Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Yasser Al Sarraj"'
Autor:
Yasser Al-Sarraj, Rowaida Z. Taha, Eman Al-Dous, Dina Ahram, Somayyeh Abbasi, Eman Abuazab, Hibah Shaath, Wesal Habbab, Khaoula Errafii, Yosra Bejaoui, Maryam AlMotawa, Namat Khattab, Yasmin Abu Aqel, Karim E. Shalaby, Amina Al-Ansari, Marios Kambouris, Adel Abouzohri, Iman Ghazal, Mohammed Tolfat, Fouad Alshaban, Hatem El-Shanti, Omar M. E. Albagha
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction: Autism spectrum disorder (ASD) is characterized by aberrations in social interaction and communication associated with repetitive behaviors and interests, with strong clinical heterogeneity. Genetic factors play an important role in ASD
Externí odkaz:
https://doaj.org/article/1cb66fb1f0d64cfb9ab254e423381745
Autor:
Nagham Nafiz Hendi, Yasser Al-Sarraj, Umm-Kulthum Ismail Umlai, Karsten Suhre, Georges Nemer, Omar Albagha
Publikováno v:
Frontiers in Nutrition, Vol 10 (2023)
IntroductionEpidemiological studies have consistently revealed that Vitamin D deficiency is most prevalent in Middle Eastern countries. However, research on the impact of genetic loci and polygenic models related to Vitamin D has primarily focused on
Externí odkaz:
https://doaj.org/article/7eb0b8d3245a4f279c6fed73df3b3fef
Autor:
Juan L. Rodriguez-Flores, Radja Messai-Badji, Amal Robay, Ramzi Temanni, Najeeb Syed, Monika Markovic, Eiman Al-khayat, Fatima Qafoud, Zafar Nawaz, Ramin Badii, Yasser Al-Sarraj, Hamdi Mbarek, Wadha Al-Muftah, Muhammad Alvi, Mahboubeh R. Rostami, Juan Carlos Martinez Cruzado, Jason G. Mezey, Alya Al Shakaki, Joel A. Malek, Matthew B. Greenblatt, Khalid A. Fakhro, Khaled Machaca, Ajayeb Al-Nabet, Nahla Afifi, Andrew Brooks, Said I. Ismail, Asmaa Althani, Ronald G. Crystal
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-21 (2022)
Abstract Risk genes for Mendelian (single-gene) disorders (SGDs) are consistent across populations, but pathogenic risk variants that cause SGDs are typically population-private. The goal was to develop “QChip1,” an inexpensive genotyping microar
Externí odkaz:
https://doaj.org/article/37726560b48d41ea9a863392829c265f
Autor:
Salman M. Toor, Eman K. Aldous, Aijaz Parray, Naveed Akhtar, Yasser Al-Sarraj, Essam M. Abdelalim, Abdelilah Arredouani, Omar El-Agnaf, Paul J. Thornalley, Sajitha V. Pananchikkal, Ghulam Jeelani Pir, Raheem Ayadathil Thazhhe Kuni, Ashfaq Shuaib, Nehad M. Alajez, Omar M. E. Albagha
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Stroke is the second leading cause of global mortality and continued efforts aim to identify predictive, diagnostic, or prognostic biomarkers to reduce the disease burden. Circulating microRNAs (miRNAs) have emerged as potential biomarkers in stroke.
