Rolf Sijmons
Rolf Sijmons
Professor of Medical Translational Genetics, dept Genetics, University Medical Center Groningen
Verified email at umcg.nl - Homepage
TitleCited byYear
DNA Commission of the International Society of Forensic Genetics (ISFG): an update of the recommendations on the use of Y-STRs in forensic analysis
L Gusmao, JM Butler, A Carracedo, P Gill, M Kayser, WR Mayr, N Morling, ...
International journal of legal medicine 120 (4), 191-200, 2006
566*2006
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
5141997
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
5102013
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
4541998
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, 1999
4481999
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
3221999
Inhibition of nitric oxide synthesis during endotoxemia promotes intrahepatic thrombosis and an oxygen radical‐mediated hepatic injury
BG Harbrecht, TR Billiar, J Stadler, AJ Demetris, J Ochoa, RD Curran, ...
Journal of leukocyte biology 52 (4), 390-394, 1992
3221992
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
3002002
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, 2014
2832014
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
2702001
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
2442013
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
2262010
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
2212004
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
2092002
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
2042011
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
1992005
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, 2001
1932001
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, ...
J Clin Oncol 30 (35), 4409-15, 2012
1912012
A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families
T Peelen, M Van Vliet, A Petrij-Bosch, R Mieremet, C Szabo, ...
American journal of human genetics 60 (5), 1041, 1997
1901997
Molecular evidence linking primary cancer of the fallopian tube to BRCA1 germline mutations
RP Zweemer, PJ Van Diest, RHM Verheijen, A Ryan, JJP Gille, ...
Gynecologic oncology 76 (1), 45-50, 2000
1812000
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