For researchers

Is your paper here?

2,673 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.

9 matches for Jonsson T.

Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31666285
11 pages
rs9927389 rs183821586 rs41282145 rs17300770 rs9621 rs138587317
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA
Nature communications · 2018 · PMID 30410027 · open access
9 pages
rs381949 rs10054105 rs200476 rs72878024 rs8853 rs1638703
Rare and Common Variants Conferring Risk of Tooth Agenesis
Journal of dental research · 2018 · PMID 29364747
4 pages
rs121908120 rs917412 rs55846652 Tooth Agenesis
Many sequence variants affecting diversity of adult human height
Nature genetics · 2008 · PMID 18391951
3 pages
rs3748069 rs12198986 rs6830062
Discovery of common variants associated with low TSH levels and thyroid cancer risk
Nature genetics · 2012 · PMID 22267200
3 pages
rs2439302 rs116909374 Thyroid Cancer
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
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Nature · 2008 · PMID 18385739
1 page
Lung Cancer
A genome-wide association study yields five novel thyroid cancer risk loci
Nature communications · 2017 · PMID 28195142 · open access
1 page
rs12129938

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.