Andries Westerveld - Publications

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

147 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
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  0.336
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  0.35
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 DOI: 10.1136/Jmg.38.7.481  0.346
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 DOI: 10.1159/000015542  0.385
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  0.382
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  0.369
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  0.313
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  0.409
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 DOI: 10.1159/000015371  0.36
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  0.354
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 DOI: 10.1159/000015204  0.393
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 DOI: 10.1016/S0964-1955(97)00031-6  0.388
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  0.398
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 DOI: 10.1159/000134602  0.309
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  0.415
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  0.326
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  0.335
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  0.399
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  0.368
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 DOI: 10.1093/Nar/24.17.3370  0.543
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/Bf02185773  0.513
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 DOI: 10.1159/000134313  0.386
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/Bf02346199  0.575
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  0.564
1996 Voesten A, Bijleveld E, Westerveld A, Hulsebos T. Determination of the smallest region of amplification in chromosomal band 17P12 in malignant astrocytomas Cancer Genetics and Cytogenetics. 91: 172. DOI: 10.1016/S0165-4608(97)82648-9  0.342
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  0.352
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  0.371
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  0.382
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 DOI: 10.1159/000133917  0.361
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  0.566
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 DOI: 10.1038/Ng1195-338  0.438
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  0.475
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  0.385
1995 van Soest S, Te Nijenhuis S, van den Born L, Bleeker-Wagemakers E, Sankuul L, Westerveld A, Bergen A. 3233 Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome IQ; exclusion of the phosducin gene Vision Research. 35: S131. DOI: 10.1016/0042-6989(95)90291-0  0.37
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  0.314
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  0.328
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  0.39
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 DOI: 10.1002/Gcc.2870110103  0.318
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 DOI: 10.1002/Gcc.2870090213  0.386
1994 Ngan Ching C, Caron H, Chan A, Beitsma M, van Sluis P, Speleman F, Westerveld A, Versteeg R. N-myc regulation in neuroblastoma Cancer Genetics and Cytogenetics. 77: 175. DOI: 10.1016/0165-4608(94)90335-2  0.459
1994 van der Drift P, Chan A, van Roy N, Laureys G, Westerveld A, Speleman F, Versteeg R. Analysis of a balanced translocation on chromosome 1p36 in a neuroblastoma patient Cancer Genetics and Cytogenetics. 77: 174. DOI: 10.1016/0165-4608(94)90334-4  0.369
1994 Alders M, Bliek J, Redeker E, Hoovers J, Feinberg A, Little P, Westerveld A, Mannens M. Characterization of the chromosomal regions involved in the Beckwith-Wiedemann syndrome Cancer Genetics and Cytogenetics. 77: 168. DOI: 10.1016/0165-4608(94)90309-3  0.357
1994 Redeker E, Hoovers J, Alders M, Bliek J, de Galan L, Feinberg A, Little P, Westerveld A, Mannens M. A physical map of the short arm of chromosome 11 involved in childhood solid tumours and the Beckwith-Wiedemann syndrome Cancer Genetics and Cytogenetics. 77: 168. DOI: 10.1016/0165-4608(94)90307-7  0.328
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  0.426
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  0.712
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 DOI: 10.1002/Gcc.2870080208  0.404
1993 Caron H, Sluis Pv, Hoeve Mv, Kraker Jd, Bras J, Slater R, Mannens M, Voûte PA, Westerveld A, Versteeg R. Erratum: Corrigendum: Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification Nature Genetics. 4: 431-431. DOI: 10.1038/Ng0893-431A  0.561
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  0.433
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  0.351
1992 Versteeg R, Caron H, van Sluis P, Chan A, van Roy N, Cheng NC, Mannens M, Laurey G, Slater R, Speleman F, Westerveld A. Tumor suppressor genes in neuroblastoma Cancer Genetics and Cytogenetics. 63: 169. DOI: 10.1016/0165-4608(92)90516-B  0.499
