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Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
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DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome | American journal of human genetics | 2016 | 512 | 159 | |||
Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing | PLOS genetics | 2015 | 647 | 232 | |||
Passive and active DNA methylation and the interplay with genetic variation in gene regulation | eLife | 2013 | 697 | 446 | |||
Transcriptome and genome sequencing uncovers functional variation in humans | Nature | 2013 | 679 | 3 | |||
Mapping cis- and trans-regulatory effects across multiple tissues in twins | Nature genetics | 2012 | 645 | 949 | |||
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis | Nature genetics | 2012 | 643 | 1,234 | |||
A systematic survey of loss-of-function variants in human protein-coding genes | Science | 2012 | 1,044 | 828 | |||
Genotype-based test in mapping cis-regulatory variants from allele-specific expression data | PloS one | 2012 | 618 | 306 | |||
Patterns of cis regulatory variation in diverse human populations | PLOS genetics | 2012 | 574 | 228 | |||
Sex-biased genetic effects on gene regulation in humans | Genome research | 2012 | 530 | 316 | |||
Rare and common regulatory variation in population-scale sequenced human genomes | PLOS genetics | 2011 | 634 | 279 | |||
Genome-wide association study identifies a common variant associated with risk of endometrial cancer | Nature genetics | 2011 | 721 | 969 | |||
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts | Genome research | 2011 | 670 | 330 | |||
From expression QTLs to personalized transcriptomics | Nature reviews. Genetics | 2011 | 539 | 1 | |||
The architecture of gene regulatory variation across multiple human tissues: the MuTHER study | PLOS genetics | 2011 | 620 | 297 | |||
Epistatic selection between coding and regulatory variation in human evolution and disease | American journal of human genetics | 2011 | 552 | 270 | |||
Integrating common and rare genetic variation in diverse human populations | Nature | 2010 | 686 | 391 | |||
Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies | Bioinformatics | 2010 | 652 | 0 | |||
Common regulatory variation impacts gene expression in a cell type-dependent manner | Science | 2009 | 652 | 2 |