Antigen Receptor Galaxy: A User-Friendly, Web-Based Tool for Analysis and Visualization of T and B Cell Receptor Repertoire Data

Por IJspeert, Hanna, van Schouwenburg, Pauline A., van Zessen, David, Pico-Knijnenburg, Ingrid, Stubbs, Andrew P., van der Burg, Mirjam
Publicado no J Immunol (2017)

Evaluation of the Antigen-Experienced B-Cell Receptor Repertoire in Healthy Children and Adults

Por IJspeert, Hanna, van Schouwenburg, Pauline A., van Zessen, David, Pico-Knijnenburg, Ingrid, Driessen, Gertjan J., Stubbs, Andrew P., van der Burg, Mirjam
Publicado no Front Immunol (2016)

Identification of CVID Patients With Defects in Immune Repertoire Formation or Specification

Por van Schouwenburg, Pauline A., IJspeert, Hanna, Pico-Knijnenburg, Ingrid, Dalm, Virgil A. S. H., van Hagen, P. Martin, van Zessen, David, Stubbs, Andrew P., Patel, Smita Y., van der Burg, Mirjam
Publicado no Front Immunol (2018)

Functional Analysis of the Anti-adalimumab Response Using Patient-derived Monoclonal Antibodies

Por van Schouwenburg, Pauline A., Kruithof, Simone, Votsmeier, Christian, van Schie, Karin, Hart, Margreet H., de Jong, Rob N., van Buren, Esther E. L., van Ham, Marieke, Aarden, Lucien, Wolbink, Gertjan, Wouters, Diana, Rispens, Theo
Publicado no J Biol Chem (2014)

Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE

Por Kienzler, Anne-Kathrin, van Schouwenburg, Pauline A., Taylor, John, Marwah, Ishita, Sharma, Richa U., Noakes, Charlotte, Thomson, Kate, Sadler, Ross, Segal, Shelley, Ferry, Berne, Taylor, Jenny C., Blair, Edward, Chapel, Helen, Patel, Smita Y.
Publicado no Clin Immunol (2016)

Repertoire Sequencing of B Cells Elucidates the Role of UNG and Mismatch Repair Proteins in Somatic Hypermutation in Humans

Por IJspeert, Hanna, van Schouwenburg, Pauline A., Pico-Knijnenburg, Ingrid, Loeffen, Jan, Brugieres, Laurence, Driessen, Gertjan J., Blattmann, Claudia, Suerink, Manon, Januszkiewicz-Lewandowska, Danuta, Azizi, Amedeo A., Seidel, Marcus G., Jacobs, Heinz, van der Burg, Mirjam
Publicado no Front Immunol (2019)

Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders

Por van Schouwenburg, Pauline A., Davenport, Emma E., Kienzler, Anne-Kathrin, Marwah, Ishita, Wright, Benjamin, Lucas, Mary, Malinauskas, Tomas, Martin, Hilary C., Lockstone, Helen E., Cazier, Jean-Baptiste, Chapel, Helen M., Knight, Julian C., Patel, Smita Y.
Publicado no Clin Immunol (2015)

A kindred with Mutant IKAROS and autoimmunity.

Por Van Nieuwenhove, Erika, Garcia-Perez, Josselyn E., Helsen, Christine, Rodriguez, Princess D., van Schouwenburg, Pauline A., Dooley, James, Schlenner, Susan, van der Burg, Mirjam, Verhoeyen, Els, Gijsbers, Rik, Frietze, Seth, Schjerven, Hilde, Meyts, Isabelle, Claessens, Frank, Humblet-Baron, Stephanie, Wouters, Carine, Liston, Adrian
Publicado no J Allergy Clin Immunol (2018)

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

Por Taylor, Jenny C, Martin, Hilary C, Lise, Stefano, Broxholme, John, Cazier, Jean-Baptiste, Rimmer, Andy, Kanapin, Alexander, Lunter, Gerton, Fiddy, Simon, Allan, Chris, Aricescu, A. Radu, Attar, Moustafa, Babbs, Christian, Becq, Jennifer, Beeson, David, Bento, Celeste, Bignell, Patricia, Blair, Edward, Buckle, Veronica J, Bull, Katherine, Cais, Ondrej, Cario, Holger, Chapel, Helen, Copley, Richard R, Cornall, Richard, Craft, Jude, Dahan, Karin, Davenport, Emma E, Dendrou, Calliope, Devuyst, Olivier, Fenwick, Aimée L, Flint, Jonathan, Fugger, Lars, Gilbert, Rodney D, Goriely, Anne, Green, Angie, Greger, Ingo H., Grocock, Russell, Gruszczyk, Anja V, Hastings, Robert, Hatton, Edouard, Higgs, Doug, Hill, Adrian, Holmes, Chris, Howard, Malcolm, Hughes, Linda, Humburg, Peter, Johnson, David, Karpe, Fredrik, Kingsbury, Zoya, Kini, Usha, Knight, Julian C, Krohn, Jonathan, Lamble, Sarah, Langman, Craig, Lonie, Lorne, Luck, Joshua, McCarthy, Davis, McGowan, Simon J, McMullin, Mary Frances, Miller, Kerry A, Murray, Lisa, Németh, Andrea H, Nesbit, M Andrew, Nutt, David, Ormondroyd, Elizabeth, Oturai, Annette Bang, Pagnamenta, Alistair, Patel, Smita Y, Percy, Melanie, Petousi, Nayia, Piazza, Paolo, Piret, Sian E, Polanco-Echeverry, Guadalupe, Popitsch, Niko, Powrie, Fiona, Pugh, Chris, Quek, Lynn, Robbins, Peter A, Robson, Kathryn, Russo, Alexandra, Sahgal, Natasha, van Schouwenburg, Pauline A, Schuh, Anna, Silverman, Earl, Simmons, Alison, Sørensen, Per Soelberg, Sweeney, Elizabeth, Taylor, John, Thakker, Rajesh V, Tomlinson, Ian, Trebes, Amy, Twigg, Stephen RF, Uhlig, Holm H, Vyas, Paresh, Vyse, Tim, Wall, Steven A, Watkins, Hugh, Whyte, Michael P, Witty, Lorna, Wright, Ben, Yau, Chris, Buck, David, Humphray, Sean, Ratcliffe, Peter J, Bell, John I, Wilkie, Andrew OM, Bentley, David, Donnelly, Peter, McVean, Gilean
Publicado no Nat Genet (2015)