For researchers

Is your paper here?

2,673 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.

53 matches for Chen S, showing the first 20.

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nature genetics · 2015 · PMID 26343387 · open access
12 pages+
rs1544935 rs1870634 rs2891168 rs56131196 rs72689147 rs2487928
Discovery of common and rare genetic risk variants for colorectal cancer
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
rs12144319 rs116353863 rs117079142 rs11884596 rs12708491 rs4901473
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+
rs10928512 rs187479321 rs6493583 rs72729623 rs115726216 rs144242131
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+
rs9899520 rs75307421 rs3780012 rs4267865 rs57634870 rs11196296
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+
rs1887200 rs11904581 rs6139109 rs1442883 rs973730 rs6020177
Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus
Nature communications · 2023 · PMID 36750564 · open access
12 pages+
rs6434435 rs9469857 rs2084654 rs1155060 rs3732421 rs16833177
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
GWA-PA Consortium · Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37679419 · open access
12 pages+
rs11146926 rs2236418 rs925095 rs11049144 rs61285514 rs17437371
A Genome-Wide Association Study of Metabolic Syndrome in the Taiwanese Population
Nutrients · 2023 · PMID 38201907 · open access
12 pages+
rs10892049 rs191655881 rs17440824 rs11601584 rs61905145 rs35732917
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1683935 rs71474196 rs72798545 rs1523539 rs7307263 rs11716527
Whole exome sequencing analyses reveal novel genes in telomere length and their biomedical implications
GeroScience · 2024 · PMID 38837026
12 pages+
rs3737194 rs4496196 rs74552928 rs962535 rs79074096 rs817330
Developing an optimal stratification model for colorectal cancer screening and reducing racial disparities in multi-center population-based studies
Genome medicine · 2024 · PMID 38872215 · open access
12 pages+
rs56270678 rs371061408 rs6507877 rs11213825 rs28774977 rs10318
Translational genomics of osteoarthritis in 1,962,069 individuals
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
rs295299 rs645019 rs2430398 rs3116615 rs4836390 rs73382475
Exploring Genetic Contributions to Prostate Cancer Risk in an Asian Population-Based Study
Cancer medicine · 2026 · PMID 42415294 · open access
12 pages+
rs11220138 rs75964872 rs13025842 rs143976741 rs55916943 rs76661218
Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci
Clinical and translational medicine · 2021 · PMID 33634981 · open access
11 pages
rs73530508 rs9204 rs9530695 rs73365860 rs117445861 rs6497488
Genetic study identifies novel genes in developmental dysplasia of the hip
Bone research · 2026 · PMID 41912496 · open access
9 pages
rs17677724 rs9835230 rs10817926 rs12350134 rs1384547 rs147057560
Genome-wide association analysis of left ventricular imaging-derived phenotypes identifies 72 risk loci and yields genetic insights into hypertrophic cardiomyopathy
Nature communications · 2023 · PMID 38036550 · open access
8 pages
rs79548216 rs9428227 rs62253183 rs62250980 rs7928419 rs9462210
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
AOGC Consortium · UK10K Consortium
Nature · 2015 · PMID 26367794
7 pages
rs188303909 rs11024028 rs148771817 rs11692564 rs6542457 Spine Bone Mineral Density
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs762517 rs12012576 rs139120857 rs5942972 rs7063103 rs62603531
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations
KidneyGen Consortium · CKDGen Consortium and 1 more consortia
Nature genetics · 2012 · PMID 22797727
6 pages
rs17730281 rs11868441 rs10767873 rs2074356 rs17730436 rs11864909
Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese
Circulation. Cardiovascular genetics · 2013 · PMID 24165912
6 pages
rs10930597 rs2030114 rs16890334 rs17135875 rs1330225 rs8002688

Showing 20 of 53 · page 1 of 3

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.