Søgeresultater - 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 af Maarten P.G. Massink, Irsan Kooi, John W.M. Martens, Quinten Waisfisz, Hanne Meijers‐Heijboer

    Udgivet 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... af Sandra van Dijk, Daniëlle R. M. Timmermans, Hanne Meijers-Heijboer, Aad Tibben, Christi J. van Asperen, Wilma Otten

    Udgivet 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 af Kyra E. Stuurman, Marieke Joosten, Ineke van der Burgt, Mariet W. Elting, Helger G. Yntema, Hanne Meijers‐Heijboer, Tuula Rinne

    Udgivet 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 af Dora Hammerl, Maarten P.G. Massink, Marcel Smid, Carolien H. M. van Deurzen, Hanne Meijers‐Heijboer, Quinten Waisfisz, Reno Debets, John W.M. Martens

    Udgivet 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 af 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

    Udgivet 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 af 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

    Udgivet 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 af 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

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

    Biallelic germline mutations of mismatch‐repair genes af 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

    Udgivet 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 af 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

    Udgivet 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 af 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

    Udgivet 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 af 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

    Udgivet 2005
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  12. 12
    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 af 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

    Udgivet 2007
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  13. 13
    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. af 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

    Udgivet 2013
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  14. 14
    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 af 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

    Udgivet 1991
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  15. 15
    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 af 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

    Udgivet 2016
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  16. 16
    Whole-genome sequencing in health care

    Whole-genome sequencing in health care af 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

    Udgivet 2013
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  17. 17
    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 af 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

    Udgivet 2019
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  18. 18
    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 af 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

    Udgivet 2004
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  19. 19
    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 af 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

    Udgivet 2014
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  20. 20
    Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis

    Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis af Henne Holstege, Wayne Pfeiffer, Daoud Sie, Marc Hulsman, Thomas J. Nicholas, Clarence Lee, Tristen Ross, Jue Lin, Mark A. Miller, Bauke Ylstra, Hanne Meijers‐Heijboer, Martijn H. Brugman, Frank J. T. Staal, Gert Holstege, Marcel J. T. Reinders, Timothy T. Harkins, Samuel Lévy, Erik A. Sistermans

    Udgivet 2014
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