Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype von Altassan, Ruqaiah, Saud, Haya Al, Masoodi, Tariq Ahmad, Dosssari, Haya Al, Khalifa, Ola, Al‐Zaidan, Hamad, Sakati, Nadia, Rhabeeni, Zuhair, Al‐Hassnan, Zuhair, Binamer, Yousef, Alhashemi, Nadia, Wade, William, Al‐Zayed, Zayed, Al‐Sayed, Moeen, Al‐Muhaizea, Mohamed A., Meyer, Brian, Al‐Owain, Mohammad, Wakil, Salma M.

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Automated SARS-COV-2 RNA extraction from patient nasopharyngeal samples using a modified DNA extraction kit for high throughput testing von Al-Saud, Haya, Al-Romaih, Khaldoun, Bakheet, Razan, Mahmoud, Lina, Al-Harbi, Najla, Alshareef, Ibtihaj, Judia, Sara Bin, Aharbi, Layla, Alzayed, Abdulaziz, Jabaan, Amjad, Alhadrami, Hani, Albarrag, Ahmed, Azhar, Essam I, Al-Mozaini, Maha Ahmad

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Favipiravir Effectiveness and Safety in Hospitalized Moderate-Severe COVID-19 Patients: Observational Prospective Multicenter Investigation in Saudi Arabia von Al-Muhsen, Saleh, Al-Numair, Nouf S, Saheb Sharif-Askari, Narjes, Basamh, Roaa, Alyounes, Banan, Jabaan, Amjad, Saheb Sharif-Askari, Fatemeh, Alosaimi, Mohammed F, Alsohime, Fahad, Halwani, Rabih, Al-Saud, Haya

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Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population von Alsmadi, Osama, Al-Rubeaan, Khalid, Mohamed, Gamal, Alkayal, Fadi, Al-Saud, Haya, Al-Saud, Nouran Abu, Al-Daghri, Nasser, Mohammad, Shahinaz, Meyer, Brian F

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Genetic Study of Saudi Diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes von Alsmadi, Osama, Al-Rubeaan, Khalid, Wakil, Salma M., Imtiaz, Faiqa, Mohamed, Gamal, Al-Saud, Haya, Al-Saud, Nouran Abu, Aldaghri, Nasser, Mohammad, Shahinaz, Meyer, Brian F

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Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia von Alsmadi, Osama, Al-Ghonaium, Abdulaziz, Al-Muhsen, Saleh, Arnaout, Rand, Al-Dhekri, Hasan, Al-Saud, Bandar, Al-Kayal, Fadi, Al-Saud, Haya, Al-Mousa, Hamoud

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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 von Zhang, Qian, Bastard, Paul, Liu, Zhiyong, Le Pen, Jérémie, Moncada-Velez, Marcela, Chen, Jie, Ogishi, Masato, Sabli, Ira K D, Hodeib, Stephanie, Korol, Cecilia, Rosain, Jérémie, Bilguvar, Kaya, Ye, Junqiang, Bolze, Alexandre, Bigio, Benedetta, Yang, Rui, Arias, Andrés Augusto, Zhou, Qinhua, Zhang, Yu, Onodi, Fanny, Korniotis, Sarantis, Karpf, Léa, Philippot, Quentin, Chbihi, Marwa, Bonnet-Madin, Lucie, Dorgham, Karim, Smith, Nikaïa, Schneider, William M, Razooky, Brandon S, Hoffmann, Hans-Heinrich, Michailidis, Eleftherios, Moens, Leen, Han, Ji Eun, Lorenzo, Lazaro, Bizien, Lucy, Meade, Philip, Neehus, Anna-Lena, Ugurbil, Aileen Camille, Corneau, Aurélien, Kerner, Gaspard, Zhang, Peng, Rapaport, Franck, Seeleuthner, Yoann, Manry, Jeremy, Masson, Cecile, Schmitt, Yohann, Schlüter, Agatha, Le Voyer, Tom, Khan, Taushif, Li, Juan, Fellay, Jacques, Roussel, Lucie, Shahrooei, Mohammad, Alosaimi, Mohammed F, Mansouri, Davood, Al-Saud, Haya, Al-Mulla, Fahd, Almourfi, Feras, Al-Muhsen, Saleh Zaid, Alsohime, Fahad, Al Turki, Saeed, Hasanato, Rana, van de Beek, Diederik, Biondi, Andrea, Bettini, Laura Rachele, D'Angio', Mariella, Bonfanti, Paolo, Imberti, Luisa, Sottini, Alessandra, Paghera, Simone, Quiros-Roldan, Eugenia, Rossi, Camillo, Oler, Andrew J, Tompkins, Miranda F, Alba, Camille, Vandernoot, Isabelle, Goffard, Jean-Christophe, Smits, Guillaume, Migeotte, Isabelle, Haerynck, Filomeen, Soler-Palacin, Pere, Martin-Nalda, Andrea, Colobran, Roger, Morange, Pierre-Emmanuel, Keles, Sevgi, Çölkesen, Fatma, Ozcelik, Tayfun, Yasar, Kadriye Kart, Senoglu, Sevtap, Karabela, Şemsi Nur, Rodríguez-Gallego, Carlos, Novelli, Giuseppe, Hraiech, Sami, Tandjaoui-Lambiotte, Yacine, Duval, Xavier, Laouénan, Cédric, Snow, Andrew L, Dalgard, Clifton L, Milner, Joshua D, Vinh, Donald C

