A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations is a research paper published in PLOS Genetics (2017). On theSindex it has a DataRank of 0.550. It has been cited 38 times.
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Base Score Contribution
0.550
From this paper's citation signal
Citation Network Contribution
0
Citation network not refreshed for this result
This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
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Grant: U01 NS077274
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Grant: UM1 AI100645
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Grant: U01 HG007672
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Grant: U01 NS053998
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Grant: U01 NS077276
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Grant: P01 HD080642
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Grant: UL1 TR000040
National Institutes of Health
Grant: 5R01HD048805-03
Beta2 adrenoceptor genotype and preterm labor
National Institutes of Health
Grant: 5K23NS069784-04
Genetics of Familial Epilepsy Syndromes
National Institutes of Health
Grant: 5K01MH098126-02
Genetics of Normal Human Variation: Implications for Disease
National Institutes of Health
Grant: 3U01NS077303-04S1
3 of 7 Epi4K: Sequencing, Biostatistics & Bioinformatics Core
National Institutes of Health
Grant: 2UL1TR001873-06
Clinical and Translational Science Award
National Institutes of Health
Grant: 5UM1AI100645-06
Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery
National Institutes of Health
Grant: 7R01MH099216-03
Identifying de novo mutations causing OCD in trios by whole exome sequencing
National Institutes of Health
Grant: 1RC2MH089915-01
Whole-genome sequencing for rare highly penetrant gene variants in schizophrenia
National Institutes of Health
Grant: 5U19AI067854-04
Structural Biology Core
National Institutes of Health
Grant: 5R01AG037212-04
Epidemiology of Biomarkers of Risk and Progression in LOAD
National Institutes of Health
Grant: 2R01DK080099-10
Genetics of human renal hypodysplasia
National Institutes of Health
Grant: 1U01NS053998-01A1
The Epilepsy Phenome/ Genome Project (EPGP)
National Institutes of Health
Grant: 5R01MH097971-04
1 of 2: Identification of Rare Variants of OCD
National Institutes of Health
Grant: 5U54NS078059-10
The North American Mitochondrial Disease Consortium (NAMDC)
National Institutes of Health
Grant: 5UM1HG006504-07
Yale Center for Mendelian Genomics
National Institutes of Health
Grant: 5UM1AI100645-03
Nonhuman primate scientific research support component
National Institutes of Health
Grant: 3U54NS078059-08S1
Mining the North American Mitochondrial Disease Consortium (NAMDC) Clinical Registry Data to Identify Phenotypes and Outcome Measures for Mitochondrial Diseases
European Commission
Grant: 602531
Development and Epilepsy - Strategies for Innovative Research to improve diagnosis, prevention and treatment in children with difficult to treat Epilepsy
National Institutes of Health
Grant: 3UL1TR001873-07S1
Clinical and Translational Science Award
National Institutes of Health
Grant: 1R56AI098588-01A1
Determinants of protection in HIV-exposed seronegative men
National Institutes of Health
Grant: 3RF1AG054023-01S1
Genetic Epidemiology of Cerebrovascular Factors in Alzheimer's Disease
National Institutes of Health
Grant: 5U01HG007672-04
An integrated and diverse genomic medicine program for undiagnosed diseases
National Institutes of Health
Grant: 1P01HD080642-01
Project #2 - Approaches to treating mtDNA-based mitochondrial disease.
National Institutes of Health
Grant: 1P30AG028377-01
DATA MANAGEMENT AND STATISTICS CORE
National Institutes of Health
Grant: 8UL1TR000040-07
Clinical and Translational Science Award
FWCI
4.22
Citation Percentile
0.9%
Citation Trend
Fields of Study
MeSH Terms
Keywords
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations