IFIH1 loss of function predisposes to inflammatory and SARS‐CoV‐2‐related infectious diseases by Najm, Rania, Yavuz, Lemis, Jain, Ruchi, El Naofal, Maha, Ramaswamy, Sathishkumar, Abuhammour, Walid, Loney, Tom, Nowotny, Norbert, Alsheikh‐Ali, Alawi, Abou Tayoun, Ahmad, Kandasamy, Richard K.

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Genetic determinants of severe COVID-19 in young Asian and Middle Eastern patients: a case series by Badla, Beshr Abdulaziz, Hanifa, Mohamed Samer, Jain, Ruchi, Naofal, Maha El, Halabi, Nour, Yaslam, Sawsan, Ramaswamy, Sathishkumar, Taylor, Alan, Alfalasi, Roudha, Shenbagam, Shruti, Khansaheb, Hamda, Al Suwaidi, Hanan, Nowotny, Norbert, Popatia, Rizwana, Al Khayat, Abdulla, Alsheikh-Ali, Alawi, Loney, Tom, AlDabal, Laila Mohamed, Abou Tayoun, Ahmad

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Heterozygous gain of function variants in a critical region of RNF13 cause congenital microcephaly, epileptic encephalopathy, blindness, and failure to thrive by Taylor, Alan, Kashyape, Pawan S., Jain, Ruchi, El Naofal, Maha, Tayoun, Ahmad Abou

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P456: Genetic testing and screening for spinal muscular atrophy in the Middle East by El Naofal, Maha, Tayoun, Ahmad Abou

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Middle Eastern Genetic Variation Improves Clinical Annotation of the Human Genome by Ramaswamy, Sathishkumar, Jain, Ruchi, El Naofal, Maha, Halabi, Nour, Yaslam, Sawsan, Taylor, Alan, Tayoun, Ahmad Abou

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Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populations by Halabi, Nour, Ramaswamy, Sathishkumar, El Naofal, Maha, Taylor, Alan, Yaslam, Sawsan, Jain, Ruchi, Alfalasi, Roudha, Shenbagam, Shruti, Bitzan, Martin, Yavuz, Lemis, Abulhoul, Hamda, Shankar, Shiva, Janjua, Dalwinder, Jadhav, Devendrasing, Al Maazmi, Munira Mahmoud, Abuhammour, Walid, Alsheikh-Ali, Alawi, Al Awadhi, Mohamed, Al Khayat, Abdulla, Abou Tayoun, Ahmad N

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Spinal muscular atrophy genetic epidemiology and the case for premarital genomic screening in Arab populations by Rabea, Fatma, El Naofal, Maha, Chekroun, Ikram, Khalaf, Mona, Zaabi, Nuha Al, AlZaabi, Khawla, ElHalik, Mahmoud, Dash, Swarup, El Saba, Yaser, Ali, Azhari, Abraham, Smitha, Fathi, Khansa, Shekhy, Jwan, Aswad, Saad G., Elbashir, Haitham, Alkuraya, Fowzan, Loney, Tom, Alsheikh-Ali, Alawi, Khayat, Abdulla Al, Abou Tayoun, Ahmad

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Utility of clinical exome sequencing in a complex Emirati pediatric cohort by Mahfouz, Nour Abu, Kizhakkedath, Praseetha, Ibrahim, Alia, El Naofal, Maha, Ramaswamy, Sathishkumar, Harilal, Divinlal, Qutub, Yasmeen, Uddin, Mohammed, Taylor, Alan, Alloub, Zeinab, AlBanna, Ammar, Abuhammour, Walid, Fathalla, Basil, Tayoun, Ahmad Abou

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Genetic and Clinical Characteristics of Patients in the Middle East With Multisystem Inflammatory Syndrome in Children by Abuhammour, Walid, Yavuz, Lemis, Jain, Ruchi, Abu Hammour, Khawla, Al-Hammouri, Ghalia F, El Naofal, Maha, Halabi, Nour, Yaslam, Sawsan, Ramaswamy, Sathishkumar, Taylor, Alan, Wafadari, Deena, Alsarhan, Ali, Khansaheb, Hamda, Deesi, Zulfa Omar, Varghese, Rupa Murthy, Uddin, Mohammed, Al Suwaidi, Hanan, Al-Hammadi, Suleiman, Alkhaja, Abdulmajeed, AlDabal, Laila Mohamed, Loney, Tom, Nowotny, Norbert, Al Khayat, Abdulla, Alsheikh-Ali, Alawi, Abou Tayoun, Ahmad

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Virtual Gene Panels Have a Superior Diagnostic Yield for Inherited Rare Diseases Relative to Static Panels by Sheikh Hassani, Massomeh, Jain, Ruchi, Ramaswamy, Sathishkumar, Sinha, Shruti, El Naofal, Maha, Halabi, Nour, Alyafei, Sawsan, Alfalasi, Roudha, Shenbagam, Shruti, Taylor, Alan, Abou Tayoun, Ahmad

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The genomic landscape of rare disorders in the Middle East by El Naofal, Maha, Ramaswamy, Sathishkumar, Alsarhan, Ali, Nugud, Ahmed, Sarfraz, Fatima, Janbaz, Hiba, Taylor, Alan, Jain, Ruchi, Halabi, Nour, Yaslam, Sawsan, Alfalasi, Roudha, Shenbagam, Shruti, Rabea, Fatma, Bitzan, Martin, Yavuz, Lemis, Wafadari, Deena, Abulhoul, Hamda, Shankar, Shiva, Al Maazmi, Munira, Rizk, Ruba, Alloub, Zeinab, Elbashir, Haitham, Babiker, Mohamed O E, Chencheri, Nidheesh, AlBanna, Ammar, Sultan, Meshal, El Bitar, Mohamed, Kherani, Safeena, Thalange, Nandu, Alshryda, Sattar, Di Donato, Roberto, Tzivinikos, Christos, Majid, Ibrar, Freeman, Alexandra F, Gonzalez, Corina, Khan, Arif O, Hamdan, Hisham, Abuhammour, Walid, AlAwadhi, Mohamed, AlKhayat, Abdulla, Alsheikh-Ali, Alawi, Abou Tayoun, Ahmad N

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Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populations by Halabi, Nour, Ramaswamy, Sathishkumar, El Naofal, Maha, Taylor, Alan, Yaslam, Sawsan, Jain, Ruchi, Alfalasi, Roudha, Shenbagam, Shruti, Bitzan, Martin, Yavuz, Lemis, Abulhoul, Hamda, Shankar, Shiva, Janjua, Dalwinder, Jadhav, Devendrasing, Al Maazmi, Munira Mahmoud, Abuhammour, Walid, Alsheikh-Ali, Alawi, Al Awadhi, Mohamed, Al Khayat, Abdulla, Abou Tayoun, Ahmad N

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