Author
University of EdinburghORCID 0000-0002-6169-6262Unclaimed ORCID profile · follow to get notified of new preprints
6 papers
Recent·Most cited
Jennifer E. Huffman, Jayna C. Nicholas, Julie M. Hahn…·Yoav Ben‐Shlomo
This study uses whole genome sequencing to identify 18 novel genetic loci associated with plasma fibrinogen levels, including variants more common in African populations and linked to liver-related traits and disease.
Laurence J Howe, Michel Guillaume Nivard, Tim Morris…·Neil M Davies
In 159,701 siblings from 17 cohorts, population GWAS overstate direct effects on height, education, smoking, cognition, depressive symptoms and age at first birth; clinical traits mostly agree across models.
Gabriel Cuéllar-Partida, Joyce Y. Tung, Nicholas Eriksson…·Gérard Waeber
This study identifies 48 genetic variants associated with handedness using a large GWAS, highlighting polygenic nature and genetic links to neuropsychiatric traits.
Andrew D. Bretherick, Oriol Canela‐Xandri, Peter K. Joshi…·Chris Haley
Patrick Wu, Aliya Gifford, Xiangrui Meng…·Wei‐Qi Wei
The paper develops and evaluates mappings from ICD-10 and ICD-10-CM codes to PheCodes, showing high coverage and reproducibility for chronic diseases.
Sodbo Sharapov, Yakov A. Tsepilov, Lucija Klarić…·Yurii S. Aulchenko
This study identifies twelve genetic loci associated with human blood plasma N-glycome composition through genome-wide association analysis, revealing both direct and indirect genetic influences on glycosylation.