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dr. ing. G. (Lars) van der Hondebrink

dr. ing. G. (Lars) van der Hondebrink

Researcher/Postdoc
dr. ing. G. (Lars) van der Hondebrink
  • Section genome diagnostics

Research Programs

Strategic Program Cancer

Research Output (34)

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.

Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome)

Monroe Glen R, Kappen Isabelle Fpm, Stokman Marijn F, Terhal Paulien A, van den Boogaard Marie-José H, Savelberg Sanne Mc, van der Veken Lars T, van Es Robert J J, Lens Susanne M, Hengeveld Rutger C, Creton Marijn A, Janssen Nard G, Mink van der Molen Aebele B, Ebbeling Michelle B, Giles Rachel H, Knoers Nine V, van Haaften Gijs 17 Aug 2016, In: European Journal of Human Genetics. 24 , p. 1752–1760

Tetraploid/Diploid Mosaicism in Cultured Genital Skin Fibroblasts:Is It Causally Related to Penoscrotal Hypospadias

Giltay Jacques C., Klijn Aart J., de Jong Tom P V M, Kats Peter, van Breugel Marjolein, Lens Susan, Vromans Martijn, Van Der Veken Lars T., Hochstenbach Ron 1 Jul 2016, In: Molecular Syndromology. 7 , p. 153-159 7 p.

An unique case of a mosaic genome-wide uniparental isodisomy in a newborn with Beckwith-Wiedemann syndrome

van der Veken LTJN, Hochstenbach PFR, Verrijn Stuart AA, Giltay JC, Hopman SMJ 5 Apr 2016,

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