Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2) by Lee, Pui Y., Kellner, Erinn S., Huang, Yuelong, Furutani, Elissa, Huang, Zhengping, Bainter, Wayne, Alosaimi, Mohammed F., Stafstrom, Kelsey, Platt, Craig D., Stauber, Tali, Raz, Somech, Tirosh, Irit, Weiss, Aaron, Jordan, Michael B., Krupski, Christa, Eleftheriou, Despina, Brogan, Paul, Sobh, Ali, Baz, Zeina, Lefranc, Gerard, Irani, Carla, Kilic, Sara S., El-Owaidy, Rasha, Lokeshwar, M.R., Pimpale, Pallavi, Khubchandani, Raju, Chambers, Eugene P., Chou, Janet, Geha, Raif S., Nigrovic, Peter A., Zhou, Qing

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Human inherited complete STAT2 deficiency underlies inflammatory viral diseases by Bucciol, Giorgia, Moens, Leen, Ogishi, Masato, Rinchai, Darawan, Matuozzo, Daniela, Momenilandi, Mana, Kerrouche, Nacim, Cale, Catherine M, Treffeisen, Elsa R, Al Salamah, Mohammad, Al-Saud, Bandar K, Lachaux, Alain, Duclaux-Loras, Remi, Meignien, Marie, Bousfiha, Aziz, Benhsaien, Ibtihal, Shcherbina, Anna, Roppelt, Anna, Gothe, Florian, Houhou-Fidouh, Nadhira, Hackett, Scott J, Bartnikas, Lisa M, Maciag, Michelle C, Alosaimi, Mohammed F, Chou, Janet, Mohammed, Reem W, Freij, Bishara J, Jouanguy, Emmanuelle, Zhang, Shen-Ying, Boisson-Dupuis, Stephanie, Béziat, Vivien, Zhang, Qian, Duncan, Christopher Ja, Hambleton, Sophie, Casanova, Jean-Laurent, Meyts, Isabelle

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Immune dysregulation caused by homozygous mutations in CBLB by Janssen, Erin, Peters, Zachary, Alosaimi, Mohammed F, Smith, Emma, Milin, Elena, Stafstrom, Kelsey, Wallace, Jacqueline G, Platt, Craig D, Chou, Janet, Ansari, Yasmeen S. El, Farsi, Tariq Al, Ameziane, Najim, Al-Ali, Ruslan, Calvo, Maria, Rocha, Maria Eugenia, Bauer, Peter, Al-Sannaa, Nouriya Abbas, Sukaiti, Nashat Faud Al, Alangari, Abdullah A, Bertoli-Avella, Aida M, Geha, Raif S

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Clinical and biochemical characteristics of people experiencing post-coronavirus disease 2019-related symptoms: A prospective follow-up investigation by Alfadda, Assim A, Rafiullah, Mohamed, Alkhowaiter, Mohammad, Alotaibi, Naif, Alzahrani, Musa, Binkhamis, Khalifa, Siddiqui, Khalid, Youssef, Amira, Altalhi, Haifa, Almaghlouth, Ibrahim, Alarifi, Mohammed, Albanyan, Saleh, Alosaimi, Mohammed F, Isnani, Arthur, Nawaz, Shaik Sarfaraz, Alayed, Khalid

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Favipiravir Effectiveness and Safety in Hospitalized Moderate-Severe COVID-19 Patients: Observational Prospective Multicenter Investigation in Saudi Arabia by 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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ITK deficiency presenting as autoimmune lymphoproliferative syndrome by Wallace, Jacqueline G., Alosaimi, Mohammed F., Khayat, Claudia Djambas, Jaber, Faris, Almutairi, Abduarahman, Beaussant-Cohen, Sarah, Pinkus, Geraldine, Fleming, Mark, Mehawej, Cybel, Chou, Janet, Geha, Raif S.

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Combined immunodeficiency in a patient with c-Rel deficiency by Beaussant-Cohen, Sarah, Jaber, Faris, Massaad, Michel J., Weeks, Sabrina, Jones, Jennifer, Alosaimi, Mohammed F., Wallace, Jacqueline, Al-Herz, Waleed, Geha, Raif S., Chou, Janet

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Immunodeficiency and EBV-induced lymphoproliferation caused by 4-1BB deficiency by Alosaimi, Mohammed F., Hoenig, Manfred, Jaber, Faris, Platt, Craig D., Jones, Jennifer, Wallace, Jacqueline, Debatin, Klaus-Michael, Schulz, Ansgar, Jacobsen, Eva, Möller, Peter, Shamseldin, Hanan E., Abdulwahab, Ferdous, Ibrahim, Niema, Alardati, Hosam, Almuhizi, Faisal, Abosoudah, Ibraheem F., Basha, Talal A., Chou, Janet, Alkuraya, Fowzan S., Geha, Raif S.

