For researchers

Is your paper here?

2,685 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.

50 matches for Estonian Biobank, 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+
rs72622585 rs13148153 rs4660885 rs61734651 rs11881070 rs11152089
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
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+
rs4515883 rs6743072 rs35073727 rs57631119 rs9380498 rs12187932
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+
rs4312054 rs6023002 rs705699 rs117137535 rs11236813 rs56308324
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+
rs2601803 rs4932352 rs36213229 rs141336511 rs406079 rs1441198
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+
rs4844565 rs12126767 rs35726795 rs56135013 rs7149218 rs2292622
Genetic determinants of plasma protein levels in the Estonian population
Estonian Biobank Research Team
Scientific reports · 2024 · PMID 38565889 · open access
12 pages+
rs4253536 rs420726 rs3135043 rs34266919 rs369634369 rs11465597
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+
rs113469203 rs7280197 rs12552930 rs12595409 rs141599192 rs6860725
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 rs78201023 rs2214230 rs7243332 rs6032660
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+
rs7170288 rs4495566 rs1790604 rs2288188 rs9494311 rs71581958
Genetic architecture reconciles linkage and association studies of complex traits
Estonian Biobank Research Team · Lifelines Cohort Study
Nature genetics · 2024 · PMID 39375568
12 pages+
rs769670 rs12440590 rs217671 rs3198123 rs4952843 rs6794389
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
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+
rs67377357 rs149780392 rs3794752 rs62233286 rs7095308 rs73048654
Atlas of genetic and phenotypic associations across 42 female reproductive health diagnoses
Estonian Biobank Research Team
Nature medicine · 2025 · PMID 40069456
12 pages+
rs12374261 rs7522710 rs1422 rs4708089 rs78602818 rs12475639
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+
rs12350099 rs1480637 rs2095140 rs13118508 rs2015110 rs509236
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+
rs58247754 rs12719514 rs34835001 rs1445566 rs17803970 rs10997841
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+
rs12206423 rs933809 rs10873079 rs1829142 rs34011920 rs8022931
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+
rs5991029 rs35485101 rs2421650 rs77608177 rs2150026 rs11564336
The genetic basis of dermatophytosis skin infection susceptibility
Estonian Biobank Research Team · FinnGen
Nature communications · 2026 · PMID 41792138 · open access
12 pages+
rs62066119 rs12958073 rs439223 rs61730306 rs12728311 rs10094888

Showing 20 of 50 · 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.