P. Tuijnenburg MD publications

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Publications MD P. Tuijnenburg

Position
Research Associate
Main activities
Research
Specialisation
Primary Immunodeficiencies, B cells
Focus of research

Investigating the cellular phenotype and function of lymphocytes in primary immunodeficiencies and determine normal B cell development and differentiation in healthy individuals.

2020

  • Lorenzini Tiziana, Fliegauf Manfred, Klammer Nils, Frede Natalie, Proietti Michele, Bulashevska Alla, Camacho-Ordonez Nadezhda, Varjosalo Markku, Kinnunen Matias, de Vries Esther, van der Meer Jos W. M., Ameratunga Rohan, Roifman Chaim M., Schejter Yael D., Kobbe Robin, Hautala Timo, Atschekzei Faranaz, Schmidt Reinhold E., Schröder Claudia, Stepensky Polina, Shadur Bella, Pedroza Luis A., van der Flier Michiel, Martínez-Gallo M. nica, Gonzalez-Granado Luis Ignacio, Allende Luis M., Shcherbina Anna, Kuzmenko Natalia, Zakharova Victoria, Neves João Farela, Svec Peter, Fischer Ute, Ip Winnie, Bartsch Oliver, Barış Safa, Klein Christoph, Geha Raif, Chou Janet, Alosaimi Mohammed, Weintraub Lauren, Boztug Kaan, Hirschmugl Tatjana, Dos Santos Vilela Maria Marluce, Holzinger Dirk, Seidl Maximilian, Lougaris Vassilios, Plebani Alessandro, Alsina Laia, Tuijnenburg Paul, Kuijpers Taco W. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations Journal of allergy and clinical immunology 2020;146 (4):901-911 [PubMed]
  • Tuijnenburg Paul Deconstructing B cell responses: Lessons learned from development, drugs and deficiencies 2020. 254p. ISBN 9789463756297. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Kuijpers T. W.; Co-supervisors: van Leeuwen Ester, de Bree G.)
  • Tuijnenburg Paul, aan de Kerk Daan J., Jansen Machiel H., Morris Ben, Lieftink Cor, Beijersbergen Roderick L., van Leeuwen Ester M. M., Kuijpers Taco W. High-throughput compound screen reveals mTOR inhibitors as potential therapeutics to reduce (auto)antibody production by human plasma cells European journal of immunology 2020;50 (1):73-85 [PubMed]
  • Thaventhiran James E. D., Lango Allen Hana, Burren Oliver S., Rae William, Greene Daniel, Staples Emily, Zhang Zinan, Farmery James H. R., Simeoni Ilenia, Rivers Elizabeth, Maimaris Jesmeen, Penkett Christopher J., Stephens Jonathan, Deevi Sri V. V., Sanchis-Juan Alba, Gleadall Nicholas S., Thomas Moira J., Sargur Ravishankar B., Gordins Pavels, Baxendale Helen E., Brown Matthew, Tuijnenburg Paul, Worth Austen, Hanson Steven, Linger Rachel J., Buckland Matthew S., Rayner-Matthews Paula J., Gilmour Kimberly C., Samarghitean Crina, Seneviratne Suranjith L., Sansom David M., Lynch Andy G., Megy Karyn, Ellinghaus Eva, Ellinghaus David, Jorgensen Silje F., Karlsen Tom H., Stirrups Kathleen E., Cutler Antony J., Kumararatne Dinakantha S., Chandra Anita, Edgar J. David M., Herwadkar Archana, Cooper Nichola, Grigoriadou Sofia, de Bree Godelieve J., Kuijpers Taco W., Sivapalaratnam Suthesh, Walsh Roddy, Kuijpers Taco W. Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1) Nature 2020;584 (7819):E2 [PubMed]
  • Thaventhiran James E. D., Lango Allen Hana, Burren Oliver S., Rae William, Greene Daniel, Staples Emily, Zhang Zinan, Farmery James H. R., Simeoni Ilenia, Rivers Elizabeth, Maimaris Jesmeen, Penkett Christopher J., Stephens Jonathan, Deevi Sri V. V., Sanchis-Juan Alba, Gleadall Nicholas S., Thomas Moira J., Sargur Ravishankar B., Gordins Pavels, Baxendale Helen E., Brown Matthew, Tuijnenburg Paul, Worth Austen, Hanson Steven, Linger Rachel J., Buckland Matthew S., Rayner-Matthews Paula J., Gilmour Kimberly C., Samarghitean Crina, Seneviratne Suranjith L., Sansom David M., Lynch Andy G., Megy Karyn, Ellinghaus Eva, Ellinghaus David, Jorgensen Silje F., Karlsen Tom H., Stirrups Kathleen E., Cutler Antony J., Kumararatne Dinakantha S., Chandra Anita, Edgar J. David M., Herwadkar Archana, Cooper Nichola, Grigoriadou Sofia, de Bree Godelieve J., Kuijpers Taco W., Sivapalaratnam Suthesh, Walsh Roddy, Kuijpers Taco W. Whole-genome sequencing of a sporadic primary immunodeficiency cohort Nature 2020;583 (7814):90-95 [PubMed]

