For researchers

Is your paper here?

2,660 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.

23 matches for Cheng Y, showing the first 20.

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
rs2820443 rs12955983 rs6737082 rs2821248 rs10840060 rs4727804
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults
CHARGE Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS genetics · 2017 · PMID 28448500 · open access
12 pages+
rs7175517 rs1406948 rs10923724 rs2371767 rs7766106 rs10101061
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+
rs6987444 rs2852151 rs9385532 rs12083537 rs67129560 rs4752829
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs924981 rs35636653 rs1078442 rs4918943 rs10096421 rs57126710
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans
GCKD Investigators
Nature genetics · 2020 · PMID 31959995
12 pages+
rs1698237 rs112992077 rs820503 rs61898064 rs77289848 rs6889699
Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine
GCKD Investigators
Nature genetics · 2023 · PMID 37277652 · open access
12 pages+
rs140188 rs11136305 rs739296 rs296377 rs473913 rs1126742
Ischemic stroke is associated with the ABO locus: the EuroCLOT study
EuroCLOT Investigators · Wellcome Trust Case Control Consortium 2 and 3 more consortia
Annals of neurology · 2013 · PMID 23381943 · open access
11 pages
rs2022309 rs10922162 rs3211770 rs1318606 rs555212 rs10982156
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness
GEFOS Any-Type of Fracture Consortium
Nature communications · 2017 · PMID 29313844 · open access
5 pages
rs72979233 rs4926611 rs11614333 rs2110927 rs80103986
Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Science China. Life sciences · 2019 · PMID 30591961
5 pages
rs17737857 rs4467035 rs12504231 rs7047871 rs11078446
Genomewide association study of leprosy
The New England journal of medicine · 2009 · PMID 20018961
4 pages
rs602875 rs40457 rs42490 Leprosy
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
rs2107595 rs879324 rs13407662 Ischaemic Stroke
Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases
JCI insight · 2022 · PMID 35446786 · open access
4 pages
rs9646256 rs7224888 rs73338360 rs10738906
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Journal of the National Cancer Institute · 2019 · PMID 29917119
3 pages
rs10911251 rs3824999 rs17094983
Large-scale meta- and cross-trait analyses uncover shared genetic risk factors for IBS and psychiatric disorders
Frontiers in psychiatry · 2026 · PMID 42221328 · open access
3 pages
rs7106434 rs20551 Irritable Bowel Syndrome
Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels
Circulation. Cardiovascular genetics · 2009 · PMID 20031604
2 pages
rs11225434 rs495366
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21909108 · open access
2 pages
rs11781551 rs17398575
A central role for GRB10 in regulation of islet function in man
PLoS genetics · 2014 · PMID 24699409 · open access
2 pages
rs12549902 rs11187144
Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans
COMPASS and METASTROKE Consortia
Stroke · 2015 · PMID 26089329
2 pages
rs4471613 rs9899375
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
Nature genetics · 2009 · PMID 19838193
1 page
rs1167796
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity
Nature communications · 2017 · PMID 28232668 · open access
1 page
rs12229892

Showing 20 of 23 · 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.