For researchers

Is your paper here?

2,645 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.

51 matches for FinnGen, showing the first 20.

Genetic architecture of human plasma lipidome and its link to cardiovascular disease
FinnGen Project
Nature communications · 2019 · PMID 31551469 · open access
12 pages+
rs139612538 rs76368648 rs13070110 rs13151374 rs117478007 rs182894584
Genetics of 35 blood and urine biomarkers in the UK Biobank
FinnGen
Nature genetics · 2021 · PMID 33462484 · open access
12 pages+
rs117038277 rs137886124 rs34473506 rs112481451 rs115282533 rs116859590
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+
rs61870251 rs34175429 rs938604 rs1893261 rs62521288 rs17146835
Genetic analyses identify widespread sex-differential participation bias
FinnGen Study · 23andMe Research Team and 1 more consortia
Nature genetics · 2021 · PMID 33888908
12 pages+
rs2814162 rs28575268 rs67624109 rs1368546 rs77966298 rs10468280
A cross-population atlas of genetic associations for 220 human phenotypes
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
rs12946693 rs11191447 rs12902050 rs62576695 rs73200263 rs9573566
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
FinnGen
Nature communications · 2022 · PMID 35347128 · open access
12 pages+
rs150615661 rs1718292 rs117217055 rs6702754 rs12923769 rs35296872
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs7076754 rs835576 rs151215 rs36575 rs6978118 rs6485462
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+
rs9594366 rs16856530 rs62283809 rs10854002 rs2276133 rs7748159
Genome-wide association analysis of plasma lipidome identifies 495 genetic associations
FinnGen
Nature communications · 2023 · PMID 37907536 · open access
12 pages+
rs34621709 rs204468 rs17395333 rs34396223 rs12763964 rs7529794
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+
rs35857242 rs11039155 rs35397778 rs10873232 rs34907038 rs61802334
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
rs10992779 rs13161130 rs868754 rs2899991 rs6802567 rs2684641
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs240471 rs12887451 rs12118203 rs11754000 rs11263445 rs17180949
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+
rs58723578 rs2551776 rs9787942 rs3849386 rs3010043 rs11848465
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+
rs2867109 rs11021409 rs2205325 rs17120227 rs11071365 rs1059698
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum
Genes & Health Research Team · Estonian Biobank Research Team and 3 more consortia
Nature genetics · 2025 · PMID 40229599 · open access
12 pages+
rs6029630 rs3790611 rs12999558 rs147039802 rs116325030 rs58282071
131 genetic loci highlight immunological pathways and tissues in nasal polyposis and asthma
FinnGen
Nature communications · 2025 · PMID 41213931 · open access
12 pages+
rs116877855 rs62408224 rs9828592 rs113372064 rs11894248 rs113752715
Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk
FinnGen
Nature genetics · 2026 · PMID 41419685 · open access
12 pages+
rs10841441 rs7001844 rs140798921 rs9826313 rs10185667 rs4368668
The genetic basis of dermatophytosis skin infection susceptibility
Estonian Biobank Research Team · FinnGen
Nature communications · 2026 · PMID 41792138 · open access
12 pages+
rs35273427 rs612057 rs640081 rs7196726 rs2236506 rs3787092
Consensus meta-analysis of genome-wide association studies for Alzheimer's disease and related dementias
EADB · EADI and 7 more consortia
Nature genetics · 2026 · PMID 42237039 · open access
12 pages+
rs8712 rs58124010 rs376291994 rs34450379 rs7232 rs7080009
Novel loci and biomedical consequences of iron homoeostasis variation
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
11 pages
rs996347 rs112856048 rs72832593 rs187669805 rs2238005 rs549876436

Showing 20 of 51 · page 1 of 3

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.