A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease von Staels, Frederik, Lorenzetti, Flaminia, De Keukeleere, Kerstin, Willemsen, Mathijs, Gerbaux, Margaux, Neumann, Julika, Tousseyn, Thomas, Pasciuto, Emanuela, De Munter, Paul, Bossuyt, Xavier, Gijsbers, Rik, Liston, Adrian, Humblet-Baron, Stephanie, Schrijvers, Rik

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Predictors of neutralizing antibody response to BNT162b2 vaccination in allogeneic hematopoietic stem cell transplant recipients von Canti, Lorenzo, Humblet-Baron, Stéphanie, Desombere, Isabelle, Neumann, Julika, Pannus, Pieter, Heyndrickx, Leo, Henry, Aurélie, Servais, Sophie, Willems, Evelyne, Ehx, Grégory, Goriely, Stanislas, Seidel, Laurence, Michiels, Johan, Willems, Betty, Liston, Adrian, Ariën, Kevin K, Beguin, Yves, Goossens, Maria E, Marchant, Arnaud, Baron, Frédéric

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OTULIN haploinsufficiency predisposes to environmentally directed inflammation von Staels, Frederik, Bücken, Leoni, De Vuyst, Leana, Willemsen, Mathijs, Van Nieuwenhove, Erika, Gerbaux, Margaux, Neumann, Julika, Malviya, Vanshika, Van Meerbeeck, Lize, Haughton, Jeason, Seldeslachts, Laura, Gouwy, Mieke, Martinod, Kimberly, Vande Velde, Greetje, Proost, Paul, Yshii, Lidia, Schlenner, Susan, Schrijvers, Rik, Liston, Adrian, Humblet-Baron, Stephanie

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Immunological phenotype of the murine Lrba knockout von Gámez‐Díaz, Laura, Neumann, Julika, Jäger, Fiona, Proietti, Michele, Felber, Felicitas, Soulas‐Sprauel, Pauline, Perruzza, Lisa, Grassi, Fabio, Kögl, Tamara, Aichele, Peter, Kilimann, Manfred, Grimbacher, Bodo, Jung, Sophie

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Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations von Staels, Frederik, De Keukeleere, Kerstin, Kinnunen, Matias, Keskitalo, Salla, Lorenzetti, Flaminia, Vanmeert, Michiel, Prezzemolo, Teresa, Pasciuto, Emanuela, Lescrinier, Eveline, Bossuyt, Xavier, Gerbaux, Margaux, Willemsen, Mathijs, Neumann, Julika, Van Loo, Sien, Corveleyn, Anniek, Willekens, Karen, Stalmans, Ingeborg, Meyts, Isabelle, Liston, Adrian, Humblet-Baron, Stephanie, Seppänen, Mikko, Varjosalo, Markku, Schrijvers, Rik

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Missense mutations in inositol 1,4,5-trisphosphate receptor type 3 result in leaky Ca2+ channels and activation of store-operated Ca2+ entry von Terry, Lara E., Arige, Vikas, Neumann, Julika, Wahl, Amanda M., Knebel, Taylor R., Chaffer, James W., Malik, Sundeep, Liston, Adrian, Humblet-Baron, Stephanie, Bultynck, Geert, Yule, David I.

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Dominant mutations in ITPR3 cause Charcot‐Marie‐Tooth disease von Rönkkö, Julius, Molchanova, Svetlana, Revah‐Politi, Anya, Pereira, Elaine M., Auranen, Mari, Toppila, Jussi, Kvist, Jouni, Ludwig, Anastasia, Neumann, Julika, Bultynck, Geert, Humblet‐Baron, Stéphanie, Liston, Adrian, Paetau, Anders, Rivera, Claudio, Harms, Matthew B., Tyynismaa, Henna, Ylikallio, Emil

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IP3R3 variants as novel form of hereditary disorders von Neumann, Julika

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DNA replication–associated inborn errors of immunity von Willemsen, Mathijs, Staels, Frederik, Gerbaux, Margaux, Neumann, Julika, Schrijvers, Rik, Meyts, Isabelle, Humblet-Baron, Stephanie, Liston, Adrian

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DNA replication-associated inborn errors of immunity von Willemsen, Mathijs, Staels, Frederik, Gerbaux, Margaux, Neumann, Julika, Schrijvers, Rik, Meyts, Isabelle, Humblet-Baron, Stephanie, Liston, Adrian

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CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 Deficiency von Gerbaux, Margaux, Roos, Evelyne, Willemsen, Mathijs, Staels, Frederik, Neumann, Julika, Bücken, Leoni, Haughton, Jeason, Yshii, Lidia, Dooley, James, Schlenner, Susan, Humblet-Baron, Stephanie, Liston, Adrian

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CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 Deficiency von Gerbaux, Margaux, Roos, Evelyne, Willemsen, Mathijs, Staels, Frederik, Neumann, Julika, Bucken, Leoni, Haughton, Jeason, Yshii, Lidia, Dooley, James, Schlenner, Susan, Humblet-Baron, Stephanie, Liston, Adrian

