Ewan Birney


Ontology type: schema:Person     


Person Info

NAME

Ewan

SURNAME

Birney

Publications in SciGraph latest 50 shown

  • 2019-02 GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals in NATURE GENETICS
  • 2019-01-18 Author Correction: Landscape of somatic mutations in 560 breast cancer whole-genome sequences in NATURE
  • 2018-11 A call for public archives for biological image data in NATURE METHODS
  • 2017-11 Corrigendum: A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers in NATURE GENETICS
  • 2017-06 Corrigendum: Common genetic variation drives molecular heterogeneity in human iPSCs in NATURE
  • 2017-06 Common genetic variation drives molecular heterogeneity in human iPSCs in NATURE
  • 2017-04 Promoter shape varies across populations and affects promoter evolution and expression noise in NATURE GENETICS
  • 2017-04 HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures in NATURE MEDICINE
  • 2017-03 A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers in NATURE GENETICS
  • 2017-01 Genetic variants regulating expression levels and isoform diversity during embryogenesis in NATURE
  • 2016-12 Genome wide association analysis of the heart using high-resolution 3D cardiac MRI identifies new genetic loci underlying cardiac structure and function in JOURNAL OF CARDIOVASCULAR MAGNETIC RESONANCE
  • 2016-09-26 Breast cancer genome and transcriptome integration implicates specific mutational signatures with immune cell infiltration in NATURE COMMUNICATIONS
  • 2016-06 Landscape of somatic mutations in 560 breast cancer whole-genome sequences in NATURE
  • 2016-05-02 The topography of mutational processes in breast cancer genomes in NATURE COMMUNICATIONS
  • 2015-12 Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel in NATURE COMMUNICATIONS
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-12 Whole-genome sequence-based analysis of thyroid function in NATURE COMMUNICATIONS
  • 2015-10 Human genomics: The end of the start for population sequencing in NATURE
  • 2015-10 Using human genetics to make new medicines in NATURE REVIEWS GENETICS
  • 2014-12 A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans in NATURE COMMUNICATIONS
  • 2014-04 Integrative knowledge management to enhance pharmaceutical R&D in NATURE REVIEWS DRUG DISCOVERY
  • 2014-01 Archaic humans: Four makes a party in NATURE
  • 2013-08 Genome-wide meta-analysis identifies new susceptibility loci for migraine in NATURE GENETICS
  • 2013-02 Towards practical, high-capacity, low-maintenance information storage in synthesized DNA in NATURE
  • 2012-12 The future of DNA sequence archiving in GIGASCIENCE
  • 2012-09 Analysis of variation at transcription factor binding sites in Drosophila and humans in GENOME BIOLOGY
  • 2012-09 The making of ENCODE: Lessons for big-data projects in NATURE
  • 2012-09 Modeling gene expression using chromatin features in various cellular contexts in GENOME BIOLOGY
  • 2012-09 Classification of human genomic regions based on experimentally determined binding sites of more than 100 transcription-related factors in GENOME BIOLOGY
  • 2012-04-04 The genomic basis of adaptive evolution in threespine sticklebacks in NATURE
  • 2011-10 A high-resolution map of human evolutionary constraint using 29 mammals in NATURE
  • 2011-09 Mouse genomic variation and its effect on phenotypes and gene regulation in NATURE
  • 2011-02 Considerations for the inclusion of 2x mammalian genomes in phylogenetic analyses in GENOME BIOLOGY
  • 2011-01 Assemblies: the good, the bad, the ugly in NATURE METHODS
  • 2010-12 Ensembl variation resources in BMC GENOMICS
  • 2010-12 A database and API for variation, dense genotyping and resequencing data in BMC BIOINFORMATICS
  • 2010-09 The BioPAX community standard for pathway data sharing in NATURE BIOTECHNOLOGY
  • 2010-07 Genomic information infrastructure after the deluge in GENOME BIOLOGY
  • 2010-04-15 International network of cancer genome projects in NATURE
  • 2010-04 Locus Reference Genomic sequences: an improved basis for describing human DNA variants in GENOME MEDICINE
  • 2010 Ensembl Genome Browser in VOGEL AND MOTULSKY'S HUMAN GENETICS
  • 2010-01 A small-cell lung cancer genome with complex signatures of tobacco exposure in NATURE
  • 2009-11 Sense from sequence reads: methods for alignment and assembly in NATURE METHODS
  • 2009-09-10 Prepublication data sharing in NATURE
  • 2009-08 Mapping identifiers for the integration of genomic datasets with the R/Bioconductor package biomaRt in NATURE PROTOCOLS
  • 2009-05-03 Reactome – a knowledgebase of human biological pathways in NATURE PRECEDINGS
  • 2009-02 Erratum to: Reactome: a knowledge base of biologic pathways and processes in GENOME BIOLOGY
  • 2009 Visualising the Epigenome in EPIGENOMICS
  • 2008-12 Integrating biological data – the Distributed Annotation System in BMC BIOINFORMATICS
  • 2008-07 A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis in NATURE BIOTECHNOLOGY
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