Characterization of a loss-of-function NSF attachment protein beta mutation in monozygotic triplets affected with epilepsy and autism using cortical neurons from proband-derived an... von Ali, Gowher, Shin, Kyung Chul, Habbab, Wesal, Alkhadairi, Ghaneya, AbdelAleem, Alice, AlShaban, Fouad A, Park, Yongsoo, Stanton, Lawrence W

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Effects of COVID-19 on Autism Spectrum Disorder in Qatar von Alshaban, Fouad A, Ghazal, Iman, Al-Harahsheh, Sanaa T, Lotfy, Mustafa, Al-Shammari, Hawraa, Al-Faraj, Fatema, Thompson, I Richard, Ratto, Allison B, Nasir, Assal, Tolefat, Mohamed

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Consanguinity as a Risk Factor for Autism von Alshaban, Fouad A., Aldosari, Mohammad, Ghazal, Iman, Al-Shammari, Hawraa, ElHag, Saba, Thompson, I. Richard, Bruder, Jennifer, Shaath, Hibah, Al-Faraj, Fatema, Tolefat, Mohamed, Nasir, Assal, Fombonne, Eric

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Validation of the Arabic version of the Social Communication Questionnaire von Aldosari, Mohammed, Fombonne, Eric, Aldhalaan, Hesham, Ouda, Mohammed, Elhag, Saba, Alshammari, Hawraa, Ghazal, Iman, Alsaleh, Asma, Alqadoumi, Tala, Thomson, Richard, Al Khasawneh, Mohanad, Tolefat, Mohamed, Alshaban, Fouad

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Prevalence and correlates of autism spectrum disorder in Qatar: a national study von Alshaban, Fouad, Aldosari, Mohammed, Al‐Shammari, Hawraa, El‐Hag, Saba, Ghazal, Iman, Tolefat, Mohamed, Ali, Mogahed, Kamal, Madeeha, Abdel Aati, Nazim, Abeidah, Mahmoud, Saad, Ahmad Hassan, Dekair, Lobna, Al Khasawneh, Mohanad, Ramsay, Katrina, Fombonne, Eric

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Identification of two novel autism genes, TRPC4 and SCFD2, in Qatar simplex families through exome sequencing von Gupta, Vijay, Ben-Mahmoud, Afif, Ku, Bonsu, Velayutham, Dinesh, Jan, Zainab, Yousef Aden, Abdi, Kubbar, Ahmad, Alshaban, Fouad, Stanton, Lawrence W., Jithesh, Puthen Veettil, Layman, Lawrence C., Kim, Hyung-Goo

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The genetic landscape of autism spectrum disorder in the Middle Eastern population von Al-Sarraj, Yasser, Taha, Rowaida Z, Al-Dous, Eman, Ahram, Dina, Abbasi, Somayyeh, Abuazab, Eman, Shaath, Hibah, Habbab, Wesal, Errafii, Khaoula, Bejaoui, Yosra, AlMotawa, Maryam, Khattab, Namat, Aqel, Yasmin Abu, Shalaby, Karim E, Al-Ansari, Amina, Kambouris, Marios, Abouzohri, Adel, Ghazal, Iman, Tolfat, Mohammed, Alshaban, Fouad, El-Shanti, Hatem, Albagha, Omar M E

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Genome Sequencing Identifies 13 Novel Candidate Risk Genes for Autism Spectrum Disorder in a Qatari Cohort von Ben-Mahmoud, Afif, Gupta, Vijay, Abdelaleem, Alice, Thompson, Richard, Aden, Abdi, Mbarek, Hamdi, Saad, Chadi, Tolefat, Mohamed, Alshaban, Fouad, Stanton, Lawrence W, Kim, Hyung-Goo

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Prevalence of Autism Spectrum Disorders in Qatar: A National Epidemiological Survey von Kamal, Madeeha, Alshaban, Fouad, Fombonne, Eric, AlShammari, Hawraa, El-Hag, Saba, Ghazal, Iman, Tolefat, Mohamed, Ali, Mogahed, AbdelAati, Nazim, Abeidah, Mahmoud, Saad, Ahmed, Dekair, Lobna, Alkhasawneh, Mohanad, Ramsey, Katrina

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Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families von Al-Sarraj, Yasser, Al-Dous, Eman, Taha, Rowaida Z., Ahram, Dina, Alshaban, Fouad, Tolfat, Mohammed, El-Shanti, Hatem, Albagha, Omar M. E.

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Autism spectrum disorder in Qatar: Profiles and correlates of a large clinical sample von Alshaban, Fouad, Aldosari, Mohammed, El Sayed, Zakaria, Tolefat, Mohammed, El Hag, Saba, Al Shammari, Hawra, Ghazal, Iman, Fombonne, Eric

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Prevalence of Autism Spectrum Disorders in Qatar von Alshaban, Fouad

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Characterization of a loss-of-function NAPB mutation in monozygotic triplets affected with epilepsy and autism using cortical neurons from proband-derived and CRISPR-corrected iPSC... von Ali, Gowher, Shin, Kyung Chul, Habbab, Wesal, Alkhadairi, Ghaneya, AbdelAleem, Alice, Alshaban, Fouad, Park, Yongsoo, Stanton, Lawrence

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Characterization of a loss-offunction NSF attachment protein beta mutation in monozygotic triplets affected with epilepsy and autism using cortical neurons from proband-derived and... von Ali, Gowher, Shin, Kyung Chul, Habbab, Wesal, Alkhadairi, Ghaneya, AbdelAleem, Alice, Alshaban, Fouad, Park, Yongsoo, Stanton, Lawrence

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