Damien Sternberg

4.1k total citations
80 papers, 2.6k citations indexed

About

Damien Sternberg is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Damien Sternberg has authored 80 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 43 papers in Cardiology and Cardiovascular Medicine and 29 papers in Cellular and Molecular Neuroscience. Recurrent topics in Damien Sternberg's work include Ion channel regulation and function (44 papers), Cardiac electrophysiology and arrhythmias (35 papers) and Genetic Neurodegenerative Diseases (21 papers). Damien Sternberg is often cited by papers focused on Ion channel regulation and function (44 papers), Cardiac electrophysiology and arrhythmias (35 papers) and Genetic Neurodegenerative Diseases (21 papers). Damien Sternberg collaborates with scholars based in France, Canada and United States. Damien Sternberg's co-authors include Bertrand Fontaine, Emmanuel Fournier, Savine Vicart, Pascal Laforêt, Nacira Tabti, B. Eymard, Jean‐Claude Willer, Anne Lombès, Claude Jardel and Michel Fardeau and has published in prestigious journals such as Journal of Biological Chemistry, Brain and Neurology.

In The Last Decade

Damien Sternberg

78 papers receiving 2.5k citations

Peers

Damien Sternberg

CMN

CCM

NEURO

Nicole Monnier France

Stefano DiDonato Italy

Nobuya Fujita Japan

Gilles Millat France

Gábor Mikala Hungary

Arvid Suls Belgium

Christopher H. Thompson United States

Andrew P. Landstrom United States

Annette Feigenbaum Canada

Sumimasa Yamashita Japan

Nicole Monnier France

Damien Sternberg

2.8k ×1.3

594 ×0.5

CMN

1.8k ×1.7

CCM

99 ×0.3

NEURO

28 ×0.1

Citations per year, relative to Damien Sternberg Damien Sternberg (= 1×) peers Nicole Monnier

Countries citing papers authored by Damien Sternberg

Since Specialization

Citations

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

Fields of papers citing papers by Damien Sternberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Damien Sternberg

This figure shows the co-authorship network connecting the top 25 collaborators of Damien Sternberg. A scholar is included among the top collaborators of Damien Sternberg 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 Damien Sternberg. Damien Sternberg 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

Li, Dong, Armelle Magot, Yann Péréon, et al.. (2024). Expanding the Spectrum of Congenital Myopathy Linked to Variants in the MYBPC1 Gene. Neurology Clinical Practice. 14(3). e200228–e200228. 1 indexed citations

Dobbertin, Alexandre, B. Eymard, Damien Sternberg, et al.. (2023). Molecular Analysis of a Congenital Myasthenic Syndrome Due to a Pathogenic Variant Affecting the C-Terminus of ColQ. International Journal of Molecular Sciences. 24(22). 16217–16217.

Wolff, Nicolas, Damien Sternberg, Anthony Béhin, et al.. (2023). New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani–Lenz syndrome. Scientific Reports. 13(1). 14054–14054. 2 indexed citations

Malfatti, Edoardo, Sonia Nouioua, Emmanuel Fournier, et al.. (2021). A TOR1AIP1 variant segregating with an early onset limb girdle myasthenia—Support for the role of LAP1 in NMJ function and disease. Neuropathology and Applied Neurobiology. 48(1). e12743–e12743. 6 indexed citations

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

Mussini, Jean‐Marie, Armelle Magot, Daniel Hantaı̈, et al.. (2015). Atypical nuclear abnormalities in a patient with Brody disease. Neuromuscular Disorders. 25(10). 773–779. 4 indexed citations

Nolent, Flora, Jérôme Maluenda, Fabienne Giuliano, et al.. (2015). Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Arthrogryposis. The American Journal of Human Genetics. 97(4). 616–620. 48 indexed citations

Eymard, B., Daniel Hantaı̈, Emmanuel Fournier, et al.. (2014). Syndromes myasthéniques congénitaux — L’expérience française. Bulletin de l Académie Nationale de Médecine. 198(2). 257–271. 1 indexed citations

Eymard, B., Tanya Stojkovic, Damien Sternberg, et al.. (2013). Syndromes myasthéniques congénitaux : difficultés diagnostiques, évolution et pronostic, thérapeutique L’expérience du réseau national « Syndromes Myasthéniques Congénitaux ». Revue Neurologique. 169. S45–S55. 18 indexed citations

10.

Simkin, Dina, Isabelle Léna, P. Landrieu, et al.. (2011). Mechanisms underlying a life‐threatening skeletal muscle Na⁺ channel disorder. The Journal of Physiology. 589(13). 3115–3124. 12 indexed citations

11.

Matthews, Emma, Doreen Fialho, S. Veronica Tan, et al.. (2009). The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment. Brain. 133(1). 9–22. 148 indexed citations

12.

Dupuis, Delphine S., Laurence Faivre, Alice Masurel‐Paulet, et al.. (2008). Severe neonatal non‐dystrophic myotonia secondary to a novel mutation of the voltage‐gated sodium channel (SCN4A) gene. American Journal of Medical Genetics Part A. 146A(3). 380–383. 53 indexed citations

13.

Schoser, Benedikt, J. M. Schröder, T. Grimm, Damien Sternberg, & Wolfram Kreß. (2007). A large german kindred with cold‐aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene. Muscle & Nerve. 35(5). 599–606. 15 indexed citations

14.

Mahjoub, S., et al.. (2007). A Novel Mitochondrial DNA tRNAIle (m.4322dupC) Mutation Associated With Idiopathic Dilated Cardiomyopathy. Diagnostic Molecular Pathology. 16(4). 238–242. 11 indexed citations

15.

Ferriby, D., et al.. (2006). A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification. Neuromuscular Disorders. 16(5). 321–324. 16 indexed citations

16.

Luce, Sandrine, et al.. (2005). A1152D mutation of the Na⁺ channel causes paramyotonia congenita and emphasizes the role of DIII/S4–S5 linker in fast inactivation. The Journal of Physiology. 565(2). 415–427. 16 indexed citations

17.

Vittecoq, Daniel, Claude Jardel, C. Barthélémy, et al.. (2002). Mitochondrial Damage Associated With Long-Term Antiretroviral Treatment: Associated Alteration or Causal Disorder?. JAIDS Journal of Acquired Immune Deficiency Syndromes. 31(3). 299–308. 45 indexed citations

18.

Sternberg, Damien. (2001). Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A. Brain. 124(6). 1091–1099. 159 indexed citations

19.

Bakker, Annette, C. Barthélémy, Paule Frachon, et al.. (2000). Functional Mitochondrial Heterogeneity in Heteroplasmic Cells Carrying the Mitochondrial DNA Mutation Associated with the MELAS Syndrome (Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes). Pediatric Research. 48(2). 143–150. 16 indexed citations

20.

Sternberg, Damien, Claude Danan, A. Lombès, et al.. (1998). Exhaustive Scanning Approach to Screen All the Mitochondrial tRNA Genes for Mutations and Its Application to the Investigation of 35 Independent Patients with Mitochondrial Disorders. Human Molecular Genetics. 7(1). 33–42. 63 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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