Rolf H. Sijmons - Concepedia

Author

Rolf H. Sijmons

University Medical Center Groningen ORCID

Also Known As

I Van Langen, J-P Plazzer, Lilian Vreede, Marjolijn Ligtenberg, R H Sijmons, R. H. SIJMONS, R. H. Sijmons, R. Sijmons, R.H Sijmons, R.H. SIJMONS

269

Publications

13.5K

Citations

H-Index

155

Concepts

All Affiliations

University Medical Center Groningen University of Groningen Leiden University Medical Center Radboud University Nijmegen University Medical Center Utrecht

About

Rolf H. Sijmons is an author at University Medical Center Groningen specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	3	3	242
2	Health Sciences	2	2	189
3	Arts	1	1	25
4	Law	1	1	34
5	Management	1	1	28

Rolf H. Sijmons

124

Publications

10.9K

Citations

H-Index

Page 1

	Year	Citations
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts Hans F. A. Vasen, Ignacio Blanco, Katja Aktan–Collan, Gut	2013	722
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database Mev Dominguez–Valentin, Julian R. Sampson, Toni T. Seppälä, Genetics in Medicine	2019	615
Cancer risk and survival in <i>path_MMR</i> carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database Pål Møller, Toni T. Seppälä, Inge Bernstein, Gut	2017	544
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database Pål Møller, Toni T. Seppälä, Inge Bernstein, Gut	2015	531
Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer Juul Wijnen, Hans F. A. Vasen, P. Meera Khan, New England Journal of Medicine	1998	397
Association of Hereditary Nonpolyposis Colorectal Cancer–Related Tumors Displaying Low Microsatellite Instability with MSH6 Germline Mutations Ying Wu, Maran J.W. Berends, Rob G.J. Mensink, The American Journal of Human Genetics Cancer PathologyMedicineGeneticsGenetic EpidemiologyPathology	1999	308
Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome Christoph Engel, Markus Loeffler, Verena Steinke, Journal of Clinical Oncology	2012	300
Molecular and Clinical Characteristics of MSH6 Variants: An Analysis of 25 Index Carriers of a Germline Variant Maran J.W. Berends, Ying Wu, Rolf H. Sijmons, The American Journal of Human Genetics Msh6 VariantsSomatic VariantGenetic DisorderMedicineGenetics	2002	296
Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics Birgit Sikkema‐Raddatz, Lennart Johansson, Eddy N. de Boer, Human Mutation Exome SequencingGeneticsMutation DetectionGenetic EpidemiologyPathology	2013	294
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study Marlies Kempers, Roland P. Kuiper, Charlotte W. Ockeloen, The Lancet Oncology Cancer RiskMedicineColorectal CancerPathologyGynecology	2010	287

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