BRCA1 -specific machine learning model predicts variant pathogenicity with high accuracy von Khandakji, Mohannad, Habish, Hind Hassan Ahmed, Abdulla, Nawal Bakheet Salem, Kusasi, Sitti Apsa Albani, Abdou, Nema Mahmoud Ghobashy, Al-Mulla, Hajer Mahmoud M A, Al Sulaiman, Reem Jawad A A, Bu Jassoum, Salha M, Mifsud, Borbala

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Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in DCAF17: Report of 58 additional patients from Qatar and literature review von Ali, Rehab, Al‐Dewik, Nader, Mohammed, Shayma, Elfituri, Mahmud, Agouba, Sahar, Musa, Sara, Mahmoud, Laila, Almulla, Mariam, El‐Akouri, Karen, Mohd, Howaida, Bux, Reem, Almulla, Hajer, Othman, Amna, Al‐Mesaifri, Fatma, Shahbeck, Noora, Al‐Muriekhi, Mariam, Khalifa, Amal, Al‐Sulaiman, Reem, Ben‐Omran, Tawfeg

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A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families von Al‐Sulaiman, Reem, Othman, Amna, El‐Akouri, Karen, Fareed, Shehab, AlMulla, Hajer, Sukik, Aseel, Al‐Mureikhi, Mariam, Shahbeck, Noora, Ali, Rehab, Al‐Mesaifri, Fatma, Musa, Sara, Al‐Mulla, Mariam, Ibrahim, Khalid, Mohamed, Khalid, Al‐Nesef, Maryam Ali, Ehlayel, Mohammad, Ben‐Omran, Tawfeg

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Clinical genetics and genomic medicine in Qatar von Al‐Dewik, Nader, Al‐Mureikhi, Mariam, Shahbeck, Noora, Ali, Rehab, Al‐Mesaifri, Fatma, Mahmoud, Laila, Othman, Amna, AlMulla, Mariam, Sulaiman, Reem Al, Musa, Sara, Abdoh, Ghassan, El‐Akouri, Karen, Solomon, Benjamin D., Ben‐Omran, Tawfeg

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Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience von Al‐Dewik, Nader, Mohd, Howaida, Al‐Mureikhi, Mariam, Ali, Rehab, Al‐Mesaifri, Fatma, Mahmoud, Laila, Shahbeck, Noora, El‐Akouri, Karen, Almulla, Mariam, Al Sulaiman, Reem, Musa, Sara, Al‐Marri, Ajayeb Al‐Nabet, Richard, Gabriele, Juusola, Jane, Solomon, Benjamin D., Alkuraya, Fowzan S., Ben‐Omran, Tawfeg

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Congenital Methemoglobinemia: First Confirmed Case in the Arab Population with a Novel Variant in the CYB5R Gene in the State of Qatar: A Case Report von Al-Abdulmalek, Abdulrahman, Al-Sulaiman, Reem, Abu-Tineh, Mohammad, Yassin, Mohamed A

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Pancytopenia And Limbic Encephalopathy Complicating Immunotherapy For Clear Cell Endometrial Cancer With Microsatellite Instability-High (MSI-H) von Kanbour, Aladdin, Rasul, Kakil Ibrahim, Bujassoum Albader, Salha, Al Sulaiman, Reem Jawad, Melikyan, Gayan, Farghaly, Hanan, Lengyel, Zsolt, Al Rimawi, Yousef, Soliman, Dina, Omar, Nabil Elhadi

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Li-Fraumeni Syndrome: The Two Faces of a Coin in Myeloid Malignancies von Sidenna, Mariem, Al Sulaiman, Reem, Ben-Omran, Tawfeg, Bujassoum, Salha, Gameil, Amna

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Clinical and Molecular Characterization of Qatari Patients with Inherited Dysfibrinogenemia von Gameil, Amna, Al-Mulla, Hajer, Amer, Aliaa, Ben-Omran, Tawfeg, Yassin, Mohamed A, Al-Sulaiman, Reem

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Exploring the effectiveness of crisis counseling and psychoeducation in relation to improving mental well-being, quality of life and treatment compliance of breast cancer patients... von Al-Sulaiman, Reem Jawad, Bener, Abdulbari, Doodson, Lisa, Bujassoum Al Bader, Salha, Ghuloum, Suhaila, Lemaux, Alain, Bugrein, Hekmat, Alassam, Reena, Karim, Aisha

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Prevalence and Genotype-Phenotype Correlation of Lynch Syndrome in a Selected High-Risk Cohort from Qatar's Population von Sidenna, Mariem, Khodjet-El-Khil, Houssein, Al Mulla, Hajar, Al-Shafai, Mashael, Habish, Hind Hassan, Al-Sulaiman, Reem, Al-Bader, Salha Bujassoum

