Canlyniadau Chwilio - Christi J. van Asperen
- Dangos 1 - 20 canlyniadau o 45
- Ewch i'r Dudalen Nesaf
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A whisper-game perspective on the family communication of DNA-test results: a retrospective study on the communication process of BRCA1/2-test results between proband and relatives gan Joël Vos, Fred H. Menko, Anna M. Jansen, Christi J. van Asperen, Anne M. Stiggelbout, Aad Tibben
Cyhoeddwyd 2010Artigo -
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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... gan Sandra van Dijk, Daniëlle R. M. Timmermans, Hanne Meijers-Heijboer, Aad Tibben, Christi J. van Asperen, Wilma Otten
Cyhoeddwyd 2006Artigo -
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Genetic testing for familial/hereditary breast cancer—comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany gan Dorothea Gadzicki, D. Gareth Evans, Hilary Harris, Claire Julian‐Reynier, Irmgard Nippert, Jörg Schmidtke, Aad Tibben, Christi J. van Asperen, Brigitte Schlegelberger
Cyhoeddwyd 2011Artigo -
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The functional impact of variants of uncertain significance in BRCA2 gan Romy L.S. Mesman, Fabienne M.G.R. Calléja, Giel Hendriks, Bruno Morolli, Branislav Mišovic, Peter Devilee, Christi J. van Asperen, Harry Vrieling, Maaike P.G. Vreeswijk
Cyhoeddwyd 2018Artigo -
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Intronic variants in<i>BRCA1</i>and<i>BRCA2</i>that affect RNA splicing can be reliably selected by splice-site prediction programs gan Maaike P.G. Vreeswijk, Jaco Kraan, Heleen M. van der Klift, Geraldine R. Vink, Cees J. Cornelisse, Juul Wijnen, Egbert Bakker, Christi J. van Asperen, Peter Devilee
Cyhoeddwyd 2008Artigo -
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Recommendations for reporting results of diagnostic genomic testing gan Zandra C. Deans, Joo Wook Ahn, Isabel M. Carreira, Elisabeth Dequeker, Mick Henderson, Luca Lovrečić, Katrin Õunap, Melody Tabiner, Rebecca J. L. Treacy, Christi J. van Asperen
Cyhoeddwyd 2022Artigo -
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Risk reduction of contralateral breast cancer and survival after contralateral prophylactic mastectomy in BRCA1 or BRCA2 mutation carriers gan T.C. van Sprundel, Marjanka K. Schmidt, Matti A. Rookus, Richard M. Brohet, Christi J. van Asperen, Emiel J. Rutgers, Laura J. vanʼt Veer, Rob A.�E.�M. Tollenaar
Cyhoeddwyd 2005Artigo -
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Effectiveness and cost-effectiveness of meaning-centered group psychotherapy in cancer survivors: protocol of a randomized controlled trial gan Nadia van der Spek, Joël Vos, Cornelia F. van Uden–Kraan, William Breitbart, Pim Cuijpers, Kitty Knipscheer-Kuipers, Vincent Willemsen, Rob A.�E.�M. Tollenaar, Christi J. van Asperen, Irma M. Verdonck‐de Leeuw
Cyhoeddwyd 2014Artigo -
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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 gan 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
Cyhoeddwyd 2019Artigo -
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Pathological characterisation of male breast cancer: Results of the EORTC 10085/TBCRC/BIG/NABCG International Male Breast Cancer Program gan Marijn A. Vermeulen, Leen Slaets, Fátima Cardoso, Sharon H. Giordano, Konstantinos Tryfonidis, P. J. van Diest, N Dijkstra, Carolien P. Schröder, Christi J. van Asperen, Barbro Linderholm, Kim Benstead, Renée Foekens, John W.M. Martens, John M.S. Bartlett, Carolien H. M. van Deurzen
