Belmabrouk S, Kharrat N, Benmarzoug R, Rebai A. (2015). Exploring proteome-wide occurrence of clusters of charged residues in Eukaryotes. Proteins: Structure, Function, and Bioinformatics, 83: 1252-61

Bouhamed H., Masmoudi A, Lecroq T, Rebai A. (2015). Reducing the Structure Space of Bayesian Classifiers Using some General Algorithms.Journal of Mathematical Modelling and Algorithms in Operations Research. 14: 197-237 .

Abdelhedi R, Bouayed NA, Alfadhli S, Abid L, Rebai A, Kharrat N. (2015). Characterization of drug-metabolizing enzymes CYP2C9, CYP2C19 polymorphisms in Tunisian, Kuwaiti and Bahraini populations.Journalof Genetics, 94: 765-70.

Bouhamed, H., Masmoudi, A., Lecroq, T.,Rebaï, A. (2015). Structure space of Bayesian networks is dramatically reduced by subdividing it in sub-networks. Journal of Computational and Applied Mathematics. 287: 46-62.

Bouhamed H, Masmoudi A, Rebai A. (2015). Bayesian classifier structure-learning using several general algorithms.Procedia Computer Science. 46: 476-482.

HadjKacemLoukil L, HadjKacem H, Bahloul A, Ayadi H. (2015). Relation between male obesity and male infertility in a Tunisian population.Andrologia,  47: 282-285.

Choura M, Rebaï A, Masmoudi K. (2015). Unraveling the WRKY transcription factors network in Arabidopsis Thaliana by integrative approach. Network Biology, 5: 55-61

Choura M, Rebaï A. (2015). Prediction of hormone response elements in the humantyrosine kinase receptors.Current Topics in Peptide & Protein Research.

Triki-Fendri S, Sánchez-Diz P, Rey-González D, Ayadi I, Carracedo Á, Rebai A. (2015). Paternal lineages in Libya inferred from Y-chromosome haplogroups. American Journal of Physical Anthropology. 157: 242-51.

Chaabane S, Marzouk S, Akrout R, Ben Hamad M, Achour Y, Rebai A, Keskes L, Fourati H, Bahloul Z, Maalej A. (2015). Genetic Determinants of Methotrexate Toxicity in  Tunisian Patients with Rheumatoid Arthritis: A Study of Polymorphisms Involved in the MTX Metabolic Pathway. Europpean Journal Of  Drug Metabolism and Pharmacokinetics.

Triki-Fendri S, Sánchez-Diz P, Rey-González D, AlFadhli S, Ayadi I, Benarzoug R, Carracedo Á, Rebai A. (2015). Genetic structure of the Kuwaiti population revealed by paternal lineages.American Journal of Human Biology, in press.

Kallel I, Rebai M, Khabir A, Rebai A. (2015).  What a common biomarkers characterize a triple-negative profile in breast cancer? PathologieBiologie, 63: 224-9

Apellániz-Ruiz M, Inglada-Pérez L, Naranjo ME, Sánchez L, Mancikova V, Currás-Freixes M, de Cubas AA, Comino-Méndez I, Triki S, Rebai A, Rasool M, Moya G, Grazina M, Opocher G, Cascón A, Taboada-Echalar P, Ingelman-Sundberg M, Carracedo A, Robledo M, Llerena A, Rodríguez-Antona C. (2015). High frequency and founder effect of the CYP3A4*20 loss-of-function allele in the Spanish population classifies CYP3A4 as a polymorphic enzyme. Pharmacogenomics J. 15: 288-92.

Mnif S, Aifa S.(2015).Cumin  (Cuminumcyminum L.) From Traditional Uses to Potentiel Biomedical Applications.Chemistry and Biodiversity. 12: 733-42.

Elloumi-Mseddi J, Jemel-Oualha I, Beji A, Hakim B, Aifa S. (2015).Effect of estradiol and clomiphene citrate on Erk activation in breast cancer cells.Journal of Receptors and Signal Transduction Research. 2015 35: 202-6.

Makki-Rmida F, Kammoun A, Mahfoudh N, Ayadi A, Gibriel AA, Mallek B, Maalej L, Hammami Z, Maatoug S, Makni H, Masmoudi S. (2015). Genetic diversity and haplotype structure of 21 Y-STRs, including nine noncore loci, in South Tunisian Population: Forensic relevance. Electrophoresis. 36: 2908-13.

