T‐cell lymphoblastic lymphoma in constitutional mismatch repair deficiency (CMMRD): Exploring treatment opportunities
Kroeze, Emma, Weijers, Dilys D., Kleisman, Michelle M., Ilan, Uri, Bladergroen, Reno S., Hagelaar, Rico, Meijerink, Jules P. P., Jongmans, Marjolijn C. J., Loeffen, Jan L. C., Kuiper, Roland P.
Published in HemaSphere (01.05.2024)
Published in HemaSphere (01.05.2024)
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Combined occurrence of filaggrin mutations and IL-10 or IL-13 polymorphisms predisposes to atopic dermatitis
Lesiak, Aleksandra, Kuna, Piotr, Zakrzewski, Marcin, van Geel, Michael, Bladergroen, Reno S., Przybylowska, Karolina, Stelmach, Iwona, Majak, Pawel, Hawro, Tomasz, Sysa-Jedrzejowska, Anna, Narbutt, Joanna
Published in Experimental dermatology (01.06.2011)
Published in Experimental dermatology (01.06.2011)
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Novel Mutations in the BHD Gene and Absence of Loss of Heterozygosity in Fibrofolliculomas of Birt-Hogg-Dubé Patients
van Steensel, Maurice A.M., Verstraeten, Valerie L.R.M., Frank, Jorge, Kelleners-Smeets, Nicole W.J., Poblete-Gutiérrez, Pamela, Marcus-Soekarman, Dominique, Bladergroen, Reno S., Steijlen, Peter M., van Geel, Michel
Published in Journal of investigative dermatology (01.03.2007)
Published in Journal of investigative dermatology (01.03.2007)
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Digenic Inheritance of Mutations in the Coproporphyrinogen Oxidase and Protoporphyrinogen Oxidase Genes in a Unique Type of Porphyria
van Tuyll van Serooskerken, Anne Moniek, de Rooij, Felix W., Edixhoven, Annie, Bladergroen, Reno S., Baron, Jens M., Joussen, Sylvia, Merk, Hans F., Steijlen, Peter M., Poblete-Gutiérrez, Pamela, te Velde, Kornelis, Paul Wilson, J.H., Koole, Rita H., van Geel, Michel, Frank, Jorge
Published in Journal of investigative dermatology (01.11.2011)
Published in Journal of investigative dermatology (01.11.2011)
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Mutational and transcriptional landscape of pediatric B-cell precursor lymphoblastic lymphoma
Kroeze, Emma, Iaccarino, Ingram, Kleisman, Michelle M., Mondal, Mayukh, Beder, Thomas, Khouja, Mouhamad, Höppner, Marc P., Scheijde-Vermeulen, Marijn A., Kester, Lennart A., Brüggemann, Monika, Baldus, Claudia D., Cario, Gunnar, Bladergroen, Reno S., Garnier, Nathalie, Attarbaschi, Andishe, Verdu-Amorós, Jaime, Sutton, Rosemary, Macintyre, Elizabeth, Scholten, Kenneth, Arias Padilla, Laura, Burkhardt, Birgit, Beishuizen, Auke, den Boer, Monique L., Kuiper, Roland P., Loeffen, Jan L. C., Boer, Judith M., Klapper, Wolfram
Published in Blood (04.07.2024)
Published in Blood (04.07.2024)
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Hereditary multiple cutaneous leiomyoma resulting from novel mutations in the fumarate hydratase gene
Badeloe, Sadhanna, Bladergroen, Reno S, Jonkman, Marcel F, Burrows, Nigel P, Steijlen, Peter M, Poblete-Gutiérrez, Pamela, van Steensel, Maurice A.M, van Geel, Michel, Frank, Jorge
Published in Journal of dermatological science (01.08.2008)
Published in Journal of dermatological science (01.08.2008)
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A recurrent mutation in variegate porphyria patients from Chile and Sweden: Evidence for a common genetic background?
