prof. dr. R.H. (Rolf) Sijmons

Professor in Medical Translational Genetics

prof. dr. R.H. (Rolf) Sijmons
E-mail:
r.h.sijmons umcg.nl

Research

  1. 2019
  2. Johansson, L. F., van Dijk-Bos, K. K., van der Hout, A. H., Knopperts, A. P., Leegte, B., ter Beest, J., ... Westers, H. (2019). What if we would turn a diagnostic multi-cancer gene panel into a screening tool? European Journal of Human Genetics, 27, 1126-1126.
  3. Drost, M., Tiersma, Y., Thompson, B. A., Frederiksen, J. H., Keijzers, G., Glubb, D., ... Tavtigian, S. V. (2019). A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome. Genetics in Medicine, 21(7), 1486-1496. https://doi.org/10.1038/s41436-018-0372-2
  4. Grolleman, J. E., de Voer, R. M., Elsayed, F. A., Nielsen, M., Weren, R. D. A., Palles, C., ... Kuiper, R. P. (2019). Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype. Cancer cell, 35(2), 256-266.e5. https://doi.org/10.1016/j.ccell.2018.12.011
  5. 2018
  6. Weren, R. D. A., van der Post, R. S., Vogelaar, I. P., van Krieken, J. H., Spruijt, L., Lubinski, J., ... Ligtenberg, M. J. L. (2018). Role of germline aberrations affecting,andin gastric cancer susceptibility. JOURNAL OF MEDICAL GENETICS, 55(10), 669-674. https://doi.org/10.1136/jmedgenet-2017-104962
  7. Schubert, S. A., Ruano, D., Elsayed, F. A., Boot, A., Crobach, S., Sarasqueta, A. F., ... van Wezel, T. (2018). Erratum: Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia (vol 117, pg 1215, 2017). British Jounal of Cancer, 118(2), e4. [e4]. https://doi.org/10.1038/bjc.2017.380
  8. 2017
  9. Vogelaar, I. P., van der Post, R. S., van Krieken, J. H. J., Spruijt, L., van Zelst-Stams, W. A., Kets, C. M., ... Hoogerbrugge, N. (2017). Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing. European Journal of Human Genetics, 25(11), 1246-1252. https://doi.org/10.1038/ejhg.2017.138
  10. Seppala, T., Pylvanainen, K., Evans, D. G., Jarvinen, H., Renkonen-Sinisalo, L., Bernstein, I., ... Collaboration Mallorca Grp (2017). Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: A Prospective Lynch Syndrome Database report. Hereditary cancer in clinical practice, 15, [18]. https://doi.org/10.1186/s13053-017-0078-5
  11. Schubert, S. A., Ruano, D., Elsayed, F. A., Boot, A., Crobach, S., Sarasqueta, A. F., ... van Wezel, T. (2017). Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia. British Jounal of Cancer, 117(8), 1215-1223. https://doi.org/10.1038/bjc.2017.240
  12. Konings, I. C. A. W., Harinck, F., Poley, J-W., Aalfs, C. M., van Rens, A., Krak, N. C., ... Dutch Res Grp Pancreatic Canc Surv (2017). Prevalence and Progression of Pancreatic Cystic Precursor Lesions Differ Between Groups at High Risk of Developing Pancreatic Cancer. PANCREAS, 46(1), 28-34. https://doi.org/10.1097/MPA.0000000000000725
  13. Møller, P., Seppälä, T., Bernstein, I., Holinski-Feder, E., Sala, P., Evans, D. G., ... Mallorca Group (http://mallorca-group.org) (2017). Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database. Gut, 66(9), 1657-1664. https://doi.org/10.1136/gutjnl-2016-311403
  14. 2016
  15. Ghorbanoghli, Z., Nieuwenhuis, M. H., Houwing-Duistermaat, J. J., Jagmohan-Changur, S., Hes, F. J., Tops, C. M., ... Wijnen, J. T. (2016). Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers. Familial Cancer, 15(4), 563-570. https://doi.org/10.1007/s10689-016-9877-5
  16. Harinck, F., Konings, I. C. A. W., Kluijt, I., Poley, J. W., van Hooft, J. E., van Dullemen, H. M., ... Dutch Res Grp Pancreatic Canc (2016). A multicentre comparative prospective blinded analysis of EUS and MRI for screening of pancreatic cancer in high-risk individuals. Gut, 65(9), 1505-1513. https://doi.org/10.1136/gutjnl-2014-308008
  17. 2015
  18. van der Post, R. S., Vogelaar, I. P., Manders, P., van der Kolk, L. E., Cats, A., van Hest, L. P., ... Ligtenberg, M. J. L. (2015). Accuracy of Hereditary Diffuse Gastric Cancer Testing Criteria and Outcomes in Patients With a Germline Mutation in CDH1. Gastroenterology, 149(4), 897-906.e19. https://doi.org/10.1053/j.gastro.2015.06.003
  19. ten Broeke, S. W., Brohet, R. M., Tops, C. M., van der Klift, H. M., Velthuizen, M. E., Bernstein, I., ... Wijnen, J. T. (2015). Lynch Syndrome Caused by Germline PMS2 Mutations: Delineating the Cancer Risk. Journal of Clinical Oncology, 33(4), 319-325. https://doi.org/10.1200/JCO.2014.57.8088
  20. 2014
  21. Monteira Ferreira, A. M., Tuominen, I., van Dijk-Bos, K., Sanjabi, B., van der Sluis, T., van der Zee, A. G., ... Hofstra, R. M. W. (2014). High Frequency of RPL22 Mutations in Microsatellite-Unstable Colorectal and Endometrial Tumors. Human Mutation, 35(12), 1442-1445. https://doi.org/10.1002/humu.22686
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