Published in Physiol Genomics on December 06, 2011
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Identification of Map4k4 as a novel suppressor of skeletal muscle differentiation. Mol Cell Biol (2012) 0.96
Identification of genes differentially expressed in myogenin knock-down bovine muscle satellite cells during differentiation through RNA sequencing analysis. PLoS One (2014) 0.96
Correlated mRNAs and miRNAs from co-expression and regulatory networks affect porcine muscle and finally meat properties. BMC Genomics (2013) 0.87
Temporal analysis of reciprocal miRNA-mRNA expression patterns predicts regulatory networks during differentiation in human skeletal muscle cells. Physiol Genomics (2014) 0.80
Network Analysis for the Identification of Differentially Expressed Hub Genes Using Myogenin Knock-down Muscle Satellite Cells. PLoS One (2015) 0.77
Identification of common regulators of genes in co-expression networks affecting muscle and meat properties. PLoS One (2015) 0.77
Deubiquitinating Enzyme USP20 Regulates Extracellular Signal-Regulated Kinase 3 Stability and Biological Activity. Mol Cell Biol (2017) 0.75
Linkages between changes in the 3D organization of the genome and transcription during myotube differentiation in vitro. Skelet Muscle (2017) 0.75
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A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature (2007) 35.08
CellProfiler: image analysis software for identifying and quantifying cell phenotypes. Genome Biol (2006) 32.51
International network of cancer genome projects. Nature (2010) 20.35
Genome-wide detection and characterization of positive selection in human populations. Nature (2007) 17.27
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet (2010) 16.96
A predominantly clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality. N Engl J Med (2005) 16.59
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Ablation in mice of the mTORC components raptor, rictor, or mLST8 reveals that mTORC2 is required for signaling to Akt-FOXO and PKCalpha, but not S6K1. Dev Cell (2006) 11.48
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nat Genet (2007) 9.88
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes. Nature (2012) 8.31
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nat Genet (2008) 6.97
Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proc Natl Acad Sci U S A (2003) 6.87
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nat Genet (2008) 6.75
Genome-wide analysis of transcript isoform variation in humans. Nat Genet (2008) 6.70
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Nat Genet (2009) 6.39
Exploration of essential gene functions via titratable promoter alleles. Cell (2004) 5.21
Scoring diverse cellular morphologies in image-based screens with iterative feedback and machine learning. Proc Natl Acad Sci U S A (2009) 5.15
A survey of genetic and epigenetic variation affecting human gene expression. Physiol Genomics (2004) 4.99
Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray. Epigenetics (2013) 4.61
Control genes and variability: absence of ubiquitous reference transcripts in diverse mammalian expression studies. Genome Res (2002) 4.49
Cis-acting regulatory variation in the human genome. Science (2004) 4.47
Characterization of a common susceptibility locus for asthma-related traits. Science (2004) 4.05
Exploring the mode-of-action of bioactive compounds by chemical-genetic profiling in yeast. Cell (2006) 4.03
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
Mapping common regulatory variants to human haplotypes. Hum Mol Genet (2005) 3.53
Characterization of variability in large-scale gene expression data: implications for study design. Genomics (2002) 3.42
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet (2012) 3.21
Susceptibility to leprosy is associated with PARK2 and PACRG. Nature (2004) 3.07
Germ-line DNA copy number variation frequencies in a large North American population. Hum Genet (2007) 2.94
Large-scale essential gene identification in Candida albicans and applications to antifungal drug discovery. Mol Microbiol (2003) 2.84
Seventy-five genetic loci influencing the human red blood cell. Nature (2012) 2.77
Heritability of alternative splicing in the human genome. Genome Res (2007) 2.76
Inhibition of mitochondrial translation as a therapeutic strategy for human acute myeloid leukemia. Cancer Cell (2011) 2.68
Common variants in the NLRP3 region contribute to Crohn's disease susceptibility. Nat Genet (2008) 2.67
Survey of allelic expression using EST mining. Genome Res (2005) 2.67
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. Gastroenterology (2012) 2.57
Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). J Infect Dis (2009) 2.53
Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region. Diabetes (2004) 2.52
MBNL proteins repress ES-cell-specific alternative splicing and reprogramming. Nature (2013) 2.49
Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies. Int J Epidemiol (2010) 2.44
Dissecting DNA damage response pathways by analysing protein localization and abundance changes during DNA replication stress. Nat Cell Biol (2012) 2.40
Functional normalization of 450k methylation array data improves replication in large cancer studies. Genome Biol (2014) 2.37
