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| Full Text | Issue Date | Title | Author(s) |  | 2011 | SNP array analysis in constitutional and cancer genome diagnostics-copy number variants, genotyping and quality control. | Leeuw, N. de; Hehir-Kwa, J.Y.; Simons, A.; Geurts van Kessel, A.H.M.; Smeets, D.F.; Faas, B.H.W.; Pfundt, R. |
 | 2011 | TET2 mutations in childhood leukemia | Langemeijer, S.M.C.; Jansen, J.H.; Hooijer, J.; Hoogen, P.C.M. van; Stevens-Linders, E.H.P.; Massop, M.; Waanders, E.; Reijmersdal, S.V. van; Stevens-Kroef, M.J.P.L.; Zwaan, C.M.; Heuvel-Eibrink, M.M. van den; Sonneveld, E.; Hoogerbrugge, P.M.; Geurts van Kessel, A.H.M.; Kuiper, R.P. |
| | 2011 | High prevalence of adverse prognostic genetic aberrations and unmutated IGHV genes in small lymphocytic lymphoma as compared to chronic lymphocytic leukemia. | Groenen, P.J.T.A.; Raymakers, R.; Rombout, P.D.M.; Prenter, M. de; Kossen, L.; Philipsen-Jansen, C.; Feuth, T.; Meijer, J.W.R.; Geurts van Kessel, A.H.M.; Krieken, J.H.J.M. van; Stevens-Kroef, M.J.P.L. |
| | 2011 | Nonstarch polysaccharide-degrading enzymes alter the microbial community and the fermentation patterns of barley cultivars and wheat products in an in vitro model of the porcine gastrointestinal tract | Bindelle, J.; Pieper, R.; Montoya, C.A.; Geurts van Kessel, A.H.M.; Leterme, P. |
| | 2011 | Genomic profiling of papillary renal cell tumours identifies small regions of DNA alterations: a possible role of HNF1B in tumour development | Szponar, A.; Yusenko, M.V.; Kuiper, R.P.; Geurts van Kessel, A.H.; Kovacs, G. |
| | 2011 | Incidental prenatal diagnosis of sex chromosome aneuploidies: health, behavior, and fertility. | Pieters, J.J.; Kooper, A.J.A.; Geurts van Kessel, A.H.M.; Braat, D.D.M.; Smits, A.P.T. |
| | 2011 | Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia | Simons, A.; Stevens-Kroef, M.J.P.L.; El Idrissi-Zaynoun, N.; Gessel, S. van; Weghuis, D.O.; Berg, E. van den; Waanders, E.; Hoogerbrugge, P.M.; Kuiper, R.P.; Geurts van Kessel, A.H.M. |
| | 2011 | Integrated use of minimal residual disease classification and IKZF1 alteration status accurately predicts 79% of relapses in pediatric acute lymphoblastic leukemia | Waanders, E.; Velden, V.H. van der; Schoot, C.E. van der; Leeuwen, F.N. van; Reijmersdal, S.V. van; Haas, V. de; Veerman, A.J.P.; Geurts van Kessel, A.H.M.; Hoogerbrugge, P.M.; Kuiper, R.P.; Dongen, J.J. van |
| | 2011 | Intra-individual stability over time of standardized anti-Mullerian hormone in FMR1 premutation carriers | Spath, M.A.; Feuth, T.; Allen, E.G.; Smits, A.P.T.; Yntema, H.G.; Geurts van Kessel, A.H.M.; Braat, D.D.M.; Sherman, S.L.; Thomas, C.M.G. |
| | 2011 | Homozygosity mapping in outbred families with mental retardation | Schuurs-Hoeijmakers, J.H.M.; Hehir, J.Y.; Pfundt, R.; Bon, B.W.M. van; Leeuw, N. de; Kleefstra, T.; Willemsen, M.A.A.P.; Geurts van Kessel, A.H.M.; Brunner, H.G.; Veltman, J.A.; Bokhoven, J.H.L.M. van; Brouwer, A.P.M. de; Vries, B.B. de |
