Diagnosis of primary antibody and complement deficiencies in young adults after a first invasive bacterial infection von Sanges, S., Wallet, F., Blondiaux, N., Theis, D., Vérin, I., Vachée, A., Dessein, R., Faure, K., Viget, N., Senneville, E., Leroy, O., Maury, F., Just, N., Poissy, J., Mathieu, D., Prévotat, A., Chenivesse, C., Scherpereel, A., Smith, G., Lopez, B., Rosain, J., Frémeaux-Bacchi, V., Hachulla, E., Hatron, P.-Y., Bahuaud, M., Batteux, F., Launay, D., Labalette, M., Lefèvre, G.

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Séquençage de l’exome chez des patients avec un syndrome d’Evans à début adulte : une cohorte de 80 patients von Crickx, E., Fadlallah, J., Cheminant, M., Rosain, J., Dion, J., Malphettes, M., Faucher, B., Terriou, L., Souchaud-Debouverie, O., Comont, T., Suarez, F., Graveleau, J., Hadjadj, J., Moulinet, T., Ronchetti, A.M., Ebbo, M., Stolzenberg, M.C., Boutboul, D., Gobert, D., Gourguechon, C., Godeau, B., Galicier, L., Viallard, J.F., Audia, S., Oksenhendler, E., Fieschi, C., Hermine, O., Michel, M., Mahevas, M., Rieux-Laucat, F.

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Syndrome de déficience en HLA de classe 1 secondaire à une mutation de TAP1 responsable d’une granulomatose chronique associé à des surinfections bronchiques von Kottler, D., Rosain, J., Picard-Dahan, C., Deschamps, L., Borie, R., Bustamante, J., Descamps, V.

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Neutralizing IFN-γ autoantibodies are rare and in HLA-DRB115:02 or 16:02 individuals von Peel, JN, Yang, R, Le, Voyer T, Gervais, A, Rosain, J, Bastard, P, Behere, A, Cederholm, A, Bodansky, A, Seeleuthner, Y

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Human T-bet governs the generation of a distinct subset of CD11c high CD21 low B cells von Yang, R, Avery, DT, Jackson, KJL, Ogishi, M, Benhsaien, I, Du, L, Ye, X, Han, J, Rosain, J, Peel, JN

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Partial human Janus kinase 1 deficiency predominantly impairs responses to interferon gamma and intracellular control of mycobacteria von Daza-Cajigal, V, Albuquerque, AS, Young, DF, Ciancanelli, MJ, Moulding, D, Angulo, I, Jeanne-Julien, V, Rosain, J, Minskaia, E, Casanova, J-L, Boisson-Dupuis, S, Bustamante, J, Randall, RE, McHugh, TD, Thrasher, AJ, Burns, SO

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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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The association of red and processed meat with gestational diabetes mellitus: Results from 2 Canadian birth cohort studies von Stennett, Rosain N, Gerstein, Hertzel C, Bangdiwala, Shrikant I, Rafiq, Talha, Teo, Koon K, Morrison, Katherine M, Atkinson, Stephanie A, Anand, Sonia S, de Souza, Russell J

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A partial form of inherited human USP18 deficiency underlies infection and inflammation von Martin-Fernandez, Marta, Buta, Sofija, Le Voyer, Tom, Li, Zhi, Dynesen, Lasse Toftdal, Vuillier, Françoise, Franklin, Lina, Ailal, Fatima, Muglia Amancio, Alice, Malle, Louise, Gruber, Conor, Benhsaien, Ibtihal, Altman, Jennie, Taft, Justin, Deswarte, Caroline, Roynard, Manon, Nieto-Patlan, Alejandro, Moriya, Kunihiko, Rosain, Jérémie, Boddaert, Nathalie, Bousfiha, Aziz, Crow, Yanick J, Jankovic, Dragana, Sher, Alan, Casanova, Jean-Laurent, Pellegrini, Sandra, Bustamante, Jacinta, Bogunovic, Dusan

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Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccine von Bastard, Paul, Michailidis, Eleftherios, Hoffmann, Hans-Heinrich, Chbihi, Marwa, Le Voyer, Tom, Rosain, Jérémie, Philippot, Quentin, Seeleuthner, Yoann, Gervais, Adrian, Materna, Marie, de Oliveira, Patricia Mouta Nunes, Maia, Maria de Lourdes S, Dinis Ano Bom, Ana Paula, Azamor, Tamiris, Araújo da Conceição, Deborah, Goudouris, Ekaterini, Homma, Akira, Slesak, Günther, Schäfer, Johannes, Pulendran, Bali, Miller, Joseph D, Huits, Ralph, Yang, Rui, Rosen, Lindsey B, Bizien, Lucy, Lorenzo, Lazaro, Chrabieh, Maya, Erazo, Lucia V, Rozenberg, Flore, Jeljeli, Mohamed Maxime, Béziat, Vivien, Holland, Steven M, Cobat, Aurélie, Notarangelo, Luigi D, Su, Helen C, Ahmed, Rafi, Puel, Anne, Zhang, Shen-Ying, Abel, Laurent, Seligman, Stephen J, Zhang, Qian, MacDonald, Margaret R, Jouanguy, Emmanuelle, Rice, Charles M, Casanova, Jean-Laurent

