For researchers

Is your paper here?

2,663 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

171 matches for Wilson J, showing the first 20.

Multi-trait genome-wide association study identifies new loci associated with optic disc parameters
International Glaucoma Genetics Consortium · NEIGHBORHOOD consortium and 1 more consortia
Communications biology · 2019 · PMID 31798171 · open access
12 pages+
rs72748148 rs10882283 rs2078555 rs6054383 rs1420993 rs2239854
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
rs11921457 rs4246224 rs59212267 rs111551996 rs3747570 rs4834347
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs8104447 rs55861089 rs17860955 rs176694 rs471994 rs8064426
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs10071837 rs4899520 rs75823898 rs112226333 rs2553033 rs7905296
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs7063597 rs3752435 rs4317621 rs4731113 rs4674280 rs138245006
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
Genetics of DNA Methylation Consortium · NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Genome biology · 2021 · PMID 34187551 · open access
12 pages+
rs3118123 rs3737843 rs117932856 rs73538174 rs10949481 rs856046
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
Mapping the serum proteome to neurological diseases using whole genome sequencing
Nature communications · 2021 · PMID 34857772 · open access
12 pages+
rs67924081 rs28483039 rs11004802 rs217053 rs1921087 rs73070113
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs3211938 rs151235402 rs73339979 rs114139997 rs10184673 rs117139027
Genetic regulation of post-translational modification of two distinct proteins
Nature communications · 2022 · PMID 35332118 · open access
12 pages+
rs8022094 rs75757016 rs11622603 rs80021729 rs35376994 rs2413592
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs7819706 rs1473781 rs6876198 rs3743140 rs3806155 rs7313668
Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits
Nature communications · 2022 · PMID 35585065 · open access
12 pages+
rs1370063 rs2110529 rs4947336 rs12430440 rs543760429 rs76395182
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
NHLBI Trans-Omics for Precision Medicine 1 Consortium
Nature communications · 2022 · PMID 35995766 · open access
12 pages+
rs76992529 rs2453544 rs74934947 rs754490766 rs77271279 rs10785996
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs30226 rs1804193 rs1658323 rs17171711 rs35283519 rs2627230
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
12 pages+
rs1160545 rs3759344 rs7067170 rs7615206 rs1691471 rs4483592
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs17105330 rs8079564 rs4813853 rs7015100 rs7522427 rs9907557
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
rs4337253 rs62321845 rs57380671 rs227728 rs9600261 rs6806825
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Nature communications · 2023 · PMID 36918541 · open access
12 pages+
rs2762049 rs55824920 rs72798148 rs8019721 rs1724411 rs12467581
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
GenOMICC Investigators · SCOURGE Consortium and 2 more consortia
Nature · 2023 · PMID 37198478 · open access
12 pages+
rs1123573 rs111837807 rs7528026 rs17713054 rs7949972 rs12046291
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets
Estonian Biobank Research Team
Nature immunology · 2023 · PMID 37563310 · open access
12 pages+
rs3811621 rs4251805 rs10733789 rs62360376 rs11265493 rs9469127

Showing 20 of 171 · page 3 of 9

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.