Dineke S. Verbeek - Concepedia

Author

Dineke S. Verbeek

Also Known As

D E P Verbeek, D. S. Verbeek, D. Verbeek, D.S. Verbeek, Dineke S Verbeek, Dineke S. Verbeek, Dineke Verbeek, Verbeek, Dineke S.

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

University of Groningen University Medical Center Groningen Radboud University Nijmegen University Medical Center Utrecht Radboud University Medical Center

About

Dineke S. Verbeek is an author at University of Groningen specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	19	864
2	Social Sciences	7	7	325
3	Natural Sciences	2	2	59
4	Biochemistry	2	2	96
5	Health Sciences	1	1	10

Dineke S. Verbeek

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Mutations in potassium channel <i>kcnd3</i> cause spinocerebellar ataxia type 19 Anna Duarri, Justyna Jezierska, Michiel R. Fokkens, Annals of Neurology	2012	134
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia Esther Nibbeling, Anna Duarri, Corien C. Verschuuren‐Bemelmans, Brain Exome SequencingGeneticsGenetic EpidemiologyNetwork Analysis IdentifiesGene Characterization	2017	121
Prodynorphin Mutations Cause the Neurodegenerative Disorder Spinocerebellar Ataxia Type 23 Georgy Bakalkin, Hiroyuki Watanabe, Justyna Jezierska, The American Journal of Human Genetics Neurodegenerative DiseasesMendelian DisorderNeurological DisorderGeneticsDegenerative Disease	2010	109
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family Bart P.C. van de Warrenburg, Dineke S. Verbeek, Sytse J. Piersma, Neurology	2003	101
Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3 Dineke S. Verbeek Brain Sca23 LocusMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	2004	90
CACNA1B mutation is linked to unique myoclonus-dystonia syndrome J Groen, Arturo Andrade, Katja Ritz, Human Molecular Genetics Cardiac MuscleExome SequencingGeneticsNeurotransmissionIdentified Mutation	2014	87
PKCγ mutations in spinocerebellar ataxia type 14 affect C1 domain accessibility and kinase activity leading to aberrant MAPK signaling Dineke S. Verbeek, Joachim Goedhart, Laurie Bruinsma, Journal of Cell Science Signal TransductionMolecular NeuroscienceBiochemistrySignaling PathwayReceptor Tyrosine Kinase	2008	86
Identification of a novel SCA locus ( SCA19 ) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21 Dineke S. Verbeek, Jurgen Schelhaas, Elly F. Ippel, Human Genetics Neurodegenerative DiseasesNovel Sca LocusChromosome RegionMendelian DisorderGenetic Disorder	2002	83
Protein kinase C gamma mutations in spinocerebellar ataxia 14 increase kinase activity and alter membrane targeting Dineke S. Verbeek Brain	2004	80
First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy Katrien Smets, Anna Duarri, Tine Deconinck, BMC Medical Genetics	2015	67

Page 1