Correction: An immunogenomic exome landscape of triple positive primary antiphospholipid patients von Guffroy, A., Jacquel, L., Seeleuthner, Y., Paul, N., Poindron, V., Maurier, F., Delannoy, V., Voegeli, A. C., Zhang, P., Nespola, B., Molitor, A., Apithy, M. J., Soulas-Sprauel, P., Martin, T., Voll, R. E., Bahram, S., Gies, V., Casanova, J. L., Cobat, A., Boisson, B., Carapito, R., Korganow, A. S.

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Qualitative and quantitative assessment of cartilage degeneration using full-field optical coherence tomography ex vivo von Pailhé, R., Mounier, A., Boisson, B., Rouchy, R.C., Voros, S., Chipon, E., Boudry, I., Medici, M., Hughes, C., Moreau-Gaudry, A.

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Anatomy and histology of the scrotal ligament in adults: inconsistency and variability of the gubernaculum testis von Cavalie, G., Bellier, Alexandre, Marnas, G., Boisson, B., Robert, Y., Rabattu, P. Y., Chaffanjon, P.

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Identification of eukaryotic peptide deformylases reveals universality of N-terminal protein processing mechanisms von Giglione, Carmela, Serero, Alexandre, Pierre, Michèle, Boisson, Bertrand, Meinnel, Thierry

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Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency von Abolhassani, Hassan, Edwards, Emily S J, Ikinciogullari, Aydan, Jing, Huie, Borte, Stephan, Buggert, Marcus, Du, Likun, Matsuda-Lennikov, Mami, Romano, Rosa, Caridha, Rozina, Bade, Sangeeta, Zhang, Yu, Frederiksen, Juliet, Fang, Mingyan, Bal, Sevgi Kostel, Haskologlu, Sule, Dogu, Figen, Tacyildiz, Nurdan, Matthews, Helen F, McElwee, Joshua J, Gostick, Emma, Price, David A, Palendira, Umaimainthan, Aghamohammadi, Asghar, Boisson, Bertrand, Rezaei, Nima, Karlsson, Annika C, Lenardo, Michael J, Casanova, Jean-Laurent, Hammarström, Lennart, Tangye, Stuart G, Su, Helen C, Pan-Hammarström, Qiang

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Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections von Dobbs, Kerry, Domínguez Conde, Cecilia, Zhang, Shen-Ying, Parolini, Silvia, Audry, Magali, Chou, Janet, Haapaniemi, Emma, Keles, Sevgi, Bilic, Ivan, Okada, Satoshi, Massaad, Michel J, Rounioja, Samuli, Alwahadneh, Adel M, Serwas, Nina K, Capuder, Kelly, Çiftçi, Ergin, Felgentreff, Kerstin, Ohsumi, Toshiro K, Pedergnana, Vincent, Boisson, Bertrand, Haskoloğlu, Şule, Ensari, Arzu, Schuster, Michael, Moretta, Alessandro, Itan, Yuval, Patrizi, Ornella, Rozenberg, Flore, Lebon, Pierre, Saarela, Janna, Knip, Mikael, Petrovski, Slavé, Goldstein, David B, Parrott, Roberta E, Savas, Berna, Schambach, Axel, Tabellini, Giovanna, Bock, Christoph, Chatila, Talal A, Comeau, Anne Marie, Geha, Raif S, Abel, Laurent, Buckley, Rebecca H, İkincioğulları, Aydan, Al-Herz, Waleed, Helminen, Merja, Doğu, Figen, Casanova, Jean-Laurent, Boztuğ, Kaan, Notarangelo, Luigi D

