Ingrid P. Vogelaar - Concepedia

Author

Ingrid P. Vogelaar

Radboud University Medical Center ORCID

Also Known As

I. P. Vogelaar, Ingrid P Vogelaar, Ingrid P. Vogelaar, International Gastric Cancer Genetics Group

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Radboud University Medical Center Radboud University Nijmegen Leiden University Medical Center Maastricht University Amsterdam UMC Location University of Amsterdam

About

Ingrid P. Vogelaar is an author at Radboud University Medical Center specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	682
2	Gastroenterology	2	2	107
3	Molecular Biology	2	2	362
4	Molecular Genetics	2	2	87
5	Biology	1	1	42

Ingrid P. Vogelaar

Publications

826

Citations

H-Index

Page 1

	Year	Citations
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
Accuracy of Hereditary Diffuse Gastric Cancer Testing Criteria and Outcomes in Patients With a Germline Mutation in CDH1 Rachel S. van der Post, Ingrid P. Vogelaar, Peggy Manders, Gastroenterology Somatic VariantCancer PathologyMedicineGeneticsGastroenterology	2015	89
Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts Ingrid P. Vogelaar, Joana Figueiredo, Iris A.L.M. van Rooij, Human Molecular Genetics GeneticsGenetic EpidemiologyPathologyGene Cdh1Disease Gene Identification	2012	75
Familial gastric cancer: detection of a hereditary cause helps to understand its etiology Ingrid P. Vogelaar, Rachel S. van der Post, Tanya M. Bisseling, Hereditary Cancer in Clinical Practice	2012	46
The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype Chau‐To Kwok, Ingrid P. Vogelaar, Wendy A. van Zelst-Stams, European Journal of Human Genetics Allelic VariantEuropean Ancestral HaplotypeGenetic DisorderGeneticsMlh1 Epimutation	2013	45
Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing Ingrid P. Vogelaar, Rachel S. van der Post, J. Han van Krieken, European Journal of Human Genetics	2017	43
Role of germline aberrations affecting <i>CTNNA1</i>, <i>MAP3K6</i> and <i>MYD88</i> in gastric cancer susceptibility Robbert D.A. Weren, Rachel S. van der Post, Ingrid P. Vogelaar, Journal of Medical Genetics	2018	43
Fine-tiling array CGH to improve diagnostics for α- and β-thalassemia rearrangements Marion Phylipsen, Attawut Chaibunruang, Ingrid P. Vogelaar, Human Mutation Breakpoint PrimersGeneticsMolecular BiologyGenomicsHigh Throughput Sequencing	2011	42
Thalassemia in Western Australia: 11 novel deletions characterized by Multiplex Ligation-dependent Probe Amplification Marion Phylipsen, John F. Prior, Erna Lim, Blood Cells Molecules and Diseases BiologyWestern AustraliaMedicineGeneticsHematology	2010	42
HNF4A immunohistochemistry facilitates distinction between primary and metastatic breast and gastric carcinoma Rachel S. van der Post, Peter Bult, Ingrid P. Vogelaar, Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin Breast OncologyOncologyGastrointestinal OncologyMedicinePathology	2014	36

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