Charlotte Dommering

DR.

20022020

Research output per year

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Research Output

  • 27 Article
  • 3 Chapter
  • 1 Review article
  • 1 Research VU University Amsterdam, graduation VU University Amsterdam
2020

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

Tonorezos, E. S., Friedman, D. N., Barnea, D., Bosscha, M. I., Chantada, G., Dommering, C. J., de Graaf, P., Dunkel, I. J., Fabius, A. W. M., Francis, J. H., Greer, M-L. C., Kleinerman, R. A., Kors, W. A., Laughlin, S., Moll, A. C., Morton, L. M., Temming, P., Tucker, M. A., van Leeuwen, F. E., Walsh, M. F. & 2 others, Oeffinger, K. C. & Abramson, D. H., 15 May 2020, In : Ophthalmology.

Research output: Contribution to journalArticleAcademicpeer-review

2019

Biochemically Silent Sympathetic Paraganglioma, Pheochromocytoma, or Metastatic Disease in SDHD Mutation Carriers

Dreijerink, K. M. A., Rijken, J. A., Compaijen, C. J., Timmers, H. J. L. M., van der Horst-Schrivers, A. N. A., van Leeuwaarde, R. S., van Dam, P. S., Leemans, C. R., van Dam, E. W. C. M., Dickhoff, C., Dommering, C. J., de Graaf, P., Zwezerijnen, G. J. C., van der Valk, P., Menke-van der Houven van Oordt, C. W., Hensen, E. F., Corssmit, E. P. M. & Eekhoff, E. M. W., 1 Nov 2019, In : The Journal of clinical endocrinology and metabolism. 104, 11, p. 5421-5426 6 p.

Research output: Contribution to journalArticleAcademicpeer-review

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

Reumkens, K., Tummers, M. H. E., Gietel-Habets, J. J. G., van Kuijk, S. M. J., Aalfs, C. M., van Asperen, C. J., Ausems, M. G. E. M., Collée, M., Dommering, C. J., Kets, C. M., van der Kolk, L. E., Oosterwijk, J. C., Tjan-Heijnen, V. C. G., van der Weijden, T., de Die-Smulders, C. E. M. & van Osch, L. A. D. M., 1 Jun 2019, In : Journal of Genetic Counseling. 28, 3, p. 533-542

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

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 study

Reumkens, K., Tummers, M. H. E., Gietel-Habets, J. J. G., van Kuijk, S. M. J., Aalfs, C. M., van Asperen, C. J., Ausems, M. G. E. M., Collée, M., Dommering, C. J., Kets, C. M., van der Kolk, L. E., Oosterwijk, J. C., Tjan-Heijnen, V. C. G., van der Weijden, T., de Die-Smulders, C. E. M. & van Osch, L. A. D. M., 15 Jan 2019, In : Familial Cancer. 18, 1, p. 137-146 10 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access
2017

Childhood tumours with a high probability of being part of a tumour predisposition syndrome; reason for referral for genetic consultation

Postema, F. A. M., Hopman, S. M. J., Aalfs, C. M., Berger, L. P. V., Bleeker, F. E., Dommering, C. J., Jongmans, M. C. J., Letteboer, T. G. W., Olderode-Berends, M. J. W., Wagner, A., Hennekam, R. C. & Merks, J. H. M., 1 Jul 2017, In : European Journal of Cancer. 80, p. 48-54 7 p.

Research output: Contribution to journalReview articleAcademicpeer-review

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

Dommering, C. J., Henneman, L., van der Hout, A. H., Jonker, M. A., Tops, C. M. J., van den Ouweland, A. M. W., Van Der Luijt, R. B., Mensenkamp, A. R., Hogervorst, F. B. L., Redeker, E. J. W., de Die-Smulders, C. E. M., Moll, A. C. & Meijers-Heijboer, H., 1 Apr 2017, In : Familial Cancer. 16, 2, p. 271-277 7 p.

Research output: Contribution to journalArticleAcademicpeer-review

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

Postema, F. A. M., Hopman, S. M. J., De Borgie, C. A. J. M., Hammond, P., Hennekam, R. C., Merks, J. H. M. & TuPS study group, 1 Jan 2017, In : BMJ Open. 7, 1, e013237.

Research output: Contribution to journalArticleAcademicpeer-review

2016

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

Kooi, I. E., Mol, B. M., Massink, M. P. G., Ameziane, N., Meijers-Heijboer, H., Dommering, C. J., van Mil, S. E., de Vries, Y., van der Hout, A. H., Kaspers, G. J. L., Moll, A. C., te Riele, H., Cloos, J. & Dorsman, J. C., 29 Apr 2016, In : Scientific Reports. 6

Research output: Contribution to journalArticleAcademicpeer-review

2015

Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome

Kelmemi, W., Teeuw, M. E., Bochdanovits, Z., Ouburg, S., Jonker, M. A., Alkuraya, F., Hashem, M., Kayserili, H., van Haeringen, A., Sheridan, E., Masri, A., Cobben, J. M., Rizzu, P., Kostense, P. J., Dommering, C. J., Henneman, L., Bouhamed-Chaabouni, H., Heutink, P., ten Kate, L. P. & Cornel, M. C., 2015, In : BMC Medical Genetics. 16, 50.

