For researchers

Is your paper here?

2,681 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.

184 matches for Van Duijn C, showing the first 20.

Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology
NEIGHBORHOOD Consortium
Genetic epidemiology · 2015 · PMID 25631615
6 pages
rs11031436 rs11651885 rs301801 rs6671926 rs9546434 rs7972528
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs16826069 rs1127787 rs7572857 rs2233580 rs56200889 rs35658696
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
Brain : a journal of neurology · 2022 · PMID 35511193 · open access
6 pages
rs3744027 rs6503417 rs12149643 rs73191849 rs13403122 Cerebral Small Vessel Disease
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
6 pages
rs56381411 rs3784634 rs5400 rs17853166 rs75619922 rs7225887
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function
Nature genetics · 2010 · PMID 20010835
5 pages
rs2070600 rs11727189 rs11168048 rs2277027 Pulmonary Function (Lung Capacity)
Genome-wide association study of intracranial aneurysm identifies three new risk loci
Nature genetics · 2010 · PMID 20364137 · open access
5 pages
rs11661542 rs9298506 rs12413409 rs9315204 Intracranial Aneurysm
A genome-wide association study of optic disc parameters
PLoS genetics · 2010 · PMID 20548946 · open access
5 pages
rs1362756 rs1547014 rs1900004 rs17146964 Glaucoma
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Nature genetics · 2010 · PMID 21076409 · open access
5 pages
rs17391905 rs1886512 rs17608766 rs1733724 Cardiac Conduction Intervals (PR Interval and QRS Duration)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
BioBank Japan Project
American journal of human genetics · 2017 · PMID 28017375
5 pages
rs10929547 rs6430549 rs2060597 rs592423 rs4535497
Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence
Nature genetics · 2017 · PMID 28530673 · open access
5 pages
rs7646501 rs10191758 rs12744310 rs12928404 rs36093924
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness
GEFOS Any-Type of Fracture Consortium
Nature communications · 2017 · PMID 29313844 · open access
5 pages
rs72979233 rs4926611 rs11614333 rs2110927 rs80103986
Large-scale association analyses identify host factors influencing human gut microbiome composition
Nature genetics · 2021 · PMID 33462485
5 pages
rs71348714 rs7605229 rs7322849 rs11110281 rs61841503
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
23andMe Research Team · International Visible Trait Genetics Consortium
Science advances · 2021 · PMID 33692100 · open access
5 pages
rs1740397 rs3809761 rs13297008 rs62330021 rs9971729
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
ENGAGE Consortium
Nature genetics · 2009 · PMID 19060911
4 pages
rs10903129 rs693 rs3905000 rs2240466
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
Genetic Factors for Osteoporosis (GEFOS) Consortium
Nature genetics · 2009 · PMID 19801982 · open access
4 pages
rs7524102 rs7932354 rs11898505 Spine Bone Mineral Density
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Nature genetics · 2010 · PMID 20081858 · open access
4 pages
rs11920090 rs7944584 rs11605924 Fasting Blood Glucose
New loci associated with kidney function and chronic kidney disease
Nature genetics · 2010 · PMID 20383146
4 pages
rs267734 rs10774021 rs7805747 rs6465825
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels
Genetic Factors for Osteoporosis Consortium · Meta Analysis of Glucose and Insulin Related Traits Consortium
PLoS genetics · 2010 · PMID 20700443 · open access
4 pages
rs3925584 rs13146355 rs11144134 Magnesium
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors
Circulation. Cardiovascular genetics · 2010 · PMID 20884846
4 pages
rs675209 rs13129697 rs1106766 Gout

Showing 20 of 184 · page 5 of 10

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.