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Haplotypes Encompassing the KIAA0391 and PSMA6 Gene Cluster Confer a Genetic Link for Myocardial Infarction and Coronary Artery Disease von Alsmadi, Osama, Muiya, Paul, Khalak, Hanif, Al‐Saud, Haya, Meyer, Brian F., Al‐Mohanna, Futwan, Alshahid, Maie, Dzimiri, Nduna

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Global Healthspan Summit 2023: closing the gap between healthspan and lifespan von Khan, Mehmood, Al Saud, Haya, Sierra, Felipe, Perez, Viviana, Greene, William, Al Asiry, Salman, Pathai, Sophia, Torres, Michael

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Clinical characteristics, risk factors, and rate of severity of a nationwide COVID-19 Saudi cohort von Al-Numair, Nouf S., Alyounes, Banan, Al-Saud, Haya, Halwani, Rabih, Al-Muhsen, Saleh

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Design of Arab Diabetes Gene-Centric Array (ADGCA) in population with an epidemic of Type 2 Diabetes: A population specific SNP evaluation von Al-Rubeaan, Khalid, Musambil, Mohthash, Wakil, Salma Majid, Al-Saud, Haya, Saeb, Amr T.M., Al-Qasim, Sara, Al-Naqeb, Dhekra

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Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases

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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 von Zhang, Qian, Bastard, Paul, Liu, Zhiyong, Le Pen, Jeremie, Moncada-Velez, Marcela, Chen, Jie, Ogishi, Masato, Sabli, Ira K.D, Hodeib, Stephanie, Korol, Cecilia, Rosain, Jeremie, Bilguvar, Kaya, Ye, Junqiang, Bolze, Alexandre, Bigio, Benedetta, Yang, Rui, Arias, Andres Augusto, Zhou, Qinhua, Zhang, Yu, Onodi, Fanny, Korniotis, Sarantis, Karpf, Lea, Philippot, Quentin, Chbihi, Marwa, Bonnet-Madin, Lucie, Dorgham, Karim, Smith, Nikaia, Schneider, William M, Razooky, Brandon S, Hoffmann, Hans-Heinrich, Michailidis, Eleftherios, Moens, Leen, Han, Ji Eun, Lorenzo, Lazaro, Bizien, Lucy, Meade, Philip, Neehus, Anna-Lena, Ugurbil, Aileen Camille, Corneau, Aurelien, Kerner, Gaspard, Zhang, Peng, Rapaport, Franck, Seeleuthner, Yoann, Manry, Jeremy, Masson, Cecile, Schmitt, Yohann, Schlueter, Agatha, Le Voyer, Tom, Khan, Taushif, Li, Juan, Fellay, Jacques, Roussel, Lucie, Shahrooei, Mohammad, Alosaimi, Mohammed F, Mansouri, Davood, Al-Saud, Haya, Al-Mulla, Fahd, Almourfi, Feras, Al-Muhsen, Saleh Zaid, Alsohime, Fahad, Al Turki, Saeed, Hasanato, Rana, van de Beek, Diederik, Biondi, Andrea, Bettini, Laura Rachele, D'Angio, Mariella, Bonfanti, Paolo, Imberti, Luisa, Sottini, Alessandra, Paghera, Simone, Quiros-Roldan, Eugenia, Rossi, Camillo, Oler, Andrew J, Tompkins, Miranda F, Alba, Camille, Vandernoot, Isabelle, Goffard, Jean-Christophe, Smits, Guillaume, Migeotte, Isabelle, Haerynck, Filomeen, Soler-Palacin, Pere, Martin-Nalda, Andrea, Colobran, Roger, Morange, Pierre-Emmanuel, Keles, Sevgi, Colkesen, Fatma, Ozcelik, Tayfun, Yasar, Kadriye Kart, Senoglu, Sevtap, Karabela, Semsi Nur, Rodriguez-Gallego, Carlos, Novelli, Giuseppe, Hraiech, Sami, Tandjaoui-Lambiotte, Yacine, Duval, Xavier, Laouenan, Cedric, Snow, Andrew L, Dalgard, Clifton L, Milner, Joshua D, Vinh, Donald C

