David Balding

Q: What Schools Are Affiliated With David Balding

David Balding is affiliated with the following schools: Imperial College London, University College London, University of Oxford, University of Melbourne, Queen Mary University of London, University of Reading

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David Balding

Mathematics

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#8028

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Statistics

#441

World Rank

#512

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Why Is David Balding Influential?

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According to Wikipedia, David Balding is Professor of Statistical Genetics at the University of Melbourne, and Director of Melbourne Integrative Genomics , having previously been the founding senior appointment at the UCL Genetics Institute in London. He was educated at the University of Newcastle, Australia, and the University of Oxford, UK, and is editor of the Handbook of Statistical Genetics.

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David Balding'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

A genome-wide association study identifies novel risk loci for type 2 diabetes (2007) (2994)
Approximate Bayesian computation in population genetics. (2002) (2720)
A tutorial on statistical methods for population association studies (2006) (1429)
Epigenome-wide association studies for common human diseases (2011) (1163)
Identifying adaptive genetic divergence among populations from genome scans (2004) (1022)
Inferring coalescence times from DNA sequence data. (1997) (925)
Inferring population history with DIY ABC: a user-friendly approach to approximate Bayesian computation (2008) (693)
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations (2009) (653)
Improved heritability estimation from genome-wide SNPs. (2012) (612)
Handbook of statistical genetics (2004) (585)
Assessment of cumulative evidence on genetic associations: interim guidelines. (2008) (559)
Common genetic variation near MC4R is associated with waist circumference and insulin resistance (2008) (523)
Bayesian statistical methods for genetic association studies (2009) (488)
Population Structure and Cryptic Relatedness in Genetic Association Studies (2009) (434)
A method for quantifying differentiation between populations at multi-allelic loci and its implications for investigating identity and paternity (2005) (422)
Re-evaluation of SNP heritability in complex human traits (2016) (371)
Simultaneous Analysis of All SNPs in Genome-Wide and Re-Sequencing Association Studies (2008) (344)
Admixture in Latin America: Geographic Structure, Phenotypic Diversity and Self-Perception of Ancestry Based on 7,342 Individuals (2014) (326)
Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots (2003) (289)
Genealogical inference from microsatellite data. (1998) (278)
Genome-wide association mapping to candidate polymorphism resolution in the unsequenced barley genome (2010) (255)
Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities (2003) (252)
MultiBLUP: improved SNP-based prediction for complex traits (2014) (232)
Patterns of human diversity, within and among continents, inferred from biallelic DNA polymorphisms. (2002) (229)
Relatedness in the post-genomic era: is it still useful? (2014) (227)
Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies (2014) (222)
Genome‐wide significance for dense SNP and resequencing data (2008) (218)
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies (2018) (213)
A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order. (2011) (211)
Interpreting low template DNA profiles. (2009) (192)
Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool. (2012) (177)
In defence of model‐based inference in phylogeography (2010) (170)
On Optimal Selection of Summary Statistics for Approximate Bayesian Computation (2010) (165)
A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation (2016) (158)
Likelihood-based inference for genetic correlation coefficients. (2003) (156)
Identification of the remains of King Richard III (2014) (153)
The genomic and phenotypic diversity of Schizosaccharomyces pombe (2015) (152)