Research output: Contribution to journalArticleAcademicpeer-review

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

Potjer, T. P., van der Stoep, N., Houwing-Duistermaat, J. J., Konings, I. C. A. W., Aalfs, C. M., van den Akker, P. C., Ausems, M. G., Dommering, C. J., van der Kolk, L. E., Maiburg, M. C., Spruijt, L., Wagner, A., Vasen, H. F. A. & Hes, F. J., 2015, In : BMC Research Notes. 8, 264.

Research output: Contribution to journalArticleAcademicpeer-review

Retinoblastoma: molecular genetics and clinical consequences

Dommering, C. J., 2015

Research output: ThesisResearch VU University Amsterdam, graduation VU University Amsterdam

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55 Downloads (Pure)

Vroegdetectie cruciaal bij oncologische patiënten met het zeldzame PTEN hamartoom tumorsyndroom

Verhoeff, J. J. C., van Tienhoven, G., Rijna, H., van der Linden, P. W. G., Dommering, C. J., Moonen, L. & van den Brink, A., 2015, In : Nederlands Tijdschrift voor Oncologie. 12, 4, p. 148-151

Research output: Contribution to journalArticleProfessional

2014

High resolution SNP array profiling identifies variability in retinoblastoma genome stability

Mol, B. M., Massink, M. P. G., van der Hout, A. H., Dommering, C. J., Zaman, J. M. A., Bosscha, M. I., Kors, W. A., Meijers-Heijboer, H. E., Kaspers, G. J. L., te Riele, H., Moll, A. C., Cloos, J. & Dorsman, J. C., 2014, In : Genes, Chromosomes and Cancer. 53, 1, p. 1-14

Research output: Contribution to journalArticleAcademicpeer-review

RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients

Dommering, C. J., Mol, B. M., Moll, A. C., Burton, M., Cloos, J., Dorsman, J. C., Meijers-Heijboer, H. & van der Hout, A. H., 2014, In : Journal of Medical Genetics. 51, 6, p. 366-374

Research output: Contribution to journalArticleAcademicpeer-review

Retinoblastoma and Reproductive Decision-Making

Dommering, C. J. & Henneman, L., 2014, Tumors of the Central Nervous System. p. 75-82

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

2013

Second malignancies and other long-term effects in retinoblastoma survivors

Moll, A. C., van Dijk, J., Bosscha, M. I., Dommering, C. J., de Graaf, P., Kors, W. A. & van Leeuwen, F. E., 2013, Retinoblastoma: Clinical advances and emerging treatment strategies. p. 109-125

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

2012

IVF and retinoblastoma revisited

Dommering, C. J., van der Hout, A. H., Meijers-Heijboer, E. J., Marees, T. & Moll, A. C., 2012, In : Fertility and Sterility. 97, 1, p. 79-81

Research output: Contribution to journalArticleAcademicpeer-review

RB1 mutations and second primary malignancies after hereditary retinoblastoma

Dommering, C. J., Marees, T., van der Hout, A. H., Imhof, S. M., Meijers-Heijboer, E. J., Ringens, P. J., van Leeuwen, F. E. & Moll, A. C., 2012, In : Familial Cancer. 11, 2, p. 225-233

Research output: Contribution to journalArticleAcademicpeer-review

Reproductive behavior of individuals with increased risk of having a child with retinoblastoma

Dommering, C. J., Garvelink, M. M., Moll, A. C., van Dijk, J., Imhof, S., Meijers-Heijboer, E. J. & Henneman, L., 2012, In : Clinical Genetics. 81, 3, p. 216-223

Research output: Contribution to journalArticleAcademicpeer-review

Risk Factors for the Incidence of Second Cancers in Survivors of Retinoblastoma With a Family History

Moll, A. C., Dommering, C. J., Bosscha, M. I., de Graaf, P., Kors, W. A. & van Leeuwen, F. E., 2012, In : Journal of Clinical Oncology. 30, 24, p. 3028-3028

Research output: Contribution to journalArticleAcademicpeer-review

Second primary malignancy

Moll, A. C., Bosscha, M. I. & Dommering, C. J., 2012, Retinoblastoma. Jaypee Highlights, p. 195-199

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

2011

Clinical utility gene card for: Retinoblastoma

Lohmann, D., Gallie, B., Dommering, C. J. & Gauthier-Villars, M., 2011, In : European Journal of Human Genetics. 19, 3

Research output: Contribution to journalArticleAcademicpeer-review

2010

Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers

Pijpe, A., Manders, P., Brohet, R. M., Collee, J. M., Verhoef, S., Vasen, HF., Hoogerbrugge, N., van Asperen, C. J., Dommering, C. J., Ausems, M. G., Aalfs, C. M., Gomez-Garcia, E. B., van 't Veer, L. J., van Leeuwen, F. E. & Rookus, M. A., 2010, In : Breast Cancer Research and Treatment. 120, 1, p. 235-244

Research output: Contribution to journalArticleAcademicpeer-review

Open Access
File
58 Downloads (Pure)

