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dr. M.C.J. (Marjolijn) Jongmans

dr. M.C.J. (Marjolijn) Jongmans

Associate Professor - medical

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Research Output (89)

Incidence of and Risk Factors for Histologically Confirmed Solid Benign Tumors among Long-term Survivors of Childhood Cancer

Kok Judith L., Teepen Jop C., Van Der Pal Helena J., Van Leeuwen Flora E., Tissing Wim J.E., Neggers Sebastian J.C.M.M., Loonen Jacqueline J., Louwerens Marloes, Versluys Birgitta, Van Den Heuvel-Eibrink Marry M., Van Dulmen-Den Broeder Eline, Jaspers Monique M.W., Van Santen Hanneke M., Van Der Heiden-Van Der Loo Margriet, Janssens Geert O., Maduro John H., Bruggink Annette H., Jongmans Marjolijn C., Kremer Leontien C.M., Ronckers Cécile M. 1 May 2019, In: JAMA Oncology. 5 , p. 671-680 10 p.

De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism

Diets Illja J., van der Donk Roos, Baltrunaite Kristina, Waanders Esmé, Reijnders Margot R.F., Dingemans Alexander J.M., Pfundt Rolph, Vulto-van Silfhout Anneke T., Wiel Laurens, Gilissen Christian, Thevenon Julien, Perrin Laurence, Afenjar Alexandra, Nava Caroline, Keren Boris, Bartz Sarah, Peri Bethany, Beunders Gea, Verbeek Nienke, van Gassen Koen, Thiffault Isabelle, Cadieux-Dion Maxime, Huerta-Saenz Lina, Wagner Matias, Konstantopoulou Vassiliki, Vodopiutz Julia, Griese Matthias, Boel Annekatrien, Callewaert Bert, Brunner Han G., Kleefstra Tjitske, Hoogerbrugge Nicoline, de Vries Bert B.A., Hwa Vivian, Dauber Andrew, Hehir-Kwa Jayne Y., Kuiper Roland P., Jongmans Marjolijn C.J. 4 Apr 2019, In: American Journal of Human Genetics. 104 , p. 758-766 9 p.

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

Grolleman Judith E., de Voer Richarda M., Elsayed Fadwa A., Nielsen Maartje, Weren Robbert D.A., Palles Claire, Ligtenberg Marjolijn J.L., Vos Janet R., ten Broeke Sanne W., de Miranda Noel F.C.C., Kuiper Renske A., Kamping Eveline J., Jansen Erik A.M., Vink-Börger M. Elisa, Popp Isabell, Lang Alois, Spier Isabel, Hüneburg Robert, James Paul A., Li Na, Staninova Marija, Lindsay Helen, Cockburn David, Spasic-Boskovic Olivera, Clendenning Mark, Sweet Kevin, Capellá Gabriel, Sjursen Wenche, Høberg-Vetti Hildegunn, Jongmans Marjolijn C., Neveling Kornelia, Geurts van Kessel Ad, Morreau Hans, Hes Frederik J., Sijmons Rolf H., Schackert Hans K., Ruiz-Ponte Clara, Dymerska Dagmara, Lubinski Jan, Rivera Barbara, Foulkes William D., Tomlinson Ian P., Valle Laura, Buchanan Daniel D., Kenwrick Sue, Adlard Julian, Dimovski Aleksandar J., Campbell Ian G., Aretz Stefan, Schindler Detlev, 11 Feb 2019, In: Cancer Cell. 35 , p. 256-266.e5

TRIM28 haploinsufficiency predisposes to Wilms tumor

Diets Illja J., Hoyer Juliane, Ekici Arif B., Popp Bernt, Hoogerbrugge Nicoline, van Reijmersdal Simon V., Bhaskaran Rajith, Hadjihannas Michel, Vasileiou Georgia, Thiel Christian T., Seven Didem, Uebe Steffen, Ilencikova Denisa, Waanders Esmé, Mavinkurve-Groothuis Annelies M.C., Roeleveld Nel, de Krijger Ronald R., Wegert Jenny, Graf Norbert, Vokuhl Christian, Agaimy Abbas, Gessler Manfred, Reis André, Kuiper Roland P., Jongmans Marjolijn C.J., Metzler Markus 29 Jan 2019, In: International Journal of Cancer. 145 , p. 941-951 11 p.

Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis

Saes Joline L, Simons Annet, de Munnik Sonja A, Nijziel Marten R, Blijlevens Nicole M A, Jongmans Marjolijn C, van der Reijden Bert A, Smit Yolba, Brons Paul P, van Heerde Waander L, Schols Saskia E M 15 Nov 2018, In: Haemophilia. 25 , p. 127-135 9 p.

Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1:consensus guidelines for testing a child without malignancy

Suerink Manon, Ripperger Tim, Messiaen Ludwine, Menko Fred H, Bourdeaut Franck, Colas Chrystelle, Jongmans Marjolijn, Goldberg Yael, Nielsen Maartje, Muleris Martine, van Kouwen Mariëtte, Slavc Irene, Kratz Christian, Vasen Hans F, Brugiѐres Laurence, Legius Eric, Wimmer Katharina 10 Nov 2018, In: Journal of Medical Genetics. 56 , p. 53-62 10 p.

Clinical and Molecular Characteristics May Alter Treatment Strategies of Thyroid Malignancies in DICER1-syndrome

van der Tuin Karin, de Kock Leanne, Kamping Eveline J, Hannema Sabine E, Pouwels Marie-Jose M, Niedziela Marek, van Wezel Tom, Hes Frederik J, Jongmans Marjolijn C, Foulkes William D, Morreau Hans 26 Sep 2018, In: Journal of Clinical Endocrinology and Metabolism. 104 , p. 277-284 8 p.

Somatic reversion events point towards RPL4 as a novel disease gene in a condition resembling Diamond-Blackfan anemia

Jongmans Marjolijn C.J., Diets Illja J., Quarello Paola, Garelli Emanuela, Kuiper Roland P., Pfundt Rolph 13 Sep 2018, In: Haematologica. 103 , p. e607-e609

Severe positional central sleep apnea in an asymptomatic adult with a PHOX2B frameshift mutation

Janssen Hennie C J P, Vulto-van Silfhout Anneke T, Jongmans Marjolijn C J, van der Hout Annemieke H, Overeem Sebastiaan 15 Aug 2018, In: Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine. 14 , p. 1427-1430 4 p.

Colorectal Adenomas and Cancers After Childhood Cancer Treatment:A DCOG-LATER Record Linkage Study

Teepen J C, Kok Judith L, van Leeuwen Flora E, Tissing Wim J E, Dolsma Wil V, van der Pal Helena J, Loonen Jacqueline J, Bresters Dorine, Versluys A B, van den Heuvel-Eibrink Marry M, van Dulmen-den Broeder Eline, van den Berg Marleen H, van der Heiden-van der Loo Margriet, Hauptmann Michael, Jongmans M C, Overbeek L I, van de Vijver M J, Kremer L C M, Ronckers C M, Aleman B M P, van den Berg M H, Caron H N, Daniels L A, Dolsma W, van Dulmen-den Broeder E, Grootenhuis M A, Haasbeek C J, den Hartogh J G, Hauptmann M, van der Heiden-van der Loo M, van den Heuvel-Eibrink Marry M, Hollema N, Janssens G O, Jongmans M C, Jaspers M W M, Kok J L, van Leeuwen F E, Loonen J, Maduro J H, Neggers S J C M M, Oldenburger F, van der Pal H J, Postma A, Ronckers C M, Tersteeg R J, Tissing Wim J E, Versluys A B, Zsíros J, 1 Jul 2018, In: Journal of the National Cancer Institute. 110 , p. 758-767 10 p.

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