20122019
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Research Output 2012 2019

  • 16 Article
  • 3 Meeting Abstract
  • 1 Research VU University Amsterdam, graduation VU University Amsterdam
2019

Next Generation Sequencing in health care and clinical research: attuning all steps

Rigter, T., Belien, J. A. M., de Wert, G. M. W. R., Ploem, C., Bunnik, E. M., Bredenoord, A. L. & Cornel, M. C., Oct 2019, In : European Journal of Human Genetics. 27, p. 1790-1791

Research output: Contribution to journalMeeting AbstractAcademic

SLCO1B1 c.521T > C genotype, sex, and initial statin treatment as contributing factors to continuous simvastatin or atorvastatin treatment in a Dutch cohort

Jansen, M. E., Rigter, T., Fleur, T. M. C., Souverein, P., Vijverberg, S. J. H., Rodenburg, W. & Cornel, M. C., Jul 2019, In : European Journal of Human Genetics. 27, p. 558-559

Research output: Contribution to journalMeeting AbstractAcademic

2018

Actions, roles, and responsibilities in implementation of pharmacogenomics in primary care

Jansen, M. E., Rigter, T., Janssen, S., Rodenburg, W. & Cornel, M. C., Oct 2018, In : European Journal of Human Genetics. 26, p. 687-688

Research output: Contribution to journalMeeting AbstractAcademic

2017

Review of the reported measures of clinical validity and clinical utility as arguments for the implementation of pharmacogenetic testing: A case study of statin-induced muscle toxicity

Jansen, M. E., Rigter, T., Rodenburg, W., Fleur, T. M. C., Houwink, E. J. F., Weda, M. & Cornel, M. C., 23 Aug 2017, In : Frontiers in Pharmacology. 8, AUG, 555.

Research output: Contribution to journalArticleAcademicpeer-review

Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape

Holtkamp, K. C. A., Vos, E. M., Rigter, T., Lakeman, P., Henneman, L. & Cornel, M. C., 16 Feb 2017, In : BMC Health Services Research. 17, 1, 146.

Research output: Contribution to journalArticleAcademicpeer-review

2016

Challenges and opportunities for ELSI early career researchers: Bmc Medical Ethics

Bell, J., Ancillotti, M., Coathup, V., Coy, S., Rigter, T., Tatum, T., Grewal, J., Akcesme, F. B., Brkic, J., Causevic-Ramosevac, A., Milovanovic, G., Nobile, M., Pavlidis, C., Finlay, T., Kaye, J. & [Unknown], E., 2016, In : BMC Medical Ethics. 17, 1 p., 37.

Research output: Contribution to journalArticleAcademicpeer-review

2015

A decade of molecular genetic testing for MODY: a retrospective study of utilization in The Netherlands

Weinreich, S. S., Bosma, A. R., Henneman, L., Rigter, T., Spruijt, C. M. J., Grimbergen, A. J. E. M., Breuning, M. H., de Koning, E. J. P., Losekoot, M. & Cornel, M. C., 2015, In : European Journal of Human Genetics. 23, 1, p. 29-33

Research output: Contribution to journalArticleAcademicpeer-review

Current and Best Practices of Genetic Testing for Maturity Onset Diabetes of the Young: Views of Professional Experts

van der Zwaag, A. M., Weinreich, S. S., Bosma, A. R., Rigter, T., Losekoot, M., Henneman, L. & Cornel, M. C., 2015, In : Public Health Genomics. 18, 1, p. 52-59

Research output: Contribution to journalArticleAcademicpeer-review

Farmacogenetica in de eerstelijnszorg. Toepassingen en toekomstverwachtingen

Houwink, E. J. F., Rigter, T., Swen, J. J., Cornel, M. C., Kienhuis, A., Rodenburg, W. & Weda, M., 2015, In : Nederlands Tijdschrift voor Geneeskunde. 159, A9204.

Research output: Contribution to journalArticleProfessional

2014

A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document

Cornel, M. C., Rigter, T., Weinreich, S. S., Burgard, P., Hoffmann, G. F., Lindner, M., Loeber, J. G., Rupp, K., Taruscio, D. & Vittozzi, L., 2014, In : European Journal of Human Genetics. 22, 1, p. 12-17

Research output: Contribution to journalArticleAcademicpeer-review

Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases

Rigter, T., Henneman, L., Broerse, J. E. W., Shepherd, M., Blanco, I., Kristoffersson, U. & Cornel, M. C., 2014, In : Journal of Community Genetics. 5, 4, p. 337-347

Research output: Contribution to journalArticleAcademicpeer-review

Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients

Rigter, T., van Aart, C. J. A., Elting, M. W., Waisfisz, Q., Cornel, M. C. & Henneman, L., 2014, In : Clinical Genetics. 85, 5, p. 417-422

Research output: Contribution to journalArticleAcademicpeer-review

Newborn screening for pompe disease? a qualitative study exploring professional views

van El, C. G., Rigter, T., Reuser, A. J. J., van der Ploeg, A. T., Weinreich, S. S. & Cornel, M. C., 2014, In : BMC Pediatrics. 14, 203.

Research output: Contribution to journalArticleAcademicpeer-review

71 Downloads (Pure)

Translating the dynamics of genetics into health care practice

Rigter, T., 2014

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

File
2013

Reflecting on Earlier Experiences with Unsolicited Findings: Points to Consider for Next-Generation Sequencing and Informed Consent in Diagnostics

Rigter, T., Henneman, L., Kristoffersson, U., Hall, A., Yntema, H. G., Borry, P., Tonnies, H., Waisfisz, Q., Elting, M. W., Dondorp, W. J. & Cornel, M. C., 2013, In : Human Mutation. 34, 10, p. 1322-1328

Research output: Contribution to journalArticleAcademicpeer-review

2012

Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 1. From blood spot to screening result

Loeber, J. G., Burgard, P., Cornel, M. C., Rigter, T., Weinreich, S. S., Rupp, K., Hoffmann, G. F. & Vittozzi, L., 2012, In : Journal of Inherited Metabolic Disease. 35, 4, p. 603-611

Research output: Contribution to journalArticleAcademicpeer-review

Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 2. From screening laboratory results to treatment, follow-up and quality assurance

Burgard, P., Rupp, K., Lindner, M., Haege, G., Rigter, T., Weinreich, S. S., Loeber, J. G., Taruscio, D., Vittozzi, L., Cornel, M. C. & Hoffmann, G. F., 2012, In : Journal of Inherited Metabolic Disease. 35, 4, p. 613-625

Research output: Contribution to journalArticleAcademicpeer-review

48 Downloads (Pure)

Public support for neonatal screening for Pompe disease, a broad-phenotype condition

Weinreich, S. S., Rigter, T., van El, C. G., Dondorp, W. J., Kostense, P. J., van der Ploeg, A. T., Reuser, A. J., Cornel, M. C. & Hagemans, M. L., 2012, In : Orphanet Journal of Rare Diseases. 7, 15.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access
File

Severely impaired health status at diagnosis of Pompe disease: A cross-sectional analysis to explore the potential utility of neonatal screening

Rigter, T., Weinreich, S. S., van El, C. G., de Vries, J. M., van Gelder, C. M., Gungor, D., Reuser, A. J. J., Hagemans, M. L. C., Cornel, M. C. & van der Ploeg, A. T., 2012, In : Molecular Genetics and Metabolism. 107, 3, p. 448-455

Research output: Contribution to journalArticleAcademicpeer-review