Serooskerken, Anne Moniek van Tuyll van, Ernst, Manon, Bladergroen, Reno S, Wolff, Carlos, Floderus, Ylva, Harper, Pauline, Poblete-Gutiérrez, Pamela, van Geel, Michel, Frank, Jorge
Published in Journal of dermatological science (01.01.2011)
Published in Journal of dermatological science (01.01.2011)
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Biallelic inactivation of protoporphyrinogen oxidase and hydroxymethylbilane synthase is associated with liver cancer in acute porphyrias
Schneider-Yin, Xiaoye, van Tuyll van Serooskerken, Anne-Moon, Siegesmund, Marko, Went, Philip, Barman-Aksözen, Jasmin, Bladergroen, Reno S, Komminoth, Paul, Cloots, Roy H.E, Winnepenninckx, Véronique J, zur Hausen, Axel, Weber, Markus, Driessen, Ann, Poblete-Gutiérrez, Pamela, Bauer, Peter, Schroeder, Christopher, van Geel, Michel, Minder, Elisabeth I, Frank, Jorge
Published in Journal of hepatology (01.03.2015)
Published in Journal of hepatology (01.03.2015)
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Comparison of clinical selection-based genetic testing with phenotype-agnostic extensive germline sequencing to diagnose genetic predisposition in children with cancer: a prospective diagnostic study
Bakhuizen, Jette J, van Dijk, Freerk, Koudijs, Marco J, Bladergroen, Reno S, Bon, Sebastian B B, Hopman, Saskia M J, Kester, Lennart A, Kranendonk, Mariëtte E G, Loeffen, Jan L C, Smetsers, Stephanie E, Sonneveld, Edwin, Tachdjian, Melissa, de Vos-Kerkhof, Evelien, Goudie, Catherine, Merks, Johannes H M, Kuiper, Roland P, Jongmans, Marjolijn C J
Published in The lancet child & adolescent health (01.10.2024)
Published in The lancet child & adolescent health (01.10.2024)
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Phenotypic variation in epidermolytic ichthyosis: clinical and functional evaluation of the novel p.(Met339Lys) mutation in the L12 domain of KRT1
Nellen, Ruud G. L., Nagtzaam, Ivo F., Hoogeboom, A. Jeannette M., Bladergroen, Reno S., Jonkman, Marcel F., Steijlen, Peter M., van Steensel, Maurice A. M., van Geel, Michel
Published in Experimental dermatology (01.11.2015)
Published in Experimental dermatology (01.11.2015)
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A Phenotype Resembling the Clouston Syndrome with Deafness Is Associated with a Novel Missense GJB2 Mutation
van Steensel, Maurice A.M., Steijlen, Peter M., Bladergroen, Reno S., Hoefsloot, Elisabeth H., van Ravenswaaij-Arts, Connie M., van Geel, Michel
Published in Journal of investigative dermatology (01.08.2004)
Published in Journal of investigative dermatology (01.08.2004)
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Functional Analysis of FLT4 Mutations Associated with Nonne–Milroy Lymphedema
Verstraeten, Valerie L.R.M., Holnthoner, Wolfgang, van Steensel, Maurice A.M., Veraart, Joep C.J.M., Bladergroen, Reno S., Heckman, Caroline A., Keskitalo, Salla, Frank, Jorge, Alitalo, Kari, van Geel, Michel, Steijlen, Peter M.
Published in Journal of investigative dermatology (01.02.2009)
Published in Journal of investigative dermatology (01.02.2009)
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Protein output for DNA computing
Henkel, Christian V., Bladergroen, Reno S., Balog, Crina I. A., Deelder, André M., Head, Tom, Rozenberg, Grzegorz, Spaink, Herman P.
Published in Natural computing (01.01.2005)
Published in Natural computing (01.01.2005)
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Phenotypic variation in epidermolytic ichthyosis: clinical and functional evaluation of the novel p.(Met339Lys) mutation in the L12 domain of KRT 1
Nellen, Ruud G. L., Nagtzaam, Ivo F., Hoogeboom, A. Jeannette M., Bladergroen, Reno S., Jonkman, Marcel F., Steijlen, Peter M., van Steensel, Maurice A. M., van Geel, Michel
Published in Experimental dermatology (01.11.2015)
Published in Experimental dermatology (01.11.2015)
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Combined occurrence of filaggrin mutations and IL-10 or IL-13 polymorphisms predisposes to atopic dermatitis: Filaggrin mutations and IL-10 or IL-13 polymorphisms
Lesiak, Aleksandra, Kuna, Piotr, Zakrzewski, Marcin, van Geel, Michael, Bladergroen, Reno S., Przybylowska, Karolina, Stelmach, Iwona, Majak, Pawel, Hawro, Tomasz, Sysa-Jedrzejowska, Anna, Narbutt, Joanna
Published in Experimental dermatology (01.06.2011)
Published in Experimental dermatology (01.06.2011)
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T-cell lymphoblastic lymphoma compared with T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Kroeze, Emma, Kleisman, Michelle M., Hagelaar, Rico, Bladergroen, Reno S., Kester, Lennart A., Scheijde-Vermeulen, Marijn A., van Dijk, Freerk, Meijerink, Jules P. P., Kuiper, Roland P., Loeffen, Jan L. C.
Published in Blood Neoplasia (01.09.2024)
Published in Blood Neoplasia (01.09.2024)
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Phenotypic variation in epidermolytic ichthyosis: clinical and functional evaluation of the novel p.(Met339Lys) mutation in the L12 domain of KRT1
Nellen, Ruud G L, Nagtzaam, Ivo F, Hoogeboom, A Jeannette M, Bladergroen, Reno S, Jonkman, Marcel F, Steijlen, Peter M, van Steensel, Maurice A M, van Geel, Michel
Published in Experimental dermatology (01.11.2015)
Published in Experimental dermatology (01.11.2015)
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Hereditary multiple cutaneous leiomyoma resulting from novel mutations in the fumarate hydratase gene
Badeloe, Sadhanna, Bladergroen, Reno S, Jonkman, Marcel F, Burrows, Nigel P, Steijlen, Peter M, Poblete-Gutiérrez, Pamela, van Steensel, Maurice A M, van Geel, Michel, Frank, Jorge
Published in Journal of dermatological science (01.08.2008)
Published in Journal of dermatological science (01.08.2008)
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Functional analysis of FLT4 mutations associated with Nonne-Milroy lymphedema
Verstraeten, Valerie L R M, Holnthoner, Wolfgang, van Steensel, Maurice A M, Veraart, Joep C J M, Bladergroen, Reno S, Heckman, Caroline A, Keskitalo, Salla, Frank, Jorge, Alitalo, Kari, van Geel, Michel, Steijlen, Peter M
Published in The Journal of investigative dermatology (01.02.2009)
Published in The Journal of investigative dermatology (01.02.2009)
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