For researchers

Is your paper here?

2,663 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.

44 matches for Rafnar T, showing the first 20.

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
rs6830062 rs3748069 rs12198986
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
Nature genetics · 2009 · PMID 19767754
3 pages
rs16902094 rs8102476 rs11228565
Discovery of common variants associated with low TSH levels and thyroid cancer risk
Nature genetics · 2012 · PMID 22267200
3 pages
rs2439302 rs116909374 Thyroid Cancer
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
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
Nature genetics · 2022 · PMID 35915169
3 pages
rs11607355 rs2413932 rs12348845
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
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations
Nature genetics · 2009 · PMID 19198613
2 pages
rs944289 Thyroid Cancer
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
Nature genetics · 2009 · PMID 19648920
2 pages
rs2294008 Bladder Cancer
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
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Nature genetics · 2010 · PMID 20972438 · open access
2 pages
rs8102137 rs798766
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
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
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
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
1 page
rs4105144
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption
Human molecular genetics · 2011 · PMID 21357676
1 page
rs6968865
Mutations in BRIP1 confer high risk of ovarian cancer
Nature genetics · 2011 · PMID 21964575
1 page
rs34289250
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Nature genetics · 2014 · PMID 24880342 · open access
1 page
rs13314271
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma
Nature communications · 2015 · PMID 26007630 · open access
1 page
rs57104699

Showing 20 of 44 · page 2 of 3

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.