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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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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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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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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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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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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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, Francois, Schlenner, Susan, Meyts, Isabelle, Yule, David, Bultynck, Geert, Schrijvers, Rik, Humblet-Baron, Stephanie, Liston, Adrian

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LATE BREAKING NEWS E-POSTER PRESENTATION: LBP 3 Dominant mutations in ITPR3 cause Charcot-Marie-Tooth disease 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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IP3R3 variants as novel form of hereditary disorders von Neumann, Julika

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A cross entropy test allows quantitative statistical comparison of t-SNE and UMAP representations von Roca, Carlos P., Burton, Oliver T., Neumann, Julika, Tareen, Samar, Whyte, Carly E., Gergelits, Vaclav, Veiga, Rafael V., Humblet-Baron, Stéphanie, Liston, Adrian

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A cross entropy test allows quantitative statistical comparison of t-SNE and UMAP representations von Roca, Carlos P, Burton, Oliver T, Neumann, Julika, Tareen, Samar, Whyte, Carly E, Gergelits, Vaclav, Veiga, Rafael V, Humblet-Baron, Stephanie, Liston, Adrian

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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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Missense mutations in inositol 1,4,5-trisphosphate receptor type 3 result in leaky Ca 2+ channels and activation of store-operated Ca 2+ 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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Author Correction: Disrupted Ca 2+ homeostasis and immunodeficiency in patients with functional IP 3 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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