Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ajayeb Al-Nabet"'
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:
Sarah L O'Beirne, Jacqueline Salit, Juan L Rodriguez-Flores, Michelle R Staudt, Charbel Abi Khalil, Khalid A Fakhro, Amal Robay, Monica D Ramstetter, Joel A Malek, Mahmoud Zirie, Amin Jayyousi, Ramin Badii, Ajayeb Al-Nabet Al-Marri, Abdulbari Bener, Mai Mahmoud, Maria J Chiuchiolo, Alya Al-Shakaki, Omar Chidiac, Dora Stadler, Jason G Mezey, Ronald G Crystal
Publikováno v:
PLoS ONE, Vol 13, Iss 9, p e0199837 (2018)
BACKGROUND:Type 2 diabetes (T2D) susceptibility is influenced by genetic and lifestyle factors. To date, the majority of genetic studies of T2D have been in populations of European and Asian descent. The focus of this study is on genetic variations u
Externí odkaz:
https://doaj.org/article/3bc29196bf8746a88fb56c0bfb23126d
Autor:
Sarah L O'Beirne, Jacqueline Salit, Juan L Rodriguez-Flores, Michelle R Staudt, Charbel Abi Khalil, Khalid A Fakhro, Amal Robay, Monica D Ramstetter, Iman K Al-Azwani, Joel A Malek, Mahmoud Zirie, Amin Jayyousi, Ramin Badii, Ajayeb Al-Nabet Al-Marri, Maria J Chiuchiolo, Alya Al-Shakaki, Omar Chidiac, Maey Gharbiah, Abdulbari Bener, Dora Stadler, Neil R Hackett, Jason G Mezey, Ronald G Crystal
Publikováno v:
PLoS ONE, Vol 11, Iss 7, p e0156834 (2016)
The prevalence of type 2 diabetes (T2D) is increasing in the Middle East. However, the genetic risk factors for T2D in the Middle Eastern populations are not known, as the majority of studies of genetic risk for T2D are in Europeans and Asians.All su
Externí odkaz:
https://doaj.org/article/23fe42e26a404d9889315c23e2c9f95d
Autor:
Sarah L O'Beirne, Jacqueline Salit, Juan L Rodriguez-Flores, Michelle R Staudt, Charbel Abi Khalil, Khalid A Fakhro, Amal Robay, Monica D Ramstetter, Iman K Al-Azwani, Joel A Malek, Mahmoud Zirie, Amin Jayyousi, Ramin Badii, Ajayeb Al-Nabet Al-Marri, Maria J Chiuchiolo, Alya Al-Shakaki, Omar Chidiac, Maey Gharbiah, Abdulbari Bener, Dora Stadler, Neil R Hackett, Jason G Mezey, Ronald G Crystal
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0161910 (2016)
[This corrects the article DOI: 10.1371/journal.pone.0156834.].
Externí odkaz:
https://doaj.org/article/83b5fcc2d5ee4b2380283a0d191ee0c8
Autor:
Fakhro, Khalid A., Staudt, Michelle R., Ramstetter, Monica Denise, Robay, Amal, Malek, Joel A., Badii, Ramin, Al-Marri, Ajayeb Al-Nabet, Khalil, Charbel Abi, Al-Shakaki, Alya, Chidiac, Omar, Stadler, Dora, Zirie, Mahmoud, Jayyousi, Amin, Salit, Jacqueline, Mezey, Jason G., Crystal, Ronald G., Rodriguez-Flores, Juan L.
Publikováno v:
Hum Genome Var. 2016 Jun 30;3:16016
Reaching the full potential of precision medicine depends on the quality of personalized genome interpretation. In order to facilitate precision medicine in regions of the Middle East and North Africa (MENA), a population-specific reference genome fo
Externí odkaz:
http://arxiv.org/abs/1805.03233
Autor:
Howaida Mohd, Karen El-Akouri, Reem Al Sulaiman, Nader Al-Dewik, Benjamin D. Solomon, Mariam Al-Mulla, Sara Musa, Mariam Almureikhi, Noora Shahbeck, Laila Mahmoud, Ajayeb Al-Nabet Al-Marri, Jane Juusola, Rehab Ali, Gabriele Richard, Fatma Al-Mesaifri, Fowzan S. Alkuraya, Tawfeg Ben-Omran
Publikováno v:
American Journal of Medical Genetics. Part a
Background Clinical exome sequencing (CES) is rapidly becoming the diagnostic test of choice in patients with suspected Mendelian diseases especially those that are heterogeneous in etiology and clinical presentation. Reporting large CES series can i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96e9ab39993688f0e70006c728ab496b
https://doi.org/10.1002/ajmg.a.61126
https://doi.org/10.1002/ajmg.a.61126
Autor:
Jacqueline Salit, Khalid A. Fakhro, Juan L. Rodriguez-Flores, Joel A. Malek, Omar Chidiac, Amin Jayyousi, Ronald G. Crystal, Amal Robay, Michelle R. Staudt, Alya Al-Shakaki, Ajayeb Al-Nabet Al-Marri, Dora J. Stadler, Jason G. Mezey, Mahmoud Zirie, Monica D. Ramstetter, Charbel Abi Khalil, Ramin Badii
Publikováno v:
Human Genome Variation
Reaching the full potential of precision medicine depends on the quality of personalized genome interpretation. In order to facilitate precision medicine in regions of the Middle East and North Africa (MENA), a population-specific reference genome fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6764e2b46d99affc57302006ce7f3e74
Akademický článek
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Autor:
Ajayeb Al-Nabet Al-Marri, Hüseyin Çaksen, Abdulbari Bener, Mamoun Elsheikh, Asma Althani, Mohammed Janahi
Publikováno v:
Journal of Pediatric Infectious Diseases. :041-045
Respiratory syncytial virus (RSV) is the major cause of acute lower respiratory tract infections in early childhood. Annual epidemics occur which are well documented in developed countries during winter months, placing considerable pressure on the pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa7768911cd1c3257ba0b70809e98001
https://doi.org/10.1055/s-0035-1556966
https://doi.org/10.1055/s-0035-1556966
Akademický článek
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