Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Lilia, Romdhane"'
Autor:
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hajer Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, CRYSTEL Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/d1f20ca9f1e041b5805610de30e16616
Autor:
Lilia Romdhane, Sameh Kefi, Nessrine Mezzi, Najla Abassi, Haifa Jmel, Safa Romdhane, Jingxuan Shan, Lotfi Chouchane, Sonia Abdelhak
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-17 (2024)
Abstract Admixture mapping has been useful in identifying genetic variations linked to phenotypes, adaptation and diseases. Copy number variations (CNVs) represents genomic structural variants spanning large regions of chromosomes reaching several me
Externí odkaz:
https://doaj.org/article/74ddedd6d9b74cfca46ce714398b9c4f
Autor:
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hager Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, Crystel Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Hearing impairment (HI) is a prevalent neurosensory condition globally, impacting 5% of the population, with over 50% of congenital cases attributed to genetic etiologies. In Tunisia, HI underdiagnosis prevails, primarily due to limited access to com
Externí odkaz:
https://doaj.org/article/d53f3da42b5b4e8f9503ec02796dd375
Autor:
Lilia Romdhane, Nessrine Mezzi, Hamza Dallali, Olfa Messaoud, Jingxuan Shan, Khalid A. Fakhro, Rym Kefi, Lotfi Chouchane, Sonia Abdelhak
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-18 (2021)
Abstract Copy number variation (CNV) is considered as the most frequent type of structural variation in the human genome. Some CNVs can act on human phenotype diversity, encompassing rare Mendelian diseases and genomic disorders. The North African po
Externí odkaz:
https://doaj.org/article/399d7564503448b8a9d14b264646b319
Autor:
Yosr Hamdi, Mariem Ben Rekaya, Shan Jingxuan, Majdi Nagara, Olfa Messaoud, Amel Benammar Elgaaied, Ridha Mrad, Lotfi Chouchane, Mohamed Samir Boubaker, Sonia Abdelhak, Hamouda Boussen, Lilia Romdhane
Publikováno v:
BMC Cancer, Vol 18, Iss 1, Pp 1-14 (2018)
Abstract Background Breast cancer is the most common cancer in women worldwide. Around 50% of breast cancer familial risk has been so far explained by known susceptibility alleles with variable levels of risk and prevalence. The vast majority of thes
Externí odkaz:
https://doaj.org/article/0957321ba9cb490d8d06cf0d499519af
Autor:
Maroua Boujemaa, Yosr Hamdi, Nesrine Mejri, Lilia Romdhane, Kais Ghedira, Hanen Bouaziz, Houda El Benna, Soumaya Labidi, Hamza Dallali, Olfa Jaidane, Sonia Ben Nasr, Abderrazek Haddaoui, Khaled Rahal, Sonia Abdelhak, Hamouda Boussen, Mohamed Samir Boubaker
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0245362 (2021)
Hereditary breast cancer accounts for 5-10% of all breast cancer cases. So far, known genetic risk factors account for only 50% of the breast cancer genetic component and almost a quarter of hereditary cases are carriers of pathogenic mutations in BR
Externí odkaz:
https://doaj.org/article/def6bd33a2214e8aa81a2ffd6005199f
Autor:
Abir Ben Haj Ali, Ahlem Amouri, Marwa Sayeb, Saloua Makni, Wajih Hammami, Chokri Naouali, Hamza Dallali, Lilia Romdhane, Anu Bashamboo, Kenneth McElreavey, Sonia Abdelhak, Olfa Messaoud
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Abstract Background Several studies have shown a high rate of consanguinity and endogamy in North African populations. As a result, the frequency of autosomal recessive diseases is relatively high in the region with the co‐occurrence of two or more
Externí odkaz:
https://doaj.org/article/ba14324bf6dd468b87e9e7ef456fff63
Autor:
Haifa Jmel, Lilia Romdhane, Yosra Ben Halima, Meriem Hechmi, Chokri Naouali, Hamza Dallali, Yosr Hamdi, Jingxuan Shan, Abdelmajid Abid, Henda Jamoussi, Sameh Trabelsi, Lotfi Chouchane, Donata Luiselli, Sonia Abdelhak, Rym Kefi
Publikováno v:
PLoS ONE, Vol 13, Iss 4, p e0194842 (2018)
Genetic variation is an important determinant affecting either drug response or susceptibility to adverse drug reactions. Several studies have highlighted the importance of ethnicity in influencing drug response variability that should be considered
Externí odkaz:
https://doaj.org/article/750c463436b44044b9ff16d1f5bbd813
Publikováno v:
Journal of Water, Sanitation and Hygiene for Development. 10:1019-1025
Sewage sludge is considered as a main product obtained from urban liquid effluents that are discharged into sanitation systems of wastewater treatment plants. The aim of this work was to reuse it as compost, after the dehydration process, to replace
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2a4d3fb73ce9d788d0f0869d702b508
https://doi.org/10.2166/washdev.2020.082
https://doi.org/10.2166/washdev.2020.082
Autor:
Melek Chaouch, Kais Ghedira, Judit Kumuthini, Yosr Hamdi, Jorge da Rocha, Alia Benkahla, Lilia Romdhane, Nicola Mulder, Sumir Panji, Maryame Azzouzi, Haifa Jmel, Sonia Abdelhak, Fouzia Radouani, Reem M. Sallam, Collen Masimirembwa, Samah Ahmed, Chaimae Samtal, Houcemeddine Othman, Phumlani Masilela, Rym Kefi, Ayoub Ksouri, Faisal M. Fadlelmola, Ichrak Benamri, Samar K. Kassim, Lyndon Zass, Rania Sibira, Balkiss Bouhaouala-Zahar
Publikováno v:
Personalized medicine
Effective interventions and treatments for complex diseases have been implemented globally, however, coverage in Africa has been comparatively lower due to lack of capacity, clinical applicability and knowledge on the genetic contribution to disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::993423de3e07b91a3c2d1ab14ddc38b5
http://europepmc.org/articles/PMC8093600
http://europepmc.org/articles/PMC8093600