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dr. L.T.J.N. (Lars) van der Veken

dr. L.T.J.N. (Lars) van der Veken

Researcher/Postdoc
dr. L.T.J.N. (Lars) van der Veken
  • Section genome diagnostics

Research Programs

Strategic Program Cancer

Research Output (37)

Prolonged Disease Course of COVID-19 in a Patient with CTLA-4 Haploinsufficiency

Hoffman T W, Leavis H L, Smits B M, van der Veken L T, van Kessel D A 22 May 2023, In: Case reports in immunology. 2023 7 p.

Heterozygous Variants in the DNA-binding Domain of c-Myb May Affect Normal B/T Cell Development

Smits Bas M., Hartley Taila, Dünnebach Ester, Bartels Marije, Boycott Kim M., Kernohan Kirstin D., Dyment David A., Giltay Jacques C., Haddad Elie, Jarinova Olga, Van Montfrans Joris, Van Royen-Kerkhof Annet, Van Der Veken Lars T., De Witte Moniek, Nierkens Stefan, Pham-Huy Anne, Leavis Helen L. 21 Oct 2022, In: HemaSphere. 6 , p. E774

Genetic care in geographically isolated small island communities:8 years of experience in the Dutch Caribbean

Verberne Eline A, Westermann Jonne M, de Vries Tamar I, Ecury-Goossen Ginette M, Lo-A-Njoe Shirley M, Manshande Meindert E, Faries Sonja, Veenhuis Hans D, Philippi Patricia, Falix Farah A, Rosina-Angelista Irsa, Ponson-Wever Maria, Rafael-Croes Louise, Thorsen Patricia, Arends Eric, de Vroomen Maartje, Nagelkerke Sietse Q, Tilanus Martijn, van der Veken Lars T, Huijsdens-van Amsterdam Karin, van der Kevie-Kersemaekers Anne-Marie, Alders Mariëlle, Mannens Marcel M A M, van Haelst Mieke M 7 Mar 2022, In: American Journal of Medical Genetics. Part A. 188 , p. 1777-1791 15 p.

Implementation of Early Next-Generation Sequencing for Inborn Errors of Immunity:A Prospective Observational Cohort Study of Diagnostic Yield and Clinical Implications in Dutch Genome Diagnostic Centers

Elsink Kim, Huibers Manon M.H., Hollink Iris H.I.M., Simons Annet, Zonneveld-Huijssoon Evelien, van der Veken Lars T., Leavis Helen L., Henriet Stefanie S.V., van Deuren Marcel, van de Veerdonk Frank L., Potjewijd Judith, Berghuis Dagmar, Dalm Virgil A.S.H., Vermont Clementien L., van de Ven Annick A.J.M., Lambeck Annechien J.A., Abbott Kristin M., van Hagen P. Martin, de Bree Godelieve J., Kuijpers Taco W., Frederix Geert W.J., van Gijn Mariëlle E., van Montfrans Joris M., 21 Dec 2021, In: Frontiers in Immunology. 12

Adult-onset autoinflammation caused by somatic mutations in UBA1:A Dutch case series of patients with VEXAS

van der Made Caspar I, Potjewijd Judith, Hoogstins Annemiek, Willems Huub P J, Kwakernaak A J, de Sevaux Ruud G L, van Daele Paul L A, Simons Annet, Heijstek Marloes, Beck David B, Netea Mihai G, van Paassen Pieter, Hak A E, van der Veken Lars T, van Gijn Marielle E, Hoischen Alexander, van der Veerdonk Frank L, Leavis Helen L, Rutgers Abraham 25 May 2021, In: The Journal of Allergy and Clinical Immunology. 149 , p. 432-439.e4

ERAP2 Increases the Abundance of a Peptide Submotif Highly Selective for the Birdshot Uveitis-Associated HLA-A29

Venema Wouter J, Hiddingh Sanne, de Boer Joke H, Claas Frans H J, Mulder Arend, den Hollander Anneke I, Stratikos Efstratios, Sarkizova Siranush, van der Veken Lars T, Janssen George M C, van Veelen Peter A, Kuiper Jonas J W 25 Feb 2021, In: Frontiers in Immunology. 12 15 p.

National external quality assessment for next-generation sequencing-based diagnostics of primary immunodeficiencies

Elsink Kim, Huibers Manon M H, Hollink Iris H I M, van der Veken Lars T, Ernst Robert F, Simons Annet, Zonneveld-Huijssoon Evelien, van der Hout Annemieke H, Abbott Kristin M, Hoischen Alexander, Pieterse Marc, Kuijpers Taco W, van Montfrans Joris M, van Gijn Mariëlle E 2020, In: European Journal of Human Genetics. 29 , p. 20-28 9 p.

Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3’ MECOM

van der Veken Lars T., Maiburg Merel C., Groenendaal Floris, van Gijn Mariëlle E., Bloem Andries C., Erpelinck Claudia, Gröschel Stefan, Sanders Mathijs A., Delwel Ruud, Bierings Marc B., Buijs Arjan 8 Feb 2018, In: Haematologica. 103 , p. e173-e176

The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs

Loviglio Maria Nicla, Arbogast Thomas, Jønch Aia Elise, Collins Stephan C., Popadin Konstantin, Bonnet Camille S., Giannuzzi Giuliana, Maillard Anne M., Jacquemont Sébastien, Loviglio Maria Nicla, Jønch Aia Elise, Popadin Konstantin, Giannuzzi Giuliana, Maillard Anne M., Fagerberg Christina, Andersen Charlotte Brasch, Doco-Fenzy Martine, Delrue Marie-Ange, Faivre Laurence, Arveiler Benoit, Geneviève David, Schneider Anouck, Gerard Marion, Andrieux Joris, El Chehadeh Salima, Schaefer Elise, Depienne Christel, Van Haelst Mieke, Brilstra Eva H., Van Binsbergen Ellen, van Harssel Jeske, van der Veken Lars T., Gusella James F, Shen Yiping, Mitchell Elyse, Kini Usha, Hawkes Lara, Campbell Carolyn, Butschi Florence Niel, Addor Marie Claude, Beckmann Jacques S., Jacquemont Sébastien, Reymond Alexandre, Yalcin Binnaz, Katsanis Nicholas, Golzio Christelle, Reymond Alexandre, 5 Oct 2017, In: American Journal of Human Genetics. 101 , p. 564-577 14 p.

Lymphoblastic lymphoma with a triple-hit profile:a rare but distinct and relevant entity

Hiemcke-Jiwa Laura S., Leguit RJ, van der Veken Lars T., Buijs A, Leeuwis JW, de Boer Mirthe, Jiwa Mehdi, Bloem AC, Clevers-Petersen E.J., de Weger Roel A., Huibers Manon M.H. May 2017, In: Human Pathology. 63 , p. 171-176 6 p.

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