Ali Benomar

4.4k citations

69 papers · 2.3k · 1 hit paper · h-index 21

Impact in

Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Neurology top 2%
- Neurological disorders and treatments
- Neurological diseases and metabolism
- Parkinson's Disease Mechanisms and Treatments

Papers in

Cellular and Molecular Neuroscience 27
- Genetic Neurodegenerative Diseases 15
- Hereditary Neurological Disorders 13
Molecular Biology 21
- Mitochondrial Function and Pathology 9
- RNA regulation and disease 5

Co-authors: Alexis Brice (20 shared papers)Giovanni Stévanin (14 shared papers)Alexandra Dürr (13 shared papers)Yves Agid (6 shared papers)Géraldine Cancel‐Tassin (4 shared papers)Nacer Abbas (2 shared papers)Ahmed Bouhouche (26 shared papers)Gilles David (5 shared papers)
Journals: Journal of Medical Genetics (3 papers)Annals of Neurology (3 papers)Journal of the Neurological Sciences (3 papers)The American Journal of Human Genetics (2 papers)Human Genetics (2 papers)
Partner nations: Morocco France United States

In The Last Decade

Ali Benomar

64 papers receiving 2.3k citations

Ali Benomar's Hit Papers

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Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion 1997 · 604 citations

Peers

Countries citing papers authored by Ali Benomar

Since Specialization

Citations

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

Fields of papers citing papers by Ali Benomar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Ali Benomar, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ali Benomar Line = papers co-authored together Ali Benomar links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 69 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion Nature Genetics ·Gilles David, Nacer Abbas, Giovanni Stévanin, Alexandra Dürr, Gaël Yvert, Géraldine Cancel‐Tassin, C. R. Weber, Georges Imbert, Frédéric Saudou, Eric Antoniou, Harry A. Drabkin, Robert M. Gemmill, Paola Giunti, Ali Benomar, (unknown), Merle Ruberg, Yves Agid, Jean‐Louis Mandel, Alexis Brice Hit paper breakdown →	1997	604
2	Spinocerebellar ataxia 3 and machado‐joseph disease: Clinical, molecular, and neuropathological features Annals of Neurology ·Alexandra Dürr, Giovanni Stévanin, Géraldine Cancel‐Tassin, Charles Duyckaerts, Nacer Abbas, Olivier Didierjean, Hervé Chneiweiss, Ali Benomar, O. Lyon‐Caen, Jean Julien, M Serdaru, Christiane Penet, Yves Agid, Alexis Brice	1996	353
3	Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome The American Journal of Human Genetics ·Sylvain Hanein, Elodie Martin, Amir Boukhris, P. Byrne, Cyril Goizet, Abdelmadjid Hamri, Ali Benomar, Alexander Lossos, Paola S. Denora, José Carlos Fernández Fernández, Nizar Elleuch, Sylvie Forlani, Alexandra Dürr, Imed Feki, Michael Hutchinson, Filippo M. Santorelli, Chokri Mhiri, Alexis Brice, Giovanni Stévanin	2008	148
4	The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1 Nature Genetics ·Ali Benomar, Luc Krols, Giovanni Stévanin, Géraldine Cancel‐Tassin, Éric Leguern, Gilles David, H. Ouhabi, Jean‐Jacques Martin, Alexandra Dürr, A. Zaǐm, N. Ravisé, C. Busque, Christiane Penet, Nicole Van Regemorter, J. Weissenbach, M. Yahyaoui, T. Chkili, Yves Agid, Christine Van Broeckhoven, Alexis Brice	1995	126
5	Non-Motor Symptoms of Parkinson’s Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients Frontiers in Neurology ·Houyam Tibar, Khalil El Bayad, Ahmed Bouhouche, El Hachmia Ait Ben Haddou, Ali Benomar, Mohamed Yahyaoui, Abdelhamid Benazzouz, Wafa Regragui	2018	93
6	An expanded CAG repeat sequence in spinocerebellar ataxia type 7. Genome Research ·K Lindblad, M L Savontaus, Giovanni Stévanin, Monica Holmberg, Kathleen B. Digre, Cecilia Zander, Hans Ehrsson, Gilles David, Ali Benomar, Eeva Nikoskelainen, Yvon Trottier, Gösta Holmgren, L J Ptácek, Anu Anttinen, Alexis Brice, Martin Schalling	1996	85
7	Vitamin D deficiency and its role in neurological conditions: A review Revue Neurologique ·Ghislain Armel Mpandzou, E. Aït Ben Haddou, Wafa Regragui, Ali Benomar, M. Yahyaoui	2016	71
8	Mutation analysis of the paraplegin gene ( SPG7 ) in patients with hereditary spastic paraplegia Neurology ·N. Elleuch, Christel Depienne, Ali Benomar, Angel Hernandez, Xavier Ferrer, Bertrand Fontaine, Djamel Grid, Chantal Tallaksen, R. Zemmouri, Giovanni Stévanin, Alexandra Dürr, Alexis Brice	2006	71