Chakchouk I, Ben Said M, Jbeli F, Benmarzoug R, Loukil S, Smeti I, ChakrounA,Gibriel AA, Ghorbel A, Hadjkacem H, Masmoudi S. (2015). NADf chip, a two-color microarray for simultaneous screening of multigene mutations associated with hearing impairment in North African Mediterranean countries. Journal ofMolecularDiagnostics. 17: 155-61.

Chakchouk I, Grati M, Bademci G, Bensaid M, Ma Q, Chakroun A, Foster J 2nd,Yan D, Duman D, Diaz-Horta O, Ghorbel A, Mittal R, Farooq A, Tekin M, Masmoudi S, Liu XZ. (2015).  Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53. Molecular Genetics and Genomics.2015, 290: 1327-34.

Grati M, Chakchouk I, Ma Q, Bensaid M, Desmidt A, Turki N, Yan D, BaanannouA,Mittal R, Driss N, Blanton S, Farooq A, Lu Z, Liu XZ, Masmoudi S. (2015). A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation. HumanMolecularGenetics; 24: 2482-91.

Elloumi-Mseddi J, Jemel-Oualha I, Beji A, Hakim B, Aifa S. (2015).Effect of estradiol and clomiphene citrate on Erk activation in breast cancer cells.Journal of Receptors and  Signal Transduction Research. 35: 202-6

Apellániz-Ruiz M, Inglada-Pérez L, Naranjo ME, Sánchez L, Mancikova V, Currás-Freixes M, de Cubas AA, Comino-Méndez I, Triki S, Rebai A, Rasool M, MoyaG,Grazina M, Opocher G, Cascón A, Taboada-Echalar P, Ingelman-Sundberg M, Carracedo A, Robledo M, Llerena A, Rodríguez-Antona C. (2015). High frequency and founder effect of the CYP3A4*20 loss-of-function allele in the Spanish population classifies CYP3A4 as a polymorphic enzyme. Pharmacogenomics Journal. 15:288-92.

Siala O, Rebai A, Fakhfakh F. (2014). Slight variations in the SC35 ESE sequence motif among human chromosomes: a computational approach. Gene. 545: 102-110.

Hamad MB, Marzouk S, Kaddour N, Masmoudi H, Fakhfakh F, Rebai A, Bahloul Z, Maalej A. (2014). Anticycliccitrullinated peptide antibody and rheumatoid factor in south Tunisian patients with rheumatoid arthritis: association with disease activity and severity. Journal Clinical Laboratory Analysis. 28: 21-26.

Khlifi R, Olmedo P, Gil F, Feki-Tounsi M, Hammami B, Rebai A, Hamza-Chaffai A. (2014). Biomonitoring of cadmium, chromium, nickel and arsenic in general population living near mining and active industrial areas in Southern Tunisia.Environmantal Monitoring and Assessment. 186: 761-779.

Khlifi R, Olmedo P, Gil F, Feki-Tounsi M, Hammami B, Rebai A, Hamza-Chaffai A. (2014). Risk of laryngeal and nasopharyngeal cancer associated with arsenic and cadmium in the Tunisian population. Environ Science Pollution Research International. in press.

Khlifi R, Kallel I, Hammami B, Hamza-Chaffai A, Rebai A. (2014). DNA repair gene polymorphisms and risk of head and neck cancer in the Tunisian population. Journal of Oral PathologyMedecine. 43: 217-224

Lasram K, Ben Halim N, Hsouna S, Kefi R, Arfa I, Ghazouani W, Jamoussi H, Benrahma H, Kharrat N, Rebai A, Ben Ammar S, Bahri S, Barakat A, Abid A, Abdelhak S. (2014). Evidence for association of the E23K variant of KCNJ11 gene with type 2 diabetes in Tunisian population: population-based study and meta-analysis. Biomedical Research International. 265-274

Feki-Tounsi M, Khlifi R, Mhiri MN, Rebai A, Hamza-Chaffai A. (2014). Cytogenetic damage in the oral mucosa cells of bladder cancer patients exposed to tobacco in Southern Tunisia. Environ Science Pollution Research International. 21:12922-7

Khlifi R, Ben Salah G, Chakroun A, Hamza-Chaffai A, Rebai A. (2014). Inter-ethnic differences in genetic polymorphisms of xenobiotic-metabolizing enzymes (CYP1A1, CYP2D6, NAT1 and  AT2) in healthy populations: correlation with the functional in silico prediction. Molecular  Biology Reports. 41: 5735-43.

