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Ad Geurts van Kessel

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Marjolijn Jongmans; Eveline J Kamping; Ernie M H F Bongers; Inderjeet Dokal; Ad Geurts van Kessel; Jayne Hehir-Kwa; Yvonne Heijdra; Nicoline Hoogerbrugge; Marjolijn J L Ligtenberg; Rolph Pfundt; Liesbeth van Emst; Koen L I van Gassen; Frank van Leeuwen; Eugene T P Verwiel; Tom Vulliamy; Roland P Kuiper
Revertant somatic mosaicism by mitotic recombination in dyskeratosis congenita.
Ad Geurts van Kessel
The 'omics' of cancer.
Ramprasath Venkatachalam; Marjolijn J L Ligtenberg; Nicoline Hoogerbrugge; Diederik R H de Bruijn; Roland P Kuiper; Ad Geurts van Kessel
The epigenetics of (hereditary) colorectal cancer.

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2012: Marjolijn Jongmans; Eveline J Kamping; Ernie M H F Bongers; Inderjeet Dokal; Ad Geurts van Kessel; Jayne Hehir-Kwa; Yvonne Heijdra; Nicoline Hoogerbrugge; Marjolijn J L Ligtenberg; Rolph Pfundt; Liesbeth van Emst; Koen L I van Gassen; Frank van Leeuwen; Eugene T P Verwiel; Tom Vulliamy; Roland P Kuiper
Revertant somatic mosaicism by mitotic recombination in dyskeratosis congenita.
American journal of human genetics 2012;90(3):426-33.
2010: Ad Geurts van Kessel
The 'omics' of cancer.
Cancer genetics and cytogenetics 2010;203(1):37-42.
2010: Ramprasath Venkatachalam; Marjolijn J L Ligtenberg; Nicoline Hoogerbrugge; Diederik R H de Bruijn; Roland P Kuiper; Ad Geurts van Kessel
The epigenetics of (hereditary) colorectal cancer.
Cancer genetics and cytogenetics 2010;203(1):1-6.
2010: Roland P Kuiper; M J L Ligtenberg; Nicoline Hoogerbrugge; Ad Geurts van Kessel
Germline copy number variation and cancer risk.
Current opinion in genetics & development 2010;20(3):282-9.
2009: Roland P Kuiper; Lilian A Vreede; Ramprasath Venkatachalam; Chris Ricketts; Eveline Kamping; Eugene Verwiel; Lutgarde Govaerts; Maria Debiec-Rychter; Evelyne Lerut; Femke van Erp; Nicoline Hoogerbrugge; Léon C L van Kempen; Eric F P M Schoenmakers; Anita Bonne; Eamonn R Maher; Ad Geurts van Kessel
The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer.
Cancer genetics and cytogenetics 2009;195(2):105-11.
2009: Marian Stevens-Kroef; Annet Simons; Hanneke Gorissen; Ton Feuth; Daniel Olde Weghuis; Arjan Buijs; Reinier A P Raymakers; Ad Geurts van Kessel
Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification.
Cancer genetics and cytogenetics 2009;195(2):97-104.
2008: Terry Vrijenhoek; Jacobine E Buizer-Voskamp; Inge van der Stelt; Eric Strengman; Chiara Sabatti; Ad Geurts van Kessel; Han G Brunner; Roel A Ophoff; Joris Veltman
Recurrent CNVs disrupt three candidate genes in schizophrenia patients.
American journal of human genetics 2008;83(4):504-10.
2008: R Venkatachalam; M J L Ligtenberg; Nicoline Hoogerbrugge; Ad Geurts van Kessel; Roland P Kuiper
Predisposition to colorectal cancer: exploiting copy number variation to identify novel predisposing genes and mechanisms.
Cytogenetic and genome research 2008;123(1-4):188-94.
2007: Anita Bonne; Lilian A Vreede; Roland P Kuiper; Daniëlle Bodmer; Corine Jansen; Marc J Eleveld; Femke van Erp; Ger Arkesteijn; Nicoline Hoogerbrugge; Conny van Ravenswaaij-Arts; Eric F P M Schoenmakers; Ad Geurts van Kessel
Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene.
