Rolf Sijmons
Rolf Sijmons
Professor of Medical Translational Genetics, dept Genetics, University Medical Center Groningen
Verified email at - Homepage
Cited by
Cited by
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
HFA Vasen, I Blanco, K Aktan-Collan, JP Gopie, A Alonso, S Aretz, ...
Gut 62 (6), 812-823, 2013
Germline Mutations in the PTEN/MMAC1 Gene in Patients With Cowden Disease
MR Nelen, WCG Van Staveren, EAJ Peeters, M Ben Hassel, RJ Gorlin, ...
Human molecular genetics 6 (8), 1383-1387, 1997
Familial endometrial cancer in female carriers of MSH6 germline mutations
J Wijnen, W de Leeuw, H Vasen, H van der Klift, P Møller, A Stormorken, ...
Nature genetics 23 (2), 142-144, 1999
Clinical findings with implications for genetic testing in families with clustering of colorectal cancer
JT Wijnen, HFA Vasen, PM Khan, AH Zwinderman, H Van Der Klift, ...
New England Journal of Medicine 339 (8), 511-518, 1998
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database
BA Thompson, AB Spurdle, JP Plazzer, MS Greenblatt, K Akagi, ...
Nature genetics 46 (2), 107-115, 2014
Association of hereditary nonpolyposis colorectal cancer–related tumors displaying low microsatellite instability with MSH6 germline mutations
Y Wu, MJW Berends, RGJ Mensink, C Kempinga, RH Sijmons, ...
The American Journal of Human Genetics 65 (5), 1291-1298, 1999
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database
P Møller, T Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 66 (3), 464-472, 2017
Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
P Møller, TT Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 67 (7), 1306-1316, 2018
Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant
MJW Berends, Y Wu, RH Sijmons, RGJ Mensink, T van der Sluis, ...
The American Journal of Human Genetics 70 (1), 26-37, 2002
Targeted next‐generation sequencing can replace Sanger sequencing in clinical diagnostics
B Sikkema‐Raddatz, LF Johansson, EN de Boer, R Almomani, LG Boven, ...
Human mutation 34 (7), 1035-1042, 2013
Reviews of evidence regarding interventions to reduce tobacco use and exposure to environmental tobacco smoke
DP Hopkins, PA Briss, CJ Ricard, CG Husten, VG Carande-Kulis, ...
American journal of preventive medicine 20 (2), 16-66, 2001
TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes
MWG Ruijs, S Verhoef, MA Rookus, R Pruntel, AH van der Hout, ...
Journal of medical genetics 47 (6), 421-428, 2010
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
MJE Kempers, RP Kuiper, CW Ockeloen, PO Chappuis, P Hutter, ...
The lancet oncology 12 (1), 49-55, 2011
Risks of less common cancers in proven mutation carriers with lynch syndrome
C Engel, M Loeffler, V Steinke, N Rahner, E Holinski-Feder, W Dietmaier, ...
Journal of Clinical Oncology 30 (35), 4409-4415, 2012
Low-penetrance genes and their involvement in colorectal cancer susceptibility
MM de Jong, IM Nolte, GJ te Meerman, WTA van der Graaf, EGE de Vries, ...
Cancer Epidemiology and Prevention Biomarkers 11 (11), 1332-1352, 2002
Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status
C Oliveira, JL Westra, D Arango, M Ollikainen, E Domingo, A Ferreira, ...
Human molecular genetics 13 (19), 2303-2311, 2004
Management of extracolonic tumours in patients with Lynch syndrome
JJ Koornstra, MJE Mourits, RH Sijmons, AM Leliveld, H Hollema, ...
The lancet oncology 10 (4), 400-408, 2009
Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome
RC Niessen, RMW Hofstra, H Westers, MJL Ligtenberg, K Kooi, ...
Genes, Chromosomes and Cancer 48 (8), 737-744, 2009
Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)
M Nielsen, PF Franken, T Reinards, MM Weiss, A Wagner, H Van der Klift, ...
Journal of medical genetics 42 (9), e54-e54, 2005
A role for MLH3 in hereditary nonpolyposis colorectal cancer
Y Wu, MJW Berends, RH Sijmons, RGJ Mensink, E Verlind, KA Kooi, ...
Nature genetics 29 (2), 137-138, 2001
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