Konrad Rawlik

Employment

Employment history is unavailable.

Education

• University of Edinburgh PhD in Machine Learning
  2008 - 2012
• University of Edinburgh MRes in Neuroinformatics
  2007 - 2008
• University of Edinburgh BSc in Mathematics and Artificial Intelligence
  2003 - 2007

Projects & Funding

Projects & funding information is unavailable.

Publications (54)

• Whole genome sequence meta-analyses reveal common and rare genetic associations with critical COVID-19
  2025 DOI: 10.1101/2025.11.19.25340573
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• Mendelian randomization study implicates inflammaging biomarkers in retinal vasculature, cardiovascular diseases and longevity
  Science Advances 2025 DOI: 10.1126/sciadv.adu1985
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• The genomic landscape of Acute Respiratory Distress Syndrome: a meta-analysis by information content of genome-wide studies of the host response
  2024 DOI: 10.1101/2024.02.13.24301089
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• Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
  Erola Pairo‐Castineira, Konrad Rawlik, Andrew D. Bretherick +97 more
  Nature 2023 DOI: 10.1038/s41586-023-06383-z
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• GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
  Erola Pairo‐Castineira, Konrad Rawlik, Andrew D. Bretherick +97 more
  Nature 2023 DOI: 10.1038/s41586-023-06034-3
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• Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes
  Communications Biology 2023 DOI: 10.1038/s42003-023-04836-9
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• Adeno-associated virus 2 infection in children with non-A-E hepatitis.
  Antonia Ying Wai Ho, Richard J Orton, Rachel Tayler +97 more
  Nature 2023 DOI: 10.1038/s41586-023-05948-2
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• Reply to: Genotype by sex interactions in ankylosing spondylitis
  Nature Genetics 2023 DOI: 10.1038/s41588-022-01251-4
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• A compendium of genetic regulatory effects across pig tissues
  2022 DOI: 10.21203/rs.3.rs-2261680/v1
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• Frequency and Phenotype Associations of Rare Variants in 5 Monogenic Cerebral Small Vessel Disease Genes in 200,000 UK Biobank Participants
  Neurology Genetics 2022 DOI: 10.1212/NXG.0000000000200015
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• A multi-tissue atlas of regulatory variants in cattle.
  Nature genetics 2022 DOI: 10.1038/s41588-022-01153-5
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• Comparative transcriptome in large-scale human and cattle populations.
  Genome biology 2022 DOI: 10.1186/s13059-022-02745-4
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• Whole-genome sequencing reveals host factors underlying critical COVID-19
  Athanasios Kousathanas, Erola Pairo‐Castineira, Konrad Rawlik +97 more
  Nature 2022 DOI: 10.1038/s41586-022-04576-6
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• Genetic Landscape of the ACE2 Coronavirus Receptor.
  Circulation 2022 DOI: 10.1161/circulationaha.121.057888
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• GWAS and meta-analysis identifies multiple new genetic mechanisms underlying severe Covid-19
  Erola Pairo‐Castineira, Konrad Rawlik, Lucija Klarić +46 more
  2022 DOI: 10.1101/2022.03.07.22271833
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• Physician-Confirmed and Administrative Definitions of Stroke in UK Biobank Reflect the Same Underlying Genetic Trait.
  Frontiers in neurology 2022 DOI: 10.3389/fneur.2021.787107
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• Expanded Analysis of Pigmentation Genetics in UK Biobank
  2022 DOI: 10.1101/2022.01.30.478418
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• Decreased retinal vascular complexity is an early biomarker of MI supported by a shared genetic control
  2021 DOI: 10.1101/2021.12.16.21267446
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• Frequency and phenotype associations of rare variants in five monogenic cerebral small vessel disease genes in 200,000 UK Biobank participants with whole exome sequencing data
  2021 DOI: 10.1101/2021.11.17.21266447
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• Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
  Nature communications 2021 DOI: 10.1038/s41467-021-26783-x
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