Martine Cohen‐Salmon

6.2k total citations
58 papers, 3.0k citations indexed

About

Martine Cohen‐Salmon is a scholar working on Molecular Biology, Neurology and Sensory Systems. According to data from OpenAlex, Martine Cohen‐Salmon has authored 58 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 19 papers in Neurology and 11 papers in Sensory Systems. Recurrent topics in Martine Cohen‐Salmon's work include Connexins and lens biology (21 papers), Barrier Structure and Function Studies (12 papers) and Hearing, Cochlea, Tinnitus, Genetics (11 papers). Martine Cohen‐Salmon is often cited by papers focused on Connexins and lens biology (21 papers), Barrier Structure and Function Studies (12 papers) and Hearing, Cochlea, Tinnitus, Genetics (11 papers). Martine Cohen‐Salmon collaborates with scholars based in France, United States and Switzerland. Martine Cohen‐Salmon's co-authors include Christine Petit, Anne Boulay, A. Amraoui, Bruno Saubaméa, Pascal Ezan, Jacques Loiselet, M’hamed Grati, Mirna Mustapha, Elie El‐Zir and Nabiha Salem and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Martine Cohen‐Salmon

57 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martine Cohen‐Salmon France 27 1.6k 1.1k 879 483 352 58 3.0k
Konrad Noben‐Trauth United States 25 1.7k 1.1× 2.0k 1.9× 550 0.6× 297 0.6× 422 1.2× 47 3.4k
Sherri M. Jones United States 33 861 0.5× 1.6k 1.5× 993 1.1× 250 0.5× 474 1.3× 80 2.6k
Anna Lysakowski United States 33 2.0k 1.2× 2.4k 2.2× 1.3k 1.5× 829 1.7× 706 2.0× 57 4.1k
Ruth Anne Eatock United States 31 1.8k 1.1× 2.9k 2.7× 1.2k 1.4× 551 1.1× 770 2.2× 57 4.1k
Stéphane Blanchard France 20 1.9k 1.1× 1.4k 1.3× 406 0.5× 227 0.5× 252 0.7× 32 2.9k
Gwenaëlle S. G. Géléoc United States 24 1.4k 0.9× 2.6k 2.4× 490 0.6× 386 0.8× 657 1.9× 39 3.3k
Saima Riazuddin United States 34 2.4k 1.5× 2.2k 2.1× 982 1.1× 170 0.4× 346 1.0× 101 4.0k
Bronya J.B. Keats United States 37 2.3k 1.4× 1.9k 1.7× 682 0.8× 420 0.9× 608 1.7× 103 4.2k
Saaïd Safieddine France 28 1.3k 0.8× 2.1k 2.0× 631 0.7× 525 1.1× 697 2.0× 52 2.8k
Xi Lin United States 27 1.4k 0.9× 1.6k 1.5× 406 0.5× 222 0.5× 392 1.1× 55 2.3k

Countries citing papers authored by Martine Cohen‐Salmon

Since Specialization
Citations

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

Fields of papers citing papers by Martine Cohen‐Salmon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martine Cohen‐Salmon. 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 Martine Cohen‐Salmon. The network helps show where Martine Cohen‐Salmon may publish in the future.

