| Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing | PLOS genetics |  | | 2015 | 737 | 348 |
|
| Domains of genome-wide gene expression dysregulation in Down's syndrome | Nature |  | | 2014 | 718 | 2 |
|
| Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature | American journal of medical genetics. Part B, Neuropsychiatric genetics |  | | 2013 | 651 | 0 |
|
| Passive and active DNA methylation and the interplay with genetic variation in gene regulation | eLife |  | | 2013 | 786 | 553 |
|
| Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications | Stem cell research |  | | 2013 | 674 | 0 |
|
| Tandem repeat sequence variation as causative cis-eQTLs for protein-coding gene expression variation: the case of CSTB | Human mutation |  | | 2012 | 604 | 0 |
|
| Extensive natural variation for cellular hydrogen peroxide release is genetically controlled | PloS one |  | | 2012 | 769 | 552 |
|
| Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele | Journal of medical genetics |  | | 2012 | 700 | 0 |
|
| Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts | Genome research |  | | 2011 | 743 | 369 |
|
| Genetic structure of Europeans: a view from the North-East | PloS one |  | | 2009 | 789 | 3,357 |
|
| Common regulatory variation impacts gene expression in a cell type-dependent manner | Science |  | | 2009 | 695 | 2 |
|
| Mapping of small RNAs in the human ENCODE regions | American journal of human genetics |  | | 2008 | 632 | 0 |
|
| Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events | American journal of medical genetics. Part A |  | | 2008 | 743 | 4 |
|
| Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance | American journal of human genetics |  | | 2007 | 726 | 0 |
|
| Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypes | American journal of human genetics |  | | 2007 | 726 | 0 |
|
| Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes | Human molecular genetics |  | | 2005 | 617 | 0 |
|