Feki-Sahnoun W, Hamza A, Mahfoudi M, Rebai A, Hassen MB.(2014). Long-term microphytoplankton variability patterns using multivariate analyses: ecological and management implications. Environ Science Pollution Research International. 19: 11481-99.

Feki-Tounsi M, Olmedo P, Gil F, Mhiri MN, Rebai A, Hamza-Chaffai A. (2014). Trace metal quantification in bladder biopsies from tumoral lesions of Tunisian cancer and controls subjects. Environ Science Pollution Research International. 19:11433-8

Jabeur H, Zribi A, Makni J, Rebai A, Abdelhedi R, Bouaziz M. (2014). Detection of Chemlali extra-virgin olive oil adulteration mixed with soybean oil, corn oil, and sunflower oil by using GC and HPLC. Journal of Agricultural Food Chemistry. 62:4893-4904.

Ben-Ayed R, Sans-Grout C, Moreau F, Grati-Kamoun N, Rebai A. (2014). Genetic Similarity Among Tunisian Olive Cultivars and Two Unknown Feral Olive Trees Estimated Through SSR Markers. Biochemical Genetics. 52: 258-68.

Louati R., Abdelmoula N.B., Trabelsi I., Abid D., Lissewski C., Kharrat N, Kamoun S., Zenker M., Rebai T. (2014). Clinical and Molecular Findings of Tunisian Patients with RASopathies.MolecularSyndromology, 5: 212-7.

Elloumi-Mseddi J, Jellali K, Villalobo A, Aifa S. (2014).A premature termination of human epidermal growth factor receptor transcription in Escherichia coli.Scientific World Journal.830923

Jemel-Oualha I, Elloumi-Mseddi J, Beji A, Hakim B, Aifa S. (2014).Controversial effect on Erk activation of some cytotoxic drugs in human LOVO colon cancer cells.Journal of Receptors and Signal Transduction Research.36: 21-5.

El Arbi M, Théolier J, Pigeon P, Jellali K, Trigui F, Top S, Aifa S, Fliss I, Jaouen G, Hammami R. (2014). Antibacterial properties and mode of action of new triarylbutene citrate compounds.European Journal ofMedicinal Chemistry.

F.Z. Ferradji, S. Mnif, A. Badis, S. Rebbani, D. Fodil, K. Eddouaouda, S. Sayadi. (2014). Naphthalene and crude oil degradation by biosurfactant producing Streptomyces spp. isolated from Mitidja plain soil (North of Algeria).International Biodeterioration and Biodegradation 86, 300-308.

28. S. Mnif, S. Aifa. (2014). Cumin (Cuminumcyminum L.) from traditional uses to potential biomedical applications.Chemistry and Biodiversity, in-press.

BenHassen H, Bouchaala, L, Masmoudi A, Rebai A. ((2013)). Analysis of breast cancer profiles using Bayesian network modeling. International Journal of Biomathematics, 6 (3).

Choura M, Rebaï A. (2013). Exploring charged biased regions in the human proteome. Gene. 515: 277-80

Khlifi R, Messaoud O, Rebai A, Hamza-Chaffai A. (2013). Polymorphisms in the human cytochrome P450 and arylamine N-acetyltransferase: susceptibility to head and neck cancers. Biomedical  Research International. 582: 76-8.

BenAyed R, Kamoun-Grati N, Rebai A. (2013).An overview of the authentification of olive tree and oil.Comprehensive reviews in Food science and food safety, 12: 218-227.

Mahfoudh N, Ayadi I, Kamoun A, Ammar R, Mallek B, Maalej L, Hakim F, Gaddour L, Rebai A, Makni H. (2013). Analysis of HLA-A, -B, -C, -DR, -DQ polymorphisms in the South Tunisian population and a comparison with other populations.Annals of  Human Biology,  40: 41-7.

