Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East

por Romdhane, Lilia, Kefi, Rym, Azaiez, Hela, Halim, Nizar Ben, Dellagi, Koussay, Abdelhak, Sonia
Publicado 2012

Decoding the genetic relationship between Alzheimer’s disease and type 2 diabetes: potential risk variants and future direction for North Africa

por Boukhalfa, Wided, Jmel, Haifa, Kheriji, Nadia, Gouiza, Ismail, Dallali, Hamza, Hechmi, Mariem, Kefi, Rym
Publicado 2023

Case report: Exome sequencing revealed disease-causing variants in a patient with spondylospinal thoracic dysostosis

por Bouchoucha, Sami, Chikhaoui, Asma, Najjar, Dorra, Zayoud, Khouloud, Zouari, Mohamed, Nessib, Mohamed Nabil, Kéfi, Rym, Yacoub-Youssef, Houda
Publicado 2023

A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa

por Romdhane, Lilia, Mezzi, Nessrine, Dallali, Hamza, Messaoud, Olfa, Shan, Jingxuan, Fakhro, Khalid A., Kefi, Rym, Chouchane, Lotfi, Abdelhak, Sonia
Publicado 2021

Adult gaucher disease in southern Tunisia: report of three cases

por Ben Rhouma, Faten, Kallel, Faten, Kefi, Rym, Cherif, Wafa, Nagara, Majdi, Azaiez, Hela, Jedidi, Ines, Elloumi, Moez, Abdelhak, Sonia, Mseddi, Sondes
Publicado 2012

Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort

por Landoulsi, Zied, Benromdhan, Sawssan, Ben Djebara, Mouna, Damak, Mariem, Dallali, Hamza, Kefi, Rym, Abdelhak, Sonia, Gargouri-Berrechid, Amina, Mhiri, Chokri, Gouider, Riadh
Publicado 2017

The Role of Dietary Intake in Type 2 Diabetes Mellitus: Importance of Macro and Micronutrients in Glucose Homeostasis

por Kheriji, Nadia, Boukhalfa, Wided, Mahjoub, Faten, Hechmi, Meriem, Dakhlaoui, Thouraya, Mrad, Mehdi, Hadj Salah Bahlous, Afef, Ben Amor, Nadia, Jamoussi, Henda, Kefi, Rym
Publicado 2022

Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa

por 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
Publicado 2020

Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis

por Dallali, Hamza, Hechmi, Meriem, Morjane, Imane, Elouej, Sahar, Jmel, Haifa, Ben Halima, Yosra, Abid, Abdelmajid, Bahlous, Afef, Barakat, Abdelhamid, Jamoussi, Henda, Abdelhak, Sonia, Kefi, Rym
Publicado 2022

Gut microbiota profile and the influence of nutritional status on bacterial distribution in diabetic and healthy Tunisian subjects

por Fassatoui, Meriem, Saffarian, Azadeh, Mulet, Céline, Jamoussi, Henda, Gamoudi, Amel, Ben Halima, Yosra, Hechmi, Meriem, Abdelhak, Sonia, Abid, Abdelmajid, Sansonetti, Philippe J., Pedron, Thierry, Kefi, Rym
Publicado 2023

Multiallelic Rare Variants in BBS Genes Support an Oligogenic Ciliopathy in a Non-obese Juvenile-Onset Syndromic Diabetic Patient: A Case Report

por Dallali, Hamza, Kheriji, Nadia, Kammoun, Wafa, Mrad, Mehdi, Soltani, Manel, Trabelsi, Hajer, Hamdi, Walid, Bahlous, Afef, Ben Ahmed, Melika, Mahjoub, Faten, Jamoussi, Henda, Abdelhak, Sonia, Kefi, Rym
Publicado 2021

Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations

por Jmel, Haifa, Romdhane, Lilia, Ben Halima, Yosra, Hechmi, Meriem, Naouali, Chokri, Dallali, Hamza, Hamdi, Yosr, Shan, Jingxuan, Abid, Abdelmajid, Jamoussi, Henda, Trabelsi, Sameh, Chouchane, Lotfi, Luiselli, Donata, Abdelhak, Sonia, Kefi, Rym
Publicado 2018