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A novel variant in STAT2 presenting with hemophagocytic lymphohistiocytosis by Alosaimi, Mohammed F., Maciag, Michelle C., Platt, Craig D., Geha, Raif S., Chou, Janet, Bartnikas, Lisa M.

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T-cell mitochondrial dysfunction and lymphopenia in DOCK2-deficient patients by Alosaimi, Mohammed F., Shendi, Hiba, Beano, Abdallah, Stafstrom, Kelsey, El Hawary, Rabab, Meshaal, Safa, Galal, Nermeen, Pai, Sung-Yun, El-Marsafy, Aisha, Geha, Raif S., Chou, Janet

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Severe combined immunodeficiency caused by inositol-trisphosphate 3-kinase B (ITPKB) deficiency by Almutairi, Abduarahman, Wallace, Jacqueline G., Jaber, Faris, Alosaimi, Mohammed F., Jones, Jennifer, Sallam, Mohamed T.H., Elnagdy, M.H., Chou, Janet, Sobh, Ali, Geha, Raif S.

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Hypomorphic variants in AK2 reveal the contribution of mitochondrial function to B-cell activation by Chou, Janet, Alazami, Anas M., Jaber, Faris, Hoyos-Bachiloglu, Rodrigo, Jones, Jennifer, Weeks, Sabrina, Alosaimi, Mohammed F., Bainter, Wayne, Cangemi, Brittney, Badran, Yousef R., Mohammed, Reem, Alroqi, Fayhan, Almutairi, Abduarahman, Al-Onazi, Noufa, AlAjaji, Sulaiman, Al-Saud, Bander, Arnaout, Rand, Elkins, Megan, Devana, Sridevi, Imperial, Juliet, Li, Betty, Drexhage, Linnea, Abdel Rahman, Anas M., Jacob, Minnie, Haddad, Hadi, Hanna-Wakim, Rima, Dbaibo, Ghassan, Massaad, Michel J., Dasouki, Majed, Mikhael, Raymond, Baz, Zeina, Geha, Raif S., Al-Mousa, Hamoud

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Rethinking newborn screening for severe combined immunodeficiency: Lessons from an international partnership for patients with primary immunodeficiencies in Pakistan by Wallace, Jacqueline G., Tipu, Hamid Nawaz, Stafstrom, Kelsey, Alosaimi, Mohammed F., Massaad, Michel J., Bainter, Wayne, Geha, Raif S., Chou, Janet

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Immunologic reconstitution following hematopoietic stem cell transplantation despite lymph node paucity in NF-κB–inducing kinase deficiency by Ben Farhat, Khaoula, Alosaimi, Mohammed F., Shendi, Hiba, Al-Hammadi, Suleiman, Jones, Jennifer, Schwarz, Klaus, Schulz, Ansgar, Alawdah, Laila S., Burchett, Sandra, Albuhairi, Sultan, Whangbo, Jennifer, Kwatra, Neha, Shamseldin, Hanan E., Alkuraya, Fowzan S., Chou, Janet, Geha, Raif S.

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Case report: A late and isolated presentation of meningoencephalomyelitis uncovers a novel pathogenic variant in the CIITA gene by Alosaimi, Mohammed F., Hamad, Muddathir H., AlShammari, Muneera J., Jamjoom, Dima Z., Musibeeh, Najd S.

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Early Cytokine Signatures of Hospitalized Mild and Severe COVID-19 Patients: A Prospective Observational Study by Alfadda, Assim A, Siddiqui, Khalid, Rafiullah, Mohamed, AlKhowaiter, Mohammad, Alotaibi, Naif, Alzahrani, Musa, Binkhamis, Khalifa, Youssef, Amira M, Altalhi, Haifa, Almaghlouth, Ibrahim, Alarifi, Mohammed, Albanyan, Saleh, Alosaimi, Mohammed F, Isnani, Arthur, Nawaz, Shaik S, Alayed, Khalid

