Functional reprogramming of regulatory T cells in the absence of Foxp3 von Charbonnier, Louis-Marie, Cui, Ye, Stephen-Victor, Emmanuel, Harb, Hani, Lopez, David, Bleesing, Jack J., Garcia-Lloret, Maria I., Chen, Karin, Ozen, Ahmet, Carmeliet, Peter, Li, Ming O., Pellegrini, Matteo, Chatila, Talal A.

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ICT penetration and life expectancy in emerging market economies: panel evidence from asymmetric causality analysis von Bayar, Yilmaz, Ozen, Ahmet, Sasmaz, Mahmut Unsal, Danilina, Marina

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Severe allergic dysregulation due to a gain of function mutation in the transcription factor STAT6 von Baris, Safa, Benamar, Mehdi, Chen, Qian, Catak, Mehmet Cihangir, Martínez-Blanco, Mónica, Wang, Muyun, Fong, Jason, Massaad, Michel J., Sefer, Asena Pinar, Kara, Altan, Babayeva, Royala, Eltan, Sevgi Bilgic, Yucelten, Ayse Deniz, Bozkurtlar, Emine, Cinel, Leyla, Karakoc-Aydiner, Elif, Zheng, Yumei, Wu, Hao, Ozen, Ahmet, Schmitz-Abe, Klaus, Chatila, Talal A.

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CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis von Ozen, Ahmet, Comrie, William A, Ardy, Rico C, Domínguez Conde, Cecilia, Dalgic, Buket, Beser, Ömer F, Morawski, Aaron R, Karakoc-Aydiner, Elif, Tutar, Engin, Baris, Safa, Ozcay, Figen, Serwas, Nina K, Zhang, Yu, Matthews, Helen F, Pittaluga, Stefania, Folio, Les R, Unlusoy Aksu, Aysel, McElwee, Joshua J, Krolo, Ana, Kiykim, Ayca, Baris, Zeren, Gulsan, Meltem, Ogulur, Ismail, Snapper, Scott B, Houwen, Roderick H.J, Leavis, Helen L, Ertem, Deniz, Kain, Renate, Sari, Sinan, Erkan, Tülay, Su, Helen C, Boztug, Kaan, Lenardo, Michael J

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Stepwise Reversal of Immune Dysregulation Due to STAT1 Gain-of-Function Mutation Following Ruxolitinib Bridge Therapy and Transplantation von Kayaoglu, Basak, Kasap, Nurhan, Yilmaz, Naz Surucu, Charbonnier, Louis Marie, Geckin, Busranur, Akcay, Arzu, Eltan, Sevgi Bilgic, Ozturk, Gulyuz, Ozen, Ahmet, Karakoc-Aydiner, Elif, Chatila, Talal A., Gursel, Mayda, Baris, Safa

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A novel approach in allergen-specific immunotherapy: Combination of sublingual and subcutaneous routes von Keles, Sevgi, MD, Karakoc-Aydiner, Elif, MD, Ozen, Ahmet, MD, Izgi, Ayse Gul, MS, Tevetoglu, Ayzer, MS, Akkoc, Tunc, PhD, Bahceciler, Nerin N., MD, Barlan, Isil, MD

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Clinical and metabolic features of urolithiasis and microlithiasis in children von Alpay, Harika, Ozen, Ahmet, Gokce, Ibrahim, Biyikli, Nese

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Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis von Yucel, Esra, Karakus, Ibrahim Serhat, Krolo, Ana, Kiykim, Ayca, Heredia, Raul Jimenez, Tamay, Zeynep, Cipe, Funda Erol, Karakoc-Aydiner, Elif, Ozen, Ahmet, Karaman, Serap, Boztug, Kaan, Baris, Safa

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CHAPLE syndrome uncovers the primary role of complement in a familial form of Waldmann's disease von Ozen, Ahmet