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Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia von Van Nieuwenhove, Erika, Barber, John S., Neumann, Julika, Smeets, Elien, Willemsen, Mathijs, Pasciuto, Emanuela, Prezzemolo, Teresa, Lagou, Vasiliki, Seldeslachts, Laura, Malengier-Devlies, Bert, Metzemaekers, Mieke, Haßdenteufel, Sarah, Kerstens, Axelle, van der Kant, Rob, Rousseau, Frederic, Schymkowitz, Joost, Di Marino, Daniele, Lang, Sven, Zimmermann, Richard, Schlenner, Susan, Munck, Sebastian, Proost, Paul, Matthys, Patrick, Devalck, Christine, Boeckx, Nancy, Claessens, Frank, Wouters, Carine, Humblet-Baron, Stephanie, Meyts, Isabelle, Liston, Adrian

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Homozygous DBF4 mutation as a cause of severe congenital neutropenia von Willemsen, Mathijs, Barber, John S., Nieuwenhove, Erika Van, Staels, Frederik, Gerbaux, Margaux, Neumann, Julika, Prezzemolo, Teresa, Pasciuto, Emanuela, Lagou, Vasiliki, Boeckx, Nancy, Filtjens, Jessica, De Visscher, Amber, Matthys, Patrick, Schrijvers, Rik, Tousseyn, Thomas, O’Driscoll, Mark, Bucciol, Giorgia, Schlenner, Susan, Meyts, Isabelle, Humblet-Baron, Stephanie, Liston, Adrian

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Homozygous DBF4 mutation as a cause of severe congenital neutropenia von Willemsen, Mathijs, Barber, John S, Van Nieuwenhove, Erika, Staels, Frederik, Gerbaux, Margaux, Neumann, Julika, Prezzemolo, Teresa, Pasciuto, Emanuela, Lagou, Vasiliki, Boeckx, Nancy, Filtjens, Jessica, De Visscher, Amber, Matthys, Patrick, Schrijvers, Rik, Tousseyn, Thomas, O'Driscoll, Mark, Bucciol, Giorgia, Schlenner, Susan, Meyts, Isabelle, Humblet-Baron, Stephanie, Liston, Adrian

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A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease von Staels, Frederik, Lorenzetti, Flaminia, De Keukeleere, Kerstin, Willemsen, Mathijs, Gerbaux, Margaux, Neumann, Julika, Tousseyn, Thomas, Pasciuto, Emanuela, De Munter, Paul, Bossuyt, Xavier, Gijsbers, Rik, Liston, Adrian, Humblet-Baron, Stephanie, Schrijvers, Rik

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OTULIN haploinsufficiency predisposes to environmentally directed inflammation von Staels, Frederik, Bucken, Leoni, De Vuyst, Leana, Willemsen, Mathijs, Van Nieuwenhove, Erika, Gerbaux, Margaux, Neumann, Julika, Malviya, Vanshika, Van Meerbeeck, Lize, Haughton, Jeason, Seldeslachts, Laura, Gouwy, Mieke, Martinod, Kimberly, Vande Velde, Greetje, Proost, Paul, Yshii, Lidia, Schlenner, Susan, Schrijvers, Rik, Liston, Adrian, Humblet-Baron, Stephanie

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Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects von Neumann, Julika, Van Nieuwenhove, Erika, Terry, Lara E., Staels, Frederik, Knebel, Taylor R., Welkenhuyzen, Kirsten, Ahmadzadeh, Kourosh, Baker, Mariah R., Gerbaux, Margaux, Willemsen, Mathijs, Barber, John S., Serysheva, Irina I., De Waele, Liesbeth, Vermeulen, François, Schlenner, Susan, Meyts, Isabelle, Yule, David I., Bultynck, Geert, Schrijvers, Rik, Humblet-Baron, Stephanie, Liston, Adrian

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Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia von Van Nieuwenhove, Erika, Barber, John S, Neumann, Julika, Smeets, Elien, Willemsen, Mathijs, Pasciuto, Emanuela, Prezzemolo, Teresa, Lagou, Vasiliki, Seldeslachts, Laura, Malengier-Devlies, Bert, Metzemaekers, Mieke, Hassdenteufel, Sarah, Kerstens, Axelle, van der Kant, Rob, Rousseau, Frederic, Schymkowitz, Joost, Di Marino, Daniele, Lang, Sven, Zimmermann, Richard, Schlenner, Susan, Munck, Sebastian, Proost, Paul, Matthys, Patrick, Devalck, Christine, Boeckx, Nancy, Claessens, Frank, Wouters, Carine, Humblet-Baron, Stephanie, Meyts, Isabelle, Liston, Adrian

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LATE BREAKING NEWS E-POSTER PRESENTATION von Rönkkö, Julius, Molchanova, Svetlana, Revah-Politi, Anya, Pereira, Elaine, Auranen, Mari, Toppila, Jussi, Kvist, Jouni, Ludwig, Anastasia, Neumann, Julika, Humblet-Baron, Stephanie, Bultynck, Geert, Liston, Adrian, Patau, Anders, Rivera, Claudio, Harms, Matthew, Tyynismaa, Henna, Ylikallio, Emil

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