Publications 2003 & younger


Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities. Vissers LE, de Vries BB, Osoegawa K, Janssen IM, Feuth T, Choy CO, Straatman H, van der Vliet W, Huys EH, van Rijk A, Smeets D, van Ravenswaaij-Arts CM, Knoers NV, van der Burgt I, de Jong PJ, Brunner HG, Geurts van Kessel A, Schoenmakers EF, and Veltman JA.
Am.J.Hum.Genet., 73: 1261-1270 (2003).

Role of gain of 12p in germ cell tumour development. Looijenga LH, Zafarana G, Grygalewicz B, Summersgill B, Debiec-Rychter M, Veltman J, Schoenmakers EF, Rodriguez S, Jafer O, Clark J, Geurts van Kessel A, Shipley J, van Gurp RJ, Gillis AJ, and Oosterhuis JW.
APMIS, 111: 161-171 (2003).

Human mitochondrial complex I deficiency: investigating transcriptional responses by microarray. van der Westhuizen FH, van den Heuvel LP, Smeets R, Veltman JA, Pfundt R, Geurts van Kessel AG, Ursing BM, and Smeitink JA.
Neuropediatrics, 34: 14-22 (2003).

Chromosomal breakpoint mapping by arrayCGH using flow-sorted chromosomes. Veltman IM, Veltman JA, Arkesteijn G, Janssen IM, Vissers LE, de Jong PJ, Geurts van Kessel A, and Schoenmakers EF
Biotechniques, 35: 1066-1070 (2003).

Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH. Veltman JA, Jonkers Y, Nuijten I, Janssen I, van der Vliet W, Huys E, Vermeesch J, van Bruggenhout G, Fryns JP, Admiraal R, Terhal P, Lacombe D, Geurts van Kessel A, Smeets D, Schoenmakers EF, and van Ravenswaaij-Arts CM.
Am.J.Hum.Genet., 72: 1578-1584 (2003).

Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors. Veltman JA, Fridlyand J, Pejavar S, Olshen AB, Korkola JE, de Vries S, Carroll P, Kuo WL, Pinkel D, Albertson D, Cordon-Cardo C, Jain AN, and Waldman FM.
Cancer Res., 63: 2872-2880 (2003)

12p-amplicon structure analysis in testicular germ cell tumors of adolescents and adults by array CGH. Zafarana G, Grygalewicz B, Gillis AJ, Vissers LE, van der Vliet W, van Gurp RJ, Stoop H, Debiec-Rychter M, Oosterhuis JW, Geurts van Kessel A, Schoenmakers EF, Looijenga LH, and Veltman JA.
Oncogene, 22: 7695-7701 (2003).

Before 2003

Array-based comparative genomic hybridization for the differential diagnosis of renal cell cancer. Wilhelm M, Veltman JA, Olshen AB, Jain AN, Moore DH, Presti JC Jr., Kovacs G, and Waldman FM.
Cancer Res., 62: 957-960 (2002).

High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization. Veltman JA, Schoenmakers EF, Eussen BH, Janssen I, Merkx G, van Cleef B, van Ravenswaaij CM, Brunner HG, Smeets D, and Geurts van Kessel A.
Am.J.Hum.Genet., 70: 1269-1276 (2002).

Specific steps in aneuploidization correlate with LOH of 9p21, 17p13 and 18q21 in the progression of premalignant laryngeal lesions. Veltman JA, van de Weert I, Aubele M, Bot FJ, Ramaekers FCS, Manni JJ, Hopman AHN.
International Journal of Cancer, 91: 193-199 (2001).

Mapping of resection margins of oral cancer for p53 overexpression and chromosome instability to detect residual (pre)malignant cells. van der Toorn PP, Veltman JA, Bot FJ, de Jong JM, Manni JJ, Ramaekers FC, and Hopman AH
J.Pathol., 193: 66-72 (2001).

Chromosome instability as an indicator of malignant progression in laryngeal mucosa. Veltman JA, Bot FJ, Huynen FC, Ramaekers FC, Manni JJ, and Hopman AH.
J.Clin.Oncol., 18: 1644-1651 (2000).

Double-target fluorescence in situ hybridization distinguishes multiple genetically aberrant clones in head and neck squamous cell carcinoma. Veltman JA, Hopman AH, van der Vliet W, Bot FJ, Ramaekers FC, and Manni JJ
Cytometry, 34: 113-120 (1998).

Detection of chromosomal aberrations in cytologic brush specimens from head and neck squamous cell carcinoma. Veltman JA, Hopman AH, Bot FJ, Ramaekers FC, and Manni JJ.
Cancer, 81: 309-314 (1997).

Anomalies of the CD8+ T cell pool in haemochromatosis: HLA-A3-linked expansions of CD8+ Clin.Exp. Arosa FA, Oliveira L, Porto G, da Silva BM, Kruijer W, Veltman J, and de Sousa M.
Immunol., 107: 548-554 (1997).