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.

58 matches for Kathiresan S, showing the first 18.

Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Nature genetics · 2012 · PMID 22544366
3 pages
rs10821415 rs10824026 rs7164883
Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor
INVENT Consortium
Circulation. Cardiovascular genetics · 2017 · PMID 28373160
3 pages
rs2519093 rs1799963 rs3136516
Genome-wide association study of peripheral artery disease in the Million Veteran Program
VA Million Veteran Program
Nature medicine · 2019 · PMID 31285632 · open access
3 pages
rs138294113 rs4722172 rs7476
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Lancet (London, England) · 2011 · PMID 21239051
2 pages
rs1994016 Coronary Artery Disease
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21909108 · open access
2 pages
rs11781551 rs17398575
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium and 1 more consortia
Arteriosclerosis, thrombosis, and vascular biology · 2014 · PMID 24578379
2 pages
rs9399599 rs3136739
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
Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts
Wellcome Trust Case Control Consortium
Circulation. Cardiovascular genetics · 2009 · PMID 20031576
1 page
rs1800789
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project
PLoS genetics · 2011 · PMID 21347282 · open access
1 page
rs7801190
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
Lancet (London, England) · 2012 · PMID 22607825 · open access
1 page
Cholesterol (LDL, HDL and Total)
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium
Nature genetics · 2012 · PMID 22751097
1 page
rs9268402
Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk
CARDIoGRAM Consortium
Arteriosclerosis, thrombosis, and vascular biology · 2012 · PMID 22982463
1 page
rs854572
FTO genotype is associated with phenotypic variability of body mass index
Nature · 2012 · PMID 22982992
1 page
rs7202116
Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies
CARDIoGRAM Consortium
Circulation. Cardiovascular genetics · 2013 · PMID 23247143
1 page
rs12564445
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
METASTROKE Consortium · CARDIoGRAM Consortium and 2 more consortia
Stroke · 2014 · PMID 24262325
1 page
rs12646447
Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia
Journal of the American College of Cardiology · 2016 · PMID 27050191
1 page
Cholesterol (LDL, HDL and Total)
Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease
CARDIoGRAMplusC4D Consortium
Nature genetics · 2017 · PMID 28714974 · open access
1 page
rs17517928
Heritability of Atrial Fibrillation
Circulation. Cardiovascular genetics · 2017 · PMID 29237688
1 page
rs117640426

Showing 18 of 58 · page 3 of 3

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.