Christiane Ben Hamida

2.2k citations

29 papers · 1.6k indexed · h-index 17

Molecular Biology top 10%
Cellular and Molecular Neuroscience top 2%
Neurology top 5%
Cell Biology top 5%
Neurology top 5%

Co-authors: Fayçal Hentati Samir Belal M. Ben Hamida Mongi Ben Hamida Haluk Topaloğlu Jeffery M. Vance Kamel Ben Othmane Beyhan Tüysüz
Topics: Genetic Neurodegenerative Diseases (9 papers)Hereditary Neurological Disorders (8 papers)Neurological diseases and metabolism (7 papers)
Cited by: Cellular and Molecular Neuroscience Neurology
Journals: Nature Genetics Neurology Human Molecular Genetics
Partner nations: Tunisia France United States

In The Last Decade

Christiane Ben Hamida

29 papers receiving 1.6k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Autosomal Recessive Ataxia Caused by Three Distinct Gene Defects in a Single Consanguineous Family 2008 ·Journal of Neurogenetics ·Yosr Bouhlal,M. Zouari,Mounir Kefi,Christiane Ben Hamida,Fayçal Hentati,Rim Amouri	17
2	Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study 2003 ·Parkinsonism & Related Disorders ·N. Gouider‐Khouja,A. Larnaout,Rim Amouri,Sana Sfar,Samir Belal,Christiane Ben Hamida,Mongi Ben Hamida,Nobutaka Hattori,Yoshikuni Mizuno,Fayçal Hentati	69
3	Linkage of a new locus for autosomal recessive axonal form of Charcot–Marie–Tooth disease to chromosome 8q21.3 2001 ·Neuromuscular Disorders ·(unknown),Rim Amouri,Christiane Ben Hamida,M. Ben Hamida,(unknown),(unknown),Fayçal Hentati	36
4	Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia) 2000 ·Nature Genetics ·Sophie Nicole,Claire-Sophie Davoine,Haluk Topaloğlu,Laurence Cattolico,Duarte C. Barral,Peter Beighton,Christiane Ben Hamida,(unknown),Corinne Cruaud,Peter S. White,Delphine Samson,J. Andoni Urtizberea,F. Lehmann‐Horn,Jean Weissenbach,Fayçal Hentati,Bertrand Fontaine	198
5	The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy 2000 ·Nature Genetics ·Pascale Bomont,L Cavalier,F Blondeau,Christiane Ben Hamida,Samir Belal,Mériem Tazir,Ercan Demir,Haluk Topaloğlu,Rudolf Korinthenberg,Beyhan Tüysüz,P. Landrieu,Fayçal Hentati,M. Kœnig	313
6	Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings 1998 ·Journal of Neurology ·A. Larnaout,Samir Belal,Christiane Ben Hamida,M. Ben Hamida,Fayçal Hentati	13
7	Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency 1998 ·Neuromuscular Disorders ·M. Zouari,Moncef Feki,Christiane Ben Hamida,A. Larnaout,Ilhem Turki,Samir Belal,Abderraouf Mebazaa,M. Ben Hamida,Fayçal Hentati	44
8	Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient 1997 ·Acta Neuropathologica ·A. Larnaout,Samir Belal,M. Zouari,Moncef Feki,Christiane Ben Hamida,Hans H. Goebel,M. Ben Hamida,Fayçal Hentati	42
9	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 1996 ·Human Genetics ·Bertrand Fontaine,Sophie Nicole,Haluk Topaloğlu,Christiane Ben Hamida,Peter Beighton,Frank Spaans,J. M. Cantú,(unknown),Norma B. Romero,K. Ricker,Patricio Barros‐Núñez,G Ponsot,M. Ben Hamida,Jean Weissenbach,Fayçal Hentati,Frank Lehmann‐Horn	20
10	Localization of the Schwartz–Jampel syndrome (SJS) locus to chromosome 1p34–p36.1 by homozygosity mapping 1995 ·Human Molecular Genetics ·Sophie Nicole,Christiane Ben Hamida,Peter Beighton,(unknown),Samir Belal,Norma B. Romero,Denis Viljoen,G Ponsot,Azza Sammoud,Jean Weissenbach,Michel Fardeau,Mongi Ben Hamida,Bertrand Fontaine,Fayçal Hentati	36
