For researchers

Is your paper here?

2,677 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.

30 matches for Kettunen J, showing the first 20.

Hundreds of variants clustered in genomic loci and biological pathways affect human height
Nature · 2010 · PMID 20881960 · open access
12 pages+
rs822552 rs12694997 rs7853377 rs7532866 rs4605213 rs4640244
Discovery and refinement of loci associated with lipid levels
Global Lipids Genetics Consortium
Nature genetics · 2013 · PMID 24097068 · open access
12 pages+
rs4883201 rs11603023 rs11136341 rs4253772 rs13315871 rs2290159
The impact of low-frequency and rare variants on lipid levels
ENGAGE Consortium
Nature genetics · 2015 · PMID 25961943
12 pages+
rs419132 rs9638182 rs115400054 rs11648003 rs12208357 rs149615216
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors
American journal of human genetics · 2017 · PMID 27989323
12 pages+
rs188740444 rs6841333 rs113831257 rs141053179 rs2070074 rs28637706
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
12 pages+
rs72622585 rs13148153 rs4660885 rs61734651 rs11881070 rs11152089
Genome-wide characterization of circulating metabolic biomarkers
China Kadoorie Biobank Collaborative Group · Estonian Biobank Research Team and 1 more consortia
Nature · 2024 · PMID 38448586 · open access
12 pages+
rs1056265 rs1265103 rs73062380 rs4844565 rs12126767 rs35726795
Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations
FinnGen · Estonian Biobank Research Team
Nature communications · 2024 · PMID 39511132 · open access
12 pages+
rs11848465 rs2224214 rs144549742 rs2164198 rs41308273 rs77651758
131 genetic loci highlight immunological pathways and tissues in nasal polyposis and asthma
FinnGen
Nature communications · 2025 · PMID 41213931 · open access
12 pages+
rs2891058 rs116877855 rs62408224 rs9828592 rs113372064 rs11894248
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
11 pages
rs543874 rs10150332 rs2241423 rs2287019 rs12444979 rs206936
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels
Circulation · 2011 · PMID 21300955
9 pages
rs6734238 rs13233571 rs1183910 rs1800961 rs10521222 rs2847281
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
DBDS Genomic Consortium · FinnGen Study and 3 more consortia
Nature genetics · 2023 · PMID 36914876
8 pages
rs2226158 rs71575922 rs1903068 rs3858429 rs4540228 rs57281976
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
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata
FinnGen
Nature communications · 2023 · PMID 36726022 · open access
7 pages
rs17119191 rs11031731 rs7986407 rs182218101 rs4864806 rs4694227
Identifying Atopic Dermatitis Risk Loci in 1,094,060 Individuals with Subanalysis of Disease Severity and Onset
FinnGen · Estonian Biobank Research Team
The Journal of investigative dermatology · 2024 · PMID 38663478
7 pages
rs933905994 rs7481797 rs763581386 rs6064053 rs538763482 rs13275449
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease
Journal of the American Heart Association · 2019 · PMID 31070104 · open access
5 pages
rs12126607 rs2364368 rs71503800 rs12003835 rs11860711
Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome
FinnGen Consortium, Estonian Biobank Research Team
Human reproduction (Oxford, England) · 2022 · PMID 34791234 · open access
5 pages
rs7564590 rs3945628 rs1672716 rs11031002 rs145598156
Hirsutism beyond PCOS: Genome-wide evidence for genetic factors
FinnGen · Estonian Biobank Research Team
The Journal of investigative dermatology · 2026 · PMID 42190866
5 pages
rs150735020 rs199649605 rs180731645 rs544265360 Hirsutism
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population
Circulation. Cardiovascular genetics · 2017 · PMID 29237677 · open access
4 pages
rs12406089 rs198379 rs11105298 rs3753584
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns
Journal of medical genetics · 2019 · PMID 31217265 · open access
4 pages
rs192716315 rs6917603 rs117960796 rs117238625

Showing 20 of 30 · 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.