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Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia von Zhang, Qian, Matuozzo, Daniela, Le Pen, Jérémie, Lee, Danyel, Moens, Leen, Asano, Takaki, Bohlen, Jonathan, Liu, Zhiyong, Moncada-Velez, Marcela, Kendir-Demirkol, Yasemin, Jing, Huie, Bizien, Lucy, Marchal, Astrid, Abolhassani, Hassan, Delafontaine, Selket, Bucciol, Giorgia, Bayhan, Gulsum Ical, Keles, Sevgi, Kiykim, Ayca, Hancerli, Selda, Haerynck, Filomeen, Florkin, Benoit, Hatipoglu, Nevin, Ozcelik, Tayfun, Morelle, Guillaume, Zatz, Mayana, Ng, Lisa F P, Lye, David Chien, Young, Barnaby Edward, Leo, Yee-Sin, Dalgard, Clifton L, Lifton, Richard P, Renia, Laurent, Meyts, Isabelle, Jouanguy, Emmanuelle, Hammarström, Lennart, Pan-Hammarström, Qiang, Boisson, Bertrand, Bastard, Paul, Su, Helen C, Boisson-Dupuis, Stéphanie, Abel, Laurent, Rice, Charles M, Zhang, Shen-Ying, Cobat, Aurélie, Casanova, Jean-Laurent

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Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases von Rosain, Jeremie, Le Voyer, Tom, Liu, Xian, Gervais, Adrian, Polivka, Laura, Cederholm, Axel, Berteloot, Laureline, Parent, Audrey V., Pescatore, Alessandra, Spinosa, Ezia, Minic, Snezana, Kiszewski, Ana Elisa, Tsumura, Miyuki, Thibault, Chloe, Azcoiti, Maria Esnaola, Martinovic, Jelena, Philippot, Quentin, Khan, Taushif, Marchal, Astrid, Charmeteau-De Muylder, Benedicte, Bizien, Lucy, Deswarte, Caroline, Hadjem, Lillia, Fauvarque, Marie-Odile, Dorgham, Karim, Eriksson, Daniel, Falcone, Emilia Liana, Puel, Mathilde, Uenal, Sinem, Geraldo, Amyrath, Le Floc'h, Corentin, Li, Hailun, Rheault, Sylvie, Muti, Christine, Bobrie-Moyrand, Claire, Welfringer-Morin, Anne, Fuleihan, Ramsay L., Levy, Romain, Roelens, Marie, Gao, Liwei, Materna, Marie, Pellegrini, Silvia, Piemonti, Lorenzo, Catherinot, Emilie, Goffard, Jean-Christophe, Fekkar, Arnaud, Sacko-Sow, Aissata, Soudee, Camille, Boucherit, Soraya, Neehus, Anna-Lena, Has, Cristina, Huebner, Stefanie, Blanchard-Rohner, Geraldine, Amador-Borrero, Blanca, Utsumi, Takanori, Taniguchi, Maki, Tani, Hiroo, Izawa, Kazushi, Yasumi, Takahiro, Kanai, Sotaro, Migaud, Melanie, Aubart, Melodie, Lambert, Nathalie, Gorochov, Guy, Picard, Capucine, Soudais, Claire, L'Honneur, Anne-Sophie, Rozenberg, Flore, Milner, Joshua D., Zhang, Shen-Ying, Vabres, Pierre, Trpinac, Dusan, Marr, Nico, Boddaert, Nathalie, Desguerre, Isabelle, Pasparakis, Manolis, Miller, Corey N., Poziomczyk, Claudia S., Abel, Laurent, Okada, Satoshi, Jouanguy, Emmanuelle, Cheynier, Remi, Zhang, Qian, Cobat, Aurelie, Beziat, Vivien, Boisson, Bertrand, Steffann, Julie, Fusco, Francesca, Ursini, Matilde Valeria, Hadj-Rabia, Smail, Bodemer, Christine, Bustamante, Jacinta, Luche, Herve, Puel, Anne, Courtois, Gilles, Bastard, Paul, Landegren, Nils, Anderson, Mark S., Casanova, Jean-Laurent

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P273 A case of agammaglobulinemia attributed to heterozygous, dominant-negative mutation in transcription factor E47 von Feuille, E., Boisson, B., Itan, Y., Casanova, J., Cunningham-Rundles, C.