Cancer genetics and cytogenetics 2007;179(1):11-8.
2007: K Medendorp; Jan J M van Groningen; Marga Schepens; Lilian A Vreede; José Thijssen; Eric F P M Schoenmakers; Wilhelmina H van den Hurk; Ad Geurts van Kessel; Roland P Kuiper
Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas.
Cytogenetic and genome research 2007;118(2-4):157-65.
2007: Stefan J White; Lisenka E L M Vissers; Ad Geurts van Kessel; Renée X de Menezes; E Kalay; A E Lehesjoki; P C Giordano; Esther van de Vosse; M H Breuning; Han G Brunner; Johan T den Dunnen; Joris Veltman
Variation of CNV distribution in five different ethnic populations.
Cytogenetic and genome research 2007;118(1):19-30.
2006: Diederik R H de Bruijn; W J M Peters; S M Chuva de Sousa Lopes; A H A van Dijk; Marieke P Willemse; Rolph Pfundt; P de Boer; Ad Geurts van Kessel
Targeted disruption of the synovial sarcoma-associated SS18 gene causes early embryonic lethality and affects PPARBP expression.
Human molecular genetics 2006;15(19):2936-44.
2006: Marjolijn Jongmans; Ronald J C Admiraal; Kim P van der Donk; Lisenka E L M Vissers; A F Baas; Livia Kapusta; J M van Hagen; D Donnai; T J de Ravel; Joris Veltman; Ad Geurts van Kessel; Bert B A de Vries; Han G Brunner; Lies Hoefsloot; Conny van Ravenswaaij-Arts
CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.
Journal of medical genetics 2006;43(4):306-14.
2006: Y M H Jonkers; S M H Claessen; Joris Veltman; Ad Geurts van Kessel; Winand N M Dinjens; B Skogseid; Frans C S Ramaekers; Ernst J M Speel
Molecular parameters associated with insulinoma progression: chromosomal instability versus p53 and CK19 status.
Cytogenetic and genome research 2006;115(3-4):289-97.
2006: David A Koolen; Jos Herbergs; Joris Veltman; Rolph Pfundt; Hans van Bokhoven; Hans Stroink; Erik A Sistermans; Han G Brunner; Ad Geurts van Kessel; Bert B A de Vries
Holoprosencephaly and preaxial polydactyly associated with a 1.24 Mb duplication encompassing FBXW11 at 5q35.1.
Journal of human genetics 2006;51(8):721-6.
2006: Diederik R H de Bruijn; Ad Geurts van Kessel
Common origin of the human synovial sarcoma associated SS18 and SS18L1 gene loci.
Cytogenetic and genome research 2006;112(3-4):222-6.
2004: Joris Veltman; Helger G Yntema; Dorien Lugtenberg; H Arts; Sylvain Briault; Erik H L P G Huys; Kazutoyo Osoegawa; Pieter de Jong; Han G Brunner; Ad Geurts van Kessel; Hans van Bokhoven; Eric F P M Schoenmakers
High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation.
Journal of medical genetics 2004;41(6):425-32.
2004: Wilhelmina H van den Hurk; Gerard J M Martens; Ad Geurts van Kessel; Jan J M van Groningen
Isolation and characterization of the Xenopus laevis orthologs of the human papillary renal cell carcinoma-associated genes PRCC and MAD2L2 (MAD2B).
Cytogenetic and genome research 2004;106(1):68-73.
2003: Daniëlle Bodmer; Marga Schepens; Marc J Eleveld; Eric F P M Schoenmakers; Ad Geurts van Kessel
Disruption of a novel gene, DIRC3, and expression of DIRC3-HSPBAP1 fusion transcripts in a case of familial renal cell cancer and t(2;3)(q35;q21).
Genes, chromosomes & cancer 2003;38(2):107-16.
2003: F Van Erp; Conny van Ravenswaaij-Arts; Daniëlle Bodmer; Marc J Eleveld; Nicoline Hoogerbrugge; P Mulders; Ad Geurts van Kessel
Chromosome 3 translocations and the risk to develop renal cell cancer: a Dutch intergroup study.
Genetic counseling (Geneva, Switzerland) 2003;14(2):149-54.
2002: Daniëlle Bodmer; Marc J Eleveld; M J L Ligtenberg; Marian A J Weterman; Adrian van der Meijden; Marianne Koolen; Christien Hulsbergen-van der Kaa; Arie P T Smits; Dominique Smeets; Ad Geurts van Kessel
Cytogenetic and molecular analysis of early stage renal cell carcinomas in a family with a translocation (2;3)(q35;q21).
Cancer genetics and cytogenetics 2002;134(1):6-12.
2001: Diederik R H de Bruijn; Nuno R. dos Santos; José Thijssen; Matthé Balemans; Silvana Debernardi; Britta Linder; Bryan D Young; Ad Geurts van Kessel
The synovial sarcoma associated protein SYT interacts with the acute leukemia associated protein AF10.
Oncogene 2001;20(25):3281-9.
2001: Marc J Eleveld; Daniëlle Bodmer; Gerard F M Merkx; A Siepman; Sandra H E Sprenger; Marian A J Weterman; M J L Ligtenberg; J Kamp; W Stapper; Judith W M Jeuken; Dominique Smeets; Arie P T Smits; Ad Geurts van Kessel
Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15).
Genes, chromosomes & cancer 2001;31(1):23-32.
2001: Marian A J Weterman; Jan J M van Groningen; A den Hartog; Ad Geurts van Kessel
Transformation capacities of the papillary renal cell carcinoma-associated PRCCTFE3 and TFE3PRCC fusion genes.
Oncogene 2001;20(12):1414-24.
2001: Marian A J Weterman; M Wilbrink; Marc J Eleveld; Gerard F M Merkx; Jan J M van Groningen; M van Rooijen; Ad Geurts van Kessel
Genomic structure, chromosomal localization, and embryonic expression of the mouse homolog of PRCC, a gene associated with papillary renal cell carcinoma.
Cytogenetics and cell genetics 2001;92(3-4):326-32.
2001: Diederik R H de Bruijn; Ellen Kater-Baats; Marc J Eleveld; Gerard F M Merkx; Ad Geurts van Kessel
Mapping and characterization of the mouse and human SS18 genes, two human SS18-like genes and a mouse Ss18 pseudogene.
Cytogenetics and cell genetics 2001;92(3-4):310-9.
2000: Martien van Asseldonk; Marga Schepens; Diederik R H de Bruijn; B Janssen; Gerard F M Merkx; Ad Geurts van Kessel
Construction of a 350-kb sequence-ready 11q13 cosmid contig encompassing the markers D11S4933 and D11S546: mapping of 11 genes and 3 tumor-associated translocation breakpoints.
Genomics 2000;66(1):35-42.
2000: Sander Rensen; Gerard F M Merkx; Pieter A Doevendans; Ad Geurts van Kessel; Guillaume J J M van Eys
Structure and chromosome location of Smtn, the mouse smoothelin gene.
Cytogenetics and cell genetics 2000;89(3-4):225-9.
1999: A Simons; Judith W M Jeuken; Marc J Eleveld; Rudolf H Boerman; Ad Geurts van Kessel
Isolation and characterization of glioblastoma-associated homozygously deleted DNA fragments from chromosomal region 9p21 suggests involvement of multiple tumour suppressor genes.
The Journal of pathology 1999;189(3):402-9.
1999: Ad Geurts van Kessel; A Simons; P P Comtesse; A Siepman; IM Janssen; Ron Suijkerbuijk; Anne Forus; Maciej Pruszczynski; R P H Veth
Ring chromosomes in a malignant mesenchymoma.
Cancer genetics and cytogenetics 1999;109(2):119-22.
