Andries Westerveld - Publications

Affiliations: 
University of Amsterdam, Amsterdam, Netherlands 
Area:
human genetics

163 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2009 Bliek J, Alders M, Maas SM, Oostra RJ, Mackay DM, van der Lip K, Callaway JL, Brooks A, van 't Padje S, Westerveld A, Leschot NJ, Mannens MM. Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells. European Journal of Human Genetics : Ejhg. 17: 1625-34. PMID 19513094 DOI: 10.1038/ejhg.2009.77  0.72
2008 Ruigrok YM, Wijmenga C, Rinkel GJ, van't Slot R, Baas F, Wolfs M, Westerveld A, Roos YB. Genomewide linkage in a large Dutch family with intracranial aneurysms: replication of 2 loci for intracranial aneurysms to chromosome 1p36.11-p36.13 and Xp22.2-p22.32. Stroke; a Journal of Cerebral Circulation. 39: 1096-102. PMID 18309175 DOI: 10.1161/STROKEAHA.107.495168  0.72
2004 Roos YB, Pals G, Struycken PM, Rinkel GJ, Limburg M, Pronk JC, van den Berg JS, Luijten JA, Pearson PL, Vermeulen M, Westerveld A. Genome-wide linkage in a large Dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13. Stroke; a Journal of Cerebral Circulation. 35: 2276-81. PMID 15331791 DOI: 10.1161/01.STR.0000141415.28155.46  0.72
2003 Struycken PM, Pals G, Limburg M, Pronk JC, Wijmenga C, Pearson PL, Luijten JA, van den Berg JS, Vermeulen M, Rinkel GJ, Westerveld A. Anticipation in familial intracranial aneurysms in consecutive generations. European Journal of Human Genetics : Ejhg. 11: 737-43. PMID 14512962 DOI: 10.1038/sj.ejhg.5201039  0.72
2002 van Dartel M, Cornelissen PW, Redeker S, Tarkkanen M, Knuutila S, Hogendoorn PC, Westerveld A, Gomes I, Bras J, Hulsebos TJ. Amplification of 17p11.2 approximately p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma. Cancer Genetics and Cytogenetics. 139: 91-6. PMID 12550767 DOI: 10.1016/S0165-4608(02)00627-1  0.72
2001 Ratsma JE, Van Stelt OD, Schoffelmeer ANM, Westerveld A, Boudewijn Gunning W. P3 event-related potential, dopamine D2 receptor A1 allele, and sensation-seeking in adult children of alcoholics Alcoholism: Clinical and Experimental Research. 25: 960-967. PMID 11505019  0.72
2001 Luijten M, Redeker S, Minoshima S, Shimizu N, Westerveld A, Hulsebos TJ. Duplication and transposition of the NF1 pseudogene regions on chromosomes 2, 14, and 22. Human Genetics. 109: 109-16. PMID 11479742 DOI: 10.1007/s004390100543  0.72
2001 Luijten M, Fahsold R, Mischung C, Westerveld A, Nürnberg P, Hulsebos TJ. Limited contribution of interchromosomal gene conversion to NF1 gene mutation. Journal of Medical Genetics. 38: 481-5. PMID 11476066  0.72
2001 van den Berg JS, Limburg M, Pals G, Arwert F, Westerveld A. Type III collagen deficiency in a family with intracranial aneurysms. Cerebrovascular Diseases (Basel, Switzerland). 11: 92-4. PMID 11223659 DOI: 10.1159/000047618  0.72
2001 Bliek J, Maas SM, Ruijter JM, Hennekam RC, Alders M, Westerveld A, Mannens MM. Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS. Human Molecular Genetics. 10: 467-76. PMID 11181570  0.72
2000 Luijten M, Redeker S, van Noesel MM, Troost D, Westerveld A, Hulsebos TJ. Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas. European Journal of Human Genetics : Ejhg. 8: 939-45. PMID 11175282 DOI: 10.1038/sj.ejhg.5200565  0.72
2000 Steenman MJ, Zijlstra N, Kruitbosch DL, Wiesmeijer C, Larizza L, Voûte PA, Westerveld A, Mannens MM. Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors. Cytogenetics and Cell Genetics. 88: 289-95. PMID 10828613  0.72
2000 Luijten M, Wang Y, Smith BT, Westerveld A, Smink LJ, Dunham I, Roe BA, Hulsebos TJ. Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22. European Journal of Human Genetics : Ejhg. 8: 209-14. PMID 10780787 DOI: 10.1038/sj.ejhg.5200434  0.72
2000 Alders M, Ryan A, Hodges M, Bliek J, Feinberg AP, Privitera O, Westerveld A, Little PF, Mannens M. Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome. American Journal of Human Genetics. 66: 1473-84. PMID 10762538 DOI: 10.1086/302892  0.72
2000 Steenman M, Westerveld A, Mannens M. Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways. Genes, Chromosomes & Cancer. 28: 1-13. PMID 10738297 DOI: 10.1002/(SICI)1098-2264(200005)28:1<1::AID-GCC1>3.0.CO;2-#  0.72
1999 van der Drift P, Chan A, Zehetner G, Westerveld A, Versteeg R. Multiple MSP pseudogenes in a local repeat cluster on 1p36.2: An expanding genomic graveyard? Genomics. 62: 74-81. PMID 10585770 DOI: 10.1006/geno.1999.5972  0.72
1999 Hulsebos TJ, Oskam NT, Bijleveld EH, Westerveld A, Hermsen MA, van den Ouweland AM, Hamel BC, Tijssen CC. Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2. British Journal of Cancer. 81: 1150-4. PMID 10584875 DOI: 10.1038/sj.bjc.6690822  0.72
1999 Steenman M, Tomlinson G, Westerveld A, Mannens M. Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma. Cytogenetics and Cell Genetics. 86: 157-61. PMID 10545709  0.72
1999 den Hollander AI, ten Brink JB, de Kok YJ, van Soest S, van den Born LI, van Driel MA, van de Pol DJ, Payne AM, Bhattacharya SS, Kellner U, Hoyng CB, Westerveld A, Brunner HG, Bleeker-Wagemakers EM, Deutman AF, et al. Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12). Nature Genetics. 23: 217-21. PMID 10508521 DOI: 10.1038/13848  0.72
