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。Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Design of Prospective Meta-Analyses of Genome-Wide Association Studies From 5 Cohorts
Bruce M. Psaty et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2009)
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
Chiara Sabatti et al.
NATURE GENETICS (2009)
Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure
Christopher Newton-Cheh et al.
NATURE GENETICS (2009)
Whole-genome association study identifies STK39 as a hypertension susceptibility gene
Ying Wang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
Andrew D. Johnson et al.
BIOINFORMATICS (2008)
A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation
Alex V. Postma et al.
CIRCULATION RESEARCH (2008)
Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population
Martin D. Tobin et al.
HYPERTENSION (2008)
New determinant for the Cavβ2 subunit modulation of the Cav1.2 calcium channel
Qi Zong Lao et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
A HapMap harvest of insights into the genetics of common disease
Teri A. Manolio et al.
JOURNAL OF CLINICAL INVESTIGATION (2008)
Global burden of blood-pressure-related disease, 2001
Carlene M. M. Lawes et al.
LANCET (2008)
Genetics of gene expression and its effect on disease
Valur Emilsson et al.
NATURE (2008)
Newly identified genetic risk variants for celiac disease related to the immune response
Karen A. Hunt et al.
NATURE GENETICS (2008)
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Jeffrey C. Barrett et al.
NATURE GENETICS (2008)
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
Mark I. McCarthy et al.
NATURE REVIEWS GENETICS (2008)
Shared and Distinct Genetic Variants in Type 1 Diabetes and Celiac Disease
Deborah J. Smyth et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Mapping the genetic architecture of gene expression in human liver
Eric E. Schadt et al.
PLOS BIOLOGY (2008)
Alcohol intake and blood pressure: A systematic review implementing a Mendelian Randomization approach
Lina Chen et al.
PLOS MEDICINE (2008)
High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project
Norihiro Kato et al.
HUMAN MOLECULAR GENETICS (2008)
A genome-wide association study of global gene expression
Anna L. Dixon et al.
NATURE GENETICS (2007)
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
Miriam F. Moffatt et al.
NATURE (2007)
Imputation-based analysis of association studies: Candidate regions and quantitative traits
Bertrand Servin et al.
PLOS GENETICS (2007)
CONTROL OF THE MEAN NUMBER OF FALSE DISCOVERIES, BONFERRONI AND STABILITY OF MULTIPLE TESTING
Alexander Gordon et al.
ANNALS OF APPLIED STATISTICS (2007)
Trying to be precise about vagueness
Stephen Senn
STATISTICS IN MEDICINE (2007)
Multiple genes for essential-hypertension susceptibility on chromosome 1q
Yen-Pei Christy Chang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-Segment elevation, short QT intervals, and sudden cardiac death
Charles Antzelevitch et al.
CIRCULATION (2007)
Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
Daniel Levy et al.
BMC MEDICAL GENETICS (2007)
Phenotype-genotype correlation in eight Chinese 17α-hydroxylase/17,20 lyase-deficiency patients with five novel mutations of CYP17A1 gene
Jun Yang et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)
Aortic smooth muscle and endothelial plasma membrane Ca2+ pump isoforms are inhibited differently by the extracellular inhibitor caloxin 1b1
J Pande et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2006)
The burden of adult hypertension in the United States 1999 to 2000 - A rising tide
LE Fields et al.
HYPERTENSION (2004)
Two prevalent CYP17 mutations and genotype-phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency
M Costa-Santos et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2004)
Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3
L Koivukoski et al.
HUMAN MOLECULAR GENETICS (2004)
The critical role of c-Src and the Shc/Grb2/ERK2 signaling pathway in angiotensin II-dependent VSMC proliferation
PP Sayeski et al.
EXPERIMENTAL CELL RESEARCH (2003)
Antihypertensive treatments obscure familial contributions to blood pressure variation
JSS Cui et al.
HYPERTENSION (2003)
Cytokine signaling and hematopoietic homeostasis are disrupted in Lnk-deficient mice
L Velazquez et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2002)
A comprehensive review of genetic association studies
JN Hirschhorn et al.
GENETICS IN MEDICINE (2002)
Prediction of deleterious human alleles
S Sunyaev et al.
HUMAN MOLECULAR GENETICS (2001)
Evidence for a gene influencing blood pressure on chromosome 17 - Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham Heart Study
D Levy et al.
HYPERTENSION (2000)
分享论文
