Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Insaf Rejeb"'
Autor:
Nizar Ben Halim, Habiba Ben Romdhane, Zinet Turki, Om Kalthoum Sallem, Insaf Rejeb, Abdelmajid Abid, Mariem Chargui, Majdi Nagara, Sahar Elouej, Dalenda Triki, Sonia Bahri, Henda Jamoussi, Sonia Abdelhak, Khaled Lasram, Redha Attaoua, Claude Ben Slama, Sana Hsouna, Ines Kamoun, Florin Grigorescu, Hanen Belfki-Benali, Rym Kefi
Publikováno v:
Journal of Diabetes and its Complications
Journal of Diabetes and its Complications, Elsevier, 2016, 30 (2), pp.206-211. ⟨10.1016/j.jdiacomp.2015.11.013⟩
Journal of Diabetes and its Complications, Elsevier, 2016, 30 (2), pp.206-211. ⟨10.1016/j.jdiacomp.2015.11.013⟩
International audience; Aims: Variants in the fat mass and obesity-associated gene (FTO) are associated with obesity and type 2 diabetes. However, the association of FTO variants in the MENA (Middle East and North Africa) region with MetS is largely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8afb1c91a25332ad641127f0b4b72a97
https://doi.org/10.1016/j.jdiacomp.2015.11.013
https://doi.org/10.1016/j.jdiacomp.2015.11.013
Autor:
Slim Ben Ammar, Neji Tebib, Farah Ouechtati, Khaled Lasram, Marie Françoise Ben Dridi, Faten Talmoudi, Rym Kefi, Houyem Ouragini, Nizar Ben Halim, Insaf Rejeb, Olfa Messaoud, Asma Walha, Yosra Bouyacoub, Sonia Abdelhak, Mourad Mokni, Ahlem Amouri, Habib Messai, Sana Hsouna, Majdi Nagara, Ahlem Sabrine Ben Brick, Wafa Cherif, Leila El Matri, Faten Ben Rhouma, I. Chouchene, Mariem Ben Rekaya
Publikováno v:
American Journal of Human Biology. 28:171-180
Objectives Consanguinity is common in Tunisia. However, little information exists on its impact on recessive disorders. In this study, we evaluate the impact of consanguineous marriages on the occurrence of some specific autosomal recessive disorders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4de7f5fa3c497e90f4264cfcb27a3572
https://doi.org/10.1002/ajhb.22764
https://doi.org/10.1002/ajhb.22764
Autor:
Crystel Bonnet, Mariem Ben Rekaya, Nizar Ben Halim, Yosra Bouyacoub, Giovanni Romeo, Insaf Rejeb, Olfa Messaoud, Faten Ben Rhouma, Lilia Romdhane, Christine Petit, Habib Messai, Zied Riahi, Sonia Abdelhak, Rym Kefi, Majdi Nagara, Ken McElreavey
Publikováno v:
Human Heredity
Human Heredity, Karger, 2014, 77 (1-4), pp.167-74. ⟨10.1159/000362167⟩
Human Heredity, 2014, 77 (1-4), pp.167-74. ⟨10.1159/000362167⟩
Human Heredity, Karger, 2014, 77 (1-4), pp.167-74. ⟨10.1159/000362167⟩
Human Heredity, 2014, 77 (1-4), pp.167-74. ⟨10.1159/000362167⟩
International audience; Located at the cross-road between Europe and Africa, Tunisia is a North African country of 11 million inhabitants. Throughout its history, it has been invaded by different ethnic groups. These historical events, and consanguin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13ae8973b9d253a7b933a1b5bf48e6ac
https://doi.org/10.1159/000362167
https://doi.org/10.1159/000362167
Autor:
Redha Attaoua, Sonia Abdelhak, Om Kalthoum Sallem, Henda Jamoussi, Habiba Ben Romdhane, Majdi Nagara, Mariem Chargui, Insaf Rejeb, Abdelmajid Abid, Rym Kefi, Zinet Turki, Sonia Bahri, Sahar Elouej, Claude Ben Slama, Ines Kamoun, Florin Grigorescu
Publikováno v:
Endocrine Research
Endocrine Research, Taylor & Francis, 2016, 41 (4), pp.300-309. ⟨10.3109/07435800.2016.1141945⟩
Endocrine Research, Taylor & Francis, 2016, 41 (4), pp.300-309. ⟨10.3109/07435800.2016.1141945⟩
International audience; AIM OF THE STUDY: Recent genome-wide association studies (GWASs) have identified many genetic variants associated with metabolic syndrome (MetS). However, their contribution to MetS in ethnic groups in Tunisia is largely unexp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef375256e573e45440bb6237b1fbffdc
https://pubmed.ncbi.nlm.nih.gov/26905813
https://pubmed.ncbi.nlm.nih.gov/26905813
Autor:
Alison Shaw, Hasan Al-Dhekri, Taisa Manuela Bonfim Machado, I. Christopher Lloyd, Fernanda Bender, Nima Rezaei, Nadia Al-Hashmi, Alessandro Gialluisi, Lihadh Al-Gazali, Christine Petit, Hanan Hamamy, Mourad Sahbatou, Mohammad Jalal Abbasi-Shavazi, Insaf Rejeb, Kristen L. Sund, Marion D. Teare, Yosra Bouyacoub, Khalid Abdulhadi, Stavit A. Shalev, Trevor J. Pemberton, Nicholas J. Schork, Diego Vozzi, Mariem Ben Rekaya, Mohamed-Ridha Barbouche, Anne-Louise Leutenegger, Simona Ferrari, Graeme C.M. Black, Khalid Yunis, Noah A. Rosenberg, Nizar Ben Halim, Paolo Giorgi Rossi, Faten Ben Rhouma, Meimanat Hosseini-Chavoshi, Ramin Badii, Majdi Nagara, Steven Gazal, Habib Messai, Martina C. Cornel, Rym Kefi, Liliana Uribe-Bruce, Laura H. Goetz, Moza Khalifa Alkowari, Danjuma Quarless, Watfa Al-Mamari, Zafar Iqbal, Hussein A. Abbas, Emmanuelle Génin, Roberto Giugliani, Crystel Bonnet, Lilia Romdhane, Rachel L. Gillespie, M. Mazharul Islam, Olfa Messaoud, Ondrej Libiger, Tatiana Boa Sorte, Lidewij Henneman, Angelina Xavier Acosta, Said A. Al-Yahyaee, Sandra Leistner-Segal, Kiyoko Abe-Sandes, Giovanni Romeo, Druckerei Stückle, Hans van Bokhoven, Thais Bomfim, Catherine Rehder, Alan H. Bittles, Zied Riahi, Fabiana Moura Costa-Motta, Satz Mengensatzproduktion, Khalid Al-Thihli, Tommaso Pippucci, Andrea Finocchi, Waleed Al-Herz, Elizabeth C. Goyder, Danniel da Silva, Valentina Di Pierro, Marieke E. Teeuw, Leo P. ten Kate, Ken McElreavey, Hervé Perdry, Ibrahim M. Gosadi, Caterina Cancrini, Massimo Mezzavilla, Sonia Abdelhak, Alberto Magi, Joël Zlotogora, Paolo Gasparini, Dragana Vuckovic, Giorgia Girotto, Anu Bashamboo, Giulia Angelino, Roberta Zuntini, Fathiya Al-Murshedi, Sébastien Letort, Alan Bittles, Peter C. Corry
Publikováno v:
Human Heredity. 77
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d54ea3e527a0f5c3a922963301a052f
https://doi.org/10.1159/000363357
https://doi.org/10.1159/000363357