Evidence for Association of the E23K Variant of KCNJ11 Gene with Type 2 Diabetes in Tunisian Population: Population-Based Study and Meta-Analysis

por Lasram, Khaled, Ben Halim, Nizar, Hsouna, Sana, Kefi, Rym, Arfa, Imen, Ghazouani, Welid, Jamoussi, Henda, Benrahma, Houda, Kharrat, Najla, Rebai, Ahmed, Ben Ammar, Slim, Bahri, Sonia, Barakat, Abdelhamid, Abid, Abdelmajid, Abdelhak, Sonia
Publicado 2014

Lactase persistence in Tunisia as a result of admixture with other Mediterranean populations

por Ben Halima, Yosra, Kefi, Rym, Sazzini, Marco, Giuliani, Cristina, De Fanti, Sara, Nouali, Chokri, Nagara, Majdi, Mengozzi, Giacomo, Elouej, Sahar, Abid, Abdelmajid, Jamoussi, Henda, Chouchane, Lotfi, Romeo, Giovanni, Abdelhak, Sonia, Luiselli, Donata
Publicado 2017

Gut microbiota imbalances in Tunisian participants with type 1 and type 2 diabetes mellitus

por Fassatoui, Meriem, Lopez-Siles, Mireia, Díaz-Rizzolo, Diana A., Jmel, Haifa, Naouali, Chokri, Abdessalem, Ghaith, Chikhaoui, Asma, Nadal, Belén, Jamoussi, Henda, Abid, Abdelmajid, Gomis, Ramon, Abdelhak, Sonia, Martinez-Medina, Margarita, Kefi, Rym
Publicado 2019

A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy

por 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
Publicado 2014

Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment

por Hechmi, Meriem, Charif, Majida, Kraoua, Ichraf, Fassatoui, Meriem, Dallali, Hamza, Desquiret-Dumas, Valerie, Bris, Céline, Goudenège, David, Drissi, Cyrine, Galaï, Saïd, Ouerhani, Slah, Procaccio, Vincent, Amati-Bonneau, Patrizia, Abdelhak, Sonia, Ben Youssef-Turki, Ilhem, Lenaers, Guy, Kefi, Rym
Publicado 2022

Prevalence and risk factors of diabetes mellitus and hypertension in North East Tunisia calling for efficient and effective actions

por Kheriji, Nadia, Dakhlaoui, Thouraya, Kamoun Rebai, Wafa, Maatoug, Sonia, Thabet, Mohamed Taher, Mellah, Thouraya, Mrad, Mehdi, Trabelsi, Hajer, Soltani, Manel, Kabbage, Maria, Hassine, Hichem Ben, Hadj Salah Bahlous, Afef, Mahjoub, Faten, Jamoussi, Henda, Abid, Abdelmajid, Abdelhak, Sonia, Kefi, Rym
Publicado 2023

Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness

por Riahi, Zied, Bonnet, Crystel, Zainine, Rim, Louha, Malek, Bouyacoub, Yosra, Laroussi, Nadia, Chargui, Mariem, Kefi, Rym, Jonard, Laurence, Dorboz, Imen, Hardelin, Jean-Pierre, Salah, Sihem Belhaj, Levilliers, Jacqueline, Weil, Dominique, McElreavey, Kenneth, Boespflug, Odile Tanguy, Besbes, Ghazi, Abdelhak, Sonia, Petit, Christine
Publicado 2014

High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis

por Amouri, Ahlem, Talmoudi, Faten, Messaoud, Olfa, d'Enghien, Catherine D, Rekaya, Mariem B, Allegui, Ines, Azaiez, Héla, Kefi, Rym, Abdelhak, Ahlem, Meseddi, Sondes H, Torjemane, Lamia, Ouederni, Monia, Mellouli, Fethi, Abid, Héla B, Aissaoui, Lamia, Bejaoui, Mohamed, Othmen, Tarek B, Lyonnet, Dominique S, Soulier, Jean, Hachicha, Mongia, Dellagi, Koussay, Abdelhak, Sonia, Fanconi, Tunisian
Publicado 2014