Rolf Sijmons

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144 Article
11 Review article
10 Meeting Abstract
7 Comment/Letter to the editor
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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 p., 6478.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
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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-Mar-2022, In: Frontiers in Genetics. 13, 13 p., 782685.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
File

2 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-Mar-2022, In: Frontiers in Genetics. 13, 7 p., 824510.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
File

1 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, p. 1-7 7 p., 10.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
File

30 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 p., 33.
Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

Open Access
File

1 Citation (Scopus)

10 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
Activity: Talk and presentation › Professional or public presentation › Professional
European Society for Medical Oncology (ESMO) , Lugano , Switzerland. (External organisation)
Rolf Sijmons (Member)
2019 → 2023
Activity: Membership › Professional
European Hereditary Tumour Group (External organisation)
Rolf Sijmons (Member of board)
2019 → 2023
Activity: Membership › Professional
9th European Multidisciplinary Colorectal Cancer Congress
Rolf Sijmons (Member of scientific committee)
2018 → 2019
Activity: Organising and attending an event › Organising and contributing to an event › Professional
Dutch Colorectal Cancer Group (DCCG) (External organisation)
Rolf Sijmons (Member of board)
2017 → 2021
Activity: Membership › Professional

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
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 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: 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 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

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

Rolf Sijmons

Network

Dive into 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. (External organisation)

European Hereditary Tumour Group (External organisation)

9th European Multidisciplinary Colorectal Cancer Congress

Dutch Colorectal Cancer Group (DCCG) (External organisation)

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

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

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

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

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

Er moet een omslag komen richting preventie

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

Rolf Sijmons

Network

Research output

Activities

Datasets

Press / Media