| | 2011 | Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients | Venkatachalam, R.; Verwiel, E.T.P.; Kamping, E.J.; Hoenselaar, E.; Gorgens, H.; Schackert, H.K.; Krieken, J.H. van; Ligtenberg, M.J.L.; Hoogerbrugge, N.; Geurts van Kessel, A.H.M.; Kuiper, R.P. |
| | 2011 | Predictors and risk model development for menopausal age in fragile X premutation carriers | Spath, M.A.; Feuth, A.B.; Smits, A.P.T.; Yntema, H.G.; Braat, D.D.M.; Thomas, C.M.G.; Geurts van Kessel, A.H.M.; Sherman, S.L.; Allen, E.G. |
| | 2011 | Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation | Jongmans, M.C.J.; Burgt, I. van der; Hoogerbrugge, P.M.; Noordam, K.; Yntema, H.G.; Nillesen, W.M.; Kuiper, R.P.; Ligtenberg, M.J.L.; Geurts van Kessel, A.H.M.; Krieken, J.H. van; Kiemeney, L.A.L.M.; Hoogerbrugge, N. |
| | 2011 | Recurrence and variability of germline EPCAM deletions in Lynch syndrome | Kuiper, R.P.; Vissers, L.E.L.M.; Venkatachalam, R.; Bodmer, D.; Hoenselaar, E.; Goossens, M.; Haufe, A.; Kamping, E.J.; Niessen, R.C.; Hogervorst, F.B.L.; Gille, J.J.P.; Redeker, B.; Tops, C.M.; Gijn, M.E. van; Ouweland, A.M. van den; Rahner, N.; Steinke, V.; Kahl, P.; Holinski-Feder, E.; Morak, M.; Kloor, M.; Stemmler, S.; Betz, B.; Hutter, P.; Bunyan, D.J.; Syngal, S.; Culver, J.O.; Graham, T.; Chan, T.L.; Nagtegaal, I.D.; Krieken, J.H. van; Schackert, H.K.; Hoogerbrugge, N.; Geurts van Kessel, A.H.M.; Ligtenberg, M.J.L. |
| | 2011 | Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study | Kempers, M.J.E.; Kuiper, R.P.; Ockeloen, C.W.; Chappuis, P.O.; Hutter, P.; Rahner, N.; Schackert, H.K.; Steinke, V.; Holinski-Feder, E.; Morak, M.; Kloor, M.; Buttner, R.; Verwiel, E.T.P.; Krieken, J.H. van; Nagtegaal, I.D.; Goossens, M.; Post, R.S. van der; Niessen, R.C.; Sijmons, R.H.; Kluijt, I.; Hogervorst, F.B.L.; Leter, E.M.; Gille, J.J.P.; Aalfs, C.M.; Redeker, E.J.; Hes, F.J.; Tops, C.M.; Nesselrooij, B.P. van; Gijn, M.E. van; Gomez Garcia, E.B.; Eccles, D.M.; Bunyan, D.J.; Syngal, S.; Stoffel, E.M.; Culver, J.O.; Palomares, M.R.; Graham, T.; Velsher, L.; Papp, J.; Olah, E.; Chan, T.L.; Leung, S.Y.; Geurts van Kessel, A.H.M.; Kiemeney, L.A.L.M.; Hoogerbrugge, N.; Ligtenberg, M.J.L. |
| | 2010 | Germline epigenetic silencing of the tumor suppressor gene PTPRJ in early-onset familial colorectal cancer. | Venkatachalam, R.; Ligtenberg, M.J.L.; Hoogerbrugge, N.; Schackert, H.K.; Gorgens, H.; Hahn, M.M.; Kamping, E.J.; Basten-Vreede, L.A.J.; Hoenselaar, E.; Looij, E. van de; Goossens, M.; Churchman, M.; Carvajal-Carmona, L.; Tomlinson, I.P.; Bruijn, D.R.H. de; Geurts van Kessel, A.H.M.; Kuiper, R.P. |
| | 2010 | Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome. | Jongmans, M.C.J.; Kuiper, R.P.; Carmichael, C.L.; Wilkins, E.J.; Dors, N.; Carmagnac, A.; Schouten-van Meeteren, A.Y.; Li, X.; Stankovic, M.; Kamping, E.J.; Bengtsson, H.; Schoenmakers, E.F.P.M.; Geurts van Kessel, A.H.M.; Hoogerbrugge, P.M.; Hahn, C.N.; Brons, P.P.T.; Scott, H.S.; Hoogerbrugge-van der Linden, N. |
| | 2010 | The 'omics' of cancer. | Geurts van Kessel, A.H.M. |
