Rolf Sijmons

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144 Article
11 Review article
10 Meeting Abstract
7 Comment/Letter to the editor
Meer

Evaluation of a seven gene mutational profile as a prognostic factor in a population-based study of clear cell renal cell carcinoma
van de Pol, J. A. A., Ferronika, P., Westers, H., van Engeland, M., Terpstra, M. M., Smits, K. M., de Lange, K., van den Brandt, P. A., Sijmons, R. H., Schouten, L. J. & Kok, K., 22-apr-2022, In: Scientific Reports. 12, 1, 12 blz., 6478.
Onderzoeksoutput › Academic › peer review

Open Access
Bestand
Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance
Ghorbani, F., Alimohamed, M. Z., Vilacha, J. F., Van Dijk, K. K., De Boer-Bergsma, J., Fokkens, M. R., Lemmink, H., Sijmons, R. H., Sikkema-Raddatz, B., Groves, M. R., Verschuuren-Bemelmans, C. C., Verbeek, D. S., Van Diemen, C. C. & Westers, H., 25-mrt-2022, In: Frontiers in Genetics. 13, 13 blz., 782685.
Onderzoeksoutput › Academic › peer review

Open Access
Bestand

5 Downloads (Pure)
Validation of New Gene Variant Classification Methods: a Field-Test in Diagnostic Cardiogenetics
Alimohamed, M. Z., Westers, H., Vos, Y. J., Van der Velde, K. J., Sijmons, R. H., Van der Zwaag, P. A., Sikkema-Raddatz, B. & Jongbloed, J. D. H., 1-mrt-2022, In: Frontiers in Genetics. 13, 7 blz., 824510.
Onderzoeksoutput › Academic › peer review

Open Access
Bestand

2 Downloads (Pure)
A rare large duplication of MLH1 identified in Lynch syndrome
Kumar, A., Paramasivam, N., Bandapalli, O. R., Schlesner, M., Chen, T., Sijmons, R., Dymerska, D., Golebiewska, K., Kuswik, M., Lubinski, J., Hemminki, K. & Försti, A., 19-jan-2021, In: Hereditary cancer in clinical practice. 19, 1, blz. 1-7 7 blz., 10.
Onderzoeksoutput › Academic › peer review

Open Access
Bestand

1 Citaat (Scopus)

32 Downloads (Pure)
Characterization of rare germline variants in familial multiple myeloma
Catalano, C., Paramasivam, N., Blocka, J., Giangiobbe, S., Huhn, S., Schlesner, M., Weinhold, N., Sijmons, R., de Jong, M., Langer, C., Preuss, K-D., Nilsson, B., Durie, B., Goldschmidt, H., Bandapalli, O. R., Hemminki, K. & Foersti, A., 13-feb-2021, In: Blood cancer journal. 11, 2, 4 blz., 33.
Onderzoeksoutput › Academic › peer review

Open Access
Bestand

2 Citaten (Scopus)

12 Downloads (Pure)

5 Membership
1 Organising and contributing to an event
1 Editorial work
1 Professional or public event

7th International Cardiovascular Genomic Medicine Conference
Yvonne Vos (Speaker), Mohamed Alimohamed (Speaker), Lennart Johansson (Speaker), Helga Westers (Speaker), Richard Sinke (Speaker), Rolf Sijmons (Speaker), Birgit Sikkema-Raddatz (Speaker), Jan Jongbloed (Speaker) & Paul Zwaag, van der (Speaker)
4-dec-2019 → 5-dec-2019
Activiteit: Professional or public presentation › Professional
European Society for Medical Oncology (ESMO) , Lugano , Switzerland. (Externe Organisatie)
Rolf Sijmons (Member)
2019 → 2023
Activiteit: Membership › Professional
European Hereditary Tumour Group (Externe Organisatie)
Rolf Sijmons (Member of board)
2019 → 2023
Activiteit: Membership › Professional
9th European Multidisciplinary Colorectal Cancer Congress
Rolf Sijmons (Member of scientific committee)
2018 → 2019
Activiteit: Organising and contributing to an event › Professional
Dutch Colorectal Cancer Group (DCCG) (Externe Organisatie)
Rolf Sijmons (Member of board)
2017 → 2021
Activiteit: Membership › Professional

