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

Researcher/Postdoc

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Research Output (30)

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

Monosomy 20 mosaicism revealed by extensive karyotyping in blood and skin cells:Case report and review of the literature

Hochstenbach Ron, Krijtenburg Pieter Jaap, Van Der Veken Lars T., Van Der Smagt Jasper, Roeleveld-Versteegh Angelique, Visser Gepke, Terhal Paulien 1 jan 2014, In: Cytogenetic and Genome Research. 144 , p. 155-162 8 p.

Elevated Infant Mortality Rate among Dutch Oral Cleft Cases: A Retrospective Analysis from 1997 to 2011

van Nunen D.P., van den Boogaard M.J.H., Don Griot J.P., Rüttermann M., van der Veken L.T.J.N., Breugem C.C. 2014, In: Frontiers in Genetics [E]. 1

Novel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure

van der Veken L.T.J.N., Bierings M.B., Maiburg M.C., Groenendaal F., Bloem A.C., Knoers N.V.A.M., Buijs A. 13 jun 2013,

Novel Bone Marrow Failure Syndrome Due to a Deletion of the EVI1/Mecom

van der Veken L.T.J.N., Bierings M.B., Maiburg M.C., Groenendaal F., Bloem A.C., Knoers N.V.A.M., Buijs A. 8 dec 2012,

Novel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure

van der Veken L.T.J.N. 6 nov 2012,

KIAA1524:A novel MLL translocation partner in acute myeloid leukemia

Coenen Eva A., Zwaan C. Michel, Meyer Claus, Marschalek Rolf, Pieters Rob, van der Veken Lars T., Beverloo H. Berna, Van den Heuvel-Eibrink Marry M. 1 jan 2011, In: Leukemia Research. 35 , p. 133-135 3 p.

Array CGH in Human Leukemia: From Somatics to Genetics

van der Veken L.T.J.N., Buijs A. 2011, In: Cytogenetic and Genome Research. 135 , p. 260-270 11 p.

Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies

Van Der Veken Lars T., Dieleman Marianne M J, Douben Hannie, Van De Brug Judith C., Van De Graaf Raoul, Hoogeboom A. Jeannette M, Poddighe Pino J., De Klein Annelies 13 jul 2010, In: Molecular Cytogenetics. 3