Bahri R, Halima AB, Ayadi I, Esteban E, Alfadhli SM, Rebai A, Moral P, Chaabani H. (2013). Genetic position of Bahrain natives among wider Middle East populations according to Alu insertion polymorphisms.Annals of  HumanBiology. 40: 35-40.

Abdelhedi R, Kharrat N, Bouayed NA, Abid L, Abdelmouleh W, Sahnoun IT, Alfadhli S, Laroussi L, Rebai A. (2013). Lack of Association of NOS3 and ACE Gene Polymorphisms with Coronary Artery Disease in Southern Tunisia.Biochemical Genetics. 51: 92-100.

Feki-Tounsi M, Olmedo P, Gil F, Khlifi R, Mhiri MN, Rebai A, Hamza-Chaffai A. (2013). Low-level arsenic exposure is associated with bladder cancer risk and cigarette smoking: a case-control study among men in Tunisia. Environnemental SciencePollution  Research International. 20:3923-31

Ben Sadok I., Moutier N., Garcia G., Dosba F. and Grati-Kamoun N., Rebai A Khadari B., Costes E. (2013).  Genetic determinism of the vegetative and reproductive traits in an F1 olive tree progeny.Evidence of tree ontogeny effect.Tree Genetics & Genomes,  9 : 205-221.

Triki-Fendri S, Sánchez-Diz P, Rey-González D, Ayadi I, Alfadhli S, Rebai A, Carracedo A. (2013). Population genetics of 17 Y-STR markers in West Libya (Tripoli region).Forensic Science International Genetics. 7: 95-61

Khlifi R, Olmedo P, Gil F, Hammami B, Chakroun A, Rebai A, Hamza-Chaffai A. (2013). Arsenic, cadmium, chromium and nickel in cancerous and healthy tissues from patients with head and neck cancer. Science Total Environnment. 452-453:58-67.

Khlifi R, Olmedo P, Gil F, Feki-Tounsi M, Chakroun A, Rebai A, Hamza-Chaffai A. (2013) Blood nickel and chromium levels in association with smoking and occupational exposure among head and neck cancer patients in Tunisia. Environnemental Science Pollution  Research International. 20: 8282-94.

Khlifi R, Trabelsi-Ksibi F, Chakroun A, Rebai A, Hamza-Chaffai A. (2013) Cytogenetic abnormality in exfoliated cells of buccal mucosa in head and neck cancer patients in the Tunisian population: impact of different exposure sources. Biomedical  Research International, 2013:905252

Fourati M, Mnif M, Kharrat N, Charfi N, Kammoun M, Fendri N, Sessi S, Abid M, Rebai A, Fakhfakh F. (2013). Association between Leptin gene polymorphisms and plasmleptin level in three consanguineous families with obesity.Gene. 527: 75-81.

Zribi, A., Gargouri, B., Jabeur, H., Rebaï, A., Abdelhedi, R., Bouaziz, M. (2013). Enrichment of pan‐frying refined oils with olive leaf phenolic‐rich extract to extend the usage life. European Journal of Lipid Science and Technology, 115: 1443-1453.

Trigui F, Pigeon P, Jalleli K, Top S, Aifa S, El Arbi M. Selection of asuitable disc bioassay for the screening of anti-tumor molecules. International Journal of  BiomedicalSciences. 9:230-6.

Elloumi-Mseddi J, Jellali K, Aifa S. (2013) In vitro activation and inhibition ofrecombinant EGFR tyrosine kinase expressed in Escherichia coli.ScientificWorldJournal. 2013: 807284..

Jellali K, Pigeon P, Trigui F, Top S, Aifa S, Jaouen G, El Arbi M. (2013) Effect ofthe amino chain length and the transformation into citric acid salts ofaryl-diphenyl-butenes and ferrocenyl-diphenyl-butenes bearing twodimethylaminoalkyl chains on their antimicrobial activities. Springerplus.2:508

Kallel R, Niasme-Grare M, Belguith-Maalej S, Mnif M, Abid M, Ayadi H, Masmoudi S, Jonard L, HadjKacem H. (2013) Screening of SLC26A4 gene in autoimmune thyroiddiseases. International Journal of Immunogenetics.40: 284-91.