Pathway Analysis of GWAS Provides New Insights into Genetic Susceptibility to 3 Inflammatory Diseases (2009) (152)
Evidence for a Common Origin of Blacksmiths and Cultivators in the Ethiopian Ari within the Last 4500 Years: Lessons for Clustering-Based Inference (2015) (148)
Population Structure and Inbreeding From Pedigree Analysis of Purebred Dogs (2008) (146)
SumHer better estimates the SNP heritability of complex traits from summary statistics (2018) (145)
A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features (2016) (142)
Analyses of infectious disease data from household outbreaks by Markov chain Monte Carlo methods (2000) (141)
Fine-scale mapping of disease loci via shattered coalescent modeling of genealogies. (2002) (137)
Weight-of-Evidence for Forensic DNA Profiles (2005) (133)
A Genome-Wide Association Study of the Metabolic Syndrome in Indian Asian Men (2010) (133)
Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation (2017) (131)
AIP mutation in pituitary adenomas in the 18th century and today. (2011) (127)
Logistic regression protects against population structure in genetic association studies. (2005) (120)
Sequence-Level Population Simulations Over Large Genomic Regions (2007) (118)
Uricotelism and Low Evaporative Water Loss in a South American Frog (1972) (112)
A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia (2019) (108)
Bayesian fine-scale mapping of disease loci, by hidden Markov models. (2000) (104)
Common Genetic Variation Near Melatonin Receptor MTNR1B Contributes to Raised Plasma Glucose and Increased Risk of Type 2 Diabetes Among Indian Asians and European Caucasians (2009) (103)
Latin Americans show wide-spread Converso ancestry and imprint of local Native ancestry on physical appearance (2018) (101)
A Comparative Survey of Non-Adaptive Pooling Designs (1996) (100)
PopABC: a program to infer historical demographic parameters (2009) (100)
Gametic phase estimation over large genomic regions using an adaptive window approach (2003) (98)
Inference in Forensic Identification (1995) (97)
Using Genetic Distance to Infer the Accuracy of Genomic Prediction (2015) (91)
Evaluating and improving heritability models using summary statistics (2019) (89)
A Genome-Wide Association Study of Neuroticism in a Population-Based Sample (2010) (88)
Genetic screening for Niemann–Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM study (2013) (85)
Applying association mapping and genomic selection to the dissection of key traits in elite European wheat (2014) (82)
Describing the genetic architecture of epilepsy through heritability analysis (2014) (82)
Statistical Evaluation of Forensic DNA Profile Evidence (2014) (81)
Fregene: Simulation of realistic sequence-level data in populations and ascertained samples (2008) (80)
Evaluation of mixed-source, low-template DNA profiles in forensic science (2013) (80)
Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study (2006) (79)
Confounding between recombination and selection, and the Ped/Pop method for detecting selection. (2008) (79)
Genetic association of the major histocompatibility complex with rheumatoid arthritis implicates two non-DRB1 loci. (2009) (79)
Measuring departures from Hardy–Weinberg: a Markov chain Monte Carlo method for estimating the inbreeding coefficient (1998) (79)
Little loss of information due to unknown phase for fine-scale linkage-disequilibrium mapping with single-nucleotide-polymorphism genotype data. (2004) (79)
Models of sequence evolution for DNA sequences containing gaps. (2001) (78)
Evaluating forensic DNA profiles using peak heights, allowing for multiple donors, allelic dropout and stutters. (2013) (78)
Multiple Quantitative Trait Analysis Using Bayesian Networks (2014) (76)
Evaluating DNA profile evidence when the suspect is identified through a database search. (1996) (75)
A method for quantifying differentiation between populations at multi-allelic loci and its implications for investigating identity and paternity (2008) (74)
Storytelling and story testing in domestication (2014) (72)
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. (2012) (71)
A genome-wide association study identifies multiple loci for variation in human ear morphology (2015) (70)
