For researchers

Is your paper here?

2,657 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.

47 matches for Estonian Biobank Research Team, showing the first 20.

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+
rs61734651 rs11881070 rs11152089 rs143796236 rs222835 rs11643684
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
rs6632109 rs8049403 rs2048528 rs1518760 rs78475244 rs76668186
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets
Estonian Biobank Research Team
Nature immunology · 2023 · PMID 37563310 · open access
12 pages+
rs13010492 rs3811621 rs4251805 rs10733789 rs62360376 rs11265493
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
23andMe Research Team · Estonian Biobank Research Team
Nature communications · 2023 · PMID 37794016 · open access
12 pages+
rs6023002 rs705699 rs117137535 rs11236813 rs56308324 rs10836538
Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2023 · PMID 37872160 · open access
12 pages+
rs1441198 rs333933 rs17198582 rs1453184 rs1861628 rs11728154
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+
rs11776164 rs11946481 rs61903423 rs633372 rs34696599 rs9306328
Genetic determinants of plasma protein levels in the Estonian population
Estonian Biobank Research Team
Scientific reports · 2024 · PMID 38565889 · open access
12 pages+
rs117694210 rs116927451 rs12512757 rs4900236 rs854624 rs9927301
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
DBDS Genomic Consortium · Regeneron Genetics Center and 3 more consortia
Nature genetics · 2024 · PMID 38632349 · open access
12 pages+
rs1818599 rs75661051 rs77510523 rs12352805 rs146420876 rs10221244
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+
rs16948230 rs6801151 rs7243332 rs6032660 rs10487459 rs175086
Uncovering the shared genetic components of thyroid disorders and reproductive health
Estonian Biobank Research Team · Health Informatics Research Team
European journal of endocrinology · 2024 · PMID 39067062
12 pages+
rs4495566 rs1790604 rs2288188 rs9494311 rs71581958 rs1516960
Genetic architecture reconciles linkage and association studies of complex traits
Estonian Biobank Research Team · Lifelines Cohort Study
Nature genetics · 2024 · PMID 39375568
12 pages+
rs16932761 rs2504674 rs6504165 rs11610621 rs11656076 rs17609347
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+
rs144549742 rs2164198 rs41308273 rs77651758 rs11914834 rs10227463
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Genes & Health Research Team · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2025 · PMID 40038546 · open access
12 pages+
rs149780392 rs3794752 rs62233286 rs7095308 rs73048654 rs143445113
Atlas of genetic and phenotypic associations across 42 female reproductive health diagnoses
Estonian Biobank Research Team
Nature medicine · 2025 · PMID 40069456
12 pages+
rs12475639 rs71648550 rs1239681 rs1935050 rs67679138 rs11123172
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+
rs2081786 rs7925720 rs913671 rs10831903 rs1515873 rs2616559
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+
rs34835001 rs1445566 rs17803970 rs10997841 rs10929759 rs3730074
Genome-wide association study and polygenic risk prediction of hypothyroidism
DBDS Genomic Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2025 · PMID 41238958 · open access
12 pages+
rs4390668 rs6678625 rs1559539 rs28607283 rs1109302 rs6467265
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Colorado Center for Personalized Medicine · DBDS Genomic Consortium and 2 more consortia
Nature genetics · 2026 · PMID 41419686 · open access
12 pages+
rs2421650 rs77608177 rs2150026 rs11564336 rs178707 rs2465417
The genetic basis of dermatophytosis skin infection susceptibility
Estonian Biobank Research Team · FinnGen
Nature communications · 2026 · PMID 41792138 · open access
12 pages+
rs439223 rs61730306 rs10094888 rs17839568 rs11642192 rs35273427
Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction
Estonian Biobank Research Team · 23andMe Research Team
Nature genetics · 2026 · PMID 42009823 · open access
12 pages+
rs1729948 rs72773791 rs113329317 rs4674113 rs77541496 rs757747

Showing 20 of 47 · 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.