Ali Benomar - Concepedia

Author

Ali Benomar

Also Known As

A BENOMAR, A Benomar, A. Becker, A. Benomar, Ali Benomar, Ali. Benomar, BENOMAR, A., Benomar Ali, Benomar, A, Benomar, A.

138

Publications

4.4K

Citations

H-Index

Concepts

All Affiliations

Inserm Sorbonne Université Mohammed V University Pitié-Salpêtrière Hospital Assistance Publique – Hôpitaux de Paris

About

Ali Benomar is an author at Inserm specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	23	2.5K
2	Natural Sciences	2	2	790
3	Public Health	2	2	40
4	Health Sciences	1	1	196
5	Social Sciences	1	1	30

Ali Benomar

Publications

Citations

H-Index

Page 1

	Year	Citations
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion Gilles David, Nacer Abbas, Giovanni Stévanin, Nature Genetics Sca7 GeneMolecular ResearchNatural SciencesGeneticsMolecular Biology	1997	769
Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders Gaia Novarino, Ali G. Fenstermaker, Maha S. Zaki, Science Neurological DisorderGeneticsNetwork AnalysisGene DiscoveryDisease Gene Identification	2014	526
Spinocerebellar ataxia 3 and machado‐joseph disease: Clinical, molecular, and neuropathological features Alexandra Dürr, Giovanni Stévanin, Géraldine Cancel‐Tassin, Annals of Neurology	1996	446
Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families Alexandra Dürr, Olivier Didierjean, G. Imbert, Human Molecular Genetics	1997	256
Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome Sylvain Hanein, Elodie Martin, Amir Boukhris, The American Journal of Human Genetics Including Kjellin SyndromeGeneticsSpg15 GeneEncoding SpastizinPathology	2008	211
Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia Christelle Tesson, Magdalena Nawara, Mustafa A. Salih, The American Journal of Human Genetics Metabolic SyndromeEnergy MetabolismMetabolic DisorderMitochondrial FunctionBiochemistry	2012	196
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1 Ali Benomar, Luc Krols, Giovanni Stévanin, Nature Genetics Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	1995	159
Non-Motor Symptoms of Parkinson’s Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients Houyam Tibar, Khalil El Bayad, Ahmed Bouhouche, Frontiers in Neurology	2018	132
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia Ziv Gan‐Or, Naïma Bouslam, Nazha Birouk, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsMolecular Genetics	2016	113
An expanded CAG repeat sequence in spinocerebellar ataxia type 7. K Lindblad, M L Savontaus, Giovanni Stévanin, Genome Research	1996	106

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