Structured Regularizers for High-Dimensional Problems : Statistical and Computational Issues (2014) (70)
Significant genetic correlations among Caucasians at forensic DNA loci (1997) (68)
Bayesian Networks and Probabilistic Inference in Forensic Science (2011) (64)
Exon sequencing and high resolution haplotype analysis of ABC transporter genes implicated in drug resistance (2006) (62)
Effects of population structure on DNA fingerprint analysis in forensic science (1991) (59)
Estimating Products in Forensic Identification Using DNA Profiles (1995) (57)
Optimal Pooling Designs with Error Detection (1994) (56)
Genetic Policing: The Use of DNA in Criminal Investigations (2009) (56)
When can a DNA profile be regarded as unique? (1999) (55)
cnvHap: an integrative population and haplotype–based multiplatform model of SNPs and CNVs (2010) (50)
Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach (2007) (49)
Estimating the Age of the Common Ancestor of Men from the ZFY Intron (1996) (49)
Mapping of Interactions in the Pitch Memory Store (2004) (47)
Inferring identify from DNA profile evidence. (1995) (45)
Variation in estimated recombination rates across human populations (2007) (43)
Heritability and genetic correlations of insulin resistance and component phenotypes in Asian Indian families using a multivariate analysis (2009) (40)
Mixed methods (2020) (38)
Functional constraint and small insertions and deletions in the ENCODE regions of the human genome (2007) (37)
How convincing is a matching Y-chromosome profile? (2017) (36)
Inferring combined CNV/SNP haplotypes from genotype data (2010) (35)
Worldwide Estimates Relative to Five Continental-Scale Populations (2014) (35)
Handbook of Statistical Genetics: Balding/Handbook of Statistical Genetics, Third Edition (2007) (35)
A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy. (2014) (35)
The DN A Database Search Controversy (2002) (34)
Multipoint linkage-disequilibrium mapping narrows location interval and identifies mutation heterogeneity (2003) (32)
Statistical analysis of DNA fingerprint data for ordered clone physical mapping of human chromosomes. (1991) (31)
Inference of haplotypic phase and missing genotypes in polyploid organisms and variable copy number genomic regions (2008) (31)
Population genetics of STR loci in Caucasians (2006) (30)
Disease association tests by inferring ancestral haplotypes using a hidden markov model (2008) (29)
A Comment on the PCAST Report: Skip the 'Match'/'Non-Match' Stage (2016) (27)
Evaluation of low-template DNA profiles using peak heights (2016) (27)
Measuring gametic disequilibrium from multilocus data. (2001) (26)
The design of pooling experiments for screening a clone map. (1997) (26)
Increased Population Risk of AIP‐Related Acromegaly and Gigantism in Ireland (2016) (25)
Risk factors and heart disease mortality: A regional perspective (1986) (25)
Improving the efficiency of genomic selection (2013) (24)
How convincing is DNA evidence? (1994) (23)
A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation (2021) (23)
Handbook of Statistical Genetics: Third Edition (2008) (23)
Verifying likelihoods for low template DNA profiles using multiple replicates (2014) (23)
Limit theorems for sequences of random trees (2004) (22)
Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicity (2015) (22)
Discrimination of half-siblings when maternal genotypes are known. (2006) (21)
Implications for DNA identification arising from an analysis of Australian forensic databases. (2002) (21)
Decision-making in familial database searching: KI alone or not alone? (2013) (21)
Interaction between gas cooking and GSTM1 null genotype in bronchial responsiveness: results from the European Community Respiratory Health Survey (2014) (21)
Weight-of-Evidence for Forensic DNA Profiles: Balding/Weight-of-Evidence for Forensic DNA Profiles (2015) (21)
Discussion on the meeting on ‘Statistical modelling and analysis of genetic data’ (2002) (21)
A comparison of software for the evaluation of complex DNA profiles. (2019) (20)
Interpreting DNA Evidence: Can Probability Theory Help? (2000) (20)
Choice of population database for forensic DNA profile analysis (2014) (19)
The association between polymorphisms in RLIP76 and drug response in epilepsy. (2007) (18)
