Genetic profiling of children with advanced cholestatic liver disease von Shagrani, M., Burkholder, J., Broering, D., Abouelhoda, M., Faquih, T., El‐Kalioby, M., Subhani, S.N., Goljan, E., Albar, R., Monies, D., Mazhar, N., AlAbdulaziz, B.S., Abdelrahman, K.A., Altassan, N., Alkuraya, F.S.

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Genetic investigation of 93 families with microphthalmia or posterior microphthalmos von Patel, N., Khan, A.O., Alsahli, S., Abdel‐Salam, G., Nowilaty, S.R., Mansour, A.M., Nabil, A., Al‐Owain, M., Sogati, S., Salih, M.A., Kamal, A.M., Alsharif, H., Alsaif, H.S., Alzahrani, S.S., Abdulwahab, F., Ibrahim, N., Hashem, M., Faquih, T., Shah, Z.A., Abouelhoda, M., Monies, D., Dasouki, M., Shaheen, R., Wakil, S.M., Aldahmesh, M.A., Alkuraya, F.S.

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Agreement of aptamer proteomics with standard methods for measuring venous thrombosis biomarkers von Faquih, T., Mook-Kanamori, D.O., Rosendaal, F.R., Baglin, T., Dijk, K.W. van, Hylckama, A. van

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Causes and consequences of the opioid epidemic in the Netherlands: a population-based cohort study von Bedene, A., Dorp, E.L.A. van, Faquih, T., Cannegieter, S.C., Mook-Kanamori, D.O., Niesters, M., Velzen, M. van, Gademan, M.G.J., Rosendaal, F.R., Bouvy, M.L., Dahan, A., Lijfering, W.M.

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Causes and consequences of the opioid epidemic in the Netherlands: a population-based cohort study von Bedene, A., Dorp, E.L.A. van, Faquih, T., Cannegieter, S.C., Mook-Kanamori, D.O., Niesters, M., Velzen, M. van, Gademan, M.G.J., Rosendaal, F.R., Bouvy, M.L., Dahan, A., Lijfering, W.M.

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A workflow for missing values imputation of untargeted metabolomics data von Faquih, T., Smeden, M. van, Luo, J., Cessie, S. le, Kastenmuller, G., Krumsiek, J., Noordam, R., Heemst, D. van, Rosendaal, F.R., Vlieg, A.V., Dijk, K.W. van, Mook-Kanamori, D.O.

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Type 2 diabetes partitioned polygenic scores associate with disease outcomes in 454,193 individuals across 13 cohorts von DiCorpo, D., LeClair, J., Cole, J.B., Sarnowski, C., Ahmadizar, F., Bielak, L.F., Blokstra, A., Bottinger, E.P., Chaker, L., Chen, Y.D.I., Chen, Y., Vries, P.S. de, Faquih, T., Ghanbari, M., Gudmundsdottir, V., Guo, X.Q., Hasbani, N.R., Ibi, D., Ikram, M.A., Kavousi, M., Leonard, H.L., Leong, A., Mercader, J.M., Morrison, A.C., Nadkarni, G.N., Nalls, M.A., Noordam, R., Preuss, M., Smith, J.A., Trompet, S., Vissink, P., Yao, J., Zhao, W., Boerwinkle, E., Goodarzi, M.O., Gudnason, V., Jukema, J.W., Kardia, S.L.R., Loos, R.J.F., Liu, C.T., Manning, A.K., Mook-Kanamori, D., Pankow, J.S., Picavet, H.S.J., Sattar, N., Simonsick, E.M., Verschuren, W.M.M., Dijk, K.W. van, Florez, J.C., Rotter, J.I., Meigs, J.B., Dupuis, J., Udler, M.S.

