For researchers

Is your paper here?

2,673 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.

9 matches for Feng J.

Whole exome sequencing analyses reveal novel genes in telomere length and their biomedical implications
GeroScience · 2024 · PMID 38837026
12 pages+
rs112333466 rs540821244 rs72695085 rs9952504 rs117238689 rs77136207
Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects
PLoS genetics · 2012 · PMID 23028341 · open access
8 pages
rs2071278 rs3763317 rs241428 rs11575839 rs2857009 rs3753394
The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders
Translational psychiatry · 2023 · PMID 37236919 · open access
7 pages
rs1108048 rs10980625 rs11621425 rs12552125 rs1110339 rs7616662
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study
Stroke · 2018 · PMID 29273593
6 pages
rs9614159 rs74388387 rs9907978 rs10782008 rs117353193 Moyamoya Disease
Genome-wide association study identified novel genetic variant on SLC45A3 gene associated with serum levels prostate-specific antigen (PSA) in a Chinese population
Human genetics · 2013 · PMID 23269536
2 pages
rs12409639 Prostate-Specific Antigen (PSA) Levels
Genome-wide association study identifies loci at ATF7IP and KLK2 associated with percentage of circulating free PSA
Neoplasia (New York, N.Y.) · 2013 · PMID 23359319
2 pages
rs1354774 Prostate-Specific Antigen (PSA) Levels
Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
Human molecular genetics · 2012 · PMID 22936694
1 page
rs72829446
Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4
Nature genetics · 2012 · PMID 23023329
1 page
rs103294
Whole exome sequencing identified six novel genes for depressive symptoms
Molecular psychiatry · 2025 · PMID 39472661
1 page
rs7853605

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.