Karine Nguyen

3.9k total citations
59 papers, 1.3k citations indexed

About

Karine Nguyen is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Karine Nguyen has authored 59 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 21 papers in Cardiology and Cardiovascular Medicine and 10 papers in Genetics. Recurrent topics in Karine Nguyen's work include Muscle Physiology and Disorders (20 papers), Cardiomyopathy and Myosin Studies (19 papers) and Congenital heart defects research (8 papers). Karine Nguyen is often cited by papers focused on Muscle Physiology and Disorders (20 papers), Cardiomyopathy and Myosin Studies (19 papers) and Congenital heart defects research (8 papers). Karine Nguyen collaborates with scholars based in France, United States and Switzerland. Karine Nguyen's co-authors include Nicolas Lévy, France Leturcq, Rafaëlle Bernard, Shahram Attarian, Guillaume Bassez, Martin Krahn, Véronique Labelle, Jean Pouget, B. Eymard and Dominique Figarella‐Branger and has published in prestigious journals such as Nucleic Acids Research, Brain and Neurology.

In The Last Decade

Karine Nguyen

54 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karine Nguyen France 19 954 337 243 235 192 59 1.3k
Luca Bello Italy 21 1.0k 1.1× 270 0.8× 249 1.0× 285 1.2× 219 1.1× 84 1.4k
Joachim Schessl Germany 22 622 0.7× 386 1.1× 265 1.1× 165 0.7× 123 0.6× 43 1.2k
Andrea Klein Switzerland 22 837 0.9× 211 0.6× 187 0.8× 513 2.2× 164 0.9× 70 1.5k
Marina Pedemonte Italy 21 1.0k 1.1× 163 0.5× 176 0.7× 243 1.0× 169 0.9× 57 1.3k
C.S.M. Straathof Netherlands 18 728 0.8× 154 0.5× 213 0.9× 250 1.1× 134 0.7× 35 1.1k
Patrizia Ciscato Italy 17 826 0.9× 176 0.5× 212 0.9× 181 0.8× 115 0.6× 47 1.1k
Sylvie Tuffery‐Giraud France 26 1.2k 1.3× 432 1.3× 221 0.9× 269 1.1× 107 0.6× 72 2.0k
Tadayuki Ishihara Japan 22 1.1k 1.1× 307 0.9× 466 1.9× 208 0.9× 219 1.1× 65 1.5k
Giuliana Galluzzi Italy 19 1.4k 1.5× 331 1.0× 411 1.7× 306 1.3× 110 0.6× 26 1.6k
Rafaëlle Bernard France 20 2.3k 2.5× 354 1.1× 237 1.0× 274 1.2× 219 1.1× 54 2.8k

Countries citing papers authored by Karine Nguyen

Since Specialization
Citations

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

Fields of papers citing papers by Karine Nguyen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karine Nguyen

