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ABDELLATIF BARAKAT

Abdellatif BARAKAT Directeur de Recherche INRAE
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Présentation

**Abdellatif Barakat (43 years) is a Research Director in Bioprocess & Chemical Engineering of Biomass at INRA Montpellier, France, which focuses on bioconversion of agro-resources and waste to biofuels, biomaterials, biofertilizers and molecules of interest. His current research interests include valorization of biomass , biofertilizers & biostimulants formulation, biopolymers functionalization (plasma, microwaves...), wasetwater treatment, electro-catalysis, mechano-catalysis and bio-catalysis. He received in 2007 his PhD in Chemistry and Physicochemical of Biopolymers from Reims University and HDR in Engineering process in 2016 from Montpellier University. He has published over 150 papers in range an international journals and 4 patents (h-Index of 42)**

Domaines de recherche


Compétences

Biorefinery, pretreatment of biomass, formulation

Publications

crystel-bonnet

Novel pathogenic WHRN variant causing hearing loss in a moroccan family

Imane Aitraise , Ghita Amalou , Salaheddine Redouane , Hicham Charoute , Khalid Snoussi
Molecular Biology Reports, 2023, ⟨10.1007/s11033-023-08901-8⟩
Article dans une revue hal-04281535v1

Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families

Imane Aitraise , Ghita Amalou , Amina Bakhchane , Amale Bousfiha , Houria Abdelghaffar
Biochemical Genetics, inPress, ⟨10.1007/s10528-023-10515-5⟩
Article dans une revue pasteur-04235312v1

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco

Imane Aitraise , Ghita Amalou , Amale Bousfiha , Hicham Charoute , Hassan Rouba
Molecular Biology Reports, 2022, 49 (5), pp.3949-3954. ⟨10.1007/s11033-022-07245-z⟩
Article dans une revue pasteur-03985530v1

Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family

Soukaina Elrharchi , Zied Riahi , Sara Salime , Hicham Charoute , Lamiae Elkhattabi
Human Heredity, 2021, 85 (1), pp.35-39. ⟨10.1159/000512712⟩
Article dans une revue pasteur-03219602v1

A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family

Ghita Amalou , Crystel Bonnet , Zied Riahi , Aymane Bouzidi , Soukaina Elrharchi
International Journal of Pediatric Otorhinolaryngology, 2021, 140, pp.110481. ⟨10.1016/j.ijporl.2020.110481⟩
Article dans une revue pasteur-03215242v1

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness

Amale Bousfiha , Zied Riahi , Lamiae Elkhattabi , Amina Bakhchane , Hicham Charoute
Human Heredity, 2020, 84 (3), pp.109-116. ⟨10.1159/000503450⟩
Article dans une revue pasteur-03219615v1

A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family

Sara Salime , Zied Riahi , Soukaina Elrharchi , Lamiae Elkhattabi , Hicham Charoute
Gene, 2018, 659, pp.89-92. ⟨10.1016/j.gene.2018.03.042⟩
Article dans une revue pasteur-03219641v1