For researchers

Is your paper here?

2,663 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.

98 matches for Mägi R, showing the first 20.

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs2252281 rs6088528 rs6087579 rs113445505 rs34468415 rs12671694
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs1227734 rs35524242 rs56084311 rs5744249 rs2922996 rs12802112
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs11718848 rs11537816 rs16859180 rs1449592 rs13196885 rs576629818
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs146474788 rs17256082 rs12784552 rs142484519 rs118164457 rs7063597
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
arcOGEN Consortium · HUNT All-In Pain and 2 more consortia
Cell · 2021 · PMID 34450027 · open access
12 pages+
rs9940278 rs7294636 rs34195470 rs17615906 rs10282983 rs17288390
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+
rs12669223 rs3768301 rs72830009 rs7100404 rs7076754 rs835576
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs9344003 rs12974635 rs10519014 rs11691472 rs2679184 rs2854915
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs56372821 rs540508277 rs6430080 rs28673808 rs78875955 rs739447
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
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
GWA-PA Consortium · Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37679419 · open access
12 pages+
rs10497347 rs4769580 rs1966228 rs17656269 rs8047053 rs6048183
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+
rs72702900 rs28520436 rs10822037 rs2415269 rs4532376 rs112385344
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs940526 rs11264734 rs7236307 rs4848397 rs11055891 rs74179816
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1475655 rs67269808 rs7304270 rs2658746 rs75417759 rs12746673
Genetic determinants of plasma protein levels in the Estonian population
Estonian Biobank Research Team
Scientific reports · 2024 · PMID 38565889 · open access
12 pages+
rs3764246 rs1918898 rs71519209 rs115944227 rs34869253 rs11507717
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+
rs11708118 rs2515236 rs13064760 rs62137009 rs1658425 rs11666906
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+
rs7072793 rs4823075 rs182787262 rs12567744 rs11865979 rs12193858
Genetic architecture reconciles linkage and association studies of complex traits
Estonian Biobank Research Team · Lifelines Cohort Study
Nature genetics · 2024 · PMID 39375568
12 pages+
rs10828248 rs11152029 rs171390 rs2012697 rs2398871 rs1440983
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+
rs11831278 rs58723578 rs2551776 rs9787942 rs3849386 rs3010043

Showing 20 of 98 · page 2 of 5

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.