Search Results - Al Shakaki, Alya

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  1. 1
    Whole-exome sequencing identifies common and rare variant metabolic QTLs in a Middle Eastern population

    Whole-exome sequencing identifies common and rare variant metabolic QTLs in a Middle Eastern population by Yousri, Noha A., Fakhro, Khalid A., Robay, Amal, Rodriguez-Flores, Juan L., Mohney, Robert P., Zeriri, Hassina, Odeh, Tala, Kader, Sara Abdul, Aldous, Eman K., Thareja, Gaurav, Kumar, Manish, Al-Shakaki, Alya, Chidiac, Omar M., Mohamoud, Yasmin A., Mezey, Jason G., Malek, Joel A., Crystal, Ronald G., Suhre, Karsten

    Published in Nature communications
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  2. 2
    Point of Care Exome Sequencing Reveals Allelic and Phenotypic Heterogeneity Underlying Mendelian disease in Qatar

    Point of Care Exome Sequencing Reveals Allelic and Phenotypic Heterogeneity Underlying Mendelian disease in Qatar by Fakhro, Khalid A, Robay, Amal, Rodrigues-Flores, Juan L, Mezey, Jason G, Al-Shakaki, Alya A, Chidiac, Omar, Stadler, Dora, Malek, Joel A, Imam, Abu Bakr, Sheikh, Arwa, Azzam, Asmaa, Janahi, Ibrahim, Khanjar, Izzat, Osman, Kamal, Ziki, Maen Abu, Mahmah, Mohamed Adnan, Selim, Mohamed, Numeiri, Nuha, Ali, Rehab, Lakhani, Shenela, Butt, Fizza, Omran, Tawfeg Ben, Crystal, Ronald G

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  3. 3
    A Novel STK4 Mutation Impairs T Cell Immunity Through Dysregulation of Cytokine-Induced Adhesion and Chemotaxis Genes

    A Novel STK4 Mutation Impairs T Cell Immunity Through Dysregulation of Cytokine-Induced Adhesion and Chemotaxis Genes by Guennoun, Andrea, Bougarn, Salim, Khan, Taushif, Mackeh, Rafah, Rahman, Mahbuba, Al-Ali, Fatima, Ata, Manar, Aamer, Waleed, Prosser, Debra, Habib, Tanwir, Chin-Smith, Evonne, Al-Darwish, Khawla, Zhang, Qian, Al-Shakaki, Alya, Robay, Amal, Crystal, Ronald G., Fakhro, Khalid, Al-Naimi, Amal, Al Maslamani, Eman, Tuffaha, Amjad, Janahi, Ibrahim, Janahi, Mohammad, Love, Donald R., Karim, Mohammed Yousuf, Lo, Bernice, Hassan, Amel, Adeli, Mehdi, Marr, Nico

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  4. 4
    Predicted deleterious variants in the human genome relevant to gene therapy with adeno-associated virus vectors

    Predicted deleterious variants in the human genome relevant to gene therapy with adeno-associated virus vectors by Rostami, Mahboubeh R., Leopold, Philip L., Vasquez, Jenifer M., de Mulder Rougvie, Miguel, Al Shakaki, Alya, Hssain, Ali Ait, Robay, Amal, Hackett, Neil R., Mezey, Jason G., Crystal, Ronald G.

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  5. 5
    Type 2 Diabetes Risk Allele Loci in the Qatari Population

    Type 2 Diabetes Risk Allele Loci in the Qatari Population by O'Beirne, Sarah L, Salit, Jacqueline, Rodriguez-Flores, Juan L, Staudt, Michelle R, Abi Khalil, Charbel, Fakhro, Khalid A, Robay, Amal, Ramstetter, Monica D, Al-Azwani, Iman K, Malek, Joel A, Zirie, Mahmoud, Jayyousi, Amin, Badii, Ramin, Al-Nabet Al-Marri, Ajayeb, Chiuchiolo, Maria J, Al-Shakaki, Alya, Chidiac, Omar, Gharbiah, Maey, Bener, Abdulbari, Stadler, Dora, Hackett, Neil R, Mezey, Jason G, Crystal, Ronald G

    Published in PloS one
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  6. 6
    Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population

    Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population by O'Beirne, Sarah L, Salit, Jacqueline, Rodriguez-Flores, Juan L, Staudt, Michelle R, Abi Khalil, Charbel, Fakhro, Khalid A, Robay, Amal, Ramstetter, Monica D, Malek, Joel A, Zirie, Mahmoud, Jayyousi, Amin, Badii, Ramin, Al-Nabet Al-Marri, Ajayeb, Bener, Abdulbari, Mahmoud, Mai, Chiuchiolo, Maria J, Al-Shakaki, Alya, Chidiac, Omar, Stadler, Dora, Mezey, Jason G, Crystal, Ronald G

    Published in PloS one
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  7. 7
    Novel MYO5B mutation in microvillous inclusion disease of Syrian ancestry

    Novel MYO5B mutation in microvillous inclusion disease of Syrian ancestry by Hassan, Kamal, Robay, Amal, Al-Maraghi, Aljazi, Nimeri, Nuha, Azzam, Asmaa Basheer, Al Shakaki, Alya, Hamid, Eman, Crystal, Ronald G, Fakhro, Khalid A

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  8. 8
    Correction: Type 2 Diabetes Risk Allele Loci in the Qatari Population

