For researchers

Is your paper here?

2,663 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.

28 matches for Ma T, showing the first 8.

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
rs9687065 rs1563788
A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder
Molecular psychiatry · 2018 · PMID 28115744 · open access
2 pages
rs4926298 rs4332037
A cross-population compendium of gene-environment interactions
BioBank Japan Project
Nature · 2026 · PMID 41606330 · open access
2 pages
rs12507330 rs730154
Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population
Diabetes · 2009 · PMID 19401414 · open access
1 page
rs2237892
A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes
Diabetes Prevention Program Research Group · Broad Genomics Platform and 2 more consortia
Diabetes · 2017 · PMID 28838971 · open access
1 page
rs149483638
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
NEIGHBORHOOD consortium
Scientific reports · 2018 · PMID 29449654 · open access
1 page
rs72815193
GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy
Carcinogenesis · 2019 · PMID 30753327
1 page
rs2920283
Comparison of the loci associated with HbA1c and blood glucose levels identified by a genome-wide association study in the Japanese population
Diabetology international · 2023 · PMID 37090135
1 page
rs2299620

Showing 8 of 28 · page 2 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.