| | 2010 | Noonan syndrome, the SOS1 gene and embryonal rhabdomyosarcoma. | Jongmans, M.C.J.; Hoogerbrugge, P.M.; Hilkens, L.; Flucke, U.E.; Burgt, C.J.A.M. van der; Noordam, C.; Ruiterkamp-Versteeg, M.; Yntema, H.G.; Nillesen, W.M.; Ligtenberg, M.J.L.; Geurts van Kessel, A.H.M.; Kuiper, R.P.; Hoogerbrugge, N. |
| | 2010 | BTG1 regulates glucocorticoid receptor autoinduction in acute lymphoblastic leukemia. | Galen, J.C. van; Kuiper, R.P.; Emst, J.E. van; Levers, M.R.; Tijchon, E.J.H.; Scheijen, B.; Waanders, E.; Reijmersdal, S.V. van; Gilissen, C.F.H.A.; Geurts van Kessel, A.H.M.; Hoogerbrugge, P.M.; Leeuwen, F.N. van |
| | 2010 | The epigenetics of (hereditary) colorectal cancer. | Venkatachalam, R.; Ligtenberg, M.J.L.; Hoogerbrugge-van der Linden, N.; Bruijn, D.R.H. de; Kuiper, R.P.; Geurts van Kessel, A.H.M. |
| | 2010 | Germline copy number variation and cancer risk. | Kuiper, R.P.; Ligtenberg, M.J.L.; Hoogerbrugge, N.; Geurts van Kessel, A.H.M. |
 | 2010 | The mitotic arrest deficient protein MAD2B interacts with the clathrin light chain A during mitosis. | Medendorp, K.; Basten-Vreede, L.A.J.; Groningen, J.J.M. van; Hetterschijt, L.; Brugmans, L.J.L.; Jansen, P.A.M.; Hurk, W.H. van den; Bruijn, D.R.H. de; Geurts van Kessel, A.H.M. |
| | 2010 | X chromosome inactivation does not define the development of premature ovarian failure in fragile X premutation carriers. | Spath, M.A.; Nillesen, W.M.; Smits, A.P.T.; Feuth, A.B.; Braat, D.D.M.; Geurts van Kessel, A.H.M.; Yntema, H.G. |
| | 2010 | IKZF1 deletions predict relapse in uniformly treated pediatric precursor B-ALL. | Kuiper, R.P.; Waanders, E.; Velden, V.H. van der; Reijmersdal, S.V. van; Venkatachalam, R.; Scheijen, B.; Sonneveld, E.; Dongen, J.J.A.M. van; Veerman, A.J.P.; Leeuwen, F.N. van; Geurts van Kessel, A.H.M.; Hoogerbrugge, P.M. |
| | 2010 | CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation. | Mukhopadhyay, A.; Kramer, J.M.; Merkx, G.F.M.; Lugtenberg, D.; Smeets, D.F.C.M.; Oortveld, M.A.W.; Blokland, E.A.W.; Agrawal, J.; Schenck, A.; Bokhoven, J.H.L.M. van; Huys, E.; Schoenmakers, E.F.P.M.; Geurts van Kessel, A.H.M.; Nouhuys, C.E. van; Cremers, F.P.M. |
| | 2009 | High-resolution genomic profiling of pediatric lymphoblastic lymphomas reveals subtle differences with pediatric acute lymphoblastic leukemias in the B-lineage. | Schraders, M.; Reijmersdal, S.V. van; Kamping, E.J.; Krieken, J.H.J.M. van; Geurts van Kessel, A.H.M.; Groenen, P.J.T.A.; Hoogerbrugge, P.M.; Kuiper, R.P. |
| | 2009 | High-resolution DNA copy number and gene expression analyses distinguish chromophobe renal cell carcinomas and renal oncocytomas. | Yusenko, M.V.; Kuiper, R.P.; Boethe, T.; Ljungberg, B.; Geurts van Kessel, A.H.M.; Kovacs, G. |
| | 2009 | Characterization of a recurrent t(1;2)(p36;p24) in human uterine leiomyoma. | Rijk, A. van; Sweers, M.A.; Huys, E.; Kersten, M.; Merkx, G.F.M.; Geurts van Kessel, A.H.M.; Debiec-Rychter, M.; Schoenmakers, E.F.P.M. |
