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Marchini, Jonathan

Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK

TitleYearPMID
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. 2018 29700475
The UK Biobank resource with deep phenotyping and genomic data. 2018 30305743
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. 2015 26423011
A general approach for haplotype phasing across the full spectrum of relatedness. 2014 24743097
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel. 2014 25653097
Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. 2013 24186853
Haplotype estimation using sequencing reads. 2013 24094745
Improved whole-chromosome phasing for disease and population genetic studies. 2013 23269371
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. 2012 22820512
Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. 2012 22868939
A linear complexity phasing method for thousands of genomes. 2011 22138821
Genotype imputation with thousands of genomes. 2011 22384356
The effect of genome-wide association scan quality control on imputation outcome for common variants. 2011 21267008
Genotype imputation for genome-wide association studies. 2010 20517342
Meta-analysis and imputation refines the association of 15q25 with smoking quantity. 2010 20418889
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. 2009 19543373
Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip. PDF 2009 19492015
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 2008 18587394
A new multipoint method for genome-wide association studies by imputation of genotypes. 2007 17572673
A second generation human haplotype map of over 3.1 million SNPs. 2007 17943122
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