1999: Arn van den Maagdenberg; Jan Schepens; M T Schepens; Gerard F M Merkx; F Darroudi; Bé Wieringa; Ad Geurts van Kessel; Wiljan Hendriks
Assignment1 of the PTP-SL/PTPBR7 gene (Ptprr/PTPRR) to mouse chromosome region 8A2 by in situ hybridization.
Cytogenetics and cell genetics 1999;84(3-4):243-4.
1998: F J Meng; Y Zhou; A Giwercman; N E Skakkebaek; Ad Geurts van Kessel; Ron Suijkerbuijk
Fluorescence in situ hybridization analysis of chromosome 12 anomalies in semen cells from patients with carcinoma in situ of the testis.
The Journal of pathology 1998;186(3):235-9.
1998: Ad Geurts van Kessel; Diederik R H de Bruijn; L Hermsen; IM Janssen; Nuno R. dos Santos; R Willems; L Makkus; H Schreuder; R P H Veth
Masked t(X;18)(p11;q11) in a biphasic synovial sarcoma revealed by FISH and RT-PCR.
Genes, chromosomes & cancer 1998;23(2):198-201.
1998: Daniëlle Bodmer; Marc J Eleveld; M J L Ligtenberg; Marian A J Weterman; B A Janssen; Dominique Smeets; P E de Wit; Anke Van den Berg; Eva van den Berg; Marianne Koolen; Ad Geurts van Kessel
An alternative route for multistep tumorigenesis in a novel case of hereditary renal cell cancer and a t(2;3)(q35;q21) chromosome translocation.
American journal of human genetics 1998;62(6):1475-83.
1998: Marianne Koolen; A P van der Meyden; Daniëlle Bodmer; Marc J Eleveld; E van der Looij; H Brunner; Arie P T Smits; Eva van den Berg; Dominique Smeets; Ad Geurts van Kessel
A familial case of renal cell carcinoma and a t(2;3) chromosome translocation.
Kidney international 1998;53(2):273-5.
1998: RJ Sinke; Martien van Asseldonk; Diederik R H de Bruijn; J A Strijk; Gerard F M Merkx; D Olde Weghuis; Bauke de Jong; J W Oosterhuis; Ad Geurts van Kessel
Towards the isolation of a human malignant extragonadal germ cell tumour-associated breakpoint in chromosome 11q13.
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 1998;106(1):73-8; discussion 78-9.
1997: Trijnie Dijkhuizen; Eva van den Berg; Stephan Störkel; Bonnie de Vries; Anneke Y van der Veen; M Wilbrink; Ad Geurts van Kessel; Bauke de Jong
Renal oncocytoma with t(5;12;11), der(1)1;8) and add(19): "true" oncocytoma or chromophobe adenoma?
International journal of cancer. Journal international du cancer 1997;73(4):521-4.
1997: A Simons; IM Janssen; Ron Suijkerbuijk; R P H Veth; Maciej Pruszczynski; Christina A Hulsbergen-van de Kaa; S du Manoir; Ad Geurts van Kessel
Isolation of osteosarcoma-associated amplified DNA sequences using representational difference analysis.
Genes, chromosomes & cancer 1997;20(2):196-200.
1997: Nuno R. dos Santos; Diederik R H de Bruijn; Matthé Balemans; B Janssen; Fátima Gärtner; J M Lopes; B de Leeuw; Ad Geurts van Kessel
Nuclear localization of SYT, SSX and the synovial sarcoma-associated SYT-SSX fusion proteins.
Human molecular genetics 1997;6(9):1549-58.
1997: RJ Sinke; Trijnie Dijkhuizen; B Janssen; D Olde Weghuis; Gerard F M Merkx; Eva van den Berg; E Schuuring; Aurelia Meloni-Ehrig; Bauke de Jong; Ad Geurts van Kessel
Fine mapping of the human renal oncocytoma-associated translocation (5;11)(q35;q13) breakpoint.
Cancer genetics and cytogenetics 1997;96(2):95-101.
1997: Eva van den Berg; Trijnie Dijkhuizen; J Wolter Oosterhuis; Ad Geurts van Kessel; Bauke de Jong; Stephan Störkel
Cytogenetic classification of renal cell cancer.
