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Title
The Epilepsy Phenome/Genome Project
Authors
Keywords
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Journal
Clinical Trials
Volume 10, Issue 4, Pages 568-586
Publisher
SAGE Publications
Online
2013-07-02
DOI
10.1177/1740774513484392
References
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Related references
Note: Only part of the references are listed.- Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes
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- (2010) Ruth Ottman et al. EPILEPSIA
- Estimating risk for developing epilepsy: A population-based study in Rochester, Minnesota
- (2010) D. C. Hesdorffer et al. NEUROLOGY
- Towards a complete resolution of the genetic architecture of disease
- (2010) Andrew B. Singleton et al. TRENDS IN GENETICS
- Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies
- (2010) Heather C. Mefford et al. PLoS Genetics
- Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
- (2009) C. G. F. de Kovel et al. BRAIN
- Novel FOXG1 mutations associated with the congenital variant of Rett syndrome
- (2009) M. A. Mencarelli et al. JOURNAL OF MEDICAL GENETICS
- Finding the missing heritability of complex diseases
- (2009) Teri A. Manolio et al. NATURE
- 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
- (2009) Ingo Helbig et al. NATURE GENETICS
- Common Genetic Variation and Human Traits
- (2009) David B. Goldstein NEW ENGLAND JOURNAL OF MEDICINE
- The three stages of epilepsy in patients withCDKL5mutations
- (2008) Nadia Bahi-Buisson et al. EPILEPSIA
- Navigating the channels and beyond: unravelling the genetics of the epilepsies
- (2008) Ingo Helbig et al. LANCET NEUROLOGY
- De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy
- (2008) Hirotomo Saitsu et al. NATURE GENETICS
- Mechanisms of human inherited epilepsies
- (2008) Christopher A. Reid et al. PROGRESS IN NEUROBIOLOGY
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