Meta-analysis of prostate cancer gene expression data identifies a novel discriminatory signature enriched for glycosylating enzymes
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Volume 7, issue 1, December 2014
73 articles in this issue
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Conserved recurrent gene mutations correlate with pathway deregulation and clinical outcomes of lung adenocarcinoma in never-smokers
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A 3-biomarker-panel predicts renal outcome in patients with proteinuric renal diseases
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Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial
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PD_NGSAtlas: a reference database combining next-generation sequencing epigenomic and transcriptomic data for psychiatric disorders
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SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay
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Heterogeneity analysis of the proteomes in clinically nonfunctional pituitary adenomas
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Overexpression of miR-21-5p as a predictive marker for complete tumor regression to neoadjuvant chemoradiotherapy in rectal cancer patients
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High throughput exome coverage of clinically relevant cardiac genes
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“Genotype-first” approaches on a curious case of idiopathic progressive cognitive decline
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Transcriptome profiling and pathway analysis of genes expressed differentially in participants with or without a positive response to topiramate treatment for methamphetamine addiction
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FLAGS, frequently mutated genes in public exomes
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Integrated differential transcriptome maps of Acute Megakaryoblastic Leukemia (AMKL) in children with or without Down Syndrome (DS)
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Evaluation of an integrated clinical workflow for targeted next-generation sequencing of low-quality tumor DNA using a 51-gene enrichment panel
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Sleep quality, BDNF genotype and gene expression in individuals with chronic abdominal pain
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A common gene expression signature in Huntington’s disease patient brain regions
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Protein and microRNA biomarkers from lavage, urine, and serum in military personnel evaluated for dyspnea
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Identification of co-expression gene networks, regulatory genes and pathways for obesity based on adipose tissue RNA Sequencing in a porcine model
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Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve
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Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes
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Identification of a prognostic signature for old-age mortality by integrating genome-wide transcriptomic data with the conventional predictors: the Vitality 90+ Study
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Global population-specific variation in miRNA associated with cancer risk and clinical biomarkers
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Biological network inferences for a protection mechanism against familial Creutzfeldt-Jakob disease with E200K pathogenic mutation
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Genetic network identifies novel pathways contributing to atherosclerosis susceptibility in the innominate artery
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Gene signatures ESC, MYC and ERG-fusion are early markers of a potentially dangerous subtype of prostate cancer
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Global transcriptome-wide analysis of CIK cells identify distinct roles of IL-2 and IL-15 in acquisition of cytotoxic capacity against tumor
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Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis
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MutaCYP: Classification of missense mutations in human cytochromes P450
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MicroRNA and mRNA expression profiling in rat acute respiratory distress syndrome
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Functional characterization of breast cancer using pathway profiles
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Measurement of absolute copy number variation reveals association with essential hypertension
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Identification of gene-based responses in human blood cells exposed to alpha particle radiation
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Placental gene-expression profiles of intrahepatic cholestasis of pregnancy reveal involvement of multiple molecular pathways in blood vessel formation and inflammation
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Complexity of the 5′UTR region of the CLCN5gene: eleven 5′UTR ends are differentially expressed in the human kidney
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Novel application of multi-stimuli network inference to synovial fibroblasts of rheumatoid arthritis patients
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Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics
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Selection of competent blastocysts for transfer by combining time-lapse monitoring and array CGH testing for patients undergoing preimplantation genetic screening: a prospective study with sibling oocytes
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Human rhinovirus infection causes different DNA methylation changes in nasal epithelial cells from healthy and asthmatic subjects
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Whole genome sequencing reveals potential targets for therapy in patients with refractory KRASmutated metastatic colorectal cancer
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A systems biology approach to understand the pathophysiological mechanisms of cardiac pathological hypertrophy associated with rosiglitazone
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On the identification of potential regulatory variants within genome wide association candidate SNP sets
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Using logistic regression to improve the prognostic value of microarray gene expression data sets: application to early-stage squamous cell carcinoma of the lung and triple negative breast carcinoma
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Overlap of expression Quantitative Trait Loci (eQTL) in human brain and blood
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Imaging genomic mapping of an invasive MRI phenotype predicts patient outcome and metabolic dysfunction: a TCGA glioma phenotype research group project
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Differential expression and role of hyperglycemia induced oxidative stress in epigenetic regulation of β1, β2 and β3-adrenergic receptors in retinal endothelial cells
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Integrative analysis of the transcriptome profiles observed in type 1, type 2 and gestational diabetes mellitus reveals the role of inflammation
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Cellular dissection of psoriasis for transcriptome analyses and the post-GWAS era
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Small non-coding RNA signature in multiple sclerosis patients after treatment with interferon-β
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Translating a gene expression signature for multiple myeloma prognosis into a robust high-throughput assay for clinical use
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Whole exome sequencing reveals concomitant mutations of multiple FA genes in individual Fanconi anemia patients
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