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Author Details

Peter Donnelly
University of Oxford
1985
156
82
PMIDPaper TitleJournal TitlePublished Year
33408411Platypus and echidna genomes reveal mammalian biology and evolution.Nature2021
33675770Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries.Am J Cardiol2021
33408411Platypus and echidna genomes reveal mammalian biology and evolution.Nature2021
34491357Altering the Binding Properties of PRDM9 Partially Restores Fertility across the Species Boundary.Mol Biol Evol2021
33675770Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries.Am J Cardiol2021
34491357Altering the Binding Properties of PRDM9 Partially Restores Fertility across the Species Boundary.Mol Biol Evol2021
32744506ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair.Elife2020
32744506ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair.Elife2020
32610038The Configuration of RPA, RAD51, and DMC1 Binding in Meiosis Reveals the Nature of Critical Recombination Intermediates.Mol Cell2020
32610038The Configuration of RPA, RAD51, and DMC1 Binding in Meiosis Reveals the Nature of Critical Recombination Intermediates.Mol Cell2020
30710075Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula.Nat Commun2019
31015479Sequencing of human genomes with nanopore technology.Nat Commun2019
30898902Factors influencing meiotic recombination revealed by whole-genome sequencing of single sperm.Science2019
30710075Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula.Nat Commun2019
30898902Factors influencing meiotic recombination revealed by whole-genome sequencing of single sperm.Science2019
31015479Sequencing of human genomes with nanopore technology.Nat Commun2019
29688544Insights into Platypus Population Structure and History from Whole-Genome Sequencing.Mol Biol Evol2018
30305743The UK Biobank resource with deep phenotyping and genomic data.Nature2018
29874223Long-read whole genome sequencing and comparative analysis of six strains of the human pathogen Orientia tsutsugamushi.PLoS Negl Trop Dis2018
30327483Phenome-wide association studies across large population cohorts support drug target validation.Nat Commun2018
30323177Identifying loci affecting trait variability and detecting interactions in genome-wide association studies.Nat Genet2018
29688544Insights into Platypus Population Structure and History from Whole-Genome Sequencing.Mol Biol Evol2018
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
29874223Long-read whole genome sequencing and comparative analysis of six strains of the human pathogen Orientia tsutsugamushi.PLoS Negl Trop Dis2018
30323177Identifying loci affecting trait variability and detecting interactions in genome-wide association studies.Nat Genet2018
30305743The UK Biobank resource with deep phenotyping and genomic data.Nature2018
30327483Phenome-wide association studies across large population cohorts support drug target validation.Nat Commun2018
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
28759005Bayesian analysis of genetic association across tree-structured routine healthcare data in the UK Biobank.Nat Genet2017
29016847A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability.Hum Mol Genet2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
28759005Bayesian analysis of genetic association across tree-structured routine healthcare data in the UK Biobank.Nat Genet2017
28566273An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.Diabetes2017
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
31105805Stochastic modelling and inference in electronic hospital databases for the spread of infections: <i>Clostridium difficile</i> transmission in Oxfordshire hospitals 2007-2010.Ann Appl Stat2017
31105805Stochastic modelling and inference in electronic hospital databases for the spread of infections: <i>Clostridium difficile</i> transmission in Oxfordshire hospitals 2007-2010.Ann Appl Stat2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
29016847A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability.Hum Mol Genet2017
28566273An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.Diabetes2017
26840484Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice.Nature2016
26840484Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice.Nature2016
27236921Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.Am J Hum Genet2016
27398621The genetic architecture of type 2 diabetes.Nature2016
27596730Multiple novel gene-by-environment interactions modify the effect of FTO variants on body mass index.Nat Commun2016
27596730Multiple novel gene-by-environment interactions modify the effect of FTO variants on body mass index.Nat Commun2016
27236921Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.Am J Hum Genet2016
27398621The genetic architecture of type 2 diabetes.Nature2016
25537359Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.Eur J Hum Genet2015
25788095The fine-scale genetic structure of the British population.Nature2015
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