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Autoantibodies against type I IFNs in humans with alternative NF-.B pathway deficiency von Le Voyer, T, Parent, AV, Liu, X, Gervais, A, Nguyen, T, Lorenzo, MP, Rackaityte, E, Zhang, P, Bizien, L, Hancioglu, G, Gueye, MS, Renkilaraj, MRLM, Ogishi, M, Soudee, C, Migaud, M, Rozenberg, F, Momenilandi, M, Riller, Q, Imberti, L, Delmonte, OM, Muller, G, Keller, B, Orrego, J, Gallego, WAF, Rubin, T, Emiroglu, M, Parvaneh, N, Eriksson, D, Aranda-Guillen, M, Vong, L, Katelaris, CH, Mustillo, P, Raedler, J, Bohlen, J, Celik, JB, Astudillo, C, Guffroy, A, DeRisi, JL, Miller, C, Guichard, A, Pan-Hammarstrom, Q, Zhang, Y, Rosen, LB, Holland, SM, Bosticardo, M, Kenney, H, Slade, CA, Abraham, RS, Lougaris, V, Hauck, F, Sediva, A, Poli, MC, Palterer, B, Keller, MD, Sullivan, A, Suan, D, Wong, M, Ma, C, Ciznar, P, Aladjidi, N, Hie, M, Lazaro, E, Franco, J, Keles, S, Malphettes, M, Meinhardt, A, Ikinciogullari, A, Shahrooei, M, Celmeli, F, Goodnow, CC, Gray, PE, Belot, A, Kuehn, HS, Rosenzweig, SD, Miyara, M, Licciardi, F, Barlogis, V, Le Guenno, G, Kuijpers, T, Ducoux, G, Sarrot-Reynauld, F, Cunningham-Rundles, C, Rieux-Laucat, F, Tangye, SG, Sobacchi, C, Doffinger, R, Grimbacher, B, Fieschi, C, Bryant, VL, Assant, ST, Su, H, Neven, B, Abel, L, Zhang, Q, Boisson, B, Cobat, A, Kampe, O, Landegren, N, Notarangelo, LD, Puel, A

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Gene silencing in mosquito salivary glands by RNAi von Boisson, Bertrand, Jacques, Jean Claude, Choumet, Valérie, Martin, Estelle, Xu, Jiannong, Vernick, Ken, Bourgouin, Catherine

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Exome and genome sequencing for inborn errors of immunity von Meyts, Isabelle, Bosch, B, Bolze, A, Boisson, B, Itan, Y, Belkadi, A, Pedergnana, V, Moens, Leen, Picard, C, Cobat, A, Bossuyt, Xavier, Abel, L, Casanova, J.L

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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 von Zhang, Q, Bastard, P, Le Pen, J, Moncada-Velez, M, Ogishi, M, Sabli, IKD, Hodeib, S, Korol, C, Philippot, Q, Chbihi, M, Smith, N, Hoffmann, H-H, Moens, L, Hasanato, R, Han, JE, Lorenzo, L, Neehus, A-L, Ugurbil, AC, Corneau, A, Zhang, P, Van de Beek, D, Seeleuthner, Y, Manry, J, Masson, C, Schlüter, A, Le Voyer, T, Khan, T, Li, J, Roussel, L, Shahrooei, M, Alosaimi, MF, Mansouri, D, Al-Saud, H, Almourfi, F, Alsohime, F, Al Turki, S, Bettini, LR, D'Angio, M, Imberti, L, Sottini, A, Paghera, S, Quiros-Roldan, E, Oler, AJ, Tompkins, MF, Vandernoot, I, Goffard, J-C, Smits, G, Haerynck, F, Amsterdam UMC Covid-19, Martin-Nalda, A, Colobran, R, Keles, S, Çölkesen, F, Ozcelik, T, Yasar, KK, Karabela, ŞN, Biobank, Novelli, G, Hraiech, S, Tandjaoui-Lambiotte, Y, Duval, X, Laouénan, C, COVID-STORM Clinicians, COVID Clinicians, French COVID Cohort Study Group, NIAID-USUHS, TAGC COVID Immunity Group, Snow, AL, Dalgard, CL, Milner, J, Vinh, DC, Mogensen, TH, Marr, N, Spaan, AN, Boisson-Dupuis, S, Bustamante, J, Puel, A, Meyts, I, Ye, J, Soumelis, V, Amara, A, Nussenzweig, M, García-Sastre, A, Krammer, F, Lifton, R, Zhang, S-Y, Gorochov, G, Bolze, A, Béziat, V, Jouanguy, E, Sancho-Shimizu, V, Abel, L, Cobat, A, Su, HC, Casanova, J-L, Yang, R, Zhou, Q, Onodi, F, Korniotis, S, Karpf, L

