Julien Barc

4.0k total citations
29 papers, 977 citations indexed

About

Julien Barc is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Julien Barc has authored 29 papers receiving a total of 977 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Cardiology and Cardiovascular Medicine, 22 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Julien Barc's work include Cardiac electrophysiology and arrhythmias (23 papers), Ion channel regulation and function (16 papers) and Cardiomyopathy and Myosin Studies (6 papers). Julien Barc is often cited by papers focused on Cardiac electrophysiology and arrhythmias (23 papers), Ion channel regulation and function (16 papers) and Cardiomyopathy and Myosin Studies (6 papers). Julien Barc collaborates with scholars based in France, Netherlands and United States. Julien Barc's co-authors include Arthur A.M. Wilde, Vincent Probst, Connie R. Bezzina, Jean‐Jacques Schott, Richard Redon, Solena Le Scouarnec, Florence Kyndt, Hervé Le Marec, Jean‐Baptiste Gourraud and Arie O. Verkerk and has published in prestigious journals such as Circulation, SHILAP Revista de lepidopterología and Journal of the American College of Cardiology.

In The Last Decade

Julien Barc

27 papers receiving 956 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Julien Barc France	14	843	662	110	46	41	29	977
Véronique Fressart France	18	879 1.0×	637 1.0×	130 1.2×	46 1.0×	44 1.1×	47	1.0k
Tamara T. Koopmann Netherlands	15	1.4k 1.7×	1.1k 1.7×	181 1.6×	74 1.6×	26 0.6×	21	1.6k
Tina S. Fong United States	6	395 0.5×	459 0.7×	100 0.9×	13 0.3×	24 0.6×	7	654
Stacie Kroboth United States	12	420 0.5×	403 0.6×	62 0.6×	17 0.4×	65 1.6×	21	676
Bi-Hua Tan United States	15	502 0.6×	570 0.9×	71 0.6×	18 0.4×	18 0.4×	18	802
Lena Refsgaard Denmark	11	555 0.7×	365 0.6×	39 0.4×	98 2.1×	12 0.3×	18	696
Nancy Ball United States	12	758 0.9×	617 0.9×	101 0.9×	14 0.3×	40 1.0×	13	927
Diana T. McCloskey United States	10	400 0.5×	364 0.5×	76 0.7×	10 0.2×	39 1.0×	10	575
Anita Alvarez‐Laviada United Kingdom	12	305 0.4×	435 0.7×	192 1.7×	20 0.4×	49 1.2×	19	613
Patric Glynn United States	11	403 0.5×	339 0.5×	69 0.6×	13 0.3×	33 0.8×	13	542

Countries citing papers authored by Julien Barc

Since Specialization

Citations

This map shows the geographic impact of Julien Barc's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Julien Barc with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Julien Barc more than expected).

Fields of papers citing papers by Julien Barc

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julien Barc. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Julien Barc. The network helps show where Julien Barc may publish in the future.

Co-authorship network of co-authors of Julien Barc

This figure shows the co-authorship network connecting the top 25 collaborators of Julien Barc. A scholar is included among the top collaborators of Julien Barc based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Julien Barc. Julien Barc is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

O’Neill, Matthew J., Joseph F. Solus, G Harvey, et al.. (2025). Automated patch clamp data improve variant classification and penetrance stratification for SCN5A –Brugada syndrome. European Heart Journal.

Proost, Virginnio, Aurélie Thollet, Julien Barc, et al.. (2024). Long-term prognosis of patients with an SCN5A loss-of-function variant and progressive cardiac conduction disorder or Brugada syndrome. Heart Rhythm. 22(5). 1321–1329. 2 indexed citations

Forest, Virginie, Pierre Lindenbaum, Estelle Baron, et al.. (2024). Generation of a patient-specific induced pluripotent stem cell line carrying the DES p.R406W mutation, an isogenic control and a DES p.R406W knock-in line. Stem Cell Research. 77. 103396–103396. 1 indexed citations

Treur, Jorien L., Dirk J. A. Smit, Rafik Tadros, et al.. (2024). Associations of schizophrenia with arrhythmic disorders and electrocardiogram traits: genetic exploration of population samples. The British Journal of Psychiatry. 226(3). 153–161. 1 indexed citations

Barc, Julien, Floriane Simonet, Estelle Baron, et al.. (2024). Role of common variants and new genes associated with arrhythmogenic cardiomyopathy. European Heart Journal. 45(Supplement_1). 1 indexed citations

Caillaud, Amandine, Aurélie Thedrez, Julien Barc, et al.. (2022). FACS-assisted CRISPR-Cas9 genome editing of human induced pluripotent stem cells. STAR Protocols. 3(4). 101680–101680. 8 indexed citations

Caillaud, Amandine, Caroline Chariau, Floriane Simonet, et al.. (2021). Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic background. Stem Cell Research. 59. 102647–102647. 2 indexed citations

Barc, Julien, Charlotte Glinge, Floriane Simonet, et al.. (2020). Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome. European Heart Journal. 41(Supplement_2).

Veerman, Christiaan C., Rafik Tadros, Elisabeth M. Lodder, et al.. (2017). The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity. Circulation Research. 121(5). 537–548. 44 indexed citations

10.

Gourraud, Jean‐Baptiste, Julien Barc, Aurélie Thollet, Hervé Le Marec, & Vincent Probst. (2017). Brugada syndrome: Diagnosis, risk stratification and management. Archives of cardiovascular diseases. 110(3). 188–195. 47 indexed citations

11.

Sacher, Frédéric, Bertrand Petit, Dominique Babuty, et al.. (2017). Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivity. Heart Rhythm. 14(10). 1442–1448. 28 indexed citations

12.

Kyndt, Florence, Philippe Mabo, Jacques Mansourati, et al.. (2017). Clinical Yield of Familial Screening After Sudden Death in Young Subjects. Circulation Arrhythmia and Electrophysiology. 10(9). 22 indexed citations

13.

Loussouarn, Gildas, Damien Sternberg, Sophie Nicole, et al.. (2016). Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison. Frontiers in Pharmacology. 6. 314–314. 48 indexed citations

14.

Veerman, Christiaan C., Isabella Mengarelli, Kaomei Guan, et al.. (2016). hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities. Scientific Reports. 6(1). 30967–30967. 53 indexed citations

15.

Shy, Diana, Ludovic Gillet, Jakob Ogrodnik, et al.. (2014). PDZ Domain–Binding Motif Regulates Cardiomyocyte Compartment-Specific Na _V 1.5 Channel Expression and Function. Circulation. 130(2). 147–160. 76 indexed citations

16.

Milano, Annalisa, Alexa M.C. Vermeer, Elisabeth M. Lodder, et al.. (2014). HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy. Journal of the American College of Cardiology. 64(8). 745–756. 126 indexed citations

17.

Marsman, Roos F., Julien Barc, Leander Beekman, et al.. (2013). A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence. Journal of the American College of Cardiology. 63(3). 259–266. 114 indexed citations

18.

Barc, Julien, Sébastien Schmitt, Florence Kyndt, et al.. (2010). Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome. Journal of the American College of Cardiology. 57(1). 40–47. 58 indexed citations

19.

Probst, Vincent, Arthur A.M. Wilde, Julien Barc, et al.. (2009). SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome. Circulation Cardiovascular Genetics. 2(6). 552–557. 211 indexed citations

20.

Barc, Julien, Vincent Probst, Arthur A.M. Wilde, et al.. (2009). G023 SCN5A mutations and the role of genetic background in the pathophysiology of brugada syndrome. Archives of cardiovascular diseases. 102. S70–S70. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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