For researchers

Is your paper here?

2,655 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.

16 matches for Gudmundsson J.

Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
Nature communications · 2018 · PMID 30194396 · open access
12 pages+
rs507139 rs6771541 rs765333492 rs12484951 rs2202282 rs551980034
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease
Nature · 2020 · PMID 32581359
12 pages+
rs654537 rs1050976 rs2069556 rs6535628 rs11079788 rs11714843
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer
Nature communications · 2020 · PMID 32769997 · open access
12 pages+
rs6721104 rs10186921 rs62174422 rs6717283 rs4571283 rs77994712
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
rs41282145 rs17300770 rs9621 rs138587317 rs62193080 rs9467148
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
rs6561599 rs381949 rs10054105 rs200476 rs72878024 rs8853
New basal cell carcinoma susceptibility loci
Nature communications · 2015 · PMID 25855136 · open access
7 pages
rs7538876 rs801114 rs11170164 rs78378222 rs57244888 rs28727938
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
Ovarian Cancer Association Consortium (OCAC) · PRACTICAL Consortium and 3 more consortia
Cancer research · 2016 · PMID 27197191
6 pages
rs11844632 rs4808075 rs56084662 rs11571833 rs186507655 rs148883465
Genetic correction of PSA values using sequence variants associated with PSA levels
Science translational medicine · 2010 · PMID 21160077
4 pages
rs401681 rs17632542 rs10788160 rs11067228
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis
Nature genetics · 2023 · PMID 37932435 · open access
4 pages
rs61914392 rs17099617 rs73217448 rs60147627
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
Nature genetics · 2008 · PMID 18264098
3 pages
rs5945572 rs721048 Prostate Cancer
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
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
Mutations in BRIP1 confer high risk of ovarian cancer
Nature genetics · 2011 · PMID 21964575
1 page
rs34289250
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.