| | 2009 | The mitotic arrest deficient protein MAD2B interacts with the small GTPase RAN throughout the cell cycle. | Medendorp, K.; Groningen, J.J.M. van; Basten-Vreede, L.A.J.; Hetterschijt, L.; Hurk, W.H. van den; Bruijn, D.R.H. de; Brugmans, L.J.L.; Geurts van Kessel, A.H.M. |
| | 2009 | Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1. | Ligtenberg, M.J.L.; Kuiper, R.P.; Chan, T.L.; Goossens, M.; Hebeda, K.M.; Voorendt, M.; Lee, T.Y.; Bodmer, D.; Hoenselaar, E.; Hendriks-Cornelissen, S.J.; Tsui, W.Y.; Kong, C.K.; Brunner, H.G.; Geurts van Kessel, A.H.M.; Yuen, S.T.; Krieken, J.H.J.M. van; Leung, S.Y.; Hoogerbrugge-van der Linden, N. |
| | 2009 | Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification. | Stevens-Kroef, M.J.P.L.; Simons, A.; Gorissen, H.; Feuth, A.B.; Weghuis, D.O.; Buijs, A.J.; Raymakers, R.A.P.; Geurts van Kessel, A.H.M. |
| | 2009 | Acquired mutations in TET2 are common in myelodysplastic syndromes. | Langemeijer, S.M.C.; Kuiper, R.P.; Berends, M.; Knops, G.H.J.N.; Aslanyan, M.G.; Massop, M.; Linders, E.H.P.; Hoogen, P.C.M. van; Geurts van Kessel, A.H.M.; Raymakers, R.A.P.; Kamping, E.J.; Verhoef, G.E.; Verburgh, E.; Hagemeijer, A.; Berghe, P. van den; Witte, T.J.M. de; Reijden, B.A. van der; Jansen, J.H. |
| | 2009 | Detection of chromosome aneuploidies in chorionic villus samples by multiplex ligation-dependent probe amplification. | Kooper, A.J.A.; Faas, B.H.W.; Feuth, A.B.; Creemers, J.W.T.; Zondervan, H.H.; Boekkooi, P.F.; Quartero, R.W.; Rijnders, R.J.; Burgt, C.J.A.M. van der; Geurts van Kessel, A.H.M.; Smits, A.P.T. |
| | 2009 | The renal cell carcinoma-associated oncogenic fusion protein PRCCTFE3 provokes p21 WAF1/CIP1-mediated cell cycle delay. | Medendorp, K.; Groningen, J.J.M. van; Basten-Vreede, L.A.J.; Hetterschijt, L.; Brugmans, L.J.L.; Hurk, W.H. van den; Geurts van Kessel, A.H.M. |
| | 2009 | The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer. | Kuiper, R.P.; Basten-Vreede, L.A.J.; Venkatachalam, R.; Ricketts, C.; Kamping, E.J.; Verwiel, E.T.P.; Govaerts, L.; Debiec-Rychter, M.; Lerut, E.; Erp, C.A. van; Hoogerbrugge-van der Linden, N.; Kempen, L.C.L.T. van; Schoenmakers, E.F.P.M.; Bonne, A.; Maher, E.R.; Geurts van Kessel, A.H.M. |
| | 2009 | Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture. | Vissers, L.E.L.M.; Bhatt, S.S.; Janssen, I.M.; Xia, Z.; Lalani, S.R.; Pfundt, R.P.; Derwinska, K.; Vries, L.B.A. de; Gilissen, C.F.H.A.; Hoischen, A.; Nesteruk, M.; Wisniowiecka-Kowalnik, B.; Smyk, M.; Brunner, H.G.; Cheung, S.W.; Geurts van Kessel, A.H.M.; Veltman, J.A.; Stankiewicz, P. |
| | 2009 | Genomic microarrays in mental retardation: a practical workflow for diagnostic applications. | Koolen, D.A.; Pfundt, R.P.; Leeuw, N. de; Hehir-Kwa, J.Y.; Nillesen, W.M.; Neefs, I.; Scheltinga, I.; Sistermans, E.A.; Smeets, D.F.C.M.; Brunner, H.G.; Geurts van Kessel, A.H.M.; Veltman, J.A.; Vries, L.B.A. de |
