For researchers

Is your paper here?

2,665 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.

20 matches for Yu L.

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+
rs13011109 rs2820443 rs12955983 rs6737082 rs2821248 rs10840060
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+
rs12787013 rs17036665 rs17040476 rs174348 rs17617811 rs17712993
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
LifeLines Cohort Study
Nature genetics · 2016 · PMID 27089181 · open access
10 pages
rs782212 rs12903563 rs12961969 rs35688236 rs2075677 rs4958581
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension
Human molecular genetics · 2015 · PMID 25249183
5 pages
rs9810888 rs2021783 rs1902859 rs13143871 rs4409766
Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations
Circulation. Cardiovascular genetics · 2016 · PMID 26582766
4 pages
rs1260333 rs2575876 rs7525649 rs9357121
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
rs4851266 rs9320913 rs1056667
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers
Nature genetics · 2010 · PMID 20676096
2 pages
rs17401966 HBV-Related Hepatocellular Carcinoma
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
rs17178006 rs6581612
Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B
Hepatology (Baltimore, Md.) · 2015 · PMID 25802187
2 pages
rs2856718 rs2853953
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
Aging cell · 2016 · PMID 27325353 · open access
2 pages
rs752045 Hand Grip Strength
Exome-Wide Association Analysis Suggests LRP2BP as a Susceptibility Gene for Endothelial Injury in Systemic Sclerosis in the Han Chinese Population
The Journal of investigative dermatology · 2021 · PMID 33069728
2 pages
rs76285340 rs45471499
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
rs1898895 rs111486601
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium
Nature genetics · 2012 · PMID 22751097
1 page
rs9268402
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
European Alzheimer's Disease Initiative (EADI) · Genetic and Environmental Risk in Alzheimer's Disease and 2 more consortia
Nature genetics · 2013 · PMID 24162737
1 page
rs10498633
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
rs139967528
Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility
International journal of cancer · 2019 · PMID 30714141
1 page
rs10842893
Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study
Diabetes care · 2019 · PMID 31152121
1 page
rs4320356
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
Molecular psychiatry · 2022 · PMID 35974141 · open access
1 page
rs11711421
Single-nucleotide polymorphism in the human mu opioid receptor gene alters beta-endorphin binding and activity: possible implications for opiate addiction
Proceedings of the National Academy of Sciences of the United States of America · 1998 · PMID 9689128
1 page
rs1799971

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.