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Multibatch Cytometry Data Integration for Optimal Immunophenotyping von Ogishi, Masato, Yang, Rui, Gruber, Conor, Zhang, Peng, Pelham, Simon J, Spaan, András N, Rosain, Jérémie, Chbihi, Marwa, Han, Ji Eun, Rao, V Koneti, Kainulainen, Leena, Bustamante, Jacinta, Boisson, Bertrand, Bogunovic, Dusan, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent

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Inherited human IFN-γ deficiency underlies mycobacterial disease von Kerner, Gaspard, Rosain, Jérémie, Guérin, Antoine, Al-Khabaz, Ahmad, Oleaga-Quintas, Carmen, Rapaport, Franck, Massaad, Michel J, Ding, Jing-Ya, Khan, Taushif, Ali, Fatima Al, Rahman, Mahbuba, Deswarte, Caroline, Martinez-Barricarte, Rubén, Geha, Raif S, Jeanne-Julien, Valentine, Garcia, Diane, Chi, Chih-Yu, Yang, Rui, Roynard, Manon, Fleckenstein, Bernhard, Rozenberg, Flore, Boisson-Dupuis, Stéphanie, Ku, Cheng-Lung, Seeleuthner, Yoann, Béziat, Vivien, Marr, Nico, Abel, Laurent, Al-Herz, Waleed, Casanova, Jean-Laurent, Bustamante, Jacinta

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Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency von Bastard, Paul, Manry, Jeremy, Chen, Jie, Rosain, Jérémie, Seeleuthner, Yoann, AbuZaitun, Omar, Lorenzo, Lazaro, Khan, Taushif, Hasek, Mary, Hernandez, Nicholas, Bigio, Benedetta, Zhang, Peng, Lévy, Romain, Shrot, Shai, Reino, Eduardo J Garcia, Lee, Yoon-Seung, Boucherit, Soraya, Aubart, Mélodie, Gijsbers, Rik, Béziat, Vivien, Li, Zhi, Pellegrini, Sandra, Rozenberg, Flore, Marr, Nico, Meyts, Isabelle, Boisson, Bertrand, Cobat, Aurélie, Bustamante, Jacinta, Zhang, Qian, Jouangy, Emmanuelle, Abel, Laurent, Somech, Raz, Casanova, Jean-Laurent, Zhang, Shen-Ying

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Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome von Béziat, Vivien, Tavernier, Simon J, Chen, Yin-Huai, Ma, Cindy S, Materna, Marie, Laurence, Arian, Staal, Jens, Aschenbrenner, Dominik, Roels, Lisa, Worley, Lisa, Claes, Kathleen, Gartner, Lisa, Kohn, Lisa A, De Bruyne, Marieke, Schmitz-Abe, Klaus, Charbonnier, Louis-Marie, Keles, Sevgi, Nammour, Justine, Vladikine, Natasha, Maglorius Renkilaraj, Majistor Raj Luxman, Seeleuthner, Yoann, Migaud, Mélanie, Rosain, Jérémie, Jeljeli, Mohamed, Boisson, Bertrand, Van Braeckel, Eva, Rosenfeld, Jill A, Dai, Hongzheng, Burrage, Lindsay C, Murdock, David R, Lambrecht, Bart N, Avettand-Fenoel, Véronique, Vogel, Tiphanie P, Esther, Charles R, Haskologlu, Sule, Dogu, Figen, Ciznar, Peter, Boutboul, David, Ouachée-Chardin, Marie, Amourette, Jean, Lebras, Marie-Noëlle, Gauvain, Clément, Tcherakian, Colas, Ikinciogullari, Aydan, Beyaert, Rudi, Abel, Laurent, Milner, Joshua D, Grimbacher, Bodo, Couderc, Louis-Jean, Butte, Manish J, Freeman, Alexandra F, Catherinot, Émilie, Fieschi, Claire, Chatila, Talal A, Tangye, Stuart G, Uhlig, Holm H, Haerynck, Filomeen, Casanova, Jean-Laurent, Puel, Anne

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Detection of emerging contaminants (UV filters, UV stabilizers and musks) in marine mussels from Portuguese coast by QuEChERS extraction and GC–MS/MS von Picot Groz, M., Martinez Bueno, M.J., Rosain, D., Fenet, H., Casellas, C., Pereira, C., Maria, V., Bebianno, M.J., Gomez, E.

