Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dima Darwish"'
Autor:
Rania Abdel‐latif, Radja Badji, Shaban Mohammed, Wadha Al‐Muftah, Hamdi Mbarek, Dima Darwish, Duha Assaf, Daoud Al‐Badriyeh, Hazem Elewa, Nahla Afifi, Naseer Ahmad Masoodi, Amr Salah Omar, Jassim Al Suwaidi, Salha Bujassoum, Moza Al Hail, Said I. Ismail, Asma Althani
Publikováno v:
Clinical and Translational Science, Vol 17, Iss 6, Pp n/a-n/a (2024)
Abstract Pharmacogenetic (PGx)‐informed medication prescription is a cutting‐edge genomic application in contemporary medicine, offering the potential to overcome the conventional “trial‐and‐error” approach in drug prescription. The abili
Externí odkaz:
https://doaj.org/article/e6b2cd6df26f43e889a40c80373d678b
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:
Mohamad Saad, Younes Mokrab, Najeeb Halabi, Jingxuan Shan, Rozaimi Razali, Khalid Kunji, Najeeb Syed, Ramzi Temanni, Murugan Subramanian, Michele Ceccarelli, Arash Rafii Tabrizi, Davide Bedognetti, Lotfi Chouchane, Said I Ismail, Wadha Al-Muftah, Radja Badji, Hamdi Mbarek, Dima Darwish, Tasnim Fadl, Heba Yasin, Maryem Ennaifar, Rania Abdellatif, Fatima Alkuwari, Muhammad Alvi, Yasser Al-Sarraj, Chadi Saad, Eleni Fethnou, Fatima Qafoud, Eiman Alkhayat, Nahla Afifi, Sara Tomei, Wei Liu, Stephan Lorenz, Hakeem Almabrazi, Fazulur R Vempalli, Tariq Abu Saqri, Mohammedhusen Khatib, Mehshad Hamza, Tariq Abu Zaid, Ahmed El Khouly, Tushar Pathare, Shafeeq Poolat, Rashid Al-Ali, Omar Albagha, Souhaila Al-Khodor, Mashael Alshafai, Ramin Badii, Xavier Estivill, Khalid Fakhro, Jithesh V Puthen, Karsten Suhre, Zohreh Tatari
Publikováno v:
The Lancet. Oncology. 23(3)
Background: Disparities in the genetic risk of cancer among various ancestry groups and populations remain poorly defined. This challenge is even more acute for Middle Eastern populations, where the paucity of genomic data could affect the clinical p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cbce6fdfc5ac4b7b3692e3302e11ded
https://pubmed.ncbi.nlm.nih.gov/35150602
https://pubmed.ncbi.nlm.nih.gov/35150602
Autor:
Dima Darwish, Tasnim Fadl, Waleed Aamer, Heba Yasin, Geethanjali Devadoss Gandhi, Yasser Al-Sarraj, Khalid A. Fakhro, Omar M. E. Albagha, Asma AlThani, Younes Mokrab, Wadha Al-Muftah, Senthil Selvaraj, Karsten Suhre, Said I. Ismail, Ikhlak Ahmed, Rozaimi Mohamad Razali, Muhammad Alvi, Fatima H. Al-Kuwari, Fatemeh Abbaszadeh, Hamdi Mbarek, Ramin Badii, Radja Badji, Chadi Saad
Despite recent biomedical breakthroughs and large genomic studies growing momentum, the Middle Eastern population, home to over 400 million people, is under-represented in the human genome variation databases. Here we describe insights from phase 1 o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99cf5d59ae85f4d62a62fc1ed7a4a1a0
https://doi.org/10.1101/2021.09.19.21263548
https://doi.org/10.1101/2021.09.19.21263548
Autor:
Dima Darwish, Waseem Hasan, Navaneethakrishnan Krishnamoorthy, Puthen Veettil Jithesh, Doua Abdelrahman, Moza Al-Kowari
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 6; Pages: 3369
Hereditary hearing loss (HHL) is a common genetic disorder accounting for at least 60% of pre-lingual deafness in children, of which 70% is inherited in an autosomal recessive pattern. The long tradition of consanguinity among the Qatari population h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dfb156caed153b00c109fbfa8f56146
https://doi.org/10.3390/ijms23063369
https://doi.org/10.3390/ijms23063369
Publikováno v:
Gastroenterology. 146:S-481
Background and aims: The presence of fibrosis on liver biopsy is a prognostic tool for management of liver disease. AST/PLT ratio index (APRI) has been shown to be a useful tool to non-invasively predict fibrosis. Hepatoportal pressure gradient (HPPG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b58fabf2862a144358bc36fa55914ce2
https://doi.org/10.1016/s0016-5085(14)61726-1
https://doi.org/10.1016/s0016-5085(14)61726-1