For researchers

Is your paper here?

2,662 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+
rs117478007 rs182894584 rs183403564 rs192268857 rs174465 rs182891158
Genetics of 35 blood and urine biomarkers in the UK Biobank
FinnGen
Nature genetics · 2021 · PMID 33462484 · open access
12 pages+
rs73667430 rs12870045 rs13419481 rs41266007 rs74652320 rs11196181
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+
rs6667536 rs12540035 rs9819278 rs2491422 rs62391632 rs66819623
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+
rs17145892 rs640494 rs11000852 rs4757388 rs57203936 rs709228
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
FinnGen
Nature communications · 2022 · PMID 35347128 · open access
12 pages+
rs199546957 rs3754835 rs1865109 rs148563337 rs191616586 rs144294115
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+
rs4267865 rs57634870 rs11196296 rs3825801 rs79495865 rs1871045
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
Genome-wide association analysis of plasma lipidome identifies 495 genetic associations
FinnGen
Nature communications · 2023 · PMID 37907536 · open access
12 pages+
rs34396223 rs12763964 rs7529794 rs189452885 rs148885848 rs150536132
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+
rs3754053 rs236984 rs4310508 rs12037485 rs111705570 rs79683221
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+
rs10865093 rs7431106 rs61946067 rs28986300 rs16948230 rs6801151
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs6574106 rs6916760 rs4506680 rs114427493 rs12274095 rs57551109
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+
rs9787942 rs3849386 rs3010043 rs11848465 rs2224214 rs144549742
Novel loci and biomedical consequences of iron homoeostasis variation
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
12 pages+
rs2238005 rs549876436 rs9739943 rs2906082 rs2600895 rs143437464
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+
rs12308843 rs9348967 rs10500759 rs7572753 rs11911487 rs1152620
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+
rs114087689 rs9643050 rs192776885 rs35118298 rs10866828 rs11956571
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
Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk
FinnGen
Nature genetics · 2026 · PMID 41419685 · open access
12 pages+
rs9826313 rs10185667 rs4368668 rs73162770 rs1271934 rs1833126
The genetic basis of dermatophytosis skin infection susceptibility
Estonian Biobank Research Team · FinnGen
Nature communications · 2026 · PMID 41792138 · open access
12 pages+
rs2236506 rs3787092 rs112088479 rs62066119 rs12958073 rs439223
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+
rs34450379 rs2070217 rs7232 rs7080009 rs34674752 rs72695404

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.