Peter Donnelly

Q: What Schools Are Affiliated With Peter Donnelly

Peter Donnelly is affiliated with the following schools: University of Queensland, University College London, University of Oxford, University of Michigan, University of Chicago, Queen Mary University of London, Massachusetts General Hospital, Harvard University

Peter Donnelly's AcademicInfluence.com Rankings

Peter Donnelly

Mathematics

#2790

World Rank

#4233

Historical Rank

Statistics

#119

World Rank

#155

Historical Rank

Measure Theory

#377

World Rank

#556

Historical Rank

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Mathematics

Why Is Peter Donnelly Influential?

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According to Wikipedia, Sir Peter James Donnelly is an Australian-British mathematician and Professor of Statistical Science at the University of Oxford, and the CEO of Genomics PLC. He is a specialist in applied probability and has made contributions to coalescent theory. His research group at Oxford has an international reputation for the development of statistical methodology to analyze genetic data.

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Peter Donnelly's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Inference of population structure using multilocus genotype data. (2000) (30260)
A global reference for human genetic variation (2015) (11857)
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) (9208)
A new statistical method for haplotype reconstruction from population data. (2001) (7601)
An integrated map of genetic variation from 1,092 human genomes (2012) (7565)
A second generation human haplotype map of over 3.1 million SNPs (2007) (4567)
A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies (2009) (3816)
The UK Biobank resource with deep phenotyping and genomic data (2018) (3653)
A comparison of bayesian methods for haplotype reconstruction from population genotype data. (2003) (3589)
A new multipoint method for genome-wide association studies by imputation of genotypes (2007) (2639)
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (2011) (2511)
Association mapping in structured populations. (2000) (1906)
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) (1839)
Transcriptome and genome sequencing uncovers functional variation in humans (2013) (1758)
Genome-wide association study identifies five new schizophrenia loci (2011) (1680)
Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) (1455)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007) (1421)
Replicating genotype–phenotype associations (2007) (1367)
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis (2013) (1170)
A Fine-Scale Map of Recombination Rates and Hotspots Across the Human Genome (2005) (1118)
Genome-wide strategies for detecting multiple loci that influence complex diseases (2005) (962)
The Fine-Scale Structure of Recombination Rate Variation in the Human Genome (2004) (961)
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 (2010) (947)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
The genetic architecture of type 2 diabetes (2016) (927)
Inferring coalescence times from DNA sequence data. (1997) (925)
The effects of human population structure on large genetic association studies (2004) (886)
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility (2011) (807)
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci (2013) (689)
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease (2011) (638)
Genome-wide genetic data on ~500,000 UK Biobank participants (2017) (630)
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (600)
Drive Against Hotspot Motifs in Primates Implicates the PRDM9 Gene in Meiotic Recombination (2010) (598)
Designing Genome-Wide Association Studies: Sample Size, Power, Imputation, and the Choice of Genotyping Chip (2009) (594)
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility (2019) (589)
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity (2012) (555)
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) (547)
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas (2013) (519)
MARKOV PROCESSES Characterization and Convergence (Wiley Series in Probability and Mathematical Statistics) (1987) (519)
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region (2009) (513)
Germline mutations in the proof-reading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas (2012) (487)
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (465)
A common sequence motif associated with recombination hot spots and genome instability in humans (2008) (440)
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction (2014) (426)
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes (2010) (421)
Bayesian refinement of association signals for 14 loci in 3 common diseases (2012) (416)
Case-control studies of association in structured or admixed populations. (2001) (406)
Genome-wide and fine-resolution association analysis of malaria in West Africa (2009) (394)
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke (2012) (392)