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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 von Zhang, Qian, Bastard, Paul, Liu, Zhiyong, Ogishi, Masato, Sabli, Ira K. D, Hodeib, Stephanie, Korol, Cecilia, Bilguvar, Kaya, Ye, Junqiang, Bolze, Alexandre, Yang, Rui, Arias, Andrés Augusto, Onodi, Fanny, Korniotis, Sarantis, Karpf, Léa, Philippot, Quentin, Chbihi, Marwa, Bonnet-Madin, Lucie, Razooky, Brandon S, Hoffmann, Hans-Heinrich, Moens, Leen, Han, Ji Eun, Lorenzo, Lazaro, Bizien, Lucy, Meade, Philip, Ugurbil, Aileen Camille, Corneau, Aurélien, Kerner, Gaspard, Zhang, Peng, Rapaport, Franck, Manry, Jeremy, Masson, Cecile, Schlüter, Agatha, Le Voyer, Tom, Khan, Taushif, Li, Juan, Alosaimi, Mohammed F, Al-Saud, Haya, Al-Mulla, Fahd, Almourfi, Feras, Al-Muhsen, Saleh Zaid, Alsohime, Fahad, Biondi, Andrea, Bettini, Laura Rachele, D’Angio, Mariella, Bonfanti, Paolo, Imberti, Luisa, Sottini, Alessandra, Paghera, Simone, Quiros-Roldan, Eugenia, Oler, Andrew J, Smits, Guillaume, Migeotte, Isabelle, Haerynck, Filomeen, Colobran, Roger, Morange, Pierre-Emmanuel, Keles, Sevgi, Senoglu, Sevtap, Karabela, Şemsi Nur, Gallego, Carlos Rodríguez, Novelli, Giuseppe, Hraiech, Sami, Tandjaoui-Lambiotte, Yacine, Duval, Xavier, Snow, Andrew L, Dalgard, Clifton L, Milner, Joshua, Mogensen, Trine H, Spaan, András N, Boisson, Bertrand, Bustamante, Jacinta, Puel, Anne, Ciancanelli, Michael, Meyts, Isabelle, Soumelis, Vassili, Amara, Ali, Nussenzweig, Michel, Krammer, Florian, Duffy, Darragh, Lifton, Richard, Gorochov, Guy, Béziat, Vivien, Sancho-Shimizu, Vanessa, Abel, Laurent, Notarangelo, Luigi D, Casanova, Jean-Laurent, Bosteels, Cedric, Hoste, Levi, Hoste, Eric, Tavernier, Simon, Van Braeckel, Eva, COVID-STORM Clinicians, [missing], COVID Clinicians, [missing], Imagine COVID Group, [missing], CoV-Contact Cohort, [missing], Amsterdam UMC Covid-19, [missing], Biobank, [missing], COVID Human Genetic Effort, [missing], NIAID-USUHS, [missing], TAGC COVID Immunity Group, [missing]

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Full-in-House Method (FinHM) for SARS-COV-2 Automated Viral RNA Extraction, Followed by in-House ‘Primer-Probe’ Based RT-qPCR Detection; Low Cost Mass Testing von Al-Romaih, Khaldoun, Alsharif, Ibtihaj, Bakheet, Razan, Mahmoud, Lina, Alharbi, Najla, Bin Judia, Sara, Alharbi, Layla, Alzayed, Abdulaziz, Jabaan, Amjad, Alotaibi, Jawahar, Ayodele, Alaiya, Shinwari, Zakiya, Alhadrami, Hani, Albarrag, Ahmed, Azhar, Esam, Al-Saud, Haya, Alrahbini, Tahani, Al-Mozaini, Maha

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Erratum to: Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases

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Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 ( ) von Alsmadi, Osama, Meyer, Brian F, Alkuraya, Fowzan, Wakil, Salma, Alkayal, Fadi, Al-Saud, Haya, Ramzan, Khushnooda, Al-Sayed, MoeenAldeen

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The KIAA0391 and PSMA6 gene cluster confers a risk factor for coronary artery disease von Dzimiri, Nduna, Muiya, Paul, Alsmadi, Osma, Al‐Saud, Haya, Meyer, Brian, Alshahid, Maie, Al‐Mohanna, Futwan

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The genetics of obesity in Saudi Arabian population von Al-Saud, Haya

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Haplotypes encompassing the PSMA6 and KIAA0391 Gene Cluster confer risk for Myocardial Infarction von Dzimiri, Nduna, Muiya, Paul, Mohamed, Gamal, Alsmadi, Osama, Al‐Saud, Haya, Al‐Mohanna, Futwan, Alshahid, Maie, Meyer, Brian

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