For researchers

Is your paper here?

2,660 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.

8 matches for Hindy G.

The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs184980867 rs10248717 rs11672003 rs149590572 rs113920320 rs111589301
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+
rs1551728 rs16832694 rs16942312 rs17093810 rs6666757 rs2032289
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Biobank Japan · EPIC-CVD and 1 more consortia
Nature genetics · 2022 · PMID 36474045 · open access
12 pages+
rs192425087 rs2492304 rs66778572 rs8124182 rs2215614 rs72836800
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data
Nature communications · 2019 · PMID 31235808 · open access
5 pages
rs7852129 rs28822480 rs6495046 rs9831002 rs2046850
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
DBDS Consortium · Regeneron Genetics Center
The Journal of clinical investigation · 2022 · PMID 36194491 · open access
4 pages
rs925411 rs9704688 rs2633313 rs2633321
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes
Regeneron Genetics Center · DiscovEHR Collaboration
Nature communications · 2022 · PMID 35999217 · open access
2 pages
rs1799816 rs61739909
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
Lancet (London, England) · 2012 · PMID 22607825 · open access
1 page
Cholesterol (LDL, HDL and Total)

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.