Cancer genetics and cytogenetics 1997;95(1):103-7.
1997: Bauke de Jong; Jannie van Echten; Leendert H J Looijenga; Ad Geurts van Kessel; J Wolter Oosterhuis
Cytogenetics of the progression of adult testicular germ cell tumors.
Cancer genetics and cytogenetics 1997;95(1):88-95.
1997: Ad Geurts van Kessel; Nuno R. dos Santos; A Simons; Diederik R H de Bruijn; Anne Forus; O Fodstad; Ola Myklebost; Matthé Balemans; E Baats; D Olde Weghuis; Ron Suijkerbuijk; Eva van den Berg; Willemina M Molenaar; B de Leeuw
Molecular cytogenetics of bone and soft tissue tumors.
Cancer genetics and cytogenetics 1997;95(1):67-73.
1997: R M Landsvater; MJ de Wit; Luke Peterson; RJ Sinke; Ad Geurts van Kessel; Cornelis J M Lips; Jo W M Höppener
Exclusion of the nuclear factor-kappa B3 (REL A) gene as candidate for the multiple endocrine neoplasia type 1 (MEN 1) gene.
Biochemical and molecular medicine 1997;60(1):76-9.
1997: M A van Kuijck; Marcel Kool; Gerard F M Merkx; Ad Geurts van Kessel; René J M Bindels; Peter M T Deen; Carel H van Os
Assignment of the canalicular multispecific organic anion transporter gene (CMOAT) to human chromosome 10q24 and mouse chromosome 19D2 by fluorescent in situ hybridization.
Cytogenetics and cell genetics 1997;77(3-4):285-7.
1997: MJ de Wit; R M Landsvater; RJ Sinke; Ad Geurts van Kessel; Cornelis J M Lips; Jo W M Höppener
Exclusion of the phosphatidylinositol-specific phospholipase C beta 3 (PLC beta 3) gene as candidate for the multiple endocrine neoplasia type 1 (MEN 1) gene.
Human genetics 1997;99(1):133-7.
1996: M A Weterman; M Wilbrink; Ad Geurts van Kessel
Fusion of the transcription factor TFE3 gene to a novel gene, PRCC, in t(X;1)(p11;q21)-positive papillary renal cell carcinomas.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(26):15294-8.
1996: M M Mostert; Martijn Van de Pol; D Olde Weghuis; Ron Suijkerbuijk; Ad Geurts van Kessel; Jannie van Echten; J Wolter Oosterhuis; Leendert H J Looijenga
Comparative genomic hybridization of germ cell tumors of the adult testis: confirmation of karyotypic findings and identification of a 12p-amplicon.
Cancer genetics and cytogenetics 1996;89(2):146-52.
1996: M A Weterman; M Wilbrink; Trijnie Dijkhuizen; Eva van den Berg; Ad Geurts van Kessel
Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation.
Human genetics 1996;98(1):16-21.
1996: Reinier A P Raymakers; F Stellink; Ad Geurts van Kessel
Derivative (y)t(Y;1)(q12;q12),+9 in a patient with polycythemia vera during transition into myelodysplasia.
Cancer genetics and cytogenetics 1996;88(1):83-5.
1996: M M Mostert; Martijn Van de Pol; Jannie van Echten; D Olde Weghuis; Ad Geurts van Kessel; J Wolter Oosterhuis; Leendert H J Looijenga
Fluorescence in situ hybridization-based approaches for detection of 12p overrepresentation, in particular i(12p), in cell lines of human testicular germ cell tumors of adults.
Cancer genetics and cytogenetics 1996;87(2):95-102.
1996: WG Degen; M A Weterman; J J van Groningen; I M H A Cornelissen; J P Lemmers; M A Agterbos; Ad Geurts van Kessel; Guido W M Swart; Henri P J Bloemers
Expression of nma, a novel gene, inversely correlates with the metastatic potential of human melanoma cell lines and xenografts.
