Michel Gugenheim

954 total citations
18 papers, 555 citations indexed

About

Michel Gugenheim is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Michel Gugenheim has authored 18 papers receiving a total of 555 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cellular and Molecular Neuroscience, 7 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in Michel Gugenheim's work include Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (5 papers) and Migraine and Headache Studies (4 papers). Michel Gugenheim is often cited by papers focused on Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (5 papers) and Migraine and Headache Studies (4 papers). Michel Gugenheim collaborates with scholars based in France, Switzerland and Japan. Michel Gugenheim's co-authors include P. Bouché, Alexis Brice, Yves Agid, Riadh Gouider, Éric Leguern, Sandrine Tardieu, Nazha Birouk, Thierry Maisonobe, H Rouger and J.M. Léger and has published in prestigious journals such as Neurology, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Michel Gugenheim

16 papers receiving 545 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michel Gugenheim France 11 424 235 158 143 71 18 555
Anne Höfer Germany 15 220 0.5× 324 1.4× 132 0.8× 131 0.9× 25 0.4× 16 565
Sinan Çomu Türkiye 8 91 0.2× 39 0.2× 39 0.2× 165 1.2× 62 0.9× 15 404
Yoko Kawazoe Japan 11 140 0.3× 56 0.2× 51 0.3× 73 0.5× 9 0.1× 14 444
J. Blake United Kingdom 9 468 1.1× 279 1.2× 124 0.8× 250 1.7× 90 1.3× 10 681
Ana L. Pelayo‐Negro Spain 13 304 0.7× 181 0.8× 99 0.6× 164 1.1× 46 0.6× 27 450
Geir J. Braathen Norway 11 326 0.8× 133 0.6× 132 0.8× 186 1.3× 73 1.0× 28 526
P. Byrne Ireland 12 373 0.9× 115 0.5× 250 1.6× 140 1.0× 120 1.7× 18 547
Karine Férraud France 9 185 0.4× 343 1.5× 11 0.1× 50 0.3× 37 0.5× 12 426
Ghassan Kabbach United States 6 97 0.2× 265 1.1× 95 0.6× 123 0.9× 40 0.6× 9 431
Natasa Schiza Cyprus 8 167 0.4× 370 1.6× 74 0.5× 190 1.3× 54 0.8× 9 578

Countries citing papers authored by Michel Gugenheim

Since Specialization
Citations

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

Fields of papers citing papers by Michel Gugenheim

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michel Gugenheim

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

All Works

18 of 18 papers shown
1.
Lantéri‐Minet, Michel, C. Collin, Michel Gugenheim, et al.. (2025). Prevalence, characteristics and management of migraine patients with triptan failure in primary care: the EMR France-Mig study. The Journal of Headache and Pain. 26(1). 153–153.
2.
Lucas, Christian, et al.. (2025). Migraine management in France: Practices of general practitioners and neurologists. Revue Neurologique. 181(7). 652–666.
3.
Ducros, Anne, et al.. (2024). Pratiques de prise en charge médicamenteuse des migraines et perception des nouveaux traitements par des médecins neurologues. Revue Neurologique. 180. S30–S30. 1 indexed citations
4.
Lucas, Christian, et al.. (2024). Pratiques de prise en charge médicamenteuse des migraines par des médecins généralistes. Revue Neurologique. 180. S31–S31. 1 indexed citations
5.
Lozeron, Pierre, Catherine Lacroix, Marie Théaudin, et al.. (2013). An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation. Amyloid. 20(3). 188–192. 24 indexed citations
6.
Kubis, Nathalie, Alexandra D�rr, Michel Gugenheim, et al.. (1999). Polyneuropathy in autosomal dominant cerebellar ataxias: Phenotype-genotype correlation. Muscle & Nerve. 22(6). 712–717. 38 indexed citations
7.
Birouk, Nazha, Éric Leguern, Thierry Maisonobe, et al.. (1998). X-linked Charcot-Marie-Tooth disease with connexin 32 mutations. Neurology. 50(4). 1074–1082. 133 indexed citations
8.
Rouger, H, Éric Leguern, Nazha Birouk, et al.. (1997). Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families. Human Mutation. 10(6). 443–450. 51 indexed citations
9.
Leguern, Éric, Riadh Gouider, Michel Gugenheim, et al.. (1996). Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12→p11 and for diagnosis. Cytogenetic and Genome Research. 72(1). 20–25. 11 indexed citations
10.
Lopes, Judith, Éric Leguern, Riadh Gouider, et al.. (1996). Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.. PubMed. 58(6). 1223–30. 44 indexed citations
11.
Lévy, Richard, et al.. (1996). [Pauci-symptomatic sensory polyneuropathy in Refsum's disease].. PubMed. 152(6-7). 469–72. 2 indexed citations
12.
Apartis, Emmanuelle, J.-M. Léger, L. Musset, et al.. (1996). Peripheral neuropathy associated with essential mixed cryoglobulinaemia: a role for hepatitis C virus infection?. Journal of Neurology Neurosurgery & Psychiatry. 60(6). 661–666. 76 indexed citations
13.
Leguern, Éric, Riadh Gouider, Judith Lopes, et al.. (1995). Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. Human Molecular Genetics. 4(9). 1673–1674. 15 indexed citations
14.
Gouider, Riadh, Éric Leguern, Michel Gugenheim, et al.. (1995). Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion. Neurology. 45(11). 2018–2023. 84 indexed citations
15.
Guern, E. Le, Michel Gugenheim, Riadh Gouider, et al.. (1994). Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP). Cytogenetic and Genome Research. 65(4). 261–264. 37 indexed citations
16.
Guern, E. Le, N. Ravisé, Michel Gugenheim, et al.. (1994). Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11–Xq21 microsatellites in a new large family: Three new markers are closely linked to the gene. Neuromuscular Disorders. 4(5-6). 463–469. 8 indexed citations
17.
Léger, Juliane, G Grateau, Michel Gugenheim, et al.. (1994). Genetic expression of a transthyretin mutation in a case of amyloidotic polyneuropathy occurring in an African. Neurology. 44(1). 181–181. 1 indexed citations
18.
Brice, Alexis, Giovanni Stévanin, Michel Gugenheim, et al.. (1992). Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.. Journal of Medical Genetics. 29(11). 807–812. 29 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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