The Influence of Knowledge Management Uses on Total Quality Management Practices in Commercial Banks of Jordan von Obeidat, Bader, Hashem, Lama, Masa’deh, Ra’ed

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The Effect of Knowledge Management Uses on Total Quality Management Practices: A Theoretical Perspective von Obeidat, Bader Yousef, Hashem, Lama, Alansari, Iman, Tarhini, Ali, Al-Salti, Zahran

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Finite-state abstractions on Arabic morphology von Narayanan, Ajit, Hashem, Lama

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Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes von Abu-Safieh, Leen, Alrashed, May, Anazi, Shamsa, Alkuraya, Hisham, Khan, Arif O, Al-Owain, Mohammed, Al-Zahrani, Jawahir, Al-Abdi, Lama, Hashem, Mais, Al-Tarimi, Salwa, Sebai, Mohammed-Adeeb, Shamia, Ahmed, Ray-Zack, Mohamed D, Nassan, Malik, Al-Hassnan, Zuhair N, Rahbeeni, Zuhair, Waheeb, Saad, Alkharashi, Abdullah, Abboud, Emad, Al-Hazzaa, Selwa A F, Alkuraya, Fowzan S

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Clinical utility of polygenic scores for cardiometabolic disease in Arabs von Shim, Injeong, Kuwahara, Hiroyuki, Chen, NingNing, Hashem, Mais O., AlAbdi, Lama, Abouelhoda, Mohamed, Won, Hong-Hee, Natarajan, Pradeep, Ellinor, Patrick T., Khera, Amit V., Gao, Xin, Alkuraya, Fowzan S., Fahed, Akl C.

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In search of triallelism in Bardet-Biedl syndrome von ABU-SAFIEH, Leen, AL-ANAZI, Shamsa, AL-SALEM, Ahmad, ALRASHED, May, FAQEIH, Eissa, SOFTAH, Ameen, AL-HASHEM, Amal, WALI, Sami, RAHBEENI, Zuhair, ALSAYED, Moeen, KHAN, Arif O, AL-GAZALI, Lihadh, AL-ABDI, Lama, TASCHNER, Peter Em, AL-HAZZAA, Selwa, ALKURAYA, Fowzan S, HASHEM, Mais, ALKURAYA, Hisham, ALAMR, Mushari, SIRELKHATIM, Mugtaba O, AL-HASSNAN, Zuhair, ALKURAYA, Basim, MOHAMED, Jawahir Y

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Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families von AlAbdi, Lama, Maddirevula, Sateesh, Shamseldin, Hanan E., Khouj, Ebtissal, Helaby, Rana, Hamid, Halima, Almulhim, Aisha, Hashem, Mais O., Abdulwahab, Firdous, Abouyousef, Omar, Alqahtani, Mashael, Altuwaijri, Norah, Jaafar, Amal, Alshidi, Tarfa, Alzahrani, Fatema, Alkuraya, Fowzan S.

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Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases von AlAbdi, Lama, Shamseldin, Hanan E, Khouj, Ebtissal, Helaby, Rana, Aljamal, Bayan, Alqahtani, Mashael, Almulhim, Aisha, Hamid, Halima, Hashem, Mais O, Abdulwahab, Firdous, Abouyousef, Omar, Jaafar, Amal, Alshidi, Tarfa, Al-Owain, Mohammed, Alhashem, Amal, Al Tala, Saeed, Khan, Arif O, Mardawi, Elham, Alkuraya, Hisham, Faqeih, Eissa, Afqi, Manal, Alkhalifi, Salwa, Rahbeeni, Zuhair, Hagos, Samya T, Al-Ahmadi, Wijdan, Nadeef, Seba, Maddirevula, Sateesh, Khabar, Khalid S A, Putra, Alexander, Angelov, Angel, Park, Changsook, Reyes-Ramos, Ana M, Umer, Husen, Ullah, Ikram, Driguez, Patrick, Fukasawa, Yoshinori, Cheung, Ming Sin, Gallouzi, Imed Eddine, Alkuraya, Fowzan S

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Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders von Ortigoza‐Escobar, Juan Darío, Zamani, Mina, Dorison, Nathalie, Sadeghian, Saeid, Azizimalamiri, Reza, Alvi, Javeria Raza, Sultan, Tipu, Galehdari, Hamid, Shariati, Gholamreza, Saberi, Alihossein, Leeuwen, Lisette, Zifarelli, Giovanni, Bauer, Peter, d'Hardemare, Vincent, Doummar, Diane, Roze, Emmanuel, Travaglini, Lorena, Nicita, Francesco, Ojea Ponce, Núria, Zahraei, Seyed Mohammadsaleh, Alabdi, Lama, Tamim, Abdullah, Hashem, Mais O., Ababneh, Faroug, Morrow, Michelle M, Curry, Cynthia, Tam, Allison, Ruedy, Jessica, Bhambhani, Vikas, Veith, Regan, Strømme, Petter, Efthymiou, Stephanie, Alkuraya, Fowzan S, Moreno‐De‐Luca, Andres, Burglen, Lydie, Houlden, Henry, Maroofian, Reza

