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。Reevaluation of SNP heritability in complex human traits
Doug Speed et al.
NATURE GENETICS (2017)
Abundant contribution of short tandem repeats to gene expression variation in humans
Melissa Gymrek et al.
NATURE GENETICS (2016)
Mapping DNA methylation across development, genotype and schizophrenia in the human frontal cortex
Andrew E. Jaffe et al.
NATURE NEUROSCIENCE (2016)
Mechanisms and Disease Associations of Haplotype-Dependent Allele-Specific DNA Methylation
Catherine Do et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
Allele-Skewed DNA Modification in the Brain: Relevance to a Schizophrenia GWAS
Sarah A. Gagliano et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
Lu Chen et al.
CELL (2016)
Genetic sources of population epigenomic variation
Aaron Taudt et al.
NATURE REVIEWS GENETICS (2016)
Gap hunting to characterize clustered probe signals in Illumina methylation array data
Shan V. Andrews et al.
EPIGENETICS & CHROMATIN (2016)
Information recovery from low coverage whole-genome bisulfite sequencing
Emanuele Libertini et al.
NATURE COMMUNICATIONS (2016)
Genetic and environmental influences interact with age and sex in shaping the human methylome
Jenny van Dongen et al.
NATURE COMMUNICATIONS (2016)
Mapping of Variable DNA Methylation Across Multiple Cell Types Defines a Dynamic Regulatory Landscape of the Human Genome
Junchen Gu et al.
G3-GENES GENOMES GENETICS (2016)
Which Genetics Variants in DNase-Seq Footprints Are More Likely to Alter Binding?
Gregory A. Moyerbrailean et al.
PLOS GENETICS (2016)
Systematic identification of genetic influences on methylation across the human life course
Tom R. Gaunt et al.
GENOME BIOLOGY (2016)
CTCF-Mediated Human 3D Genome Architecture Reveals Chromatin Topology for Transcription
Zhonghui Tang et al.
CELL (2015)
Retrotransposition creates sloping shores: a graded influence of hypomethylated CpG islands on flanking CpG sites
Fiorella C. Grandi et al.
GENOME RESEARCH (2015)
Integrative analysis of haplotype-resolved epigenomes across human tissues
Danny Leung et al.
NATURE (2015)
Function and information content of DNA methylation
Dirk Schuebeler
NATURE (2015)
Competition between DNA methylation and transcription factors determines binding of NRF1
Silvia Domcke et al.
NATURE (2015)
Transcription factor binding dynamics during human ES cell differentiation
Alexander M. Tsankov et al.
NATURE (2015)
A copy number variation map of the human genome
Mehdi Zarrei et al.
NATURE REVIEWS GENETICS (2015)
FTO Obesity Variant Circuitry and Adipocyte Browning in Humans
Melina Claussnitzer et al.
NEW ENGLAND JOURNAL OF MEDICINE (2015)
Global diversity, population stratification, and selection of human copy-number variation
Peter H. Sudmant et al.
SCIENCE (2015)
High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction
Joseph L. McClay et al.
GENOME BIOLOGY (2015)
Reducing the risk of false discovery enabling identification of biologically significant genome-wide methylation status using the HumanMethylation450 array
Haroon Naeem et al.
BMC GENOMICS (2014)
The landscape of human STR variation
Thomas Willems et al.
GENOME RESEARCH (2014)
Dissection of thousands of cell type-specific enhancers identifies dinucleotide repeat motifs as general enhancer features
J. Omar Yanez-Cuna et al.
GENOME RESEARCH (2014)
An atlas of active enhancers across human cell types and tissues
Robin Andersson et al.
NATURE (2014)
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
Danielle Welter et al.
NUCLEIC ACIDS RESEARCH (2014)
Quantitative Genetics of CTCF Binding Reveal Local Sequence Effects and Different Modes of X-Chromosome Association
Zhihao Ding et al.
PLOS GENETICS (2014)
Using high-density DNA methylation arrays to profile copy number alterations
Andrew Feber et al.
GENOME BIOLOGY (2014)
A beta-mixture quantile normalization method for correcting probe design bias in Illumina Infinium 450 k DNA methylation data
Andrew E. Teschendorff et al.
