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Author Details
Full Name
Graham R S Ritchie
Affiliation
Wellcome Sanger Institute
ORCID
Career Start Year
2008
Papers
31
H Index
26
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
30692680
GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals.
Nat Genet
2019
31675503
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Cell
2019
30576415
Very low-depth whole-genome sequencing in complex trait association studies.
Bioinformatics
2019
28552196
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.
Am J Hum Genet
2017
28934396
Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus.
Hum Mol Genet
2017
28643794
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations.
Nat Commun
2017
28827734
Integrative epigenomics, transcriptomics and proteomics of patient chondrocytes reveal genes and pathways involved in osteoarthritis.
Sci Rep
2017
27049301
Whole-exome sequencing in an isolated population from the Dalmatian island of Vis.
Eur J Hum Genet
2016
27268795
The Ensembl Variant Effect Predictor.
Genome Biol
2016
27146844
Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation.
Hum Mol Genet
2016
27111036
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences.
Nat Genet
2016
25236461
The Ensembl REST API: Ensembl Data for Any Language.
Bioinformatics
2015
26229585
Improving the Sequence Ontology terminology for genomic variant annotation.
J Biomed Semantics
2015
26110515
Comparison of GENCODE and RefSeq gene annotation and the impact of reference geneset on variant effect prediction.
BMC Genomics
2015
25470054
The African Genome Variation Project shapes medical genetics in Africa.
Nature
2015
24412096
Revisiting the thrifty gene hypothesis via 65 loci associated with susceptibility to type 2 diabetes.
Am J Hum Genet
2014
25473426
Computational approaches to interpreting genomic sequence variation.
Genome Med
2014
25373335
Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants.
Nat Commun
2014
24514567
A genome-wide association study of anorexia nervosa.
Mol Psychiatry
2014
24487584
Functional annotation of noncoding sequence variants.
Nat Methods
2014
23203987
Ensembl 2013.
Nucleic Acids Res
2013
24343240
A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates.
Nat Commun
2013
24092746
Integrative annotation of variants from 1092 humans: application to cancer genomics.
Science
2013
23900255
Computational approaches to identify functional genetic variants in cancer genomes.
Nat Methods
2013
22086963
Ensembl 2012.
Nucleic Acids Res
2012
22843499
Genome-wide meta-analysis of common variant differences between men and women.
Hum Mol Genet
2012
22261837
A combined functional annotation score for non-synonymous variants.
Hum Hered
2012
21045057
Ensembl 2011.
Nucleic Acids Res
2011
21750661
Modernizing reference genome assemblies.
PLoS Biol
2011
19740461
Signalling signalhood and the emergence of communication.
Cognition
2009
18294656
Song learning as an indicator mechanism: modelling the developmental stress hypothesis.
J Theor Biol
2008
1 - 31 of 31
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Co-authored papers
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Co-authored papers
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University of Cambridge
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Nigel W Rayner
Co-authored papers
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Angela Matchan
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Tim Hubbard
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European Bioinformatics Institute
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Samuli Ripatti
Co-authored papers
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Andrew D Yates
European Bioinformatics Institute
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3
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Co-authored papers
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Ioanna Ntalla
Co-authored papers
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Oncology R&D
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Jennifer L Asimit
Co-authored papers
3
Aarno Palotie
Co-authored papers
3
Susan Fairley
European Bioinformatics Institute
Co-authored papers
3
Shane McCarthy
Wellcome Sanger Institute
Co-authored papers
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Michael Schuster
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Stephen M J Searle
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