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Partial human Janus kinase 1 deficiency predominantly impairs responses to interferon gamma and intracellular control of mycobacteria von Daza-Cajigal, Vanessa, Albuquerque, Adriana S, Young, Dan F, Ciancanelli, Michael J, Moulding, Dale, Angulo, Ivan, Jeanne-Julien, Valentine, Rosain, Jérémie, Minskaia, Ekaterina, Casanova, Jean-Laurent, Boisson-Dupuis, Stéphanie, Bustamante, Jacinta, Randall, Richard E, McHugh, Timothy D, Thrasher, Adrian J, Burns, Siobhan O

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Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency von Li, Juan, Lei, Wei-Te, Zhang, Peng, Rapaport, Franck, Seeleuthner, Yoann, Lyu, Bingnan, Asano, Takaki, Rosain, Jérémie, Hammadi, Boualem, Zhang, Yu, Pelham, Simon J, Spaan, András N, Migaud, Mélanie, Hum, David, Bigio, Benedetta, Chrabieh, Maya, Béziat, Vivien, Bustamante, Jacinta, Zhang, Shen-Ying, Jouanguy, Emmanuelle, Boisson-Dupuis, Stephanie, El Baghdadi, Jamila, Aimanianda, Vishukumar, Thoma, Katharina, Fliegauf, Manfred, Grimbacher, Bodo, Korganow, Anne-Sophie, Saunders, Carol, Rao, V Koneti, Uzel, Gulbu, Freeman, Alexandra F, Holland, Steven M, Su, Helen C, Cunningham-Rundles, Charlotte, Fieschi, Claire, Abel, Laurent, Puel, Anne, Cobat, Aurélie, Casanova, Jean-Laurent, Zhang, Qian, Boisson, Bertrand

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A culturally tailored personaliseD nutrition intErvention in South ASIan women at risk of Gestational Diabetes Mellitus (DESI-GDM): a randomised controlled trial protocol von Stennett, Rosain N, Adamo, Kristi B, Anand, Sonia S, Bajaj, Harpreet S, Bangdiwala, Shrikant I, Desai, Dipika, Gerstein, Hertzel C, Kandasamy, Sujane, Khan, Farah, Lear, Scott A, McDonald, Sarah D, Pocsai, Tayler, Ritvo, Paul, Rogge, Andrea, Schulze, Karleen M, Sherifali, Diana, Stearns, Jennifer C, Wahi, Gita, Williams, Natalie C, Zulyniak, Michael A, de Souza, Russell J

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Helper T cell immunity in humans with inherited CD4 deficiency von Guérin, Antoine, Moncada-Vélez, Marcela, Jackson, Katherine, Ogishi, Masato, Rosain, Jérémie, Mancini, Mathieu, Langlais, David, Nunez, Andrea, Webster, Samantha, Goyette, Jesse, Khan, Taushif, Marr, Nico, Avery, Danielle T, Rao, Geetha, Waterboer, Tim, Michels, Birgitta, Neves, Esmeralda, Iracema Morais, Cátia, London, Jonathan, Mestrallet, Stéphanie, Quartier Dit Maire, Pierre, Neven, Bénédicte, Rapaport, Franck, Seeleuthner, Yoann, Lev, Atar, Simon, Amos J, Montoya, Jorge, Barel, Ortal, Gómez-Rodríguez, Julio, Orrego, Julio C, L'Honneur, Anne-Sophie, Soudée, Camille, Rojas, Jessica, Velez, Alejandra C, Sereti, Irini, Terrier, Benjamin, Marin, Nancy, García, Luis F, Abel, Laurent, Boisson-Dupuis, Stéphanie, Reis, Joel, Marinho, Antonio, Lisco, Andrea, Faria, Emilia, Goodnow, Christopher C, Vasconcelos, Julia, Béziat, Vivien, Ma, Cindy S, Somech, Raz, Casanova, Jean-Laurent, Bustamante, Jacinta, Franco, Jose Luis, Tangye, Stuart G

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Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents von Lévy, Romain, Langlais, David, Béziat, Vivien, Rapaport, Franck, Rao, Geetha, Lazarov, Tomi, Bourgey, Mathieu, Zhou, Yu J., Briand, Coralie, Moriya, Kunihiko, Ailal, Fatima, Avery, Danielle T., Markle, Janet, Lim, Ai Ing, Ogishi, Masato, Yang, Rui, Pelham, Simon, Emam, Mehdi, Migaud, Mélanie, Deswarte, Caroline, Habib, Tanwir, Saraiva, Luis R., Moussa, Eman A., Guennoun, Andrea, Boisson, Bertrand, Belkaya, Serkan, Martinez-Barricarte, Ruben, Rosain, Jérémie, Belkadi, Aziz, Breton, Sylvain, Payne, Kathryn, Benhsaien, Ibtihal, Plebani, Alessandro, Lougaris, Vassilios, Di Santo, James P., Neven, Bénédicte, Abel, Laurent, Ma, Cindy S., Bousfiha, Ahmed Aziz, Marr, Nico, Bustamante, Jacinta, Liu, Kang, Gros, Philippe, Geissmann, Frédéric, Tangye, Stuart G., Casanova, Jean-Laurent, Puel, Anne

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