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cancer breast family mutation breast cancer study patient brca 1 tumor analysis variant linkage number chromosome genet region control syndrome susceptibility disease model score brca 2 association identi brca 2 mutations marker paraganglioma table result netherland identi fied breast cancer risk university allele department brcax genetic germline individual pathway research candidate population factor frequency center carrier genome-wide genomic phaeochromocytoma protein anomaly citation purposes page number linkage analysis chek 2*1100delc sample women signi analyses figure deletion information group chek 2 aneurysm sequence ratio candidate regions foxc 1 value brcax tumors locus stage haplotype family history approach er-negative osteoarthritis
10 Most Recent Publications
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Excess breast cancer risk in first degree relatives of CHEK2* 1100delC positive familial breast cancer cases
(Article)
Adank, M.A. Verhoef, S. Jonker, M.A. Meijers-Heijboer, E.J. Oldenburg, R. Schmidt, M.K. Hooning, M. Martens, J.W.M. Broeks, A. Rookus, M.A. Waisfisz, Q. Witte, B.I. |
2013-05-01
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SDHA mutations in adult and pediatric wild-type gastrointestinal stromal tumors
(Article)
Oudijk, L. Gaal, J. Loon, R.L.E. van O'Sullivan, M.J. Krijger, R.R. de Dinjens, W.N.M. Korpershoek, E. Nederveen, F.H. van Kelly, L. Schiavon, G. Verweij, J. Mathijssen, R.H.J. Bakker, M.A. den Oldenburg, R. |
2013-03-01
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Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndrome
(Article)
Laar, I.M.B.H. van de Linde, D. van der Moelker, A. Graaf, B.M. de Matyas, G. Frohn-Mulder, I.M.E. Timmermans, J. Hilhorst-Hofstee, Y. Cobben, J.M. Brüggenwirth, H.T. Laer, L. van Loeys, B. Oei, E.H.G. Backer, J. de Coucke, P. Dietz, H.C. Willems, P.J. Oostra, B.A. Paepe, A. de Roos-Hesselink, J.W. Bertoli Avella, A.M. Wessels, M.W. Bos, P.K. Bessems, J.H.J.M. Bierma-Zeinstra, S.M.A. Meer, B.L. van Pals, G. Oldenburg, R. Bekkers, J.A. |
2012-01-01
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A non-BRCA1/2 hereditary breast cancer sub-group defined by aCGH profiling of genetically related patients
(Article)
Didraga, M.A. Beers, E.H. van Devilee, P. Nederlof, P.M. Joosse, S.A. Brandwijk, K.I.M. Oldenburg, R. Wessels, L.F.A. Hogervorst, F.B.L. Ligtenberg, M. Hoogerbrugge, N. Verhoef, S. |
2011-11-01
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Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis
(Article)
Laar, I.M.B.H. van de Oldenburg, R. Vriend, G. Pattynama, P.M.T. Collee, J.M. Majoor-Krakauer, D.F. Poldermans, D. Frohn-Mulder, I.M.E. Micha, D. Timmermans, J. Hilhorst-Hofstee, Y. Bierma-Zeinstra, S.M.A. Pals, G. Willems, P.J. Kros, J.M. Oei, E.H.G. Oostra, B.A. Wessels, M.W. Bertoli Avella, A.M. Roos-Hesselink, J.W. Graaf, B.M. de Verhagen, J.M.A. Hoedemaekers, Y.M. Willemsen, R. Severijnen, L.A. Venselaar, H. |
2011-02-01
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Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations
(Article)
D'Haene, B. Meire, F. Wuyts, W. Ende, J. van den Roulez, F. Veenstra-Knol, H.E. Oldenburg, R. Giltay, J. Verheij, J.B.G.M. Faber, J.-T. de Menten, B. Paepe, A. de Claerhout, I. Kestelyn, P. Leroy, B.P. Baere, E. de Kroes, H.Y. Plomp, A. Arens, Y.H.J.M. Ravel, T. de Casteels, I. Jaegere, S. de Hooghe, S. |
2011-01-01
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A genome-wide association scan on estrogen receptor-negative breast cancer
(Article)
Li, J. Humphreys, M.K. Ahmed, S. Hooning, M. Hollestelle, A. Oldenburg, R. Alfredsson, L. Palotie, A. Peltonen-Palotie, L. Irwanto, A. Low, H.Q. Teoh, G.H.K. Darabi, H. Thalamuthu, A. Kere, J. D'Amato, M. Easton, D.F. Nevanlinna, H. Liu, J. Czene, k. Hall, A.S. Rosin, G. Hannelius, U. Heikinen, T. Aittomäki, K. Blomqvist, C. Pharoah, P.D.P. Dunning, A.M. |
2010-11-09
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Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome
(Article)
Gaal, J. Nederveen, F.H. van Erlic, Z. Korpershoek, E. Oldenburg, R. Boedeker, C.C. Kontny, U. Neumann, H.P. Dinjens, W.N.M. Krijger, R.R. de |
2009-11-01
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An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis
(Article)
Nederveen, F.H. van Gaal, J. Petri, B.J. Komminoth, P. Pacak, K. Hop, W.C.J. Pollard, P.J. Mannelli, M. Bayley, J.P. Perren, A. Niemann, S. Verhofstad, A.A. Favier, J. Bruïne, A.P. de Maher, E.R. Tissier, F. Méatchi, T. Badoual, C. Bertherat, J. Amar, L. Alataki, D. Marck, E. van Ferrau, F. Korpershoek, E. François, J.F. Herder, W.W. de Peeters, M.P.F.V. Linge, A. van Lenders, J.W. Gimenez-Roqueplo, A.P. Krijger, R.R. de Dinjens, W.N.M. Oldenburg, R. Bruyn, E.M. de Sleddens, H.F. Derkx, P. Rivière, J. Dannenberg, H. |
2009-08-01
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Premature ovarian failure and gene polymorphisms
(Article)
Dooren, M.F. van Bertoli Avella, A.M. Oldenburg, R. |
2009-08-01
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