Better estimation of SNP heritability from summary statistics provides a new understanding of the genetic architecture of complex traits (2018) (18)
How many individuals share a mitochondrial genome? (2018) (18)
Multiple single nucleotide polymorphism analysis using penalized regression in nonlinear mixed-effect pharmacokinetic models (2013) (17)
Fine-scale Mapping (2004) (17)
Comment: Some causes for concern about DNA profiles (1994) (16)
Response to Lee et al.: SNP-based heritability analysis with dense data. (2013) (16)
Dysregulation of Complement System and CD4+ T Cell Activation Pathways Implicated in Allergic Response (2013) (15)
Handbook of Statistical Systems Biology: Stumpf/Handbook of Statistical Systems Biology (2011) (15)
Apolipoprotein E, CI and B Gene Polymorphisms in a Sample of Patients with Coronary Heart Disease in the Kuwaiti Population (2009) (14)
Diffusion-reaction in one dimension (1988) (14)
Integrated analysis of genome-wide genetic and epigenetic association data for identification of disease mechanisms (2013) (14)
Handbook of Statistical Systems Biology (2011) (13)
Clustering of protein domains in the human genome. (2004) (13)
Y-profile evidence: Close paternal relatives and mixtures. (2019) (12)
In-frame seven amino-acid duplication in AIP arose over the last 3000 years, disrupts protein interaction and stability and is associated with gigantism (2017) (12)
Probability and Proof in State v. Skipper: An Internet Exchange (1995) (11)
Comment on: Why the effect of prior odds should accompany the likelihood ratio when reporting DNA evidence (2004) (11)
Invasion processes and binary annihilation in one dimension (1988) (11)
Family‐based association analysis with ordered categorical phenotypes, covariates and interactions (2007) (11)
Review of: Forensic DNA Evidence Interpretation (2005) (10)
Disentangling Signatures of Selection Before and After European Colonization in Latin Americans (2021) (9)
Using League Table Rankings in Public Policy Formation : Statistical Issues (2014) (9)
Introduction to population genetics 1: single locus (2004) (8)
Summary statistic analyses can mistake confounding bias for heritability (2019) (8)
MAC5: Bayesian inference of phylogenetic trees from DNA sequences incorporating gaps (2001) (8)
Paternity index calculations when some individuals share common ancestry. (2005) (7)
Assessing the Forensic Value of DNA Evidence from Y Chromosomes and Mitogenomes (2021) (6)
Evaluating DNA evidence in a genetically complex population. (2018) (6)
Genome‐wide association mapping of Hagberg falling number, protein content, test weight, and grain yield in U.K. wheat (2021) (5)
Genetic and isotopic analysis and the UK Border Agency (2010) (5)
GWAlpha: genome‐wide estimation of additive effects (alpha) based on trait quantile distribution from pool‐sequencing experiments (2016) (5)
Including diverse and admixed populations in genetic epidemiology research (2022) (5)
SNP‐based heritability and selection analyses: Improved models and new results (2022) (5)
Exposing flaws in S-LDSC; reply to Gazal et al. (2018) (5)
A general framework for moment-based analysis of genetic data (2019) (5)
Comprar Handbook of Statistical Genetics | Martin Bishop | 9780470058305 | Wiley (2007) (5)
Worldwide F ST Estimates Relative to Five Continental-Scale Populations (2014) (5)
Inference in complex systems (2011) (5)
Integrating dynamic mixed-effect modelling and penalized regression to explore genetic association with pharmacokinetics (2015) (4)
Statistical analysis of DNA fingerprint data for ordered clone physical mapping of human chromosomes (1991) (4)
The impact of low-cost, genome-wide resequencing on association studies. (2005) (4)
How can courts take into account the uncertainty in a likelihood ratio? (2020) (4)
A genome‐wide association study identifies novel gene associations with facial skin wrinkling and mole count in Latin Americans (2021) (4)
Prediction of eye, hair and skin colour in Latin Americans. (2021) (4)
A Simulation Approach for Change-Points on Phylogenetic Trees (2014) (3)
Using common genetic variants to find drugs for common epilepsies (2021) (3)
Multiple Quantitative Trait Analysis Using (2014) (3)