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Characterizing the morbid genome of ciliopathies von Shaheen, R, Szymanska, K, Basu, B, Patel, N, Ewida, N, Faqeih, E, Al Hashem, A, Derar, N, Alsharif, H, Aldahmesh, MA, Alazami, AM, Hashem, M, Ibrahim, N, Abdulwahab, FM, Sonbul, R, Alkuraya, H, Alnemer, M, Al Tala, S, Al-Husain, M, Morsy, H, Seidahmed, MZ, Meriki, N, Al-Owain, M, AlShahwan, S, Tabarki, B, Salih, MA, Faquih, T, El-Kalioby, M, Ueffing, M, Boldt, K, Logan, CV, Parry, DA, Al Tassan, N, Monies, D, Megarbane, A, Abouelhoda, M, Halees, A, Johnson, CA, Alkuraya, FS

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The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes von Monies, Dorota, Abouelhoda, Mohamed, AlSayed, Moeenaldeen, Alhassnan, Zuhair, Alotaibi, Maha, Al-Owain, Mohammed, Shah, Ayaz, Rahbeeni, Zuhair, Al-Muhaizea, Mohammad A., Alzaidan, Hamad I., Cupler, Edward, Bohlega, Saeed, Faqeih, Eissa, Faden, Maha, Alyounes, Banan, Jaroudi, Dyala, Goljan, Ewa, Elbardisy, Hadeel, Akilan, Asma, Albar, Renad, Aldhalaan, Hesham, Gulab, Shamshad, Chedrawi, Aziza, Al Saud, Bandar K, Kurdi, Wesam, Makhseed, Nawal, Alqasim, Tahani, El Khashab, Heba Y., Al-Mousa, Hamoud, Kanaan, Imaduddin, Algoufi, Talal, Alsaleem, Khalid, Basha, Talal A., Al-Murshedi, Fathiya, Al-Kindy, Adila, Al-Hajjar, Sami, Alyamani, Suad, Aldhekri, Hasan, Al-Mehaidib, Ali, Arnaout, Rand, Dabbagh, Omar, Shagrani, Mohammad, Broering, Dieter, Alqassmi, Amal, Almugbel, Maisoon, AlQuaiz, Mohammed, Alsaman, Abdulaziz, Al-Thihli, Khalid, Sulaiman, Raashda A., Al-Dekhail, Wajeeh, Alsaegh, Abeer, Bashiri, Fahad A., Qari, Alya, Alhomadi, Suzan, Alkuraya, Hisham, Alsebayel, Mohammed, Hamad, Muddathir H, Szonyi, Laszlo, Abaalkhail, Faisal, Al-Mayouf, Sulaiman M., Almojalli, Hamad, Alqadi, Khalid S., Elsiesy, Hussien, Shuaib, Taghreed M., Seidahmed, Mohammed Zain, Abosoudah, Ibraheem, Akleh, Hana, AlGhonaium, Abdulaziz, Alkharfy, Turki M., Al Mutairi, Fuad, Eyaid, Wafa, Alshanbary, Abdullah, Sheikh, Farrukh R., Alsohaibani, Fahad I., Al Tala, Saeed, Balkhy, Soher, Bassiouni, Randa, Alenizi, Ahmed S., Hussein, Maged H., Hassan, Saeed, Khalil, Mohamed, Tabarki, Brahim, Alshahwan, Saad, Oshi, Amira, Sabr, Yasser, Alsaadoun, Saad, Salih, Mustafa A., Mohamed, Sarar, Sultana, Habiba, Tamim, Abdullah, El-Haj, Moayad, Alshahrani, Saif, Bubshait, Dalal K., Alfadhel, Majid, Faquih, Tariq, El-Kalioby, Mohamed, Shah, Zeeshan, Moghrabi, Nabil, Meyer, Brian F., Alkuraya, Fowzan S.

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Characterizing the morbid genome of ciliopathies von Shaheen, Ranad, Szymanska, Katarzyna, Basu, Basudha, Patel, Nisha, Ewida, Nour, Faqeih, Eissa, Al Hashem, Amal, Derar, Nada, Alsharif, Hadeel, Aldahmesh, Mohammed A, Alazami, Anas M, Hashem, Mais, Ibrahim, Niema, Abdulwahab, Firdous M, Sonbul, Rawda, Alkuraya, Hisham, Alnemer, Maha, Al Tala, Saeed, Al-Husain, Muneera, Morsy, Heba, Seidahmed, Mohammed Zain, Meriki, Neama, Al-Owain, Mohammed, AlShahwan, Saad, Tabarki, Brahim, Salih, Mustafa A, Faquih, Tariq, El-Kalioby, Mohamed, Ueffing, Marius, Boldt, Karsten, Logan, Clare V, Parry, David A, Al Tassan, Nada, Monies, Dorota, Megarbane, Andre, Abouelhoda, Mohamed, Halees, Anason, Johnson, Colin A, Alkuraya, Fowzan S

