标题
The Epilepsy Phenome/Genome Project
作者
关键词
-
出版物
Clinical Trials
Volume 10, Issue 4, Pages 568-586
出版商
SAGE Publications
发表日期
2013-07-02
DOI
10.1177/1740774513484392
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes
- (2010) Erin L. Heinzen et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Copy number variants--an unexpected risk factor for the idiopathic generalized epilepsies
- (2010) I. E. Scheffer et al. BRAIN
- Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
- (2010) Dalia Kasperavičiūtė et al. BRAIN
- Genetic testing in the epilepsies-Report of the ILAE Genetics Commission
- (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
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started