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Ali Benomar

Observed names: A BENOMAR, A Benomar, A. Benomar, Abdeljalil Benomar, Ali. Benomar, BENOMAR, A., Benomar, A.
Observed institutions: Mohammed V University, Karolinska University Hospital, Inserm, Mario Negri Institute for Pharmacological Research, Université Paris Cité, Centre Hospitalier Universitaire de Grenoble, Centre Hospitalier Universitaire de Bordeaux, Assistance Publique – Hôpitaux de Paris, Institut National d'Hygiène du Maroc, International University of Rabat, Pitié-Salpêtrière Hospital, Centre Hospitalier Ibn Sina, Centre Hospitalier Universitaire Ibn Rochd, Centre Hospitalier Universitaire de Rabat-Salé, Ibn Sina Hospital, Hôpital Tenon, Université Internationale Abulcasis des Sciences de la Santé, Université Pierre-et-Marie-Curie, Physiopathologie des Comportements, University of Tübingen, Sidi Mohamed Ben Abdellah University
OpenAlex ID: A5111540255
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
1997 · Gilles David, Nacer Abbas, et al. · Nature Genetics · 769
Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders
2014 · Gaia Novarino, Ali G. Fenstermaker, et al. · Science · 540
Spinocerebellar ataxia 3 and machado‐joseph disease: Clinical, molecular, and neuropathological features
1996 · Alexandra Durr, Giovanni Stevanin, et al. · Annals of Neurology · 436
Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families
1997 · G. Cancel, A. Durr, et al. · Human Molecular Genetics · 254
Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome
2008 · Sylvain Hanein, Elodie Martin, et al. · The American Journal of Human Genetics · 217
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Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia
2012 · Christelle Tesson, Magdalena Nawara, et al. · The American Journal of Human Genetics · 205
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The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1
1995 · A. Benomar, L. Krols, et al. · Nature Genetics · 160
Non-Motor Symptoms of Parkinson’s Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients
2018 · Houyam Tibar, Khalil El Bayad, et al. · Frontiers in Neurology · 132
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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
2016 · Ziv Gan-Or, Naima Bouslam, et al. · The American Journal of Human Genetics · 117
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Mutation analysis of the paraplegin gene ( SPG7 ) in patients with hereditary spastic paraplegia
2006 · N. Elleuch, C. Depienne, et al. · Neurology · 106
An expanded CAG repeat sequence in spinocerebellar ataxia type 7.
1996 · K Lindblad, M L Savontaus, et al. · Genome Research · 105
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Vitamin D deficiency and its role in neurological conditions: A review
2016 · G. Mpandzou, E. Aït Ben Haddou, et al. · Revue Neurologique · 100
A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3
1999 · Ahmed Bouhouche, Ali Benomar, et al. · The American Journal of Human Genetics · 93
KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction
2013 · Talya Dor, Yuval Cinnamon, et al. · Journal of Medical Genetics · 82
Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene
2003 · Nazha Birouk, Hamid Azzedine, et al. · Archives of Neurology · 80
Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)
2005 · Naima Bouslam, Ali Benomar, et al. · Annals of Neurology · 71
Autosomal‐dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I
1994 · A. Benomar, E. Le Guern, et al. · Annals of Neurology · 67
LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease
2017 · Ahmed Bouhouche, Houyam Tibar, et al. · Parkinson s Disease · 66
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Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families
2002 · Ali Benomar, Mohammed Yahyaoui, et al. · Journal of the Neurological Sciences · 60
Vitamin E deficiency ataxia with (744 del A) mutation on α-TTP gene: genetic and clinical peculiarities in Moroccan patients
2005 · Naima Marzouki, Ali Benomar, et al. · European Journal of Medical Genetics · 52
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
2020 · Thomas Roux, Mathieu Barbier, et al. · Genetics in Medicine · 49
Neuromarketing: Where marketing and neuroscience meet
2011 · Zineb Ouazzani Touhami, Larbi Benlafkih, et al. · AFRICAN JOURNAL OF BUSINESS MANAGEMENT · 44
Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31–14.1
2005 · Ahmed Bouhouche, Ali Benomar, et al. · European Journal of Human Genetics · 38
Stroke and syphilis: A retrospective study of 53 patients
2018 · N. Ahbeddou, K. El Alaoui Taoussi, et al. · Revue Neurologique · 34
Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families
2006 · A. Bouhouche, N. Birouk, et al. · Brain · 34
Works count: 145
Citation count: 4,492
H-index: 29
I10-index: 48
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