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Navigating the Labyrinth: Chylothorax and Chylous Ascites Unveiled After Abdominal Surgery for an Exceptionally Rare Tumor von Umar, Anam, Faquih, Amber E, Bilal, Muhammad, Garner, Jeffery

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Normal range CAG repeat size variations in the HTT gene are associated with an adverse lipoprotein profile partially mediated by body mass index von Faquih, Tariq O, Aziz, N Ahmad, Gardiner, Sarah L, Li-Gao, Ruifang, de Mutsert, Renée, Milaneschi, Yuri, Trompet, Stella, Jukema, J Wouter, Rosendaal, Frits R, van Hylckama Vlieg, Astrid, van Dijk, Ko Willems, Mook-Kanamori, Dennis O

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0032 Metabolomic Profile of Excessive Daytime Sleepiness in the Hispanic Community Health Study/Study of Latinos von Faquih, Tariq, Yu, Bing, Kaplan, Robert, Isasi, Carmen, Redline, Susan, Sofer, Tamar, Wang, Heming

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A Novel Tool for Configurable Process Evolution and Service Derivation von Sbai, Hanae, El Faquih, Loubna, Fredj, Mounia

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Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases von Al-Mousa, Hamoud, MD, Abouelhoda, Mohamed, PhD, Monies, Dorota M., PhD, Al-Tassan, Nada, PhD, Al-Ghonaium, Abdulaziz, MD, Al-Saud, Bandar, MD, Al-Dhekri, Hasan, MD, Arnaout, Rand, MD, Al-Muhsen, Saleh, MD, Ades, Nazema, BN, Elshorbagi, Sahar, MD, Al Gazlan, Sulaiman, MD, Sheikh, Farrukh, MD, Dasouki, Majed, MD, El-Baik, Lina, BSc, Elamin, Tanzeil, MS, Jaber, Amal, BSc, Kheir, Omnia, BPharm, El-Kalioby, Mohamed, MS, Subhani, Shazia, MS, Al Idrissi, Eman, MD, Al-Zahrani, Mofareh, MD, Alhelale, Maryam, MD, Alnader, Noukha, BSc, Al-Otaibi, Afaf, BSc, Kattan, Rana, BSc, Al Abdelrahman, Khalid, BSc, Al Breacan, Muna M., BSc, Bin Humaid, Faisal S., BSc, Wakil, Salma Majid, PhD, Alzayer, Fadi, BSc, Al-Dusery, Haya, BSc, Faquih, Tariq, MS, Al-Hissi, Safa, BSc, Meyer, Brian F., PhD, Hawwari, Abbas, PhD

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Multi-omics in research: epidemiology, methodology, and advanced data analysis von Faquih, T.O.

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When Pain Relief Turns Perilous: Uncovering the Hidden Dangers and Advanced Management of Benzocaine-Induced Methemoglobinemia von Umar, Anam, Bilal, Muhammad, Jawed, Bilal, Faquih, Amber E

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Complex Neurological Sequelae: Axonal Guillain-Barré Syndrome Post COVID-19 in a Young Patient von Umar, Anam, Faquih, Amber E, Jawed, Bilal, Bilal, Muhammad

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Perceptions of Healthcare Providers and Caregivers Regarding Procedures for Early Detection of Developmental Delays in Infants and Toddlers in Saudi Arabia von Gmmash, Afnan Sohail, Faquih, Nada Osama

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Revisiting the morbid genome of Mendelian disorders von Abouelhoda, Mohamed, Faquih, Tariq, El-Kalioby, Mohamed, Alkuraya, Fowzan S

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