| | 2008 | Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype. | Swinkels, M.E.; Simons, A.; Smeets, D.F.C.M.; Vissers, L.E.L.M.; Veltman, J.A.; Pfundt, R.P.; Vries, L.B.A. de; Faas, B.H.W.; Schrander-Stumpel, C.T.; McCann, E.; Sweeney, E.; May, P.; Draaisma, J.M.T.; Knoers, N.V.A.M.; Geurts van Kessel, A.H.M.; Ravenswaaij-Arts, C.M.A. van |
| | 2008 | Recurrent CNVs disrupt three candidate genes in schizophrenia patients. | Vrijenhoek, T.; Buizer-Voskamp, J.E.; Stelt, I van der; Strengman, E.; Sabatti, C.; Geurts van Kessel, A.H.M.; Brunner, H.G.; Ophoff, R.A.; Veltman, J.A. |
| | 2008 | CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy. | Friedman, J.I.; Vrijenhoek, T.; Markx, S.; Janssen, I.M.; Vliet, W.A. van der; Faas, B.H.W.; Knoers, N.V.A.M.; Cahn, W.; Kahn, R.S.; Edelmann, L.; Davis, K.L.; Silverman, J.M.; Brunner, H.G.; Geurts van Kessel, A.H.M.; Wijmenga, C.; Ophoff, R.A.; Veltman, J.A. |
| | 2008 | The C terminus of the synovial sarcoma-associated SSX proteins interacts with the LIM homeobox protein LHX4. | Bruijn, D.R.H. de; Dijk, A.H.A.; Willemse, M.P.; Geurts van Kessel, A.H.M. |
| | 2008 | Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cells. | Kooper, A.J.A.; Faas, B.H.W.; Kater-Baats, E.; Feuth, T.; Janssen, J.C.; Burgt, I. van der; Lotgering, F.K.; Geurts van Kessel, A.H.M.; Smits, A.P.T. |
| | 2008 | Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches. | Koolen, D.A.; Sistermans, E.A.; Nilessen, W.; Knight, S.J.; Regan, R.; Liu, Y.T.; Kooy, R.F.; Rooms, L.; Romano, C.; Fichera, M.; Schinzel, A.; Baumer, A.; Anderlid, B.M.; Schoumans, J.; Geurts van Kessel, A.H.M.; Nordenskjold, M.; Vries, L.B.A. de |
| | 2008 | Histone deacetylase inhibitors reverse SS18-SSX-mediated polycomb silencing of the tumor suppressor early growth response 1 in synovial sarcoma. | Lubieniecka, J.M.; Bruijn, D.R.H. de; Su, L.; Dijk, A.H.A.; Subramanian, S.; Rijn, M van de; Poulin, N.; Geurts van Kessel, A.H.M.; Nielsen, T.O. |
| | 2007 | The (epi)genetics of human synovial sarcoma. | Bruijn, D.R.H. de; Nap, J.P.; Geurts van Kessel, A.H.M. |
| | 2007 | Variation of CNV distribution in five different ethnic populations. | White, S.J.; Vissers, L.E.L.M.; Geurts van Kessel, A.H.M.; Menezes, R.X. de; Kalay, E.; Lehesjoki, A.E.; Giordano, P.C.; Vosse, E. van de; Breuning, M.H.; Brunner, H.G.; Dunnen, J.T. den; Veltman, J.A. |
| | 2007 | Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas. | Medendorp, K.; Groningen, J.J.M. van; Schepens, M.T.M.; Basten-Vreede, L.A.J.; Thijssen, J.; Schoenmakers, E.F.P.M.; Hurk, W.H. van den; Geurts van Kessel, A.H.M.; Kuiper, R.P. |
| | 2007 | Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene. | Bonne, A.; Basten-Vreede, L.A.J.; Kuiper, R.P.; Bodmer, D.; Jansen, C.; Eleveld, M.J.; Erp, F. van; Arkesteijn, G.; Hoogerbrugge, N.; Ravenswaaij-Arts, C.M.A. van; Schoenmakers, E.F.P.M.; Geurts van Kessel, A.H.M. |
| | 2007 | Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis. | Hehir-Kwa, J.Y.; Egmont-Peterson, M.; Janssen, I.M.; Smeets, D.F.C.M.; Geurts van Kessel, A.H.M.; Veltman, J.A. |
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