    Correction: Type 2 Diabetes Risk Allele Loci in the Qatari Population by O'Beirne, Sarah L, Salit, Jacqueline, Rodriguez-Flores, Juan L, Staudt, Michelle R, Abi Khalil, Charbel, Fakhro, Khalid A, Robay, Amal, Ramstetter, Monica D, Al-Azwani, Iman K, Malek, Joel A, Zirie, Mahmoud, Jayyousi, Amin, Badii, Ramin, Al-Nabet Al-Marri, Ajayeb, Chiuchiolo, Maria J, Al-Shakaki, Alya, Chidiac, Omar, Gharbiah, Maey, Bener, Abdulbari, Stadler, Dora, Hackett, Neil R, Mezey, Jason G, Crystal, Ronald G

    Published in PloS one
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  9. 9
    The Qatar genome: a population-specific tool for precision medicine in the Middle East

    The Qatar genome: a population-specific tool for precision medicine in the Middle East by 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

    Published in Human genome variation
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  10. 10
    Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotype

    Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotype by Fadda, Abeer, Butt, Fiza, Tomei, Sara, Deola, Sara, Lo, Bernice, Robay, Amal, Al-Shakaki, Alya, Al-Hajri, Noor, Crystal, Ronald, Kambouris, Marios, Wang, Ena, Marincola, Francesco M, Fakhro, Khalid A, Cugno, Chiara

    Published in BMC medical genetics
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  11. 11
    The Qatar Genome: A Population-Specific Tool for Precision Medicine in the Middle East

    The Qatar Genome: A Population-Specific Tool for Precision Medicine in the Middle East by Fakhro, Khalid A, Staudt, Michelle R, Ramstetter, Monica Denise, Robay, Amal, Malek, Joel A, Badii, Ramin, Ajayeb Al-Nabet Al-Marri, Charbel Abi Khalil, Al-Shakaki, Alya, Chidiac, Omar, Stadler, Dora, Zirie, Mahmoud, Amin Jayyousi, Salit, Jacqueline, Mezey, Jason G, Crystal, Ronald G, Rodriguez-Flores, Juan L

    Published in arXiv.org
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  12. 12
    Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population

    Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population by O'Beirne, Sarah L, Salit, Jacqueline, Rodriguez-Flores, Juan L, Staudt, Michelle R, Abi Khalil, Charbel, Fakhro, Khalid A, Robay, Amal, Ramstetter, Monica D, Malek, Joel A, Zirie, Mahmoud, Jayyousi, Amin, Badii, Ramin, Al-Nabet Al-Marri, Ajayeb, Bener, Abdulbari, Mahmoud, Mai, Chiuchiolo, Maria J, Al-Shakaki, Alya, Chidiac, Omar, Stadler, Dora, Mezey, Jason G, Crystal, Ronald G

    Published in PLoS ONE
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  13. 13
    Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population

    Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population by O'Beirne, Sarah L, Salit, Jacqueline, Rodriguez-Flores, Juan L, Staudt, Michelle R, Abi Khalil, Charbel, Fakhro, Khalid A, Robay, Amal, Ramstetter, Monica D, Malek, Joel A, Zirie, Mahmoud, Jayyousi, Amin, Badii, Ramin, Al-Nabet Al-Marri, Ajayeb, Bener, Abdulbari, Mahmoud, Mai, Chiuchiolo, Maria J, Al-Shakaki, Alya, Chidiac, Omar, Stadler, Dora, Mezey, Jason G, Crystal, Ronald G

    Published in PLoS ONE
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  14. 14
    Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotype

    Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotype by Fadda, Abeer, Butt, Fiza, Tomei, Sara, Deola, Sara, Lo, Bernice, Robay, Amal, Al-Shakaki, Alya, Al-Hajri, Noor, Crystal, Ronald, Kambouris, Marios, Wang, Ena, Marincola, Francesco M, Fakhro, Khalid A, Cugno, Chiara

    Published in BMC Medical Genetics
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  15. 15
    Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotype

    Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotype by Fadda, Abeer, Butt, Fiza, Tomei, Sara, Deola, Sara, Lo, Bernice, Robay, Amal, Al-Shakaki, Alya, Al-Hajri, Noor, Crystal, Ronald, Kambouris, Marios, Wang, Ena, Marincola, Francesco M, Fakhro, Khalid A, Cugno, Chiara

    Published in BMC Medical Genetics
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  16. 16
    Type 2 Diabetes Risk Allele Loci in the Qatari Population

    Type 2 Diabetes Risk Allele Loci in the Qatari Population by O'Beirne, Sarah L, Salit, Jacqueline, Rodriguez-Flores, Juan L, Staudt, Michelle R, Abi Khalil, Charbel, Fakhro, Khalid A, Robay, Amal, Ramstetter, Monica D, Al-Azwani, Iman K, Malek, Joel A, Zirie, Mahmoud, Jayyousi, Amin, Badii, Ramin, Al-Nabet Al-Marri, Ajayeb, Chiuchiolo, Maria J, Al-Shakaki, Alya, Chidiac, Omar, Gharbiah, Maey, Bener, Abdulbari, Stadler, Dora, Hackett, Neil R, Mezey, Jason G, Crystal, Ronald G

    Published in PLoS ONE
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  17. 17
    Type 2 Diabetes Risk Allele Loci in the Qatari Population

    Type 2 Diabetes Risk Allele Loci in the Qatari Population by O'Beirne, Sarah L, Salit, Jacqueline, Rodriguez-Flores, Juan L, Staudt, Michelle R, Abi Khalil, Charbel, Fakhro, Khalid A, Robay, Amal, Ramstetter, Monica D, Al-Azwani, Iman K, Malek, Joel A, Zirie, Mahmoud, Jayyousi, Amin, Badii, Ramin, Al-Nabet Al-Marri, Ajayeb, Chiuchiolo, Maria J, Al-Shakaki, Alya, Chidiac, Omar, Gharbiah, Maey, Bener, Abdulbari, Stadler, Dora, Hackett, Neil R, Mezey, Jason G, Crystal, Ronald G

    Published in PLoS ONE
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