For researchers

Is your paper here?

2,657 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.

22 matches for Reilly MP, showing the first 20.

Biological, clinical and population relevance of 95 loci for blood lipids
Nature · 2010 · PMID 20686565 · open access
12 pages+
rs1042034 rs439401 rs2929282 rs9686661 rs11613352 rs2412710
Discovery and refinement of loci associated with lipid levels
Global Lipids Genetics Consortium
Nature genetics · 2013 · PMID 24097068 · open access
12 pages+
rs4883201 rs11603023 rs11136341 rs4253772 rs13315871 rs2290159
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nature genetics · 2015 · PMID 26343387 · open access
12 pages+
rs1544935 rs1870634 rs2891168 rs56131196 rs72689147 rs2487928
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
VTE Consortium · STROKE Consortium and 3 more consortia
Circulation · 2013 · PMID 23969696
9 pages
rs434943 rs2106854 rs7968440 rs1938492 rs1019670 rs4817986
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Nature genetics · 2009 · PMID 19820697
8 pages
rs11970772 rs9609565 rs9402686 rs11602954 rs1668873 rs7961894
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease
The American journal of clinical nutrition · 2013 · PMID 23824729
8 pages
rs2275565 rs7130284 rs154657 rs234709 rs548987 rs12780845
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
7 pages
rs12526453 rs17114036 rs3798220 rs3825807 rs1231206 rs12936587
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
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways
WTCCC
Diabetes · 2010 · PMID 20858683 · open access
5 pages
rs1799884 rs1046896 rs6474359 rs7998202 Type 2 Diabetes
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19198609
4 pages
rs1746048 rs6725887 rs1122608 Coronary Artery Disease
Genetic variants influencing circulating lipid levels and risk of coronary artery disease
Wellcome Trust Case Control Consortium
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20864672
3 pages
rs964184 rs2304130 rs10105606
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Nature genetics · 2009 · PMID 19198610
2 pages
rs4857855 rs12619285
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels
GIANT Consortium
PLoS genetics · 2009 · PMID 20011104 · open access
2 pages
rs1648707 Adiponectin Levels
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
Nature genetics · 2010 · PMID 20622881
2 pages
rs7025486 Abdominal Aortic Aneurysm
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
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
INVENT Consortium · CHARGE Consortium Hemostasis Working Group and 2 more consortia
European heart journal · 2021 · PMID 33532862
2 pages
rs6694258 rs12897285
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)

Showing 20 of 22 · 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.