1999 van den Berg JS, Pals G, Arwert F, Hennekam RC, Albrecht KW, Westerveld A, Limburg M. Type III collagen deficiency in saccular intracranial aneurysms. Defect in gene regulation? Stroke; a Journal of Cerebral Circulation. 30: 1628-31. PMID 10436112  0.72
1999 van Soest S, van Rossem MJ, Heckenlively JR, van den Born LI, de Meulemeester TM, Vliex S, de Jong PT, Bleeker-Wagemakers EM, Westerveld A, Bergen AA. Integrated genetic and physical map of the 1q31-->q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenes. Cytogenetics and Cell Genetics. 84: 22-7. PMID 10343093  0.72
1999 van Soest S, Westerveld A, de Jong PT, Bleeker-Wagemakers EM, Bergen AA. Retinitis pigmentosa: defined from a molecular point of view. Survey of Ophthalmology. 43: 321-34. PMID 10025514 DOI: 10.1016/S0039-6257(98)00046-0  0.72
1998 van den Berg JS, Limburg M, Kappelle LJ, Pals G, Arwert F, Westerveld A. The role of type III collagen in spontaneous cervical arterial dissections. Annals of Neurology. 43: 494-8. PMID 9546331 DOI: 10.1002/ana.410430413  0.72
1997 Hermsen MA, Joenje H, Arwert F, Braakhuis BJ, Baak JP, Westerveld A, Slater R. Assessment of chromosomal gains and losses in oral squamous cell carcinoma by comparative genomic hybridisation. Oral Oncology. 33: 414-8. PMID 9509125  0.72
1997 van den Berg JS, Limburg M, Pals G, Arwert F, Westerveld A, Hennekam RC, Albrecht KW. Some patients with intracranial aneurysms have a reduced type III/type I collagen ratio. A case-control study. Neurology. 49: 1546-51. PMID 9409344  0.72
1997 Voesten AM, Bijleveld EH, Westerveld A, Hulsebos TJ. Fine mapping of a region of common deletion on chromosome arm 10p in human glioma. Genes, Chromosomes & Cancer. 20: 167-72. PMID 9331567 DOI: 10.1002/(SICI)1098-2264(199710)20:2<167::AID-GCC7>3.0.CO;2-1  0.72
1997 Steenman M, Redeker B, de Meulemeester M, Wiesmeijer K, Voûte PA, Westerveld A, Slater R, Mannens M. Comparative genomic hybridization analysis of Wilms tumors. Cytogenetics and Cell Genetics. 77: 296-303. PMID 9284942  0.72
1997 Alders M, Hodges M, Hadjantonakis AK, Postmus J, van Wijk I, Bliek J, de Meulemeester M, Westerveld A, Guillemot F, Oudejans C, Little P, Mannens M. The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts. Human Molecular Genetics. 6: 859-67. PMID 9175731 DOI: 10.1093/hmg/6.6.859  0.72
1997 Hulsebos TJ, Bijleveld EH, Oskam NT, Westerveld A, Leenstra S, Hogendoorn PC, Bras J. Malignant astrocytoma-derived region of common amplification in chromosomal band 17p12 is frequently amplified in high-grade osteosarcomas. Genes, Chromosomes & Cancer. 18: 279-85. PMID 9087567 DOI: 10.1002/(SICI)1098-2264(199704)18:4<279::AID-GCC5>3.0.CO;2-Y  0.72
1996 Cheng NC, Beitsma M, Chan A, Op den Camp I, Westerveld A, Pronk J, Versteeg R. Lack of class I HLA expression in neuroblastoma is associated with high N-myc expression and hypomethylation due to loss of the MEMO-1 locus. Oncogene. 13: 1737-44. PMID 8895520  0.72
1996 Cheng NC, Chan AJ, Beitsma MM, Speleman F, Westerveld A, Versteeg R. A human modifier of methylation for class I HLA genes (MEMO-1) maps to chromosomal bands 1p35-36.1. Human Molecular Genetics. 5: 309-17. PMID 8852654 DOI: 10.1093/hmg/5.3.309  0.72
1996 Alders M, Bliek J, Redeker B, Ryan A, Feinberg A, Westerveld A, Little P, Mannens M. Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors. Medical and Pediatric Oncology. 27: 495-7. PMID 8827080 DOI: 10.1002/(SICI)1096-911X(199611)27:5<495::AID-MPO18>3.0.CO;2-9  0.72
1996 Mannens M, Alders M, Redeker B, Bliek J, Steenman M, Wiesmeyer C, de Meulemeester M, Ryan A, Kalikin L, Voûte T, De Kraker J, Hoovers J, Slater R, Feinberg A, Little P, ... Westerveld A, et al. Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors. Medical and Pediatric Oncology. 27: 490-4. PMID 8827079 DOI: 10.1002/(SICI)1096-911X(199611)27:5<490::AID-MPO17>3.0.CO;2-E  0.72
1996 Hermsen MA, Joenje H, Arwert F, Welters MJ, Braakhuis BJ, Bagnay M, Westerveld A, Slater R. Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma. Genes, Chromosomes & Cancer. 15: 1-9. PMID 8824719 DOI: 10.1002/(SICI)1098-2264(199601)15:1<1::AID-GCC1>3.0.CO;2-8  0.72
1996 Sijbers AM, van der Spek PJ, Odijk H, van den Berg J, van Duin M, Westerveld A, Jaspers NG, Bootsma D, Hoeijmakers JH. Mutational analysis of the human nucleotide excision repair gene ERCC1. Nucleic Acids Research. 24: 3370-80. PMID 8811092  0.72
1996 Hofstra RM, Cheng NC, Hansen C, Stulp RP, Stelwagen T, Clausen N, Tommerup N, Caron H, Westerveld A, Versteeg R, Buys CH. No mutations found by RET mutation scanning in sporadic and hereditary neuroblastoma. Human Genetics. 97: 362-4. PMID 8786083 DOI: 10.1007/s004390050052  0.72
1996 van Soest S, te Nijenhuis S, van den Born LI, Bleeker-Wagemakers EM, Sharp E, Sandkuijl LA, Westerveld A, Bergen AA. Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC). Cytogenetics and Cell Genetics. 73: 81-5. PMID 8646891  0.72
1996 Caron H, van Sluis P, Buschman R, Pereira do Tanque R, Maes P, Beks L, de Kraker J, Voûte PA, Vergnaud G, Westerveld A, Slater R, Versteeg R. Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus. Human Genetics. 97: 834-7. PMID 8641706 DOI: 10.1007/s004390050146  0.72
