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Hammadi AYADI
Informations génerales
Coordonnées
Grade
Professeur Productions
Brevet Propriétés probiotiques de la souche Lactobacillus plantarum CTM 50371 lui permettant d’être appliquée comme additif en alimentation animale. Brevet d’invention TN2010/0246 du 31 Mai 2010 de wasim_bejar, Maguin E.,Abdelmalek B, Hichem Chouayekh , Samir BEJAR, Lotfi MELLOULI, Hammadi AYADI, Slim Smaoui , Articles scientifiques The genetics of autoimmune thyroid disease. Trends in Endocrinol and Metabolism. 15: 234-239. de Hammadi AYADI, FARID NR., Ahmed Rebai, Hassen HADJ KACEM, Lack of Association of VDR gene polymorphisms with Thyroid autoimmune disorders: Familial and case/control studies. Journal of Clinical Immunology. 28: 21-25 de MAALEJ A., PETIT-TEIXEIRA E., CHABCHOUB G., BEN HAMAD M., FARID NR., CORNELIS F ., Hammadi AYADI, Ahmed Rebai, Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation. Clin. Genet. 68: 188-189. de hanen_belguith, HAJJI S., SALEM N., CHARFEDDINE I., LAHMAR I., AMOR MB., OULDIM K., CHOUERY E., DRISS N., DRIRA M., MEGARBANE A.,SEFIANI A., Hammadi AYADI, Saber Masmoudi, Ahmed Rebai, Association study of VDR gene with Rheumatoid Arthritis in the French population. Genes and Immunity. 6: 707-711. de MAALEJ A., PETIT-TEIEXIERA E., MICHOU L., CORNELIS F. , Hammadi AYADI, Ahmed Rebai, Allelic structure and distribution of 103 STR loci in a Southern Tunisian population. Journal of Genetics. 83: 65-71. de MAALEJ A., AYADI A., JOUIDA J., MAKNI H., Hammadi AYADI, Ahmed Rebai, Evidence of association between FKBP1B and thyroid autoimmune disorders in a large Tunisian family. Autoimmunity. 37: 237-239. de MAALEJ A_, MBARKI F., JOUIDA J., ABID M. , Hammadi AYADI, Fatma Karray, Ahmed Rebaï , TMC1 but not TMC2 is responsible for autosomal recessive nonsyndromic hearing impairment in Tunisian families. Audiol Neurootol. 2008; 13(4):213-8. PMID: 18259073 de abdelaziz_tlili, TLILI-CHOUCHÈNE J., LAHMAR I., BENZINA Z., CHARFEDINE I., DRISS N., GHORBEL A., Hammadi AYADI, Saber Masmoudi, Mariem ben said, Mounira HMANI , Imen BENREBEH , Two missense mutations in SLC26A4 gene: a molecular and functional study. Clin Genet. (in press). de imen_benrebeh, YOSHIMI N., YANOHCO S., HAMMAMI B., ARAKI M., GHORBEL A., MIYAZAKI H., Saber Masmoudi, Hammadi AYADI, Mouna MNIF, Hassen HADJ KACEM, Association analysis of interleukin gene polymorphisms in autoimmune thyroid diseases in the Tunisian population. Eur Cytokine Netw. 18: 196-200. de KAMMOUN-KRICHEN M., ABID M., JOUIDA J., Hammadi AYADI, Mouna MNIF, Ahmed Rebai, Sylvie PERALDI ROUX, Maha Rebai, Kaouthar MAKNI, Noura BOUGACHA, Association and linkage studies of the 20q11.2 region (GRD-2 locus) with Graves' disease in the Tunisian population. Ann Hum Biol. 34: 566-72. de Kaouthar MAKNI, ABID M. , Hammadi AYADI, Ahmed Rebai, Hassen HADJ KACEM, Analysis of MHC genes in a Tunisian isolate with autoimmune thyroid diseases: implication of TNF -308 gene polymorphism. Journal of Autoimmunity. 23: 75-80. de Noura BOUGACHA, MAKNI H., BELLASSOUAD M., JOUIDA J., ABID M. , Hammadi AYADI, Mouna MNIF, Ahmed Rebai, Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. Nat Genet, 40(11),1335-1340. de AHMED ZM_, KALAY E., BELYANTSEVA IA., COLLIN RWJ., RIAZUDDIN S., VENZELAAR H., KAWAR MN., TLILI A., VAN DER ZWAAG B., KHAN SY., AYADI L., RIKARAGUZEL A., GHORBEL A., RIAZUDDIN S., FRIEDMAN TB., KREMER H., Hammadi AYADI, Mohamed Ali EL MOSRATI, Saber Masmoudi, Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. Eur J Hum Genet. 17(4):474-82. de mounira_hmani, BENZINA Z., ZULFIQAR F., DHOUIB H., SHAHZADI A., GHORBEL A., SÖDERKVIST P., RIAZUDDIN S., KIMBERLING WJ., Hammadi AYADI, Ahmed Rebaï , A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1. Hum Genet. 126 (4) :575-87 de mounira_hmani, BENZINA Z., BOUASSIDA W., MESSAOUD R., TURKI K., KHAIRALLAH M., FAKHFEKH F., SÖDERKVIST P, Salma BENSELEM , Ahmed Rebaï , Hammadi AYADI, Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. Eur J Hum Genet. 17: 474-482. de mounira_hmani, BENZINA Z., ZULFIQAR F., SHAHZADI A., GHORBEL A., SÖDERKVIST P., RIAZUDDIN S., KIMBERLING WJ. , Ahmed Rebaï , Hammadi AYADI, Hafeth Belghith, Association of calpain-10 polymorphisms with type 2 diabetes in the Tunisian population. Diabetes Metab. 