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Risk factors and predictors that influence SARS-Cov-2 IgG positivity by Alosaimi, Mohammed F, Alhetheel Abdulkarim, Aleisa, Khalid A, Altwerki, Abdullah A, Alenezy, Njoud M, Almutairi, Ebtisam M, Alothaim, Leen O, Khalid Abdul Manan A, Alayed, Khalid M, Almazyad, Mohammed A, BinMoammar, Turki A, Alshobaili, Fahdah A, Al-Shahrani, Fatimah S, Alsubaie, Sarah, Hasanato, Rana M

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Risk factors and predictors that influence SARS-Cov-2 IgG positivity: A cross-sectional study of blood donors in Riyadh, Saudi Arabia by Alosaimi, Mohammed F, Alhetheel, Abdulkarim, Aleisa, Khalid A, Altwerki, Abdullah A, Alenezy, Njoud M, Almutairi, Ebtisam M, Alothaim, Leen O, Khalid, Abdul Manan A, Alayed, Khalid M, Almazyad, Mohammed A, BinMoammar, Turki A, Alshobaili, Fahdah A, Al-Shahrani, Fatimah S, Alsubaie, Sarah, Hasanato, Rana M

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Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency by Lévy, Romain, Gothe, Florian, Momenilandi, Mana, Magg, Thomas, Materna, Marie, Peters, Philipp, Raedler, Johannes, Philippot, Quentin, Rack-Hoch, Anita Lena, Langlais, David, Bourgey, Mathieu, Lanz, Anna-Lisa, Ogishi, Masato, Rosain, Jérémie, Martin, Emmanuel, Latour, Sylvain, Vladikine, Natasha, Distefano, Marco, Khan, Taushif, Rapaport, Franck, Schulz, Marian S, Holzer, Ursula, Fasth, Anders, Sogkas, Georgios, Speckmann, Carsten, Troilo, Arianna, Bigley, Venetia, Roppelt, Anna, Dinur-Schejter, Yael, Toker, Ori, Bronken Martinsen, Karen Helene, Sherkat, Roya, Somekh, Ido, Somech, Raz, Shouval, Dror S, Kühl, Jörn-Sven, Ip, Winnie, McDermott, Elizabeth M, Cliffe, Lucy, Ozen, Ahmet, Baris, Safa, Rangarajan, Hemalatha G, Jouanguy, Emmanuelle, Puel, Anne, Bustamante, Jacinta, Alyanakian, Marie-Alexandra, Fusaro, Mathieu, Wang, Yi, Kong, Xiao-Fei, Cobat, Aurélie, Boutboul, David, Castelle, Martin, Aguilar, Claire, Hermine, Olivier, Cheminant, Morgane, Suarez, Felipe, Yildiran, Alisan, Bousfiha, Aziz, Al-Mousa, Hamoud, Alsohime, Fahad, Cagdas, Deniz, Abraham, Roshini S, Knutsen, Alan P, Fevang, Borre, Bhattad, Sagar, Kiykim, Ayca, Erman, Baran, Arikoglu, Tugba, Unal, Ekrem, Kumar, Ashish, Geier, Christoph B, Baumann, Ulrich, Neven, Bénédicte, Rohlfs, Meino, Walz, Christoph, Abel, Laurent, Malissen, Bernard, Marr, Nico, Klein, Christoph, Casanova, Jean-Laurent, Hauck, Fabian, Béziat, Vivien

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Human inherited complete STAT2 deficiency underlies inflammatory viral diseases by Bucciol, Giorgia, Moens, Leen, Ogishi, Masato, Rinchai, Darawan, Matuozzo, Daniela, Momenilandi, Mana, Kerrouche, Nacim, Cale, Catherine M, Treffeisen, Elsa R, Al Salamah, Mohammad, Al-Saud, Bandar K, Lachaux, Alain, Duclaux-Loras, Remi, Meignien, Marie, Bousfiha, Aziz, Benhsaien, Ibtihal, Shcherbina, Anna, Roppelt, Anna, Gothe, Florian, Houhou-Fidouh, Nadhira, Hackett, Scott J, Bartnikas, Lisa M, Maciag, Michelle C, Alosaimi, Mohammed F, Chou, Janet, Mohammed, Reem W, Freij, Bishara J, Jouanguy, Emmanuelle, Zhang, Shen-Ying, Boisson-Dupuis, Stephanie, Béziat, Vivien, Zhang, Qian, Duncan, Christopher J A, Hambleton, Sophie, Casanova, Jean-Laurent, Meyts, Isabelle

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