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  0.383
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  0.357
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  0.335
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 DOI: 10.1002/Ijc.2910470604  0.343
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  0.629
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 DOI: 10.1128/Mcb.10.11.5806  0.587
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 DOI: 10.1128/Mcb.10.6.2570  0.615
1990 BRUL S, WIEMER E, WESTERVELD A, STRIJLAND A, WANDERS R, TAGER J, SLATER E. A simple selection procedure for cells deficient in peroxisomes Cell Biology International Reports. 14: 64. DOI: 10.1016/0309-1651(90)90363-4  0.617
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.  0.552
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  0.594
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: 10.1159/000132865  0.605
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  0.458
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  0.357
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  0.384
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  0.638
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  0.566
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 DOI: 10.1093/Nar/16.12.5305  0.56
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  0.537
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  0.653
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  0.556
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  0.647
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  0.356
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  0.549
1987 Zdzienicka M, Westerveld A, Simons J, Bootsma D. Biological and biochemical consequences of the human ERCC1 repair gene in a repair-deficient Chinese hamster ovary cell line Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 181: 353. DOI: 10.1016/0027-5107(87)90206-5  0.536
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  0.445
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 DOI: 10.1101/Sqb.1986.051.01.012  0.553
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  0.584
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  0.563
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  0.348
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  0.58
1984 Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 7 of 11) Cytogenetic and Genome Research. 37: 525-545. DOI: 10.1159/000316931  0.521
1984 Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 11 of 11) Cytogenetic and Genome Research. 37: 609-616. DOI: 10.1159/000316928  0.521
1984 Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 10 of 11) Cytogenetic and Genome Research. 37: 588-608. DOI: 10.1159/000316927  0.521
1984 Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 9 of 11) Cytogenetic and Genome Research. 37: 567-587. DOI: 10.1159/000316926  0.521
1984 Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 8 of 11) Cytogenetic and Genome Research. 37: 546-566. DOI: 10.1159/000316925  0.521
1984 Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 6 of 11) Cytogenetic and Genome Research. 37: 504-524. DOI: 10.1159/000316924  0.521
1984 Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Contents, Vol. 37, 1984 Cytogenetic and Genome Research. 37. DOI: 10.1159/000132002  0.479
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  0.575
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  0.628
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  0.503
1982 Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 1 of 11) Cytogenetic and Genome Research. 32: 247-267. PMID 7140367 DOI: 10.1159/000131703  0.521
1982 Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 2 of 11) Cytogenetic and Genome Research. 32: 268-288. DOI: 10.1159/000316914  0.521
1982 McKusick VA, Ferguson-Smith MA, Aitken DA, Edwards JH, Southern EM, Skolnick MH, White R, Klinger HP, Attardi G, Chomyn A, Montoya J, Ojala D, Taggart RT, Francke U, McAlpine PJ, ... ... Westerveld A, et al. Subject Index Vol. 32, 1982 Cytogenetic and Genome Research. 32: 338-341. DOI: 10.1159/000131706  0.48
1982 McKusick VA, Ferguson-Smith MA, Aitken DA, Edwards JH, Southern EM, Skolnick MH, White R, Klinger HP, Attardi G, Chomyn A, Montoya J, Ojala D, Taggart RT, Francke U, McAlpine PJ, ... ... Westerveld A, et al. Contents, Vol. 32, 1982 Cytogenetic and Genome Research. 32. DOI: 10.1159/000131683  0.479
1982 McKusick VA, Ferguson-Smith MA, Aitken DA, Edwards JH, Southern EM, Skolnick MH, White R, Klinger HP, Attardi G, Chomyn A, Montoya J, Ojala D, Taggart RT, Francke U, McAlpine PJ, ... ... Westerveld A, et al. Peter John Langford Cook, BA, MB Cantab., PhD Lond. Cytogenetic and Genome Research. 32: 5-6. DOI: 10.1159/000131681  0.503
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  0.605
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  0.574