Admixture provides new insights into recombination (2011) (3)
Fine‐scale mapping of disease loci (2000) (3)
Comprar Handbook Of Statistical Systems Biology | Michael P. H. Stumpf | 9780470710869 | Wiley (2011) (3)
Genome-wide association, prediction and heritability in bacteria with application to Streptococcus pneumoniae (2022) (3)
Understanding complex traits: from farmers to pharmas (2012) (3)
Bayesian inference of ancestral recombination graphs (2022) (3)
Interpreting DNA evidence: statistical genetics for forensic scientists. By I. W. EVETT and B. S. WEIR. Sinauer Associates Inc. 1998. ISBN 0 87893 155 4. 278 pages. Price £25.95. (1999) (3)
Encoding of low-quality DNA profiles as genotype probability matrices for improved profile comparisons, relatedness evaluation and database searches. (2016) (3)
ZOOM: a genetic screening study of Niemann-Pick disease type C in adults with neurological and psychiatric signs (2011) (3)
A high density genome-wide association study identifies novel susceptibility genes for type 2 diabetes mellitus and reveals new mechanisms for glucose intolerance (2007) (2)
DISCUSSION OF THE PAPER (1993) (2)
RETRACTED ARTICLE: Design of an efficient and complete elicitation decision process in contingent valuation method (2019) (2)
Optimizing sampling design and sequencing strategy for the genomic analysis of quantitative traits in natural populations (2021) (2)
Genome-wide association, prediction and heritability in bacteria (2021) (2)
Summary statistic analyses do not correct confounding bias (2019) (2)
Editorial (2005) (2)
Bridging trees for posterior inference on ancestral recombination graphs (2018) (2)
Reply: On the value of haplotype-based genotype–phenotype analysis and on data transformation in pharmacogenetics and -genomics (2007) (2)
LDAK-GBAT: fast and powerful gene-based association testing using summary statistics (2022) (1)
Retraction of a peer reviewed article suggests ongoing problems with Australian forensic science (2021) (1)
The Rise and Fall of BritainsDNA: A Tale of Misleading Claims, Media Manipulation and Threats to Academic Freedom (2018) (1)
Interpretation of DNA evidence as a paradigm for speaker recognition (2010) (1)
Latin Americans show wide-spread Converso ancestry and imprint of local Native ancestry on physical appearance (2018) (1)
Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicity (2015) (1)
Sequence-level population genomic simulations (2005) (1)
Prediction of Eye, Hair and Skin Color in Admixed Populations of Latin America (2020) (1)
Confounding between recombination and selection, and a novel genome-wide method for detecting selection (2007) (1)
SumHer better estimates the SNP heritability of complex traits from summary statistics (2018) (1)
School of Mathematical Sciences , Queen Mary and Westfield College , Mile End Road , London , El 4 NS , United Kingdom (2006) (1)
Invited Speaker: Evaluation of low-copy number forensic DNA profiles (2012) (0)
Using haplotype clustering techniques to perform genome-wide disease association studies (2007) (0)
The interplay between recombination and selection can confound their inference from population data - But suggests a novel genome-wide method for detecting selection (2007) (0)
Coalescent-based LD fine-mapping narrows location interval and identifies mutation heterogeneity. (2003) (0)
A shrinkage regression approach to tackle the HLA region (2007) (0)
Estimating the Age of the Common Ancestor of Men from the ZFY Intron (1996) (0)
A spatial clustering approach to fine-mapping of disease genes (2005) (0)
Introduction to population genetics 2: linkage disequilibrium (2004) (0)
A question of identity (2005) (0)
ZOOM: Observational genetic screening study of Niemann-Pick Disease Type C in adults with neurological and psychiatric signs (2011) (0)
Forensic Genetics Module Evaluating DNA evidence (2016) (0)
Inferences of identity (2015) (0)
Featuring a collection of papers on forensic statistics - Introduction (2003) (0)
Crime on An Island (2009) (0)
Inference in complex systems INTRODUCTION (2011) (0)
Probabilistic evaluation of low-quality DNA profiles (2016) (0)
Evaluating and improving heritability models using summary statistics (2020) (0)