1996 Caron H, van Sluis P, de Kraker J, Bökkerink J, Egeler M, Laureys G, Slater R, Westerveld A, Voûte PA, Versteeg R. Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. The New England Journal of Medicine. 334: 225-30. PMID 8531999 DOI: 10.1056/NEJM199601253340404  0.72
1995 Hoovers JM, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, Steenman M, Benedict M, Wiegant J, Lengauer C, Taillon-Miller P, Schlessinger D, Edwards MC, Elledge SJ, ... ... Westerveld A, et al. Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proceedings of the National Academy of Sciences of the United States of America. 92: 12456-60. PMID 8618920 DOI: 10.1073/pnas.92.26.12456  0.72
1995 Hulsebos TJ, Gilbert DJ, Delattre O, Smink LJ, Dunham I, Westerveld A, Thomas G, Jenkins NA, Copeland NG. Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5. Genomics. 29: 712-8. PMID 8575764 DOI: 10.1006/geno.1995.9947  0.72
1995 van der Drift P, Chan A, Laureys G, van Roy N, Sickmann G, den Dunnen J, Westerveld A, Speleman F, Versteeg R. Balanced translocation in a neuroblastoma patient disrupts a cluster of small nuclear RNA U1 and tRNA genes in chromosomal band 1p36. Genes, Chromosomes & Cancer. 14: 35-42. PMID 8527382 DOI: 10.1002/gcc.2870140107  0.72
1995 Redeker E, Alders M, Hoovers JM, Richard CW, Westerveld A, Mannens M. Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3. Cytogenetics and Cell Genetics. 68: 222-5. PMID 7842740  0.72
1995 Cheng NC, Van Roy N, Chan A, Beitsma M, Westerveld A, Speleman F, Versteeg R. 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. Oncogene. 10: 291-7. PMID 7838528  0.72
1995 Fontijn R, Hop C, Brinkman HJ, Slater R, Westerveld A, van Mourik JA, Pannekoek H. Maintenance of vascular endothelial cell-specific properties after immortalization with an amphotrophic replication-deficient retrovirus containing human papilloma virus 16 E6/E7 DNA. Experimental Cell Research. 216: 199-207. PMID 7813621 DOI: 10.1006/excr.1995.1025  0.72
1995 Caron H, Peter M, van Sluis P, Speleman F, de Kraker J, Laureys G, Michon J, Brugières L, Voûte PA, Westerveld A. Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification. Human Molecular Genetics. 4: 535-9. PMID 7633401 DOI: 10.1093/hmg/4.4.535  0.72
1995 Bijlsma EK, Merel P, Fleury P, van Asperen CJ, Westerveld A, Delattre O, Thomas G, Hulsebos TJ. Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 gene. Human Genetics. 96: 1-5. PMID 7607639 DOI: 10.1007/BF00214177  0.72
1995 Pronk JC, Gibson RA, Savola A, Wijker M, Morgan NV, Melchionda S, Ford D, Temtamy S, Ortega JJ, Jansen S, Havenga C, Cohn RJ, De Ravel TJ, Roberts I, Westerveld A, et al. Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3 Nature Genetics. 11: 338-340. PMID 7581462  0.72
1995 Versteeg R, Caron H, Cheng NC, van der Drift P, Slater R, Westerveld A, Voûte PA, Delattre O, Laureys G, Van Roy N. 1p36: every subband a suppressor? European Journal of Cancer (Oxford, England : 1990). 31: 538-41. PMID 7576962 DOI: 10.1016/0959-8049(95)00037-J  0.72
1995 Bijlsma EK, Voesten AM, Bijleveld EH, Troost D, Westerveld A, Mérel P, Thomas G, Hulsebos TJ. Molecular analysis of genetic changes in ependymomas. Genes, Chromosomes & Cancer. 13: 272-7. PMID 7547635 DOI: 10.1002/gcc.2870130407  0.72
1994 Caron H, van Sluis P, van Roy N, de Kraker J, Speleman F, Voûte PA, Westerveld A, Slater R, Versteeg R. Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity. American Journal of Human Genetics. 55: 341-7. PMID 8037211  0.72
1994 van Soest S, van den Born LI, Gal A, Farrar GJ, Bleeker-Wagemakers LM, Westerveld A, Humphries P, Sandkuijl LA, Bergen AA. Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population. Genomics. 22: 499-504. PMID 8001962 DOI: 10.1006/geno.1994.1422  0.72
1994 Redeker E, Hoovers JM, Alders M, van Moorsel CJ, Ivens AC, Gregory S, Kalikin L, Bliek J, de Galan L, van den Bogaard R. An integrated physical map of 210 markers assigned to the short arm of human chromosome 11. Genomics. 21: 538-50. PMID 7959730 DOI: 10.1006/geno.1994.1312  0.72
1994 Leenstra S, Bijlsma EK, Troost D, Oosting J, Westerveld A, Bosch DA, Hulsebos TJ. Allele loss on chromosomes 10 and 17p and epidermal growth factor receptor gene amplification in human malignant astrocytoma related to prognosis. British Journal of Cancer. 70: 684-9. PMID 7917918 DOI: 10.1038/bjc.1994.373  0.72
1994 van der Drift P, Chan A, van Roy N, Laureys G, Westerveld A, Speleman F, Versteeg R. A multimegabase cluster of snRNA and tRNA genes on chromosome 1p36 harbours an adenovirus/SV40 hybrid virus integration site. Human Molecular Genetics. 3: 2131-6. PMID 7881409 DOI: 10.1093/hmg/3.12.2131  0.72
1994 Bijlsma EK, Merel P, Bosch DA, Westerveld A, Delattre O, Thomas G, Hulsebos TJ. Analysis of mutations in the SCH gene in schwannomas. Genes, Chromosomes & Cancer. 11: 7-14. PMID 7529050  0.72
1994 Bijlsma EK, Leenstra S, Westerveld A, Bosch DA, Hulsebos TJ. Amplification of the anonymous marker D17S67 in malignant astrocytomas. Genes, Chromosomes & Cancer. 9: 148-52. PMID 7513547  0.72
1993 De Schepper GG, Vander Perk C, Westerveld A, Oosting J, Van Noorden CJ. In situ glucose-6-phosphate dehydrogenase activity during development of pre-implantation mouse embryos. The Histochemical Journal. 25: 299-303. PMID 8491670 DOI: 10.1007/BF00159121  0.72
