For researchers

Is your paper here?

2,675 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.

156 matches for Chen Y, showing the first 20.

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs149165710 rs145441283 rs187207161 rs767105335 rs77357563 rs2306899
Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups
Nature communications · 2021 · PMID 33536424 · open access
12 pages+
rs1016140 rs7815944 rs405858 rs9630991 rs9899849 rs12093154
Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology
Nature communications · 2021 · PMID 33547301 · open access
12 pages+
rs7953767 rs10080411 rs2292553 rs8176279 rs151401 rs10456200
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus
Communications biology · 2021 · PMID 33649486 · open access
12 pages+
rs1200108 rs6669560 rs116792882 rs12515400 rs840464 rs35523808
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+
rs10180829 rs672769 rs10071837 rs4899520 rs75823898 rs112226333
A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic aetiology with obesity
The European respiratory journal · 2021 · PMID 33766948
12 pages+
rs6730783 rs5742653 rs28366282 rs6063386 rs16828537 rs73995038
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+
rs118164457 rs182859029 rs7063597 rs3752435 rs4317621 rs4731113
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+
rs10248717 rs11672003 rs149590572 rs113920320 rs111589301 rs12992267
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+
rs4267865 rs57634870 rs11196296 rs3825801 rs79495865 rs1871045
Genome-Wide Integration of Genetic and Genomic Studies of Atopic Dermatitis: Insights into Genetic Architecture and Pathogenesis
The Journal of investigative dermatology · 2022 · PMID 35577104
12 pages+
rs4821563 rs74692781 rs6010675 rs11697497 rs8957 rs3787103
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+
rs2901260 rs5999721 rs112166402 rs11893881 rs116471547 rs151266052
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+
rs13010821 rs13164873 rs16826031 rs16995249 rs17128737 rs17202814
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs17071170 rs2394120 rs2467111 rs4879465 rs1013339 rs10901373
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases
Nature genetics · 2023 · PMID 36635386
12 pages+
rs9469582 rs10422369 rs174458 rs201393623 rs113425878 rs2074798
Comprehensive genetic study of the insulin resistance marker TG:HDL-C in the UK Biobank
Nature genetics · 2024 · PMID 38200128
12 pages+
rs34934360 rs12927305 rs111831594 rs7966846 rs79859462 rs7298135
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1614264 rs10198943 rs3095633 rs7458670 rs9358927 rs4548860
Causal relevance of different blood pressure traits on risk of cardiovascular diseases: GWAS and Mendelian randomisation in 100,000 Chinese adults
China Kadoorie Biobank Collaborative Group
Nature communications · 2024 · PMID 39048560 · open access
12 pages+
rs10477399 rs9847595 rs6585252 rs75268076 rs62175706 rs67913572
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+
rs16989540 rs536240710 rs181676594 rs6974288 rs3846663 rs12939051
Genetic architecture and risk prediction of gestational diabetes mellitus in Chinese pregnancies
Nature communications · 2025 · PMID 40325049 · open access
12 pages+
rs76154673 rs72554664 rs182573065 rs61160304 rs146844151 rs2971667
Multiscale analysis and functional validation of the cellular and genetic determinants of skeletal disease
International Federation of Musculoskeletal Research Societies (IFMRS) Big Data Working Group
Nature genetics · 2026 · PMID 42432248 · open access
12 pages+
rs148243584 rs189567770 rs73400424 rs61872090 rs59500178 rs11992435

Showing 20 of 156 · page 2 of 8

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.