Psychosocial impact of Von Hippel-Lindau disease: levels and sources of distress

Lammens, C. R. M., Bleiker, E. M. A., Verhoef, S., Hes, F. J., Ausems, M. G. E. M., Majoor-Krakauer, D., Sijmons, RH., van der Luijt, R. B., van den Ouweland, A. M. W., Van Os, T., Hoogerbrugge, N., Garcia, E. B. G., Dommering, C. J., Gundy, C. & Aaronson, N. K., 2010, In : Clinical Genetics. 77, 5, p. 483-491

Research output: Contribution to journalArticleAcademicpeer-review

Reproductive decision-making: a qualitative study among couples at increased risk of having a child with retinoblastoma

Dommering, C. J., van den Heuvel, M. R., Acmoll, A. C., Imhof, S. M., Meijers-Heijboer, E. J. & Henneman, L., 2010, In : Clinical Genetics. 78, 4, p. 334-341

Research output: Contribution to journalArticleAcademicpeer-review

2009

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

Gomez Garcia, E. B., Oosterwijk, J. C., Timmermans, M. W. H., van Asperen, C. J., Hogervorst, FB., Hoogerbrugge, N., Oldenburg, R., Verhoef, S., Dommering, C. J., Ausems, M. G., van Os, T. A. M., van der Hout, A. H., Ligtenberg, M. J. L., van den Ouweland, A. M. W., van der Luijt, R., Wijnen, J. G., Gille, J. J. P., Lindsey, P. J., Devilee, P., Blok, M. M. & 1 others, van Vreeswijk, M., 2009, In : Breast Cancer Research. 11, 1, R8.

Research output: Contribution to journalArticleAcademicpeer-review

File
60 Downloads (Pure)

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

Mohammadi, L., van Vreeswijk, M., Oldenburg, R., van den Ouweland, A. M. W., Oosterwijk, J. C., van der Hout, A. H., Hoogerbrugge, N., Ligtenberg, M. J. L., Ausems, M. G., van der Luijt, R., Dommering, C. J., Gille, J. J. P., Verhoef, S., Hogervorst, FB., van Os, T. A. M., Gomez Garcia, E. B., Blok, M. M., Wijnen, J. G., Helmer, Q., Devilee, P. & 2 others, van Asperen, C. J. & Houwelingen, HJ., 2009, In : BMC Cancer. 9, 211.

Research output: Contribution to journalArticleAcademicpeer-review

File
49 Downloads (Pure)

Incidence of retinoblastoma in Dutch children conceived by IVF: an expanded study

Marees, T., Dommering, C. J., Imhof, S. M., Kors, W. A., Ringens, P. J., van Leeuwen, F. E. & Moll, A. C., 2009, In : Human Reproduction. 24, 12, p. 3220-3224

Research output: Contribution to journalArticleAcademicpeer-review

2008

Functional characterisation of the TSC1-TSC2 complex to assess multiple TSC2 variants identified in single families affected by tuberous sclerosis complex

Nellist, M., Sancak, O., Goedbloed, M., Adriaans, A., Wessels, M., Maat-Kievit, A., Baars, M., Dommering, C. J., van den Ouweland, A. & Halley, D., 2008, In : BMC Medical Genetics. 9, p. 10

Research output: Contribution to journalArticleAcademicpeer-review

Open Access
File
66 Downloads (Pure)

Mutation screening of fumarate hydratase by multiplex ligation-dependent probe amplification: detection of exonic deletion in a patient with leiomyomatosis and renal cell cancer

Ahvenainen, T., Lehtonen, H. J., Lehtonen, R., Vahteristo, P., Aittomaki, K., Baynam, G., Dommering, C. J., Eng, C., Gruber, S. B., Gronberg, H., Harvima, R., Herva, R., Hietala, M., Kujala, M., Kaariainen, H., Sunde, L., Vierimaa, O., Pollard, P. J., Tomlinson, I. P. M., Bjorck, E. & 2 others, Aaltonen, L. A. & Launonen, V., 2008, In : Cancer Genetics and Cytogenetics. 183, 2, p. 83-88

Research output: Contribution to journalArticleAcademicpeer-review

2003

Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method

Hogervorst, F. B. L., Nederlof, P. M., Gille, J. J. P., McElgunn, C. J., Grippeling, M., Pruntel, R., Regnerus, R., van Welsem, T., van Spaendonk, R., Menko, F. H., Kluijt, I., Dommering, C., Verhoef, S., Schouten, J. P., van't Veer, L. J. & Pals, G., 1 Apr 2003, In : Cancer Research. 63, 7, p. 1449-53 5 p.

Research output: Contribution to journalArticleAcademicpeer-review

2002

Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach

Gille, J. J. P., Hogervorst, F. B. L., Pals, G., Wijnen, J. T., van Schooten, R. J., Dommering, C. J., Meijer, G. A., Craanen, M. E., Nederlof, P. M., de Jong, D., McElgunn, C. J., Schouten, J. P. & Menko, F. H., 7 Oct 2002, In : British Journal of Cancer. 87, 8, p. 892-7 6 p.

Research output: Contribution to journalArticleAcademicpeer-review