For researchers

Is your paper here?

2,661 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.

25 matches for Karjalainen J, showing the first 20.

Genome-wide association analyses identify variants in developmental genes associated with hypospadias
Nature genetics · 2014 · PMID 25108383
12 pages+
rs988958 rs3816183 rs2999052 rs13124827 rs1801085 rs4554617
Defining the role of common variation in the genomic and biological architecture of adult human height
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
12 pages+
rs6485978 rs4332428 rs1562975 rs17807185 rs12120956 rs3739707
New genetic loci link adipose and insulin biology to body fat distribution
ADIPOGen Consortium · CARDIOGRAMplusC4D Consortium and 11 more consortia
Nature · 2015 · PMID 25673412 · open access
12 pages+
rs6060717 rs11989744 rs4646404 rs319564 rs2179129 rs16996700
The impact of low-frequency and rare variants on lipid levels
ENGAGE Consortium
Nature genetics · 2015 · PMID 25961943
12 pages+
rs72959041 rs7759633 rs9988450 rs419132 rs9638182 rs115400054
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
rs13011109 rs2820443 rs12955983 rs6737082 rs2821248 rs10840060
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
ICBP Consortium · AGEN Consortium and 3 more consortia
Nature communications · 2016 · PMID 26831199 · open access
12 pages+
rs6795744 rs228611 rs3750082 rs10491967 rs11666497 rs1800615
Genetic architecture of human plasma lipidome and its link to cardiovascular disease
FinnGen Project
Nature communications · 2019 · PMID 31551469 · open access
12 pages+
rs117478007 rs182894584 rs183403564 rs192268857 rs174465 rs182891158
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer
Nature communications · 2020 · PMID 32769997 · open access
12 pages+
rs6721104 rs10186921 rs62174422 rs6717283 rs4571283 rs77994712
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
NEIGHBORHOOD consortium · ANZRAG consortium and 5 more consortia
Nature communications · 2021 · PMID 33627673 · open access
12 pages+
rs12540035 rs9819278 rs2491422 rs62391632 rs66819623 rs8141610
Genetic analyses identify widespread sex-differential participation bias
FinnGen Study · 23andMe Research Team and 1 more consortia
Nature genetics · 2021 · PMID 33888908
12 pages+
rs10964391 rs6917190 rs10965400 rs1792358 rs7809752 rs10040110
A cross-population atlas of genetic associations for 220 human phenotypes
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
rs4844261 rs653320 rs829562 rs11072799 rs146718647 rs8121417
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs147660927 rs7209222 rs9272456 rs4515883 rs6743072 rs35073727
Translational genomics of osteoarthritis in 1,962,069 individuals
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
rs10500759 rs7572753 rs11911487 rs1152620 rs2738292 rs11726937
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
FinnGen · 23andMe Research Team
Nature · 2020 · PMID 33057200 · open access
10 pages
rs77249081 rs74676712 rs9847631 rs116466979 rs1327494 rs1633768
Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation
FINNGEN
Nature communications · 2023 · PMID 36653354 · open access
10 pages
rs12128267 rs573841223 rs6884870 rs189411872 rs1663680 rs4648051
Genome-wide meta-analysis identifies genetic drivers of bile acid metabolism in intrahepatic cholestasis of pregnancy
FinnGen · Estonian Biobank research team and 1 more consortia
Nature communications · 2026 · PMID 42178310 · open access
8 pages
rs10773287 rs2021095 rs6733156 rs4148211 rs2788095 rs4805129
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure
FinnGen
Nature communications · 2023 · PMID 36653343 · open access
5 pages
rs7995158 rs791903 rs4636903 rs11868207 Otosclerosis
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
Proceedings of the National Academy of Sciences of the United States of America · 2014 · PMID 25201988
4 pages
rs1487441 rs9858213 rs13401104 rs3789044
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
rs4851266 rs9320913 rs1056667
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839

Showing 20 of 25 · page 1 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.