Author details

Full Name

James F Wilson

Affiliation

ORCID

Career Start Year

1998

Papers

309

H Index

105

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36658113	Large scale phenotype imputation and in vivo functional validation implicate ADAMTS14 as an adiposity gene.	Nat Commun	2023
36349687	Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing.	Hum Mol Genet	2023
37749248	Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.	Nat Genet	2023
37563310	Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets.	Nat Immunol	2023
37881452	Typing myalgic encephalomyelitis by infection at onset: A DecodeME study.	NIHR Open Res	2023
37550624	Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases.	Clin Proteomics	2023
36842216	Mendelian randomization and clinical trial evidence supports TYK2 inhibition as a therapeutic target for autoimmune diseases.	EBioMedicine	2023
37034613	Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric Disorders.	Res Sq	2023
37402774	Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.	Commun Biol	2023
36959410	Comparative analysis of transferrin and IgG N-glycosylation in two human populations.		2023
36824751	Genetic mechanisms of 184 neuro-related proteins in human plasma.	medRxiv	2023
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
36798092	Guidelines for genetic ancestry inference created through roundtable discussions.	HGG Adv	2023
36737699	Mendelian randomisation identifies priority groups for prophylactic EBV vaccination.		2023
37172216	Combining serum metabolomic profiles with traditional risk factors improves 10-year cardiovascular risk prediction in people with type 2 diabetes.		2023
36927983	Clinical case study meets population cohort: identification of a BRCA1 pathogenic founder variant in Orcadians.	Eur J Hum Genet	2023
36991119	An atlas of genetic scores to predict multi-omic traits.	Nature	2023
36918541	Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.	Nat Commun	2023
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
35073279	A catalogue of omics biological ageing clocks reveals substantial commonality and associations with disease risk.	Aging	2022
35974141	Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning.	Mol Psychiatry	2022
35653391	Using genetic variation to disentangle the complex relationship between food intake and health outcomes.	PLoS Genet	2022
35585065	Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits.	Nat Commun	2022
35504531	Gene-based whole genome sequencing meta-analysis of 250 circulating proteins in three isolated European populations.	Molecular Metabolism	2022
36062073	Cystatin C is associated with adverse COVID-19 outcomes in diverse populations.	iScience	2022
35477395	Serum metabolomic profiles associated with subclinical and clinical cardiovascular phenotypes in people with type 2 diabetes.	Cardiovascular Diabetology	2022
35357430	Genetic and phenotypic links between obesity and extracellular vesicles.	Hum Mol Genet	2022
35854226	DecodeME: community recruitment for a large genetics study of myalgic encephalomyelitis / chronic fatigue syndrome.	BMC Neurology	2022
35534559	Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects.	Nat Genet	2022
37118362	Mendelian randomization of genetically independent aging phenotypes identifies LPA and VCAM1 as biological targets for human aging.	Nat Aging	2022
35320144	Genome-wide Association Study of Liking for Several Types of Physical Activity in the UK Biobank and Two Replication Cohorts.	Med Sci Sports Exerc	2022
35332118	Genetic regulation of post-translational modification of two distinct proteins.	Nature Communications	2022
34673976	Inbreeding, Native American ancestry and child mortality: linking human selection and paediatric medicine.	Human Molecular Genetics	2022
35228297	Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin.	J Am Soc Nephrol	2022
35022422	A multi-omics study of circulating phospholipid markers of blood pressure.	Sci Rep	2022
35131896	Ancient DNA at the edge of the world: Continental immigration and the persistence of Neolithic male lineages in Bronze Age Orkney.	Proc Natl Acad Sci U S A	2022
34651315	Genome-wide analysis identifies gallstone-susceptibility loci including genes regulating gastrointestinal motility.	Hepatology	2022
34535985	Genome-Wide Association Study of NAFLD Using Electronic Health Records.	Hepatology Communications	2022
34883445	Lifestyle and Genetic Factors Modify Parent-of-Origin Effects on the Human Methylome.	eBioMedicine	2021
33851187	Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19.	medRxiv	2021
34115965	Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.	Am J Hum Genet	2021
34160658	Retinal arteriolar tortuosity and fractal dimension are associated with long-term cardiovascular outcomes in people with type 2 diabetes.	Diabetologia	2021
33613642	Nontrivial Replication of Loci Detected by Multi-Trait Methods.	Front Genet	2021
34088990	Contribution of common risk variants to multiple sclerosis in Orkney and Shetland.	European Journal of Human Genetics	2021
33710309	Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function.	Human Molecular Genetics	2021
33307546	Genetic mechanisms of critical illness in COVID-19.	Nature	2021
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
34857772	Mapping the serum proteome to neurological diseases using whole genome sequencing.	Nat Commun	2021
34790224	Mendelian Randomization Identifies the Potential Causal Impact of Dietary Patterns on Circulating Blood Metabolites.	Frontiers in Genetics	2021
34499657	Genome-wide methylation data improves dissection of the effect of smoking on body mass index.	PLoS Genetics	2021