For researchers

Is your paper here?

2,652 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.

19 matches for Polašek O.

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
rs17460657 rs347272 rs164133 rs545833 rs10919070 rs12079745
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
rs13011109 rs2820443 rs12955983 rs6737082 rs2821248 rs10840060
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2018 · PMID 29760442 · open access
12 pages+
rs3808520 rs7026684 rs10980623 rs7040970 rs7308752 rs11553764
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
CREAM Consortium · 23andMe Research Team and 1 more consortia
Nature genetics · 2018 · PMID 29808027 · open access
12 pages+
rs2162488 rs4332760 rs41393947 rs10879211 rs1346720 rs55684140
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
12 pages+
rs71490394 rs12497779 rs74053129 rs12634907 rs35505 rs268717
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters
International Glaucoma Genetics Consortium · NEIGHBORHOOD consortium and 1 more consortia
Communications biology · 2019 · PMID 31798171 · open access
12 pages+
rs2239854 rs114537871 rs28503222 rs61045038 rs7868669 rs4074178
Genetic regulation of post-translational modification of two distinct proteins
Nature communications · 2022 · PMID 35332118 · open access
12 pages+
rs11622603 rs80021729 rs35376994 rs2413592 rs4543384 rs7153753
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs3212861 rs3916033 rs12212322 rs4589542 rs16853414 rs2710329
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Million Veteran Program · Lifelines Cohort Study and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
rs10521146 rs11000864 rs73046010 rs139919 rs55715288 rs17562391
Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers
PLoS genetics · 2013 · PMID 23382691 · open access
10 pages
rs11710456 rs7652995 rs4878639 rs6583437 rs2072209 rs2186369
Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk
International journal of molecular sciences · 2023 · PMID 37108169 · open access
10 pages
rs13358188 rs146072725 rs17587821 rs188290902 rs189257688 rs554596237
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
LifeLines Cohort Study · EchoGen consortium and 6 more consortia
Nature genetics · 2011 · PMID 21909110 · open access
6 pages
rs1327235 rs2071518 rs11222084 rs13082711 rs11191593 rs319690
Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation
Nature communications · 2017 · PMID 28878392 · open access
5 pages
rs8013055 rs35590487 rs2659009 rs58087925 rs12019136
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
LifeLines Cohort Study · CARDIoGRAM Consortium and 3 more consortia
Nature genetics · 2013 · PMID 23263486
3 pages
rs1481012 rs4475146 Gout
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation
PLoS genetics · 2010 · PMID 21203500 · open access
2 pages
rs3760776 rs10483776
Genetic Landscape of the ACE2 Coronavirus Receptor
GenOMICC Consortium† · IMI-DIRECT Consortium†
Circulation · 2022 · PMID 35387486 · open access
2 pages
rs5992134 rs3094087
Genetic predictors of fibrin D-dimer levels in healthy adults
Circulation · 2011 · PMID 21502573
1 page
rs12029080
Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone
Journal of endocrinological investigation · 2019 · PMID 30843173
1 page
rs67142165

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.