At What Age Could Screening for Familial Retinoblastoma Be Discontinued? A Systematic Review

nork van Hoefen Wijsard, Milo, Serné, Saskia H., Otten, René H., Bosscha, Machteld I., Dommering, Charlotte J., Fabius, Armida W., Moll, Annette C.
Argitaratua izan da Cancers (Basel) (2021)

RB1 mutations and second primary malignancies after hereditary retinoblastoma

nork Dommering, Charlotte J., Marees, Tamara, van der Hout, Annemarie H., Imhof, Saskia M., Meijers-Heijboer, Hanne, Ringens, Peter J., van Leeuwen, Flora E., Moll, Annette C.
Argitaratua 2011

Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes

nork Kooi, Irsan E., Mol, Berber M., Massink, Maarten P. G., Ameziane, Najim, Meijers-Heijboer, Hanne, Dommering, Charlotte J., van Mil, Saskia E., de Vries, Yne, van der Hout, Annemarie H., Kaspers, Gertjan J. L., Moll, Annette C., te Riele, Hein, Cloos, Jacqueline, Dorsman, Josephine C.
Argitaratua izan da Sci Rep (2016)

Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case–control study

nork Potjer, Thomas P, van der Stoep, Nienke, Houwing-Duistermaat, Jeanine J, Konings, Ingrid C A W, Aalfs, Cora M, van den Akker, Peter C, Ausems, Margreet G, Dommering, Charlotte J, van der Kolk, Lizet E, Maiburg, Merel C, Spruijt, Liesbeth, Wagner, Anja, Vasen, Hans F A, Hes, Frederik J
Argitaratua izan da BMC Res Notes (2015)

Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands

nork Dommering, Charlotte J., Henneman, Lidewij, van der Hout, Annemarie H., Jonker, Marianne A., Tops, Carli M. J., van den Ouweland, Ans M. W., van der Luijt, Rob B., Mensenkamp, Arjen R., Hogervorst, Frans B. L., Redeker, Egbert J. W., de Die-Smulders, Christine E. M., Moll, Annette C., Meijers-Heijboer, Hanne
Argitaratua izan da Fam Cancer (2016)

A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history

nork Gómez García, Encarna B, Oosterwijk, Jan C, Timmermans, Maarten, van Asperen, Christi J, Hogervorst, Frans BL, Hoogerbrugge, Nicoline, Oldenburg, Rogier, Verhoef, Senno, Dommering, Charlotte J, Ausems, Margreet GEM, van Os, Theo AM, van der Hout, Annemarie H, Ligtenberg, Marjolijn, van den Ouweland, Ans, van der Luijt, Rob B, Wijnen, Juul T, Gille, Jan JP, Lindsey, Patrick J, Devilee, Peter, Blok, Marinus J, Vreeswijk, Maaike PG
Argitaratua 2009

A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example

nork Mohammadi, Leila, Vreeswijk, Maaike P, Oldenburg, Rogier, van den Ouweland, Ans, Oosterwijk, Jan C, van der Hout, Annemarie H, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn, Ausems, Margreet G, van der Luijt, Rob B, Dommering, Charlotte J, Gille, Johan J, Verhoef, Senno, Hogervorst, Frans B, van Os, Theo A, Gómez García, Encarna, Blok, Marinus J, Wijnen, Juul T, Helmer, Quinta, Devilee, Peter, van Asperen, Christi J, van Houwelingen, Hans C
Argitaratua 2009

The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot...

nork Reumkens, Kelly, Tummers, Marly H. E., Gietel-Habets, Joyce J. G., van Kuijk, Sander M. J., Aalfs, Cora M., van Asperen, Christi J., Ausems, Margreet G. E. M., Collée, Margriet, Dommering, Charlotte J., Kets, C. Marleen, van der Kolk, Lizet E., Oosterwijk, Jan C., Tjan-Heijnen, Vivianne C. G., van der Weijden, Trudy, de Die-Smulders, Christine E. M., van Osch, Liesbeth A. D. M.
Argitaratua izan da Fam Cancer (2018)

