For researchers

Is your paper here?

2,657 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.

11 matches for Dei M.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Nature genetics · 2013 · PMID 23563607 · open access
12 pages+
rs10182181 rs1412239 rs1421085 rs538656 rs1514177 rs3101336
Complex genetic signatures in immune cells underlie autoimmunity and inform therapy
Nature genetics · 2020 · PMID 32929287
12 pages+
rs59738549 rs858551 rs4959028 rs115780495 rs3002600 rs181878688
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways
WTCCC
Diabetes · 2010 · PMID 20858683 · open access
5 pages
rs1799884 rs1046896 rs6474359 rs7998202 Type 2 Diabetes
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Nature genetics · 2009 · PMID 19305409
4 pages
rs17779747 rs10919071 rs2968863 rs11970286
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
rs1055144 rs6784615 rs6861681
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
PLoS genetics · 2007 · PMID 17658951 · open access
2 pages
rs9930506 Obesity and Body Weight
The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts
PLoS genetics · 2007 · PMID 17997608 · open access
2 pages
rs6855911 Gout
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia
Proceedings of the National Academy of Sciences of the United States of America · 2008 · PMID 18245381
2 pages
rs11886868 Blood Cell Counts
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia
Human molecular genetics · 2009 · PMID 19419973
1 page
rs887829
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis
Nature genetics · 2010 · PMID 20453840
1 page
rs2040406
Overexpression of the Cytokine BAFF and Autoimmunity Risk
The New England journal of medicine · 2017 · PMID 28445677
1 page
rs12253981

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.