Alexandre Janin

928 total citations
38 papers, 505 citations indexed

About

Alexandre Janin is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Immunology. According to data from OpenAlex, Alexandre Janin has authored 38 papers receiving a total of 505 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Cardiology and Cardiovascular Medicine, 17 papers in Molecular Biology and 5 papers in Immunology. Recurrent topics in Alexandre Janin's work include Cardiomyopathy and Myosin Studies (15 papers), Cardiac electrophysiology and arrhythmias (10 papers) and Cardiovascular Effects of Exercise (9 papers). Alexandre Janin is often cited by papers focused on Cardiomyopathy and Myosin Studies (15 papers), Cardiac electrophysiology and arrhythmias (10 papers) and Cardiovascular Effects of Exercise (9 papers). Alexandre Janin collaborates with scholars based in France, United States and Switzerland. Alexandre Janin's co-authors include Gilles Millat, Philippe Chevalier, Valérie Chanavat, Alexandre Méjat, Vincent Gache, Francesca Ratti, Francis Bessière, Claire Dauphin, Élodie Morel and Véronique Schaeffer and has published in prestigious journals such as Circulation, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Alexandre Janin

35 papers receiving 502 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexandre Janin France 15 285 254 53 50 46 38 505
Nicolas Duquesnes France 9 235 0.8× 103 0.4× 26 0.5× 19 0.4× 21 0.5× 10 322
Alejandro Giraldo United Kingdom 10 263 0.9× 124 0.5× 32 0.6× 20 0.4× 102 2.2× 26 410
Shuangshuang Lu China 12 259 0.9× 62 0.2× 42 0.8× 34 0.7× 19 0.4× 28 409
Emad Muhammad Israel 8 199 0.7× 85 0.3× 29 0.5× 18 0.4× 15 0.3× 12 297
Yuanqing Feng China 7 261 0.9× 69 0.3× 34 0.6× 32 0.6× 43 0.9× 9 392
Milagros C. Romay United States 9 192 0.7× 138 0.5× 16 0.3× 24 0.5× 60 1.3× 11 367
Catherine Brunel‐Guitton Canada 14 454 1.6× 36 0.1× 56 1.1× 24 0.5× 38 0.8× 28 621
Shi-Jie Xu China 7 453 1.6× 633 2.5× 99 1.9× 86 1.7× 81 1.8× 10 890
Shu Shi United States 7 214 0.8× 45 0.2× 52 1.0× 93 1.9× 24 0.5× 13 349
Ziwen Li United Kingdom 9 191 0.7× 66 0.3× 18 0.3× 77 1.5× 16 0.3× 25 333

Countries citing papers authored by Alexandre Janin

Since Specialization
Citations

This map shows the geographic impact of Alexandre Janin'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 Alexandre Janin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexandre Janin more than expected).

Fields of papers citing papers by Alexandre Janin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexandre Janin. 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 Alexandre Janin. The network helps show where Alexandre Janin may publish in the future.