Ali Mosrati M, Schrauwen I, Ben Saiid M, Aifa-Hmani M, Fransen E, Mneja M,Ghorbel A, Van Camp G, Masmoudi S. (2013) Genome-wide analysis reveals a novelautosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21. Human Genetics.58:98-101

Hammami I.,  Jaouadi B., Ben Bacha A., Rebai A., Bejar S., Nesme X. and Rhouma A. (2012). Bacillus subtilis broad-spectrum bacteriocinBac14B : Purification, amino acid sequence and physico-chemical characterization. Biotechnology and Bioprocess Engineering. 17: 41–49.

Khlifi R, Rebai A, Hamza-Chaffai A.(2012) Polymorphisms in human DNA repair genes and head and neck squamous cell carcinoma. Journal of  Genetics.91:375-384.

Rebaï M, Kallel I, Rebaï A. (2012)Genetic features of thyroid hormone receptors. Journal of Genetics. 91:367-374.

Kallel I, Rebai M, Rebai A.(2012).Mutations and polymorphisms of estrogens receptors genes and diseases susceptibility. Journal of Receptors and  Signal Transduction  Research. 32:304-313.

Kammoun-Krichen M, Bougacha-Elleuch N, Mnif M, Bougacha F, Charffedine I, Rebuffat S, Rebai A, Glasson E, Abid M, Ayadi F, Péraldi-Roux S, Ayadi H. (2012).IL-1β a potential factor for discriminating between thyroid carcinoma and atrophic thyroiditis.European  Cytokine Network. 23:101-116.

Kharrat N, Abdelmouleh W, Abdelhedi R, Alfadhli S, Rebai A. (2012). The linkage disequilibrium pattern of the angiotensin converting enzyme gene in Arabic and asian population groups. Annals of  Human Biology.39:538-540.

Choura M, Rebaï A. (2012). Topological features of cancer proteins in the human NR-RTK interaction network. Journal of  Receptors and  Signal Transduction  Research. 32:257-262.

Fourati H, Bouzid D, Abida O, Kharrat N, Mnif F, Haddouk S, Fesel C, Costa J, Ben Ayed M, Abid M, Rebai A, Penha-Gonçalves C, Masmoudi H. (2012). Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients. Human  Immunology. 73:740-746.

Zouari N, Ayadi I, Fakhfakh N, Rebai A, Zouari S. (2012). Variation of chemical composition of essential oils in wild populations of Thymus algeriensisBoiss.etReut., a North African endemic species. Lipids Health and Diseases.11:28.

Kallel I, Khabir A, Boujelbene N, Abdennadher R, Daoud J, Frikha M, Aifa S, Sallemi-Boudawara T, Rebaï A. (2012). EGFR overexpression relates to triple negative profile and poor prognosis in breast cancer patients in Tunisia. Journal  of Receptors and  Signal Transduction  Research. 32:142-149.

Ben Hamad M, Cornelis F, Marzouk S, Chabchoub G, Bahloul Z, Rebai A, Fakhfakh F, Ayadi H, Petit-Teixeira E, Maalej A. (2012). Association study of CARD8 (p.C10X) and NLRP3 (p.Q705K) variants with rheumatoid arthritis in French and Tunisian populations.International JournalImmunogenetics. 39:131-6.

Kallel R, Niasme-Grare M, Belguith-Maalej S, Mnif M, Abid M, Ayadi H, Masmoudi S, Jonard L, HadjKacem H. (2012). Screening of SLC26A4 gene in autoimmune thyroid diseases.InternationalJournal ofImmunogenetics.

Mosrati MA, Schrauwen I, Ben Saiid M, Aifa-Hmani M, Fransen E, Mneja M, Ghorbel A, Van Camp G, Masmoudi S. (2012). Genome-wide analysis reveals a novel autosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21. Journal OfHuman Genetics.

Mosrati MA, Schrauwen I, Kamoun H, Charfeddine I, Fransen E, Ghorbel A, Van Camp G, Masmoudi S. (2012). Genome wide analysis in a family with sensorineural hearing loss, autism and mental retardation.Gene. 510:102-106.

