Maartje Nielsen - Concepedia

Author

Maartje Nielsen

Also Known As

Bernard J. Pope, D Mollerup, Demi van Egmond, Edward M. Leter, Floor Duijkers, Hans Morreau, M Abdulrahman, M Nielsen, M. Nielsen, Maartje Nielsen

206

Publications

6.6K

Citations

H-Index

Concepts

All Affiliations

Leiden University Medical Center University Medical Center Groningen Cardiff University Leiden University University of Bonn

About

Maartje Nielsen is an author at Leiden University Medical Center specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	21	2K
2	Engineering	2	2	29
3	Natural Sciences	2	2	365
4	Arts	1	1	139
5	Health Sciences	1	1	166

Maartje Nielsen

Publications

Citations

H-Index

Page 1

	Year	Citations
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
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome Gijs W.E. Santen, Emmelien Aten, Yu Sun, Nature Genetics ChromatinGenome InstabilitySwi/snf ChromatinChromatin StructureChromatin Remodeling	2012	348
Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis Stefanie Vogt, Natalie Jones, Daria Christian, Gastroenterology Tumor BiologyTumoral PathologyMedicineSurgical PathologyPathology	2009	343
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
Lynch Syndrome Caused by Germline <i>PMS2</i> Mutations: Delineating the Cancer Risk Sanne W. ten Broeke, Richard M. Brohet, Carli M.J. Tops, Journal of Clinical Oncology	2014	189
Analysis of MUTYH Genotypes and Colorectal Phenotypes in Patients With MUTYH-Associated Polyposis Maartje Nielsen, Mirjam C. Joerink - van de Beld, Natalie Jones, Gastroenterology GeneticsGenetic EpidemiologyGastroenterologyPathologyMutyh Genotypes	2008	171
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype Judith E. Grolleman, Richarda M. de Voer, Fadwa A. Elsayed, Cancer Cell Tumor BiologyMulti-tumor PhenotypeSomatic VariantTumor HeterogeneityMedicine	2019	166
Germline mutations in <i>APC</i> and <i>MUTYH</i> are responsible for the majority of families with attenuated familial adenomatous polyposis Maartje Nielsen, FM Nagengast, EM Mathus‐Vliegen, Clinical Genetics	2007	158
Somatic <i>APC</i> mosaicism: an underestimated cause of polyposis coli Frederik J. Hes, Maartje Nielsen, Elsa C. Bik, Gut	2007	155
Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of <i>ARID1B</i> Christina Halgren, Mads Bak, Christine Søholm Hansen, Clinical Genetics GeneticsDisabilityMolecular BiologyMolecular GeneticsDisease Gene Identification	2011	139

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