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.

86 matches for Pedersen O, showing the first 20.

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets
PLoS genetics · 2013 · PMID 23754956 · open access
6 pages
rs7788053 rs1131603 rs41281112 rs2270655 rs2336573 rs3742801
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Nature communications · 2016 · PMID 26818947 · open access
6 pages
rs1116357 rs1575972 rs9309245 rs67156297 rs7107784 rs78627331
Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci
Diabetes · 2016 · PMID 27416945
6 pages
rs13422522 rs7578326 rs6027072 rs12583553 rs10483182 rs6013915
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
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
rs3784634 rs5400 rs17853166 rs75619922 rs7225887 rs56381411
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
Wellcome Trust Case Control Consortium
Nature genetics · 2008 · PMID 18372903
5 pages
rs12779790 rs864745 rs7961581 rs7578597 rs10923931
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
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
Early Growth Genetics Consortium
Human molecular genetics · 2019 · PMID 31504550
5 pages
rs6567160 rs4077678 rs10493544 rs114670539 rs74583214
Large-scale association analyses identify host factors influencing human gut microbiome composition
Nature genetics · 2021 · PMID 33462485
5 pages
rs7605229 rs7322849 rs11110281 rs61841503 rs71348714
Genetic insight into sick sinus syndrome
DBDS Genomic Consortium
European heart journal · 2021 · PMID 33580673 · open access
5 pages
rs7689774 rs11554495 rs12932445 rs35813871 Sick Sinus Syndrome
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
Brain : a journal of neurology · 2022 · PMID 35022648 · open access
5 pages
rs244620 rs62023078 rs1518111 rs4974130 rs3001038
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
Members of the DBDS Genomic Consortium · Danish RA Genetics Working Group and 1 more consortia
Annals of the rheumatic diseases · 2022 · PMID 35470158 · open access
5 pages
rs67574266 rs1471293 rs10261758 rs1538981 rs7320598
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
DBDS Consortium · Regeneron Genetics Center
The Journal of clinical investigation · 2022 · PMID 36194491 · open access
5 pages
rs9704688 rs56172805 rs2633313 rs2633321 rs925411
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
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Nature communications · 2018 · PMID 29358691 · open access
4 pages
rs1708302 rs2943656 rs71320321 rs115918645
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Genome biology · 2018 · PMID 30012220 · open access
4 pages
rs11588271 rs116202356 rs3746435 rs11848785
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
DBDS Consortium · 23andMe Research Team
Gut · 2021 · PMID 33888516 · open access
4 pages
rs11585073 rs11176001 rs722587 Haemorrhoidal Disease
Genetic effects on the timing of parturition and links to fetal birth weight
Early Growth Genetics Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2023 · PMID 37012456 · open access
4 pages
rs113828443 rs34555419 rs6472846 rs28654158
Genomics of chronic dry cough unravels neurological pathways
Genes and Health Research Team
The European respiratory journal · 2025 · PMID 40675770 · open access
4 pages
rs1544730 rs7761208 rs5924943 rs78598167

Showing 20 of 86 · page 3 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.