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A Westerveld
A Westerveld
Hoogleraar emeritus genetica AMC
Verified email at awesterveld.nl
Title
Cited by
Cited by
Year
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)
AI den Hollander, JB ten Brink, YJM de Kok, S van Soest, LI van den Born, ...
Nature genetics 23 (2), 217-221, 1999
5601999
Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma
H Caron, P Van Sluis, J De Kraker, J Bökkerink, M Egeler, G Laureys, ...
New England Journal of Medicine 334 (4), 225-230, 1996
4911996
Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10
M van Duin, J de Wit, H Odijk, A Westerveld, A Yasui, MHM Koken, ...
Cell 44 (6), 913-923, 1986
4161986
Retinitis pigmentosa: defined from a molecular point of view
S Van Soest, A Westerveld, PTVM De Jong, EM Bleeker-Wagemakers, ...
Survey of ophthalmology 43 (4), 321-334, 1999
3671999
Molecular cloning of a human DNA repair gene
A Westerveld, JHJ Hoeijmakers, M Van Duin, J De Wit, H Odijk, A Pastink, ...
Nature 310 (5976), 425-429, 1984
3671984
Loss of human genetic markers in man-Chinese hamster somatic cell hybrids
A Westerveld, R Visser, PM Khan, D Bootsma
Nature New Biology 234 (44), 20-24, 1971
2271971
Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS
J Bliek, SM Maas, JM Ruijter, RCM Hennekam, M Alders, A Westerveld, ...
Human molecular genetics 10 (5), 467-476, 2001
2132001
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using …
S Brul, A Westerveld, A Strijland, RJ Wanders, AW Schram, HS Heymans, ...
The Journal of clinical investigation 81 (6), 1710-1715, 1988
2011988
High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered
JMN Hoovers, M Mannens, R John, J Bliek, V Van Heyningen, ...
Genomics 12 (2), 254-263, 1992
1901992
Human Antigen and Enzyme Markers in Man-Chinese Hamster Somatic Cell Hybrids: Evidence for Synteny Between the HL-A, PGM3, ME1, and IPO-B Loci
H Someren, A Westerveld, A Hagemeijer, JR Mees, PM Khan, ...
Proceedings of the National Academy of Sciences 71 (3), 962-965, 1974
1881974
Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N–myc amplification
H Caron, P van Sluis, M van Hoeve, J de Kraker, J Bras, R Slater, ...
Nature genetics 4 (2), 187-190, 1993
1811993
Molecular cloning of the human DNA excision repair gene ERCC-6
C Troelstra, H Odijk, J De Wit, A Westerveld, LH Thompson, D Bootsma, ...
Molecular and cellular biology, 1990
1641990
Evidence for two tumour suppressor loci on chromosomal bands 1p35–36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification
H Caron, M Peter, P van Sluis, F Speleman, J de Kraker, G Laureys, ...
Human molecular genetics 4 (4), 535-539, 1995
1621995
Molecular cloning and biological characterization of the human excision repair gene ERCC-3
G Weeda, RCA van Ham, R Masurel, AW Veld, H Odijk, J de Wit, ...
Molecular and cellular biology, 1990
1511990
Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids: Assignment of PGM3 to chromosome C6 and regional mapping of …
A Jongsma, H van Someren, A Westerveld, A Hagemeijer, P Pearson
Humangenetik 20, 195-202, 1973
1511973
Assignment of the gene coding for human β-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies
RA Barneveld, W Keiizer, FPW Tegelaers, EI Ginns, AG van Kessel, ...
Human genetics 64, 227-231, 1983
1471983
Parental imprinting of human chromosome region 11p15. 3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
M Mannens, JMN Hoovers, E Redeker, M Verjaal, AP Feinberg, P Little, ...
European Journal of Human Genetics 2 (1), 3-23, 1994
1401994
Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification.
NC Cheng, N Van Roy, A Chan, M Beitsma, A Westerveld, F Speleman, ...
Oncogene 10 (2), 291-297, 1995
1391995
Maintenance of vascular endothelial cell-specific properties after immortalization with an amphotrophic replication-deficient retrovirus containing human papilloma virus 16 E6 …
R Fontijn, C Hop, HJ Brinkman, R Slater, A Westerveld, JA van Mourik, ...
Experimental cell research 216 (1), 199-207, 1995
1381995
Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma
MAJA Hermsen, H Joenje, F Arwert, MJP Welters, BJM Braakhuis, ...
Genes, Chromosomes and Cancer 15 (1), 1-9, 1996
1351996
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