For researchers

Is your paper here?

2,676 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.

13 matches for Adams HHH.

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs743134 rs10914462 rs6074798 rs3129977 rs79582714 rs62037363
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function
Nature communications · 2018 · PMID 30061609 · open access
12 pages+
rs252746 rs143246821 rs916888 rs963406 rs79294353 rs111898810
The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs114489117 rs62399042 rs6554054 rs11070185 rs76470478 rs2301718
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+
rs56881390 rs77631946 rs2010871 rs940922629 rs117047468 rs11758358
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+
rs7973282 rs11655686 rs6722682 rs6841071 rs6850035 rs7440928
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
Communications biology · 2023 · PMID 37402774 · open access
11 pages
rs12107945 rs113622822 rs34814687 rs13204469 rs11030009 rs55963900
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
10 pages
rs9505301 rs9818981 rs2410767 rs10439607 rs10217651 rs35200015
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
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
Brain : a journal of neurology · 2022 · PMID 35511193 · open access
6 pages
rs3744027 rs6503417 rs12149643 rs73191849 rs13403122 Cerebral Small Vessel Disease
The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages
Brain communications · 2020 · PMID 33345186 · open access
3 pages
rs75945125 rs71329093 rs2242882
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
CHARGE consortium
Nature medicine · 2023 · PMID 37069360 · open access
3 pages
rs72485816 rs6011998 rs112407396
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Stroke · 2020 · PMID 32517579
2 pages
rs2598420 rs3758575
Heritability and genome-wide association study of diffusing capacity of the lung
The European respiratory journal · 2018 · PMID 30049742
1 page
rs17280293

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.