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。Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
Costin Leu et al.
EPILEPSIA (2012)
Exome Sequencing of Ion Channel Genes Reveals Complex Profiles Confounding Personal Risk Assessment in Epilepsy
Tara Klassen et al.
CELL (2011)
Blinders, phenotype, and fashionable genetic analysis: A critical examination of the current state of epilepsy genetic studies
David A. Greenberg et al.
EPILEPSIA (2011)
Finding disease genes: a fast and flexible approach for analyzing high-throughput data
William C. L. Stewart et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
Computer Simulation Is an Undervalued Tool for Genetic Analysis: A Historical View and Presentation of SHIMSHON - A Web-Based Genetic Simulation Package
David A. Greenberg
HUMAN HEREDITY (2011)
KELVIN: A Software Package for Rigorous Measurement of Statistical Evidence in Human Genetics
Veronica J. Vieland et al.
HUMAN HEREDITY (2011)
Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009
Anne T. Berg et al.
EPILEPSIA (2010)
Pleiotropic effects of the 11p13 locus on developmental verbal dyspraxia and EEG centrotemporal sharp waves
D. K. Pal et al.
GENES BRAIN AND BEHAVIOR (2010)
Multiple Subsampling of Dense SNP Data Localizes Disease Genes with Increased Precision
William C. L. Stewart et al.
HUMAN HEREDITY (2010)
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)
Lisa J. Strug et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2009)
A multilocus model of the genetic architecture of Autoimmune Thyroid Disorder, with clinical implications
Veronica J. Vieland et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Multipoint Lods Provide Reliable Linkage Evidence Despite Unknown Limiting Distribution: Type I Error Probabilities Decrease With Sample Size for Multipoint Lods and Mods
Susan E. Hodge et al.
GENETIC EPIDEMIOLOGY (2008)
Dissecting genetic heterogeneity in autoimmune thyroid diseases by subset analysis
Yaron Tomer et al.
JOURNAL OF AUTOIMMUNITY (2007)
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy
Gianpiero L. Cavalleri et al.
EPILEPSIA (2007)
Association between D18S474 locus on chromosome 18q12 and idiopathic generalized epilepsy
Paola Lucarelli et al.
BRAIN & DEVELOPMENT (2007)
Possible interaction between HLA-DRβ1 and thyroglobulin variants in Graves' disease
Susan E. Hodge et al.
THYROID (2006)
Familial clustering of seizure types within the idiopathic generalized epilepsies
MR Winawer et al.
NEUROLOGY (2005)
Malic enzyme 2 may underlie susceptibility to adolescent-onset idiopathic generalized epilepsy
DA Greenberg et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy
DK Pal et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Identification of a variant associated with adult-type hypolactasia
NS Enattah et al.
NATURE GENETICS (2002)
HLODs, trait models, and ascertainment: Implications of admixture for parameter estimation and linkage detection
VJ Vieland et al.
HUMAN HEREDITY (2002)
Evaluating genetic heterogeneity in complex disorders
DK Pal et al.
HUMAN HEREDITY (2002)
Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure type
M Durner et al.
ANNALS OF NEUROLOGY (2001)
Reproducibility and complications in gene searches: Linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy
DA Greenberg et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
分享论文