Co-authorship network of co-authors of Martine Cohen‐Salmon

This figure shows the co-authorship network connecting the top 25 collaborators of Martine Cohen‐Salmon. A scholar is included among the top collaborators of Martine Cohen‐Salmon 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 Martine Cohen‐Salmon. Martine Cohen‐Salmon 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.
Cohen‐Salmon, Martine, et al.. (2025). Development of perivascular astrocyte processes. Frontiers in Neuroscience. 19. 1585340–1585340. 3 indexed citations
2.
Boulay, Anne, Sabrina Martín, Corinne Blugeon, et al.. (2024). Vascular dysfunction is at the onset of oxaliplatin-induced peripheral neuropathy symptoms in mice. Life Science Alliance. 8(2). e202402791–e202402791.
3.
Tortuyaux, Romain, Noémie Mazaré, Philippe Mailly, et al.. (2022). Physiopathological changes of ferritin mRNA density and distribution in hippocampal astrocytes in the mouse brain. Journal of Neurochemistry. 164(6). 847–857. 3 indexed citations
4.
Vasile, Flora, Elena Dossi, Julien Moulard, et al.. (2022). Pannexin 1 activity in astroglia sets hippocampal neuronal network patterns. PLoS Biology. 20(12). e3001891–e3001891. 9 indexed citations
5.
Fouet, Agnès, Guillaume Bouvier, Abdelouhab Bouaboud, et al.. (2021). CC17 group B Streptococcus exploits integrins for neonatal meningitis development. Journal of Clinical Investigation. 131(5). 34 indexed citations
6.
Cohen‐Salmon, Martine, et al.. (2021). Astroglial Cx30 differentially impacts synaptic activity from hippocampal principal cells and interneurons. Glia. 69(9). 2178–2198. 8 indexed citations
7.
Elorza‐Vidal, Xabier, Aida Castellanos, Gina La Sala, et al.. (2021). Identification of the GlialCAM interactome: the G protein-coupled receptors GPRC5B and GPR37L1 modulate megalencephalic leukoencephalopathy proteins. Human Molecular Genetics. 30(17). 1649–1665. 17 indexed citations
8.
Tortuyaux, Romain, et al.. (2020). AstroDot – a new method for studying the spatial distribution of mRNA in astrocytes. Journal of Cell Science. 133(7). 15 indexed citations
9.
Delavallée, Laure, Lauriane Cabon, Aurélien Mazeraud, et al.. (2020). Mitochondrial AIF loss causes metabolic reprogramming, caspase-independent cell death blockade, embryonic lethality, and perinatal hydrocephalus. Molecular Metabolism. 40. 101027–101027. 20 indexed citations
10.
Ghézali, Grégory, Flora Vasile, Nathan Curry, et al.. (2019). Neuronal Activity Drives Astroglial Connexin 30 in Perisynaptic Processes and Shapes Its Functions. Cerebral Cortex. 30(2). 753–766. 17 indexed citations
11.
Boulay, Anne, Aurélien Mazeraud, Salvatore Cisternino, et al.. (2015). Immune Quiescence of the Brain Is Set by Astroglial Connexin 43. Journal of Neuroscience. 35(10). 4427–4439. 56 indexed citations
12.
Boulay, Anne, Salvatore Cisternino, Virginie Mignon, et al.. (2015). The Sarcoglycan complex is expressed in the cerebrovascular system and is specifically regulated by astroglial Cx30 channels. Frontiers in Cellular Neuroscience. 9. 36 indexed citations
13.
Boulay, Anne, Bruno Saubaméa, Xavier Declèves, & Martine Cohen‐Salmon. (2015). Purification of Mouse Brain Vessels. Journal of Visualized Experiments. e53208–e53208. 69 indexed citations
14.
Boulay, Anne, Francisco Castillo, Fabrice Giraudet, et al.. (2013). Hearing Is Normal without Connexin30. Journal of Neuroscience. 33(2). 430–434. 67 indexed citations
15.
Ezan, Pascal, Pascal André, Salvatore Cisternino, et al.. (2012). Deletion of Astroglial Connexins Weakens the Blood–Brain Barrier. Journal of Cerebral Blood Flow & Metabolism. 32(8). 1457–1467. 177 indexed citations
16.
Castillo, Francisco, Martine Cohen‐Salmon, Anne Charollais, et al.. (2009). Consortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexins. Human Molecular Genetics. 19(2). 262–275. 35 indexed citations
17.
Cohen‐Salmon, Martine, et al.. (2004). Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear. Cell and Tissue Research. 316(1). 15–22. 53 indexed citations
18.
Simmler, Marie‐Christine, Martine Cohen‐Salmon, A. Amraoui, et al.. (2000). Targeted disruption of Otog results in deafness and severe imbalance. Nature Genetics. 24(2). 139–143. 122 indexed citations
19.
Yasunaga, Shin’ichiro, M’hamed Grati, Martine Cohen‐Salmon, et al.. (1999). A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness. Nature Genetics. 21(4). 363–369. 429 indexed citations
20.
Cohen‐Salmon, Martine, Marie‐Geneviève Mattéi, & Christine Petit. (1999). Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18. Mammalian Genome. 10(5). 520–522. 15 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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