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.

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+
rs72698571 rs2246469 rs56288844 rs149520992 rs6987444 rs2852151
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+
rs2009598 rs9708177 rs139055942 rs6848906 rs533030436 rs181718607
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+
rs6897196 rs75211492 rs76738175 rs922 rs10423120 rs10493441
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs4700436 rs6595714 rs72843867 rs7356611 rs7810260 rs79709502
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+
rs10025456 rs8032301 rs1624825 rs145502455 rs273592 rs11937432
Genetic determinants of daytime napping and effects on cardiometabolic health
23andMe Research Team
Nature communications · 2021 · PMID 33568662 · open access
12 pages+
rs11224896 rs2417268 rs35011311 rs60222088 rs11615756 rs2786547
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+
rs7688264 rs7100709 rs12470495 rs1801197 rs6125826 rs12479470
An Amish founder population reveals rare-population genetic determinants of the human lipidome
Communications biology · 2022 · PMID 35393526 · open access
12 pages+
rs77552380 rs549461 rs11536895 rs75651060 rs17226901 rs491242
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+
rs72771840 rs13067940 rs146962013 rs2292644 rs7075988 rs11218744
Novel loci and biomedical consequences of iron homoeostasis variation
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
12 pages+
rs112856048 rs72832593 rs187669805 rs2238005 rs549876436 rs9739943
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
rs11647428 rs2276724 rs62051533 rs13299380 rs62202111 rs9923732
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
rs6060752 rs1027013 rs13126656 rs11773714 rs1265093 rs11186505
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.