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Lethal variants in humans: lessons learned from a large molecular autopsy cohort von Shamseldin, Hanan E, AlAbdi, Lama, Maddirevula, Sateesh, Alsaif, Hessa S, Alzahrani, Fatema, Ewida, Nour, Hashem, Mais, Abdulwahab, Firdous, Abuyousef, Omar, Kuwahara, Hiroyuki, Gao, Xin, Alkuraya, Fowzan S

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The Perception of Spectacles Use Among the General Population in Ha’il Region, Saudi Arabia: A Cross-Sectional Study von Alrashidi, Nawaf Osaywid, Albrak, Wafy Abdulrahman, Alreshidi, Shaker Osaywid, Alaradi, Lama Abdulrahman, Adam, Hatim Adam Nagi, Alali, Naif Mamdouh, Hashem, Faris, Albalawi, Hani Basher, Alothman, Ahmed Yousef, Alharbi, Shaima Sulaiman

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Abstract 15842: Interplay of Genomic and Conventional Risk for Cardiometabolic Disease in Saudi Arabia von Shim, Injeong, Kuwahara, Hiroyuki, Chen, NingNing, Hashem, Mais, AlAbdi, Lama, Gao, Xin, AbouElHoda, Mohamed, Won, Hong-Hee, Natarajan, Pradeep, Ellinor, Patrick T, Khera, Amit V, Alkuraya, Fowzan S, FAHED, AKL C

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Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update von Maddirevula, Sateesh, Shamseldin, Hanan E, Sirr, Amy, AlAbdi, Lama, Lo, Russell S, Ewida, Nour, Al-Qahtani, Mashael, Hashem, Mais, Abdulwahab, Firdous, Aboyousef, Omar, Kaya, Namik, Monies, Dorota, Salem, May H, Al Harbi, Naffaa, Aldhalaan, Hesham M, Alzaidan, Hamad, Almanea, Hadeel M, Alsalamah, Abrar K, Al Mutairi, Fuad, Ismail, Samira, Abdel-Salam, Ghada M H, Alhashem, Amal, Asery, Ali, Faqeih, Eissa, AlQassmi, Amal, Al-Hamoudi, Waleed, Algoufi, Talal, Shagrani, Mohammad, Dudley, Aimée M, Alkuraya, Fowzan S

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Mutation of IGFBP7 Causes Upregulation of BRAF/MEK/ERK Pathway and Familial Retinal Arterial Macroaneurysms von Abu-Safieh, Leen, Abboud, Emad B., Alkuraya, Hisham, Shamseldin, Hanan, Al-Enzi, Shamsa, Al-Abdi, Lama, Hashem, Mais, Colak, Dilek, Jarallah, Abdullah, Ahmad, Hala, Bobis, Steve, Nemer, Georges, Bitar, Fadi, Alkuraya, Fowzan S.

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Genetic testing results of children suspected to have Stickler syndrome type collagenopathy after ocular examination von Khan, Arif O., AlAbdi, Lama, Patel, Nisha, Helaby, Rana, Hashem, Mais, Abdulwahab, Firdous, AlBadr, Fahad B., Alkuraya, Fowzan S.

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Arab founder variants: Contributions to clinical genomics and precision medicine von AlAbdi, Lama, Maddirevula, Sateesh, Aljamal, Bayan, Hamid, Halima, Almulhim, Aisha, Hashem, Mais O, Algoos, Yusra, Alqahtani, Mashael, Albaloshi, Shahad, Alghamdi, Mohammed, Alduaylij, Mohammed, Shamseldin, Hanan E, Nadeef, Seba, Patel, Nisha, Abdulwahab, Firdous, Abouyousef, Omar, Alshidi, Tarfa, Jaafar, Amal, Abouelhoda, Mohamed, Alhazzani, Adel, Alfares, Ahmed, Qudair, Ahmad, Alsulaiman, Ahood, Alhashem, Amal, Khan, Arif O, Chedrawi, Aziza, Alebdi, Basel, AlAjlan, Fahad, Alotaibi, Fawaz, Alzaidan, Hamad, Banjar, Hanaa, Abdelraouf, Hanem, Alkuraya, Hisham, Abumansour, Iman, Alfayez, Khowlah, Tulbah, Maha, Alowain, Mohammed, Alqahtani, Mohammed, El-Kalioby, Mohammed, Shboul, Mohammad, Sulaiman, Raashda, Al Tala, Saed, Khan, Sameena, Coskun, Serdar, Mrouge, Sobaihi, Alenazi, Walaa, Rahbeeni, Zuhair, Alkuraya, Fowzan S

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Additional file 1 of Lethal variants in humans: lessons learned from a large molecular autopsy cohort von Shamseldin, Hanan E., AlAbdi, Lama, Maddirevula, Sateesh, Alsaif, Hessa S., Alzahrani, Fatema, Ewida, Nour, Hashem, Mais, Abdulwahab, Firdous, Abuyousef, Omar, Kuwahara, Hiroyuki, Gao, Xin, Alkuraya, Fowzan S.

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Additional file 3 of Lethal variants in humans: lessons learned from a large molecular autopsy cohort von Shamseldin, Hanan E., AlAbdi, Lama, Maddirevula, Sateesh, Alsaif, Hessa S., Alzahrani, Fatema, Ewida, Nour, Hashem, Mais, Abdulwahab, Firdous, Abuyousef, Omar, Kuwahara, Hiroyuki, Gao, Xin, Alkuraya, Fowzan S.

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