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.

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2014 · PMID 25241763 · open access
2 pages
rs17658229 rs17756712
Genetic studies of body mass index yield new insights for obesity biology
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
rs16851483 rs2121279
Common and rare variants associated with kidney stones and biochemical traits
Nature communications · 2015 · PMID 26272126 · open access
2 pages
rs1256328 Kidney Stones
Genome-wide analysis yields new loci associating with aortic valve stenosis
Nature communications · 2018 · PMID 29511194 · open access
2 pages
rs1830321 Aortic Stenosis
Genetic Associations and Architecture of Asthma-COPD Overlap
Chest · 2022 · PMID 35104449 · open access
2 pages
rs9273410 rs7312770
Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect
Annals of the rheumatic diseases · 2023 · PMID 36931692 · open access
2 pages
rs1800801 rs17013495
Genome-wide association study in 21,271 individuals identifies 9 novel loci associated with circulating CD34<sup>+</sup> hematopoietic stem and progenitor cell levels
HemaSphere · 2026 · PMID 42388415 · open access
2 pages
rs78502025 rs772557
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Nature · 2008 · PMID 18385739
1 page
Lung Cancer
Two newly identified genetic determinants of pigmentation in Europeans
Nature genetics · 2008 · PMID 18488028
1 page
rs1408799
Variants in MTNR1B influence fasting glucose levels
Nature genetics · 2009 · PMID 19060907
1 page
rs560887
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
American journal of human genetics · 2009 · PMID 19836008
1 page
rs31489
Several common variants modulate heart rate, PR interval and QRS duration
Nature genetics · 2010 · PMID 20062063
1 page
rs365990
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
Nature genetics · 2010 · PMID 20835238
1 page
rs4236601
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption
Human molecular genetics · 2011 · PMID 21357676
1 page
rs6968865
A variant in MCF2L is associated with osteoarthritis
arcOGEN Consortium
American journal of human genetics · 2011 · PMID 21871595
1 page
rs11842874
A genome-wide association search for type 2 diabetes genes in African Americans
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
1 page
rs7560163
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
Lancet (London, England) · 2012 · PMID 22607825 · open access
1 page
Cholesterol (LDL, HDL and Total)
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases
MAGIC · DIAGRAM Consortium and 1 more consortia
PLoS genetics · 2012 · PMID 22693455 · open access
1 page
rs3802177
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
FTO genotype is associated with phenotypic variability of body mass index
Nature · 2012 · PMID 22982992
1 page
rs7202116

Showing 20 of 136 · page 6 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.