M. Mayer

4.2k total citations
49 papers, 1.5k citations indexed

About

M. Mayer is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, M. Mayer has authored 49 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 12 papers in Genetics and 8 papers in Surgery. Recurrent topics in M. Mayer's work include Neurogenetic and Muscular Disorders Research (10 papers), Muscle Physiology and Disorders (9 papers) and RNA Research and Splicing (7 papers). M. Mayer is often cited by papers focused on Neurogenetic and Muscular Disorders Research (10 papers), Muscle Physiology and Disorders (9 papers) and RNA Research and Splicing (7 papers). M. Mayer collaborates with scholars based in France, United States and Germany. M. Mayer's co-authors include Isabelle Desguerre, Catherine Chiron, France Leturcq, Gisèle Bonne, Pascale Guicheney, Romain K. Gherardi, Michel Fardeau, Christo Christov, Reinhard Zeller and Xavier Ferrer and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and Blood.

In The Last Decade

M. Mayer

47 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Mayer France 21 1.0k 333 210 202 172 49 1.5k
Antonella Pini Italy 16 800 0.8× 297 0.9× 111 0.5× 109 0.5× 292 1.7× 55 1.2k
Andrea Klein Switzerland 22 837 0.8× 513 1.5× 96 0.5× 301 1.5× 211 1.2× 70 1.5k
Sabrina W. Yum United States 25 880 0.8× 225 0.7× 174 0.8× 187 0.9× 543 3.2× 63 1.8k
Cheryl Longman United Kingdom 16 907 0.9× 183 0.5× 133 0.6× 73 0.4× 263 1.5× 46 1.2k
A. Reha United States 11 953 0.9× 281 0.8× 157 0.7× 60 0.3× 100 0.6× 29 1.5k
Adnan Y. Manzur United Kingdom 26 1.5k 1.4× 535 1.6× 215 1.0× 217 1.1× 351 2.0× 63 2.1k
Edmar Zanoteli Brazil 22 933 0.9× 587 1.8× 242 1.2× 413 2.0× 222 1.3× 159 1.8k
Mariacristina Scoto United Kingdom 23 1.2k 1.2× 817 2.5× 154 0.7× 441 2.2× 173 1.0× 70 2.0k
Umbertina Conti Reed Brazil 19 520 0.5× 323 1.0× 57 0.3× 170 0.8× 109 0.6× 81 956
Valeria Ricotti United Kingdom 23 1.2k 1.1× 224 0.7× 70 0.3× 69 0.3× 203 1.2× 57 1.5k

Countries citing papers authored by M. Mayer

Since Specialization
Citations

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

Fields of papers citing papers by M. Mayer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Mayer