BIOINFORMATICS (2013)
Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets
T. A. Dayeh et al.
DIABETOLOGIA (2013)
Charting a dynamic DNA methylation landscape of the human genome
Michael J. Ziller et al.
NATURE (2013)
Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis
Yun Liu et al.
NATURE BIOTECHNOLOGY (2013)
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Kyriaki Michailidou et al.
NATURE GENETICS (2013)
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity
Eleanor Wheeler et al.
NATURE GENETICS (2013)
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Jean-Charles Lambert et al.
NATURE GENETICS (2013)
Integrative annotation of chromatin elements from ENCODE data
Michael M. Hoffman et al.
NUCLEIC ACIDS RESEARCH (2013)
Probing DNA shape and methylation state on a genomic scale with DNase I
Allan Lazarovici et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
Extensive Variation in Chromatin States Across Humans
Maya Kasowski et al.
SCIENCE (2013)
Additional annotation enhances potential for biologically-relevant analysis of the Illumina Infinium HumanMethylation450 BeadChip array
E. Magda Price et al.
EPIGENETICS & CHROMATIN (2013)
DNA methylation arrays as surrogate measures of cell mixture distribution
Eugene Andres Houseman et al.
BMC BIOINFORMATICS (2012)
Linking disease associations with regulatory information in the human genome
Marc A. Schaub et al.
GENOME RESEARCH (2012)
FTO genotype is associated with phenotypic variability of body mass index
Jian Yang et al.
NATURE (2012)
An integrated encyclopedia of DNA elements in the human genome
Ian Dunham et al.
NATURE (2012)
The accessible chromatin landscape of the human genome
Robert E. Thurman et al.
NATURE (2012)
Systematic Localization of Common Disease-Associated Variation in Regulatory DNA
Matthew T. Maurano et al.
SCIENCE (2012)
EpiExplorer: live exploration and global analysis of large epigenomic datasets
Konstantin Halachev et al.
GENOME BIOLOGY (2012)
MEME-ChIP: motif analysis of large DNA datasets
Philip Machanick et al.
BIOINFORMATICS (2011)
New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort
Robert K. Nam et al.
CANCER BIOLOGY & THERAPY (2011)
Mapping and analysis of chromatin state dynamics in nine human cell types
Jason Ernst et al.
NATURE (2011)
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Stephen Sawcer et al.
NATURE (2011)
Genome-wide association study identifies three new melanoma susceptibility loci
Jennifer H. Barrett et al.
NATURE GENETICS (2011)
Allelic Skewing of DNA Methylation Is Widespread across the Genome
Leonard C. Schalkwyk et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
LocusZoom: regional visualization of genome-wide association scan results
Randall J. Pruim et al.
BIOINFORMATICS (2010)
BEDTools: a flexible suite of utilities for comparing genomic features
Aaron R. Quinlan et al.
BIOINFORMATICS (2010)
Allele-specific methylation is prevalent and is contributed by CpG-SNPs in the human genome
Robert Shoemaker et al.
GENOME RESEARCH (2010)
Computational analysis of genome-wide DNA methylation during the differentiation of human embryonic stem cells along the endodermal lineage
Lukas Chavez et al.
GENOME RESEARCH (2010)
GREAT improves functional interpretation of cis-regulatory regions
Cory Y. McLean et al.
NATURE BIOTECHNOLOGY (2010)
Integrated Genetic and Epigenetic Analysis Identifies Haplotype-Specific Methylation in the FTO Type 2 Diabetes and Obesity Susceptibility Locus
Christopher G. Bell et al.
PLOS ONE (2010)
Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX, SOX4, and IRX3
Anja Ragvin et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain
J. Raphael Gibbs et al.
PLOS GENETICS (2010)
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
Lucia A. Hindorff et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Active Alu retrotransposons in the human genome
E. Andrew Bennett et al.
GENOME RESEARCH (2008)
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
Albert Tenesa et al.
NATURE GENETICS (2008)
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
Robert M. Plenge et al.
NATURE GENETICS (2007)
Quantifying similarity between motifs
Shobhit Gupta et al.
GENOME BIOLOGY (2007)
Opinion - Inherited epigenetic variation - revisiting soft inheritance
EJ Richards
NATURE REVIEWS GENETICS (2006)