AN
Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
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Estimating the causal tissues for complex traits and diseases | Nature Genetics | 2017 | 438 | 821 | |||
Cell-type, allelic and genetic signatures in the human pancreatic beta cell transcriptome | Genome research | 2013 | 662 | 454 | |||
Expression quantitative trait loci: present and future | Philosophical transactions - Royal Society. Biological sciences | 2013 | 455 | 0 | |||
Gene expression changes with age in skin, adipose tissue, blood and brain | GenomeBiology.com | 2013 | 544 | 222 | |||
Mapping cis- and trans-regulatory effects across multiple tissues in twins | Nature genetics | 2012 | 645 | 949 | |||
Patterns of cis regulatory variation in diverse human populations | PLOS genetics | 2012 | 574 | 228 | |||
Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population | PLOS genetics | 2012 | 670 | 336 | |||
Extent, causes, and consequences of small RNA expression variation in human adipose tissue | PLOS genetics | 2012 | 653 | 363 | |||
Sex-biased genetic effects on gene regulation in humans | Genome research | 2012 | 529 | 316 | |||
Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes | Nature genetics | 2011 | 732 | 786 | |||
The architecture of gene regulatory variation across multiple human tissues: the MuTHER study | PLOS genetics | 2011 | 619 | 297 | |||
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes | Diabetes | 2011 | 621 | 1,480 | |||
Epistatic selection between coding and regulatory variation in human evolution and disease | American journal of human genetics | 2011 | 551 | 270 | |||
Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size | PLOS genetics | 2009 | 1,025 | 347 | |||
Using gene expression to investigate the genetic basis of complex disorders | Human molecular genetics | 2008 | 542 | 0 |