1993 Hoovers JM, Redeker E, Speleman F, Höppener JW, Bhola S, Bliek J, van Roy N, Leschot NJ, Westerveld A, Mannens M. High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members. Genomics. 15: 525-9. PMID 8468047 DOI: 10.1006/geno.1993.1104  0.72
1993 Caron H, van Sluis P, van Hoeve M, de Kraker J, Bras J, Slater R, Mannens M, Voûte PA, Westerveld A, Versteeg R. Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification. Nature Genetics. 4: 187-90. PMID 8102298 DOI: 10.1038/ng0693-187  0.72
1993 Bijlsma EK, Delattre O, Juyn JA, Melot T, Westerveld A, Dumanski JP, Thomas G, Hulsebos TJ. Regional fine mapping of the beta crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2. Genes, Chromosomes & Cancer. 8: 112-8. PMID 7504514  0.72
1992 Hoovers JM, Mannens M, John R, Bliek J, van Heyningen V, Porteous DJ, Leschot NJ, Westerveld A, Little PF. High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered. Genomics. 12: 254-63. PMID 1740334 DOI: 10.1016/0888-7543(92)90372-Y  0.72
1992 Bijlsma EK, Brouwer-Mladin R, Bosch DA, Westerveld A, Hulsebos TJ. Molecular characterization of chromosome 22 deletions in schwannomas. Genes, Chromosomes & Cancer. 5: 201-5. PMID 1384671 DOI: 10.1002/gcc.2870050305  0.72
1992 Leenstra S, Troost D, Westerveld A, Bosch DA, Hulsebos TJ. Molecular characterization of areas with low grade tumor or satellitosis in human malignant astrocytomas. Cancer Research. 52: 1568-72. PMID 1311634  0.72
1991 Hulsebos TJ, Bijlsma EK, Geurts van Kessel AH, Brakenhoff RH, Westerveld A. Direct assignment of the human beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2. Cytogenetics and Cell Genetics. 56: 171-5. PMID 2055112 DOI: 10.1159/000133080  0.72
1991 Arwert F, Rooimans MA, Westerveld A, Simons JW, Zdzienicka MZ. The Chinese hamster cell mutant V-H4 is homologous to Fanconi anemia (complementation group A). Cytogenetics and Cell Genetics. 56: 23-6. PMID 1900747 DOI: 10.1159/000133038  0.72
1991 Mannens M, Hoovers JMN, Bleeker-Wagemakers EM, Redeker E, Bliek J, Overbeeke-Melkert M, Saunders G, Williams B, van Heynigen V, Junien C, Haber D, Speleman F, Heyting C, Slater RM, Leschot NJ, ... Westerveld A, et al. The distal region of 11p13 and associated genetic diseases Genomics. 11: 284-293. PMID 1769647 DOI: 10.1016/0888-7543(91)90134-Z  0.72
1991 Hulsebos TJ, Oostra BA, Broersen S, Smits A, van Oost BA, Westerveld A. New distal marker closely linked to the fragile X locus. Human Genetics. 87: 369-72. PMID 1677926 DOI: 10.1007/BF00200922  0.72
1991 Devilee P, van den Broek M, Mannens M, Slater R, Cornelisse CJ, Westerveld A, Khan PM. Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhood. International Journal of Cancer. Journal International Du Cancer. 47: 817-21. PMID 1672665  0.72
1990 Bolhuis PA, Bleeker-Wagemakers EM, Ponne NJ, Van Schooneveld MJ, Westerveld A, Van den Bogert C, Tabak HF. Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy. Biochemical and Biophysical Research Communications. 170: 994-7. PMID 2390098 DOI: 10.1016/0006-291X(90)90490-E  0.72
1990 Tager JM, Brul S, Wiemer EA, Strijland A, Van Driel R, Schutgens RB, Van den Bosch H, Wanders RJ, Westerveld A. Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes. Progress in Clinical and Biological Research. 321: 545-58. PMID 2183242  0.72
1990 Klein B, Pastink A, Odijk H, Westerveld A, van der Eb AJ. Transformation and immortalization of diploid xeroderma pigmentosum fibroblasts. Experimental Cell Research. 191: 256-62. PMID 2175267 DOI: 10.1016/0014-4827(90)90012-Y  0.72
1990 Troelstra C, Odijk H, de Wit J, Westerveld A, Thompson LH, Bootsma D, Hoeijmakers JH. Molecular cloning of the human DNA excision repair gene ERCC-6. Molecular and Cellular Biology. 10: 5806-13. PMID 2172786  0.72
1990 Mannens M, Devilee P, Bliek J, Mandjes I, de Kraker J, Heyting C, Slater RM, Westerveld A. Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11. Cancer Research. 50: 3279-83. PMID 2159377  0.72
1990 Weeda G, van Ham RC, Masurel R, Westerveld A, Odijk H, de Wit J, Bootsma D, van der Eb AJ, Hoeijmakers JH. Molecular cloning and biological characterization of the human excision repair gene ERCC-3. Molecular and Cellular Biology. 10: 2570-81. PMID 2111438  0.72
1990 Hulsebos TJ, Slater RM, Westerveld A. Inheritance of glomus tumours. Lancet (London, England). 335: 660. PMID 1969034 DOI: 10.1016/0140-6736(90)90446-C  0.72
1990 Hoek FJ, Tabak HF, De Vijlder JJM, Westerveld A. Symposium: The clinical application of recombinant DNA techniques | SYMPOSIUM: KLINISCHE TOEPASSINGEN VAN RECOMBINANT DNA-TECHNIEKEN: INLEIDING Tijdschrift Van De Nederlandse Vereniging Voor Klinische Chemie. 15: 180.  0.72
1990 Tager JM, Brul S, Wiemer EAC, Heikoop JC, Middelkoop E, Bout A, Westerveld A, Wanders RJA. Peroxisomal disorders: An updating Adrenoleukodystrophy and Other Peroxisomal Disorders. Clinical, Biochemical, Genetic and Therapeutic Aspects: Proceedings of the International Workshop. Ics898. 3-15.  0.72
1989 van Duin M, Vredeveldt G, Mayne LV, Odijk H, Vermeulen W, Klein B, Weeda G, Hoeijmakers JH, Bootsma D, Westerveld A. The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I. Mutation Research. 217: 83-92. PMID 2918869 DOI: 10.1016/0921-8777(89)90059-1  0.72
1989 Bout A, Hoovers JM, Bakker E, Mannens MM, Geurts van Kessel A, Westerveld A, Tager JM, Benne R. Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23. Cytogenetics and Cell Genetics. 52: 147-50. PMID 2630187 DOI: 10.1159/000132861  0.72
1989 Thompson LH, Bachinski LL, Stallings RL, Dolf G, Weber CA, Westerveld A, Siciliano MJ. Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19. Genomics. 5: 670-9. PMID 2591959 DOI: 10.1016/0888-7543(89)90107-9  0.72
1989 Mannens M, Bleeker-Wagemakers EM, Bliek J, Hoovers J, Mandjes I, van Tol S, Frants RR, Heyting C, Westerveld A, Slater RM. Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family. Cytogenetics and Cell Genetics. 52: 32-6. PMID 2575483 DOI: 10.1159/000132834  0.72
1989 Darroudi F, Westerveld A, Natarajan AT. Cytogenetical characterisation of Chinese hamster 43-3B transferants with the amplified or non-amplified human DNA repair gene ERCC-1. Mutation Research. 212: 113-22. PMID 2499774 DOI: 10.1016/0027-5107(89)90062-6  0.72
1988 Brul S, Wiemer EA, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, Van den Bosch H, Tager JM. Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders. Biochemical and Biophysical Research Communications. 152: 1083-9. PMID 3377768 DOI: 10.1016/S0006-291X(88)80395-4  0.72
1988 van Duin M, Janssen JH, de Wit J, Hoeijmakers JH, Thompson LH, Bootsma D, Westerveld A. Transfection of the cloned human excision repair gene ERCC-1 to UV-sensitive CHO mutants only corrects the repair defect in complementation group-2 mutants. Mutation Research. 193: 123-30. PMID 3347205 DOI: 10.1016/0167-8817(88)90042-9  0.72
1988 Zdzienicka MZ, van der Schans GP, Westerveld A, van Zeeland AA, Simons JW. Phenotypic heterogeneity within the first complementation group of UV-sensitive mutants of Chinese hamster cell lines. Mutation Research. 193: 31-41. PMID 3336370 DOI: 10.1016/0167-8817(88)90005-3  0.72
1988 van Duin M, van den Tol J, Warmerdam P, Odijk H, Meijer D, Westerveld A, Bootsma D, Hoeijmakers JH. Evolution and mutagenesis of the mammalian excision repair gene ERCC-1. Nucleic Acids Research. 16: 5305-22. PMID 3290851  0.72
1988 Bootsma D, Westerveld A, Hoeijmakers JH. DNA repair in human cells: from genetic complementation to isolation of genes. Cancer Surveys. 7: 303-15. PMID 3066477  0.72
1988 Brul S, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, van den Bosch H, Tager JM. Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis. The Journal of Clinical Investigation. 81: 1710-5. PMID 2454948 DOI: 10.1172/JCI113510  0.72
1987 van Duin M, Koken MH, van den Tol J, ten Dijke P, Odijk H, Westerveld A, Bootsma D, Hoeijmakers JH. Genomic characterization of the human DNA excision repair gene ERCC-1. Nucleic Acids Research. 15: 9195-213. PMID 3684592 DOI: 10.1093/nar/15.22.9195  0.72
1987 Keijzer W, Stefanini M, Bootsma D, Verkerk A, Geurts van Kessel AH, Jongkind JF, Westerveld A. Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1. Experimental Cell Research. 169: 490-501. PMID 3556430 DOI: 10.1016/0014-4827(87)90209-6  0.72
1987 Hoeijmakers JH, Odijk H, Westerveld A. Differences between rodent and human cell lines in the amount of integrated DNA after transfection. Experimental Cell Research. 169: 111-9. PMID 3028842 DOI: 10.1016/0014-4827(87)90230-8  0.72
1987 Zdzienicka MZ, Roza L, Westerveld A, Bootsma D, Simons JW. Biological and biochemical consequences of the human ERCC-1 repair gene after transfection into a repair-deficient CHO cell line. Mutation Research. 183: 69-74. PMID 3025723 DOI: 10.1016/0167-8817(87)90047-2  0.72
1986 Arwert F, Porck HJ, Fràter-Schröder M, Brahe C, Geurts van Kessel A, Westerveld A, Meera Khan P, Zang K, Frants RR, Kortbeek HT. Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells. Human Genetics. 74: 378-81. PMID 3466852 DOI: 10.1007/BF00280489  0.72
1986 Hoeijmakers JH, van Duin M, Westerveld A, Yasui A, Bootsma D. Identification of DNA repair genes in the human genome. Cold Spring Harbor Symposia On Quantitative Biology. 51: 91-101. PMID 3034490  0.72
1986 van Duin M, de Wit J, Odijk H, Westerveld A, Yasui A, Koken MH, Hoeijmakers JH, Bootsma D. Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10. Cell. 44: 913-23. PMID 2420469 DOI: 10.1016/0092-8674(86)90014-0  0.72
1986 Wanders RJ, Saelman D, Heymans HS, Schutgens RB, Westerveld A, Poll-Thé BT, Saudubray JM, Van den Bosch H, Strijland A, Schram AW. Genetic relation between the Zellweger syndrome, infantile Refsum's disease, and rhizomelic chondrodysplasia punctata. The New England Journal of Medicine. 314: 787-8. PMID 2419755 DOI: 10.1056/NEJM198603203141216  0.72
1985 Stefanini M, Keijzer W, Westerveld A, Bootsma D. Interspecies complementation analysis of xeroderma pigmentosum and UV-sensitive Chinese hamster cells. Experimental Cell Research. 161: 373-80. PMID 4065224 DOI: 10.1016/0014-4827(85)90094-1  0.72
1985 van Duin M, Westerveld A, Hoeijmakers JH. UV stimulation of DNA-mediated transformation of human cells. Molecular and Cellular Biology. 5: 734-41. PMID 3990693  0.72
1985 Sips HJ, de Wit-Verbeek HA, de Wit J, Westerveld A, Galjaard H. The chromosomal localization of human beta-galactosidase revisited: a locus for beta-galactosidase on human chromosome 3 and for its protective protein on human chromosome 22. Human Genetics. 69: 340-4. PMID 3921454 DOI: 10.1007/BF00291653  0.72
