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Author Details

Graham R S Ritchie
Wellcome Sanger Institute
2008
31
26
PMIDPaper TitleJournal TitlePublished Year
30692680GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals.Nat Genet2019
31675503Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.Cell2019
30576415Very low-depth whole-genome sequencing in complex trait association studies.Bioinformatics2019
28552196Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.Am J Hum Genet2017
28934396Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus.Hum Mol Genet2017
28643794Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations.Nat Commun2017
28827734Integrative epigenomics, transcriptomics and proteomics of patient chondrocytes reveal genes and pathways involved in osteoarthritis.Sci Rep2017
27049301Whole-exome sequencing in an isolated population from the Dalmatian island of Vis.Eur J Hum Genet2016
27268795The Ensembl Variant Effect Predictor.Genome Biol2016
27146844Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation.Hum Mol Genet2016
27111036Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences.Nat Genet2016
25236461The Ensembl REST API: Ensembl Data for Any Language.Bioinformatics2015
26229585Improving the Sequence Ontology terminology for genomic variant annotation.J Biomed Semantics2015
26110515Comparison of GENCODE and RefSeq gene annotation and the impact of reference geneset on variant effect prediction.BMC Genomics2015
25470054The African Genome Variation Project shapes medical genetics in Africa.Nature2015
24412096Revisiting the thrifty gene hypothesis via 65 loci associated with susceptibility to type 2 diabetes.Am J Hum Genet2014
25473426Computational approaches to interpreting genomic sequence variation.Genome Med2014
25373335Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants.Nat Commun2014
24514567A genome-wide association study of anorexia nervosa.Mol Psychiatry2014
24487584Functional annotation of noncoding sequence variants.Nat Methods2014
23203987Ensembl 2013.Nucleic Acids Res2013
24343240A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates.Nat Commun2013
24092746Integrative annotation of variants from 1092 humans: application to cancer genomics.Science2013
23900255Computational approaches to identify functional genetic variants in cancer genomes.Nat Methods2013
22086963Ensembl 2012.Nucleic Acids Res2012
22843499Genome-wide meta-analysis of common variant differences between men and women.Hum Mol Genet2012
22261837A combined functional annotation score for non-synonymous variants.Hum Hered2012
21045057Ensembl 2011.Nucleic Acids Res2011
21750661Modernizing reference genome assemblies.PLoS Biol2011
19740461Signalling signalhood and the emergence of communication.Cognition2009
18294656Song learning as an indicator mechanism: modelling the developmental stress hypothesis.J Theor Biol2008
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Collaborators

Co-authored papers 16
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Co-authored papers 6
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European Bioinformatics Institute (EMBL-EBI)
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Oncology R&D
Co-authored papers 3
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Co-authored papers 3
Wellcome Sanger Institute
Co-authored papers 3
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
Co-authored papers 3
Wellcome Trust Sanger Institute
Co-authored papers 3
University Medical Center Rotterdam
Co-authored papers 3
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