Online decision support for persons having a genetic predisposition to cancer and their partners during reproductive decision‐making

nork Reumkens, Kelly, Tummers, Marly H. E., Gietel‐Habets, Joyce J. G., van Kuijk, Sander M. J., Aalfs, Cora M., van Asperen, Christi J., Ausems, Margreet G. E. M., Collée, Margriet, Dommering, Charlotte J., Kets, C. Marleen, van der Kolk, Lizet E., Oosterwijk, Jan C., Tjan‐Heijnen, Vivianne C. G., van der Weijden, Trudy, de Die‐Smulders, Christine E. M., van Osch, Liesbeth A. D. M.
Argitaratua izan da J Genet Couns (2018)

Recommendations for long-term follow-up of adults with heritable retinoblastoma

nork Tonorezos, Emily S., Friedman, Danielle Novetsky, Barnea, Dana, Bosscha, Machteld I., Chantada, Guillermo, Dommering, Charlotte J., de Graaf, Pim, Dunkel, Ira J., Fabius, Armida W.M., Francis, Jasmine H., Greer, Mary-Louise C., Kleinerman, Ruth A., Kors, Wijnanda A., Laughlin, Suzanne, Moll, Annette C., Morton, Lindsay M., Temming, Petra, Tucker, Margaret A., van Leeuwen, Flora E., Walsh, Michael F., Oeffinger, Kevin C., Abramson, David H.
Argitaratua izan da Ophthalmology (2020)

Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making

nork Reumkens, Kelly, Tummers, Marly H. E., Severijns, Yil, Gietel-Habets, Joyce J. G., van Kuijk, Sander M. J., Aalfs, Cora M., van Asperen, Christi J., Ausems, Margreet G. E. M., Collée, Margriet, Dommering, Charlotte J., Kets, Marleen, van der Kolk, Lizet E., Oosterwijk, Jan C., Tjan-Heijnen, Vivianne C. G., van der Weijden, Trudy, de Die-Smulders, Christine E. M., van Osch, Liesbeth A. D. M.
Argitaratua izan da J Community Genet (2020)

Validation of a clinical screening instrument for tumour predisposition syndromes in patients with childhood cancer (TuPS): protocol for a prospective, observational, multicentre s...

nork Postema, Floor A M, Hopman, Saskia M J, de Borgie, Corianne A J M, Hammond, Peter, Hennekam, Raoul C, Merks, Johannes H M, Aalfs, Cora M, Anninga, Jakob K, Berger, Lieke PV, Bleeker, Fonnet E, de Bont, Eveline SJM, de Borgie, Corianne AJM, Dommering, Charlotte J, van Eijkelenburg, Natasha KA, Hammond, Peter, Hennekam, Raoul C, van den Heuvel-Eibrink, Marry M, Hopman, Saskia MJ, Jongmans, Marjolijn CJ, Kors, Wijnanda A, Letteboer, Tom GW, Loeffen, Jan LCM, Merks, Johannes HM, Olderode-Berends, Maran JW, Postema, Floor AM, Wagner, Anja
Argitaratua izan da BMJ Open (2017)

The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations

nork Terry, Mary Beth, Liao, Yuyan, Kast, Karin, Antoniou, Antonis C, McDonald, Jasmine A, Mooij, Thea M, Engel, Christoph, Nogues, Catherine, Buecher, Bruno, Mari, Véronique, Moretta-Serra, Jessica, Gladieff, Laurence, Luporsi, Elisabeth, Barrowdale, Daniel, Frost, Debra, Henderson, Alex, Brewer, Carole, Evans, D Gareth, Eccles, Diana, Cook, Jackie, Ong, Kai-ren, Izatt, Louise, Ahmed, Munaza, Morrison, Patrick J, Dommering, Charlotte J, Oosterwijk, Jan C, Ausems, Margreet G E M, Kriege, Mieke, Buys, Saundra S, Andrulis, Irene L, John, Esther M, Daly, Mary, Friedlander, Michael, McLachlan, Sue Anne, Osorio, Ana, Caldes, Trinidad, Jakubowska, Anna, Simard, Jacques, Singer, Christian F, Tan, Yen, Olah, Edith, Navratilova, Marie, Foretova, Lenka, Gerdes, Anne-Marie, Roos-Blom, Marie-José, Arver, Brita, Olsson, Håkan, Schmutzler, Rita K, Hopper, John L, van Leeuwen, Flora E, Goldgar, David, Milne, Roger L, Easton, Douglas F, Rookus, Matti A, Andrieu, Nadine
Argitaratua izan da JNCI Cancer Spectr (2019)