Published in Genome Med on December 22, 2009
Pharmacogenomics of the RNA world: structural RNA polymorphisms in drug therapy. Clin Pharmacol Ther (2011) 1.15
Missing heritability of common diseases and treatments outside the protein-coding exome. Hum Genet (2014) 1.00
Genetically complex epilepsies, copy number variants and syndrome constellations. Genome Med (2010) 0.98
Evidence of allelic imbalance in the schizophrenia susceptibility gene ZNF804A in human dorsolateral prefrontal cortex. Schizophr Res (2013) 0.85
Genome-wide search for exonic variants affecting translational efficiency. Nat Commun (2013) 0.82
Analyzing allele specific RNA expression using mixture models. BMC Genomics (2015) 0.75
Unravelling genes and pathways implicated in working memory of schizophrenia in Han Chinese. Int J Mol Sci (2015) 0.75
Finding the missing heritability of complex diseases. Nature (2009) 67.95
Alternative isoform regulation in human tissue transcriptomes. Nature (2008) 52.76
Population genomics of human gene expression. Nat Genet (2007) 24.49
Histone modifications at human enhancers reflect global cell-type-specific gene expression. Nature (2009) 24.41
Gene regulation for higher cells: a theory. Science (1969) 14.19
Common regulatory variation impacts gene expression in a cell type-dependent manner. Science (2009) 11.28
Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes. Nat Genet (2007) 11.09
The evolutionary significance of cis-regulatory mutations. Nat Rev Genet (2007) 9.35
Common genetic variants account for differences in gene expression among ethnic groups. Nat Genet (2007) 9.04
Widespread monoallelic expression on human autosomes. Science (2007) 7.12
The antisense transcriptomes of human cells. Science (2008) 6.29
Global patterns of cis variation in human cells revealed by high-density allelic expression analysis. Nat Genet (2009) 4.72
Digital RNA allelotyping reveals tissue-specific and allele-specific gene expression in human. Nat Methods (2009) 4.38
Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression. PLoS Genet (2008) 3.92
Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing. Hum Mol Genet (2010) 3.50
Recent acceleration of human adaptive evolution. Proc Natl Acad Sci U S A (2007) 3.13
Polymorphisms in human dopamine D2 receptor gene affect gene expression, splicing, and neuronal activity during working memory. Proc Natl Acad Sci U S A (2007) 2.62
Implications of chimaeric non-co-linear transcripts. Nature (2009) 2.52
Extreme clonality in lymphoblastoid cell lines with implications for allele specific expression analyses. PLoS One (2008) 2.28
Regulatory polymorphism in vitamin K epoxide reductase complex subunit 1 (VKORC1) affects gene expression and warfarin dose requirement. Blood (2008) 2.18
Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues. Pharmacogenet Genomics (2008) 1.51
Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons. Mol Psychiatry (2006) 1.27
Polymorphisms affecting gene regulation and mRNA processing: broad implications for pharmacogenetics. Pharmacol Ther (2004) 1.26
Validating discovered Cis-acting regulatory genetic variants: application of an allele specific expression approach to HapMap populations. PLoS One (2008) 1.20
Correlation between nucleotide composition and folding energy of coding sequences with special attention to wobble bases. Theor Biol Med Model (2008) 0.88