Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study is a research paper published in Epilepsia (2022). On theSindex it has a DataRank of 0. It has been cited 13 times.
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National Institutes of Health
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National Institutes of Health
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National Institutes of Health
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National Institutes of Health
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National Institutes of Health
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National Institutes of Health
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National Institutes of Health
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National Institute of Neurological Disorders and Stroke
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National Institute of Neurological Disorders and Stroke
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National Institute of Neurological Disorders and Stroke
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National Institute of Neurological Disorders and Stroke
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National Institute of Neurological Disorders and Stroke
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Deutscher Akademischer Austauschdienst
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Deutsche Forschungsgemeinschaft
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Deutsche Forschungsgemeinschaft
Grant: Le1030/11‐1/2
Deutsche Forschungsgemeinschaft
Grant: Nu50/8‐1
Deutsche Forschungsgemeinschaft
Grant: Sa434/5‐1
Deutsche Forschungsgemeinschaft
Grant: He5415/3‐1
Epilepsy Research UK
Grant: P1104
Fonds National de la Recherche Luxembourg
Grant: FNR11264123
Fonds National de la Recherche Luxembourg
Grant: INTER/DFG/17/11583046
Fonds National de la Recherche Luxembourg
Grant: INTER/ESF/10/02/CoGIE
Academy of Finland
Grant: 141549
Complex genetics of idiopathic epilepsies
Ministerio de Ciencia y Tecnología
Grant: EUI‐EURC‐2011‐4325
Ministerio de Ciencia y Tecnología
Grant: SAF2010‐18586
Türkiye Bilimsel ve Teknolojik Araştirma Kurumu
Grant: 110S518
Nadir Epilepsi Sendromları Genetiği: GEFS+ Fenotipi Görülen Büyük Bir Ailede Yeni Yatkınlık Bölgeleri İçin Genom Bazında Bağlantı Taraması
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Medical Research Council
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NHGRI NIH HHS
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Grant: U24 AG021886
NINDS NIH HHS
Grant: K02 NS112600
NIA NIH HHS
Grant: U01 AG032984
NHGRI NIH HHS
Grant: U54 HG003079
NINDS NIH HHS
Grant: U24 NS120854
National Institutes of Health
Grant: 7R01MH099216-03
Identifying de novo mutations causing OCD in trios by whole exome sequencing
National Institutes of Health
Grant: 5U01NS077274-03
1 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes - Administrative Core
National Institutes of Health
Grant: 5U01NS077276-04
2 of 7 EPI4K - Phenotyping Clinical Informatics Core
National Institutes of Health
Grant: 5P01AG007232-09
POPULATION BASED STUDY OF THE COURSE AND OUTCOME OF ALZHEIMERS DISEASE
National Institutes of Health
Grant: 1R56AI098588-01A1
Determinants of protection in HIV-exposed seronegative men
Deutsche Forschungsgemeinschaft
Grant: 377782854/FOR 2715
Epileptogenesis of genetic epilepsies
National Institutes of Health
Grant: 1U01NS053998-01A1
The Epilepsy Phenome/ Genome Project (EPGP)
National Institutes of Health
Grant: 5R01AG037212-04
Epidemiology of Biomarkers of Risk and Progression in LOAD
Deutsche Forschungsgemeinschaft
Grant: unidentified
unidentified
National Institutes of Health
Grant: 5TL1TR001875-02
NRSA Training Core
Seventh Framework Programme
Genome Canada
European Science Foundation
Génome Québec
Sixth Framework Programme
FWCI
1.83
Citation Percentile
0.8%
Citation Trend
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Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study