1984 Westerveld A, Hoeijmakers JH, van Duin M, de Wit J, Odijk H, Pastink A, Wood RD, Bootsma D. Molecular cloning of a human DNA repair gene. Nature. 310: 425-9. PMID 6462228 DOI: 10.1038/310425a0  0.72
1984 Westerveld A, Naylor S. Report of the Committee on the Genetic Constitution of Chromosomes 18, 19, 20, 21, and 22. Cytogenetics and Cell Genetics. 37: 155-75. PMID 6360557 DOI: 10.1159/000132008  0.72
1983 Barneveld RA, Keijzer W, Tegelaers FP, Ginns EI, Geurts van Kessel A, Brady RO, Barranger JA, Tager JM, Galjaard H, Westerveld A, Reuser AJ. Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies. Human Genetics. 64: 227-31. PMID 6885065 DOI: 10.1007/BF00279398  0.72
1982 de Jonge AJ, Abrahams PJ, Westerveld A, Bootsma D. Expression of human hprt gene on the inactive X chromosome after DNA-mediated gene transfer. Nature. 295: 624-6. PMID 7199123 DOI: 10.1038/295624a0  0.72
1982 Ruddle FH, Bootsma D, Stefani M, Keijzer W, Westerveld A, Van Cong N, Weil D, Hors-Cayla MC, Gross MS, Heuertz S, Foubert C, Frézal J, Solomon E, Shows TB, Sakaguchi AY, et al. Workshop on mapping by somatic cell hybridization. Progress in Clinical and Biological Research. 103: 145-53. PMID 7163192  0.72
1982 Ferguson-Smith MA, Westerveld A. Report of the committee on the genetic constitution of chromosomes 13 to 22. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. Cytogenetics and Cell Genetics. 32: 161-78. PMID 7140359  0.72
1982 Ferguson-Smith MA, Westerveld A. Report of the committee on the genetic constitution of chromosomes 13 to 22. Birth Defects Original Article Series. 18: 161-78. PMID 6760918  0.72
1981 Ropers HH, Migl B, Zimmer J, Fraccaro M, Maraschio PP, Westerveld A. Activity of steroid sulfatase in fibroblasts with numerical and structural X chromosome aberrations. Human Genetics. 57: 354-6. PMID 6945285 DOI: 10.1007/BF00281683  0.72
1981 De Groot PG, Ovde Elferink RO, Hollemans M, Strijland A, Westerveld A, Meera Khan P, Tager JM. Inactivation by chloroquine of alpha-galactosidase in cultured human skin fibroblasts. Experimental Cell Research. 136: 327-33. PMID 6273196 DOI: 10.1016/0014-4827(81)90011-2  0.72
1980 Geurts van Kessel AH, Westerveld A, de Groot PG, Meera Khan P, Hagemeijer A. Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22. Cytogenetics and Cell Genetics. 28: 169-72. PMID 7192199 DOI: 10.1159/000131527  0.72
1980 Müller CR, Westerveld A, Migl B, Franke W, Ropers HH. Regional assignment of the gene locus for steroid sulfatase. Human Genetics. 54: 201-4. PMID 6985463 DOI: 10.1007/BF00278972  0.72
1980 Ferguson-Smith MA, Westerveld A. Report of the committee on the genetic constitution of chromosomes 13, 14, 15, 16, 17, 18, 19, 20, 21, and 22. Birth Defects Original Article Series. 15: 59-73. PMID 6938256  0.72
1980 Hoeksema HL, De Wit J, Westerveld A. The genetic defect in the various types of human beta-galactosidase deficiency. Human Genetics. 53: 241-7. PMID 6766901  0.72
1980 Suárez HG, Persuy MA, Westerveld A, Ermonval M, Kay A, Cassingena R. Linkage relationship between TK and SV40 T-antigen genes in the SV40-transformed WI98VaD human cell line. Experimental Cell Research. 129: 127-32. PMID 6253304 DOI: 10.1016/0014-4827(80)90337-7  0.72
1980 de Groot PG, Strijland A, Kalsbeek R, Meera Khan P, Westerveld A, Hamers MN, Tager JM. Effect of 2-deoxyglucose on lysosomal enzymes in cultured human skin fibroblasts. Experimental Cell Research. 126: 207-16. PMID 6244168 DOI: 10.1016/0014-4827(80)90487-5  0.72
1979 Ferguson-Smith MA, Westerveld A. Report of the committee on the genetic constitution of chromosomes 13, 14, 15, 16, 17, 18, 19, 20, 21, and 22. Cytogenetics and Cell Genetics. 25: 59-73. PMID 396129  0.32
1979 de Wit J, Hoeksema HL, Bootsma D, Westerveld A. Assignment of structural beta-galactosidase loci to human chromosomes 3 and 22. Human Genetics. 51: 259-67. PMID 116956 DOI: 10.1007/BF00283392  0.72
1979 Meager A, Graves HE, Walker JR, Burke DC, Swallow DM, Westerveld A. Somatic cell genetics of human interferon production in human-rodent cell hybrids. The Journal of General Virology. 45: 309-21. PMID 94346  0.72
1978 Herbschleb-Voogt E, Monteba-van Heuvel M, Wijnen LM, Westerveld A, Pearson PL, Meera Khan P. Chromosomal assignment and regional localization of CS, ENO2, GAPDH, LDHB, PEPB, and TPI in man-rodent cell hybrids. Cytogenetics and Cell Genetics. 22: 482-6. PMID 318158 DOI: 10.1159/000131003  0.72
1978 Westerveld A, Garver J, Nijman MA, Pearson PL. Regional localization of the genes coding for human red cell adenylate kinase, aconitase, and galactose-1-phosphate uridylyltransferase on chromosome 9. Cytogenetics and Cell Genetics. 22: 465-7. PMID 222548  0.72
1978 de Groot PG, Westerveld A, Meera Khan P, Tager JM. Localization of a gene for human alpha-galactosidase B (= n-acetyl-alpha-d-galactosaminidase) on chromosome 22. Human Genetics. 44: 305-12. PMID 215508 DOI: 10.1007/BF00394295  0.72
1978 Garver JJ, Pearson PL, Estop A, Dijksman TM, Wijnen LMM, Westerveld A, Khan PM. Gene assignments to the presumptive homologs of human chromosomes 1, 6,11,12, and X in the Pongidae and Cercopithecoidea Cytogenetic and Genome Research. 22: 564-569. PMID 110528 DOI: 10.1159/000131024  0.72
