Author: Ulf Gyllensten

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Preprints

Amplification-free, CRISPR-Cas9 Targeted Enrichment and SMRT Sequencing of Repeat-Expansion Disease Causative Genomic Regions

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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SweGen: A whole-genome map of genetic variability in a cross-section of the Swedish population

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Genomic evaluation of circulating proteins for drug target characterisation and precision medicine

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Amplification-free long read sequencing reveals unforeseen CRISPR-Cas9 off-target activity

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New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

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De novo assembly of two Swedish genomes reveals missing segments from the human GRCh38 reference and improves variant calling of population-scale sequencing data

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The Medical Genome Reference Bank: Whole genomes and phenotype of 2,570 healthy elderly

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Immune cells lacking Y chromosome have widespread dysregulation of autosomal genes

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High throughput proteomics identifies 484 high-accuracy plasma protein biomarker signatures for ovarian cancer

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Meta-analysis of exome array data identifies six novel genetic loci for lung function

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SweHLA: the high confidence HLA typing bio-resource drawn from 1 000 Swedish genomes

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Genome-wide CNV study and functional evaluation identified CTDSPL as tumour suppressor gene for cervical cancer

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