This figure shows the co-authorship network connecting the top 25 collaborators of M. Mayer. A scholar is included among the top collaborators of M. Mayer 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 M. Mayer. M. Mayer 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.
McMillan, Hugh J., Thomas E. Cowling, Wayne Khuu, et al.. (2021). Burden of Spinal Muscular Atrophy (SMA) on Patients and Caregivers in Canada. Journal of Neuromuscular Diseases. 8(4). 553–568. 40 indexed citations
2.
Mayer, M., et al.. (2017). Satisfacción en pacientes con corrección de pene curvo congénito. Actas Urológicas Españolas. 42(6). 414–419. 6 indexed citations
3.
Vadrot, Nathalie, Patrick Vicart, Ana Ferreiro, et al.. (2017). A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus. PLoS ONE. 12(1). e0169189–e0169189. 20 indexed citations
4.
Chabrol, B. & M. Mayer. (2015). Principes de prise en charge multidisciplinaire des dystrophies musculaires de Duchenne. Archives de Pédiatrie. 22(12). 12S69–12S72. 3 indexed citations
5.
Labus, Jennifer S., Arpana Gupta, Iris Posserud, et al.. (2012). Randomised clinical trial: symptoms of the irritable bowel syndrome are improved by a psycho‐education group intervention. Alimentary Pharmacology & Therapeutics. 37(3). 304–315. 49 indexed citations
6.
Servais, Laurent, Nicolas Deconinck, A. Moraux, et al.. (2012). Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients. Neuromuscular Disorders. 23(2). 139–148. 62 indexed citations
7.
Mignot, Cyril, Delphine Héron, Joseph Bursztyn, et al.. (2012). Novel mutation in SLC9A6 gene in a patient with Christianson syndrome and retinitis pigmentosum. Brain and Development. 35(2). 172–176. 30 indexed citations
8.
Salleron, Julia, M. Mayer, Jean‐Marie Cuisset, et al.. (2011). Natural evolution of weight status in Duchenne muscular dystrophy: a retrospective audit. British Journal Of Nutrition. 105(10). 1486–1491. 45 indexed citations
9.
Béhin, Anthony, M. Mayer, Myriam Jugie, et al.. (2008). Severe neonatal myasthenia due to maternal anti-MuSK antibodies. Neuromuscular Disorders. 18(6). 443–446. 35 indexed citations
10.
Bahi‐Buisson, Nadia, Anna Kamińska, Rima Nabbout, et al.. (2006). Epilepsy in Menkes Disease: Analysis of Clinical Stages. Epilepsia. 47(2). 380–386. 56 indexed citations
11.
Quijano‐Roy, Susana, Itxaso Martì, S. Makri, et al.. (2005). Brain MRI abnormalities in muscular dystrophy due to FKRP mutations. Brain and Development. 28(4). 232–242. 26 indexed citations
12.
Barois, A, M. Mayer, Isabelle Desguerre, et al.. (2005). Amyotrophie spinale infantile Étude multicentrique prospective et longitudinale de 168 cas suivis 4 ans. Bulletin de l Académie Nationale de Médecine. 189(6). 1181–1199. 20 indexed citations
13.
Vitte, Jérémie, Natacha Roblot, M. Mayer, et al.. (2004). Deletion of Murine Smn Exon 7 Directed to Liver Leads to Severe Defect of Liver Development Associated with Iron Overload. American Journal Of Pathology. 165(5). 1731–1741. 84 indexed citations
14.
Viollet, Louis, Mohammed Zarhrate, Isabelle Maystadt, et al.. (2004). Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families. European Journal of Human Genetics. 12(6). 483–488. 12 indexed citations
15.
Moghadaszadeh, Behzad, Isabelle Desguerre, Haluk Topaloğlu, et al.. (1998). Identification of a New Locus for a Peculiar Form of Congenital Muscular Dystrophy with Early Rigidity of the Spine, on Chromosome 1p35-36. The American Journal of Human Genetics. 62(6). 1439–1445. 62 indexed citations
16.
Lopes, Judith, N. Ravisé, A. Vandenberghe, et al.. (1998). Fine mapping of de novo CMT1A and HNPP rearrangements within CMTIA-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination. Human Molecular Genetics. 7(1). 141–148. 66 indexed citations
17.
Krüger, Jürgen & M. Mayer. (1990). Two types of neuronal synchrony in monkey striate cortex. Biological Cybernetics. 64(2). 135–140. 12 indexed citations
18.
Mayer, M., et al.. (1989). Pharmacokinetics of mezlocillin in pleural fluid. International Journal of Clinical Practice. 43(7). 246–248. 1 indexed citations
19.
Sapin, Emmanuel, et al.. (1988). Trifid Pelvis and Controlatéral Bifid Ureter withBilateral Ureteropelvic Junction Obstruction(With 1 color plate). European Urology. 15(1-2). 144–145. 1 indexed citations
20.
Chiron, Catherine, P. Plouin, Olivier Dulac, M. Mayer, & G Ponsot. (1988). Epilepsies myocloniques des encephalopathies non progressives avec etats de mal myocloniques. Neurophysiologie Clinique. 18(6). 513–524. 4 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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