Yvette J.M. de Kok - Concepedia

Concepedia

Author

Yvette J.M. de Kok

Radboud University Nijmegen

Also Known As

Yvette J. M. de Kok, Yvette J.M. de Kok

12

Publications

1.7K

Citations

9

H-Index

29

Concepts

All Affiliations

Radboud University Nijmegen University of London University of Oxford Freie Universität Berlin Radboud University Medical Center

YJ

About

Yvette J.M. de Kok is an author at Radboud University Nijmegen specializing in medicine, molecular genetics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	1.1K
2	Biology	2	2	580
3	Cell Biology	2	2	96
4	Arts	1	1	36
5	Natural Sciences	1	1	110

Yvette J.M. de Kok

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9

Publications

1.7K

Citations

9

H-Index

	Year	Citations
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12) Anneke I. den Hollander, Jacoline B. ten Brink, Yvette J.M. de Kok, Nature Genetics BiologyDevelopmental BiologyGeneticsGenomic MechanismGenetic Mechanism	1999	470
Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene <i>POU3F4</i> Yvette J.M. de Kok, Silvère M. van der Maarel, Maria Bitner‐Glindzicz, Science	1995	446
Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene Anneke I. den Hollander, John R. Heckenlively, L. Ingeborgh van den Born, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderRetinitis PigmentosaGenetics	2001	361
Isolation of Crb1, a mouse homologue of Drosophila crumbs, and analysis of its expression pattern in eye and brain Anneke I. den Hollander, Michela Ghiani, Yvette J.M. de Kok, Mechanisms of Development BiologyMouse HomologueCell LineageMolecular NeuroscienceDevelopmental Biology	2002	110
Further mutations in <i>Brain 4</i> (POU3F4) clarify the phenotype in the X-linked deafness, DFN3 Maria Bitner‐Glindzicz, Peter D. Turnpenny, Pia Höglund, Human Molecular Genetics	1995	84
Tissue- and cell-specific distribution of creatine kinase B: A new and highly specific monoclonal antibody for use in immunohistochemistry Erik A. Sistermans, Yvette J.M. de Kok, Wilma Peters, Cell and Tissue Research Immunocytochemical TechniqueSignal TransductionAutoimmune DiseaseSpecific Monoclonal AntibodyReceptor Tyrosine Kinase	1995	61
Isolation and Mapping of Novel Candidate Genes for Retinal Disorders Using Suppression Subtractive Hybridization Anneke I. den Hollander, Marc A. van Driel, Yvette J.M. de Kok, Genomics Ocular DiseaseRetinaNovel Candidate GenesOphthalmologyGenetic Disorder	1999	50
X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions I Huber, Maria Bitner-Gllndzicz, Yvette J.M. de Kok, Human Molecular Genetics GeneticsX-linked Mixed DeafnessMolecular GeneticsNovel MicrodeletionsDisease Gene Identification	1994	36
The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: Identification of a somatic mosaicism for aPOU3F4 missense mutation Yvette J.M. de Kok, Cor W. R. J. Cremers, Hans‐Hilger Ropers, Human Mutation Pou DomainsDevelopmental BiologyPoint MutationsSomatic VariantGenetic Disorder	1997	35

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