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Broadly effective metabolic and immune recovery with C5 inhibition in CHAPLE disease von Ozen, Ahmet, Kasap, Nurhan, Vujkovic-Cvijin, Ivan, Apps, Richard, Cheung, Foo, Karakoc-Aydiner, Elif, Akkelle, Bilge, Sari, Sinan, Tutar, Engin, Ozcay, Figen, Uygun, Dilara Kocacik, Islek, Ali, Akgun, Gamze, Selcuk, Merve, Sezer, Oya Balci, Zhang, Yu, Kutluk, Gunsel, Topal, Erdem, Sayar, Ersin, Celikel, Cigdem, Houwen, Roderick H. J., Bingol, Aysen, Ogulur, Ismail, Eltan, Sevgi Bilgic, Snow, Andrew L., Lake, Camille, Fantoni, Giovanna, Alba, Camille, Sellers, Brian, Chauvin, Samuel D., Dalgard, Clifton L., Harari, Olivier, Ni, Yan G., Wang, Ming-Dauh, Devalaraja-Narashimha, Kishor, Subramanian, Poorani, Ergelen, Rabia, Artan, Reha, Guner, Sukru Nail, Dalgic, Buket, Tsang, John, Belkaid, Yasmine, Ertem, Deniz, Baris, Safa, Lenardo, Michael J.

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Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency von Cagdas, Deniz, Mayr, Daniel, Baris, Safa, Worley, Lisa, Langley, David B., Metin, Ayse, Aytekin, Elif Soyak, Atan, Raziye, Kasap, Nurhan, Bal, Sevgi Köstel, Dmytrus, Jasmin, Heredia, Raul Jimenez, Karasu, Gulsun, Torun, Selda Hancerli, Toyran, Muge, Karakoc-Aydiner, Elif, Christ, Daniel, Kuskonmaz, Baris, Uçkan-Çetinkaya, Duygu, Uner, Aysegul, Oberndorfer, Felicitas, Schiefer, Ana-Iris, Uzel, Gulbu, Deenick, Elissa K., Keller, Baerbel, Warnatz, Klaus, Neven, Bénédicte, Durandy, Anne, Sanal, Ozden, Ma, Cindy S., Özen, Ahmet, Stepensky, Polina, Tezcan, Ilhan, Boztug, Kaan, Tangye, Stuart G.

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COVID-19 Vaccine Boosters: The Good, the Bad, and the Ugly von Rzymski, Piotr, Camargo, Carlos A., Fal, Andrzej, Flisiak, Robert, Gwenzi, Willis, Kelishadi, Roya, Leemans, Alexander, Nieto, Juan J., Ozen, Ahmet, Perc, Matjaz, Poniedzialek, Barbara, Sedikides, Constantine, Sellke, Frank, Skirmuntt, Emilia C., Stashchak, Anzhela, Rezaei, Nima

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Primary school teachers' knowledge about and attitudes toward anaphylaxis von Ercan, Hulya, Ozen, Ahmet, Karatepe, Hande, Berber, Mustafa, Cengizlier, Reha

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Pozelimab for CHAPLE disease: results from in-trial interviews and clinical outcome assessments von Litcher-Kelly, Leighann, Ozen, Ahmet, Ollis, Sarah, Feldman, Hagit Baris, Yaworsky, Andrew, Medrano, Paolo, Chongsrisawa, Voranush, Brackin, Taylor, Perlee, Lorah, Walker, Marisa, Pradeep, Sharanya, Lenardo, Michael J, Harari, Olivier A, Jalbert, Jessica J

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A Patient with Novel ICOS Mutation Presented with Progressive Loss of B Cells von Sefer, Asena Pınar, Charbonnier, Louis Marie, Kasap, Nurhan, Akcam, Bengu, Demirkol, Yasemin Kendir, Eltan, Sevgi Bilgic, Ozen, Ahmet, Karakoc-Aydiner, Elif, Baris, Safa

