Jacoline B. ten Brink

Author

Netherlands Institute for Neuroscience ORCID

Also Known As

J B ten Brink, J. B. t. Brink, J. B. ten Brink, J.B. Ten Brink, Jacoline B ten Brink, Jacoline B. Ten Brink, Jacoline B. ten Brink, Jacoline ten Brink, Sovann Kaing, ten Brink, J. B.

Publications

Citations

H-Index

Concepts

All Affiliations

Netherlands Institute for Neuroscience Amsterdam UMC Location University of Amsterdam University of Amsterdam Amsterdam University Medical Centers Erasmus MC

About

Jacoline B. ten Brink is an author at Netherlands Institute for Neuroscience specializing in medicine, ophthalmology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	14	1.5K
2	Cell Biology	4	4	100
3	Biology	3	3	509
4	Natural Sciences	2	2	625
5	Cellular Physiology	2	2	46

Jacoline B. ten Brink

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
Mutations in ABCC6 cause pseudoxanthoma elasticum Arthur A. Bergen, Astrid S. Plomp, Ellen J. Schuurman, Nature Genetics Somatic VariantNatural SciencesGeneticsProtein X-ray CrystallographyDna Replication	2000	597
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
Frequent Mutation in the ABCC6 Gene (R1141X) Is Associated With a Strong Increase in the Prevalence of Coronary Artery Disease Mieke D. Trip, Yvo M. Smulders, Jurgen Wegman, Circulation	2002	140
Complement Component C3 and Risk of Age-Related Macular Degeneration Dominiek D. G. Despriet, Cornelia M. van Duijn, Ben A. Oostra, Ophthalmology Complement Component C3Complement SystemOcular DiseaseOphthalmologyAge-related Diseases	2009	95
Genotypic and Phenotypic Characteristics of CRB1 -Associated Retinal Dystrophies Mays Talib, Mary J. van Schooneveld, Maria M. van Genderen, Ophthalmology Ocular DiseaseRetinaPhotoreceptor CellOphthalmologyGenetics	2017	93
CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES Mays Talib, Mary J. van Schooneveld, Alberta A. H. J. Thiadens, Retina	2018	86
A New Strategy to Identify and Annotate Human RPE-Specific Gene Expression Judith C. Booij, Jacoline B. ten Brink, Sigrid Swagemakers, PLoS ONE	2010	81
X-Linked Retinoschisis Leo C. Hahn, Mary J. van Schooneveld, Nieneke L. Wesseling, Ophthalmology	2021	73
Comparison of human retinal pigment epithelium gene expression in macula and periphery highlights potential topographic differences in Bruch's membrane. Simone S van Soest, Gerard M.J. de Wit, Anke H. W. Essing, PubMed	2007	70
A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome Jacqueline J.M. Assink, Nel Tijmes, Jacoline B. ten Brink, The American Journal of Human Genetics OphthalmologyCytogeneticsX ChromosomeGeneticsGenetic Disorder	1997	67

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