For researchers

Is your paper here?

2,677 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.

136 matches for Thorleifsson G, showing the first 20.

Genome-wide analysis identifies 12 loci influencing human reproductive behavior
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
4 pages
rs10908557 rs6885307 rs2347867 rs2721195
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
23andMe Research Team
PLoS genetics · 2018 · PMID 30566500 · open access
4 pages
rs9696009 rs1784692 rs1795379 rs8043701
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
rs6472846 rs28654158 rs113828443 rs34555419
Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights
UROMOL Consortium
European urology · 2023 · PMID 37210288
4 pages
rs1414253 rs411482 rs4743687 rs17863783
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis
Nature genetics · 2023 · PMID 37932435 · open access
4 pages
rs17099617 rs73217448 rs60147627 rs61914392
The genetic architecture of fibromyalgia across 2.5 million individuals
Chronic Pain Genomics Consortium · FinnGen and 3 more consortia
Nature medicine · 2026 · PMID 42521817 · open access
4 pages
rs62194170 rs2734833 rs34683740 Fibromyalgia
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
Nature genetics · 2008 · PMID 18264098
3 pages
rs5945572 rs721048 Prostate Cancer
Many sequence variants affecting diversity of adult human height
Nature genetics · 2008 · PMID 18391951
3 pages
rs3748069 rs12198986 rs6830062
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Wellcome Trust Case Control Consortium · Procardis Consortia and 1 more consortia
PLoS genetics · 2009 · PMID 19557161 · open access
3 pages
rs987237 rs7826222 rs2605100
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
rs1055144 rs6784615 rs6861681
Discovery of common variants associated with low TSH levels and thyroid cancer risk
Nature genetics · 2012 · PMID 22267200
3 pages
rs2439302 rs116909374 Thyroid Cancer
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
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures
Nature communications · 2016 · PMID 26733130 · open access
3 pages
rs577721086 rs71382995 rs115242848
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci
Circulation research · 2017 · PMID 27899403 · open access
3 pages
rs12133641 rs9316871 Abdominal Aortic Aneurysm
Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma
Nature communications · 2020 · PMID 32041948 · open access
3 pages
rs6791479 rs10399947 Cutaneous Squamous Cell Carcinoma
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
3 pages
rs3783347 rs6072275 rs4869272
Variants conferring risk of atrial fibrillation on chromosome 4q25
Nature · 2007 · PMID 17603472
2 pages
rs10033464 Atrial Fibrillation
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Nature genetics · 2009 · PMID 19079260
2 pages
rs6499640 rs7647305
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Nature genetics · 2009 · PMID 19198610
2 pages
rs4857855 rs12619285
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
Nature genetics · 2010 · PMID 20622881
2 pages
rs7025486 Abdominal Aortic Aneurysm

Showing 20 of 136 · page 5 of 7

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.