For researchers

Is your paper here?

2,675 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 18.

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
rs9902453 rs7800944
Genetic studies of body mass index yield new insights for obesity biology
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
rs16851483 rs2121279
GWAS meta-analysis identifies five susceptibility loci for endometrial cancer
Estonian Biobank Research Team
EBioMedicine · 2025 · PMID 40633141 · open access
2 pages
rs148261157 rs7579014
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
1 page
rs4105144
CUBN is a gene locus for albuminuria
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
1 page
Kidney Function
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption
Human molecular genetics · 2011 · PMID 21357676
1 page
rs6968865
A genome-wide association search for type 2 diabetes genes in African Americans
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
1 page
rs7560163
FTO genotype is associated with phenotypic variability of body mass index
Nature · 2012 · PMID 22982992
1 page
rs7202116
Modulation of genetic associations with serum urate levels by body-mass-index in humans
PloS one · 2015 · PMID 25811787 · open access
1 page
rs898534
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
Age at Menarche
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
rs60780116
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia
23andMe Research Team · Substance Use Disorders Working Group of the Psychiatric Genomics Consortium and 1 more consortia
Nature neuroscience · 2018 · PMID 30150663
1 page
rs17761723
Large-scale meta-analysis highlights the hypothalamic-pituitary-gonadal axis in the genetic regulation of menstrual cycle length
Human molecular genetics · 2018 · PMID 30202859 · open access
1 page
rs6670899
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
rs492571
Genome-wide association study meta-analysis supports association between MUC1 and ectopic pregnancy
Estonian Biobank Research Team
Human reproduction (Oxford, England) · 2023 · PMID 37877466 · open access
1 page
rs11598956
Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry
Estonian Biobank Research Team · FinnGen and 1 more consortia
BMC genomics · 2024 · PMID 38408933 · open access
1 page
rs12000707
Circulating anti-Müllerian hormone levels in pre-menopausal women: novel genetic insights from a genome-wide association meta-analysis
Human reproduction (Oxford, England) · 2024 · PMID 38815977 · open access
1 page
rs6729614
Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development
DBDS Genomic Consortium, Estonian Biobank Research Team
JHEP reports : innovation in hepatology · 2025 · PMID 40823170 · open access
1 page
rs3179778

Showing 18 of 98 · page 5 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.