Works matching IS 1756994X AND DT 2019
Results: 93
Relating the gut metagenome and metatranscriptome to immunotherapy responses in melanoma patients.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0672-4
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- Publication type:
- Article
Identifying Crohn's disease signal from variome analysis.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0670-6
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- Publication type:
- Article
The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants—a multi-site prospective cohort study.
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- Genome Medicine, 2019, p. 1, doi. 10.1186/s13073-023-01223-1
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- Article
Genetic underpinnings of recovery after stroke: an opportunity for gene discovery, risk stratification, and precision medicine.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0671-5
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- Publication type:
- Article
The relationship between insomnia and complex diseases—insights from genetic data.
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- 2019
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- Publication type:
- Letter
Best practices for bioinformatic characterization of neoantigens for clinical utility.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0666-2
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- Publication type:
- Article
Comprehensive characterization of circular RNAs in ~ 1000 human cancer cell lines.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0663-5
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- Publication type:
- Article
Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0667-1
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- Publication type:
- Article
Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0664-4
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- Publication type:
- Article
Identifying chemogenetic interactions from CRISPR screens with drugZ.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0665-3
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- Publication type:
- Article
A validated single-cell-based strategy to identify diagnostic and therapeutic targets in complex diseases.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0657-3
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- Publication type:
- Article
Advancing cancer immunotherapy: a vision for the field.
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- 2019
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- Publication type:
- Editorial
Correction to: Molecular and pharmacological modulators of the tumor immune contexture revealed by deconvolution of RNA-seq data.
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- 2019
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- Publication type:
- Correction Notice
Hidden Markov models lead to higher resolution maps of mutation signature activity in cancer.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0659-1
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- Publication type:
- Article
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0658-2
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- Publication type:
- Article
Deciphering drug resistance in Mycobacterium tuberculosis using whole-genome sequencing: progress, promise, and challenges.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0660-8
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- Publication type:
- Article
Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0651-9
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- Publication type:
- Article
The good, the bad, and the ugly: hyperprogression in cancer patients following immune checkpoint therapy.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0661-7
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- Publication type:
- Article
Identification of intermediate-sized deletions and inference of their impact on gene expression in a human population.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0656-4
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- Publication type:
- Article
Evolving neoantigen profiles in colorectal cancers with DNA repair defects.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0654-6
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- Publication type:
- Article
Integrating informatics tools and portable sequencing technology for rapid detection of resistance to anti-tuberculous drugs.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0650-x
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- Publication type:
- Article
Radiation therapy and anti-tumor immunity: exposing immunogenic mutations to the immune system.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0653-7
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- Publication type:
- Article
Mechanisms of immune-related adverse events associated with immune checkpoint blockade: using germline genetics to develop a personalized approach.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0652-8
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- Publication type:
- Article
Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0649-3
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- Publication type:
- Article
Somatic mutation and clonal expansions in human tissues.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0648-4
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- Publication type:
- Article
Prognostic value of B cells in cutaneous melanoma.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0647-5
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- Publication type:
- Article
Associating somatic mutations to clinical outcomes: a pan-cancer study of survival time.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0643-9
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- Publication type:
- Article
Clinical utility of custom-designed NGS panel testing in pediatric tumors.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0644-8
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- Publication type:
- Article
Dissecting lung development and fibrosis at single-cell resolution.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0645-7
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- Publication type:
- Article
Molecular and pharmacological modulators of the tumor immune contexture revealed by deconvolution of RNA-seq data.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0638-6
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- Publication type:
- Article
Points-to-consider on the return of results in epigenetic research.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0646-6
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- Publication type:
- Article
Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0639-5
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- Publication type:
- Article
Discovery and characterization of actionable tumor antigens.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0642-x
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- Publication type:
- Article
Evidence from genome wide association studies implicates reduced control of Epstein-Barr virus infection in multiple sclerosis susceptibility.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0640-z
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- Publication type:
- Article
A modular transcriptome map of mature B cell lymphomas.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0637-7
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- Publication type:
- Article
Multi-omics discovery of exome-derived neoantigens in hepatocellular carcinoma.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0636-8
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- Publication type:
- Article
TCF21 and AP-1 interact through epigenetic modifications to regulate coronary artery disease gene expression.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0635-9
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- Publication type:
- Article
Molecular basis for phenotypic similarity of genetic disorders.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0641-y
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- Publication type:
- Article
Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0633-y
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- Publication type:
- Article
Designing circulating tumor DNA-based interventional clinical trials in oncology.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0634-x
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- Publication type:
- Article
CRISPR-SONIC: targeted somatic oncogene knock-in enables rapid in vivo cancer modeling.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0627-9
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- Publication type:
- Article
Translating insights into tumor evolution to clinical practice: promises and challenges.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0632-z
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- Publication type:
- Article
Loss of BAP1 as a candidate predictive biomarker for immunotherapy of mesothelioma.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0631-0
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- Publication type:
- Article
Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0628-8
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- Publication type:
- Article
Encircling the regions of the pharmacogenomic landscape that determine drug response.
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- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0626-x
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- Publication type:
- Article
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Circular RNAs as promising biomarkers in cancer: detection, function, and beyond.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0629-7
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- Publication type:
- Article
Correction to: NSAID use and somatic exomic mutations in Barrett's esophagus.
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- 2019
- By:
- Publication type:
- Correction Notice
A decade of Genome Medicine: toward precision medicine.
- Published in:
- 2019
- By:
- Publication type:
- Editorial
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0623-0
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- Publication type:
- Article