11	Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy 1994 ·Journal of the Neurological Sciences ·Christiane Ben Hamida,Nadia Soussi‐Yanicostas,Khemissa Bejaoui,Gillian Butler‐Browne,Fayçal Hentati,M. Ben Hamida	4
12	Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus 1994 ·Neurology ·Samir Belal,Géraldine Cancel‐Tassin,Giovanni Stévanin,Fayçal Hentati,(unknown),Christiane Ben Hamida,(unknown),Yves Agid,M. Ben Hamida,Alexis Brice	42
13	Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35 1994 ·Nature Genetics ·Afif Hentati,Khemissa Bejaoui,Margaret A. Pericak‐Vance,Fayçal Hentati,Marcy C. Speer,Wu-Yen Hung,Denise A. Figlewicz,Jonathan L. Haines,(unknown),Christiane Ben Hamida,Mongi Ben Hamida,Robert H. Brown,Teepu Siddique	164
14	Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping 1993 ·Nature Genetics ·Christiane Ben Hamida,Nathalie Doerflinger,Samir Belal,(unknown),Laurence Reutenauer,Colette Dib,Gàbor Gyapay,Alain Vignal,Denis Le Paslier,Daniel Cohen,Massimo Pandolfo,Vahe Mokini,Giuseppe Novelli,F. Hentati,M. Ben Hamida,Jean‐Louis Mandel,Michel Kœnig	163
15	Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q 1993 ·Human Molecular Genetics ·Kamel Ben Othmane,(unknown),Felicia Lennon,Christiane Ben Hamida,(unknown),A.D. Roses,Margaret A Pericak‐Vance,M. Ben Hamida,Jeffery M. Vance	136
16	Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q 1992 ·Nature Genetics ·Kamel Ben Othmane,Mongi Ben Hamida,Margaret A. Pericak‐Vance,Christiane Ben Hamida,(unknown),(unknown),A. Bowcock,(unknown),T. Conrad Gilliam,Allen D. Roses,Fayçal Hentati,Jeffery M. Vance	144
17	Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum 1992 ·Neuromuscular Disorders ·(unknown),Christiane Ben Hamida,(unknown),Mohamed Ridha Kamoun,(unknown),Mongi Ben Hamida	7
18	Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome 1991 ·Journal of the Neurological Sciences ·Nadia Soussi‐Yanicostas,Christiane Ben Hamida,Gillian Butler‐Browne,Fayçal Hentati,Khemissa Bejaoui,M. Ben Hamida	10
19	Hypertrophic neuropathy in spinocerebellar degeneration 1987 ·Acta Neuropathologica ·M. Ben Hamida,(unknown),F. Hentati,Christiane Ben Hamida	2
20	Les atrophies péronières en Tunisie 1981 ·Journal of the Neurological Sciences ·Mongi Ben Hamida,(unknown),Christiane Ben Hamida,(unknown)	5

About Christiane Ben Hamida

Christiane Ben Hamida is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology, having authored 29 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (9 papers), Hereditary Neurological Disorders (8 papers) and Neurological diseases and metabolism (7 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (736 citations), Neurology (292 citations) and Neurology (427 citations). Christiane Ben Hamida has collaborated with scholars based in Tunisia, France and United States. Frequent co-authors include Fayçal Hentati, Samir Belal, M. Ben Hamida, Mongi Ben Hamida, Haluk Topaloğlu, Jeffery M. Vance, Kamel Ben Othmane, Beyhan Tüysüz, M. Kœnig and P. Landrieu. Their work appears in journals such as Nature Genetics, Neurology and Human Molecular Genetics.

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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