Coalescents and genealogical structure under neutrality. (1995) (390)
Progress and challenges in genome-wide association studies in humans (2008) (385)
The fine-scale genetic structure of the British population (2015) (376)
Comparison of Fine-Scale Recombination Rates in Humans and Chimpanzees (2005) (375)
Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (2015) (349)
A comparison of phasing algorithms for trios and unrelated individuals. (2006) (337)
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders (2015) (319)
New models of collaboration in genome-wide association studies: the Genetic Association Information Network (2007) (313)
Inference in molecular population genetics (2000) (310)
HAPGEN2: simulation of multiple disease SNPs (2011) (287)
Particle Representations for Measure-Valued Population Models (1999) (274)
The Influence of Recombination on Human Genetic Diversity (2006) (270)
A Fine-Scale Chimpanzee Genetic Map from Population Sequencing (2012) (265)
Class II HLA interactions modulate genetic risk for multiple sclerosis (2015) (262)
Evolutionary dynamics of Staphylococcus aureus during progression from carriage to disease (2012) (259)
A pilot study of rapid benchtop sequencing of Staphylococcus aureus and Clostridium difficile for outbreak detection and surveillance (2012) (258)
Multiple Instances of Ancient Balancing Selection Shared Between Humans and Chimpanzees (2013) (253)
The ages of alleles and a coalescent (1986) (249)
The mutation rate in the human mtDNA control region. (2000) (236)
Assessing population differentiation and isolation from single‐nucleotide polymorphism data (2002) (234)
Pairwise comparisons of mitochondrial DNA sequences in subdivided populations and implications for early human evolution. (1994) (231)
Effect of predicted protein-truncating genetic variants on the human transcriptome (2015) (226)
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis (2014) (218)
Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21 (2010) (215)
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer (2012) (213)
Microevolutionary analysis of Clostridium difficile genomes to investigate transmission (2012) (209)
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins (2014) (207)
Strong approximations for epidemic models (1995) (203)
Estimating recombination rates from population genetic data. (2001) (193)
Human recombination hot spots hidden in regions of strong marker association (2005) (191)
A statistical method for predicting classical HLA alleles from SNP data. (2008) (183)
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett’s esophagus (2012) (176)
A countable representation of the Fleming-Viot measure-valued diffusion (1996) (175)
Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice (2016) (173)
Choice of transcripts and software has a large effect on variant annotation (2014) (166)
Is Mate Choice in Humans MHC-Dependent? (2008) (165)
The coalescent process with selfing. (1997) (161)
Heterogeneity of microsatellite mutations within and between loci, and implications for human demographic histories. (1998) (156)
Optimal sequencing strategies for surveying molecular genetic diversity. (1996) (152)
Recombination and Population Structure in Salmonella enterica (2011) (151)
Human metabolic profiles are stably controlled by genetic and environmental variation (2011) (151)
Progress and promise in understanding the genetic basis of common diseases (2015) (150)
Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction (2014) (147)
Genealogical processes for Fleming-Viot models with selection and recombination (1999) (140)
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype (2008) (135)
Presynaptic NMDARs in the Hippocampus Facilitate Transmitter Release at Theta Frequency (2010) (133)
A Genome-Wide Metabolic QTL Analysis in Europeans Implicates Two Loci Shaped by Recent Positive Selection (2011) (129)
Sequencing of human genomes with nanopore technology (2019) (129)
Efficient computation with a linear mixed model on large-scale data sets with applications to genetic studies (2012) (128)
Superfamilies of Evolved and Designed Networks (2004) (127)
Including known covariates can reduce power to detect genetic effects in case-control studies (2012) (120)
Genome Sequencing of an Extended Series of NDM-Producing Klebsiella pneumoniae Isolates from Neonatal Infections in a Nepali Hospital Characterizes the Extent of Community- versus Hospital-Associated Transmission in an Endemic Setting (2014) (116)
Approximate likelihood methods for estimating local recombination rates (2002) (115)
Congenital myasthenic syndromes due to mutations in ALG2 and ALG14 (2013) (114)
Partition structures, Polya urns, the Ewens sampling formula, and the ages of alleles. (1986) (110)
Pneumococcal genome sequencing tracks a vaccine escape variant formed through a multi-fragment recombination event (2012) (109)
Progress in population genetics and human evolution (1997) (109)
Multiple novel gene-by-environment interactions modify the effect of FTO variants on body mass index (2016) (106)
