IL1-receptor accessory protein-like 1 (IL1RAPL1), a protein involved in cognitive functions, regulates N-type Ca2+-channel and neurite elongation F Gambino, A Pavlowsky, A Béglé, JL Dupont, N Bahi, R Courjaret, ... Proceedings of the National Academy of Sciences 104 (21), 9063-9068, 2007 | 100 | 2007 |
IL1-receptor accessory protein-like 1 (IL1RAPL1), a protein involved in cognitive functions, regulates N-type Ca2+-channel and neurite elongation F Gambino, A Pavlowsky, A Béglé, JL Dupont, N Bahi, R Courjaret, ... Proceedings of the National Academy of Sciences 104 (21), 9063-9068, 2007 | 100 | 2007 |
CTLA-4 gene polymorphisms in Tunisian patients with Graves' disease HH Kacem, M Bellassoued, N Bougacha-Elleuch, M Abid, H Ayadi Clinical Immunology 101 (3), 361-365, 2001 | 94 | 2001 |
Autoimmune thyroid diseases: genetic susceptibility of thyroid‐specific genes and thyroid autoantigens contributions H Hadj‐Kacem, S Rebuffat, M Mnif‐Féki, S Belguith‐Maalej, H Ayadi, ... International journal of immunogenetics 36 (2), 85-96, 2009 | 86 | 2009 |
HLA‐DQB1 CAR1/CAR2, TNFa IR2/IR4 and CTLA‐4 polymorphisms in Tunisian patients with rheumatoid arthritis and Sjögren's syndrome HH Kacem, N Kaddour, FZ Adyel, Z Bahloul, H Ayadi Rheumatology 40 (12), 1370-1374, 2001 | 61 | 2001 |
Genetic investigation of FOXE1 polyalanine tract in thyroid diseases: new insight on the role of FOXE1 in thyroid carcinoma R Kallel, S Belguith-Maalej, A Akdi, M Mnif, I Charfeddine, P Galofré, ... Cancer Biomarkers 8 (1), 43-51, 2011 | 44 | 2011 |
The genetics of autoimmune thyroid disease H Ayadi, HH Kacem, A Rebai, NR Farid Trends in Endocrinology & Metabolism 15 (5), 234-239, 2004 | 43 | 2004 |
PDS Is a New Susceptibility Gene to Autoimmune Thyroid Diseases: Association and Linkage Study HH Kacem, A Rebai, N Kaffel, S Masmoudi, M Abid, H Ayadi The Journal of Clinical Endocrinology & Metabolism 88 (5), 2274-2280, 2003 | 42 | 2003 |
Relation between male obesity and male infertility in a T unisian population L Hadjkacem Loukil, H Hadjkacem, A Bahloul, H Ayadi Andrologia 47 (3), 282-285, 2015 | 33 | 2015 |
Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population A Khalfallah, I Schrauwen, M Mnejja, H HadjKacem, L Dhouib, ... Annals of human genetics 75 (5), 598-604, 2011 | 30 | 2011 |
Significant transcriptomic changes are associated with differentiation of bone marrow-derived mesenchymal stem cells into neural progenitor-like cells in the presence of bFGF … AA Khan, TJ Huat, A Al Mutery, AT El-Serafi, HH Kacem, SH Abdallah, ... Cell & bioscience 10, 1-18, 2020 | 26 | 2020 |
Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss A Tlili, A Al Mutery, W Kamal Eddine Ahmad Mohamed, M Mahfood, ... Genetic testing and molecular biomarkers 21 (11), 686-691, 2017 | 25 | 2017 |
Screening of Y chromosome microdeletions in Tunisian infertile men L Hadj-Kacem, H Hadj-Kacem, N Chakroun-Fki, A Bahloul, MN Mhiri, ... Archives of andrology 52 (3), 169-174, 2006 | 22 | 2006 |
The A/T mutation in exon 2 of the DNASE1 gene is not present in Tunisian patients with systemic lupus erythematosus or in healthy subjects P Chakraborty, HH Kacem, K Makni‐Karray, F Jarraya, J Hachicha, ... Arthritis & Rheumatism 48 (11), 3297-3298, 2003 | 22 | 2003 |
Androgen receptor gene CAG repeats length in fertile and infertile Tunisian men L Hadjkacem, H Hadj-Kacem, A Boulila, A Bahloul, H Ayadi, ... Annales de génétique 47 (3), 217-224, 2004 | 21 | 2004 |
NADf chip, a two-color microarray for simultaneous screening of multigene mutations associated with hearing impairment in North African Mediterranean countries I Chakchouk, MB Said, F Jbeli, R Benmarzoug, S Loukil, I Smeti, ... The Journal of Molecular Diagnostics 17 (2), 155-161, 2015 | 20 | 2015 |
Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD) S Belguith-Maalej, HH Kacem, A Rebai, M Mnif, M Abid, H Ayadi Immunobiology 213 (7), 577-583, 2008 | 19 | 2008 |
PCR–RFLP and species-specific PCR efficiency for the identification of adulteries in meat and meat products H Gargouri, N Moalla, HH Kacem European Food Research and Technology 247 (9), 2183-2192, 2021 | 18 | 2021 |
Two missense mutations in SLC26A4 gene: a molecular and functional study IB Rebeh, N Yoshimi, H Hadj‐Kacem, S Yanohco, B Hammami, M Mnif, ... Clinical genetics 78 (1), 74-80, 2010 | 16 | 2010 |
DNase1 exon2 analysis in Tunisian patients with rheumatoid arthritis, systemic lupus erythematosus and Sjögren syndrome and healthy subjects S Belguith-Maalej, H Hadj-Kacem, N Kaddour, Z Bahloul, H Ayadi Rheumatology International 30, 69-74, 2009 | 16 | 2009 |