Works matching IS 1756994X AND DT 2016 AND VI 8
Results: 132
Implementation of next generation sequencing into pediatric hematologyoncology practice: moving beyond actionable alterations.
- Published in:
- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0389-6
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- Article
Allele-specific expression in the human heart and its application to postoperative atrial fibrillation and myocardial ischemia.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0381-1
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- Article
Mitochondrial replacement approaches: challenges for clinical implementation.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0380-2
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- Article
Looking beyond the cancer cell for effective drug combinations.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0379-8
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- Article
Potential contribution of the uterine microbiome in the development of endometrial cancer.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0368-y
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- Article
Erratum to: Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens.
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- 2016
- Publication type:
- Correction Notice
iCAGES: integrated CAncer GEnome Score for comprehensively prioritizing driver genes in personal cancer genomes.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0390-0
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- Publication type:
- Article
Genomic landscape of colorectal cancer in Japan: clinical implications of comprehensive genomic sequencing for precision medicine.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0387-8
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- Article
The variability and reproducibility of whole genome sequencing technology for detecting resistance to anti-tuberculous drugs.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0385-x
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- Article
Reconciling evidence-based medicine and precision medicine in the era of big data: challenges and opportunities.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0388-7
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- Article
Truncating de novo mutations in the Krüppel-type zinc-finger gene ZNF148 in patients with corpus callosum defects, developmental delay, short stature, and dysmorphisms.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0386-9
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- Article
XGR software for enhanced interpretation of genomic summary data, illustrated by application to immunological traits.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0384-y
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- Article
Alternate-locus aware variant calling in whole genome sequencing.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0383-z
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- Article
Non-coding single nucleotide variants affecting estrogen receptor binding and activity.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0382-0
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- Publication type:
- Article
High-specificity bioinformatics framework for epigenomic profiling of discordant twins reveals specific and shared markers for ACPA and ACPA-positive rheumatoid arthritis.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0374-0
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- Publication type:
- Article
Genome editing: progress and challenges for medical applications.
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- 2016
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- Publication type:
- Opinion
Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0375-z
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- Publication type:
- Article
Low heritability in pharmacokinetics of talinolol: a pharmacogenetic twin study on the heritability of the pharmacokinetics of talinolol, a putative probe drug of MDR1 and other membrane transporters.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0372-2
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- Article
Erratum to: Making sense of big data in health research: towards an EU action plan.
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- 2016
- Publication type:
- Correction Notice
Somatic cancer variant curation and harmonization through consensus minimum variant level data.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0367-z
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- Publication type:
- Article
MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0360-6
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- Article
Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0359-z
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- Publication type:
- Article
Integrative network analysis of nineteen brain regions identifies molecular signatures and networks underlying selective regional vulnerability to Alzheimer's disease.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0355-3
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- Article
A case study of an integrative genomic and experimental therapeutic approach for rare tumors: identification of vulnerabilities in a pediatric poorly differentiated carcinoma.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0366-0
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- Article
Approaches to modernize the combination drug development paradigm.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0369-x
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- Publication type:
- Article
Application of RNAi-induced gene expression profiles for prognostic prediction in breast cancer.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0363-3
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- Article
Integrating cancer genomic data into electronic health records.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0371-3
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- Article
Technological considerations for genome-guided diagnosis and management of cancer.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0370-4
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- Article
Delivering on the promise of precision cancer medicine.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0373-1
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- Publication type:
- Article
Transmission of methicillin-resistant Staphylococcus aureus in long-term care facilities and their related healthcare networks.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0353-5
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- Article
Acquired resistance to anti-PD1 therapy: checkmate to checkpoint blockade?
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0365-1
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- Article
Integrating precision cancer medicine into healthcare—policy, practice, and research challenges.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0362-4
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- Publication type:
- Article
Genome-wide methylation profiling of ovarian cancer patient-derived xenografts treated with the demethylating agent decitabine identifies novel epigenetically regulated genes and pathways.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0361-5
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- Publication type:
- Article
Germline, hematopoietic, mosaic, and somatic variation: interplay between inherited and acquired genetic alterations in disease assessment.
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- 2016
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- Publication type:
- Opinion
Altered gut microbiota in female mice with persistent low body weights following removal of post-weaning chronic dietary restriction.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0357-1
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- Publication type:
- Article
Molecular profiling of advanced solid tumors and patient outcomes with genotype-matched clinical trials: the Princess Margaret IMPACT/COMPACT trial.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0364-2
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- Article
Rational design of cancer gene panels with OncoPaD.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0349-1
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- Publication type:
- Article
Topological analysis of metabolic networks integrating co-segregating transcriptomes and metabolomes in type 2 diabetic rat congenic series.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0352-6
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- Publication type:
- Article
qKAT: a high-throughput qPCR method for KIR gene copy number and haplotype determination.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0358-0
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- Publication type:
- Article
Mobile real-time surveillance of Zika virus in Brazil.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0356-2
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- Article
Genetic and epigenetic analysis of schizophrenia in blood-a no-brainer?
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- 2016
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- Publication type:
- Opinion
A missing link in the bench-to-bedside paradigm: engaging regulatory stakeholders in clinical genomics research.
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- 2016
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- Publication type:
- Opinion
Genomic analysis of the molecular neuropathology of tuberous sclerosis using a human stem cell model.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0347-3
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- Publication type:
- Article
Epigenomic and metabolic responses of hypothalamic POMC neurons to gestational nicotine exposure in adult offspring.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0348-2
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- Publication type:
- Article
Recent advances in malaria genomics and epigenomics.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0343-7
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- Publication type:
- Article
Migraine genetics: from genome-wide association studies to translational insights.
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- 2016
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- Publication type:
- Opinion
The multi-omic landscape of transcription factor inactivation in cancer.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0342-8
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- Publication type:
- Article
VARPRISM: incorporating variant prioritization in tests of de novo mutation association.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0341-9
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- Publication type:
- Article
Characterisation of the global transcriptional response to heat shock and the impact of individual genetic variation.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0345-5
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- Publication type:
- Article
Cancer network activity associated with therapeutic response and synergism.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0340-x
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- Publication type:
- Article