People of the British Isles: preliminary analysis of genotypes and surnames in a UK-control population (2011) (105)
Phenome-wide association studies across large population cohorts support drug target validation (2018) (105)
A Reassessment of Genetic Diversity in Icelanders: Strong Evidence from Multiple Loci for Relative Homogeneity Caused by Genetic Drift (2003) (104)
Common variants in the HLA-DRB1-HLA-DQA1 Class II region are associated with susceptibility to visceral leishmaniasis (2013) (97)
Inference in Forensic Identification (1995) (97)
Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden (2014) (95)
The distribution and causes of meiotic recombination in the human genome. (2006) (94)
Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
Recessive Mutations in SPTBN2 Implicate β-III Spectrin in Both Cognitive and Motor Development (2012) (90)
High recombination rate in herpes simplex virus type 1 natural populations suggests significant co-infection. (2004) (88)
The correlation between reading and mathematics ability at age twelve has a substantial genetic component (2014) (87)
Assessing allele-specific expression across multiple tissues from RNA-seq read data (2015) (80)
Conditional genealogies and the age of a neutral mutant. (1999) (78)
Finite particle systems and infection models (1983) (78)
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process (2014) (75)
Evaluating DNA profile evidence when the suspect is identified through a database search. (1996) (75)
On the asymptotic distribution of large prime factors (1993) (72)
Application of Coalescent Methods to Reveal Fine-Scale Rate Variation and Recombination Hotspots (2004) (69)
Continuity and weak convergence of ranked and size-biased permutations on the infinite simplex (1989) (69)
A robust clustering algorithm for identifying problematic samples in genome-wide association studies (2011) (68)
Genomic Tools for Evolution and Conservation in the Chimpanzee: Pan troglodytes ellioti Is a Genetically Distinct Population (2012) (66)
Factors influencing meiotic recombination revealed by whole-genome sequencing of single sperm (2019) (66)
Recombination in the Human Pseudoautosomal Region PAR1 (2014) (65)
Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I (2013) (64)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (61)
Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula (2018) (59)
Platypus and echidna genomes reveal mammalian biology and evolution (2021) (56)
Bayesian analysis of genetic association across tree-structured routine healthcare data in the UK Biobank (2017) (53)
Estimating the Age of the Common Ancestor of Men from the ZFY Intron (1996) (49)
Dissection of the genetics of Parkinson ’ s disease identifies an additional association 5 ′ of SNCA and multiple associated haplotypes at 17 q 21 The UK Parkinson ’ s Disease Consortium and The Wellcome Trust Case Control Consortium 2 (2010) (48)
The transient behaviour of the Moran model in population genetics (1984) (47)
DNA database searches and the legal consumption of scientific evidence. (1999) (46)
A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation (2014) (46)
Inferring identify from DNA profile evidence. (1995) (45)
Quantifying the Underestimation of Relative Risks from Genome-Wide Association Studies (2011) (44)
The Configuration of RPA, RAD51, and DMC1 Binding in Meiosis Reveals the Nature of Critical Recombination Intermediates (2020) (43)
Identifying loci affecting trait variability and detecting interactions in genome-wide association studies (2018) (43)
A new multipoint method for genome-wide association studies via imputation of genotypes : Supplementary Methods (2007) (43)
Consistent ordered sampling distributions : characterization and convergence (1991) (43)
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
Gene-gene interactions in breast cancer susceptibility. (2012) (42)
Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children (2016) (41)
The heaps process, libraries, and size-biased permutations (1991) (40)
Integrated Polygenic Tool Substantially Enhances Coronary Artery Disease Prediction (2021) (39)
Nonindependence of matches at different loci in DNA profiles: quantifying the effect of close relatives on the match probability (1995) (39)
Erythrocytosis associated with a novel missense mutation in the BPGM gene (2010) (37)
Ancestral Inference in Population Genetics Models with Selection (with Discussion) (2003) (37)
CONTINUUM-SITES STEPPING-STONE MODELS, COALESCING EXCHANGEABLE PARTITIONS AND RANDOM TREES (1998) (35)
Genes, fossils and behaviour : an integrated approach to human evolution (2001) (35)
The population genealogy of the infinitely-many neutral alleles model (1987) (35)
Likelihoods and simulation methods for a class of nonneutral population genetics models. (2001) (35)
Microsatellite mutations and inferences about human demography. (2000) (35)
Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus (2013) (35)
Congenital myasthenic syndromes due to mutations in ALG 2 and ALG 14 (2013) (34)