1978 de Groot PG, Hamers MN, Westerveld A, Schram AW, Meera Khan P, Tager JM. A new immunochemical method for the quantitative measurement of specific gene products in man-rodent somatic cell hybrids. Human Genetics. 44: 295-304. PMID 83282 DOI: 10.1007/BF00394294  0.72
1978 Khan PM, Robson EB, Aitken DA, Arias S, Brown JA, Bruns GAP, Chu EHY, Cook PJL, Croce CM, Ferguson-Smith MA, Grzeschik KH, Harris H, Kaita H, Kucherlapati R, Lewis M, ... ... Westerveld A, et al. Report of the committee on the genetic constitution of chromosome 9 Cytogenetic and Genome Research. 22: 106-110. DOI: 10.1159/000130921  0.72
1978 Bootsma D, Ruddle FH, Aitken DA, Brown JA, Bruns GAP, Chu EHY, Croce CM, Craig IW, Francke U, Gedde-Dahl T, George DL, German JL, Grzeschik KH, Hellkuhl B, Jones CA, ... ... Westerveld A, et al. Report of the committee on the genetic constitution of chromosomes 2, 3, 4, 5, 7, 8, 10, 11, and 12 Cytogenetic and Genome Research. 22: 74-91. DOI: 10.1159/000130919  0.72
1977 Hoeksema HL, Reuser AJJ, Hoogeveen A, Westerveld A, Braidman I, Robinson D. Characterization of β D N acetylhexosaminidase isoenzymes in man Chinese hamster somatic cell hybrids American Journal of Human Genetics. 29: 14-23. PMID 835571  0.72
1977 De Wit J, Hoeksema HL, Halley D, Hagemeijer A, Bootsma D, Westerveld A. Regional localization of a beta-galactosidase locus on human chromosome 22. Somatic Cell Genetics. 3: 351-63. PMID 414365 DOI: 10.1007/BF01542965  0.72
1977 Hoeksema HL, Reuser AJJ, Hoogeveen AT, Westerveld A, Galjaard H. Characterization of residual hexosaminidase activity in Sandhoff's disease using man-Chinese hamster cell hybrids Human Genetics. 39: 315-319. PMID 413781 DOI: 10.1007/BF00295426  0.72
1977 Hamers MN, Westerveld A, Khan M, Tager JM. Characterization of α-galactosidase isoenzymes in normal and fabry human-Chinese hamster somatic cell hybrids Human Genetics. 36: 289-297. PMID 404232 DOI: 10.1007/BF00446279  0.72
1976 Wullems G, Van der Horst J, Westerveld A, Bootsma D. Expression of human X-chromosomal markers in man-Chinese hamster hybrids treated with isolated human chromosomes. Birth Defects Original Article Series. 12: 409-11. PMID 1024646  0.72
1976 Wullems G, van der Horst J, Westerveld A, Bootsma D. Expression of human X-chromosomal markers in man-Chinese hamster hybrids treated with isolated human chromosomes. Cytogenetics and Cell Genetics. 16: 409-11. PMID 975919 DOI: 10.1159/000130645  0.72
1976 Meera Khan P, Pearson PL, Wijnen LL, Doppert BA, Westerveld A, Bootsma D. Assignment of inosine triphosphatase gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybrids. Birth Defects Original Article Series. 12: 420-1. PMID 828864  0.72
1976 Westerveld A, Jongsma AP, Meera Khan P, Someren H, Bootsma D. Chromosomal assignment of the gene for human red cell adenylate kinase (AK1) in man-Chinese hamster somatic cell hybrids. Birth Defects Original Article Series. 12: 247-51. PMID 192371  0.72
1976 Meera Khan P, Pearson PL, Wijnen LL, Doppert BA, Westerveld A, Bootsma D. Assignment of inosine triphosphatase gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybrids. Cytogenetics and Cell Genetics. 16: 420-1. PMID 185023 DOI: 10.1159/000130648  0.72
1976 Westerveld A, Jongsma AP, Meera Khan P, van Someren H, Bootsma D. Chromosomal assignment of the gene for human red cell adenylate kinase (AK1) in man-Chinese hamster somatic cell hybrids. Cytogenetics and Cell Genetics. 16: 247-51. PMID 185020 DOI: 10.1159/000130603  0.72
1976 Westerveld A, Jongsma AP, Meera Khan P, van Someren H, Bootsma D. Assignment of the AK1:Np:ABO linkage group to human chromosome 9. Proceedings of the National Academy of Sciences of the United States of America. 73: 895-9. PMID 176661  0.72
1975 De Wit J, Bootsma D, Pearson PL, Westerveld A. Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocation. Cytogenetics and Cell Genetics. 15: 129-37. PMID 1238234 DOI: 10.1159/000130511  0.72
1975 Westerveld A, Van Someren H, Beyersbergen Van Henegouwen and Oosterbaan HMARA. Synteny relationship between the human loci for hexosaminidase A, mannose phosphate isomerase, and pyruvate kinase 3 studied in man Chinese hamster somatic cell hybrids Birth Defects: Original Article Series. 11: 285-287. PMID 1203498  0.72
1975 Westerveld A, Beyersbergen Van Henegouwen HMA, Van Someren H. Evidence for synteny between the human loci for galactose 1 phosphate uridyl transferase and aconitase in man Chinese hamster somatic cell hybrids Birth Defects: Original Article Series. 11: 283-284. PMID 1203497  0.72
1975 Westerveld A, Beyersbergen van Henegouwen HM, van Someren H. Evidence for synteny between the human loci for galactose-1-phosphate uridyl transferase and aconitase in man-Chinese hamster somatic cell hybrids Cytogenetics and Cell Genetics. 14: 453-454. PMID 1192837 DOI: 10.1159/000130405  0.72
1975 Meera Khan P, Westerveld A, Wurzer-Figurelli EM, Bootsma D. Alpha-galactosidase in man-Chinese hamster somatic cell hybrids. Cytogenetics and Cell Genetics. 14: 375-80. PMID 1192822  0.72
1975 Meera Khan P, Westerveld A, Wurzer-Figurelli EM, Bootsma D. Alpha-galactosidase in man-Chinese hamster somatic cell hybrids. Birth Defects Original Article Series. 11: 205-10. PMID 812566  0.72
