Marjolijn J. L. Ligtenberg

Author

Also Known As

Andreas Rump, B. Lemley, C M Aalfs, C. Seynaeve, Elizabeth M. Dequeker, Elke Holinski-Feder, F. M. Nagengast, Hans Morreau, Ingrid P. Vogelaar, Kathleen B.M. Claes

312

Publications

16.1K

Citations

H-Index

125

Concepts

All Affiliations

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

About

Marjolijn J. L. Ligtenberg is an author at Radboud University Nijmegen specializing in medicine, pathology, and oncology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	40	65	7K
2	Engineering	5	5	450
3	Natural Sciences	5	5	1.3K
4	Health Sciences	4	4	553
5	Law	1	1	34

Marjolijn J. L. Ligtenberg

160

Publications

12.5K

Citations

H-Index

Page 1

	Year	Citations
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
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients Anne Petrij-Bosch, Tamara Peelen, Margreethe van Vliet, Nature Genetics Breast OncologySomatic VariantMedicineGeneticsMajor Founder Mutations	1997	445
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
A Post-Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases Kornelia Neveling, Ilse Feenstra, Christian Gilissen, Human Mutation Exome SequencingGeneticsGenetic EpidemiologyDiagnosisPathology	2013	336
Suppression of cellular aggregation by high levels of episialin. Marjolijn J. L. Ligtenberg, F Buijs, Hans L. Vos, PubMed Apical SurfaceCell InteractionCarcinoma Cell LinesCell LinesCell-matrix Interaction	1992	321
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
Targeted sequencing by proximity ligation for comprehensive variant detection and local haplotyping Paula J. P. de Vree, Elzo de Wit, Monique van de Heijning, Nature Biotechnology Long-read SequencingSequencingFunctional GenomicsProximity LigationComprehensive Variant Detection	2014	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
Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers Antonis C. Antoniou, Amanda B. Spurdle, Olga M. Sinilnikova, The American Journal of Human Genetics Allelic VariantBreast OncologyBreast Cancer RiskCancer RiskGenetics	2008	284

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