International journal of cancer. Journal international du cancer 1996;65(4):460-5.
1996: M A Weterman; M Wilbrink; I Janssen; H A Janssen; Eva van den Berg; Simon E Fisher; I Craig; Ad Geurts van Kessel
Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.
Cytogenetics and cell genetics 1996;75(1):2-6.
1996: Arn van den Maagdenberg; D Olde Weghuis; JP Rijss; Gerard F M Merkx; Bé Wieringa; Ad Geurts van Kessel; Wiljan Hendriks
The gene (PTPN13) encoding the protein tyrosine phosphatase PTP-BL/PTP-BAS is located in mouse chromosome region 5E/F and human chromosome region 4q21.
Cytogenetics and cell genetics 1996;74(1-2):153-5.
1996: B de Leeuw; Matthé Balemans; Ad Geurts van Kessel
A novel Krüppel-associated box containing the SSX gene (SSX3) on the human X chromosome is not implicated in t(X;18)-positive synovial sarcomas.
Cytogenetics and cell genetics 1996;73(3):179-83.
1996: Arn van den Maagdenberg; D Olde Weghuis; JP Rijss; R A van de Wetering; Bé Wieringa; Ad Geurts van Kessel; Wiljan Hendriks
Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35 --> q36.1 and identification of an intragenic genetic marker.
Cytogenetics and cell genetics 1996;73(1-2):145-8.
1995: Arn van den Maagdenberg; H H van den Hurk; D Weghuis; Bé Wieringa; Ad Geurts van Kessel; Wiljan Hendriks
Assignment of the human protein tyrosine phosphatase epsilon (PTPRE) gene to chromosome 10q26 by fluorescence in situ hybridization.
Genomics 1995;30(1):128-9.
1995: Trijnie Dijkhuizen; Eva van den Berg; M Wilbrink; M Weterman; Ad Geurts van Kessel; Stephan Störkel; R P Folkers; A Braam; Bauke de Jong
Distinct Xp11.2 breakpoints in two renal cell carcinomas exhibiting X;autosome translocations.
Genes, chromosomes & cancer 1995;14(1):43-50.
1995: Anne Forus; D O Weghuis; Dominique Smeets; Oystein Fodstad; Ola Myklebost; Ad Geurts van Kessel
Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomas.
Genes, chromosomes & cancer 1995;14(1):15-21.
1995: A van den Wijngaard; D O Weghuis; CJ Boersma; Everardus J J van Zoelen; Ad Geurts van Kessel; Wiebe Olijve
Fine mapping of the human bone morphogenetic protein-4 gene (BMP4) to chromosome 14q22-q23 by in situ hybridization.
Genomics 1995;27(3):559-60.
1995: B de Leeuw; Matthé Balemans; D Olde Weghuis; Ad Geurts van Kessel
Identification of two alternative fusion genes, SYT-SSX1 and SYT-SSX2, in t(X;18)(p11.2;q11.2)-positive synovial sarcomas.
Human molecular genetics 1995;4(6):1097-9.
1995: R Q Schaapveld; Arn van den Maagdenberg; Jan Schepens; D O Weghuis; Ad Geurts van Kessel; Bé Wieringa; Wiljan Hendriks
The mouse gene Ptprf encoding the leukocyte common antigen-related molecule LAR: cloning, characterization, and chromosomal localization.
Genomics 1995;27(1):124-30.
1995: René F M de Coo; P Buddiger; H J M Smeets; Ad Geurts van Kessel; J Morgan-Hughes; D O Weghuis; J Overhauser; BA van Oost
Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene.
Genomics 1995;26(3):461-6.
1995: M Janz; B De Leeuw; D O Weghuis; Martin Werner; M Nolte; Ad Geurts van Kessel; Alfred Nordheim; R A Hipskind
Interphase cytogenetic analysis of distinct X-chromosomal translocation breakpoints in synovial sarcoma.
The Journal of pathology 1995;175(4):391-6.