Smeti I, Assou S, Savary E, Masmoudi S, Zine A. (2012). Transcriptomic analysis of the developing and adult mouse cochlear sensory epithelia.PLoS One.7(8):e42987

Schrauwen I, Khalfallah A, Ealy M, Fransen E, Claes C, Huber A, Murillo LR, Masmoudi S, Smith RJ, Van Camp G. (2012). COL1A1 association and otosclerosis: a meta-analysis. American Journal of MedicalGenetics. 158:1066-1070.

Ben Said M, Dhouib H, BenZina Z, Ghorbel A, Moreno F, Masmoudi S, Ayadi H, Hmani-Aifa M. (2012). Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome. International Journal Of PediatrOtorhinolaryngol, 76:832-836.

Elloumi J, Jellali K, Jemel I, Aifa S. (2012). Monoclonal antibodies as cancer therapeutics.Recent Patents on Biotechnology. 6:45-56.

Choura M, Rebaï A. (2011). Receptor tyrosine kinases: from biology to pathology. Journal of  Receptors and  Signal Transduction. 31: 387-394

Choura M, Rebai A. (2011). Structural analysis of hubs in human NR-RTK network.Biology  Direct, 6 :49.

Louhichi A, Fourati A, Rebaï A.(2011). IGD: A resource for intronless genes in the human genome. Gene. 488: 35-40.

Bougacha-Elleuch N, Ben Arab S, Rebai A, Mnif M, Maalej A, Charfi N, Ben Lassouad M, Jouida J, Abid M, Ayadi H.(2011). No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisia pedigree. Journal of  Genetics. 90: 333-337.

Daneshpour MS, Rebai A, Houshmand M, Alfadhli S, Zeinali S, Hedayati M, Zarkesh M, Azizi F.(2011). 8q24.3 and 11q25 chromosomal loci association with low HDL-C  in metabolic syndrome. European  Journal of  Clinical  Investigation. 41: 1105-1112.

Ben Hamad M, Cornelis F, Mbarek H, Chabchoub G, Marzouk S, Bahloul Z, Rebai A, Fakhfakh F, Ayadi H, Petit-Teixeira E, Maalej A. (2011). Signal transducer and activator  of  transcription and the risk of rheumatoid arthritis and thyroid autoimmune disorders. Clinical Experimental Rheumatology. 29: 269-274.

Ouechtati F, Merdassi A, Bouyacoub Y, Largueche L, Derouiche K, Ouragini H, Nouira S, Tiab L, Baklouti K, Rebai A, Schorderet DF, Munier FL, Zografos L, Abdelhak S, El Matri L. (2011). Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in  GNAT2 gene. Journal of  Human Genetics. 56: 22-28.

El Arbi M, Pigeon P, Top S, Rhouma A, Aifa S, Rebai A, Vessières A, Plamont A, Jaouen G.(2011). Evaluation of bactericidal and fungicidal activity of ferrocenyl or phenyl derivatives in the diphenylbuteneseries.Journal of Organometallic Chemistry, 696 : 1038-1048.

El Arbi M, Pigeon P, Chaari-Rkhis A, Top S, Rhouma A, Rebai A, Jaouen G, Aifa S. (2011). Antimicrobial effect of ferrocenyldiarylbutenes against olive plantlet diseases.Journal of  Plant Pathology. 93 : 651-657.

Salah GB, Kamoun H, Rebai A, Youssef AB, Ayadi H, Belghith-Mahfoudh N, Fourati A, Ayadi H, Fakhfakh F. (2011). Sister chromatid exchange (SCE) and high-frequency cells (HFC) in peripheral blood lymphocytes of healthy Tunisian smokers. Mutation Research, 719 :1-6

Kallel-Bayoudh I, Ben Hassen H, Khabir A, Boujelbene N, Daoud J, Frikha M, Sallemi-Boudawara T, Aifa S. Rebaï A. (2011). Bcl-2 expression and Triple negative profile in Breast carcinoma.Medical Oncology, 28: 55-61.

Ouechtati F, Merdassi A, Bouyacoub Y, Largueche L, Derouiche K, Ouragini H, Nouira S, Tiab L, Baklouti K, Rebai A, Schorderet DF, Munier FL, Zografos L, Abdelhak S, Matri LE. (2011). Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene. Journal of  Human Genetics. 56: 22-8.

Fendri-Kriaa N, Kammoun F, Salem IH, Kifagi C, Mkaouar-Rebai E, Hsairi I, Rebai A, Triki C, Fakhfakh F.(2011). New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizure.European  Journal of  Neurology. 18: 695-702.