Y-profile evidence: close paternal relatives and mixtures (2018) (0)
Heritability-based models for prediction of complex traits (2015) (0)
Methods for Analysing Complex Trait GWAS Data (2019) (0)
Multiple Quantitative Trait Analysis Using Bayesian Networks A "Methods, Technology, and Resources" Article submitted to Genetics (2014) (0)
Encyclopedia of Statistical Sciences: Update Volume 1 (1998) (0)
Short Tandem Repeats: Interpretation (2009) (0)
Applying association mapping and genomic selection to the dissection of key traits in elite European wheat (2014) (0)
REFEREES (2009) (0)
Reference Author Index (2007) (0)
Genetic association studies (2009) (0)
Fast and accurate joint inference of coancestry parameters for populations and/or individuals (2022) (0)
Low‐template DNA profiles (2015) (0)
Analysing complex canine pedigrees (2008) (0)
Assessing evidence using likelihoods (2015) (0)
Probability and Statistics in Forensic Science (2014) (0)
Kinship, Heritability, and Prediction (2013) (0)
Some issues for the courtroom (2015) (0)
Adjusting for population structure in genetic association studies (2007) (0)
Bayesian shrinkage priors for detecting multiple causal variants from genome-wide association studies (2007) (0)
Holt Biology Mendels Theory Directed Answer Key (2020) (0)
Alopecia-hypogonadism-extrapyramidal disorder in a new family? A novel gene (2008) (0)
Solutions to exercises (2009) (0)
Encoding of low-quality DNA profiles as genotype probability matrices for improved profile comparisons, relatedness evalation and database searches (Vol 227, pg 239, 2016) (2017) (0)
Can Probability Theory Help (2000) (0)
Erratum to 'Encoding of low-quality DNA profiles as genotype probability matrices for improved profile comparisons, relatedness evalation and database searches'. Forensic Science International: Genetics (2016) 227-239. (2017) (0)
P.5.e.003 ZOOM: observational genetic screening study of Niemann-Pick disease type C in adults with neurological/psychiatric signs (2010) (0)
Assessing Evidence via Likelihood Ratios (2009) (0)
Understanding complex traits: from farmers to pharmas (2012) (0)
Optimising sampling design and sequencing strategy for the genomic analysis of quantitative traits in natural populations (2021) (0)
The founder R304* AIP mutation is prevalent in Irish acromegaly and gigantism patients as well as in the general population of Ireland (2015) (0)
Are Indian Asians genetically homogeneous? Implications for genetic association studies (2008) (0)
Special Issue: Modern Statistical Methods for Disease Gene Mapping (2000) (0)
A general framework for moment-based analysis of genetic data (2019) (0)
Estimating heritabilities and genetic correlations of insulin resistance and related metabolic traits in Indian families using a multivariate maximum likelihood approach (2007) (0)
Optimising sampling design for the genomic analysis of quantitative traits in natural populations (2020) (0)
DNA and the law in Italy: the experience of "the Perugia case" (2013) (0)
Issues for the Courtroom (2009) (0)
A Practical Overview on Comparison Discrete and Continuous Probability Distributions (2019) (0)
Some Population Genetics for DNA Evidence (2009) (0)
Does genetic variation in FTO account for the increased risk of obesity and type 2 diabetes in UK Indian Asians (2008) (0)
Statistical Approaches for Genome-Wide Association Studies (2008) (0)
Genetic Clues to Dispersal in Human Populations: Retracing the Past from the Present (2001) (0)
Some Annihilating Particle Systems. (1989) (0)
Other approaches to weight of evidence (2009) (0)
Challenges in Screening Rare Diseases: The ZOOM Experience (2012) (0)
A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressure. (2022) (0)
Simultaneous analysis of genome-wide SNP data (2007) (0)
Introduction (2003) (0)
Introduction to likeLTD (2015) (0)
Biomolecular Function and Evolution in the Context of the Genome Project (July to December 1998) (2014) (0)
Acknowledgement to the Reviewers (2011) (0)
DURRETT, R. Probability Models for DNA Sequence Evolution. Springer, New York, 2002. viii + 240 pp. $69.95/£52.50. ISBN 0‐387‐95435‐X. (2003) (0)
Linkage disequilibrium mapping via coalescent modelling. (2001) (0)

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