WEAK CONVERGENCE TO A MARKOV CHAIN WITH AN ENTRANCE BOUNDARY: ANCESTRAL PROCESSES IN POPULATION GENETICS' (1991) (34)
Disease Model Distortion in Association Studies (2011) (34)
THE PROSECUTORS FALLACY AND DNA EVIDENCE (1994) (33)
Practical Use of Methods for Imputation of HLA Alleles from SNP Genotype Data (2016) (32)
A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
Long-read whole genome sequencing and comparative analysis of six strains of the human pathogen Orientia tsutsugamushi (2018) (30)
A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability (2017) (29)
Replicating genotype – phenotype associations What constitutes replication of a genotype – phenotype association , and how best can it be achieved ? (2007) (29)
Multicohort analysis of the maternal age effect on recombination (2015) (28)
Interpreting genetic variability: the effects of shared evolutionary history. (1996) (27)
Quantum operators in classical probability theory: I. “Quantum spin” techniques and the exclusion model of diffusion (1996) (25)
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment (2014) (25)
MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls (2017) (24)
The correlation structure of epidemic models. (1993) (23)
Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries. (2021) (23)
How convincing is DNA evidence? (1994) (23)
Insights into Platypus Population Structure and History from Whole-Genome Sequencing (2017) (23)
Patterns of Eurasian HSV-1 molecular diversity and inferences of human migrations. (2006) (22)
A Bayesian Method for Detecting and Characterizing Allelic Heterogeneity and Boosting Signals in Genome-Wide Association Studies (2009) (22)
Discussion on the meeting on ‘Statistical modelling and analysis of genetic data’ (2002) (21)
Reply to Zhang et al. (2001) (21)
Approach to Stationarity of the Bernoulli–Laplace Diffusion Model (1994) (20)
THE INAUGURAL EDITOR'S INVITED PAPER FOR 2002 ANCESTRAL INFERENCE IN POPULATION GENETICS MODELS WITH SELECTION (2003) (19)
Appealing statistics (2005) (19)
Dual processes in population genetics (1986) (19)
A genealogical approach to variable-population-size models in population genetics (1986) (18)
On conditional intensities and on interparticle correlation in non-linear death processes (1993) (17)
CONSTANT PREDATOR-PREY RATIOS: AN ARITHMETICAL ARTIFACT? (1993) (17)
The role of ATM in response to metformin treatment and activation of AMPK. (2012) (17)
Bayesian hierarchical mixture modeling to assign copy number from a targeted CNV array (2011) (17)
On the Functional Central Limit Theorem for the Ewens Sampling Formula (1991) (16)
The Wright-Fisher model with temporally varying selection and population size (1985) (16)
Interparticle correlation in death processes with application to variability in compartmental models (1987) (16)
Comment: Some causes for concern about DNA profiles (1994) (16)
UK Biobank release and systematic evaluation of optimised polygenic risk scores for 53 diseases and quantitative traits (2022) (15)
Experiments with the Site Frequency Spectrum (2011) (15)
Assessing association between protein truncating variants and quantitative traits (2013) (14)
The asymptotic behavior of an urn model arising in population genetics (1996) (14)
ZCWPW1 is recruited to recombination hotspots by PRDM9, and is essential for meiotic double strand break repair (2019) (14)
Discussion: Recent Common Ancestors of all Present-Day Individuals (1999) (14)
Making Sense of the Data (2011) (13)
Branching Process Approximation of Epidemic Models (1993) (13)
Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073 (2010) (13)
A ‘‘Candidate-Interactome’’ Aggregate Analysis of Genome-Wide Association Data in Multiple Sclerosis (2013) (12)
Where Next for Genetics and Genomics? (2015) (11)
A model-based approach to capture genetic variation for future association studies. (2006) (11)
Probability and Proof in State v. Skipper: An Internet Exchange (1995) (11)
On the stochastic approach to cluster size distribution during particle coagulation. I. Asymptotic expansion in the deterministic limit (1993) (11)
An integrated polygenic and clinical risk tool enhances coronary artery disease prediction (2020) (9)
Convergence to stationarity in the Moran model (2000) (9)
Phenome-wide association studies (PheWAS) across large “real-world data” population cohorts support drug target validation (2017) (9)
Zhou et al. reply (2012) (8)
Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease (2012) (8)
ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair (2020) (8)
A unified approach to variability in compartmental models (1988) (8)
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype [Corrigendum] (2010) (7)
Correlation and variability in birth processes (1993) (7)
Weak Convergence of Population Genealogical Processes to the Coalescent with Ages (1992) (7)
Genotyping and population structure of the China Kadoorie Biobank (2022) (7)
The coalescent and its descendants (2010) (6)
Genomic control to the extreme - Reply (2004) (6)
