High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands
Hensen, EF, van Duinen, N, Jansen, JC, Corssmit, EPM, Tops, CMJ, Romijn, JA, Vriends, AHJT, van der Mey, AGL, Cornelisse, CJ, Devilee, P, Bayley, JP
Published in Clinical genetics (01.03.2012)
Published in Clinical genetics (01.03.2012)
Get full text
Journal Article
Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK21100delC variant
de Bock, G H, Schutte, M, Krol-Warmerdam, E M M, Seynaeve, C, Blom, J, Brekelmans, C T M, Meijers-Heijboer, H, van Asperen, C J, Cornelisse, C J, Devilee, P, Tollenaar, R A E M, Klijn, J G M
Published in Journal of medical genetics (01.10.2004)
Published in Journal of medical genetics (01.10.2004)
Get full text
Journal Article
Mutations in SDHD, A Mitochondrial Complex II Gene, in Hereditary Paraganglioma
Baysal, Bora E., Ferrell, Robert E., Willett-Brozick, Joan E., Lawrence, Elizabeth C., Myssiorek, David, Bosch, Anne, van der Mey, Andel, Peter E. M. Taschner, Rubinstein, Wendy S., Myers, Eugene N., Richard, Charles W., Cornelisse, Cees J., Devilee, Peter, Devlin, B.
Published in Science (American Association for the Advancement of Science) (04.02.2000)
Published in Science (American Association for the Advancement of Science) (04.02.2000)
Get full text
Journal Article
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree
Wagner, A, Hendriks, Y, Meijers-Heijboer, E J, de Leeuw, W J F, Morreau, H, Hofstra, R, Tops, C, Bik, E, Bröcker-Vriends, A H J T, van der Meer, C, Lindhout, D, Vasen, H F A, Breuning, M H, Cornelisse, C J, van Krimpen, C, Niermeijer, M F, Zwinderman, A H, Wijnen, J, Fodde, R
Published in Journal of medical genetics (01.05.2001)
Published in Journal of medical genetics (01.05.2001)
Get full text
Journal Article
Quantifying measures to limit wind-driven resuspension of sediments for improvement of the ecological quality in some shallow Dutch lakes
Penning, W. E., Genseberger, M., Uittenbogaard, R. E., Cornelisse, J. C.
Published in Hydrobiologia (01.06.2013)
Published in Hydrobiologia (01.06.2013)
Get full text
Journal Article
Conference Proceeding
E‐cadherin is a tumour/invasion suppressor gene mutated in human lobular breast cancers
Berx, G., Cleton‐Jansen, A. M., Nollet, F., Leeuw, W. J., Vijver, M., Cornelisse, C., Roy, F.
Published in The EMBO journal (15.12.1995)
Published in The EMBO journal (15.12.1995)
Get full text
Journal Article
EXT-Mutation Analysis and Loss of Heterozygosity in Sporadic and Hereditary Osteochondromas and Secondary Chondrosarcomas
Bovée, Judith V.M.G., Cleton-Jansen, Anne-Marie, Wuyts, Wim, Caethoven, Goedele, Taminiau, Antonie H.M., Bakker, Egbert, Van Hul, Wim, Cornelisse, Cees J., Hogendoorn, Pancras C.W.
Published in American journal of human genetics (01.09.1999)
Published in American journal of human genetics (01.09.1999)
Get full text
Journal Article
Instability of short tandem repeats (microsatellites) in human cancers
Wooster, R, Cleton-Jansen, A.-M, Collins, N, Mangion, J, Cornelis, R.S, Cooper, C.S, Gusterson, B.A, Ponder, B.A.J, von Deimling, A, Wiestler, O.D, Cornelisse, C.J, Devilee, P, Stratton, M.R
Published in Nature genetics (01.02.1994)
Published in Nature genetics (01.02.1994)
Get full text
Journal Article
Rapid detection of BRCA1 mutations by the protein truncation test
Hogervorst, Frans B.L, Vasen, Hans F.A, van Ommen, Gert-Jan B, Cornelis, Renée S, Vliet, Margreethe van, Oosterwijk, Jan C, Olmer, Renske, Menko, Fred H, Cornelisse, Cees J, Meijers-Heijboer, Hanna, den Dunnen, Johan T, Devilee, Peter, Bakker, Bert, Klijn, Jan G.M, Bout, Mattie
Published in Nature genetics (01.06.1995)
Published in Nature genetics (01.06.1995)
Get full text
Journal Article
Presymptomatic testing for BRCA1 and BRCA2: how distressing are the pre-test weeks?