This figure shows the co-authorship network connecting the top 25 collaborators of Karine Nguyen. A scholar is included among the top collaborators of Karine Nguyen 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 Karine Nguyen. Karine Nguyen 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.
Nguyen, Karine, et al.. (2023). Genetic profile and genotype–phenotype correlations in childhood cardiomyopathy. Archives of cardiovascular diseases. 116(6-7). 309–315. 4 indexed citations
2.
Paulsen, Ole, et al.. (2023). (112) Treatment Options for Female Sexual Dysfunction in Patients with Epilepsy: A Systematic Review. The Journal of Sexual Medicine. 20(Supplement_2).
3.
Audic, Frédérique, Annie Verschueren, Shahram Attarian, et al.. (2023). Retrospective clinical and genetic analysis of COL6-RD patients with a long-term follow-up at a single French center. Frontiers in Genetics. 14. 1242277–1242277. 2 indexed citations
4.
Théron, Alexis, Jérôme Hourdain, Hélène Martel, et al.. (2023). SCN5A variants as genetic arrhythmias triggers for familial bileaflet mitral valve prolapse. Archives of Cardiovascular Diseases Supplements. 15(2). 224–224.
5.
Dion, Camille, David Hirst, Leslie Caron, et al.. (2023). In skeletal muscle and neural crest cells, SMCHD1 regulates biological pathways relevant for Bosma syndrome and facioscapulohumeral dystrophy phenotype. Nucleic Acids Research. 51(14). 7269–7287. 3 indexed citations
6.
Théron, Alexis, Jérôme Hourdain, Hélène Martel, et al.. (2022). SCN5A Variants as Genetic Arrhythmias Triggers for Familial Bileaflet Mitral Valve Prolapse. International Journal of Molecular Sciences. 23(22). 14447–14447. 1 indexed citations
7.
Bartoli, Marc, Nathalie Bonello‐Palot, Christophe Pécheux, et al.. (2021). Retrospective analysis and reclassification of DYSF variants in a large French series of dysferlinopathy patients. Genetics in Medicine. 23(8). 1574–1577. 14 indexed citations
8.
Germain, Dominique P., Thierry Levade, Bertrand Knebelmann, et al.. (2021). Challenging the traditional approach for interpreting genetic variants: Lessons from Fabry disease. Clinical Genetics. 101(4). 390–402. 46 indexed citations
9.
Donghi, Valeria, Farouk Tradi, Andreina Carbone, et al.. (2020). Left-ventricular non-compaction–comparison between different techniques of quantification of trabeculations: Should the diagnostic thresholds be modified?. Archives of cardiovascular diseases. 113(5). 321–331. 2 indexed citations
10.
Essayagh, Benjamin, Noémie Resseguier, Nicolas Michel, et al.. (2020). Left atrial dysfunction as marker of poor outcome in patients with hypertrophic cardiomyopathy. Archives of cardiovascular diseases. 114(2). 96–104. 24 indexed citations
11.
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
12.
Boyer, Anthony, R. Bellance, Martin Krahn, et al.. (2019). Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth disease. Journal of Human Genetics. 65(3). 313–323. 7 indexed citations
13.
Eyries, Mélanie, David Montani, Sophie Nadaud, et al.. (2018). Widening the landscape of heritable pulmonary hypertension mutations in paediatric and adult cases. European Respiratory Journal. 53(3). 1801371–1801371. 66 indexed citations
14.
Nguyen, Karine, Francesca Puppo, Stéphane Roche, et al.. (2017). Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy. Human Mutation. 38(10). 1432–1441. 30 indexed citations
15.
Puppo, Francesca, Stéphane Roche, Camille Dion, et al.. (2016). Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report. BMC Medical Genetics. 17(1). 66–66. 9 indexed citations
16.
Blandin, Gaëlle, Christophe Béroud, Véronique Labelle, et al.. (2011). UMD-DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene. Human Mutation. 33(3). E2317–E2331. 36 indexed citations
17.
Krahn, Martin, Nicolas Wein, Marc Bartoli, et al.. (2010). A Naturally Occurring Human Minidysferlin Protein Repairs Sarcolemmal Lesions in a Mouse Model of Dysferlinopathy. Science Translational Medicine. 2(50). 50ra69–50ra69. 59 indexed citations
18.
Barat‐Houari, Mouna, Karine Nguyen, Rafaëlle Bernard, et al.. (2009). New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?. European Journal of Human Genetics. 18(5). 533–538. 11 indexed citations
19.
Nguyen, Karine, Guillaume Bassez, Martin Krahn, et al.. (2007). Phenotypic Study in 40 Patients With Dysferlin Gene Mutations. Archives of Neurology. 64(8). 1176–1176. 184 indexed citations
20.
Villard, Laurent, Karine Nguyen, Carlos Cardoso, et al.. (2002). A Locus for Bilateral Perisylvian Polymicrogyria Maps to Xq28. The American Journal of Human Genetics. 70(4). 1003–1008. 79 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Luca Bello Breakdown of academic impact, for papers by Joachim Schessl Breakdown of academic impact, for papers by Andrea Klein Breakdown of academic impact, for papers by Marina Pedemonte Breakdown of academic impact, for papers by C.S.M. Straathof Breakdown of academic impact, for papers by Patrizia Ciscato Breakdown of academic impact, for papers by Sylvie Tuffery‐Giraud Breakdown of academic impact, for papers by Tadayuki Ishihara Breakdown of academic impact, for papers by Giuliana Galluzzi Breakdown of academic impact, for papers by Rafaëlle Bernard
Rankless by CCL
2026