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.

8 matches for Rentería ME.

Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci
23andMe Research Team · International Glaucoma Genetics Consortium
Nature genetics · 2023 · PMID 37386247 · open access
12 pages+
rs10139172 rs955934 rs10947614 rs73250939 rs67349114 rs11187315
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
rs324901 rs534415 rs1526193 rs7415357 rs72786643 rs3091404
Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank
Nature communications · 2020 · PMID 32060260 · open access
10 pages
rs10878269 rs57222984 rs61597598 rs725861 rs13251292 rs11018488
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
9 pages
rs3133370 rs2206656 rs4784256 rs196807 rs9505301 rs2410767
Genome-wide association meta-analysis identifies 29 new acne susceptibility loci
Nature communications · 2022 · PMID 35132056 · open access
7 pages
rs72803831 rs34560261 rs3849154 rs16874036 rs17265703 rs6658708
GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association
Twin research and human genetics : the official journal of the International Society for Twin Studies · 2013 · PMID 23725790
4 pages
rs11933531 rs7931462 rs10497324 rs13135284
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
Genetic Susceptibility to Pneumonia: A GWAS Meta-Analysis Between the UK Biobank and FinnGen
Twin research and human genetics : the official journal of the International Society for Twin Studies · 2021 · PMID 34340725
1 page
rs76474922

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.