| Molecular and Clinical Correlations in Autosomal Dominant Cerebellar Ataxia with Progressive Macular Dystrophy (SCA7) G David, A Dürr, G Stevanin, G Cancel, N Abbas, A Benomar, S Belal, ... Human molecular genetics 7 (2), 165-170, 1998 | 332 | 1998 |
| Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families G Cancel, A Dürr, O Didierjean, G Imbert, K Bürk, A Lezin, S Belal, ... Human molecular genetics 6 (5), 709-715, 1997 | 287 | 1997 |
| Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients I Le Ber, N Bouslam, S Rivaud‐Péchoux, J Guimarães, A Benomar, ... Brain 127 (4), 759-767, 2004 | 230 | 2004 |
| The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21. 1 A Benomar, L Krols, G Stevanin, G Cancel, E LeGuern, G David, ... Nature genetics 10 (1), 84-88, 1995 | 220 | 1995 |
| Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia C Tesson, M Nawara, MAM Salih, R Rossignol, MS Zaki, M Al Balwi, ... The American Journal of Human Genetics 91 (6), 1051-1064, 2012 | 214 | 2012 |
| Characterisation of whey proteins of camel (Camelus dromedarius) milk and colostrum H El-Hatmi, JM Girardet, JL Gaillard, MH Yahyaoui, H Attia Small Ruminant Research 70 (2-3), 267-271, 2007 | 187 | 2007 |
| Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic … A Bouhouche, A Benomar, N Bouslam, T Chkili, M Yahyaoui Journal of medical genetics 43 (5), 441-443, 2006 | 145 | 2006 |
| Non-motor symptoms of Parkinson’s disease and their impact on quality of life in a cohort of Moroccan patients H Tibar, K El Bayad, A Bouhouche, EH Ait Ben Haddou, A Benomar, ... Frontiers in neurology 9, 170, 2018 | 134 | 2018 |
| Vitamin D deficiency and its role in neurological conditions: A review G Mpandzou, EAB Haddou, W Regragui, A Benomar, M Yahyaoui Revue neurologique 172 (2), 109-122, 2016 | 132 | 2016 |
| Characterization and genotyping of the caprine κ-casein variants MH Yahyaoui, A Angiolillo, F Pilla, A Sanchez, JM Folch Journal of Dairy Science 86 (8), 2715-2720, 2003 | 128 | 2003 |
| A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21. 2-q21. 3 A Bouhouche, A Benomar, N Birouk, A Mularoni, F Meggouh, J Tassin, ... The American Journal of Human Genetics 65 (3), 722-727, 1999 | 121 | 1999 |
| Mutations in CAPN1 cause autosomal-recessive hereditary spastic paraplegia Z Gan-Or, N Bouslam, N Birouk, A Lissouba, DB Chambers, J Vérièpe, ... The American Journal of Human Genetics 98 (5), 1038-1046, 2016 | 115 | 2016 |
| Genetic polymorphism of the caprine kappa casein gene MH Yahyaoui, A COLL, A SANCHEZ, JM FOLCH Journal of Dairy Research 68 (2), 209-216, 2001 | 90 | 2001 |
| Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene N Birouk, H Azzedine, O Dubourg, MP Muriel, A Benomar, T Hamadouche, ... Archives of neurology 60 (4), 598-604, 2003 | 84 | 2003 |
| Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families N Doerflinger, C Linder, K Ouahchi, G Gyapay, J Weissenbach, ... American journal of human genetics 56 (5), 1116, 1995 | 82 | 1995 |
| Autosomal‐dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I A Benomar, E Le Guern, A Dürr, H Ouhabi, G Stevanin, M Yahyaoui, ... Annals of Neurology: Official Journal of the American Neurological …, 1994 | 79 | 1994 |
| Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28) N Bouslam, A Benomar, H Azzedine, A Bouhouche, M Namekawa, ... Annals of neurology 57 (4), 567-571, 2005 | 78 | 2005 |
| Fahr syndrome and dysparathyroidism. 3 cases A El Maghraoui, N Birouk, A Zaim, I Slassi, M Yahyaoui, T Chkili Presse Medicale (Paris, France: 1983) 24 (28), 1301-1304, 1995 | 77 | 1995 |
| Characterization of a new genetic variant in the caprine k-casein gene A Angiolillo, MH Yahyaoui, A Sanchez, F Pilla, JM Folch Journal of Dairy Science 85 (10), 2679-2680, 2002 | 66 | 2002 |
| Vitamin E deficiency ataxia with (744 del A) mutation on α-TTP gene: genetic and clinical peculiarities in Moroccan patients N Marzouki, A Benomar, M Yahyaoui, N Birouk, M Elouazzani, T Chkili, ... European journal of medical genetics 48 (1), 21-28, 2005 | 59 | 2005 |
