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.

12 matches for Tinker A.

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
rs112019128 rs6900627 rs4585546 rs3768419 rs7552783 rs62441680
Genetically Determined Serum Calcium Levels and Markers of Ventricular Repolarization: A Mendelian Randomization Study in the UK Biobank
Circulation. Genomic and precision medicine · 2021 · PMID 33887147
12 pages+
rs1184556173 rs34422500 rs3011642 rs111712978 rs75153054 rs4506486
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs4346013 rs7540968 rs1034809 rs10028613 rs17538230 rs72912375
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Nature communications · 2023 · PMID 36918541 · open access
12 pages+
rs13029206 rs330944 rs77903023 rs11047438 rs72825047 rs11195260
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
rs16982520 rs7406910 rs34591516 rs1126930 rs10407022 rs470113
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
AOCS study group · EMBRACE Study and 4 more consortia
Nature genetics · 2017 · PMID 28346442
9 pages
rs1879586 rs7207826 rs11651755 rs688187 rs7902587 rs9886651
Genomic and pleiotropic analyses of resting QT interval identifies novel loci and overlap with atrial electrical disorders
Human molecular genetics · 2021 · PMID 34274964 · open access
6 pages
rs1009674 rs2793409 rs4399570 rs1805120 rs9933198 rs2832274
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Genome biology · 2018 · PMID 30012220 · open access
4 pages
rs11588271 rs116202356 rs3746435 rs11848785
Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system
Nature communications · 2018 · PMID 29769521 · open access
3 pages
rs35118522 rs1343676 rs1384590
Common Genetic Variants Modulate the Electrocardiographic Tpeak-to-Tend Interval
American journal of human genetics · 2020 · PMID 32386560 · open access
3 pages
rs2486695 rs196064 rs113843864
Genetic Basis and Prognostic Value of Exercise QT Dynamics
Circulation. Genomic and precision medicine · 2020 · PMID 32527199 · open access
3 pages
rs1591734 rs28436726 rs12941598
Cardiovascular Predictive Value and Genetic Basis of Ventricular Repolarization Dynamics
Circulation. Arrhythmia and electrophysiology · 2019 · PMID 31607149
2 pages
rs2072412 rs1396206

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.