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Identifying driver genes involving gene dysregulated expression, tissue-specific expression and gene-gene network.
- Published in:
- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0619-z
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- Article
A network clustering based feature selection strategy for classifying autism spectrum disorder.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0598-0
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- Article
MECoRank: cancer driver genes discovery simultaneously evaluating the impact of SNVs and differential expression on transcriptional networks.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0582-8
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Directional association test reveals high-quality putative cancer driver biomarkers including noncoding RNAs.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0565-9
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- Article
A new method for mining information of co-expression network based on multicancers integrated data.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1
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HiSSI: high-order SNP-SNP interactions detection based on efficient significant pattern and differential evolution.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0584-6
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- Article
MEG3 promotes proliferation and inhibits apoptosis in osteoarthritis chondrocytes by miR-361-5p/FOXO1 axis.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0649-6
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Analysis of gene expression profiles and protein-protein interaction networks in multiple tissues of systemic sclerosis.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0632-2
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Prediction of comorbid diseases using weighted geometric embedding of human interactome.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0605-5
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A network view of microRNA and gene interactions in different pathological stages of colon cancer.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0597-1
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Region-based interaction detection in genome-wide case-control studies.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0583-7
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- Article
Genome analysis and knowledge-driven variant interpretation with TGex.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0647-8
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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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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0639-8
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- Article
Genepanel.iobio - an easy to use web tool for generating disease- and phenotype-associated gene lists.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0641-1
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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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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0642-0
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Competitive endogenous RNA (ceRNA) regulation network of lncRNAs, miRNAs, and mRNAs in Wilms tumour.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0644-y
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RNA-seq from archival FFPE breast cancer samples: molecular pathway fidelity and novel discovery.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0643-z
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- Article
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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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0640-2
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- Article
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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- 2019
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- Correction Notice
Reinterpretation, reclassification, and its downstream effects: challenges for clinical laboratory geneticists.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0612-6
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Return of genetic and genomic research findings: experience of a pediatric biorepository.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0618-0
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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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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0616-2
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- Article
MySeq: privacy-protecting browser-based personal Genome analysis for genomics education and exploration.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0615-3
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Identification and ranking of recurrent neo-epitopes in cancer.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0611-7
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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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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0614-4
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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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- 2019
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- Publication type:
- Correction Notice
Significant random signatures reveals new biomarker for breast cancer.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0609-1
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- Article
Integrative molecular analysis of metastatic hepatocellular carcinoma.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0586-4
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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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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0610-8
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- Article
Medroxyprogesterone acetate causes the alterations of endoplasmic reticulum related mRNAs and lncRNAs in endometrial cancer cells.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0601-9
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- Article
Classification of glioma based on prognostic alternative splicing.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0603-7
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- Publication type:
- Article
A functional polymorphism in the promoter of miR-17-92 cluster is associated with decreased risk of ischemic stroke.
- Published in:
- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0589-1
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- Publication type:
- Article
Preimplantation genetic testing for a family with usher syndrome through targeted sequencing and haplotype analysis.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0600-x
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- Publication type:
- Article
Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0606-4
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- Article
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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- 2019
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- Publication type:
- Correction Notice
Potential risks and solutions for sharing genome summary data from African populations.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0604-6
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- Publication type:
- Article
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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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0590-8
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- Article
A comparison of machine learning classifiers for dementia with Lewy bodies using miRNA expression data.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0607-3
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- Article
Gene expression profiling in blood from cerebral malaria patients and mild malaria patients living in Senegal.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0599-z
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- Article
Epigenetic landscapes suggest that genetic risk for intracranial aneurysm operates on the endothelium.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0591-7
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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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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0595-3
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- Publication type:
- Article
A comprehensive genome-wide profiling comparison between HBV and HCV infected hepatocellular carcinoma.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0580-x
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- Publication type:
- Article
ATXN1 N-terminal region explains the binding differences of wild-type and expanded forms.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0594-4
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- Article
Whole-genome bisulfite sequencing in systemic sclerosis provides novel targets to understand disease pathogenesis.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0602-8
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- Article
Gene-based analysis of ADHD using PASCAL: a biological insight into the novel associated genes.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s12920-019-0593-5
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- Article
A novel genomic panel as an adjunctive diagnostic tool for the characterization and profiling of breast Fibroepithelial lesions.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0588-2
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- Article
Genome-wide discovery and characterization of long noncoding RNAs in patients with multiple myeloma.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0577-5
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- Article
Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0587-3
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- Publication type:
- Article
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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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0592-6
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- Article
The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington's disease brain.
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- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0581-9
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- Article