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 | 561 | 1999 |
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 | 492 | 1996 |
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 | 416 | 1986 |
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 | 367 | 1999 |
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 | 367 | 1984 |
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 | 227 | 1971 |
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 | 213 | 2001 |
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 | 201 | 1988 |
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 | 191 | 1992 |
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 | 188 | 1974 |
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 | 181 | 1993 |
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 | 164 | 1990 |
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 | 162 | 1995 |
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 | 152 | 1990 |
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 | 151 | 1973 |
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 | 147 | 1983 |
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 | 140 | 1994 |
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 | 139 | 1995 |
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 | 138 | 1995 |
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 | 135 | 1996 |