| Identity-by-descent–guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy F Coppieters, K Van Schil, M Bauwens, H Verdin, A De Jaegher, D Syx, ... Genetics in Medicine 16 (9), 671-680, 2014 | 76 | 2014 |
| Skewed X-chromosome inactivation pattern in SRY positive XX maleness: a case report and review of literature NB Abdelmoula, MF Portnoi, L Keskes, D Recan, A Bahloul, T Boudawara, ... Annales de genetique 46 (1), 11-18, 2003 | 53 | 2003 |
| Cytogenetics and fluorescence in situ hybridization assessment of sex-chromosome mosaicism in Klinefelter’s syndrome NB Abdelmoula, A Amouri, MF Portnoi, A Saad, T Boudawara, MN Mhiri, ... Annales de genetique 47 (2), 163-175, 2004 | 46 | 2004 |
| Endocrine disruption and ovarian morphometric responses in rats following exposure to tetradifon R Badraoui, NB Abdelmoula, N Feki, HB Nasr, T Rebai General and comparative endocrinology 166 (2), 268-272, 2010 | 30 | 2010 |
| May antioxidants status depletion by Tetradifon induce secondary genotoxicity in female Wistar rats via oxidative stress? R Badraoui, Z Sahnoun, NB Abdelmoula, A Hakim, M Fki, T Rebaï Pesticide biochemistry and physiology 88 (2), 149-155, 2007 | 27 | 2007 |
| Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivation MF Portnoï, N Bouayed‐Abdelmoula, M Mirc, R Zemni, H Castaing, ... Clinical genetics 58 (2), 116-122, 2000 | 26 | 2000 |
| Effect of subchronic exposure to tetradifon on bone remodelling and metabolism in female rat R Badraoui, NB Abdelmoula, Z Sahnoun, Z Fakhfakh, T Rebai Comptes Rendus Biologies 330 (12), 897-904, 2007 | 25 | 2007 |
| Dicentric Y chromosome NB Abdelmoula, A Amouri Annales de Biologie Clinique 63 (4), 363-375, 2005 | 19 | 2005 |
| Cytogenetic abnormalities in Tunisian women with premature ovarian failure W Ayed, A Amouri, W Hammami, O Kilani, Z Turki, F Harzallah, ... Comptes Rendus. Biologies 337 (12), 691-694, 2014 | 18 | 2014 |
| Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis NB Abdelmoula, MF Portnoi, A Amouri, A Arladan, M Chakroun, A Saad, ... Annales de genetique 47 (3), 305-313, 2004 | 15 | 2004 |
| Nonclassical human leukocyte antigen (HLA-G, HLA-E, and HLA-F) in coronary artery disease I Zidi, N Kharrat, R Abdelhedi, AB Hassine, AB Laaribi, HB Yahia, ... Human Immunology 77 (4), 325-329, 2016 | 14 | 2016 |
| Epidémiologie du kyste hydatique en Tunisie: apport de l'échographie systématique dans cinq zones en dehors de la capitale. A propos de 9122 sujets explorés HA Gharbi, F Ben Chehida, A Hammou-Jeddi, B Abdelmoula, ... Tunisie médicale 64 (4), 313-320, 1986 | 14 | 1986 |
| Characterization of drug-metabolizing enzymes CYP2C9, CYP2C19 polymorphisms in Tunisian, Kuwaiti and Bahraini populations R Abdelhedi, NA Bouayed, S Alfadhli, L Abid, A Rebai, N Kharrat Journal of genetics 94, 765-770, 2015 | 13 | 2015 |
| Lack of Association of NOS3 and ACE Gene Polymorphisms with Coronary Artery Disease in Southern Tunisia R Abdelhedi, N Kharrat, NA Bouayed, L Abid, W Abdelmouleh, ... Biochemical genetics 51, 92-100, 2013 | 12 | 2013 |
| Dicentric Y chromosomes: first part: cytogenetic and molecular aspects. NB Abdelmoula, A Amouri Annales de biologie clinique 63 (3), 263-278, 2005 | 12* | 2005 |
| A potential oral microbiome signature associated with coronary artery disease in Tunisia N Bouzid, Fériel Gtif, Imen Alfadhli, Suad Charfeddine, Salma Ghorbel, Walid ... Biosci Rep, 2022 | 11* | 2022 |
| The FXII c.-4T> C polymorphism as a disease modifier in patients with hereditary angioedema due to the FXII p. Thr328Lys variant F Corvillo, ME Morena-Barrio, C Marcos-Bravo, M López-Trascasa, ... Frontiers in Genetics 11, 1033, 2020 | 9 | 2020 |
| Xipho-omphalopagus conjoined twins in a spontaneous triplet pregnancy: autopsy findings A Sellami, N Chakroun, R Frikha, NA Bouayed, H Amouri, T Rebai APSP Journal of Case Reports 4 (3), 49, 2013 | 9 | 2013 |
| Comprehensive analysis of Methylenetetrahydrofolate reductase C677T in younger acute lymphoblastic leukemia patients: A single-center experience R Frikha, T Rebai, BM Lobna, F Frikha, M Mdhaffar, I Frikha, M Elloumi, ... Journal of Oncology Pharmacy Practice 25 (5), 1182-1186, 2019 | 8 | 2019 |
| A duplex polymerase chain reaction‐restriction fragment length polymorphism for rapid screening of methylenetetrahydrofolate reductase gene variants: Genotyping in acute leukemia R Frikha, N Bouayed, B Ben Rhouma, L Keskes, T Rebai Journal of clinical laboratory analysis 32 (1), e22198, 2018 | 8 | 2018 |
