William Camu

3.5k total citations
16 papers, 957 citations indexed

About

William Camu is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, William Camu has authored 16 papers receiving a total of 957 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Neurology, 9 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in William Camu's work include Amyotrophic Lateral Sclerosis Research (13 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Genetic Neurodegenerative Diseases (3 papers). William Camu is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (13 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Genetic Neurodegenerative Diseases (3 papers). William Camu collaborates with scholars based in France, Canada and United States. William Camu's co-authors include Vincent Meininger, Guy A. Rouleau, François Salachas, Lucette Lacomblez, Nicolas Dupré, Paul N. Valdmanis, Patrick A. Dion, Hussein Daoud, Philippe Corcia and Véronique Belzil and has published in prestigious journals such as Neurology, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

William Camu

16 papers receiving 944 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
William Camu France	12	787	416	293	217	152	16	957
Geert Joris Belgium	8	755 1.0×	364 0.9×	319 1.1×	189 0.9×	256 1.7×	11	926
Maura Brunetti Italy	17	1.1k 1.4×	596 1.4×	294 1.0×	264 1.2×	255 1.7×	38	1.2k
Pegah Masrori Belgium	10	642 0.8×	331 0.8×	345 1.2×	144 0.7×	135 0.9×	17	919
Anissa Fergani France	10	635 0.8×	373 0.9×	271 0.9×	85 0.4×	141 0.9×	10	843
Rubika Balendra United Kingdom	9	607 0.8×	331 0.8×	354 1.2×	88 0.4×	130 0.9×	16	837
Javier H. Jara United States	14	434 0.6×	271 0.7×	249 0.8×	140 0.6×	106 0.7×	15	677
Sandra Pereson Belgium	5	545 0.7×	267 0.6×	236 0.8×	118 0.5×	171 1.1×	6	662
Denise Levitch United States	6	635 0.8×	302 0.7×	264 0.9×	161 0.7×	226 1.5×	8	766
Stefania Battistini Italy	18	543 0.7×	299 0.7×	411 1.4×	139 0.6×	199 1.3×	51	1.0k
Jenna M. Gregory United Kingdom	15	474 0.6×	229 0.6×	346 1.2×	113 0.5×	153 1.0×	38	739

Countries citing papers authored by William Camu

Since Specialization

Citations

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

Fields of papers citing papers by William Camu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of William Camu

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

All Works

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16 of 16 papers shown

Delaby, Constance, Elisa De La Cruz, Jens Kühle, et al.. (2025). Comparative Performances of 4 Serum NfL Assays, pTau181, and GFAP in Patients With Amyotrophic Lateral Sclerosis. Neurology. 104(6). e213400–e213400. 6 indexed citations

Palmer, Valerie S., Glen E. Kisby, É. Lagrange, et al.. (2023). Early-onset, conjugal, twin-discordant, and clusters of sporadic ALS: Pathway to discovery of etiology via lifetime exposome research. Frontiers in Neuroscience. 17. 1005096–1005096. 7 indexed citations

Lagrange, É., Jean‐Paul Vernoux, J. Reis, et al.. (2021). An amyotrophic lateral sclerosis hot spot in the French Alps associated with genotoxic fungi. Journal of the Neurological Sciences. 427. 117558–117558. 20 indexed citations

Bowerman, Mélissa, et al.. (2013). Neuroimmunity dynamics and the development of therapeutic strategies for amyotrophic lateral sclerosis. Frontiers in Cellular Neuroscience. 7. 214–214. 36 indexed citations

Kabashi, Edor, Hajer El Oussini, Valérie Bercier, et al.. (2013). Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis. Human Molecular Genetics. 22(12). 2350–2360. 75 indexed citations

Daoud, Hussein, Mike Sabbagh, Véronique Belzil, et al.. (2012). C9orf72 Hexanucleotide Repeat Expansions as the Causative Mutation for Chromosome 9p21–Linked Amyotrophic Lateral Sclerosis and Frontotemporal Dementia. Archives of Neurology. 69(9). 1159–63. 22 indexed citations

Daoud, Hussein, Paul N. Valdmanis, François Gros‐Louis, et al.. (2011). Resequencing of 29 Candidate Genes in Patients With Familial and Sporadic Amyotrophic Lateral Sclerosis. Archives of Neurology. 68(5). 587–93. 41 indexed citations

Daoud, Hussein, Véronique Belzil, Sandra Martins, et al.. (2011). Association of Long ATXN2 CAG Repeat Sizes With Increased Risk of Amyotrophic Lateral Sclerosis. Archives of Neurology. 68(6). 739–42. 67 indexed citations

Benajiba, Lina, Isabelle Le Ber, Agnès Camuzat, et al.. (2009). TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Annals of Neurology. 65(4). 470–473. 239 indexed citations

10.

Belzil, Véronique, Paul N. Valdmanis, Patrick A. Dion, et al.. (2009). Mutations in FUS cause FALS and SALS in French and French Canadian populations. Neurology. 73(15). 1176–1179. 114 indexed citations

11.

Gil, J., Benoît Funalot, Annie Verschueren, et al.. (2008). Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective study. European Journal of Neurology. 15(11). 1245–1251. 127 indexed citations

12.

Valdmanis, Paul N., Nicolas Dupré, Jean‐Pierre Bouchard, et al.. (2007). Three Families With Amyotrophic Lateral Sclerosis and Frontotemporal Dementia With Evidence of Linkage to Chromosome 9p. Archives of Neurology. 64(2). 240–240. 76 indexed citations

13.

Corcia, Philippe, Jawad Khoris, Bertrand de Toffol, et al.. (2002). Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis. Annals of Neurology. 51(2). 243–246. 87 indexed citations

14.

Corne, P., P. Massanet, Laurent Amigues, et al.. (2001). Neuropathie axonale motrice aiguë et méningite aseptique révélant une endocardite à. La Revue de Médecine Interne. 22(7). 660–663. 9 indexed citations

15.

Hivert, Bruno, Catherine Cerruti, & William Camu. (1998). Hydrogen peroxide-induced motoneuron apoptosis is prevented by poly ADP ribosyl synthetase inhibitors. Neuroreport. 9(8). 1835–1838. 30 indexed citations

16.

Olive, P. J. W., et al.. (1998). [Cyst of the conus masquerading as motor neuron disease].. PubMed. 154(12). 859–61. 1 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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