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Genetics and meta-analysis of recessive non-syndromic hearing impairment and Usher syndrome in Maghreb population: lessons from the past, contemporary actualities and future challenges

Human genetics, 2022-04, Vol.141 (3-4), p.583-593

2022

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Compound Analytical Model Dedicated to the Prediction of the Features of Fractional-Slot PMSMs

IEEE access, 2023, Vol.11, p.99438-99451

2023

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On the Analysis and Torque Enhancement of Flux-Switching Permanent Magnet Machines in Electric Power Steering Systems

World electric vehicle journal, 2022-04, Vol.13 (4), p.64

2022

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Investigation of the Effects of the Pole Shoe Geometry on the IPM T-LSM Features: Application to Free Piston Engines

IEEE access, 2022, Vol.10, p.17748-17759

2022

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Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population

Journal of advanced research, 2021-07, Vol.31, p.13-24

2021

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Evidence of SARS-CoV-2 symptomatic reinfection in four healthcare professionals from the same hospital despite the presence of antibodies

International journal of infectious diseases, 2022-04, Vol.117, p.146-154

2022

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Linear Synchronous Machines: Application to Sustainable Energy and Mobility

1, 2018

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Case report: Functional analysis of the p.Arg507Trp variant of the PIGT gene supporting the moderate epilepsy phenotype of mutations in the C-terminal region

Frontiers in neurology, 2023-03, Vol.14, p.1092887

2023

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Correction to: Gene duplication and functional divergence of the zebrafish otospiralin genes

Development genes and evolution, 2020, Vol.230 (1), p.37-37

2020

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Gene duplication and functional divergence of the zebrafish otospiralin genes

Development genes and evolution, 2020, Vol.230 (1), p.27-36

2020

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8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects

Molecular genetics & genomic medicine, 2021-11, Vol.9 (11), p.e1811-n/a

2021

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Analytical Investigation of the Air Gap Flux Density of Surface-Mounted PMSMs With Irregular Pole Shapes

IEEE transactions on industrial electronics (1982), 2024-07, p.1-13

2024

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IEEE_Xplore

Custom Next‐Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys

Molecular genetics & genomic medicine, 2022-02, Vol.10 (2), p.e1868-n/a

2022

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MEC-Based Modeling and Sizing of a Tubular Linear PM Synchronous Machine

IEEE transactions on industry applications, 2015-05, Vol.51 (3), p.2181-2194

2015

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IEEE_Xplore

Analytical Prediction of the No-Load Operation Features of Tubular-Linear Permanent Magnet Synchronous Machines

IEEE transactions on magnetics, 2016-01, Vol.52 (1), p.1-7

2016

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IEEE_Xplore

Computational identification of new TKI as potential noncovalent reversible EGFRL858R/T790M inhibitors: VHTS, molecular docking, DFT study and molecular dynamic simulation

Journal of biomolecular structure & dynamics, 2024-06, Vol.42 (9), p.4870-4887

2024

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Computational identification of new TKI as potential noncovalent reversible EGFR L858R/T790M inhibitors: VHTS, molecular docking, DFT study and molecular dynamic simulation

Journal of biomolecular structure & dynamics, 2024-06, Vol.42 (9), p.4870-4887

2024

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Expanding the Clinical and Molecular Spectrum of HARS2-Perrault Syndrome: Identification of a Novel Homozygous Missense Variant in the HARS2 gene

Genetic testing and molecular biomarkers, 2021-08, Vol.25 (8), p.528

2021

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Feature Investigation of a T-LPMSM Following the Selection of Its Slot-Pole Combination

IEEE transactions on industry applications, 2017-03, Vol.53 (2), p.1009-1017

2017

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IEEE_Xplore

SARS-CoV-2 tracking in Tunisia through next-generation sequencing: lessons for the future

Euro-Mediterranean journal for environmental integration, 2021-09, Vol.6 (2), p.40-40, Article 40

2021

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Pole Shape-Based Reduction of the Harmonic Content of the IPM T-LSM Air Gap Flux Density

IEEE transactions on industrial electronics (1982), 2018-02, Vol.65 (2), p.1429-1438

2018

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IEEE_Xplore

A new case with the recurrent PURA p.(Phe233del) pathogenic variant: Expansion of the phenotype and review of the literature

International journal of developmental neuroscience, 2023-06, Vol.83 (4), p.383-395

2023

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SRD5A3‐CDG: 3D structure modeling, clinical spectrum, and computer‐based dysmorphic facial recognition

American journal of medical genetics. Part A, 2021-04, Vol.185 (4), p.1081-1090

2021

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Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment

Journal of biomolecular structure & dynamics, 2022-01, Vol.40 (21), p.10940-10951

2022

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Further insights into the spectrum phenotype of TRAPPC9 and CDK5RAP2 genes, segregating independently in a large Tunisian family with intellectual disability and microcephaly

European journal of medical genetics, 2021-12, Vol.64 (12), p.104373-104373, Article 104373

2021

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Genetics and meta-analysis of recessive non-syndromic hearing impairment and Usher syndrome in Maghreb population: lessons from the past, contemporary actualities and future challenges

Compound Analytical Model Dedicated to the Prediction of the Features of Fractional-Slot PMSMs

On the Analysis and Torque Enhancement of Flux-Switching Permanent Magnet Machines in Electric Power Steering Systems

Investigation of the Effects of the Pole Shoe Geometry on the IPM T-LSM Features: Application to Free Piston Engines

Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population

Evidence of SARS-CoV-2 symptomatic reinfection in four healthcare professionals from the same hospital despite the presence of antibodies

Linear Synchronous Machines: Application to Sustainable Energy and Mobility

Case report: Functional analysis of the p.Arg507Trp variant of the PIGT gene supporting the moderate epilepsy phenotype of mutations in the C-terminal region

Correction to: Gene duplication and functional divergence of the zebrafish otospiralin genes

Gene duplication and functional divergence of the zebrafish otospiralin genes

8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects

Analytical Investigation of the Air Gap Flux Density of Surface-Mounted PMSMs With Irregular Pole Shapes

Custom Next‐Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys

MEC-Based Modeling and Sizing of a Tubular Linear PM Synchronous Machine

Analytical Prediction of the No-Load Operation Features of Tubular-Linear Permanent Magnet Synchronous Machines

Computational identification of new TKI as potential noncovalent reversible EGFRL858R/T790M inhibitors: VHTS, molecular docking, DFT study and molecular dynamic simulation

Computational identification of new TKI as potential noncovalent reversible EGFR L858R/T790M inhibitors: VHTS, molecular docking, DFT study and molecular dynamic simulation

Expanding the Clinical and Molecular Spectrum of HARS2-Perrault Syndrome: Identification of a Novel Homozygous Missense Variant in the HARS2 gene

Feature Investigation of a T-LPMSM Following the Selection of Its Slot-Pole Combination

SARS-CoV-2 tracking in Tunisia through next-generation sequencing: lessons for the future

Pole Shape-Based Reduction of the Harmonic Content of the IPM T-LSM Air Gap Flux Density

A new case with the recurrent PURA p.(Phe233del) pathogenic variant: Expansion of the phenotype and review of the literature

SRD5A3‐CDG: 3D structure modeling, clinical spectrum, and computer‐based dysmorphic facial recognition

Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment

Further insights into the spectrum phenotype of TRAPPC9 and CDK5RAP2 genes, segregating independently in a large Tunisian family with intellectual disability and microcephaly

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