| Gut microbiota imbalances in Tunisian participants with type 1 and type 2 diabetes mellitus M Fassatoui, M Lopez-Siles, DA Díaz-Rizzolo, H Jmel, C Naouali, ... Bioscience reports 39 (6), BSR20182348, 2019 | 54 | 2019 |
| Identification of a ERCC5 c. 2333T> C (L778P) variant in two Tunisian siblings with mild xeroderma pigmentosum phenotype A Chikhaoui, S Elouej, I Nabouli, M Jones, A Lagarde, M Ben Rekaya, ... Frontiers in Genetics 10, 111, 2019 | 15 | 2019 |
| Clinical and genetic heterogeneity in six Tunisian families with horizontal gaze palsy with progressive scoliosis: a retrospective study of 13 cases S Bouchoucha, A Chikhaoui, D Najjar, H Dallali, M Khammessi, ... Frontiers in pediatrics 8, 172, 2020 | 8 | 2020 |
| Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations A Chikhaoui, I Kraoua, N Calmels, S Bouchoucha, C Obringer, K Zayoud, ... Orphanet Journal of Rare Diseases 17 (1), 121, 2022 | 7 | 2022 |
| Identification and Characterization of a Novel Recurrent ERCC6 Variant in Patients with a Severe Form of Cockayne Syndrome B K Zayoud, I Kraoua, A Chikhaoui, N Calmels, S Bouchoucha, C Obringer, ... Genes 12 (12), 1922, 2021 | 5 | 2021 |
| Combining gene mutation with expression of candidate genes to improve diagnosis of Escobar syndrome D Najjar, A Chikhaoui, S Zarrouk, S Azouz, W Kamoun, N Nassib, ... Genes 13 (10), 1748, 2022 | 2 | 2022 |
| Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype I Nabouli, A Chikhaoui, H Othman, S Elouej, M Jones, A Lagarde, ... Frontiers in Genetics 12, 650639, 2021 | 2 | 2021 |
| Differential Expression of ATM, NF-KB, PINK1 and Foxo3a in Radiation-Induced Basal Cell Carcinoma R Jenni, A Chikhaoui, I Nabouli, A Zaouak, F Khanchel, ... International Journal of Molecular Sciences 24 (8), 7181, 2023 | 1 | 2023 |
| Immunity in the Progeroid Model of Cockayne Syndrome: Biomarkers of Pathological Aging K Zayoud, A Chikhaoui, I Kraoua, A Tebourbi, D Najjar, S Ayari, I Safra, ... Cells 13 (5), 402, 2024 | | 2024 |
| Case report: Exome sequencing revealed disease-causing variants in a patient with spondylospinal thoracic dysostosis S Bouchoucha, A Chikhaoui, D Najjar, K Zayoud, M Zouari, MN Nessib, ... Frontiers in Pediatrics 11, 1132023, 2023 | | 2023 |
| Inflammatory landscape in Xeroderma pigmentosum patients with cutaneous melanoma A Chikhaoui, M Jones, T Režen, M Ben Ahmed, C Naouali, R Komel, ... Scientific reports 12 (1), 13854, 2022 | | 2022 |
| Heterogeneous clinical features in Cockayne syndrome-A patients with the same mutation and in siblings A Chikhaoui, I Kraoua, N Calmels, S Bouchoucha, C Obringer, K Zayoud, ... | | 2022 |
| Combining Gene Mutation with Expression of Candidate Genes to Improve Diagnosis of Escobar Syndrome. Genes 2022, 13, 1748 D Najjar, A Chikhaoui, S Zarrouk, S Azouz, W Kamoun, N Nassib, ... s Note: MDPI stays neutral with regard to jurisdictional claims in published …, 2022 | | 2022 |
| Identification and Characterization of a Novel Recurrent ERCC6 Variant in Patients with a Severe Form of Cockayne Syndrome B. Genes 2021, 12, 1922 K Zayoud, I Kraoua, A Chikhaoui, N Calmels, S Bouchoucha, C Obringer, ... s Note: MDPI stays neutral with regard to jurisdictional claims in published …, 2021 | | 2021 |
| GENETIC, CELLULAR AND TISSULAR INVESTIGATION OF HEREDITARY DEGENERATIVE MUSCULAR DISEASES IN TUNISIA. M KHAMMASSI, A CHIKHAOUI, S BOUCHOUCHA, G BELDI, ... Archives de l'Institut Pasteur de Tunis 97, 2020 | | 2020 |
| MULTI-PARAMETRIC APPROACH FOR THE INVESTIGATION OF INFLAMMATORY BIOMARKERS IN CUTANEOUS MELANOMA MICROENVIRONMENT XERODERMA PIGMENTOSUM AS A MODEL. A CHIKHAOUI, I NABOULI, M JONES, M BENAHMED, C NAOUALI, ... Archives de l'Institut Pasteur de Tunis 97, 2020 | | 2020 |
| Assessment of inflammatory response and fibrosis during muscle degeneration in elderly and patients with muscle dystrophies A Chikhaoui, S Bouchoucha, I Kraoua, N Ben Achour, S Boubaker, ... EUROPEAN JOURNAL OF IMMUNOLOGY 49, 1411-1411, 2019 | | 2019 |
| Clinical and genetic investigation of Xeroderma pigmentosum in Tunisia: current situation and perspectives O Messaoud, M Ben Rekaya, M Jones, C Naouali, M Chargui, I Nabouli, ... BRITISH JOURNAL OF DERMATOLOGY 180 (6), E217-E218, 2019 | | 2019 |
| Identification of XP-G complementation group by targeted gene sequencing in two Tunisian patients A Chikhaoui, S Elouaj, I Nabouli, M Jones, A Lagarde, O Massoud, ... Frontiers in Genetics 10, 111, 2019 | | 2019 |
| Particular forms of xeroderma pigmentosum and Cockayne syndrome in the Tunisian population A Chikhaoui, I Krawa, N Calmels, C Obringer, S Elouej, ... British Journal of Dermatology 180 (6), E224-E225, 2019 | | 2019 |
