Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tasnim, Fadl"'
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
Publikováno v:
Otologyneurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 41(2)
Hearing loss (HL) is a heterogeneous condition that causes partial or complete hearing impairment. Hundreds of variants in more than 60 genes have been reported to be associated with Hereditary HL (HHL). The HHL prevalence is thought to be high in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e5ca8e83f506487d723b054595435580
https://pubmed.ncbi.nlm.nih.gov/31860473
https://pubmed.ncbi.nlm.nih.gov/31860473
Background: Colorectal cancer (CRC) is the third most common cancer worldwide and the third leading cause of cancer-related death. It is a heterogeneous disease that develops through different genetic and epigenetic mechanisms. To date, no comprehens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7052dbc22fde6774eac77112713f6525
https://hdl.handle.net/10576/12133
https://hdl.handle.net/10576/12133