Co-authorship network of co-authors of Alexandre Janin

This figure shows the co-authorship network connecting the top 25 collaborators of Alexandre Janin. A scholar is included among the top collaborators of Alexandre Janin 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 Alexandre Janin. Alexandre Janin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Sebbag, Laurent, Cécile Cazeneuve, Nathan Mewton, et al.. (2025). Arrhythmogenic Cardiomyopathy Is a New Phenotype Associated With the CACNA1C p.Arg518Cys (R518C) Variant. JACC. Clinical electrophysiology. 11(11). 2509–2512.
2.
Li, Jin, Alexandre Janin, Nathalie Gaudreault, et al.. (2024). Circulating Autoantibodies Targeting TREK-1 in Patients With Short-Coupled Ventricular Fibrillation. Circulation. 150(24). 1944–1954. 1 indexed citations
3.
Ader, Flavie, Guillaume Jedraszak, Alexandre Janin, et al.. (2024). Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy. Clinical Genetics. 105(6). 676–682. 4 indexed citations
4.
Delinière, Antoine, Claudia Herrera‐Siklody, Alexis Hermida, et al.. (2023). Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant. Circulation Genomic and Precision Medicine. 16(3). 280–282. 5 indexed citations
5.
Janin, Alexandre, Audrey Putoux, Philippe Chevalier, et al.. (2023). Biallelic PRKAG2 Truncating Variants Are Associated with Severe Neonatal Cardiomyopathies. Circulation Genomic and Precision Medicine. 16(3). 277–279.
6.
Janin, Alexandre, Karine Nguyen, Émilie Consolino, et al.. (2022). Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing: A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants. Molecular Diagnosis & Therapy. 26(5). 551–560. 7 indexed citations
7.
Chanavat, Valérie, et al.. (2021). Whole Sequencing of Most Prevalent Dilated Cardiomyopathy-Causing Genes as a Molecular Strategy to Improve Molecular Diagnosis Efficiency?. DNA and Cell Biology. 40(3). 491–498. 1 indexed citations
8.
Tanno, Pauline Le, Laurence Faivre, Gabriel Laurent, et al.. (2021). Characterization of Loss-Of-Function KCNJ2 Mutations in Atypical Andersen Tawil Syndrome. Frontiers in Genetics. 12. 773177–773177. 2 indexed citations
9.
Janin, Alexandre, et al.. (2021). Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center’s Experience Over 5 Years. Molecular Diagnosis & Therapy. 25(3). 373–385. 14 indexed citations
10.
Chevalier, Philippe, Adrien Moreau, Sylvain Richard, et al.. (2021). Short QT interval as a harbinger of an arrhythmogenic cardiomyopathy. HeartRhythm Case Reports. 7(11). 734–738. 4 indexed citations
11.
Janin, Alexandre, Nicolas Chatron, Luc Dauchet, et al.. (2020). PCSK9 post-transcriptional regulation: Role of a 3′UTR microRNA-binding site variant in linkage disequilibrium with c.1420G. Atherosclerosis. 314. 63–70. 10 indexed citations
12.
Janin, Alexandre, Valérie Chanavat, Pierre‐Antoine Rollat‐Farnier, et al.. (2019). Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy. Human Mutation. 41(2). 465–475. 17 indexed citations
13.
Filippo, Mathilde Di, Sophie Collardeau‐Frachon, Alexandre Janin, et al.. (2019). Normal serum ApoB48 and red cells vitamin E concentrations after supplementation in a novel compound heterozygous case of abetalipoproteinemia. Atherosclerosis. 284. 75–82. 9 indexed citations
14.
Janin, Alexandre, et al.. (2018). First identification of homozygous truncating CSRP3 variants in two unrelated cases with hypertrophic cardiomyopathy. Gene. 676. 110–116. 19 indexed citations
15.
Janin, Alexandre, Francesca Ratti, A. Bertrand, et al.. (2018). SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells. Scientific Reports. 8(1). 5618–5618. 5 indexed citations
16.
Janin, Alexandre, et al.. (2018). TRPM4 mutations to cause autosomal recessive and not autosomal dominant Brugada type 1 syndrome. European Journal of Medical Genetics. 62(6). 103527–103527. 24 indexed citations
17.
Charrière, Sybil, Thomas Simonet, Véronique Bonnet, et al.. (2018). Single, short in‐del, and copy number variations detection in monogenic dyslipidemia using a next‐generation sequencing strategy. Clinical Genetics. 94(1). 132–140. 15 indexed citations
18.
Mallet, Delphine, Alexandre Janin, Rita Menassa, et al.. (2018). Aberrant Splicing Is the Pathogenicity Mechanism of the p.Glu314Lys Variant in CYP11A1 Gene. Frontiers in Endocrinology. 9. 491–491. 15 indexed citations
19.
Chanavat, Valérie, Alexandre Janin, & Gilles Millat. (2015). A fast and cost-effective molecular diagnostic tool for genetic diseases involved in sudden cardiac death. Clinica Chimica Acta. 453. 80–85. 27 indexed citations
20.
Schaeffer, Véronique, et al.. (1998). Sequencing‐based typing reveals six novel MHC class I chain‐related gene B (MICB) alleles. Tissue Antigens. 51(6). 649–652. 32 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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