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van der Drift, Miep A, Prinsen, Clemens F M, Knuiman, G Jimmy, Janssen, Julius P, Dekhuijzen, P N Richard, Thunnissen, Frederic B J M
Published in Chest (01.01.2012)
Published in Chest (01.01.2012)
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DNA Microarray Format for Detection and Subtyping of Human Papillomavirus
KLAASSEN, Corné H. W, PRINSEN, Clemens F. M, DE VALK, Hanneke A, HORREVORTS, Alphons M, JEUNINK, Marcel A. F, THUNNISSEN, Frederik B. J. M
Published in Journal of Clinical Microbiology (01.05.2004)
Published in Journal of Clinical Microbiology (01.05.2004)
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Methylation analysis in spontaneous sputum for lung cancer diagnosis
Hubers, A. Jasmijn, van der Drift, Miep A, Prinsen, Clemens F.M, Witte, Birgit I, Wang, Yinghui, Shivapurkar, Narayan, Stastny, Victor, Bolijn, Anne S, Hol, Bernard E.A, Feng, Ziding, Dekhuijzen, P.N. Richard, Gazdar, Adi F, Thunnissen, Erik
Published in Lung cancer (Amsterdam, Netherlands) (01.05.2014)
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Circulating DNA is a non-invasive prognostic factor for survival in non-small cell lung cancer
van der Drift, Miep A, Hol, Bernard E.A, Klaassen, Corné H.W, Prinsen, Clemens F.M, van Aarssen, Yvonne A.W.G, Donders, Rogier, van der Stappen, Jos W.J, Dekhuijzen, P.N. Richard, van der Heijden, Henricus F.M, Thunnissen, Frederik B.J.M
Published in Lung cancer (Amsterdam, Netherlands) (01.05.2010)
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Whole-exome sequencing of a meningeal melanocytic tumour reveals activating CYSLTR2 and EIF1AX hotspot mutations and similarities to uveal melanoma
Küsters-Vandevelde, Heidi V. N., Germans, Menno R., Rabbie, Roy, Rashid, Mamunur, Ten Broek, Roel, Blokx, Willeke A. M., Prinsen, Clemens F. M., Adams, David J., Ter Laan, Mark
Published in Brain tumor pathology (01.04.2018)
Published in Brain tumor pathology (01.04.2018)
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SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas
Küsters-Vandevelde, Heidi V N, Creytens, David, van Engen-van Grunsven, Adriana C H, Jeunink, Marcel, Winnepenninckx, Veronique, Groenen, Patricia J T A, Küsters, Benno, Wesseling, Pieter, Blokx, Willeke A M, Prinsen, Clemens F M
Published in Acta neuropathologica communications (15.01.2016)
Published in Acta neuropathologica communications (15.01.2016)
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EGFR and KRAS quality assurance schemes in pathology: generating normative data for molecular predictive marker analysis in targeted therapy
Thunnissen, Erik, Bovée, Judith V M G, Bruinsma, Hans, van den Brule, Adriaan J C, Dinjens, Winand, Heideman, Daniëlle A M, Meulemans, Els, Nederlof, Petra, van Noesel, Carel, Prinsen, Clemens F M, Scheidel, Karen, van de Ven, Peter M, de Weger, Roel, Schuuring, Ed, Ligtenberg, Marjolijn
Published in Journal of clinical pathology (01.10.2011)
Published in Journal of clinical pathology (01.10.2011)
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Lessons from 10 years' experience running the Fiom KID-DNA database, a voluntary DNA-linking register for donor-conceived people and donors in The Netherlands
Indekeu, Astrid, Prinsen, Clemens F. M., Maas, A. Janneke. B. M.
Published in Human fertility (Cambridge, England) (01.12.2023)
Published in Human fertility (Cambridge, England) (01.12.2023)
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DNA hypermethylation analysis in sputum of asymptomatic subjects at risk for lung cancer participating in the NELSON trial: argument for maximum screening interval of 2years
Hubers, A Jasmijn, Heideman, Danielle A M, Duin, Sylvia, Witte, Birgit I, de Koning, Harry J, Groen, Harry J M, Prinsen, Clemens F M, Bolijn, Anne S, Wouters, Mandy, van der Meer, Susanne E, Steenbergen, Renske D M, Snijders, Peter J F, Uyterlinde, Anne, Berkhof, Hans, Smit, Egbert F, Thunnissen, Erik
Published in Journal of clinical pathology (05.03.2017)
Published in Journal of clinical pathology (05.03.2017)
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Quantification of human DNA in feces as a diagnostic test for the presence of colorectal cancer
KLAASSEN, Corne H, JEUNINK, Marcel A. F, PRINSEN, Clemens F. M, RUERS, Theo J. M, TAN, Adriaan C. I. T. L, STROBBE, Luc J. A, THUNNISSEN, Frederik B. I. M
Published in Clinical chemistry (Baltimore, Md.) (01.07.2003)
Published in Clinical chemistry (Baltimore, Md.) (01.07.2003)
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Mutated Alleles of the Rod and Cone Na-Ca+K-Exchanger Genes in Patients with Retinal Diseases
Sharon, Dror, Yamamoto, Hiroyuki, McGee, Terri L, Rabe, Vivian, Szerencsei, Robert T, Winkfein, Robert J, Prinsen, Clemens F. M, Barnes, Claire S, Andreasson, Sten, Fishman, Gerald A, Schnetkamp, Paul P. M, Berson, Eliot L, Dryja, Thaddeus P
Published in Investigative ophthalmology & visual science (01.06.2002)
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Published in Investigative ophthalmology & visual science (01.06.2002)
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DNA hypermethylation analysis in sputum of asymptomatic subjects at risk for lung cancer participating in the NELSON trial: argument for maximum screening interval of 2 years
Hubers, A Jasmijn, Heideman, Daniëlle A M, Duin, Sylvia, Witte, Birgit I, de Koning, Harry J, Groen, Harry J M, Prinsen, Clemens F M, Bolijn, Anne S, Wouters, Mandy, van der Meer, Susanne E, Steenbergen, Renske D M, Snijders, Peter J F, Uyterlinde, Anne, Berkhof, Hans, Smit, Egbert F, Thunnissen, Erik
Published in Journal of clinical pathology (01.03.2017)
Published in Journal of clinical pathology (01.03.2017)
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Mutations in NYX , encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
Bech-Hansen, N.Torben, Naylor, Margaret J, Maybaum, Tracy A, Sparkes, Rebecca L, Koop, Ben, Birch, David G, Bergen, Arthur A.B, Prinsen, Clemens F.M, Polomeno, Robert C, Gal, Andreas, Drack, Arlene V, Musarella, Maria A, Jacobson, Samuel G, Young, Rockefeller S.L, Weleber, Richard G
Published in Nature genetics (01.11.2000)
Published in Nature genetics (01.11.2000)
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Whole-exome sequencing of a meningeal melanocytic tumour reveals activating CYSLTR2 and EIF1AX hotspot mutations and similarities to uveal melanoma
Küsters-Vandevelde, Heidi V N, Germans, Menno R, Rabbie, Roy, Rashid, Mamunur, Ten Broek, Roel, Blokx, Willeke A M, Prinsen, Clemens F M, Adams, David J, Ter Laan, Mark
Published in Brain tumor pathology (01.04.2018)
Published in Brain tumor pathology (01.04.2018)
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