1. A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy. (3rd May 2014) Authors: Ben Rekaya, Mariem; Laroussi, Nadia; Messaoud, Olfa; Jones, Mariem; Jerbi, Manel; Naouali, Chokri; Bouyacoub, Yosra; Chargui, Mariem; Kefi, Rym; Fazaa, Becima; Boubaker, Mohamed Samir; Boussen, Hamouda; Mokni, Mourad; Abdelhak, Sonia; Zghal, Mohamed; Khaled, Aida; Yacoub-Youssef, Houda Other Names: Burmeister Margit Academic Editor. Journal: BioMed research international Issue: Volume 2014(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa. Issue 8 (13th August 2020) Authors: Hechmi, Meriem; Dallali, Hamza; Gharbi, Meriem; Jmel, Haifa; Fassatoui, Meriem; Ben Halima, Yossra; Bahri, Sonia; Bahlous, Afaf; Abid, Abdelmajid; Jamoussi, Henda; Barakat, Abdelhamid; Kefi, Rym Journal: Bioscience reports Issue: Volume 40:Issue 8(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Association study of HNF1A polymorphisms with metabolic syndrome in the Moroccan population. (December 2017) Authors: Morjane, Imane; Kefi, Rym; Charoute, Hicham; Lakbakbi el Yaagoubi, Fouzia; Hechmi, Meryem; Saile, Rachid; Abdelhak, Sonia; Barakat, Abdelhamid Journal: Diabetes & metabolic syndrome Issue: Volume 11(2017)Supplement 2 Page Start: S853 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Association Study of HNF1A Polymorphisms with Metabolic Syndrome in the Moroccan Population. (June 2018) Authors: Morjane, Imane; Charoute, Hicham; El Yaagoubi, Fouzia L.; Hechmi, Meryem; Rachid, Saile; Kefi, Rym; Abdelhak, Sonia; Barakat, Abdelhamid Journal: Atherosclerosis Issue: Volume 32(2018) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Association study of mitochondrial DNA polymorphisms with type 2 diabetes in Tunisian population. (June 2015) Authors: Hsouna, Sana; Ben Halim, Nizar; Lasram, Khaled; Arfa, Imen; Jamoussi, Henda; Bahri, Sonia; Ammar, Slim Ben; Miladi, Najoua; Abid, Abdelmajid; Abdelhak, Sonia; Kefi, Rym Journal: Mitochondrial DNA Issue: Volume 26:Number 3(2015:Jun.) Page Start: 367 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Contribution of CDKAL1 rs7756992 and IGF2BP2 rs4402960 polymorphisms in type 2 diabetes, diabetic complications, obesity risk and hypertension in the Tunisian population 在突尼斯人群中，CDKAL1 rs7756992与IGF2BP2 rs4402960的多态性对2型糖尿病、糖尿病并发症、肥胖风险以及高血压的影响. (21st April 2014) Authors: Lasram, Khaled; Ben Halim, Nizar; Benrahma, Houda; Mediene‐Benchekor, Sounnia; Arfa, Imen; Hsouna, Sana; Kefi, Rym; Jamoussi, Henda; Ben Ammar, Slim; Bahri, Sonia; Abid, Abdelmajid; Benhamamouch, Soraya; Barakat, Abdelhamid; Abdelhak, Sonia Journal: Journal of diabetes Issue: Volume 7:Number 1(2015:Jan.) Page Start: 102 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Contribution of CDKAL1 rs7756992 and IGF2BP2 rs4402960 polymorphisms in type 2 diabetes, diabetic complications, obesity risk and hypertension in the Tunisian population 在突尼斯人群中，CDKAL1 rs7756992与IGF2BP2 rs4402960的多态性对2型糖尿病、糖尿病并发症、肥胖风险以及高血压的影响. (21st April 2014) Authors: Lasram, Khaled; Ben Halim, Nizar; Benrahma, Houda; Mediene‐Benchekor, Sounnia; Arfa, Imen; Hsouna, Sana; Kefi, Rym; Jamoussi, Henda; Ben Ammar, Slim; Bahri, Sonia; Abid, Abdelmajid; Benhamamouch, Soraya; Barakat, Abdelhamid; Abdelhak, Sonia Journal: Journal of diabetes Issue: Volume 7:Number 1(2015:Jan.) Page Start: 102 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. CYP1B1 Gene Mutations Causing Primary Congenital Glaucoma in Tunisia. (July 2014) Authors: Bouyacoub, Yosra; Ben Yahia, Salim; Abroug, Nesrine; Kahloun, Rim; Kefi, Rym; Khairallah, Moncef; Abdelhak, Sonia Journal: Annals of human genetics Issue: Volume 78:Number 4(2014:Jul.) Page Start: 255 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia. Issue 2 (16th July 2015) Authors: Ben Halim, Nizar; Hsouna, Sana; Lasram, Khaled; Rejeb, Insaf; Walha, Asma; Talmoudi, Faten; Messai, Habib; Sabrine Ben Brick, Ahlem; Ouragini, Houyem; Cherif, Wafa; Nagara, Majdi; Rhouma, Faten Ben; Chouchene, Ibtissem; Ouechtati, Farah; Bouyacoub, Yosra; Ben Rekaya, Mariem; Messaoud, Olfa; Ben A... Journal: American journal of human biology Issue: Volume 28:Issue 2(2016:Mar./Apr.) Page Start: 171 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity. (29th September 2015) Authors: Ben Halim, Nizar; Nagara, Majdi; Regnault, Béatrice; Hsouna, Sana; Lasram, Khaled; Kefi, Rym; Azaiez, Hela; Khemira, Laroussi; Saidane, Rachid; Ammar, Slim Ben; Besbes, Ghazi; Weil, Dominique; Petit, Christine; Abdelhak, Sonia; Romdhane, Lilia Journal: Annals of human genetics Issue: Volume 79:Number 6(2015:Nov.) Page Start: 402 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