Additional file 1: Table S1. of GAVIN: Gene-Aware Variant INterpretation for medical sequencing
van der Velde, J. (Contributor), de Boer, E. N. (Contributor), van Diemen, C. (Contributor), Raddatz, B. (Contributor), Abbott, K. (Contributor), Knopperts, A. (Contributor), Franke, L. (Contributor), Sijmons, R. (Contributor), de Koning, T. (Contributor), Wijmenga, C. (Contributor), Sinke, R. (Contributor) & Swertz, M. (Contributor), University of Groningen, 16-jan-2017
DOI: 10.6084/m9.figshare.c.3666643_d4.v1
Dataset
Additional file 3: Table S3. of GAVIN: Gene-Aware Variant INterpretation for medical sequencing
van der Velde, J. (Contributor), de Boer, E. (Contributor), van Diemen, C. (Contributor), Raddatz, B. (Contributor), Abbott, K. (Contributor), Knopperts, A. (Contributor), Franke, L. (Contributor), Sijmons, R. (Contributor), de Koning, T. (Contributor), Wijmenga, C. (Contributor), Sinke, R. (Contributor) & Swertz, M. (Contributor), University of Groningen, 16-jan-2017
DOI: 10.6084/m9.figshare.c.3666643_d3.v1
Dataset
Additional file 4: of NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing
Johansson, L. (Contributor), Weerd ,de, H. (Contributor), de Boer, E. (Contributor), van Dijk, F. (Contributor), te Meerman, G. (Contributor), Sijmons, R. (Contributor), Raddatz, B. (Contributor) & Swertz, M. (Contributor), University of Groningen, 17-dec-2018
DOI: 10.6084/m9.figshare.7479074.v1
Dataset
Additional file 3: of NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing
Johansson, L. (Contributor), Weerd, H. (Contributor), de Boer, E. (Contributor), van Dijk, F. (Contributor), te Meerman, G. (Contributor), Sijmons, R. (Contributor), Raddatz, B. (Contributor) & Swertz, M. (Contributor), University of Groningen, 17-dec-2018
DOI: 10.6084/m9.figshare.7479071.v1
Dataset
Additional file 5: of NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing
Johansson, L. (Contributor), Weerd, H. (Contributor), de Boer, E. (Contributor), van Dijk, F. (Contributor), te Meerman, G. (Contributor), Sijmons, R. (Contributor), Raddatz, B. (Contributor) & Swertz, M. (Contributor), University of Groningen, 17-dec-2018
DOI: 10.6084/m9.figshare.7479080.v1
Dataset

Er moet een omslag komen richting preventie
Rolf Sijmons
22/11/2019
1 Mediabijdrage
Pers / media: Expert Comment › Popular
Will your DNA change if you receive a donor organ or bloodtransfusion?
Rolf Sijmons
13/12/2018
1 Mediabijdrage
Pers / media: Expert Comment › Popular

Rolf Sijmons

Netwerk

Duik in details

Evaluation of a seven gene mutational profile as a prognostic factor in a population-based study of clear cell renal cell carcinoma

Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance

Validation of New Gene Variant Classification Methods: a Field-Test in Diagnostic Cardiogenetics

A rare large duplication of MLH1 identified in Lynch syndrome

Characterization of rare germline variants in familial multiple myeloma

7th International Cardiovascular Genomic Medicine Conference

European Society for Medical Oncology (ESMO) , Lugano , Switzerland. (Externe Organisatie)

European Hereditary Tumour Group (Externe Organisatie)

9th European Multidisciplinary Colorectal Cancer Congress

Dutch Colorectal Cancer Group (DCCG) (Externe Organisatie)

Additional file 1: Table S1. of GAVIN: Gene-Aware Variant INterpretation for medical sequencing

Additional file 3: Table S3. of GAVIN: Gene-Aware Variant INterpretation for medical sequencing

Additional file 4: of NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing

Additional file 3: of NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing

Additional file 5: of NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing

Er moet een omslag komen richting preventie

Will your DNA change if you receive a donor organ or bloodtransfusion?

Rolf Sijmons

Netwerk

Onderzoeksoutput

Activiteiten

Datasets

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