Fendri-Kriaa N. Boujilbene S, Kammoun F, Ben Mahmoud A; Hsairi I, Rebai A, TrikiC, FaizaFakhfakh F. (2011). A putative disease-associated haplotype within the SCN1A gene in Dravet syndrome.Biochemical and Biophysical Research Communications. 408: 654-7.

Amouri M, Masmoudi A, Borgi N, Rebai A, Turki H. (2011). Atopic dermatitis in Tunisian schoolchildren.Pan African  Medical Journal. 9:34.

Blibech I, KsantiniM, Chaieb I, Jlassi B, Rhouma A, Jaoua S, Aifa S.(2011). Isolation of entomopathogenic Bacillus from a biodynamic olive farm and their pathogenicity to lepidopteran and coleopteran insect pests.Crop Protection 31: 72-77 .

Jemel I, Jellali K, Elloumi J and Aifa S. (2011).The Offer of Chemistry to Targeted Therapy in Cancer.Recent Patents on Biotechnology, 5: 174-182.

Bensaïd M, Hmani-Aifa M, Hammami B, Tlili A, Hakim B, Charfeddine I, Ayadi H, Ghorbel A, Castillo ID, Masmoudi S. (2011). DFNB66 and DFNB67 loci are non allelic and rarely contribute to autosomal recessive nonsyndromic hearing loss. European Journal of  Medical  Genetics. 54 : 565-9.

Ben Saïd M, Ayedi L, Mnejja M, Hakim B, Khalfallah A, Charfeddine I, Khifagi C, Turki K, Ayadi H, Benzina Z, Ghorbel A, Castillo ID, Masmoudi S, Aifa MH. (2011). A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family. European  Journal of  Medical  Genetics. 54: 535-41.

Khalfallah A, Schrauwen I, Mnejja M, HadjKacem H, Dhouib L, Mosrati MA, Hakim B, Lahmar I, Charfeddine I, Driss N, Ayadi H, Ghorbel A, Van Camp G, Masmoudi S.(2011). Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population. Annals of  Human Genetics. 75:598-604.

Mosrati MA, Hammami B, Rebeh IB, Ayadi L, Dhouib L, Ben Mahfoudh K, Hakim B, Charfeddine I, Mnif J, Ghorbel A, Masmoudi S. (2011). A novel dominant mutation in SIX1, affecting a highly conserved residue, result in only auditory defects in humans. European  Journal of  Medical Genetics. 54: 484-8.

Nair KS, Hmani-Aifa M, Ali Z, Kearney AL, Ben Salem S, Macalinao DG, Cosma IM, Bouassida W, Hakim B, Benzina Z, Soto I, Söderkvist P, Howell GR, Smith RS, Ayadi H, John SW. (2011). Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice. Nature Genetics. 43:579-84.

Belguith-Maalej S, Rebuffat SA, Charfeddine I, Mnif M, Nadir RF, Abid M, Ghorbel A, Peraldi-Roux S, Ayadi H, Hadj-Kacem H.(2011). SLC26A4 expression among autoimmune thyroid tissues.Immunobiology. 216:571-578.

Choura M, Rebai A. (2010). Application of computational approaches to study signalling networks of nuclear and Tyrosine kinase receptors.Biology Direct. 5: 58.

Triki-Fendri S, Alfadhli S, Ayadi I, Kharrat N, Ayadi H, Rebai A. (2010). Genetic structure of Kuwaiti population revealed by Y-STR diversity.Annals of Human Biology. 37: 827-835

Siala O, Rebai A, Baklouti F, Fakhfakh F. (2010). Subtle discrepancies of SF2/ASF ESE sequence motif among human tissues: A computational approach. Computational Biological  Chemistry. 34: 203-209.