1994: Diederik R H de Bruijn; Frank Oerlemans; W Hendriks; E Baats; R Ploemacher; Bé Wieringa; Ad Geurts van Kessel
Normal development, growth and reproduction in cellular retinoic acid binding protein-I (CRABPI) null mutant mice.
Differentiation; research in biological diversity 1994;58(2):141-8.
1994: Ron Suijkerbuijk; RJ Sinke; D E Weghuis; L Roque; Anne Forus; F Stellink; A Siepman; C van de Kaa; J Soares; Ad Geurts van Kessel
Amplification of chromosome subregion 12p11.2-p12.1 in a metastasis of an i(12p)-negative seminoma: relationship to tumor progression?
Cancer genetics and cytogenetics 1994;78(2):145-52.
1994: M Janz; U Lehmann; D Olde Weghuis; B de Leeuw; Ad Geurts van Kessel; S Gilgenkrantz; R A Hipskind; Alfred Nordheim
Refined mapping of the human Ets-related gene Elk-1 to Xp11.2-p11.4, distal to the OATL1 region.
Human genetics 1994;94(4):442-4.
1994: B de Leeuw; Matthé Balemans; D O Weghuis; Raquel Seruca; M Janz; M T Geraghty; S Gilgenkrantz; Hans-Hilger Ropers; Ad Geurts van Kessel
Molecular cloning of the synovial sarcoma-specific translocation (X;18)(p11.2;q11.2) breakpoint.
Human molecular genetics 1994;3(5):745-9.
1994: Ron Suijkerbuijk; D E Olde Weghuis; M Van den Berg; Florence Pedeutour; Anne Forus; Ola Myklebost; C Glier; Claude Turc-Carel; Ad Geurts van Kessel
Comparative genomic hybridization as a tool to define two distinct chromosome 12-derived amplification units in well-differentiated liposarcomas.
Genes, chromosomes & cancer 1994;9(4):292-5.
1994: D Olde Weghuis; M E Stoepker; B de Leeuw; Eva van den Berg; Ron Suijkerbuijk; W M Molenaar; Bauke de Jong; Ad Geurts van Kessel
A synovial sarcoma with a complex t(X;18;5;4) and a break in the ornithine aminotransferase (OAT)L1 cluster on Xp11.2.
Genes, chromosomes & cancer 1994;9(4):288-91.
1994: Ad Geurts van Kessel; F Stellink; J van Gaal; W van de Klundert; A Siepman; H R Oosten
Translocation (12;22)(p13;q12) as sole karyotypic abnormality in a patient with nonlymphocytic leukemia.
Cancer genetics and cytogenetics 1994;72(2):105-8.
1994: Peter M T Deen; D O Weghuis; RJ Sinke; Ad Geurts van Kessel; Bé Wieringa; Carel H van Os
Assignment of the human gene for the water channel of renal collecting duct Aquaporin 2 (AQP2) to chromosome 12 region q12-->q13.
Cytogenetics and cell genetics 1994;66(4):260-2.
1993: Ron Suijkerbuijk; Aurelia Meloni-Ehrig; RJ Sinke; B de Leeuw; M Wilbrink; H A Janssen; M T Geraghty; Anthony P Monaco; A A Sandberg; Ad Geurts van Kessel
Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2.
Cancer genetics and cytogenetics 1993;71(2):164-9.
1993: Ron Suijkerbuijk; RJ Sinke; Aurelia Meloni-Ehrig; J M Parrington; Jannie van Echten; Bauke de Jong; J Wolter Oosterhuis; A A Sandberg; Ad Geurts van Kessel
Overrepresentation of chromosome 12p sequences and karyotypic evolution in i(12p)-negative testicular germ-cell tumors revealed by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1993;70(2):85-93.
1993: RJ Sinke; A Tanigami; Y Nakamura; Ad Geurts van Kessel
Reverse mapping of the gene encoding the human fos-related antigen-1 (fra-1) within chromosome band 11q13.
Genomics 1993;18(1):165.
1993: RJ Sinke; Ron Suijkerbuijk; Bauke de Jong; J Wolter Oosterhuis; Ad Geurts van Kessel
Uniparental origin of i(12p) in human germ cell tumors.
