Boudour Khabou

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 11

Top Topics

Intellectual Disability

Cancer Stem Cells

Ejection Fraction

Top Venues

Metabolic brain disease

Annals of human genetics

Experimental dermatology

This page only lists publications with an associated author ORCID identifier.

Publications

Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi, Boudour Khabou, Marwa Ammar, Rahma Felhi, Marwa Kharrat, Jihen Chouchen, Thouraya Kammoun, Abdelaziz Tlili, Faiza Fakhfakh
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity. Metabolic brain disease 39 (4) (2024)
Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi, Boudour Khabou, Marwa Ammar, Rahma Felhi, Marwa Kharrat, Jihen Chouchen, Thouraya Kammoun, Abdelaziz Tlili, Faiza Fakhfakh
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity. Metabolic brain disease 39 (4) (2024)
Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi, Boudour Khabou, Marwa Ammar, Rahma Felhi, Marwa Kharrat, Jihen Chouchen, Thouraya Kammoun, Abdelaziz Tlili, Faiza Fakhfakh
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity. Metabolic brain disease 39 (4) (2024)
Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi, Boudour Khabou, Marwa Ammar, Rahma Felhi, Marwa Kharrat, Jihen Chouchen, Thouraya Kammoun, Abdelaziz Tlili, Faiza Fakhfakh
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity. Metabolic brain disease 39 (4) (2024)
Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi, Boudour Khabou, Marwa Ammar, Rahma Felhi, Marwa Kharrat, Jihen Chouchen, Thouraya Kammoun, Abdelaziz Tlili, Faiza Fakhfakh
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity. Metabolic brain disease (2024)
Boudour Khabou, Raouia Fakhfakh, Safa Tahri, Emna Bahloul, Hassen Hadj Kacem, Sabrine Belmabrouk, Hend Hachicha, Khadija Sellami, Hamida Turki, Hatem Masmoudi, Olfa Abida
miRNA implication in the pathogenesis and the outcome of Tunisian endemic pemphigus foliaceous. Experimental dermatology (2023)
Boudour Khabou, Fakhri Kallabi, Rim Ben Abdelaziz, Ines Maaloul, Hajer Aloulou, Amel Ben Chehida, Thouraya Kammoun, Veronique Barbu, Tahya Sellami Boudawara, Faiza Fakhfakh, Bassem Khemakhem, Olfa Siala Sahnoun
Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low-GGT intrahepatic cholestasis: Genetic diagnosis and genotype-phenotype correlation assessment. Annals of human genetics (2023)
Boudour Khabou, Raouia Fakhfakh, Safa Tahri, Emna Bahloul, Hassen Hadj Kacem, Sabrine Belmabrouk, Hend Hachicha, Khadija Sellami, Hamida Turki, Hatem Masmoudi, Olfa Abida
miRNA implication in the pathogenesis and the outcome of Tunisian endemic pemphigus foliaceus. Experimental dermatology (2023)
Boudour Khabou, Fakhri Kallabi, Rim Ben Abdelaziz, Ines Maaloul, Hajer Aloulou, Amel Ben Chehida, Thouraya Kammoun, Veronique Barbu, Tahya Sellami Boudawara, Faiza Fakhfakh, Bassem Khemakhem, Olfa Siala Sahnoun
Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low-GGT intrahepatic cholestasis: Genetic diagnosis and genotype-phenotype correlation assessment. Annals of human genetics 88 (3) (2023)
Boudour Khabou, Fakhri Kallabi, Rim Ben Abdelaziz, Ines Maaloul, Hajer Aloulou, Amel Ben Chehida, Thouraya Kammoun, Veronique Barbu, Tahya Sellami Boudawara, Faiza Fakhfakh, Bassem Khemakhem, Olfa Siala Sahnoun
Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low-GGT intrahepatic cholestasis: Genetic diagnosis and genotype-phenotype correlation assessment. Annals of human genetics 88 (3) (2023)
Boudour Khabou, Mouna Tabebi, Olfa Siala-Sahnoun, Emna Mkaouar-Rebai, Ahmed Rebai, Faiza Fakhfakh
Potential dysfunctional effects of synonymous variants: Insights from an exhaustive in silico analysis of the ABCB4 gene. Annals of human genetics 82 (6) (2018)