Meta-analysis of new genome-wide association studies of colorectal cancer risk. Hum Genet (2011) 2.35
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. PLoS Genet (2012) 2.34
A survey of genes differentially expressed in subcutaneous and visceral adipose tissue in men. Obes Res (2004) 2.33
Influence of human genome polymorphism on gene expression. Hum Mol Genet (2006) 2.14
Association of vitamin D receptor genetic variants with susceptibility to asthma and atopy. Am J Respir Crit Care Med (2004) 2.08
TFCat: the curated catalog of mouse and human transcription factors. Genome Biol (2009) 2.06
A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis. Nat Genet (2005) 2.03
The genetic basis for cancer treatment decisions. Cell (2012) 2.03
Significant conservation of synthetic lethal genetic interaction networks between distantly related eukaryotes. Proc Natl Acad Sci U S A (2008) 2.01
Genetic variants associated with myocardial infarction risk factors in over 8000 individuals from five ethnic groups: The INTERHEART Genetics Study. Circ Cardiovasc Genet (2009) 1.83
CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup. Am J Hum Genet (2009) 1.78
Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol. Am J Hum Genet (2007) 1.77
Genome-wide fitness test and mechanism-of-action studies of inhibitory compounds in Candida albicans. PLoS Pathog (2007) 1.74
1alpha,25-dihydroxy-vitamin D3 stimulation of bronchial smooth muscle cells induces autocrine, contractility, and remodeling processes. Physiol Genomics (2007) 1.73
A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One (2012) 1.72
Cancer genomics: technology, discovery, and translation. J Clin Oncol (2012) 1.70
Developmentally programmed nuclear destruction during yeast gametogenesis. Dev Cell (2012) 1.69
The growth factor midkine is modulated by both glucocorticoid and retinoid in fetal lung development. Am J Respir Cell Mol Biol (2003) 1.62
A Pan-BCL2 inhibitor renders bone-marrow-resident human leukemia stem cells sensitive to tyrosine kinase inhibition. Cell Stem Cell (2013) 1.59
Correction of population stratification in large multi-ethnic association studies. PLoS One (2008) 1.59
Characterization of gene-environment interactions for colorectal cancer susceptibility loci. Cancer Res (2012) 1.58
Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). J Infect Dis (2009) 1.57
A genome-wide approach to identifying novel-imprinted genes. Hum Genet (2007) 1.55
Genome-wide scan for linkage to obesity-associated hypertension in French Canadians. Hypertension (2005) 1.55
Skin barrier function and allergic risk. Nat Genet (2006) 1.50
Feasibility of real time next generation sequencing of cancer genes linked to drug response: results from a clinical trial. Int J Cancer (2012) 1.49
Analyses of associations with asthma in four asthma population samples from Canada and Australia. Hum Genet (2009) 1.48
An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population. PLoS Genet (2006) 1.47
Sex-stratified linkage analysis identifies a female-specific locus for IgE to cockroach in Costa Ricans. Am J Respir Crit Care Med (2008) 1.43
A strategy for modulation of enzymes in the ubiquitin system. Science (2013) 1.43
A lentiviral functional proteomics approach identifies chromatin remodeling complexes important for the induction of pluripotency. Mol Cell Proteomics (2010) 1.41
cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs. Nat Methods (2010) 1.41
Is rigorous retrospective harmonization possible? Application of the DataSHaPER approach across 53 large studies. Int J Epidemiol (2011) 1.41
Microarray analysis of uterine gene expression in mouse and human pregnancy. Mol Endocrinol (2003) 1.41
Toward further mapping of the association between the IL2RA locus and type 1 diabetes. Diabetes (2007) 1.38
Wanted: regulatory SNPs. Nat Genet (2003) 1.37
A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis. Am J Hum Genet (2002) 1.35
Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduria. Hum Mol Genet (2002) 1.34
The molecular and cellular heterogeneity of pancreatic ductal adenocarcinoma. Nat Rev Gastroenterol Hepatol (2011) 1.32
Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes. Diabetes (2004) 1.32
Functional classes of bronchial mucosa genes that are differentially expressed in asthma. BMC Genomics (2004) 1.32
Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord. PLoS Genet (2008) 1.32
Expression profiling in squamous carcinoma cells reveals pleiotropic effects of vitamin D3 analog EB1089 signaling on cell proliferation, differentiation, and immune system regulation. Mol Endocrinol (2002) 1.30
Small deletion variants have stable breakpoints commonly associated with alu elements. PLoS One (2008) 1.30
Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population. Nat Genet (2003) 1.30
A role for the TGFbeta-Par6 polarity pathway in breast cancer progression. Proc Natl Acad Sci U S A (2009) 1.29
Prediction and uncertainty in the analysis of gene expression profiles. In Silico Biol (2002) 1.27
Unraveling the genetics of cancer: genome sequencing and beyond. Annu Rev Genomics Hum Genet (2011) 1.27
Replication of an association between 17q21 SNPs and asthma in a French-Canadian familial collection. Hum Genet (2007) 1.26