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

Structural analysis of hubs in human NR-RTK network. Biol Direct. 6 :49.

Lack of association between the angiotensin-converting enzyme gene (I/D) polymorphism and diabetic nephropathy in Tunisian type 2 diabetic patients. Journal of Renin Angiotensin Aldosterone system 9:32-36.

Lack of Association of VDR gene polymorphisms with Thyroid autoimmune disorders: Familial and case/control studies. Journal of Clinical Immunology. 28: 21-25

Dinucleotide (AC) repeat polymorphism in intron1 of human EGFR shows ethnic specificities and high evidence for association with breast cancer. International Journal of Biological Markers. 22: 258-264

Severe MDC1A congenital muscular dystrophy due to a splicing mutation in the LAMA2 gene resulting in exon skipping and significant decrease of mRNA level. Genet Test. 11: 199-207.

Electrostatic interactions of peptides flanking the tyrosine kinase domain in the epidermal growth factor receptor (EGFR) provides a model for intracellular dimerization and autophosphorylation. Proteins: Structure, Function and Bioinformatics. 62: 1036-1

Identification and characterization of new members of vacuolar H+-pyrophosphatase family from Oryza sativa genome. Russian Journal of Plant Physiology. 52: 926-930.

Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation. Clin. Genet. 68: 188-189.

Analysis of Genetic Diversity in Tunisian Durum Wheat Cultivars and related wild species by SSR and AFLP markers. Genetic Resources and Crop Evolution, 52: 21-31.

Association study of VDR gene with Rheumatoid Arthritis in the French population. Genes and Immunity. 6: 707-711.

SSR-based Genetic diversity Assessment among tunisian barley cultivars and relationship with morphological traits. Euphytica. 135: 107-118.

Allelic structure and distribution of 103 STR loci in a Southern Tunisian population. Journal of Genetics. 83: 65-71.

Application of computational approaches to study signalling networks of nuclear and Tyrosine kinase receptors. Biology Direct. 5: 58

Association analysis of interleukin gene polymorphisms in autoimmune thyroid diseases in the Tunisian population. Eur Cytokine Netw. 18: 196-200.

Linkage disequilibrium in the human genome and its applications: between myth and reality. Archives de l?Institut Pasteur de Tunis, 82: 9-21

Causal inference in Biomolecular Pathways using a Bayesian network approach and an Implicit method. Journal of Theoretical Biology, 253: 717-723.

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.

Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients. J Hum Genet. 52: 262-70.

Cleavage of the human thyrotropin receptor by ADAM10 is regulated by thyrotropin. Journal of Molecular Recognition. 20:392-404.

Genetic diversity assessment of Tunisian olive tree (Olea europaea L.) cultivars using AFLP markers. Genetic Resources and Crop Evolution. 53: 265-275

Sample size computation for association studies using case-parents design. J Genet. 85: 187-191.

Analysis of MHC genes in a Tunisian isolate with autoimmune thyroid diseases: implication of TNF -308 gene polymorphism. Journal of Autoimmunity. 23: 75-80.

IGD: A resource for intronless genes in the human genome. Gene. 488: 35-40.79

Receptor tyrosine kinases: from biology to pathology. 2011. J Recept Signal Transduct. 31 : 387-394

Association of calpain-10 polymorphisms with type 2 diabetes in the Tunisian population. Diabetes Metab. 34: 273-278.

Optimization of alkaline protease production by Aspergillus clavatus ES1 in Mirabilis jalap tuber powder using statistical experimental design. Applied Microbiol Biotechnol. 79: 915-923.

Combining Autosomal and Y-Chromosomal Short Tandem Repeat Data in Paternity Testing with Male Child: Methods and Application. J Forensic Sci. 52: 1068-1072.

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.

Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean region. J Hum Genet. 51: 841-845.

Haplotype structure of five SNPs within the ACE gene in the Tunisian population. Annals of Human Biology, 33: 319-329

Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers. Clinical Genetics. 66: 358-364.

Investigating the function of three nonsynonymous SNPs in EGFR gene: Structural modelling and association with breast cancer. Protein Journal, 29: 50-54

Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD). Immunobiology. 213: 577-583

Haplotypes for 13 Y-chromosomal STR loci in South Tunisian population (Sfax region). Forensic Science International. 164: 249-253

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

Data for 10 autosomal STR markers in South Tunisian population. Forensic Sci Int. 164: 254-256.

The genetics of autoimmune thyroid disease. Trends in Endocrinol and Metabolism. 15: 234-239.