Výsledky vyhledávání - Hanne Meijers‐Heijboer

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  1. 1
    Genomic profiling of CHEK2*1100delC-mutated breast carcinomas

    Genomic profiling of CHEK2*1100delC-mutated breast carcinomas Autor Maarten P.G. Massink, Irsan Kooi, John W.M. Martens, Quinten Waisfisz, Hanne Meijers‐Heijboer

    Vydáno 2015
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  2. 2
    Clinical Characteristics Affect the Impact of an Uninformative DNA Test Result: The Course of Worry and Distress Experienced by Women Who Apply for Genetic Testing for Breast Cancer

    Clinical Characteristics Affect the Impact of an Uninformative DNA Test Result: The Course of Worry and Distress Experienced by Women Who Apply for Genetic Testing for Breast Cance... Autor Sandra van Dijk, Daniëlle R. M. Timmermans, Hanne Meijers-Heijboer, Aad Tibben, Christi J. van Asperen, Wilma Otten

    Vydáno 2006
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  3. 3
    Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era

    Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era Autor Kyra E. Stuurman, Marieke Joosten, Ineke van der Burgt, Mariet W. Elting, Helger G. Yntema, Hanne Meijers‐Heijboer, Tuula Rinne

    Vydáno 2019
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  4. 4
    Clonality, Antigen Recognition, and Suppression of CD8+ T Cells Differentially Affect Prognosis of Breast Cancer Subtypes

    Clonality, Antigen Recognition, and Suppression of CD8+ T Cells Differentially Affect Prognosis of Breast Cancer Subtypes Autor Dora Hammerl, Maarten P.G. Massink, Marcel Smid, Carolien H. M. van Deurzen, Hanne Meijers‐Heijboer, Quinten Waisfisz, Reno Debets, John W.M. Martens

    Vydáno 2019
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  5. 5
    RB1 mutations and second primary malignancies after hereditary retinoblastoma

    RB1 mutations and second primary malignancies after hereditary retinoblastoma Autor Charlotte J. Dommering, Tamara Marees, Annemarie H. van der Hout, Saskia M. Imhof, Hanne Meijers‐Heijboer, Peter J. Ringens, Flora E. van Leeuwen, Annette C. Moll

    Vydáno 2011
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  6. 6
    Leptin receptor deficiency: a systematic literature review and prevalence estimation based on population genetics

    Leptin receptor deficiency: a systematic literature review and prevalence estimation based on population genetics Autor Lotte Kleinendorst, Ozair Abawi, H.J. van der Kamp, Mariëlle Alders, Hanne Meijers‐Heijboer, Elisabeth F. C. van Rossum, Erica L T van den Akker, Mieke M. van Haelst

    Vydáno 2019
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  7. 7
    The 100-plus Study of cognitively healthy centenarians: rationale, design and cohort description

    The 100-plus Study of cognitively healthy centenarians: rationale, design and cohort description Autor Henne Holstege, Nina Beker, Tamara Dijkstra, Karlijn Pieterse, Elizabeth Wemmenhove, Kimja Schouten, Linette Thiessens, Debbie Horsten, Sterre Rechtuijt, Sietske A.M. Sikkes, Frans van Poppel, Hanne Meijers‐Heijboer, Marc Hulsman, Philip Scheltens

    Vydáno 2018
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  8. 8
    Biallelic germline mutations of mismatch‐repair genes

    Biallelic germline mutations of mismatch‐repair genes Autor Jan‐Werner Poley, Anja Wagner, Monique M. C. P. Hoogmans, Fred H. Menko, Carli M.J. Tops, Johan M. Kros, Roel E. Reddingius, Hanne Meijers‐Heijboer, Ernst J. Kuipers, Winand N.M. Dinjens

    Vydáno 2007
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  9. 9
    Centenarian controls increase variant effect sizes by an average twofold in an extreme case–extreme control analysis of Alzheimer’s disease

    Centenarian controls increase variant effect sizes by an average twofold in an extreme case–extreme control analysis of Alzheimer’s disease Autor Niccoló Tesi, Sven J. van der Lee, Marc Hulsman, Iris E. Jansen, Najada Stringa, Natasja M. van Schoor, Hanne Meijers‐Heijboer, Martijn Huisman, Philip Scheltens, Marcel J. T. Reinders, Wiesje M. van der Flier, Henne Holstege

    Vydáno 2018
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  10. 10
    Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis

    Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis Autor Tessa van Dijk, Sacha Ferdinandusse, Jos P.N. Ruiter, Mariëlle Alders, Inge B. Mathijssen, Jillian S. Parboosingh, A. Micheil Innes, Hanne Meijers-Heijboer, Bwee Tien Poll‐The, François Bernier, Ronald J. A. Wanders, Ryan E. Lamont, Frank Baas

    Vydáno 2018
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  11. 11
    Survival and prognostic factors in BRCA1-associated breast cancer

