For researchers

Is your paper here?

2,677 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.

76 matches for Munroe P, showing the first 20.

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
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
rs2793409 rs4399570 rs1805120 rs9933198 rs2832274 rs1009674
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
6 pages
rs56381411 rs3784634 rs5400 rs17853166 rs75619922 rs7225887
Genome-wide association analysis identifies 20 loci that influence adult height
Diabetes Genetics Initiative · Wellcome Trust Case Control Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18391952
5 pages
rs6060373 rs1390401 rs6724465 rs2814993 rs2282978
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Nature genetics · 2010 · PMID 21076409 · open access
5 pages
rs17391905 rs1886512 rs17608766 rs1733724 Cardiac Conduction Intervals (PR Interval and QRS Duration)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Genome-wide association study identifies eight loci associated with blood pressure
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · open access
4 pages
rs12946454 rs1530440 rs16948048 rs17367504
Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1
Hypertension (Dallas, Tex. : 1979) · 2013 · PMID 23381795
4 pages
rs2957692 rs2731672 rs5370 rs4253238
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
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
4 pages
rs9308788 rs141962517 rs75535814 rs113809930
Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function
Nature genetics · 2022 · PMID 35697868
4 pages
rs78529941 rs9856926 rs501740 rs55834511
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations
EUROSPAN Consortium · ENGAGE Consortium and 3 more consortia
PLoS genetics · 2009 · PMID 19503597 · open access
3 pages
rs12356193 rs742132 rs780094
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Wellcome Trust Case Control Consortium · Procardis Consortia and 1 more consortia
PLoS genetics · 2009 · PMID 19557161 · open access
3 pages
rs987237 rs7826222 rs2605100
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
rs1055144 rs6784615 rs6861681
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
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
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
3 pages
rs3783347 rs6072275 rs4869272
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure
VA Million Veteran Program
Nature communications · 2023 · PMID 37429843 · open access
3 pages
rs2832275 rs7795282 rs34163229

Showing 20 of 76 · page 3 of 4

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.