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

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

Researcher/Postdoc

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Research Output (38)

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,

De Novo Trisomy 1q10q23.3 Mosaicism Causes Microcephaly, Severe Developmental Delay, and Facial Dysmorphic Features but No Cardiac Anomalies

Lo-A-Njoe Shirley, van der Veken Lars T, Vermont Clementien, Rafael-Croes Louise, Keizer Vincent, Hochstenbach Ron, Knoers Nine, van Haelst Mieke M 6 Jan 2016, In: Case reports in genetics. 2016 , p. 1-5

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

van der Veken LTJN, Hochstenbach P., Verrijn Stuart AA, Giltay JC, Hopman SMJ 2016,

Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring

de Pagter MS, van Roosmalen Markus J., Baas AF, Renkens Ivo, Duran KJ, van Binsbergen E, Tavakoli-Yaraki Masoumeh, Hochstenbach PFR, van der Veken LTJN, Cuppen EPJG, Kloosterman WP 8 Jun 2015,

Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring

de Pagter MS, van Roosmalen Markus J., Baas AF, Renkens Ivo, Duran KJ, van Binsbergen E, Tavakoli-Yaraki Masoumeh, Hochstenbach PFR, van der Veken LTJN, Cuppen EPJG, Kloosterman WP 22 Apr 2015,

Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring

de Pagter Mirjam S., van Roosmalen Markus J., Baas AF, Renkens I.J., Duran KJ, van Binsbergen E, Tavakoli-Yaraki Masoumeh, Hochstenbach Ron, van der Veken Lars T., Cuppen Edwin, Kloosterman Wigard P. 2 Apr 2015, In: American Journal of Human Genetics. 96 , p. 651-656 6 p.

Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management

Bayindir Baran, Dehaspe Luc, Brison Nathalie, Brady Paul, Ardui Simon, Kammoun Molka, van der Veken Lars, Lichtenbelt Klaske, van den Bogaert Kris, van Houdt Jeroen, Peeters Hilde, van Esch Hilde, de Ravel Thomy, Legius Eric, Devriendt Koen, Vermeesch Joris R. 14 Jan 2015, In: European Journal of Human Genetics. 23 , p. 1286-1293

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