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.

9 matches for Magnusson OT.

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
rs183821586 rs41282145 rs17300770 rs9621 rs138587317 rs62193080
Physical and neurobehavioral determinants of reproductive onset and success
Nature genetics · 2016 · PMID 27089180
10 pages
rs1040124 rs12522910 rs4840367 rs658385 rs2248699 rs538498277
New basal cell carcinoma susceptibility loci
Nature communications · 2015 · PMID 25855136 · open access
7 pages
rs7538876 rs801114 rs11170164 rs78378222 rs57244888 rs28727938
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
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
Nature communications · 2016 · PMID 26838040 · open access
6 pages
rs11559024 rs2930191 rs4072797 rs17412833 rs150956780 rs116841148
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
Nature genetics · 2019 · PMID 30643255
5 pages
rs34210653 rs17718444 rs6543124 rs1050152 Chronic Rhinosinusitis and the Bitter Taste Receptor
Discovery of common variants associated with low TSH levels and thyroid cancer risk
Nature genetics · 2012 · PMID 22267200
3 pages
rs2439302 rs116909374 Thyroid Cancer
Mutations in BRIP1 confer high risk of ovarian cancer
Nature genetics · 2011 · PMID 21964575
1 page
rs34289250
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy
Nature communications · 2019 · PMID 30992453 · open access
1 page
rs73112142

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.