For researchers

Is your paper here?

2,677 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.

22 matches for Yan S, showing the first 20.

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
12 pages+
rs149520992 rs6987444 rs2852151 rs9385532 rs12083537 rs67129560
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Understanding Society Scientific Group · International Consortium for Blood Pressure and 2 more consortia
Nature genetics · 2019 · PMID 30578418 · open access
12 pages+
rs34797797 rs6797165 rs2366264 rs12506184 rs162366 rs11187844
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
rs114846969 rs6029549 rs556107 rs117753190 rs6489786 rs217358
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
rs181269956 rs35873233 rs473068 rs4842316 rs56337010 rs77182156
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs35513223 rs4808566 rs5744168 rs62006258 rs62246445 rs6588417
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+
rs184289122 rs149165710 rs145441283 rs187207161 rs767105335 rs77357563
Genetic determinants of daytime napping and effects on cardiometabolic health
23andMe Research Team
Nature communications · 2021 · PMID 33568662 · open access
12 pages+
rs2786547 rs2893323 rs35039375 rs13033444 rs9309116 rs13023587
Joint Genome-Wide Association Analyses Identified 49 Novel Loci For Age at Natural Menopause
The Journal of clinical endocrinology and metabolism · 2021 · PMID 34050765
12 pages+
rs11711203 rs12622788 rs2282851 rs638600 rs1628578 rs8053204
An Amish founder population reveals rare-population genetic determinants of the human lipidome
Communications biology · 2022 · PMID 35393526 · open access
12 pages+
rs1056391806 rs145703167 rs149621053 rs542120882 rs67241885 rs117070489
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+
rs1056265 rs1265103 rs73062380 rs4844565 rs12126767 rs35726795
Novel loci and biomedical consequences of iron homoeostasis variation
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
12 pages+
rs2906082 rs2600895 rs143437464 rs186044114 rs113000093 rs485073
Genome-wide association studies reveal new insights into the genetic basis of IgG4-related disease in the Chinese Han population
Annals of the rheumatic diseases · 2026 · PMID 41298177
10 pages
rs28371251 rs116353692 rs9348878 rs2233964 rs57235233 rs4717156
Assessing the causal association of glycine with risk of cardio-metabolic diseases
Nature communications · 2019 · PMID 30837465 · open access
8 pages
rs2276724 rs62051533 rs13299380 rs62202111 rs9923732 rs9862438
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
rs115234772 rs62319742 rs148772934 rs138973557 rs148753653 rs12135881
The genetic architecture of age at menarche and its causal effects on other traits
Journal of human genetics · 2024 · PMID 39147824
6 pages
rs1265093 rs11186505 rs6060752 rs1027013 rs13126656 rs11773714
Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate
Pharmacogenetics and genomics · 2012 · PMID 22890011
2 pages
rs11766298 Cholesterol (LDL, HDL and Total)
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Nature genetics · 2016 · PMID 27064256
1 page
rs3739821
Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy
Scientific reports · 2018 · PMID 29618737 · open access
1 page
rs7545860
The influence of rare variants in circulating metabolic biomarkers
INTERVAL Study
PLoS genetics · 2020 · PMID 32150548 · open access
1 page
rs12191266
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · open access
1 page
rs11265618

Showing 20 of 22 · page 1 of 2

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.