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Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 von Matuozzo, D, Talouarn, E, Marchal, A, Zhang, P, Manry, J, Seeleuthner, Y, Zhang, Y, Milisavljevic, B, Bastard, P, Asano, T, Barzaghi, F, Abolhassani, H, Tayoun, AA, Aiuti, A, Darazam, IA, Allende, LM, Arias, AA, Aytekin, G, Bondesan, S, Bryceson, YT, Bustos, IG, Cabrera-Marante, O, Carcel, S, Carrera, P, Casari, G, Chaïbi, K, Colobran, R, Condino-Neto, A, Covill, LE, Delmonte, OM, Zein, LE, Flores, C, Gregersen, PK, Gut, M, Haerynck, F, Halwani, R, Hancerli, S, Hatipoğlu, N, Karbuz, A, Keles, S, Leon-Lopez, R, Franco, JL, Mansouri, D, Martinez-Picado, J, Akcan, OM, Migeotte, I, Morelle, G, Martin-Nalda, A, Novelli, G, Novelli, A, Ozcelik, T, Palabiyik, F, De Diego, RP, Planas-Serra, L, Prando, C, Pujol, A, Rodriguez-Gallego, C, Rojas, J, Rovere-Querini, P, Shahrooei, M, Tresoldi, C, Troya, J, Van de Beek, D, Zatz, M, Zawadzki, P, Alosaimi, MF, Baris-Feldman, H, Butte, MJ, Constantinescu, SN, Cooper, MA, Dalgard, CL, Heath, JR, Maniatis, T, Mogensen, TH, Von Bernuth, H, Lermine, A, Vidaud, M, Boland, A, Nussbaum, R, Kahn-Kirby, A, Mentre, F, Tubiana, S, Gorochov, G, Hausfater, P, COVID Human Genetic Effort, COVIDeF Study Group, French COVID Cohort Study Group, COVID Clinicians, Orchestra Working Group, Meyts, I, Zhang, S-Y, Notarangelo, LD, Boisson-Dupuis, S, Su, HC, Boisson, B, Jouanguy, E, Casanova, J-L, Zhang, Q, Abel, L, Cobat, A

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Catharanthus roseus G-box binding factors 1 and 2 act as repressors of strictosidine synthase gene expression in cell cultures von Sibéril, Y, Benhamron, S, Memelink, J, Giglioli-Guivarc'h, N, Thiersault, M, Boisson, B, Doireau, P, Gantet, P

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Valeur diagnostique et pronostique de NDRG2 et NDRG4, cibles de miR-483-5p et miR-139-5p dans le carcinome corticosurrénalien von Boisson, B., David-Boudet, L., Col, E., Agosta, C., Gervais, M., Denis, J., Chaffanjon, P., Chabre, O., Sturm, N., Cherradi, N.

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COMBINED IMMUNODEFICIENCY AND EPSTEIN-BARR VIRUS-INDUCED B CELL MALIGNANCY IN HUMANS WITH INHERITED CD70 DEFICIENCY von Jing, HE, Abolhassani, H, Edwards, ESJ, Ikinciogullari, KA, Borte, S, Buggert, M, Du, LK, Lennikov, M, Romano, R, Caridha, R, Bade, S, Zhang, Y, Frederiksen, J, Fang, MY, Bal, SK, Haskologlu, S, Dogu, F, Tacyildiz, N, Matthews, HF, McElwee, JJ, Gostick, E, Price, DA, Palendira, U, Aghamohammadi, A, Boisson, B, Rezaei, N, Karlsson, A, Lenardo, MJ, Casanova, JL, Hammarstrom, L, Tangye, SG, Pan-Hammarstrom, Q, Su, HC

