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。Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population
Shintaro Mori et al.
DIABETES (2008)
A second generation human haplotype map of over 3.1 million SNPs
Kelly A. Frazer et al.
NATURE (2007)
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
Valgerdur Steinthorsdottir et al.
NATURE GENETICS (2007)
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
Laura J. Scott et al.
SCIENCE (2007)
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
Richa Saxena et al.
SCIENCE (2007)
Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene
Arthur J. Moss et al.
CIRCULATION (2007)
A genome-wide association study identifies novel risk loci for type 2 diabetes
Robert Sladek et al.
NATURE (2007)
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Eleftheria Zeggini et al.
SCIENCE (2007)
Principal components analysis corrects for stratification in genome-wide association studies
Alkes L. Price et al.
NATURE GENETICS (2006)
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
SFA Grant et al.
NATURE GENETICS (2006)
Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies
AD Skol et al.
NATURE GENETICS (2006)
KCNQ1-dependent transport in renal and gastrointestinal epithelia
V Vallon et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
A note on exact tests of Hardy-Weinberg equilibrium
JE Wigginton et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: Application to HLA in type 1 diabetes
HJ Cordell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190562 genetic variations in the human genome
H Haga et al.
JOURNAL OF HUMAN GENETICS (2002)
Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome
MC Casimiro et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
A high-throughput SNP typing system for genome-wide association studies
Y Ohnishi et al.
JOURNAL OF HUMAN GENETICS (2001)
Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice
MP Lee et al.
JOURNAL OF CLINICAL INVESTIGATION (2000)
分享论文
