Journal of Clinical Investigation(2021)10.1172/jci142148

N/A

1.2DataRank · unranked

27 citations

Alex V. Postma, Christian Salazar, Daniel M. De Laughter, Fleur V.Y. Tjong, Lenka Piherová +51 more

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Nature Genetics(2025)10.1038/s41588-025-02074-9

N/A

0.628DataRank · unranked

28 citations

Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson +95 more

Targeting the Microtubule EB1-CLASP2 Complex Modulates Na V 1.5 at Intercalated Discs

Circulation Research(2021)10.1161/circresaha.120.318643

N/A

0DataRank · unranked

38 citations

Mariam Jouni, David Y. Chiang, Marta Pérez-Hernández, Svitlana Podliesna, Nuo Yu +21 more

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

Genetics in Medicine(2021)10.1038/s41436-021-01212-y

N/A

0DataRank · unranked

17 citations

Najim Lahrouchi, Fernanda M. Bosada, Gregor Dombrowsky, Simon G. Williams, Robert Lesurf +49 more

Animal models and animal-free innovations for cardiovascular research: current status and routes to be explored. Consensus document of the ESC Working Group on Myocardial Function and the ESC Working Group on Cellular Biology of the Heart

Cardiovascular Research(2022)10.1093/cvr/cvab370

N/A

0DataRank · unranked

78 citations

Folkert W. Asselbergs, Jeroen Bakkers, Sandor Batkai, Luc Bertrand, Connie R. Bezzina +56 more

Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies

Nature Cardiovascular Research(2023)10.1038/s44161-023-00346-3

N/A

0DataRank · unranked

34 citations

Sean J. Jurgens, Francesco Mazzarotto, Mona Allouba, James P. Pirruccello, Yasmine Aguib +6 more

The Role of MAPRE2 and Microtubules in Maintaining Normal Ventricular Conduction

Circulation Research(2023)10.1161/circresaha.123.323231

N/A

0DataRank · unranked

10 citations

Arie O. Verkerk, Rachelle Victorio, Boris Shneyer, Babet van der Vaart, Mariam Jouni +14 more

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

medRxiv(2023)10.1101/2023.01.28.23285147

N/A

0DataRank · unranked

12 citations

Sean Zheng, Christopher Grace, Paloma Jordà, Catherine Francis, Sean J. Jurgens +57 more

Common and Rare Variant Contributions to Bradyarrhythmias from Multi-Ancestry Meta-Analyses

medRxiv(2023)10.1101/2023.09.24.23295485

N/A

0DataRank · unranked

0 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +56 more

The role of MAPRE2 and microtubules in Brugada syndrome pathogenesis

European Heart Journal(2023)10.1093/eurheartj/ehad655.3059

N/A

0DataRank · unranked

0 citations

Boris Shneyer, Arie O. Verkerk, Babet van der Vaart, Rachelle Victorio, Nirodhini Narendran +6 more

Rare coding variant analysis for human diseases across biobanks and ancestries

Nature Genetics(2024)10.1038/s41588-024-01894-5

N/A

0DataRank · unranked

58 citations

Xin Wang, Seung Hoan Choi, Lu‐Chen Weng, Satoshi Koyama, James P. Pirruccello +20 more

Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

Nature Genetics(2024)10.1038/s41588-024-01975-5

N/A

0DataRank · unranked

51 citations

Joel Rämö, Daria R. Kramarenko, Leonoor F. J. M. Wijdeveld, Jan Haas, Mark Chaffin +55 more

Genetic testing in early-onset atrial fibrillation

European Heart Journal(2024)10.1093/eurheartj/ehae298

N/A

0DataRank · unranked

39 citations

Sean J. Jurgens, Joel Rämö, Ingrid E. Christophersen, Michiel Rienstra, Mina K. Chung +14 more

Genetic modifiers and ascertainment drive variable expressivity of complex disorders

medRxiv(2024)10.1101/2024.08.27.24312158

N/A

0DataRank · unranked

5 citations

Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Deepro Banerjee, Matthew T. Oetjens +65 more

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

medRxiv(2024)10.1101/2024.07.04.24309755

N/A

0DataRank · unranked

0 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +65 more

The impact of common and rare genetic variants on bradyarrhythmia development

Nature Genetics(2025)10.1038/s41588-024-01978-2

N/A

0DataRank · unranked

19 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +95 more

Automated patch clamp data improve variant classification and penetrance stratification for SCN5A –Brugada syndrome

European Heart Journal(2025)10.1093/eurheartj/ehaf874

N/A

0DataRank · unranked

4 citations

G. Joanne, Jessa L. Aldridge, Joseph F. Solus, Genevieve R Harvey, Paige H Roberson +8 more

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016

N/A

0DataRank · unranked

2 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 more

Multi-trait polygenic risk scores improve genomic prediction of atrial fibrillation across diverse ancestries

Research Square(2025)10.21203/rs.3.rs-7713077/v1

N/A

0DataRank · unranked

0 citations

Daria Kramarenko, Marre Corver, Nobuyuki Enzan, Dominic S. Zimmerman, Patrick T. Ellinor +3 more

Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity

Nature Genetics(2021)10.1038/s41588-020-00764-0

N/A

0DataRank · unranked

344 citations

Anuj Goel, Christopher Grace, Kate Thomson, Steffen E. Petersen, Xiao Hua Xu +64 more

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Nature Genetics(2021)10.1038/s41588-020-00762-2

N/A

0DataRank · unranked

296 citations

Catherine Francis, Xiao Yun Xu, Alexa M.C. Vermeer, Andrew R. Harper, Roy Huurman +65 more