Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies is a research paper published in EBioMedicine (2022). On theSindex it has a DataRank of 0. It has been cited 21 times.
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European Science Foundation
Grant: DFG Le1030/11-1/2
European Science Foundation
Grant: INTER/ESF/10/02/CoGIE
National Institutes of Health
Grant: U01NS077367
National Human Genome Research Institute
Grant: 5U01HG009088-02
Powering whole genome sequence-based genetic discovery for common human diseases
National Human Genome Research Institute
Grant: UM1 HG008895
NHGRI NIH HHS
Grant: U01 HG009088
Deutsche Forschungsgemeinschaft
Grant: unidentified
unidentified
Deutsche Forschungsgemeinschaft
Grant: 377782854/FOR 2715
Epileptogenesis of genetic epilepsies
National Institutes of Health
Grant: 5UM1HG008895-04
Center for Common Disease Genetics
National Institutes of Health
Grant: 4U01NS077367-03
5 of 7 Epi4K: Multiplex Families & Pairs Project
Fonds National de la Recherche Luxembourg
Broad Institute
Bundesministerium für Bildung und Forschung
National Institute of Neurological Disorders and Stroke
Université du Luxembourg
Deutsche Forschungsgemeinschaft
Eberhard Karls Universität Tübingen
FWCI
2.97
Citation Percentile
0.9%
Influential Citations
2
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies