Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

For researchers

Is your paper here?

3,192 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 MuTHER.

An atlas of genetic influences on human blood metabolites
Multiple Tissue Human Expression Resource (MuTHER) Consortium
Nature genetics · 2014 · PMID 24816252 · open access
12 pages+
rs2547231 rs2066938 rs316020 rs296396 rs11950562 rs9393915
New genetic loci link adipose and insulin biology to body fat distribution
ADIPOGen Consortium · CARDIOGRAMplusC4D Consortium and 11 more consortia
Nature · 2015 · PMID 25673412 · open access
12 pages+
rs7759742 rs1385167 rs7733331 rs6090583 rs4846565 rs3902751
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Multiple Tissue Human Expression Resource (MUTHER) Consortium
Nature genetics · 2012 · PMID 22581228
8 pages
rs35747 rs4691380 rs2785980 rs1371614 rs13179048 rs6048205
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs2590838 rs6488898 rs182052 rs2980879 rs4805885 Adiponectin Levels
Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms
MuTHER Consortium
PLoS genetics · 2011 · PMID 21533175 · open access
3 pages
rs2637125 rs740160 rs2185570
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Diabetes · 2011 · PMID 21873549 · open access
3 pages
rs6235 rs11558471 rs1549318
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
3 pages
rs6815464 rs7041847 rs9470794
Genetic studies of body mass index yield new insights for obesity biology
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
3 pages
rs16851483 rs2121279 rs16951275
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes
FIND Consortium · eMERGE Consortium and 3 more consortia
PLoS genetics · 2014 · PMID 25102180 · open access
2 pages
rs2283228 rs3842770
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
DIAGRAM · MuTHER
Nature genetics · 2011 · PMID 21874001
1 page
rs4812829
Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India
DIAGRAM · MuTHER and 1 more consortia
Diabetes · 2013 · PMID 23300278 · open access
1 page
rs9552911

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.