Externí odkaz:
https://doaj.org/article/14182f8bb886419da0388089a89ec258
Autor:
Ilhame Diboun, Yasser Al-Sarraj, Salman M. Toor, Shaban Mohammed, Nadeem Qureshi, Moza S. H. Al Hail, Amin Jayyousi, Jassim Al Suwaidi, Omar M. E. Albagha
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Familial hypercholesterolemia (FH) is an inherited disease characterized by reduced efficiency of low-density lipoprotein-cholesterol (LDL-C) removal from the blood and, consequently, an increased risk of life-threatening early cardiovascular complic
Externí odkaz:
https://doaj.org/article/24e107776a2c4f2a8e333ab37ad49833
Autor:
Gaurav Thareja, Yasser Al-Sarraj, Aziz Belkadi, Maryam Almotawa, The Qatar Genome Program Research (QGPR) Consortium, Karsten Suhre, Omar M. E. Albagha
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
The genetic basis for traits can vary between populations. Here the authors report a genome wide association study with 45 clinically-relevant traits in individuals from Qatar, replicating many known loci and identifying new Qatari-predominant signal
Externí odkaz:
https://doaj.org/article/550716d2d177482ca7de149aa5671de9
Autor:
Fatiha M. Benslimane, Hebah A. Al Khatib, Ola Al-Jamal, Dana Albatesh, Sonia Boughattas, Ayeda A Ahmed, Meryem Bensaad, Shameem Younuskunju, Yasmin A. Mohamoud, Mashael Al Badr, Abdalla A. Mohamed, Reham A. El-Kahlout, Tasneem Al-Hamad, Dina Elgakhlab, Fatima H. Al-Kuwari, Chadi Saad, Andrew Jeremijenko, Abdullatif Al-Khal, Muna A. Al-Maslamani, Roberto Bertollini, Einas A. Al-Kuwari, Hamad E. Al-Romaihi, Salih Al-Marri, Mohammed Al-Thani, Radja M. Badji, Hamdi Mbarek, Yasser Al-Sarraj, Joel A. Malek, Said I. Ismail, Laith J. Abu-Raddad, Peter V. Coyle, Asmaa A. Al Thani, Hadi M. Yassine
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 11 (2021)
Qatar, a country with a strong health system and a diverse population consisting mainly of expatriate residents, has experienced two large waves of COVID-19 outbreak. In this study, we report on 2634 SARS-CoV-2 whole-genome sequences from infected pa
Externí odkaz:
https://doaj.org/article/9bc184c8503742488eed928ed0480af6
Autor:
Hamdi, Mbarek, Geethanjali, Devadoss Gandhi, Senthil, Selvaraj, Wadha, Al-Muftah, Radja, Badji, Yasser, Al-Sarraj, Chadi, Saad, Dima, Darwish, Muhammad, Alvi, Tasnim, Fadl, Heba, Yasin, Fatima, Alkuwari, Rozaimi, Razali, Waleed, Aamer, Fatemeh, Abbaszadeh, Ikhlak, Ahmed, Younes, Mokrab, Karsten, Suhre, Omar, Albagha, Khalid, Fakhro, Ramin, Badii, Said I, Ismail, Asma, Althani
Publikováno v:
Human mutationREFERENCES. 43(4)
Despite recent biomedical breakthroughs and large genomic studies growing momentum, the Middle Eastern population, home to over 400 million people, is underrepresented in the human genome variation databases. Here we describe insights from Phase 1 of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f7cfb01e5d209e148487863e48da967
https://pubmed.ncbi.nlm.nih.gov/35112413
https://pubmed.ncbi.nlm.nih.gov/35112413
Autor:
Clemence Lepelletier, Yasser Al-Sarraj, Christine Bodemer, Hibbah Shaath, Sylvie Fraitag, Marios Kambouris, Dominique Hamel-Teillac, Hatem El Shanti, Smail Hadj-Rabia
Publikováno v:
Acta Dermato-Venereologica, Vol 97, Iss 7, Pp 858-859 (2017)
Externí odkaz:
https://doaj.org/article/4b71ecc8f615404ba58ee0189cc84c36
Autor:
Salman M. Toor, Eman K. Aldous, Aijaz Parray, Naveed Akhtar, Yasser Al-Sarraj, Essam M. Abdelalim, Abdelilah Arredouani, Omar El-Agnaf, Paul J. Thornalley, Sajitha V. Pananchikkal, Ghulam Jeelani Pir, Raheem Ayadathil, Ashfaq Shuaib, Nehad M. Alajez, Omar M. E. Albagha
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 1; Pages: 108
Transient ischemic attack (TIA) refers to a momentary neurologic deficit caused by focal cerebral, spinal or retinal ischemic insult. TIA is associated with a high risk of impending acute ischemic stroke (AIS), a neurologic dysfunction characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a73cfeb2872f189e13639ba5193c559c
https://doi.org/10.3390/ijms24010108
https://doi.org/10.3390/ijms24010108