Salah GB, Kamoun H, Rebai A, Youssef AB, Ayadi H, Belghith-Mahfoudh N, FouratiA, Ayadi H, Fakhfakh F. (2010). Sister chromatid exchange (SCE) and high-frequency cells (HFC) in peripheral blood lymphocytes of healthy Tunisian smokers. Mutation Research, 719 : 1-6

Fendri-Kriaa N, Louhichi N, Mkaouar-Rebai E, Chabchoub G, Kammoun F, Hadj Salem I, Rebai A, Triki C, Fakhfakh F. (2010). The First Genome-Wide Scan in a Tunisian Family With Generalized Epilepsy With Febrile Seizure Plus (GEFS+). Journal of  Child Neurology. 1468

Bouchaala L, Masmoudi A and Rebai A. (2010).Improving algorithms for structure learning in Bayesian Networks using a new implicit score.Expert Systems With Applications, 37: 5470-5475.

Masmoudi Y, Chabchoub H, Hanafi S, and Rebaï A. (2010). A new classification procedure based on mathematical programming: Application to breast cancer classification. Journal of Mathematical Modeling and Algorithms, 9: 247-255.

AlFadhli S, AlTamimy B, Kharrat N, AlSaeid K, Haider MZ, Rebai A. (2010). Molecular analysis of HumDN1 VNTR polymorphism of the human deoxyribonuclease I in systemic lupus erythematosus.International Journal of  Immunogenetics. 37: 5-8.

Choura M, Frikha F, Rebai A. (2010). Investigating the function of three non-synonymous SNPs in EGFR gene: Structural modelling and association with breast cancer.Protein Journal, 29: 50-54

Al’Fadhli S, Kharrat N, Rebai A. (2010). Genome Scan Meta-Analysis in Systemic Lupus Erythematosus Strong linkage with loci 6p22.3-p21.1, and 2q31.1-34. Journal of Medical Genetics and Genomics, 2: 1-7

Rekik-Hakim I, Grati-Kammoun N, Makhloufi E and Rebaï A. (2010).Discovery and potential of SNP markers in characterization of Tunisian olive germplasm.Diversity, 2: 17-27

Kallel I, Kharrat N, Al-Fadhly S, Rebai M, Khabir A, Boudawara TS, Rebaï A. (2010). HER2 Polymorphisms and Breast Cancer in Tunisian Women.Genetic  Testing and  Molecular Biomarkers, 14 : 29-35.

Hadj-Kacem H, Kallel R, Belguith-Maalej S, Mnif M, Charfeddine I, Ghorbel A, Abid M, Ayadi H, Masmoudi S. (2010)  SLC26A4 variations among Graves' hyper-functioning thyroid gland. Disease  Markers. 29:63-69.

Belguith-Maalej S, Rebuffat SA, Charfeddine I, Mnif M, Nadir RF, Abid M, Ghorbel A, Peraldi-Roux S, Ayadi H, Hadj-Kacem H. (2010) SLC26A4 expression among autoimmune thyroid tissues. Immunobiology.

Ben Rebeh I, Morinière M, Ayadi L, Benzina Z, Charfedine I, Feki J, Ayadi H, Ghorbel A, Baklouti F, Masmoudi S.(2010)  Reinforcement of a minor alternative splicing  event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness. Molecular  Vision. 16:1898-1906.

Belguith-Maalej S, Hadj-Kacem H, Rebuffat SA, Mnif-Feki M, Nguyen B, Abid M, Gross R, Ayadi H, Peraldi-Roux S. (2010) Absence of anti-pendrin auto-antibodies in the  sera of Tunisian patients with autoimmune thyroid diseases. Clinical  Laboratory.  56:335-343.

Khalfallah A, Schrauwen I, Mnaja M, Fransen E, Lahmar I, Ealy M, Dhouib L, Ayadi H, Charfedine I, Driss N, Ghorbel A, Smith RJ, Masmoudi S, Van Camp G. (2010) Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia. Annals of  Human Genetics, 74: 399-405.

Ben Saïd M, Hmani-Aifa M, Amar I, Baig SM, Mustapha M, Delmaghani S, Tlili A,  Ghorbel A, Ayadi H, Van Camp G, Smith RJ, Tekin M, Masmoudi S. (2010) High frequency of  the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects. Genetic Testing and  Molecular Biomarkers, 14:307-311.

Rebeh IB, Yoshimi N, Hadj-Kacem H, Yanohco S, Hammami B, Mnif M, Araki M, Ghorbel A, Ayadi H, Masmoudi S, Miyazaki H. (2010). Two missense mutations in SLC26A4 gene: a molecular and functional study. Clinical  Genetics.78: 74-80.