For researchers

Is your paper here?

2,692 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.

21 matches for Ye L, showing the first 20.

Genetics of rheumatoid arthritis contributes to biology and drug discovery
RACI consortium · GARNET consortium
Nature · 2014 · PMID 24390342 · open access
12 pages+
rs9653442 rs71508903 rs9372120 rs72634030 rs11933540 rs2561477
Genome-wide association study identifies 74 loci associated with educational attainment
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
rs142328051 rs12143094 rs34305371 rs17504614 rs56158183 rs4851251
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+
rs7628338 rs7175517 rs1406948 rs10923724 rs2371767 rs7766106
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
Alzheimer’s Disease Neuroimaging Initiative · Pediatric Imaging, Neurocognition and Genetics Study
Molecular psychiatry · 2020 · PMID 30279459 · open access
12 pages+
rs58499557 rs6675690 rs13188633 rs1861979 rs57246240 rs12218858
The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs62002282 rs117892760 rs4706392 rs72722993 rs28496034 rs11789773
The genetic architecture of the human thalamus and its overlap with ten common brain disorders
Nature communications · 2021 · PMID 34006833 · open access
12 pages+
rs57977776 rs12924872 rs11175916 rs2774406 rs34316881 rs1316356
Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology
NeuroImage · 2021 · PMID 34560273
12 pages+
rs62360696 rs4506217 rs11695197 rs7295050 rs35694396 rs11191839
The genetic architecture of human cortical folding
Science advances · 2021 · PMID 34910505 · open access
12 pages+
rs12880832 rs7919525 rs2381939 rs2675613 rs4655025 rs78068712
The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition
Communications biology · 2022 · PMID 36402844 · open access
12 pages+
rs11892032 rs908611 rs2854152 rs60258355 rs6723391 rs646026
The genetic architecture of human cerebellar morphology supports a key role for the cerebellum in human evolution and psychopathology
Communications biology · 2026 · PMID 41703085 · open access
12 pages+
rs8182773 rs1569270 rs4891263 rs61618811 rs4843226 rs62029094
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
rs4938021 rs3756290 rs782212 rs12903563 rs12961969 rs35688236
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
10 pages
rs10217651 rs35200015 rs3133370 rs2206656 rs4784256 rs196807
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
9 pages
rs10218452 rs10456100 rs17857135 rs7775721 rs2506142 rs4081947
The genetic landscape of basal ganglia and implications for common brain disorders
Nature communications · 2024 · PMID 39353893 · open access
9 pages
rs2817145 rs56000151 rs1953352 rs4938400 rs6138937 rs10414860
Large-scale brainstem neuroimaging and genetic analyses provide new insights into the neuronal mechanisms of hypertension
HGG advances · 2025 · PMID 39663699 · open access
8 pages
rs111423688 rs13140033 rs783622 rs76344126 rs1863244 rs11243203
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
Genome-wide meta-analysis identifies new susceptibility loci for migraine
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
rs11759769 rs12134493 rs4379368
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
2 pages
rs1854853 rs12525220
Identification of common variants associated with human hippocampal and intracranial volumes
Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium and 4 more consortia
Nature genetics · 2012 · PMID 22504417
1 page
rs10784502
Genome-wide significant association signals in IPO11-HTR1A region specific for alcohol and nicotine codependence
Alcoholism, clinical and experimental research · 2013 · PMID 23216389
1 page
rs7445832

Showing 20 of 21 · 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.