Genes, chromosomes & cancer 1993;6(3):161-5.
1993: Ron Suijkerbuijk; M F Gebbink; Wouter H Moolenaar; Ad Geurts van Kessel
Fine mapping of the human receptor-like protein tyrosine phosphatase gene (PTPRM) to 18p11.2 by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1993;64(3-4):245-6.
1993: Ad Geurts van Kessel; Ron Suijkerbuijk; RJ Sinke; Leendert H J Looijenga; J Wolter Oosterhuis; Bauke de Jong
Molecular cytogenetics of human germ cell tumours: i(12p) and related chromosomal anomalies.
European urology 1993;23(1):23-8; discussion 29.
1992: Wolfgang Berger; Alfons Meindl; B de Leeuw; A de Roos; T J van de Pol; Thomas Meitinger; Saskia D van der Velde-Visser; H Achatz; Ad Geurts van Kessel; Frans P M Cremers
Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosome.
Human genetics 1992;90(3):243-6.
1992: Ron Suijkerbuijk; Leendert H J Looijenga; Bauke de Jong; J Wolter Oosterhuis; J J Cassiman; Ad Geurts van Kessel
Verification of isochromosome 12p and identification of other chromosome 12 aberrations in gonadal and extragonadal human germ cell tumors by bicolor double fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1992;63(1):8-16.
1992: RJ Sinke; Ron Suijkerbuijk; J Herbergs; H Janssen; J J Cassiman; Ad Geurts van Kessel
Generation of a panel of somatic cell hybrids containing fragments of human chromosome 12P by X-ray irradiation and cell fusion.
Genomics 1992;12(2):206-13.
1991: A Hamers; Bauke de Jong; Ron Suijkerbuijk; Ad Geurts van Kessel; J Wolter Oosterhuis; Jannie van Echten; J Evers; F Bosman
A 46,XY female with mixed gonadal dysgenesis and a 48,XY, +7, +i(12p) chromosome pattern in a primary gonadal tumor.
Cancer genetics and cytogenetics 1991;57(2):219-24.
1991: M F Gebbink; I van Etten; G Hateboer; Ron Suijkerbuijk; R L Beijersbergen; Ad Geurts van Kessel; Wouter H Moolenaar
Cloning, expression and chromosomal localization of a new putative receptor-like protein tyrosine phosphatase.
FEBS letters 1991;290(1-2):123-30.
1991: Ad Geurts van Kessel; H de Leeuw; E J Dekker; L Rijks; N Spurr; David Ledbetter; E Kootwijk; M J Vaessen
Localization of the cellular retinoic acid binding protein (CRABP) gene relative to the acute promyelocytic leukemia-associated breakpoint on human chromosome 15.
Human genetics 1991;87(2):201-4.
1991: Ron Suijkerbuijk; A Y van de Veen; Jannie van Echten; C H Buys; Bauke de Jong; J Wolter Oosterhuis; D A Warburton; J J Cassiman; D Schonk; Ad Geurts van Kessel
Demonstration of the genuine iso-12p character of the standard marker chromosome of testicular germ cell tumors and identification of further chromosome 12 aberrations by competitive in situ hybridization.
American journal of human genetics 1991;48(2):269-73.
1991: Ad Geurts van Kessel; Ron Suijkerbuijk; Bauke de Jong; J Wolter Oosterhuis
Molecular analysis of isochromosome 12p in testicular germ cell tumors.
Recent results in cancer research. Fortschritte der Krebsforschung. Progrès dans les recherches sur le cancer 1991;123():113-8.
1990: D Schonk; P van Dijk; P Riegmann; Jan Trapman; C Holm; T C Willcocks; P Sillekens; Walther J van Venrooij; E Wimmer; Ad Geurts van Kessel
Assignment of seven genes to distinct intervals on the midportion of human chromosome 19q surrounding the myotonic dystrophy gene region.
Cytogenetics and cell genetics 1990;54(1-2):15-9.