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M. Bensaid · SciRah

Researcher profile · Semantic Scholar

M. Bensaid

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M. Bensaid — researcher profile on SciRah

h-index: 9
Works: 14
Citations: 889

Most-cited papers

A Novel Function for Fragile X Mental Retardation Protein in Translational Activation
Elias Bechara, Marie-Cécile Didiot, Mireille Melko, L. Davidovic +7 more
2009PLoS Biology215 citations Open access
Semantic Scholar
Duodenal mRNA expression of iron related genes in response to iron loading and iron deficiency in four strains of mice
F. Dupic, S. Fruchon, M. Bensaid, O. Loréal +4 more
2002Gut120 citations Open access
Semantic Scholar
Inactivation of the hemochromatosis gene differentially regulates duodenal expression of iron-related mRNAs between mouse strains.
F. Dupic, S. Fruchon, M. Bensaid, N. Borot +7 more
2002Gastroenterology107 citations Open access
Semantic Scholar
The fragile X syndrome: exploring its molecular basis and seeking a treatment
B. Bardoni, L. Davidovic, M. Bensaid, É. W. Khandjian
2006Expert Reviews in Molecular Medicine95 citations
Semantic Scholar
Functional characterization of the AFF (AF4/FMR2) family of RNA-binding proteins: insights into the molecular pathology of FRAXE intellectual disability.
Mireille Melko, D. Douguet, M. Bensaid, Samantha Zongaro +3 more
2011Human Molecular Genetics84 citations
Semantic Scholar
FRAXE-associated mental retardation protein (FMR2) is an RNA-binding protein with high affinity for G-quartet RNA forming structure
M. Bensaid, Mireille Melko, Elias Bechara, L. Davidovic +5 more
2009Nucleic Acids Research82 citations Open access
Semantic Scholar
Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure
Elias Bechara, L. Davidovic, Mireille Melko, M. Bensaid +5 more
2006Nucleic Acids Research59 citations Open access
Semantic Scholar
Multigenic control of hepatic iron loading in a murine model of hemochromatosis.
M. Bensaid, S. Fruchon, Christine Mazères, S. Bahram +2 more
2004Gastroenterology56 citations Open access
Semantic Scholar
Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenarians
H. Coppin, M. Bensaid, S. Fruchon, N. Borot +2 more
2003British medical journal54 citations Open access
Semantic Scholar
Effect of CYP2C9, VKORC1, CYP4F2, and GGCX gene variants and patient characteristics on acenocoumarol maintenance dose: Proposal for a dosing algorithm for Moroccan patients.
A. Elkhazraji, E. Bouaiti, Hassan Boulahyaoui, Christiana Philippa Nahmtchougli +4 more
2018Drug Discoveries & Therapeutics8 citations Open access
Semantic Scholar
Use of denaturing HPLC and a heteroduplex generator to detect the HFE C282Y mutation associated with genetic hemochromatosis.
S. Fruchon, M. Bensaid, N. Borot, M. Roth +1 more
2003Clinical Chemistry5 citations
Semantic Scholar
Multi-hit autism genomic architecture evidenced from consanguineous families with involvement of FEZF2 and mutations in high-risk genes
M. Bensaid, Yann Loe-Mie, A. Lepagnol-Bestel, Wenqi Han +13 more
2019bioRxiv2 citations Open access
Semantic Scholar
AUTS2 gene dosage affects synaptic AMPA receptors via a local dendritic spine AUTS2-TTC3-AKT-mTORC1 signaling dysfunction
A. Lepagnol-Bestel, A. Duchon, J. Viard, M. Kvajo +20 more
2022bioRxiv1 citations Open access
Semantic Scholar
AUTS2 expression within mammalian lineage: A predictor of neural networks involved in autism spectrum disorders
A. Lepagnol-Bestel, Yann Loe-Mie, M. Bensaid, M. Simonneau
2022bioRxiv1 citations Open access
Semantic Scholar

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