MEG3 promotes proliferation and inhibits apoptosis in osteoarthritis chondrocytes by miR-361-5p/FOXO1 axis
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Volume 12, issue 1, December 2019
130 articles in this issue
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Genome analysis and knowledge-driven variant interpretation with TGex
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Analysis of gene expression profiles and protein-protein interaction networks in multiple tissues of systemic sclerosis
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CDK1 and CCNB1 as potential diagnostic markers of rhabdomyosarcoma: validation following bioinformatics analysis
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Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review
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Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13
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RNA-seq from archival FFPE breast cancer samples: molecular pathway fidelity and novel discovery
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Competitive endogenous RNA (ceRNA) regulation network of lncRNAs, miRNAs, and mRNAs in Wilms tumour
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Systematic computational identification of prognostic cytogenetic markers in neuroblastoma
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Genepanel.iobio - an easy to use web tool for generating disease- and phenotype-associated gene lists
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A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report
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Correction to: A functional polymorphism in the promoter of miR-17-92 cluster is associated with decreased risk of ischemic stroke
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High-throughput RNA sequencing from paired lesional- and non-lesional skin reveals major alterations in the psoriasis circRNAome
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Return of genetic and genomic research findings: experience of a pediatric biorepository
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MySeq: privacy-protecting browser-based personal Genome analysis for genomics education and exploration
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Identification and ranking of recurrent neo-epitopes in cancer
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Reinterpretation, reclassification, and its downstream effects: challenges for clinical laboratory geneticists
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Clinical, cytogenetic, and molecular findings in a patient with ring chromosome 4: case report and literature review
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Correction to: RNA sequencing identifies novel non-coding RNA and exon-specific effects associated with cigarette smoking
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Classification of glioma based on prognostic alternative splicing
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Integrative molecular analysis of metastatic hepatocellular carcinoma
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Medroxyprogesterone acetate causes the alterations of endoplasmic reticulum related mRNAs and lncRNAs in endometrial cancer cells
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Accurate detection of KRAS, NRAS and BRAF mutations in metastatic colorectal cancers by bridged nucleic acid-clamp real-time PCR
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Significant random signatures reveals new biomarker for breast cancer
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A functional polymorphism in the promoter of miR-17-92 cluster is associated with decreased risk of ischemic stroke
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Preimplantation genetic testing for a family with usher syndrome through targeted sequencing and haplotype analysis
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Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family
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Correction to: Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits
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Detection of fetal trisomy and single gene disease by massively parallel sequencing of extracellular vesicle DNA in maternal plasma: a proof-of-concept validation
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A comparison of machine learning classifiers for dementia with Lewy bodies using miRNA expression data
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Epigenetic landscapes suggest that genetic risk for intracranial aneurysm operates on the endothelium
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Gene expression profiling in blood from cerebral malaria patients and mild malaria patients living in Senegal
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A comprehensive genome-wide profiling comparison between HBV and HCV infected hepatocellular carcinoma
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Genetic and epigenetic modifications induced by chemotherapeutic drugs: human amniotic fluid stem cells as an in-vitro model
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ATXN1 N-terminal region explains the binding differences of wild-type and expanded forms
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Whole-genome bisulfite sequencing in systemic sclerosis provides novel targets to understand disease pathogenesis
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Gene-based analysis of ADHD using PASCAL: a biological insight into the novel associated genes
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A novel genomic panel as an adjunctive diagnostic tool for the characterization and profiling of breast Fibroepithelial lesions
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Intrinsic and extrinsic epigenetic age acceleration are associated with hypertensive target organ damage in older African Americans
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Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing
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The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington’s disease brain
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Co-mutations of TP53 and KRAS serve as potential biomarkers for immune checkpoint blockade in squamous-cell non-small cell lung cancer: a case report
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Genome-wide discovery and characterization of long noncoding RNAs in patients with multiple myeloma
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Transcriptome analysis identified a novel 3-LncRNA regulatory network of transthyretin attenuating glucose induced hRECs dysfunction in diabetic retinopathy
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Deconvolution of transcriptomes and miRNomes by independent component analysis provides insights into biological processes and clinical outcomes of melanoma patients
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Integrative genomic analyses of APOBEC-mutational signature, expression and germline deletion of APOBEC3 genes, and immunogenicity in multiple cancer types
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Host genetic variability and pneumococcal disease: a systematic review and meta-analysis
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Enhancer variants associated with Alzheimer’s disease affect gene expression via chromatin looping
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Transcriptome analysis of human monocytic cells infected with Burkholderia species and exploration of pentraxin-3 as part of the innate immune response against the organisms
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