1975 Westerveld A, Van Someren H, Beyersbergen Van Henegouwen H, Oosterbaan RA. Synteny relationship between the human loci for hexosaminidase-A, mannose phosphate isomerase, and pyruvate kinase-3 studied in man-Chinese hamster somatic cell hybrids Cytogenetic and Genome Research. 14: 285-287. DOI: 10.1159/000130406  0.72
1975 Meera Khan P, Westerveld A, Wurzer-Figurelli EM, Bootsma D. α-Galactosidase in man-Chinese hamster somatic cell hybrids Cytogenetic and Genome Research. 14: 205-210. DOI: 10.1159/000130389  0.72
1974 van Someren H, Kahn PM, Westerveld A, Bootsma D. Claim that two human linkage groups carry different loci for GPT and LDH withdrawn. Nature. 249: 279-80. PMID 4833247 DOI: 10.1038/249279a0  0.72
1974 van Someren H, van Henegouwen HB, Westerveld A, Bootsma D. Synteny of the human loci for fumarate hydratase and UDPG pyrophosphorylase with chromosome 1 markers in somatic cell hybrids Cytogenetic and Genome Research. 13: 551-557. PMID 4549862 DOI: 10.1159/000130306  0.72
1974 Paterson MC, Lohman PHM, Westerveld A, Sluyter ML. DNA repair in human/embryonic chick heterokaryons. Ability of each species to aid the other in the removal of ultraviolet induced damage Biophysical Journal. 14: 835-845. PMID 4474028  0.72
1974 Galjaard H, Hoogeveen A, de Wit-Verbeek HA, Reuser AJ, Keijzer W, Westerveld A, Bootsma D. Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization. Experimental Cell Research. 87: 444-8. PMID 4416048 DOI: 10.1016/0014-4827(74)90515-1  0.72
1974 Khan PM, Los WRT, Los WR, Pearson PL, Westerveld A, Bootsma D. Genetical studies on the multiple forms of human guanylate kinase in man-chinese hamster somatic cell hybrids Human Heredity. 24: 415-423. PMID 4377261 DOI: 10.1159/000152700  0.72
1974 Westerveld A, van Someren H, Zaalberg OB. Evidence for synteny between the human loci for the HLA histocompatibility antigen, phosphoglucomutase3, malic enzyme (Cytoplasmic), and indophenol oxidase B (tetrameric) Cytogenetic and Genome Research. 13: 185-186. PMID 4363869 DOI: 10.1159/000130269  0.72
1974 Khan PM, Doppert BA, Hagemeijer A, Westerveld A. The human loci for phosphopyruvate hydratase and guanylate kinase are syntenic with the PGD-PGM1 linkage group in man-chinese hamster somatic cell hybrids Cytogenetic and Genome Research. 13: 130-131. PMID 4363865 DOI: 10.1159/000130255  0.72
1974 van Someren H, Westerveld A, Hagemeijer A, Mees JR, Meera Khan P, Zaalberg OB. Human antigen and enzyme markers in man; Chinese hamster somatic cell hybrids: evidence for synteny between the HL A, PGM 3, ME 1, and IPO B loci Proceedings of the National Academy of Sciences of the United States of America. 71: 962-965. PMID 4362641 DOI: 10.1073/pnas.71.3.962  0.72
1974 Paterson MC, Lohman PHM, Westerveld A, Sluyter ML. DNA repair monitored by an enzymatic assay in multinucleate xeroderma pigmentosum cells after fusion Nature. 248: 50-52. PMID 4274220 DOI: 10.1038/248050a0  0.72
1974 Paterson MC, Lohman PHM, De Weerd Kastelein EA, Westerveld A. Photoreactivation and excision repair of ultraviolet radiation injured DNA in primary embryonic chick cells Biophysical Journal. 14: 454-466. PMID 4134590  0.72
1973 Jongsma A, van Someren H, Westerveld A, Hagemeijer A, Pearson P. 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 the PGD, PGM1 and Pep-C genes on chromosome A1 Humangenetik. 20: 195-202. PMID 4358963 DOI: 10.1007/BF00385730  0.72
1972 Westerveld A, Visser RPLS, Freeke MA, Bootsma D. Evidence for linkage of 3-phosphoglycerate kinase, hypoxanthine-guanine-phosphoribosyl transferase, and glucose 6-phosphate dehydrogenase loci in Chinese hamster cells studied by using a relationship between gene multiplicity and enzyme activity Biochemical Genetics. 7: 33-40. PMID 5064956 DOI: 10.1007/BF00487007  0.72
1972 Westerveld A, Khan PM. Evidence for linkage between human loci for 6-phosphogluconate dehydrogenase and phosphoglucomutase1 in man-Chinese hamster somatic cell hybrids Nature. 236: 30-32. PMID 4553635 DOI: 10.1038/236030a0  0.72
1972 van Someren H, Meera Khan P, Westerveld A, Bootsma D. Two new linkage groups in man, both carrying different loci for lactate dehydrogenase and glutamic-pyruvic transaminase Nature: New Biology. 240: 221-223. PMID 4509147  0.72
1972 Grzeschik KH, Grzeschik AM, Banhof S, Romeo G, Siniscalco M, van Someren H, Meera Khan P, Westerveld A, Bootsma D. X-linkage of human -galactosidase Nature: New Biology. 240: 48-50. PMID 4508394  0.72
1971 Westerveld A, Freeke MA. Cell cycle of multinucleate cells after cell fusion Experimental Cell Research. 65: 140-144. PMID 5549540 DOI: 10.1016/S0014-4827(71)80059-9  0.72
1971 Westerveld A, Visser RP, Meera Khan P, Bootsma D. Loss of human genetic markers in man--Chinese hamster somatic cell hybrids Nature: New Biology. 234: 20-24. PMID 5286856  0.72
1971 Meera Khan P, Westerveld A, Grzeschik KH, Deys BF, Garson OM, Siniscalco M. X-linkage of human phosphoglycerate kinase confirmed in man-mouse and man-Chinese hamster somatic cell hybrids American Journal of Human Genetics. 23: 614-623. PMID 5132070  0.72
1971 Westerveld A, Visser RPLS, Freeke MA. Evidence for linkage between glucose 6-phosphate dehydrogenase and hypoxanthine-guanine-phosphoribosyl transferase loci in Chinese hamster cells Biochemical Genetics. 5: 591-599. PMID 5116523 DOI: 10.1007/BF00485676  0.72
Show low-probability matches.