TL
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome | American journal of human genetics | 2016 | 628 | 189 | |||
| Sequence variation between 462 human individuals fine-tunes functional sites of RNA processing | Scientific reports | 2016 | 576 | 235 | |||
| Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing | PLOS genetics | 2015 | 723 | 288 | |||
| Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins | Nature genetics | 2015 | 546 | 0 | |||
| Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome | Science | 2015 | 540 | 1 | |||
| Assessing allele-specific expression across multiple tissues from RNA-seq read data | Bioinformatics | 2015 | 547 | 1 | |||
| Human genomics. The human transcriptome across tissues and individuals | Science | 2015 | 417 | 0 | |||
| Gene Age Predicts the Strength of Purifying Selection Acting on Gene Expression Variation in Humans | American journal of human genetics | 2014 | 665 | 1 | |||
| Tandem RNA chimeras contribute to transcriptome diversity in human population and are associated with intronic genetic variants | PloS one | 2014 | 648 | 321 | |||
| Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data | Bioinformatics | 2014 | 518 | 0 | |||
| Allelic mapping bias in RNA-sequencing is not a major confounder in eQTL studies | GenomeBiology.com | 2014 | 544 | 238 | |||
| Genetic interactions affecting human gene expression identified by variance association mapping | eLife | 2014 | 515 | 475 | |||
| High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms | PLOS genetics | 2014 | 544 | 229 | |||
| Passive and active DNA methylation and the interplay with genetic variation in gene regulation | eLife | 2013 | 775 | 523 | |||
| Transcriptome and genome sequencing uncovers functional variation in humans | Nature | 2013 | 720 | 3 | |||
| Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcription | Science | 2013 | 543 | 1 | |||
| Integrative annotation of variants from 1092 humans: application to cancer genomics | Science | 2013 | 477 | 1 | |||
| Insights into hominid evolution from the gorilla genome sequence | Nature | 2012 | 780 | 1,150 | |||
| Sex-biased genetic effects on gene regulation in humans | Genome research | 2012 | 568 | 356 | |||
| Rare and common regulatory variation in population-scale sequenced human genomes | PLOS genetics | 2011 | 674 | 358 | |||
| Epistatic selection between coding and regulatory variation in human evolution and disease | American journal of human genetics | 2011 | 599 | 310 | |||
| Evolutionary history of regulatory variation in human populations | Human molecular genetics | 2010 | 594 | 1 |
