MG
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Title Published in Access level OA Policy Year Views Downloads
Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicingPLOS genetics
accessLevelPublic
2015 723 286
Domains of genome-wide gene expression dysregulation in Down's syndromeNature
accessLevelRestricted
2014 706 2
Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literatureAmerican journal of medical genetics. Part B, Neuropsychiatric genetics
accessLevelRestricted
2013 637 0
Passive and active DNA methylation and the interplay with genetic variation in gene regulationeLife
accessLevelPublic
2013 775 523
Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modificationsStem cell research
accessLevelRestricted
2013 657 0
Tandem repeat sequence variation as causative cis-eQTLs for protein-coding gene expression variation: the case of CSTBHuman mutation
accessLevelRestricted
2012 594 0
Extensive natural variation for cellular hydrogen peroxide release is genetically controlledPloS one
accessLevelPublic
2012 758 452
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleJournal of medical genetics
accessLevelRestricted
2012 690 0
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblastsGenome research
accessLevelPublic
2011 733 350
Genetic structure of Europeans: a view from the North-EastPloS one
accessLevelPublic
2009 778 1,784
Common regulatory variation impacts gene expression in a cell type-dependent mannerScience
accessLevelRestricted
2009 683 2
Mapping of small RNAs in the human ENCODE regionsAmerican journal of human genetics
accessLevelRestricted
2008 620 0
Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of eventsAmerican journal of medical genetics. Part A
accessLevelRestricted
2008 727 4
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalanceAmerican journal of human genetics
accessLevelRestricted
2007 709 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 phenotypesAmerican journal of human genetics
accessLevelRestricted
2007 713 0
Gene expression variation and expression quantitative trait mapping of human chromosome 21 genesHuman molecular genetics
accessLevelRestricted
2005 606 0
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