Review: Alan F. Karr, Point Processes and their Statistical Inference (1987) (5)
Bayesian analysis of DNA profiling data in forensic identification applications - Discussion (1997) (5)
Reply to "Genomic Control to the extreme" (2004) (5)
Do Eve's alleles live on? (1992) (5)
Reply to Pembrey et al: ‘ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis' (2014) (5)
Reply to "Comment on 'Nodal infection in Markovian susceptible-infected-susceptible and susceptible-infected-removed epidemics on networks are non-negatively correlated' ". (2018) (5)
Particle representations for measure-valued population models 1 June 1 , 1998 (1998) (4)
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
[The Growth and Stabilization of Populations]: Comment (1991) (4)
The effect on genetic sampling distributions of correlations in reproduction (1989) (4)
Germline mutations in the proofreading domains of POLE and POLD 1 predispose to colorectal adenomas and carcinomas (4)
Stochastic modelling and inference in electronic hospital databases for the spread of infections: Clostridium difficile transmission in Oxfordshire hospitals 2007-2010. (2017) (3)
On reinforcement-depletion compartmental urn models (1989) (3)
Altering the Binding Properties of PRDM9 Partially Restores Fertility across the Species Boundary (2021) (3)
Coalescent experiments I: Unlabeled n-coalescent and the site frequency spectrum (2009) (2)
Assessing allele specific expression across multiple tissues from RNA-seq read data (2014) (2)
Modelling genes: mathematical and statistical challenges in genomics (2006) (2)
Alu insertion polymorphisms in humans: A review (2001) (2)
Match probability calculations for multi-locus DNA profiles (2005) (2)
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (2019) (2)
Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula (2019) (2)
A genealogical description of the infinitely-many neutral alleles model (1987) (1)
Kingman's unlabelled n-coalescent (2008) (1)
Approximation, Comparison, and Bayesian Reasoning in Juridical Proof (1997) (1)
Assessing population structure and its effects on association studies in a genome wide SNP dataset. (2002) (1)
Consistent ordered sampling distributions: characterization and convergence (1991) (1)
Choice of transcripts and software has a large effect on variant annotation (2014) (1)
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (2018) (0)
A model-based approach to capture genetic variation for future Material Supplemental (2006) (0)
Edinburgh Research Explorer Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer (2018) (0)
BIOINFORMATICS A robust clustering algorithm for identifying problematic samples in genome-wide association studies (2011) (0)
APPROACH TO STATIONARITY OF THE BERNOULLI (1994) (0)
Abstract 11316: Analytical Validation for an Integrated Risk Tool for Cardiovascular Disease Combining Conventional Risk Factors and Polygenic Risk Inferred from Snp Array and Low-Pass Whole Genome Sequencing (2021) (0)
Reprogramming meiotic recombination in the mouse (2014) (0)
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (2019) (0)
Bayesian Methods for Statistical Reconstruction of Haplotypes (2002) (0)
Genomic analysis of sporadic neurological disease using family trios: learning to expect the unexpected (2012) (0)
Identifying loci affecting trait variability and detecting interactions in genome-wide association studies (2018) (0)
Talk in ASHG 2008 Philadelphia PA (2008) (0)
A Greedy Homotopy Method for Regression with Nonconvex Constraints (2014) (0)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (0)
University of Dundee Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children Rautanen, (2017) (0)
Haplotype phase inference (2004) (0)
Evolutionary modeling in haplotype analysis (2005) (0)
Rare loss of function variants in candidate genes and risk of colorectal cancer (2018) (0)
Bayesian and frequentist methods and analyses of genome-wide association studies (2009) (0)
Labellings, size-biased permutations and the GEM distribution (1992) (0)
Author response: ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair (2020) (0)
Estimating the Age of the Common Ancestor of Men from the ZFY Intron (1996) (0)
Phenome-wide association studies across large population cohorts support drug target validation (2018) (0)
Mathematical and statistical aspects of DNA and protein sequence analysis - Preface (1994) (0)
STOCHASTIC MODELLING AND INFERENCE IN ELECTRONIC HOSPITAL DATABASES FOR THE SPREAD OF INFECTIONS: CLOSTRIDIUM DIFFICILE TRANSMISSION IN OXFORDSHIRE HOSPITALS 2007–2010 1 (2017) (0)
Recombination in the human pseudoautosomal region PAR 1 Text S 1 (2014) (0)
Genetic Clues to Dispersal in Human Populations: Retracing the Past from the Present (2001) (0)
Versus Hospital-associated Transmission in an Endemic Setting 3 4 (2014) (0)
Sequencing of human genomes with nanopore technology (2019) (0)
DNA as Evidence: Viewing Science through the Prism of the Law (2000) (0)

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