9	A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3 The American Journal of Human Genetics ·Ahmed Bouhouche, Ali Benomar, Nazha Birouk, Angélique Mularoni, Farid Meggouh, (unknown), D. Grid, Antoon Vandenberghe, Mohamed Yahyaoui, T. Chkili, Alexis Brice, Éric Leguern	1999	68
10	KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction Journal of Medical Genetics ·Talya Dor, Yuval Cinnamon, Laure Raymond, Avraham Shaag, Naïma Bouslam, Ahmed Bouhouche, Marion Gaussen, Vincent Meyer, Alexandra Dürr, Alexis Brice, Ali Benomar, Giovanni Stévanin, Markus Schuelke, Simon Edvardson	2013	52
11	Autosomal‐dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I Annals of Neurology ·Ali Benomar, E. Le Guern, Alexandra Dürr, H. Ouhabi, Giovanni Stévanin, M. Yahyaoui, T. Chkili, Yves Agid, Alexis Brice	1994	47
12	Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene Archives of Neurology ·Nazha Birouk, Hamid Azzedine, O. Dubourg, Marie‐Paule Muriel, Ali Benomar, Tarik Hamadouche, Thierry Maisonobe, Réda Ouazzani, Alexis Brice, Mohamed Yahyaoui, T Chkili, E. Le Guern	2003	45
13	Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28) Annals of Neurology ·Naïma Bouslam, Ali Benomar, Hamid Azzedine, Ahmed Bouhouche, Michito Namekawa, Stephan Klebe, Céline Charon, Alexandra Dürr, Merle Ruberg, Alexis Brice, Mohamed Yahyaoui, Giovanni Stévanin	2005	44
14	Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families Journal of the Neurological Sciences ·Ali Benomar, Mohammed Yahyaoui, Farid Meggouh, Ahmed Bouhouche, M. Boutchich, Naïma Bouslam, A. Zaǐm, M. Schmitt, Halima Belaïdi, Réda Ouazzani, T Chkili, Michel Kœnig	2002	41
15	LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease Parkinson s Disease ·Ahmed Bouhouche, Houyam Tibar, Rafiqua Ben El Haj, Khalil El Bayad, Rachid Razıne, S. Tazrout, A. Skalli, Naïma Bouslam, Loubna Elouardi, Ali Benomar, Mohammed Yahyaoui, Wafa Regragui	2017	35
16	Vitamin E deficiency ataxia with (744 del A) mutation on α-TTP gene: genetic and clinical peculiarities in Moroccan patients European Journal of Medical Genetics ·Naïma Marzouki, Ali Benomar, Mohamed Yahyaoui, Nezha Birouk, Mohamed Elouazzani, T Chkili, Mohamed Benlemlih	2005	34
17	Chemotactic factor and P15E-related chemotaxis inhibitor in human melanoma cell lines with different macrophage content and tumorigenicity in nude mice. The Journal of Immunology ·Ali Benomar, W J Ming, Giulia Taraboletti, Pietro Ghezzi, Claudia Balotta, Giuseppe Cianciolo, Ralph Snyderman, J F Doré, Alberto Mantovani	1987	33
18	Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G3145TG/A3145TG) European Journal of Human Genetics ·Giovanni Stévanin, Gilles David, Alexandra Dürr, Paola Giunti, Ali Benomar, M. Abada-Bendib, M S Lee, Yves Agid, Alexis Brice	1999	28
19	Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families Brain ·Ahmed Bouhouche, N. Birouk, H. Azzedine, Ali Benomar, G. Durosier, D. Ente, M.-P. Muriel, Merle Ruberg, I. Slassi, M. Yahyaoui, O. Dubourg, Réda Ouazzani, E. LeGuern	2006	26
20	Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31–14.1 European Journal of Human Genetics ·Ahmed Bouhouche, Ali Benomar, Naïma Bouslam, Réda Ouazzani, T. Chkili, Mohamed Yahyaoui	2005	26

About Ali Benomar

Ali Benomar is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Pathology and Forensic Medicine and Neurology, having authored 69 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (15 papers), Hereditary Neurological Disorders (13 papers), Mitochondrial Function and Pathology (9 papers), Neurological diseases and metabolism (8 papers), Parkinson's Disease Mechanisms and Treatments (7 papers), RNA regulation and disease (5 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Lysosomal Storage Disorders Research (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.7k citations), Neurology (585 citations), Neurology (293 citations), Molecular Biology (1.3k citations) and Clinical Biochemistry (83 citations). Ali Benomar has collaborated with scholars based in Morocco, France and United States. Frequent co-authors include Alexis Brice, Giovanni Stévanin, Alexandra Dürr, Yves Agid, Géraldine Cancel‐Tassin, Nacer Abbas, Ahmed Bouhouche, Gilles David, Mohamed Yahyaoui and Merle Ruberg. Their work appears in journals such as Journal of Medical Genetics, Annals of Neurology, Journal of the Neurological Sciences, The American Journal of Human Genetics and Human 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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Ali Benomar

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