For researchers

Is your paper here?

2,673 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.

41 matches for Evangelou E, showing the first 20.

Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
Lifelines Cohort Study · VA Million Veteran Program
Nature communications · 2021 · PMID 33972514 · open access
12 pages+
rs62463430 rs187345738 rs202155306 rs5747734 rs529876271 rs17710
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer
Scientific reports · 2021 · PMID 34021172 · open access
12 pages+
rs2535326 rs4925133 rs6045908 rs67017503 rs74513896 rs7571231
Genetic analysis of over half a million people characterises C-reactive protein loci
Nature communications · 2022 · PMID 35459240 · open access
12 pages+
rs12428361 rs7455288 rs72799498 rs6595549 rs11653826 rs7801838
Pleiotropic genetic architecture and novel loci for C-reactive protein levels
Nature communications · 2022 · PMID 36376304 · open access
12 pages+
rs12797544 rs144780071 rs73196883 rs35091123 rs11643744 rs11165468
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Million Veteran Program · Lifelines Cohort Study and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
rs28734123 rs7151849 rs10040811 rs13270541 rs16852778 rs1878825
Multi-trait association analysis reveals shared genetic loci between Alzheimer's disease and cardiovascular traits
Nature communications · 2024 · PMID 39537608 · open access
12 pages+
rs73517027 rs12372344 rs34873381 rs56145652 rs7081664 rs112961583
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
rs16982520 rs7406910 rs34591516 rs1126930 rs10407022 rs470113
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus
Nature communications · 2017 · PMID 28743860 · open access
11 pages
rs3765350 rs6726821 rs2110281 rs12283755 rs6684375 rs13245690
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders
Nature human behaviour · 2019 · PMID 31358974
9 pages
rs2277499 rs10496076 rs71414193 rs57281063 rs227179 rs4794015
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
8 pages
rs11230661 rs2050058 rs79624003 rs55809639 rs4847240 rs4660303
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
rs1566045 rs7953528 rs163879 rs1864325 rs344081 rs3905706
Seven new loci associated with age-related macular degeneration
AMD Gene Consortium
Nature genetics · 2013 · PMID 23455636 · open access
7 pages
rs1864163 rs920915 rs8135665 rs8017304 rs9542236 rs13081855
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
rs115234772 rs62319742 rs148772934 rs138973557 rs148753653 rs12135881
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis
PLoS genetics · 2016 · PMID 27701424 · open access
4 pages
rs11880992 rs10948155 rs12206662 rs10471753
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
4 pages
rs9308788 rs141962517 rs75535814 rs113809930
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
arcOGEN Consortium
Annals of the rheumatic diseases · 2014 · PMID 23989986 · open access
3 pages
rs3757837 rs6094710 Hip Osteoarthritis
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
rs12599112 rs11940694 Alcohol Consumption
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
2 pages
rs60839105 rs116843064
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
arcOGEN Consortium · arcOGEN Collaborators
Lancet (London, England) · 2012 · PMID 22763110 · open access
1 page
rs11177

Showing 20 of 41 · page 2 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.