Publications 2005

Diagnostic genome profiling in mental retardation. de Vries BB, Pfundt R, Leisink M, Koolen DA, Vissers LE, Janssen IM, Reijmersdal S, Nillesen WM, Huys EH, Leeuw N, Smeets D, Sistermans EA, Feuth T, van Ravenswaaij-Arts CM, Geurts van Kessel A, Schoenmakers EF, Brunner HG, and Veltman JA.
Am.J.Hum.Genet., 77: 606-616 (2005).


Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications. Heidenblad M, Lindgren D, Veltman JA, Jonson T, Mahlamaki EH, Gorunova L, Geurts van Kessel A, Schoenmakers EF, and Hoglund M.
Oncogene, 24: 1794-1801 (2005).


CHARGE - Op jacht naar ziektegenen met behulp van array CGH. Janssen I, Veltman J.
Analyse, oktober (8): 224-228 (2005).

Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation Koolen DA, Reardon W, Rosser EM, Lacombe D, Hurst JA, Law CJ, Bongers EM, van Ravenswaaij-Arts CM, Leisink MA, Geurts van Kessel A, Veltman JA, and de Vries BB.
Eur.J.Hum.Genet., 13: 1019-1024 (2005).


Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses Cancer Genet. Magnani I, Moroni RF, Roversi G, Beghini A, Pfundt R, Schoenmakers EF, and Larizza L.
Cytogenet., 161: 140-145 (2005).


Identification of androgen-responsive genes that are alternatively regulated in androgen-dependent and androgen-independent rat prostate tumors.Pfundt R, Smit F, Jansen C, Aalders T, Straatman H, van der Vliet W, Isaacs J, Geurts van Kessel A, and Schalken J.
Genes Chromosomes Cancer, 43: 273-283 (2005).


Novel chromosomal imbalances in mantle cell lymphoma detected by genome-wide array-based comparative genomic hybridization Schraders M, Pfundt R, Straatman HM, Janssen IM, Geurts van Kessel A, Schoenmakers EF, van Krieken JH, and Groenen PJ.
Blood, 105: 1686-1693 (2005).


Identification of recurrent chromosomal aberrations in germ cell tumors of neonates and infants using genomewide array-based comparative genomic hybridization.Veltman I, Veltman J, Janssen I, Hulsbergen-van de KC, Oosterhuis W, Schneider D, Stoop H, Gillis A, Zahn S, Looijenga L, Gobel U, and Geurts van Kessel A.
Genes Chromosomes Cancer, 43: 367-376 (2005).


Identification of disease genes by whole genome CGH arrays. Vissers LE, Veltman JA, Geurts van Kessel A, and Brunner HG.
Hum.Mol.Genet., 14 Spec No. 2: R215-R223 (2005).