34: 273-278. de Chamseddine Kifagi, MNIF F., BOUDAWARA M., HAMZA N., REKIK N., ABID M., GRANIER C., Kaouthar MAKNI, Ahmed Rebai, Fatma Karray, Hammadi AYADI, Polymorphisms in the protein tyrosine phosphatase (PTPN22) gene is not associated with autoimmune thyroid in a large affected Tunisian family. Clin Immunol. 120: 235-236. de CHABCHOUB G., MAALEJ A., PETIT-TEIXEIRA E., GLIKMANS E., FARID NR., CORNELIS F. , Hammadi AYADI, Ahmed Rebai, Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD). Immunobiology. 2008;213(7):577-83. PMID: 18656705 de BELGUITH-MAALEJ S_, MNIF M., ABID M., Hammadi AYADI, Ahmed Rebaï , Hassen HADJ KACEM, A potential role of TNFR gene polymorphisms in autoimmune thyroid diseases in the Tunisian population. Cytokine. 2008 Aug;43(2):110-3. PMID: 18571427 de KAMMOUN-KRICHEN M_, MNIF M, JOUIDA J, ABID M., Hammadi AYADI, Ahmed Rebaï , Kaouthar MAKNI, Noura BOUGACHA, Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers. Clinical Genetics. 66: 358-364. de Saber Masmoudi, CHARFEDINE I., GHORBEL A., PETIT C., DRIRA M., Hammadi AYADI, Hanen Belguith, Abdelaziz TLILI, Ahmed Rebai, Imen BENREBEH , Identification of candidate regions for a novel Usher syndrome type II locus. Mol Vis. 2008 Sep 19;14:1719-26. PMID: 18806881 de imen_benrebeh, BENZINA Z., DHOUIB H., HADJAMOR I., AMYERE M., TURKI K., HAMMAMI B., KMIHA N., KAMMOUN H., CHARFEDINE I., VIKKULA M., GHORBEL A, Saber Masmoudi, Hammadi AYADI, Leila AYADI , Bochra Hakim, Association of calpain-10 polymorphisms with type 2 diabetes in the Tunisian population. Diabetes Metab. 2008 Jun;34(3):273-8. PMID: 18487065 de Chamseddine Kifagi, MNIF F., BOUDAWARA M., HAMZA N., REKIK N., ABID M., Claude GRANIER, Faiçal JARRAYA, Hammadi AYADI, Ahmed Rebaï , Kaouthar MAKNI, Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus. Genet Test Mol Biomarkers. 13 (1) 147-51. de hanen_belguith, DHOUIB H., LAHMAR I., MOALLA J., CHARFEDDINE I., DRISS N., ARAB SB., GHORBEL A., Saber Masmoudi, Hammadi AYADI, Mohamed Ali EL MOSRATI, Mariem ben said, Mounira HMANI , Autoimmune thyroid diseases: genetic susceptibility of thyroid-specific genes and thyroid autoantigens contributions. Int J Immunogenet. Apr;36(2):85-96. Review. PubMed PMID: 19284442. de Hassen HADJ KACEM, PERALDI-ROUX S., Hammadi AYADI, Salima BELGUITH, Mouna MNIF, Sandra Rebuffat, Mutation in gap and tight junctions in patients with non-syndromic hearing loss. Biochem Biophys Res Commun. Jul 17; 385(1):1-5. PubMed PMID: 19254696. de hanen_belguith, DHOUIB H., LAHMAR I., CHARFEDDINE I., DRISS N., GHORBEL A., Hammadi AYADI, Imen BENREBEH , Saber Masmoudi, Abdelaziz TLILI, Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD). Immunobiology. 213: 577-583 de BELGUITH-MAALEJ S., ABID M., Hammadi AYADI, Mouna MNIF, Ahmed Rebai, Hassen HADJ KACEM, Evidence for linkage and association between autoimmune thyroid diseases and the 18q12-q21 region in a large Tunisian family. International Journal of Immunogenetics, 33: 25-32 de Hassen HADJ KACEM, KAFFEL N., ABID M., Hammadi AYADI, Ahmed Rebai, Gene and protein markers of diabetic nephropathy. Nephrol Dial Transplant. 2008 Mar;23(3):792-9. PMID: 18065784 de GRANIER C_, Faiçal JARRAYA, Hammadi AYADI, Bénédicte JARDIN, Laurence MOLINA, Kaouthar MAKNI, TNF gene polymorphisms in Graves? disease: TNF-308 A/G meta-analysis. Ann Hum Biol, 35(6):656-61. de KAMMOUN-KRICHEN M_, ABID M., Hammadi AYADI, Mouna MNIF, Ahmed Rebaï , Noura BOUGACHA, Renal alpha-smooth muscle actin: a new prognostic factor for lupus nephritis. Nephrology (Carlton). Aug; 14(5):499-505. PubMed PMID: 19674318. de Kaouthar MAKNI, HENTATI B., HMIDA MB., MAKNI H., BOUDAWARA T., JLIDI R., HACHICHA J., Hammadi AYADI, Abdelmajid Khabir , Faiçal JARRAYA, DNase1 exon2 analysis in Tunisian patients with rheumatoid arthritis, systemic lupus erythematosus and Sjögren syndrome and healthy subjects. Rheumatol Int. Apr. (In press). de BELGUITH-MAALEJ S_, KADDOUR N., BAHLOUL Z., Hammadi AYADI, Hassen HADJ KACEM, Spatial and temporal variations of microphytoplankton composition related to hydrographic conditions in the Gulf of Gabes. Journal of the Marine Biological Association of the United Kingdom.( In press). de DRIRA Z_, BEL HASSEN M., HAMZA A., BOUAIN A., ALEYA L., Hammadi AYADI, Ahmed Rebaï , |