D. J. Balding
Balding, D.J.
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Balding, D. J., 1961-
Balding, David J.
Balding, David
Balding, David 1961-
Balding, David J. 1961-
VIAF ID: 100859111 (Personal)
Permalink: http://viaf.org/viaf/100859111
Preferred Forms
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Balding
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David J.
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100 1 _ ‡a Balding, D. J.
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100 1 _
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Balding, D. J.
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100 1 _ ‡a Balding, D. J.
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Balding, D. J.
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Balding, D. J.
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100 1 _ ‡a Balding, D. J. ‡d (1961- ).
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100 1 _ ‡a Balding, D. J., ‡d 1961-
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100 1 _ ‡a Balding, D.J.
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Balding, David
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100 1 _ ‡a Balding, David J
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100 1 _ ‡a Balding, David J.
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100 1 _
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Balding, David J.
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1961-
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100 1 _
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Balding, David
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1961-
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D. J. Balding
4xx's: Alternate Name Forms (13)
5xx's: Related Names (3)
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Kiama
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New South Wales
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ortg
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https://d-nb.info/standards/elementset/gnd#placeOfBirth
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Melbourne
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orts
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https://d-nb.info/standards/elementset/gnd#placeOfDeath
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University of Melbourne
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affi
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https://d-nb.info/standards/elementset/gnd#affiliation
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Affiliation
Works
| Title | Sources |
|---|---|
| Fine-scale mapping of disease loci via shattered coalescent modeling of genealogies. |
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| Functional constraint and small insertions and deletions in the ENCODE regions of the human genome |
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| Gametic phase estimation over large genomic regions using an adaptive window approach |
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| Genetic and isotopic analysis and the UK Border Agency |
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| Genetic association of the major histocompatibility complex with rheumatoid arthritis implicates two non-DRB1 loci |
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| Genome-wide association mapping to candidate polymorphism resolution in the unsequenced barley genome |
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| Genome-wide association, prediction and heritability in bacteria with application to <i>Streptococcus pneumoniae</i> |
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| Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations |
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| Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP |
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| A genome-wide association study of the metabolic syndrome in Indian Asian men |
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| Genome-wide linkage disequilibrium modeling using hierarchical latent Bayesian networksand applications. |
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| Genome-wide significance for dense SNP and resequencing data |
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| The genomic and phenotypic diversity of Schizosaccharomyces pombe |
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| GWAlpha: genome-wide estimation of additive effects (alpha) based on trait quantile distribution from pool-sequencing experiments |
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| Handbook of statistical genetics |
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| Heritability and genetic correlations of insulin resistance and component phenotypes in Asian Indian families using a multivariate analysis |
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| How convincing is a matching Y-chromosome profile? |
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| How many individuals share a mitochondrial genome? |
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| Identification of the remains of King Richard III |
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| Identifying adaptive genetic divergence among populations from genome scans. |
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| Improved heritability estimation from genome-wide SNPs |
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| Improving the efficiency of genomic selection |
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| In defence of model-based inference in phylogeography. |
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| In-frame seven amino-acid duplication in AIP arose over the last 3000 years, disrupts protein interaction and stability and is associated with gigantism |
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| Increased Population Risk of AIP-Related Acromegaly and Gigantism in Ireland |
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| Inference in complex systems |
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| Inference in Forensic Identification |
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| Inference of haplotypic phase and missing genotypes in polyploid organisms and variable copy number genomic regions |
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| Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities |
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| Inferring combined CNV/SNP haplotypes from genotype data |
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| Inferring identify from DNA profile evidence. |
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| Inferring population history with DIY ABC: a user-friendly approach to approximate Bayesian computation |
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| Integrated analysis of genome-wide genetic and epigenetic association data for identification of disease mechanisms |
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| Interaction between gas cooking and GSTM1 null genotype in bronchial responsiveness: results from the European Community Respiratory Health Survey |
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| Latin Americans show wide-spread Converso ancestry and imprint of local Native ancestry on physical appearance |
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| Likelihood-based inference for genetic correlation coefficients |
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| Limit theorems for sequences of random trees |
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| Little loss of information due to unknown phase for fine-scale linkage-disequilibrium mapping with single-nucleotide-polymorphism genotype data. |
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| MAC5: Bayesian inference of phylogenetic trees from DNA sequences incorporating gaps. |
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| A mathematical model of tumour-induced capillary growth. |
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| Measuring departures from Hardy-Weinberg: a Markov chain Monte Carlo method for estimating the inbreeding coefficient |
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| A method for quantifying differentiation between populations at multi-allelic loci and its implications for investigating identity and paternity |
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| Modélisation pangénomique du déséquilibre de liaison à l'aide de réseaux bayésiens hiérarchiques latents et applications |
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| MultiBLUP: improved SNP-based prediction for complex traits |
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| Multiple quantitative trait analysis using bayesian networks |
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| Multiple single nucleotide polymorphism analysis using penalized regression in nonlinear mixed-effect pharmacokinetic models |
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| Multipoint linkage-disequilibrium mapping narrows location interval and identifies mutation heterogeneity |
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| On Optimal Selection of Summary Statistics for Approximate Bayesian Computation |
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| Optimal Pooling Designs with Error Detection |
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| Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation |
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| Optimizing sampling design and sequencing strategy for the genomic analysis of quantitative traits in natural populations |
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| Paternity index calculations when some individuals share common ancestry |
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| Pathway analysis of GWAS provides new insights into genetic susceptibility to 3 inflammatory diseases |
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| Patterns of human diversity, within and among continents, inferred from biallelic DNA polymorphisms |
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| PopABC: a program to infer historical demographic parameters. |
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| Population genetics of STR loci in Caucasians |
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| Population Structure and Cryptic Relatedness in Genetic Association Studies |
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| Population structure and inbreeding from pedigree analysis of purebred dogs |
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| A question of identity |
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| Re-evaluation of SNP heritability in complex human traits |
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| Relatedness in the post-genomic era: is it still useful? |
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| Reply |
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| Reply: On the value of haplotype-based genotype–phenotype analysis and on data transformation in pharmacogenetics and -genomics |
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| Response to Lee et al.: SNP-based heritability analysis with dense data |
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| The Rise and Fall of BritainsDNA: A Tale of Misleading Claims, Media Manipulation and Threats to Academic Freedom |
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| Sequence-level population simulations over large genomic regions |
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| Significant genetic correlations among Caucasians at forensic DNA loci |
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| A simulation approach for change-points on phylogenetic trees |
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| Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies |
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| Special Issue: Modern Statistical Methods for Disease Gene Mapping |
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| Storytelling and story testing in domestication |
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| Summary statistic analyses can mistake confounding bias for heritability |
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| Time for DNA disclosure |
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| A tutorial on statistical methods for population association studies |
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| Understanding complex traits: from farmers to pharmas |
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| Using Genetic Distance to Infer the Accuracy of Genomic Prediction |
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| Using Penalised Logistic Regression to Fine Map HLA Variants for Rheumatoid Arthritis |
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| Variation in estimated recombination rates across human populations |
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| Verifying likelihoods for low template DNA profiles using multiple replicates |
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| Weight-of-evidence for forensic DNA profiles |
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| When can a DNA profile be regarded as unique? |
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| Worldwide F(ST) estimates relative to five continental-scale populations |
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| Y-profile evidence: close paternal relatives and mixtures |
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| ZOOM: Observational genetic screening study of Niemann-Pick Disease Type C in adults with neurological and psychiatric signs |
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| প্রত্যুত্তর |
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