For researchers

Is your paper here?

2,671 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.

39 matches for Ehret G, showing the first 19.

Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior
Swiss Kidney Project on Genes in Hypertension (SKIPOGH) team
Human molecular genetics · 2016 · PMID 27702941
7 pages
rs10275488 rs12909047 rs35107470 rs2892838 rs2470893 rs66500423
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
rs115234772 rs62319742 rs148772934 rs138973557 rs148753653 rs12135881
Genome-wide association study of PR interval
Nature genetics · 2010 · PMID 20062060 · open access
6 pages
rs3807989 rs11047543 rs251253 rs11708996 rs6800541 Cardiac Conduction Intervals (PR Interval and QRS Duration)
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
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
Nature communications · 2017 · PMID 28613276 · open access
6 pages
rs12974440 rs12980262 rs1812835 rs2529471 rs4899412 rs12974991
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa
Cell · 2019 · PMID 31675503
6 pages
rs151330263 rs115231893 rs569795903 rs7564935 rs148228241 rs1088639
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
rs1173771 rs13139571 rs6015450 rs11191548 rs7129220
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Nature genetics · 2009 · PMID 19305409
4 pages
rs17779747 rs10919071 rs2968863 rs11970286
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels
Genetic Factors for Osteoporosis Consortium · Meta Analysis of Glucose and Insulin Related Traits Consortium
PLoS genetics · 2010 · PMID 20700443 · open access
4 pages
rs3925584 rs13146355 rs11144134 Magnesium
Genome-wide association study of blood pressure and hypertension
Nature genetics · 2009 · PMID 19430479
3 pages
rs2681472 rs2384550 Blood Pressure
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia
LifeLines Cohort Study
American journal of human genetics · 2014 · PMID 24954895
3 pages
rs12416687 rs16833934 rs4842666
Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes
Journal of the American Society of Nephrology : JASN · 2018 · PMID 29093028
3 pages
rs35929 rs3824347 rs4460629
Genetic determinants of zinc homeostasis and its role in cardiometabolic diseases
INSPIRE Consortium
PLoS genetics · 2025 · PMID 41325371 · open access
3 pages
rs138587215 rs12734494 rs41305769
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
PLoS genetics · 2007 · PMID 17658951 · open access
2 pages
rs9930506 Obesity and Body Weight
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
2 pages
rs17428471 rs17080102
Genetic studies of body mass index yield new insights for obesity biology
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
rs16851483 rs2121279
Multiple loci associated with indices of renal function and chronic kidney disease
Nature genetics · 2009 · PMID 19430482
1 page
rs17319721
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Nature genetics · 2009 · PMID 19597492 · open access
1 page
rs17042171
Common variants in KCNN3 are associated with lone atrial fibrillation
Nature genetics · 2010 · PMID 20173747 · open access
1 page
rs13376333

Showing 19 of 39 · page 2 of 2

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.