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A founderRAB27Avariant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families von Al-Sulaiman, Reem, Othman, Amna, El-Akouri, Karen, Fareed, Shehab, AlMulla, Hajer, Sukik, Aseel, Al-Mureikhi, Mariam, Shahbeck, Noora, Ali, Rehab, Al-Mesaifri, Fatma, Musa, Sara, Al-Mulla, Mariam, Ibrahim, Khalid, Mohamed, Khalid, Al-Nesef, Maryam Ali, Ehlayel, Mohammad, Ben-Omran, Tawfeg

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Qatar’s genetic counseling landscape: Current insights and future prospects von Abiib, Sumaya, Khodjet-El-khil, Houssein, El-Akouri, Karen, Bux, Reem Ibrahim, Rezoug, Zoulikha, Abualainin, Wafa, Alkowari, Moza, Musa, Sara Osman, Al Mulla, Mariam, Al Saleh, Rehab, Shahbeck, Noora, Farag, Maria, Ismail, Said I., Al Sulaiman, Reem, Ben-Omran, Tawfeg, Al-Thani, Asma, Al-Shafai, Mashael

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QATAR’S EXPERIENCE WITH HEREDITARY BREAST AND OVARIAN CANCER AND HIGH RISK CLINIC: A RETROSPECTIVE STUDY 2013-2016 von Bujassoum, Salha Mohammed, Bugrein, HekmetAbubaker, Al-Sulaiman, Reem Jawad, Ghazouani, Hafedh

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Congenital Methemoglobinemia: First Confirmed Case in the Arab Population with a Novel Variant in the CYB5R Gene in the State of Qatar: A Case Report von Al-Abdulmalek, Abdulrahman, Al-Sulaiman, Reem, Abu-Tineh, Mohammad, Yassin, Mohamed A

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BRCA1-specific machine learning model predicts variant pathogenicity with high accuracy - Supplementary material von Khandakji, Mohannad, Habish, Hind Hassan Ahmed, Abdulla, Nawal Bakheet Salem, Kusasi, Sitti Apsa Albani, Abdou, Nema Mahmoud Ghobashy, Al-Mulla, Hajer Mahmoud, Al Sulaiman, Reem Jawad, Bu Jassoum, Salha, Mifsud, Borbala

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Advances in Enzyme and Ionic Liquid Immobilization for Enhanced in MOFs for Biodiesel Production von Shomal, Reem, Ogubadejo, Babatunde, Shittu, Toyin, Mahmoud, Eyas, Du, Wei, Al-Zuhair, Sulaiman

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Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus von Alkuraya, Fowzan S, Al-Mayouf, Sulaiman M, Sunker, Asma, Abdwani, Reem, Abrawi, Safiya Al, Almurshedi, Fathiya, Alhashmi, Nadia, Al Sonbul, Abdullah, Sewairi, Wafaa, Qari, Aliya, Abdallah, Eiman, Al-Owain, Mohammed, Al Motywee, Saleh, Al-Rayes, Hanan, Hashem, Mais, Khalak, Hanif, Al-Jebali, Latifa

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Statins and Risk of Thrombosis in Critically ill Patients with COVID-19: A Multicenter Cohort Study von Al Harbi, Shmeylan, Kensara, Raed, Aljuhani, Ohoud, Korayem, Ghazwa B., Altebainawi, Ali F., Al Harthi, Abdullah, Vishwakarma, Ramesh, Alenazi, Alaa M., Almutairi, Abdulmajed, Alshaya, Omar, Alraddadi, Sultan, Al Sulaiman, Tareq, Aldakkan, Latifah, Mahboob, Reem, Alaamer, Kholoud, Alissa, Abdulrahman, Hafiz, Awatif, Aldhayyan, Nada, Althewaibi, Sara, Alenezi, Farhan, Alkhotani, Nadeen Y., Alghamdi, Sara A., Alenazi, Abeer A., Al Sulaiman, Khalid

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Cumulative Damage in Juvenile Idiopathic Arthritis: A Multicenter Study From the Pediatric Rheumatology Arab Group von Al‐Mayouf, Sulaiman M., Hashad, Soad, Khawaja, Khulood, Alrasheedi, Abeer, Abdwani, Reem, Abushhaiwia, Awatif, AlSuwaiti, Muatasem, Alzyoud, Raed, AL Abrawi, Safiya, Asiri, Abdulrahman, Alshaikh, Manal, Sharif, Elsadeg, Muzaffer, Mohammed, Alsewairi, Wafa, Zlenti, Mabruka, Kawaja, Ebtisam, Almutairi, Muna, Majeed, Mahmoud, Lotfy, Hala, AlMarri, Munira, Almutairi, Nora

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