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ILC3 deficiency and generalized ILC abnormalities in DOCK8‐deficient patients von Eken, Ahmet, Cansever, Murat, Okus, Fatma Zehra, Erdem, Serife, Nain, Ercan, Azizoglu, Zehra Busra, Haliloglu, Yesim, Karakukcu, Musa, Ozcan, Alper, Devecioglu, Omer, Aksu, Guzide, Arikan Ayyildiz, Zeynep, Topal, Erdem, Karakoc Aydiner, Elif, Kiykim, Ayca, Metin, Ayse, Cipe, Funda, Kaya, Aysenur, Artac, Hasibe, Reisli, Ismail, Guner, Sukru N., Uygun, Vedat, Karasu, Gulsun, Dönmez Altuntas, Hamiyet, Canatan, Halit, Oukka, Mohamed, Ozen, Ahmet, Chatila, Talal A., Keles, Sevgi, Baris, Safa, Unal, Ekrem, Patiroglu, Turkan

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Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency von Sefer, Asena Pinar, Abolhassani, Hassan, Ober, Franziska, Kayaoglu, Basak, Bilgic Eltan, Sevgi, Kara, Altan, Erman, Baran, Surucu Yilmaz, Naz, Aydogmus, Cigdem, Aydemir, Sezin, Charbonnier, Louis-Marie, Kolukisa, Burcu, Azizi, Gholamreza, Delavari, Samaneh, Momen, Tooba, Aliyeva, Simuzar, Kendir Demirkol, Yasemin, Tekin, Saban, Kiykim, Ayca, Baser, Omer Faruk, Cokugras, Haluk, Gursel, Mayda, Karakoc-Aydiner, Elif, Ozen, Ahmet, Krappmann, Daniel, Chatila, Talal A., Rezaei, Nima, Baris, Safa

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DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans von Azizoglu, Zehra Busra, Babayeva, Royala, Haskologlu, Zehra Sule, Acar, Mustafa Burak, Ayaz-Guner, Serife, Okus, Fatma Zehra, Alsavaf, Mohammad Bilal, Can, Salim, Basaran, Kemal Erdem, Canatan, Mehmed Fatih, Ozcan, Alper, Erkmen, Hasret, Leblebici, Can Berk, Yilmaz, Ebru, Karakukcu, Musa, Kose, Mehmet, Canoz, Ozlem, Özen, Ahmet, Karakoc-Aydiner, Elif, Ceylaner, Serdar, Gümüş, Gülsüm, Per, Huseyin, Gumus, Hakan, Canatan, Halit, Ozcan, Servet, Dogu, Figen, Ikinciogullari, Aydan, Unal, Ekrem, Baris, Safa, Eken, Ahmet

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Lymphopenia with Low T and NK Cells in a Patient with USB1 Mutation, Rare Findings in Clericuzio-Type Poikiloderma with Neutropenia von Bilgic Eltan, Sevgi, Sefer, Asena Pınar, Karakus, İbrahim Serhat, Ozen, Ahmet, Karakoc-Aydiner, Elif, Baris, Safa

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Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease von Kubo, Satoshi, Fritz, Jill M., Raquer-McKay, Hayley M., Kataria, Rhea, Vujkovic-Cvijin, Ivan, Al-Shaibi, Ahmad, Yao, Yikun, Zheng, Lixin, Zou, Juan, Waldman, Alex D., Jing, Xinyi, Farley, Taylor K., Park, Ann Y., Oler, Andrew J., Charles, Adrian K., Makhlouf, Melanie, AbouMoussa, Eman H., Hasnah, Reem, Saraiva, Luis R., Ganesan, Sundar, Al-Subaiey, Abdulrahman Ahmed, Matthews, Helen, Flano, Emilio, Lee, Hyun Hee, Freeman, Alexandra F., Sefer, Asena Pınar, Sayar, Ersin, Çakır, Erkan, Karakoc-Aydiner, Elif, Baris, Safa, Belkaid, Yasmine, Ozen, Ahmet, Lo, Bernice, Lenardo, Michael J.

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