Christiane Ben Hamida

2.2k total citations
29 papers, 1.6k citations indexed

About

Christiane Ben Hamida is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Christiane Ben Hamida has authored 29 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 10 papers in Neurology. Recurrent topics in Christiane Ben Hamida's work include Genetic Neurodegenerative Diseases (9 papers), Hereditary Neurological Disorders (8 papers) and Neurological diseases and metabolism (7 papers). Christiane Ben Hamida is often cited by papers focused on Genetic Neurodegenerative Diseases (9 papers), Hereditary Neurological Disorders (8 papers) and Neurological diseases and metabolism (7 papers). Christiane Ben Hamida collaborates with scholars based in Tunisia, France and United States. Christiane Ben Hamida's co-authors include Fayçal Hentati, Samir Belal, M. Ben Hamida, Mongi Ben Hamida, Haluk Topaloğlu, Kamel Ben Othmane, Jeffery M. Vance, F Blondeau, L Cavalier and Rudolf Korinthenberg and has published in prestigious journals such as Nature Genetics, Neurology and Human Molecular Genetics.

In The Last Decade

Christiane Ben Hamida

29 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christiane Ben Hamida Tunisia 17 901 736 427 384 292 29 1.6k
W.‐Y. Hung United States 14 621 0.7× 362 0.5× 562 1.3× 85 0.2× 305 1.0× 29 1.3k
Barbara Castellotti Italy 25 987 1.1× 757 1.0× 670 1.6× 100 0.3× 252 0.9× 65 1.8k
Rim Amouri Tunisia 24 702 0.8× 667 0.9× 541 1.3× 146 0.4× 345 1.2× 58 1.5k
Faisal Fecto United States 13 669 0.7× 287 0.4× 984 2.3× 132 0.3× 314 1.1× 19 1.6k
Hiroyuki Ishiura Japan 25 844 0.9× 633 0.9× 627 1.5× 177 0.5× 383 1.3× 146 1.8k
Norma B. Romero France 22 1.2k 1.3× 291 0.4× 304 0.7× 182 0.5× 97 0.3× 44 1.7k
Andrew A. Jarjour Canada 17 750 0.8× 499 0.7× 59 0.1× 167 0.4× 343 1.2× 21 1.5k
Alessandra Tessa Italy 29 1.6k 1.8× 1.0k 1.4× 251 0.6× 271 0.7× 496 1.7× 139 2.5k
Nathalie Doerflinger France 11 753 0.8× 349 0.5× 60 0.1× 127 0.3× 58 0.2× 13 1.2k
Jun Mitsui Japan 24 860 1.0× 480 0.7× 582 1.4× 212 0.6× 281 1.0× 115 1.7k

Countries citing papers authored by Christiane Ben Hamida

Since Specialization
Citations

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

Fields of papers citing papers by Christiane Ben Hamida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christiane Ben Hamida. 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 Christiane Ben Hamida. The network helps show where Christiane Ben Hamida may publish in the future.

Co-authorship network of co-authors of Christiane Ben Hamida

This figure shows the co-authorship network connecting the top 25 collaborators of Christiane Ben Hamida. A scholar is included among the top collaborators of Christiane Ben Hamida 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 Christiane Ben Hamida. Christiane Ben Hamida 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.
Bouhlal, Yosr, M. Zouari, Mounir Kefi, et al.. (2008). Autosomal Recessive Ataxia Caused by Three Distinct Gene Defects in a Single Consanguineous Family. Journal of Neurogenetics. 22(2). 139–148. 17 indexed citations
2.
Gouider‐Khouja, N., A. Larnaout, Rim Amouri, et al.. (2003). Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study. Parkinsonism & Related Disorders. 9(5). 247–251. 69 indexed citations
3.
Nicole, Sophie, Claire-Sophie Davoine, Haluk Topaloğlu, et al.. (2000). Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia). Nature Genetics. 26(4). 480–483. 198 indexed citations
4.
Bomont, Pascale, L Cavalier, F Blondeau, et al.. (2000). The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy. Nature Genetics. 26(3). 370–374. 313 indexed citations
5.
Zouari, M., Moncef Feki, Christiane Ben Hamida, et al.. (1998). Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency. Neuromuscular Disorders. 8(6). 416–425. 44 indexed citations
6.
Larnaout, A., Samir Belal, Christiane Ben Hamida, M. Ben Hamida, & Fayçal Hentati. (1998). Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings. Journal of Neurology. 245(4). 231–235. 13 indexed citations
7.
Larnaout, A., Samir Belal, M. Zouari, et al.. (1997). Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient. Acta Neuropathologica. 93(6). 633–637. 42 indexed citations
8.
Fontaine, Bertrand, Sophie Nicole, Haluk Topaloğlu, et al.. (1996). Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval. Human Genetics. 98(3). 380–385. 20 indexed citations
9.
Nicole, Sophie, Christiane Ben Hamida, Peter Beighton, et al.. (1995). Localization of the Schwartz–Jampel syndrome (SJS) locus to chromosome 1p34–p36.1 by homozygosity mapping. Human Molecular Genetics. 4(9). 1633–1636. 36 indexed citations
10.
Hamida, Christiane Ben, Nadia Soussi‐Yanicostas, Khemissa Bejaoui, et al.. (1994). Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy. Journal of the Neurological Sciences. 123(1-2). 114–121. 4 indexed citations
11.
Belal, Samir, Géraldine Cancel‐Tassin, Giovanni Stévanin, et al.. (1994). Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus. Neurology. 44(8). 1423–1423. 42 indexed citations
12.
Hentati, Afif, Khemissa Bejaoui, Margaret A. Pericak‐Vance, et al.. (1994). Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35. Nature Genetics. 7(3). 425–428. 164 indexed citations
13.
Hamida, Christiane Ben, Nadia Soussi‐Yanicostas, Gillian Butler‐Browne, et al.. (1994). Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy. Muscle & Nerve. 17(4). 400–410. 7 indexed citations
14.
Othmane, Kamel Ben, Felicia Lennon, Christiane Ben Hamida, et al.. (1993). Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Human Molecular Genetics. 2(10). 1625–1628. 136 indexed citations
15.
Othmane, Kamel Ben, Mongi Ben Hamida, Margaret A. Pericak‐Vance, et al.. (1992). Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q. Nature Genetics. 2(4). 315–317. 144 indexed citations
16.
Hamida, Christiane Ben, et al.. (1992). Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum. Neuromuscular Disorders. 2(5-6). 361–369. 7 indexed citations
17.
Soussi‐Yanicostas, Nadia, Christiane Ben Hamida, Gillian Butler‐Browne, et al.. (1991). Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome. Journal of the Neurological Sciences. 104(1). 64–73. 10 indexed citations
18.
Hamida, M. Ben, et al.. (1987). Hypertrophic neuropathy in spinocerebellar degeneration. Acta Neuropathologica. 75(1). 51–61. 2 indexed citations
19.
Hamida, Christiane Ben, et al.. (1983). Postnatal maturation of the vascularisation of the suprasylvian gyrus of the cat.. PubMed. 137 (Pt 2). 371–85. 8 indexed citations
20.
Hamida, Mongi Ben, et al.. (1981). Les atrophies péronières en Tunisie. Journal of the Neurological Sciences. 50(3). 335–356. 5 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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