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  0.339
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 DOI: 10.1007/Bf00273505  0.423
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  0.389
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  0.598
1979 Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Catalog of mapped human gene markers Cytogenetic and Genome Research. 25: 3-8. PMID 295267 DOI: 10.1159/000131393  0.561
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  0.596
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 DOI: 10.1099/0022-1317-45-2-309  0.332
1979 Menlove LA, Robson EB, Lamm LU, Hamerton JL, Povey S, Morton NE, Bootsma D, Kidd KK, Shows TB, McAlpine PJ, Miller RL, Partridge CW, Ruddle FH, Gerald PS, Grzeschik KH, ... ... Westerveld A, et al. Abstracts of meeting presentations (Part 4 of 11) Cytogenetic and Genome Research. 37: 462-482. DOI: 10.1159/000316922  0.521
1979 Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Abstracts of meeting presentations (Part 5 of 11) Cytogenetic and Genome Research. 25: 205-221. DOI: 10.1159/000316912  0.521
1979 Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Abstracts of meeting presentations (Part 3 of 11) Cytogenetic and Genome Research. 25: 170-190. DOI: 10.1159/000316910  0.521
1979 Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Abstracts of meeting presentations (Part 2 of 5) Cytogenetic and Genome Research. 25: 149-169. DOI: 10.1159/000316909  0.521
1979 Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Subject Index Vol. 25, 1979 Cytogenetic and Genome Research. 25: 232-236. DOI: 10.1159/000131409  0.48
1979 Bootsma D, McAlpine PJ, Francke U, Weitkamp LR, Shows TB, Chapelle Adl, Miller OJ, Ferguson-Smith MA, Westerveld A, McKusick VA, Edwards JH, Steffensen DM, Gosden JR, Pearson PL, Roderick TH, et al. Contents, Vol. 25, 1979 Cytogenetic and Genome Research. 25. DOI: 10.1159/000131395  0.479
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  0.398
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  0.642
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  0.414
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  0.637
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  0.535
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  0.606
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  0.344
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  0.541
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  0.569
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  0.569
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  0.598
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  0.596
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  0.639
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  0.637
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 DOI: 10.1073/Pnas.73.3.895  0.612
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  0.591
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 DOI: 10.1159/000130406  0.37
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  0.304
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  0.418
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 DOI: 10.1159/000130389  0.548
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  0.497
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  0.508
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  0.621
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  0.631
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  0.563
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  0.611
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  0.381
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  0.381
1974 Boer Pd, Groen A, Gropp A, Giers D, Kolbus U, Miller DA, Firschein IL, Dev VG, Tantravahi R, Miller OJ, Someren Hv, Henegouwen HBv, Westerveld A, Bootsma D, Miklos GLG. Human Genetic Mutant Cell Repository Index / Book Review Index Cytogenetic and Genome Research. 13: 584-584. DOI: 10.1159/000130310  0.545
1974 Boer Pd, Groen A, Gropp A, Giers D, Kolbus U, Miller DA, Firschein IL, Dev VG, Tantravahi R, Miller OJ, Someren Hv, Henegouwen HBv, Westerveld A, Bootsma D, Miklos GLG. Subject Index Vol. 13, 1974 Cytogenetic and Genome Research. 13: 581-583. DOI: 10.1159/000130309  0.48
1974 Boer Pd, Groen A, Gropp A, Giers D, Kolbus U, Miller DA, Firschein IL, Dev VG, Tantravahi R, Miller OJ, Someren Hv, Henegouwen HBv, Westerveld A, Bootsma D, Miklos GLG. Contents, Vol. 13, 1974 Cytogenetic and Genome Research. 13. DOI: 10.1159/000130302  0.479
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  0.44
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  0.533
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  0.446
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 DOI: 10.1038/Newbio240221A0  0.643
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 DOI: 10.1038/Newbio240048A0  0.546
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 DOI: 10.1038/Newbio234020A0  0.635
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