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。Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population
Ken Suzuki et al.
NATURE GENETICS (2019)
Genome-wide association study of type 2 diabetes in Africa
Ji Chen et al.
DIABETOLOGIA (2019)
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Jason Flannick et al.
NATURE (2019)
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies
Huaying Fang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2019)
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
Yun J. Sung et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
Economic Costs of Diabetes in the US in 2017
Wenya Yang et al.
DIABETES CARE (2018)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Anubha Mahajan et al.
NATURE GENETICS (2018)
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types
Hilary K. Finucane et al.
NATURE GENETICS (2018)
An atlas of genetic associations in UK Biobank
Oriol Canela-Xandri et al.
NATURE GENETICS (2018)
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Anubha Mahajan et al.
NATURE GENETICS (2018)
Genetics of blood lipids among ∼300,000 multi-ethnic participants of the Million Veteran Program
Derek Klarin et al.
NATURE GENETICS (2018)
Genomic Risk Stratification Predicts All-Cause Mortality After Cardiac Catheterization
Michael G. Levin et al.
CIRCULATION-GENOMIC AND PRECISION MEDICINE (2018)
Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity
Danish Saleheen et al.
NATURE (2017)
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
Eleanor Wheeler et al.
PLOS MEDICINE (2017)
Interrogating islets in health and disease with single-cell technologies
Andrea C. Carrano et al.
MOLECULAR METABOLISM (2017)
Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series
Martina Buse et al.
ITALIAN JOURNAL OF PEDIATRICS (2017)
Genetic-Variation-Driven Gene-Expression Changes Highlight Genes with Important Functions for Kidney Disease
Yi-An Ko et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
The SIDER database of drugs and side effects
Michael Kuhn et al.
NUCLEIC ACIDS RESEARCH (2016)
Million Veteran Program: A mega-biobank to study genetic influences on health and disease
John Michael Gaziano et al.
JOURNAL OF CLINICAL EPIDEMIOLOGY (2016)
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
Georg B. Ehret et al.
NATURE GENETICS (2016)
Next-generation genotype imputation service and methods
Sayantan Das et al.
NATURE GENETICS (2016)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Cristian Pattaro et al.
NATURE COMMUNICATIONS (2016)
Integration of ATAC-seq and RNA-seq identifies human alpha cell and beta cell signature genes
Amanda M. Ackermann et al.
MOLECULAR METABOLISM (2016)
GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach
Ellen M. Schmidt et al.
BIOINFORMATICS (2015)
XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome
Feng Gao et al.
JOURNAL OF HEREDITY (2015)
Integrative analysis of 111 reference human epigenomes
Anshul Kundaje et al.
NATURE (2015)
A global reference for human genetic variation
David M. Altshuler et al.
NATURE (2015)
PDE3A mutations cause autosomal dominant hypertension with brachydactyly
Philipp G. Maass et al.
NATURE GENETICS (2015)
Partitioning heritability by functional annotation using genome-wide association summary statistics
Hilary K. Finucane et al.
NATURE GENETICS (2015)
An atlas of genetic correlations across human diseases and traits
Brendan Bulik-Sullivan et al.
NATURE GENETICS (2015)
Gene expression analysis identifies global gene dosage sensitivity in cancer
Rudolf S. N. Fehrmann et al.
NATURE GENETICS (2015)
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
Brendan K. Bulik-Sullivan et al.
NATURE GENETICS (2015)
Second-generation PLINK: rising to the challenge of larger and richer datasets
Christopher C. Chang et al.
GIGASCIENCE (2015)
Genetic Association Analysis under Complex Survey Sampling: The Hispanic Community Health Study/Study of Latinos
Dan-Yu Lin et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
An atlas of active enhancers across human cell types and tissues
Robin Andersson et al.
NATURE (2014)
Meta-Analysis of Genome-Wide Association Studies in African Americans Provides Insights into the Genetic Architecture of Type 2 Diabetes
Maggie C. Y. Ng et al.
PLOS GENETICS (2014)
CREB mediates the insulinotropic and anti-apoptotic effects of GLP-1 signaling in adult mouse β-cells
Soona Shin et al.
MOLECULAR METABOLISM (2014)
Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataract
Donna S. Mackay et al.
HUMAN GENOMICS (2014)
TCF7L2 Variation and Proliferative Diabetic Retinopathy
Jing Luo et al.
DIABETES (2013)
An integrated encyclopedia of DNA elements in the human genome
Ian Dunham et al.
NATURE (2012)
A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
Nicholette D. Palmer et al.
PLOS ONE (2012)
Toxic optic neuropathy
Pradeep Sharma et al.
INDIAN JOURNAL OF OPHTHALMOLOGY (2011)
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies
Muredach P. Reilly et al.
LANCET (2011)
Behavior of QQ-Plots and Genomic Control in Studies of Gene-Environment Interaction
Arend Voorman et al.
PLOS ONE (2011)
Alterations in cyclic nucleotide phosphodiesterase activities in omental and subcutaneous adipose tissues in human obesity
B. Omar et al.
NUTRITION & DIABETES (2011)
Robust relationship inference in genome-wide association studies
Ani Manichaikul et al.
BIOINFORMATICS (2010)
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations
Joshua C. Denny et al.
BIOINFORMATICS (2010)
METAL: fast and efficient meta-analysis of genomewide association scans
Cristen J. Willer et al.
BIOINFORMATICS (2010)
Integrating common and rare genetic variation in diverse human populations
David M. Altshuler et al.
NATURE (2010)
Effect of valproic acid on body weight, food intake, physical activity and hormones: results of a randomized controlled trial
C. K. Martin et al.
JOURNAL OF PSYCHOPHARMACOLOGY (2009)
A transcriptome database for astrocytes, neurons, and oligodendrocytes: A new resource for understanding brain development and function
John D. Cahoy et al.
JOURNAL OF NEUROSCIENCE (2008)
The Immunological Genome Project: networks of gene expression in immune cells
Tracy S. P. Heng et al.
NATURE IMMUNOLOGY (2008)
The vesicular amine transporter family (SLC18):: amine/proton antiporters required for vesicular accumulation and regulated exocytotic secretion of monoamines and acetylcholine
LE Eiden et al.
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2004)
Validating administrative data in stroke research
DL Tirschwell et al.
STROKE (2002)