Cyhoeddwyd 2017Artigo -
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Clinical correlates of low-risk variants in FGFR2, TNRC9, MAP3K1, LSP1 and 8q24 in a Dutch cohort of incident breast cancer cases gan Petra E.A. Huijts, Maaike P.G. Vreeswijk, Karin Kroeze‐Jansema, Catharina E. Jacobi, Caroline Seynaeve, Elly MM Krol-Warmerdam, Pauline M. Wijers‐Koster, Jannet Blom, Karen A. Pooley, Jan G.M. Klijn, Rob A.�E.�M. Tollenaar, Peter Devilee, Christi J. van Asperen
Cyhoeddwyd 2007Artigo -
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A Genotypic and Histopathological Study of a Large Dutch Kindred with Hyperparathyroidism-Jaw Tumor Syndrome1 gan Carola J. Haven, Fung Ki Wong, Eveline W. C. M. van Dam, Rob B. van der Luijt, Christi J. van Asperen, Joke Jansen, Carla Rosenberg, Mireille de Wit, Janine Roijers, Jo W.M. Höppener, Cornelis J.M. Lips, Catharina Larsson, Bin Tean Teh, Hans Morreau
Cyhoeddwyd 2000Artigo -
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Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers gan Anouk Pijpe, Peggy Manders, Richard M. Brohet, J. Margriet Collée, Senno Verhoef, Hans F. A. Vasen, Nicoline Hoogerbrugge, Christi J. van Asperen, Charlotte J. Dommering, Margreet G.E.M. Ausems, Cora M. Aalfs, E. Gómez, Laura J. vanʼt Veer, Flora E. van Leeuwen, Matti A. Rookus
Cyhoeddwyd 2009Artigo -
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Guidance Statement On BRCA1/2 Tumor Testing in Ovarian Cancer Patients gan Ettore Capoluongo, Gillian Ellison, José Antonio López‐Guerrero, Frédérique Penault‐Llorca, Marjolijn J. L. Ligtenberg, Susana Banerjee, Christian F. Singer, Eitan Friedman, Birgid Markiefka, Peter Schirmacher, Reinhard Büttner, Christi J. van Asperen, Isabelle Ray‐Coquard, Volker Endris, Suzanne Kamel‐Reid, Natalie Percival, Jane Bryce, Benno Röthlisberger, Richie Soong, David González de Castro
Cyhoeddwyd 2017Revisão -
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Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases gan Inge M. M. Lakeman, Mar D M Rodríguez-Girondo, Andrew Lee, Nandi Celosse, Merel E. Braspenning, Klaartje van Engelen, Irma van de Beek, Annemiek H van der Hout, E. Gómez, Arjen R. Mensenkamp, Margreet G.E.M. Ausems, Maartje J. Hooning, Muriel A. Adank, Antoinette Hollestelle, Marjanka K. Schmidt, Christi J. van Asperen, Peter Devilee
Cyhoeddwyd 2022Artigo -
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BRCA1 and BRCA2 genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance gan Diana Eccles, Gillian Mitchell, Álvaro N.A. Monteiro, Rita K. Schmutzler, Fergus J. Couch, Amanda B. Spurdle, E. Gómez, Ronald H. Driessen, Noralane M. Lindor, Marinus J. Blok, Pål Møller, Miguel de la Hoya, Tuya Pal, S. M. Domchek, Katherine L. Nathanson, Christi J. van Asperen, Orland Dı́ez, K. Rheim, Dominique Stoppa‐Lyonnet, Michael T. Parsons, David E. Goldgar
Cyhoeddwyd 2015Revisão
Offerynnau Chwilio:
Pynciau Perthynol
Medicine
Biology
Cancer
Genetics
Internal medicine
Gene
Breast cancer
Oncology
Mutation
Gynecology
Allele
Genotype
Germline mutation
Cancer research
Family history
Genetic testing
Ovarian cancer
Cohort
Single-nucleotide polymorphism
Bioinformatics
Computer science
Confidence interval
Family medicine
Phenotype
BRCA mutation
BRCA2 Protein
Cohort study
Computational biology
Environmental health
Missense mutation