MG
Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
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Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing | PLOS genetics | 2015 | 629 | 225 | |||
Domains of genome-wide gene expression dysregulation in Down's syndrome | Nature | 2014 | 622 | 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 | 581 | 0 | |||
Passive and active DNA methylation and the interplay with genetic variation in gene regulation | eLife | 2013 | 644 | 433 | |||
Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications | Stem cell research | 2013 | 577 | 0 | |||
Tandem repeat sequence variation as causative cis-eQTLs for protein-coding gene expression variation: the case of CSTB | Human mutation | 2012 | 536 | 0 | |||
Extensive natural variation for cellular hydrogen peroxide release is genetically controlled | PloS one | 2012 | 684 | 376 | |||
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 | 617 | 0 | |||
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts | Genome research | 2011 | 647 | 327 | |||
Genetic structure of Europeans: a view from the North-East | PloS one | 2009 | 650 | 497 | |||
Common regulatory variation impacts gene expression in a cell type-dependent manner | Science | 2009 | 638 | 2 | |||
Mapping of small RNAs in the human ENCODE regions | American journal of human genetics | 2008 | 563 | 0 | |||
Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events | American journal of medical genetics. Part A | 2008 | 640 | 4 | |||
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance | American journal of human genetics | 2007 | 638 | 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 | 616 | 0 | |||
Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes | Human molecular genetics | 2005 | 552 | 0 |