Works matching IS 1756994X AND DT 2017 AND VI 9
Results: 118
Within-host evolution of Enterococcus faecium during longitudinal carriage and transition to bloodstream infection in immunocompromised patients.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0507-0
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- Article
Bugs, drugs, and HIV: the role of the vaginal microbiome in HIV risk and antiretroviral efficacy for HIV prevention.
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- Genome Medicine, 2017, v. 9, n. 1, p. 1, doi. 10.1186/s13073-017-0469-2
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Genetic variation in human drug-related genes.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0502-5
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- Article
The potential of circulating tumor DNA methylation analysis for the early detection and management of ovarian cancer.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0500-7
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Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0497-y
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Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0463-8
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- Article
B3GALNT2 mutations associated with nonsyndromic autosomal recessive intellectual disability reveal a lack of genotype- phenotype associations in the muscular dystrophy-dystroglycanopathies.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0505-2
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Defining the role of Lgr5<sup>+ </sup> stem cells in colorectal cancer: from basic research to clinical applications.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0460-y
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- Article
Methylation patterns in serum DNA for early identification of disseminated breast cancer.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0499-9
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Mapping genetic variations to threedimensional protein structures to enhance variant interpretation: a proposed framework.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0509-y
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- Article
Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0494-1
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Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0486-1
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Clinical implications and considerations for evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0508-z
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- Article
Challenges in understanding common disease.
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- 2017
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- Publication type:
- Interview
Narrowing the spectrum: the new frontier of precision antimicrobials.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0504-3
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- Article
Mapping a shared genetic basis for neurodevelopmental disorders.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0503-4
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Granatum: a graphical single-cell RNA-Seq analysis pipeline for genomics scientists.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0492-3
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Emerging mechanisms and novel targets in allergic inflammation and asthma.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0501-6
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A practical guide to single-cell RNA-sequencing for biomedical research and clinical applications.
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- Genome Medicine, 2017, v. 9, n. 1, p. 1, doi. 10.1186/s13073-017-0467-4
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- Article
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0488-z
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- Article
Predicting cancer type from tumour DNA signatures.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0493-2
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The genomic road to invasion--examining the similarities and differences in the genomes of associated oral pre-cancer and cancer samples.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/S13073-017-0442-0
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- Article
A novel Ruminococcus gnavus clade enriched in inflammatory bowel disease patients.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0490-5
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Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0498-x
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Neuroimaging genomics in psychiatry—a translational approach.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0496-z
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- Article
A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0491-4
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Cohort-specific imputation of gene expression improves prediction of warfarin dose for African Americans.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0495-0
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- Article
Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0487-0
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Prospects for using risk scores in polygenic medicine.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0489-y
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- Article
The circadian clock system's influence in health and disease.
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- 2017
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- Publication type:
- Interview
Actionable gene-based classification toward precision medicine in gastric cancer.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0484-3
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- Article
Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns.
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- Genome Medicine, 2017, v. 9, p. 14, doi. 10.1186/s13073-017-0482-5
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- Article
Public health surveillance in the UK revolutionises our understanding of the invasive Salmonella Typhimurium epidemic in Africa.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0480-7
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Cancer gene profiling in non-small cell lung cancers reveals activating mutations in JAK2 and JAK3 with therapeutic implications.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0478-1
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- Article
Nuclear Wiskott-Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cells.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0481-6
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- Article
Next-generation mapping: a novel approach for detection of pathogenic structural variants with a potential utility in clinical diagnosis.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0479-0
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Breathing new life into an old target: pulmonary disease drugs for Parkinson's disease therapy.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0483-4
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Three-dimensional genome architecture and emerging technologies: looping in disease.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0477-2
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HLAProfiler utilizes k-mer profiles to improve HLA calling accuracy for rare and common alleles in RNA-seq data.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0473-6
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Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0475-4
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Creating a data resource: what will it take to build a medical information commons?
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0476-3
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Identification of novel candidate disease genes from de novo exonic copy number variants.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0472-7
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- Article
Genetic and epigenetic studies of adiposity and cardiometabolic disease.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0474-5
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Whole genome sequencing of ESBL-producing Escherichia coli isolated from patients, farm waste and canals in Thailand.
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- Genome Medicine, 2017, v. 9, n. 1, p. 1, doi. 10.1186/s13073-017-0471-8
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Clinical implications of neoepitope landscapes for adult and pediatric cancers.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0470-9
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- Article
The neoepitope landscape in pediatric cancers.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0468-3
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- Article
Parkinson's disease is associated with DNA methylation levels in human blood and saliva.
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- Genome Medicine, 2017, v. 9, n. 1, p. 1, doi. 10.1186/s13073-017-0466-5
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- Article
Differential analysis between somatic mutation and germline variation profiles reveals cancer-related genes.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0465-6
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Genomic technologies--from tools to therapies.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0462-9
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Longitudinal genomic surveillance of multidrug-resistant Escherichia coli carriage in a long-term care facility in the United Kingdom.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0457-6
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- Article