A CD40 variant is associated with systemic bone loss among patients with rheumatoid arthritis von Sghiri, Rim, Benhassine, Hana, Baccouche, Khadija, Ghozzi, Meriem, Jriri, Sarra, Shakoor, Zahid, Almogren, Adel, Slama, Foued, Idriss, Nadia, Benlamine, Zeineb, Bouajina, Elyes, Zemni, Ramzi

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IRAK2 is associated with systemic lupus erythematosus risk von Boumiza, Asma, Zemni, Ramzi, Sghiri, Rim, Idriss, Nadia, Hassine, Hana Ben, Chabchoub, Elyes, Mzabi, Anis, Ghannouchi, Neirouz, Bouajina, Elyes, Ben Hadj Slama, Foued

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A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation von Carrié, Alain, Jun, Lin, Bienvenu, Thierry, Vinet, Marie-Claude, McDonell, Nathalie, Couvert, Philippe, Zemni, Ramzi, Cardona, Ana, Van Buggenhout, Griet, Frints, Suzanna, Hamel, Ben, Moraine, Claude, Ropers, Hans H., Strom, Tim, Howell, Gareth R., Whittaker, Adam, Ross, Mark T., Kahn, Axel, Fryns, Jean-Pierre, Beldjord, Cherif, Marynen, Peter, Chelly, Jamel

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Sousse: extreme genetic heterogeneity in North Africa von Fadhlaoui-Zid, Karima, Garcia-Bertrand, Ralph, Alfonso-Sánchez, Miguel A, Zemni, Ramzi, Benammar-Elgaaied, Amel, Herrera, Rene J

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Sera Levels of microRNA-124 in Newly Diagnosed Patients with Type 2 Diabetes Mellitus in Iraqi Population von Al-Lami, Huda B., ZEMNI, Ramzi, Yassin, Ammar Gany

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Interleukin‐21 receptor gene polymorphism (rs2285452 A/G) is associated with susceptibility to Behçet's disease von Lahmar, Rajaa, Chabchoub, Elyes, Zemni, Ramzi, Anis, Mzabi, Ghannouchi, Neirouz, Slama, Foued Ben Hadj

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A TRAF6 genetic variant is associated with low bone mineral density in rheumatoid arthritis von Hassine, Hana Ben, Zemni, Ramzi, Nacef, Imen Ben, Boumiza, Asma, Slama, Foued, Baccouche, Khadija, Amri, Najla, Melayah, Sarra, Shakoor, Zahid, Almogren, Adel, Bouajina, Elyes, Sghiri, Rim

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Micro RNA-146a But Not IRAK1 is Associated with Rheumatoid Arthritis in the Tunisian Population von Hassine, Hana Ben, Boumiza, Asma, Sghiri, Rim, Baccouche, Khadija, Boussaid, Imen, Atig, Ahlem, Shakoor, Zahid, Bouajina, Elyes, Zemni, Ramzi

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IRAK2 is associated with susceptibility to rheumatoid arthritis von Hassine, Hana Ben, Sghiri, Rim, Chabchoub, Elyes, Boumiza, Asma, Slama, Foued, Baccouche, Khadija, Shakoor, Zahid, Almogren, Adel, Mariaselvam, Christina, Tamouza, Ryad, Bouajina, Elyes, Zemni, Ramzi

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Association of the IL-10 Receptor A536G (S138G) Loss-of-Function Variant with Recurrent Miscarriage von Magdoud, Kalthoum, Hellal, Radhia, Zemni, Ramzi, Touraine, Renaud, Mahjoub, Touhami, Almawi, Wassim Y.

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Sousse, Tunisia: Tumultuous history and high Y-STR diversity von Fadhlaoui-Zid, Karima, Chennakrishnaiah, Shilpa, Zemni, Ramzi, Grinberg, Sagy, Herrera, Rene J., Benammar-Elgaaied, Amel

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S ousse, T unisia: Tumultuous history and high Y ‐ STR diversity von Fadhlaoui‐Zid, Karima, Chennakrishnaiah, Shilpa, Zemni, Ramzi, Grinberg, Sagy, Herrera, Rene J., Benammar‐Elgaaied, Amel

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ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation von Bienvenu, Thierry, Poirier, Karine, Friocourt, Gaelle, Bahi, Nadia, Beaumont, Delphine, Fauchereau, Fabien, Ben Jeema, Lamia, Zemni, Ramzi, Vinet, Marie-Claude, Francis, Fiona, Couvert, Philippe, Gomot, Marie, Moraine, Claude, van Bokhoven, Hans, Kalscheuer, Vera, Frints, Suzanne, Gecz, Josef, Ohzaki, Kanae, Chaabouni, Habiba, Fryns, Jean-Pierre, Desportes, Vincent, Beldjord, Cherif, Chelly, Jamel

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Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation von Billuart, Pierre, Bienvenu, Thierry, Ronce, Nathalie, des Portes, Vincent, Vinet, Marie Claude, Zemni, Ramzi, Crollius, Hugues Roest, Carrié, Alain, Fauchereau, Fabien, Cherry, Michele, Briault, Sylvain, Hamel, Ben, Fryns, Jean-Pierre, Beldjord, Cherif, Kahn, Axel, Moraine, Claude, Chelly, Jamel

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Lack of association between PADI4 polymorphisms and rheumatoid arthritis in the Tunisian population von Ben Hassine, Hana, Zemni, Ramzi, Bouagina, Elyes, Zaglaoui, Hala, Ben Fradj, Hosni, Slama, Foued, Boukadida, Jalel, Sghiri, Rim

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Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria von Jellouli, Nadege Kammoun, Hadj Salem, Ikhlass, Ellouz, Emna, Kamoun, Zeineb, kamoun, Fatma, tlili, Abdelaziz, Kaabachi, Naziha, Triki, Chanez, Fakhfakh, Faiza

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Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease von Kammoun Jellouli, Nadege, Hadj Salem, Ikhlass, Ellouz, Emna, Louhichi, Nacim, tlili, Abdelaziz, Kammoun, Fatma, Triki, Chanez, Fakhfakh, Faiza

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A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation von Zemni, Ramzi, Bienvenu, Thierry, Vinet, Marie C., Sefiani, Aziz, Carrié, Alain, Billuart, Pierre, McDonell, Nathalie, Couvert, Philippe, Francis, Fiona, Chafey, Philippe, Fauchereau, Fabien, Friocourt, Gaelle, Portes, Vincent des, Cardona, Anna, Frints, Suzanna, Meindl, Alfonse, Brandau, Oliver, Ronce, Nathalie, Moraine, Claude, Bokhoven, Han van, Ropers, Hans H., Sudbrak, Ralf, Kahn, Axel, Fryns, Jean P, Beldjord, Cherif, Chelly, Jamel

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Mutational Analysis of the MECP2 Gene in Tunisian Patients With Rett Syndrome: A Novel Double Mutation von Fendri-Kriaa, Nourhene, Mkaouar-Rebai, Emna, Moalla, Dorsaf, Belguith, Neila, Louhichi, Nacim, Zemni, Ramzi, Slama, Foued, Triki, Chahnez, Fakhfakh, Faiza

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A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene von Fendri-Kriaa, Nourhene, Hsairi, Ines, Kifagi, Chamseddine, Ellouze, Emna, Mkaouar-Rebai, Emna, Triki, Chahnez, Fakhfakh, Faiza

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