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The Tetrafigap survey on the long-term outcome of tetraplegic spinal cord injured persons: Part III. Medical complications and associated factors von KLOTZ, R, JOSEPH, P. A, RAVAUD, J. F, WIART, L, BARAT, M

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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 von Matuozzo, D, Marchal, A, Manry, J, Seeleuthner, Y, Bolze, A, Chaldebas, M, Milisavljevic, B, Zhang, P, Gervais, A, Bastard, P, Asano, T, Abolhassani, H, Tayoun, AA, Aiuti, A, Darazam, IA, Allende, LM, Alonso-Arias, R, Arias, AA, Bergman, P, Bondesan, S, Bryceson, YT, Bustos, IG, Cabrera-Marante, O, Carcel, S, Carrera, P, Casari, G, Colobran, R, Covill, LE, El Zein, L, Flores, C, Gregersen, PK, Gut, M, Haerynck, F, Hancerli, S, Hammarström, L, Hatipoğlu, N, Keles, S, Kyheng, C, Leon-Lopez, R, Franco, JL, Mansouri, D, Martinez-Picado, J, Akcan, OM, Migeotte, I, Martin-Nalda, A, Novelli, A, Ozcelik, T, Pan-Hammarström, Q, Pérez de Diego, R, Planas-Serra, L, Pleguezuelo, DE, Prando, C, Pujol, A, Reyes, LF, Rivière, JG, Rodriguez-Gallego, C, Rojas, J, Rovere-Querini, P, Schlüter, A, Shahrooei, M, Sobh, A, Soler-Palacin, P, Tandjaoui-Lambiotte, Y, Tipu, I, Tresoldi, C, Troya, J, van de Beek, D, Zatz, M, Zawadzki, P, Al-Muhsen, SZ, Baris-Feldman, H, Butte, MJ, Constantinescu, SN, Cooper, MA, Dalgard, CL, Fellay, J, Heath, JR, Lau, YL, Lifton, RP, Maniatis, T, von Bernuth, H, Lermine, A, Vidaud, M, Deleuze, JF, Nussbaum, R, Kahn-Kirby, A, Mentre, F, Tubiana, S, Gorochov, G, Tubach, F, Hausfater, P, Meyts, I, Zhang, SY, Puel, A, Notarangelo, LD, Jouanguy, E, Casanova, JL, Zhang, Q, Abel, L, Cobat, A

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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 von Zhang, Q, Liu, Z, Moncada-Velez, M, Chen, J, Ogishi, M, Bigio, B, Yang, R, Arias, AA, Zhou, Q, Han, JE, Ugurbil, AC, Zhang, P, Rapaport, F, Li, J, Spaan, AN, Boisson, B, Boisson-Dupuis, S, Bustamante, J, Puel, A, Ciancanelli, MJ, Zhang, SY, Béziat, V, Jouanguy, E, Abel, L, Cobat, A, Casanova, JL, Bastard, P, Korol, C, Rosain, J, Philippot, Q, Chbihi, M, Lorenzo, L, Bizien, L, Neehus, AL, Kerner, G, Seeleuthner, Y, Manry, J, Le Voyer, T, Le Pen, J, Schneider, WM, Razooky, BS, Hoffmann, HH, Michailidis, E, Rice, CM, Sabli, IKD, Hodeib, S, Sancho-Shimizu, V, Bilguvar, K, Ye, J, Maniatis, T, Bolze, A, Zhang, Y, Notarangelo, LD, Su, HC, Onodi, F, Korniotis, S, Karpf, L, Soumelis, V, Bonnet-Madin, L, Amara, A, Dorgham, K, Gorochov, G, Smith, N, Duffy, D, Moens, L, Meyts, I, Meade, P, Darley, David, Tangye, Stuart, Matthews, Gail

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