LODDER, L. N, FRETS, P. G, CORNELISSE, C. J, NIERMEIJER, M. F, TRIJSBURG, R. W, MEIJERS-HEIJBOER, E. J, KLIJN, J. G. M, DUIVENVOORDEN, H. J, TIBBEN, A, WAGNER, A, VAN DER MEER, C. A, DEVILEE, P
Published in Journal of medical genetics (01.12.1999)
Get full text
Published in Journal of medical genetics (01.12.1999)
Journal Article
Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families
HENSEN, Erik F, JORDANOVA, Ekaterina S, VAN MINDERHOUT, Ivonne J. H. M, HOGENDOORN, Pancras C. W, TASCHNER, Peter E. M, VAN DER MEY, Andel G. L, DEVILEE, Peter, CORNELISSE, Cees J
Published in Oncogene (20.05.2004)
Published in Oncogene (20.05.2004)
Get full text
Journal Article
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients
Petrij-Bosch, A, Peelen, T, van Vliet, M, van Eijk, R, Olmer, R, Drüsedau, M, Hogervorst, F B, Hageman, S, Arts, P J, Ligtenberg, M J, Meijers-Heijboer, H, Klijn, J G, Vasen, H F, Cornelisse, C J, van 't Veer, L J, Bakker, E, van Ommen, G J, Devilee, P
Published in Nature genetics (01.11.1997)
Published in Nature genetics (01.11.1997)
Get full text
Journal Article
Extending the p16-Leiden tumour spectrum by respiratory tract tumours
Oldenburg, R A, de Vos tot Nederveen Cappel, W H, van Puijenbroek, M, van den Ouweland, A, Bakker, E, Griffioen, G, Devilee, P, Cornelisse, C J, Meijers-Heijboer, H, Vasen, H F A, Morreau, H
Published in Journal of medical genetics (01.03.2004)
Published in Journal of medical genetics (01.03.2004)
Get full text
Journal Article
Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q
Devilee, P, van Vliet, M, van Sloun, P, Kuipers Dijkshoorn, N, Hermans, J, Pearson, P L, Cornelisse, C J
Published in Oncogene (01.09.1991)
Get more information
Published in Oncogene (01.09.1991)
Journal Article
A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families
PEELEN, T, VAN VLIET, M, VAN DER LUIJT, R, VAN DER HOUT, A. H, GILLE, J. J. P, PALS, G, JEDEMA, I, OLMER, R, VAN LEEUWEN, I, NEWMAN, B, PLANDSOEN, M, VAN DER EST, M, PETRIJ-BOSCH, A, BRINK, G, HAGEMAN, S, ARTS, P. J. W, BAKKER, M. M, WILLEMS, H. W, VAN DER LOOIJ, E, NEYNS, B, BONDUELLE, M, JANSEN, R, OOSDERWIJK, J. C, MIEREMET, R, SIJMONS, R, SMEETS, H. J. M, VAN ASPEREN, C. J, MEIJERS-HEIJBOER, H, KLIJN, J. G. M, DE GREVE, J, KING, M.-C, MENKO, F. H, BRUNNER, H. G, HALLEY, D, SZABO, C, VAN OMMEN, G.-J. B, VASEN, H. F. A, CORNELISSE, C. J, VAN'VEER, L. J, DE KNIJFF, P, BAKKER, E, DEVILEE, P, VAN DEN OUWELAND, A. M. W, HOGERVORST, F, BROHET, R, LIGTENBERG, M. J. L, TEUGELS, E
Published in American journal of human genetics (01.05.1997)
Get full text
Published in American journal of human genetics (01.05.1997)
Journal Article
Ever since Knudson
Devilee, Peter, Cleton-Jansen, Anne-Marie, Cornelisse, Cees J.
Published in Trends in genetics (01.10.2001)
Published in Trends in genetics (01.10.2001)
Get full text
Journal Article
Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene
Taschner, Peter E.M., Jansen, Jeroen C., Baysal, Bora E., Bosch, Anne, Rosenberg, Efraim H., Bröcker-Vriends, Annette H.J.T., van der Mey, Andel G.L., van Ommen, Gert-Jan B., Cornelisse, Cees J., Devilee, Peter
Published in Genes chromosomes & cancer (01.07.2001)
Published in Genes chromosomes & cancer (01.07.2001)
Get full text
Journal Article