For researchers

Is your paper here?

2,681 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.

195 matches for Rotter JI, showing the first 20.

A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium
Diabetes · 2011 · PMID 21386085 · open access
7 pages
rs173539 rs11820589 rs301 rs11823543 rs2954033 rs1919128
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation
Nature genetics · 2017 · PMID 27918534
7 pages
rs2434264 rs7374732 rs6689335 rs912056 rs10060123 rs2123685
Fifteen Genetic Loci Associated With the Electrocardiographic P Wave
Circulation. Cardiovascular genetics · 2017 · PMID 28794112
7 pages
rs1467026 rs12090194 rs4839185 rs11099412 rs4276421 rs3801995
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals
Scientific reports · 2017 · PMID 29213071 · open access
7 pages
rs73017364 rs12035622 rs55863869 rs35760656 rs12271931 rs12626657
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
Common variants at ten loci influence QT interval duration in the QTGEN Study
Nature genetics · 2009 · PMID 19305408 · open access
6 pages
rs37062 rs12576239 rs2968864 rs12029454 rs8049607 rs11756438
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)
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci
PLoS genetics · 2012 · PMID 22412388 · open access
6 pages
rs6545946 rs7705924 rs9258260 rs12677663 rs11229030 rs3091338
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
Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci
Diabetes · 2016 · PMID 27416945
6 pages
rs13422522 rs7578326 rs6027072 rs12583553 rs10483182 rs6013915
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
Nature communications · 2017 · PMID 28613276 · open access
6 pages
rs12980262 rs1812835 rs2529471 rs4899412 rs12974991 rs12974440
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations
The Journal of clinical endocrinology and metabolism · 2018 · PMID 29325163
6 pages
rs1526692 rs719700 rs1410656 rs13107347 rs17767445 Vitamin D Deficiency and the GC Gene
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs16826069 rs1127787 rs7572857 rs2233580 rs56200889 rs35658696
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
Brain : a journal of neurology · 2022 · PMID 35511193 · open access
6 pages
rs3744027 rs6503417 rs12149643 rs73191849 rs13403122 Cerebral Small Vessel Disease
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Cell genomics · 2024 · PMID 38190104 · open access
6 pages
rs10993435 rs2016708 rs13392691 rs35790011 rs11753349 rs73392143
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
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function
Nature genetics · 2010 · PMID 20010835
5 pages
rs2070600 rs11727189 rs11168048 rs2277027 Pulmonary Function (Lung Capacity)
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 Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
BioBank Japan Project
American journal of human genetics · 2017 · PMID 28017375
5 pages
rs10929547 rs6430549 rs2060597 rs592423 rs4535497

Showing 20 of 195 · page 5 of 10

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.