For researchers

Is your paper here?

2,663 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.

135 matches for Harris T, showing the first 20.

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
rs35658696 rs16826069 rs1127787 rs7572857 rs2233580 rs56200889
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
rs17853166 rs75619922 rs7225887 rs56381411 rs3784634 rs5400
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)
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population
PLoS genetics · 2011 · PMID 21738478 · open access
5 pages
rs11018874 rs9373124 rs12988934 rs2516399 rs7275212
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
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
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
The Journal of clinical investigation · 2017 · PMID 28394258
5 pages
rs6702619 rs17696696 rs7127129 rs2649 rs11207426
New loci associated with kidney function and chronic kidney disease
Nature genetics · 2010 · PMID 20383146
4 pages
rs267734 rs10774021 rs7805747 rs6465825
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
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors
Circulation. Cardiovascular genetics · 2010 · PMID 20884846
4 pages
rs675209 rs13129697 rs1106766 Gout
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
International Lung Cancer Consortium · GIANT consortium
Nature genetics · 2011 · PMID 21946350 · open access
4 pages
rs1036429 rs2798641 rs12447804 rs6903823
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans
Human molecular genetics · 2012 · PMID 23001564 · open access
4 pages
rs3027234 rs412658 rs1317082 Telomere Length and Epigenetic Age Acceleration
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium
Human molecular genetics · 2014 · PMID 24430505
4 pages
rs2982552 rs10416265 rs7902708 rs3020331
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Nature genetics · 2014 · PMID 24929828
4 pages
rs1430193 rs6923462 rs2863171 rs6501431
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
4 pages
rs10908557 rs6885307 rs2347867 rs2721195
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function
Scientific reports · 2017 · PMID 28452372 · open access
4 pages
rs700236 rs4500972 rs12451586 rs10874312
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 study of blood pressure and hypertension
Nature genetics · 2009 · PMID 19430479
3 pages
rs2681472 rs2384550 Blood Pressure
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
Lancet (London, England) · 2010 · PMID 20541252
3 pages
rs2282679 Vitamin D Deficiency and the GC Gene Vitamin D

Showing 20 of 135 · page 4 of 7

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.