B. Redeker - Concepedia

Author

B. Redeker

Amsterdam UMC Location University of Amsterdam

Also Known As

B Redeker, B. Redeker, Bert E.J.W. Redeker, Bert Redeker

Publications

840

Citations

H-Index

Concepts

All Affiliations

Amsterdam UMC Location University of Amsterdam University of Amsterdam University of Groningen Institute of Human Genetics University Medical Center Groningen

About

B. Redeker is an author at Amsterdam UMC Location University of Amsterdam specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	585
2	Pathology	4	4	489
3	Molecular Genetics	3	3	464
4	Biology	1	1	218
5	Immunology	1	1	63

B. Redeker

Publications

790

Citations

H-Index

Page 1

	Year	Citations
Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype Judy Fantes, B. Redeker, Matthew Breen, Human Molecular Genetics Aniridia-associated Cytogenetic RearrangementsCytogeneticsGeneticsPathologyMolecular Genetics	1995	218
Recurrence and variability of germline <i>EPCAM</i> deletions in Lynch syndrome Roland P. Kuiper, Lisenka E.L.M. Vissers, Ramprasath Venkatachalam, Human Mutation Genome InstabilityGene Deletion DataEpcam GeneMedicineGenetics	2011	150
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. J.M.N. Hoovers, Linda M. Kalikin, Laura A. Johnson, Proceedings of the National Academy of Sciences	1995	106
Mutations in ZBTB20 cause Primrose syndrome Viviana Cordeddu, B. Redeker, Emilia Stellacci, Nature Genetics Genetic DisorderGeneticsInherited Metabolic DiseaseMolecular GeneticsMedicine	2014	96
A specific mutation in <i>TBL1XR1</i> causes Pierpont syndrome Charlotte A. Heinen, Aldo Jongejan, Peter J. Watson, Journal of Medical Genetics	2016	67
Comprehensive Mutation Analysis of<i>PMS2</i>in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome Heleen M. van der Klift, Arjen R. Mensenkamp, Mark Drost, Human Mutation Probands SuspectedSomatic VariantMendelian DisorderGenetic DisorderMedicine	2016	63
Comparative genomic hybridization analysis of Wilms tumors Marja Steenman, B. Redeker, Maurice de Meulemeester, Cytogenetic and Genome Research Somatic VariantHybridisationCytogeneticsHybridizationGenetics	1997	58
Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma Frank Speleman, Eva van den Berg, Catharina Dhooge, Genes Chromosomes and Cancer	1998	20
Characterization of a de novo duplication of 11p14→p13, using fluorescent in situ hybridization and Southern hybridization Frank Speleman, M. Mannens, B. Redeker, Cytogenetic and Genome Research	1991	12

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