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.

29 matches for Larson M, showing the first 20.

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
rs17460657 rs347272 rs164133 rs545833 rs10919070 rs12079745
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
BIOS Consortium · Understanding Society Scientific Group
Hypertension (Dallas, Tex. : 1979) · 2017 · PMID 28739976
12 pages+
rs35783704 rs73075659 rs73099903 rs36047283 rs871524 rs337100
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Million Veteran Program
Nature genetics · 2018 · PMID 30224653
12 pages+
rs61653296 rs7187540 rs77692990 rs75902664 rs7976167 rs10873612
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs10025456 rs8032301 rs1624825 rs145502455 rs273592 rs11937432
Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations
NHLBI Trans-Omics for Precision Medicine (TOPMed)
Nature communications · 2023 · PMID 37253714 · open access
12 pages+
rs6722867 rs7075655 rs2296435 rs55916375 rs224799 rs72853921
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels
Circulation · 2011 · PMID 21300955
9 pages
rs6734238 rs13233571 rs1183910 rs1800961 rs10521222 rs2847281
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling
CARDIoGRAM Consortium · CHARGE Inflammation Working Group and 1 more consortia
The Journal of clinical investigation · 2013 · PMID 23999434
9 pages
rs12999542 rs13019803 rs2302612 rs11693697 rs13029918 rs1014286
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
CHD Exome+ Consortium · ExomeBP Consortium and 4 more consortia
Nature genetics · 2016 · PMID 27618448
9 pages
rs2493292 rs11639856 rs1925153 rs3755652 rs11014166 rs11024074
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
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)
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
rs2071518 rs11222084 rs13082711 rs11191593 rs319690 rs1327235
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
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
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 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
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies
European heart journal · 2012 · PMID 22003152
2 pages
rs7528419 rs6511720
Clinical and genetic correlates of growth differentiation factor 15 in the community
Clinical chemistry · 2012 · PMID 22997280
2 pages
rs888663 rs1054564
Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels
Human molecular genetics · 2014 · PMID 25080503
2 pages
rs1425053 rs704

Showing 20 of 29 · page 1 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.