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An interactive genome browser of association results from the UK10K cohorts project
Oxford University Press | 2015| -
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Free accessBASE | 2015| -
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Free accessBASE | 2015| -
An Organismal CNV Mutator Phenotype Restricted to Early Human Development
British Library Online Contents | 2017| -
An Organismal CNV Mutator Phenotype Restricted to Early Human Development
British Library Online Contents | 2017| -
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
British Library Online Contents | 2016| -
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
British Library Online Contents | 2016| -
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
British Library Online Contents | 2016| -
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
British Library Online Contents | 2016| -
Origins and functional impact of copy number variation in the human genome
Online Contents | 2010|Contributors: Walter, Klaudia -
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
Free accessBASE | 2022|Contributors: Walter, Klaudia
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