For researchers

Is your paper here?

2,676 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.

173 matches for Duijn CM, showing the first 20.

The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs56881390 rs77631946 rs2010871 rs940922629 rs117047468 rs11758358
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs12109259 rs11671130 rs2971871 rs1136774 rs1662340 rs10028665
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
12 pages+
rs68049022 rs56151256 rs13201721 rs58541850 rs9867121 rs114590429
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+
rs7973282 rs11655686 rs6722682 rs6841071 rs6850035 rs7440928
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Nature communications · 2023 · PMID 36918541 · open access
12 pages+
rs10793848 rs2066626 rs1873164 rs2762049 rs55824920 rs72798148
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+
rs67507374 rs62523081 rs11925442 rs138917529 rs721156 rs11767259
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+
rs1457553 rs3765618 rs57917116 rs7003445 rs6964590 rs10819313
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
11 pages
rs543874 rs10150332 rs2241423 rs2287019 rs12444979 rs206936
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
11 pages
rs1364063 rs4840086 rs9939609 rs10980926 rs7642134 rs17188434
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
Communications biology · 2023 · PMID 37402774 · open access
11 pages
rs12107945 rs113622822 rs34814687 rs13204469 rs11030009 rs55963900
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
Alcohol Genome-wide Association (AlcGen) Consortium · Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study and 5 more consortia
Nature genetics · 2011 · PMID 22001757
10 pages
rs7267979 rs6834314 rs2954021 rs1976403 rs1883415 rs7923609
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
NEIGHBOR Consortium
Nature genetics · 2013 · PMID 23291589
10 pages
rs2307121 rs1007000 rs1536482 rs11145951 rs4938174 rs1564892
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
rs10853531 rs11145488 rs12511037 rs1649081 rs16949788 rs10089517
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
LifeLines Cohort Study
Nature genetics · 2016 · PMID 27089181 · open access
10 pages
rs2075677 rs4958581 rs7554469 rs4938021 rs3756290 rs782212
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
International Visible Trait Genetics Consortium
Nature genetics · 2018 · PMID 29662168 · open access
10 pages
rs6440008 rs10960765 rs58979150 rs11041426 rs72917317 rs10899501
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
10 pages
rs9505301 rs9818981 rs2410767 rs10439607 rs10217651 rs35200015
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels
Circulation · 2011 · PMID 21300955
9 pages
rs6734238 rs13233571 rs1183910 rs1800961 rs10521222 rs2847281
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
9 pages
rs2506142 rs4081947 rs6791480 rs6693567 rs10155855 rs10218452
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
CHD Exome+ Consortium · ExomeBP Consortium and 4 more consortia
Nature genetics · 2016 · PMID 27618448
9 pages
rs2493292 rs11639856 rs1925153 rs3755652 rs11014166 rs11024074
New insights into the genetic etiology of Alzheimer's disease and related dementias
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
9 pages
rs3848143 rs62374257 rs3851179 rs6605556 rs7767350 rs6586028

Showing 20 of 173 · page 3 of 9

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.