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Daniëlle Bodmer

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Peggy Manders; L Spruijt; Carolien M Kets; H W Willems; Daniëlle Bodmer; Konnie Hebeda; Iris Nagtegaal; J H J M van Krieken; M J L Ligtenberg; Nicoline Hoogerbrugge
Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome.
R S van der Post; Lambertus A L M Kiemeney; M J L Ligtenberg; J Alfred Witjes; Christina A Hulsbergen-van de Kaa; Daniëlle Bodmer; L Schaap; Carolien M Kets; J H J M van Krieken; Nicoline Hoogerbrugge
Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers.
Sascha Vermeer; Rowdy P P Meijer; Tom G J Hofste; Daniëlle Bodmer; Ermanno A J Bosgoed; Frans P M Cremers; Berry H P Kremer; Nine V A M Knoers; Hans Scheffer
Design and validation of a conformation sensitive capillary electrophoresis-based mutation scanning system and automated data analysis of the more than 15 kbp-spanning coding sequence of the SACS gene.

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All Publications

2011: Peggy Manders; L Spruijt; Carolien M Kets; H W Willems; Daniëlle Bodmer; Konnie Hebeda; Iris Nagtegaal; J H J M van Krieken; M J L Ligtenberg; Nicoline Hoogerbrugge
Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome.
European journal of cancer (Oxford, England : 1990) 2011;47(9):1407-13.
2010: R S van der Post; Lambertus A L M Kiemeney; M J L Ligtenberg; J Alfred Witjes; Christina A Hulsbergen-van de Kaa; Daniëlle Bodmer; L Schaap; Carolien M Kets; J H J M van Krieken; Nicoline Hoogerbrugge
Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers.
Journal of medical genetics 2010;47(7):464-70.
2009: Sascha Vermeer; Rowdy P P Meijer; Tom G J Hofste; Daniëlle Bodmer; Ermanno A J Bosgoed; Frans P M Cremers; Berry H P Kremer; Nine V A M Knoers; Hans Scheffer
Design and validation of a conformation sensitive capillary electrophoresis-based mutation scanning system and automated data analysis of the more than 15 kbp-spanning coding sequence of the SACS gene.
The Journal of molecular diagnostics : JMD 2009;11(6):514-23.
2009: M J L Ligtenberg; Roland P Kuiper; Tsun Leung Chan; Monique Goossens; Konnie Hebeda; Marsha Voorendt; Tracy Y H Lee; Daniëlle Bodmer; Eveline Hoenselaar; Sandra J B Hendriks-Cornelissen; Wai Yin Tsui; Chi Kwan Kong; Han G Brunner; Ad Geurts van Kessel; Siu Tsan Yuen; J Han J M van Krieken; Suet Yi Leung; Nicoline Hoogerbrugge
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.
Nature genetics 2009;41(1):112-7.
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: L I H Overbeek; Carolien M Kets; Konnie Hebeda; Daniëlle Bodmer; E van der Looij; Riki Willems; M Goossens; Neeltje J W Arts; Han G Brunner; J H J M van Krieken; Nicoline Hoogerbrugge; M J L Ligtenberg
Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer.
British journal of cancer 2007;96(10):1605-12.
2006: Carolien M Kets; Nicoline Hoogerbrugge; Daniëlle Bodmer; Riki Willems; Han G Brunner; J H J M van Krieken; M J L Ligtenberg
Unfavorable pathological characteristics in familial colorectal cancer with low-level microsatellite instability.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2006;19(12):1624-30.
2006: Daniëlle Bodmer; M J L Ligtenberg; Annemarie H Van Der Hout; S Gloudemans; K Ansink; Jan C Oosterwijk; Nicoline Hoogerbrugge
Optimal selection for BRCA1 and BRCA2 mutation testing using a combination of 'easy to apply' probability models.
British journal of cancer 2006;95(6):757-62.
2006: Annemarie H Van Der Hout; Ans M W van den Ouweland; Rob B van der Luijt; Hans J P Gille; Daniëlle Bodmer; Hennie T Brüggenwirth; Inge M Mulder; Pieter van der Vlies; Peter Elfferich; Maarten Huisman; Annelies M ten Berge; Joan Kromosoeto; Rumo P M Jansen; Patrick H A van Zon; Thyrsa Vriesman; Neeltje J W Arts; Majella Boutmy-de Lange; Jan C Oosterwijk; Hanne Meijers-Heijboer; Margreet G E M Ausems; Nicoline Hoogerbrugge; Senno Verhoef; D J J Halley; Yvonne J Vos; Frans B L Hogervorst; M J L Ligtenberg; Robert M W Hofstra
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
Human mutation 2006;27(7):654-66.
2004: Anita C M Bonné; Daniëlle Bodmer; Eric F P M Schoenmakers; Conny van Ravenswaaij-Arts; Nicoline Hoogerbrugge; Ad Geurts van Kessel
Chromosome 3 translocations and familial renal cell cancer.
Current molecular medicine 2004;4(8):849-54.
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; Wilhelmina H van den Hurk; Jan J M van Groningen; Marc J Eleveld; Gerard J M Martens; Marian A J Weterman; Ad Geurts van Kessel
Understanding familial and non-familial renal cell cancer.
Human molecular genetics 2002;11(20):2489-98.
2002: Daniëlle Bodmer; Irene M Janssen; Yvonne Jonkers; Eva van den Berg; Trijnie Dijkhuizen; Maria Debiec-Rychter; Eric F P M Schoenmakers; Ad Geurts van Kessel
Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13 approximately q22 breakpoints.
Cancer genetics and cytogenetics 2002;136(2):95-100.
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.
2002: Daniëlle Bodmer; Marc J Eleveld; Ellen Kater-Baats; Irene M Janssen; Bert Janssen; Marian A J Weterman; Eric F P M Schoenmakers; Michael L Nickerson; Marston Linehan; Berton Zbar; Ad Geurts van Kessel
Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21).
Human molecular genetics 2002;11(6):641-9.
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.
1999: Ad Geurts van Kessel; H Wijnhoven; Daniëlle Bodmer; Marc J Eleveld; L Kiemeney; P Mulders; Marian A J Weterman; M J L Ligtenberg; Dominique Smeets; Arie P T Smits
Renal cell cancer: chromosome 3 translocations as risk factors.
Journal of the National Cancer Institute 1999;91(13):1159-60.
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.