Nicoline Hoogerbrugge

Author

Also Known As

Ad Geurts van Kessel, Andreas Rump, Annemarie H. van der Hout, Anthony J. Brookes, C.J. van Asperen, Carla Oliveira, Christi J. van Asperen, Hagenkord, Jill, Hans F. A. Vasen, Hans Scheffer

437

Publications

18.3K

Citations

H-Index

134

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center University Medical Center Groningen The Netherlands Cancer Institute Leiden University Medical Center

About

Nicoline Hoogerbrugge is an author at Radboud University Nijmegen specializing in medicine, pathology, and oncology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	36	72	6.1K
2	Health Sciences	9	9	477
3	Engineering	3	3	226
4	Management	1	1	63
5	Natural Sciences	1	1	803

Nicoline Hoogerbrugge

184

Publications

13.2K

Citations

H-Index

Page 1

	Year	Citations
Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results Sharon E. Plon, Diana Eccles, Douglas F. Easton, Human Mutation Genetic TestingCancer PathologySequence Variant ClassificationGeneticsGenetic Epidemiology	2008	897
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1 Marjolijn J. L. Ligtenberg, Roland P. Kuiper, Tsun Leung Chan, Nature Genetics Heritable Somatic MethylationSomatic VariantMendelian DisorderGenetic DisorderMedicine	2008	803
Deficient mismatch repair system in patients with sporadic advanced colorectal cancer Miriam Koopman, Guus A. M. Kortman, Leonie J. Mekenkamp, British Journal of Cancer	2009	509
A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer Robbert D.A. Weren, Marjolijn J. L. Ligtenberg, C. Marleen Kets, Nature Genetics Genome InstabilityMedicineGeneticsColorectal CancerPathology	2015	372
Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors Arjen R. Mensenkamp, Ingrid P. Vogelaar, Wendy A.G. van Zelst–Stams, Gastroenterology Genome InstabilitySomatic VariantSomatic MutationsGenetic DisorderLynch Syndrome-like Tumors	2013	320
The effect of growth hormone administration in growth hormone deficient adults on bone, protein, carbohydrate and lipid homeostasis, as well as on body composition Arjen Binnerts, G. Roel Swart, J. H. P. Wilson, Clinical Endocrinology	1992	316
Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome Christoph Engel, Markus Loeffler, Verena Steinke, Journal of Clinical Oncology	2012	300
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
Cancer Risks for <i>PMS2</i>-Associated Lynch Syndrome Sanne W. ten Broeke, Heleen M. van der Klift, Carli M.J. Tops, Journal of Clinical Oncology	2018	205
Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among <i>MSH2</i> mutation carriers Rachel S. van der Post, Lambertus A. Kiemeney, Marjolijn J. L. Ligtenberg, Journal of Medical Genetics	2010	190

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