For researchers

Is your paper here?

2,671 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.

15 matches for Cheng S.

Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort
Nature genetics · 2022 · PMID 35115689
12 pages+
rs3940549 rs160329 rs141975840 rs76416179 rs187475866 rs79317201
Genome-wide association studies of thyroid-related hormones, dysfunction, and autoimmunity among 85,421 Chinese pregnancies
Nature communications · 2024 · PMID 39266554 · open access
12 pages+
rs231770 rs1348003 rs9393917 rs2234036 rs1051365311 rs2288187
Genetic architecture and risk prediction of gestational diabetes mellitus in Chinese pregnancies
Nature communications · 2025 · PMID 40325049 · open access
12 pages+
rs72554664 rs182573065 rs61160304 rs146844151 rs2971667 rs732360
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling
CARDIoGRAM Consortium · CHARGE Inflammation Working Group and 1 more consortia
The Journal of clinical investigation · 2013 · PMID 23999434
9 pages
rs12999542 rs13019803 rs2302612 rs11693697 rs13029918 rs1014286
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
rs1566045 rs7953528 rs163879 rs1864325 rs344081 rs3905706
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals
Scientific reports · 2017 · PMID 29213071 · open access
7 pages
rs73017364 rs12035622 rs55863869 rs35760656 rs12271931 rs12626657
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
The Journal of clinical investigation · 2017 · PMID 28394258
5 pages
rs6702619 rs17696696 rs7127129 rs2649 rs11207426
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs75031349 rs137884934 rs682888 rs10901793 rs71467682
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium
Human molecular genetics · 2014 · PMID 24430505
4 pages
rs2982552 rs10416265 rs7902708 rs3020331
The STROMICS genome study: deep whole-genome sequencing and analysis of 10K Chinese patients with ischemic stroke reveal complex genetic and phenotypic interplay
Cell discovery · 2023 · PMID 37479695 · open access
3 pages
rs12718465 rs12081480 rs866262287
Clinical and genetic correlates of growth differentiation factor 15 in the community
Clinical chemistry · 2012 · PMID 22997280
2 pages
rs888663 rs1054564
GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations
PloS one · 2019 · PMID 31251759 · open access
2 pages
rs62241190 rs9856387
Genetic determinants of IgG antibody response to COVID-19 vaccination
American journal of human genetics · 2024 · PMID 38181733 · open access
2 pages
rs10947290 rs35986240
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Human molecular genetics · 2016 · PMID 26732429
1 page
rs7741164
Identification of susceptibility loci and relevant cell type for IgA nephropathy in Han Chinese by integrative genome-wide analysis
Frontiers of medicine · 2024 · PMID 39343836
1 page
rs13332545

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.