Sahar Elouej

Saclay, 91190, France

Last Updated: 09/26/2026

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Found 26 publications

Identifying Therapeutic Targets for Amyotrophic Lateral Sclerosis Through Modeling of Multi-Omics Data.

Identifying Therapeutic Targets for Amyotrophic Lateral Sclerosis Through Modeling of Multi-Omics Data.

Journal: International journal of molecular sciences

Published: May 05, 2025

Antibody-mediated neutralization of galectin-3 as a strategy for the treatment of systemic sclerosis.

Antibody-mediated neutralization of galectin-3 as a strategy for the treatment of systemic sclerosis.

Journal: Nature communications

Published: October 28, 2022

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma.

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma.

Journal: Genes

Published: June 02, 2022

Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case-control study in the Tunisian population and a meta-analysis.

Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case-control study in the Tunisian population and a meta-analysis.

Journal: Diabetology & metabolic syndrome

Published: October 20, 2021

Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism.

Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism.

Journal: Frontiers in genetics

Published: February 07, 2021

The Potential of Induced Pluripotent Stem Cells to Test Gene Therapy Approaches for Neuromuscular and Motor Neuron Disorders.

The Potential of Induced Pluripotent Stem Cells to Test Gene Therapy Approaches for Neuromuscular and Motor Neuron Disorders.

Journal: Frontiers in cell and developmental biology

Published: February 01, 2021

Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype.

Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype.

Journal: Frontiers in genetics

Published: January 07, 2021

Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.

Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.

Journal: Nature communications

Published: October 20, 2020

FANCA Gene Mutations in North African Fanconi Anemia Patients.

FANCA Gene Mutations in North African Fanconi Anemia Patients.

Journal: Frontiers in genetics

Published: September 24, 2020

Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype.

Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype.

Journal: European journal of human genetics : EJHG

Published: May 28, 2020

Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.

Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.

Journal: Nature communications

Published: August 23, 2019

Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young.

Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young.

Journal: Herz

Published: August 15, 2019

Showing 1-12 of 26

Last Updated: 09/26/2026