For researchers

Is your paper here?

2,676 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.

228 matches for Ang W, showing the first 20.

Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study
Blood Cell Consortium
BMC genomics · 2021 · PMID 34107879 · open access
12 pages+
rs76676074 rs9659479 rs2768762 rs11240092 rs28873209 rs11264765
A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects
23andMe Research Team
Nature communications · 2021 · PMID 34127677 · open access
12 pages+
rs2686878 rs17172647 rs4814857 rs9842371 rs1014607 rs10210444
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+
rs56881390 rs77631946 rs2010871 rs940922629 rs117047468 rs11758358
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs12363019 rs72934602 rs1866862 rs2238304 rs7701188 rs9597388
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+
rs11196296 rs3825801 rs79495865 rs1871045 rs80102379 rs7819706
Your height affects your health: genetic determinants and health-related outcomes in Taiwan
BMC medicine · 2022 · PMID 35831902 · open access
12 pages+
rs11170631 rs938608 rs185053690 rs57454081 rs61016611 rs12230367
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
rs6632109 rs8049403 rs2048528 rs1518760 rs78475244 rs76668186
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+
rs7973282 rs11655686 rs6722682 rs6841071 rs6850035 rs7440928
A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses
Osteoarthritis and cartilage · 2023 · PMID 36889626
12 pages+
rs6029202 rs35739367 rs17760596 rs2640909 rs2681781 rs4858223
Genetically adjusted PSA levels for prostate cancer screening
Nature medicine · 2023 · PMID 37264206 · open access
12 pages+
rs7129424 rs80122351 rs9933507 rs10193919 rs11709611 rs34388051
Using human genetics to understand the phenotypic association between chronotype and breast cancer
Journal of sleep research · 2024 · PMID 37380357
12 pages+
rs115356840 rs62467945 rs139909 rs695459 rs61863443 rs7907439
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs11892008 rs6151589 rs4713343 rs2485662 rs78416326 rs17804499
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs60128210 rs244080 rs2534653 rs4932747 rs6073369 rs11576244
Genome-wide characterization of circulating metabolic biomarkers
China Kadoorie Biobank Collaborative Group · Estonian Biobank Research Team and 1 more consortia
Nature · 2024 · PMID 38448586 · open access
12 pages+
rs13221253 rs28396910 rs11065397 rs11668477 rs145679432 rs10260300
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs114427493 rs12274095 rs57551109 rs501842 rs12113633 rs62169409
iGWAS: Image-based genome-wide association of self-supervised deep phenotyping of retina fundus images
PLoS genetics · 2024 · PMID 38728357 · open access
12 pages+
rs2703950 rs11638265 rs7481199 rs1942486 rs1635166 rs2003176
A genome-wide association analysis reveals new pathogenic pathways in gout
FAST Study Group · Japan Gout Genomics Consortium and 3 more consortia
Nature genetics · 2024 · PMID 39406924
12 pages+
rs2503700 rs11191479 rs12152850 rs72680102 rs732819 rs9896098
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries
VA Million Veteran Program · International AMD Genomics Consortium (IAMDGC)
Nature genetics · 2024 · PMID 39623103
12 pages+
rs7663219 rs444189 rs11569415 rs9973159 rs334362 rs56123646
Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves prediction across ancestry groups
Nature genetics · 2025 · PMID 39930085 · open access
12 pages+
rs59426030 rs930782 rs72655532 rs113431408 rs13194407 rs4567770
Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits
DIAMANTE Hispanic/Latino Consortium · Global Hispanic Lipids Consortium
Nature communications · 2025 · PMID 40210677 · open access
12 pages+
rs536240710 rs181676594 rs6974288 rs3846663 rs12939051 rs58458113

Showing 20 of 228 · page 3 of 12

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.