Konrad Rawlik

Roslin Institute — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

32h-index7.3kcitations112works28.52yr avg
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Research Topics

Genetic and phenotypic traits in livestock(33), Genetic Associations and Epidemiology(27), Epigenetics and DNA Methylation(17), Genetic Mapping and Diversity in Plants and Animals(15), Cancer-related molecular mechanisms research(14)

Publications107 total

Whole genome sequence meta-analyses reveal common and rare genetic associations with critical COVID-19
2025Open Access
Mendelian randomization study implicates inflammaging biomarkers in retinal vasculature, cardiovascular diseases, and longevity
Science Advances·2025Open Access
Same model, better performance: the impact of shuffling on DNA Language Models benchmarking
arXiv (Cornell University)·2025Open Access
Use of polygenic risk scores in the prediction of COVID-19 non-recovery
2025
Data Resource Profile: Whole-Blood DNA Methylation Resource in Generation Scotland (MeGS)
International Journal of Epidemiology·2025· 7 citedOpen Access
Genetic Landscape of the ACE2 Coronavirus Receptor
UNC Libraries·2025Open Access
The Farm Animal Genotype–Tissue Expression (FarmGTEx) Project
Nature Genetics·2025· 30 citedOpen Access
Proteome-wide Mendelian randomization study implicates inflammaging biomarkers in retinal vasculature, cardiometabolic diseases and longevity
2024Open Access
Data Resource Profile: Whole Blood DNA Methylation Resource in Generation Scotland (MeGS)
2024· 4 citedOpen Access
The genomic landscape of Acute Respiratory Distress Syndrome: a meta-analysis by information content of genome-wide studies of the host response
2024· 4 citedOpen Access
A compendium of genetic regulatory effects across pig tissues
Nature Genetics·2024· 233 citedOpen Access
Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
Nature·2023· 10 citedOpen Access
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
Nature·2023· 182 citedOpen Access
Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes
Communications Biology·2023· 8 citedOpen Access
Adeno-associated virus 2 infection in children with non-A–E hepatitis
Nature·2023· 163 citedOpen Access
Reply to: Genotype by sex interactions in ankylosing spondylitis
Nature Genetics·2023· 5 citedOpen Access
A compendium of genetic regulatory effects across pig tissues
2022· 13 citedOpen Access
Frequency and Phenotype Associations of Rare Variants in 5 Monogenic Cerebral Small Vessel Disease Genes in 200,000 UK Biobank Participants
Neurology Genetics·2022· 15 citedOpen Access
Comparative transcriptome in large-scale human and cattle populations
Genome biology·2022· 38 citedOpen Access
cGTEx_dataset:A multi-tissue atlas of regulatory variants in cattle
2022Open Access
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Frequent Co-authors

Albert Tenesa(32), Oriol Canela‐Xandri(21), Erola Pairo‐Castineira(14), Andrew D. Bretherick(10), Chris Haley(10), Manu Shankar‐Hari(10), Wilna Oosthuyzen(9), David J. Porteous(9), J. Kenneth Baillie(9), Caroline Hayward(8), Charley Xia(8), Fiona Griffiths(7), Athanasios Kousathanas(7), Julian C. Knight(7), Charlotte Summers(7), Charles Hinds(7), Alistair Nichol(7), David M. Maslove(7), Hugh Montgomery(7), Timothy Walsh(7)