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.

7 matches for Moore A.

Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
Genetics of DNA Methylation Consortium · NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Genome biology · 2021 · PMID 34187551 · open access
12 pages+
rs72633672 rs75462778 rs3118123 rs3737843 rs117932856 rs73538174
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs6139332 rs2014307 rs630839 rs6514424 rs6677770 rs505317
Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors
The Journal of biological chemistry · 2022 · PMID 36395887 · open access
12 pages+
rs1438480 rs28603189 rs16879947 rs73264680 rs71308182 rs28418405
Biological and genetic determinants of glycolysis: Phosphofructokinase isoforms boost energy status of stored red blood cells and transfusion outcomes
Cell metabolism · 2024 · PMID 38964323
12 pages+
rs636889 rs116703563 rs9910909 rs139287365 rs5987022 rs140657308
Seven new loci associated with age-related macular degeneration
AMD Gene Consortium
Nature genetics · 2013 · PMID 23455636 · open access
7 pages
rs1864163 rs920915 rs8135665 rs8017304 rs9542236 rs13081855
Beyond factor H: The impact of genetic-risk variants for age-related macular degeneration on circulating factor-H-like 1 and factor-H-related protein concentrations
American journal of human genetics · 2021 · PMID 34260948 · open access
6 pages
rs72732232 rs70620 rs10801561 rs10801586 rs150313019 rs78606172
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes
Genetic epidemiology · 2019 · PMID 31407831
1 page
rs16947122

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.