    Survival and prognostic factors in BRCA1-associated breast cancer Autor Cecile T.M. Brekelmans, Caroline Seynaeve, M. Menke-Pluymers, Hennie T. Brüggenwirth, Madeleine M.A. Tilanus‐Linthorst, C.C.M. Bartels, Mieke Kriege, Albertus N. van Geel, C. Crépin, Jannet Blom, Hanne Meijers-Heijboer, J.G.M. Klijn

    Vydáno 2005
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  12. 12
    Increased prevalence of BRCA1/2 mutations in women with macrotextured breast implants and anaplastic large cell lymphoma of the breast

    Increased prevalence of BRCA1/2 mutations in women with macrotextured breast implants and anaplastic large cell lymphoma of the breast Autor Mintsje de Boer, Michael Hauptmann, Nathalie J. Hijmering, Carel J.M. van Noesel, Hinne A. Rakhorst, Hanne Meijers‐Heijboer, Jan Paul de Boer, René R. W. J. van der Hulst, Daphne de Jong, Flora E. van Leeuwen

    Vydáno 2020
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  13. 13
    Prophylactic Mastectomy in BRCA1/2 Mutation Carriers and Women at Risk of Hereditary Breast Cancer: Long-Term Experiences at the Rotterdam Family Cancer Clinic

    Prophylactic Mastectomy in BRCA1/2 Mutation Carriers and Women at Risk of Hereditary Breast Cancer: Long-Term Experiences at the Rotterdam Family Cancer Clinic Autor Bernadette A. M. Heemskerk‐Gerritsen, Cecile T.M. Brekelmans, Marian B. E. Menke‐Pluymers, A.N. van Geel, Madeleine M.A. Tilanus‐Linthorst, Carina C. M. Bartels, Murly Tan, Hanne Meijers‐Heijboer, Jan G.M. Klijn, Caroline Seynaeve

    Vydáno 2007
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  14. 14
    Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.

    Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. Autor Carla van El, Martina C. Cornel, Pascal Borry, Ros Hastings, Florence Fellmann, Shirley V. Hodgson, Heidi Howard, Anne Cambon‐Thomsen, Bartha Maria Knoppers, Hanne Meijers‐Heijboer, Hans Scheffer, Lisbeth Tranebjærg, Wybo Dondorp, Guido M. W. R. de Wert

    Vydáno 2013
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  15. 15
    Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

    Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region Autor Carl C.T. Ton, Harri Hirvonen, Hiroshi Miwa, Michael M. Weil, Paula Monaghan, Tim Jordan, Veronica van Heyningen, Nicholas D. Hastie, Hanne Meijers‐Heijboer, Matthias Drechsler, Brigitte Royer‐Pokora, Francis S. Collins, Anand Swaroop, Louise C. Strong, Grady F. Saunders

    Vydáno 1991
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  16. 16
    A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression

    A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression Autor Irsan Kooi, Berber M. Mol, Maarten P.G. Massink, Marcus C. de Jong, Pim de Graaf, Paul van der Valk, Hanne Meijers‐Heijboer, Gertjan J.L. Kaspers, Annette C. Moll, Hein te Riele, Jacqueline Cloos, Josephine C. Dorsman

    Vydáno 2016
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  17. 17
    Whole-genome sequencing in health care

    Whole-genome sequencing in health care Autor Carla van El, Martina C. Cornel, Pascal Borry, Ros Hastings, Florence Fellmann, Shirley V. Hodgson, Heidi Howard, Anne Cambon‐Thomsen, Bartha Maria Knoppers, Hanne Meijers‐Heijboer, Hans Scheffer, Lisbeth Tranebjærg, Wybo Dondorp, Guido M. W. R. de Wert

    Vydáno 2013
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  18. 18
    Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-<i>BRCA1/2</i>breast cancer families

    Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-<i>BRCA1/2</i>breast cancer families Autor Inge M. M. Lakeman, Florentine Hilbers, Mar Rodríguez‐Girondo, Andrew Lee, Maaike P.G. Vreeswijk, Antoinette Hollestelle, Caroline Seynaeve, Hanne Meijers‐Heijboer, Jan C. Oosterwijk, Nicoline Hoogerbrugge, Edith Oláh, Hans F. A. Vasen, Christi J. van Asperen, Peter Devilee

    Vydáno 2019
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  19. 19
    Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer

    Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer Autor Andrea E. van der Meulen–de Jong, Marjo van Puijenbroek, Yvonne Hendriks, Carli Tops, Juul Wijnen, Margreet G.E.M. Ausems, Hanne Meijers‐Heijboer, Anja Wagner, Theo A.M. van Os, Annette Bröcker‐Vriends, Hans F. A. Vasen, Hans Morreau

    Vydáno 2004
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  20. 20
    Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence

    Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence Autor Maria B. Tan-Sindhunata, Inge B. Mathijssen, Margriet Smit, Frank Baas, Johanna I. de Vries, J. Patrick van der Voorn, Irma Kluijt, Marleen A. Hagen, Eveline W Blom, Erik A. Sistermans, Hanne Meijers‐Heijboer, Quinten Waisfisz, Marjan M. Weiss, Alexander J. Groffen

    Vydáno 2014
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