2019

  • Volpi Stefano, Cicalese Maria Pia, Tuijnenburg Paul, Tool Anton T. J., Cuadrado Eloy, Abu-Halaweh Marwan, Ahanchian Hamid, Alzyoud Raed, Akdemir Zeynep Coban, Barzaghi Federica, Blank Alexander, Boisson Bertrand, Bottino Cristina, Brigida Immacolata, Caorsi Roberta, Casanova Jean-Laurent, Chiesa Sabrina, Chinn Ivan Kingyue, Dückers Gregor, Enders Anselm, Erichsen Hans Christian, Forbes Lisa R., Gambin Tomasz, Gattorno Marco, Karimiani Ehsan Ghayoor, Giliani Silvia, Gold Michael S., Jacobsen Eva-Maria, Jansen Machiel H., King Jovanka R., Laxer Ronald M., Lupski James R., Mace Emily, Marcenaro Stefania, Maroofian Reza, Meijer Alexander B., Niehues Tim, Notarangelo Luigi D., Orange Jordan, Pannicke Ulrich, Pearson Chris, Picco Paolo, Quinn Patrick J., Schulz Ansgar, Seeborg Filiz, Stray-Pedersen Asbjørg, Tawamie Hasan, van Leeuwen Ester M. M., Aiuti Alessandro, Yeung Rae, Schwarz Klaus, Kuijpers Taco W. A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency Journal of allergy and clinical immunology 2019;143 (6):2296-2299 [PubMed]
  • Tuijnenburg Paul, Lango Allen Hana, de Bree Godelieve J., Savic Sinisa, Jansen Machiel H., Stockdale Claire, Simeoni Ilenia, ten Berge Ineke J. M., van Leeuwen Ester M. M., Thaventhiran James E., Kuijpers Taco W. Pathogenic NFKB2 variant in the ankyrin repeat domain (R635X) causes a variable antibody deficiency Clinical immunology (Orlando, Fla.) 2019;203:23-27 [PubMed]

2018

  • Tuijnenburg Paul, Lango Allen Hana, Burns Siobhan O., Greene Daniel, Jansen Machiel H., Staples Emily, Stephens Jonathan, Carss Keren J., Biasci Daniele, Baxendale Helen, Thomas Moira, Chandra Anita, Kiani-Alikhan Sorena, Longhurst Hilary J., Seneviratne Suranjith L., Oksenhendler Eric, Simeoni Ilenia, de Bree Godelieve J., Tool Anton T. J., van Leeuwen Ester M. M., Ebberink Eduard H. T. M., Meijer Alexander B., Tuna Salih, Whitehorn Deborah, Brown Matthew, Turro Ernest, Thrasher Adrian J., Smith Kenneth G. C., Thaventhiran James E., Kuijpers Taco W. Loss of function NFKB1 variants are the most common monogenic cause of CVID in Europeans Journal of allergy and clinical immunology 2018;142 (4):1285-1296 [PubMed]

2017

  • Tuijnenburg Paul, Cuadrado Eloy, Bosch Annet M., Kindermann Angelika, Jansen Machiel H., Alders Marielle, van Leeuwen Ester M. M., Kuijpers Taco W. Humoral Immunodeficiency with Hypotonia, Feeding Difficulties, enteropathy, and Mild eczema Caused by a Classical FOXP3 Mutation Frontiers in pediatrics 2017;5:37 [PubMed]
  • Oud Machteld M., Tuijnenburg Paul, Hempel Maja, van Vlies Naomi, Ren Zemin, Ferdinandusse Sacha, Jansen Machiel H., Santer René, Johannsen Jessika, Bacchelli Chiara, Alders Marielle, Li Rui, Davies Rosalind, Dupuis Lucie, Cale Catherine M., Wanders Ronald J. A., Pals Steven T., Ocaka Louise, James Chela, Müller Ingo, Lehmberg Kai, Strom Tim, Engels Hartmut, Williams Hywel J., Beales Phil, Roepman Ronald, Dias Patricia, Brunner Han G., Cobben Jan-Maarten, Hall Christine, Hartley Taila, Le Quesne Stabej Polona, Mendoza-Londono Roberto, Davies E. Graham, de Sousa Sérgio B., Lessel Davor, Arts Heleen H., Kuijpers Taco W. Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome American journal of human genetics 2017;100 (2):281-296 [PubMed]
  • Vasanthakumar Ajithkumar, Liao Yang, teh Peggy, Pascutti Maria F., Oja Anna E., Garnham Alexandra L., Gloury Renee, Tempany Jessica C., Sidwell Tom, Cuadrado Eloy, Tuijnenburg Paul, Kuijpers Taco W., Lalaoui Najoua, Mielke Lisa A., Bryant Vanessa L., Hodgkin Philip D., Silke John, Smyth Gordon K., Nolte Martijn A., Shi Wei, Kallies Axel The TNF Receptor Superfamily-NF-kappa B Axis Is Critical to Maintain Effector Regulatory T Cells in Lymphoid and Non-lymphoid Tissues Cell reports 2017;20 (12):2906-2920 [PubMed]