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.

66 matches for Cupples L, showing the first 20.

Genetic variation associated with circulating monocyte count in the eMERGE Network
CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
2 pages
rs2124440 Monocyte Count
Genome-wide association of body fat distribution in African ancestry populations suggests new loci
PLoS genetics · 2013 · PMID 23966867 · open access
2 pages
rs6931262 rs2075064
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
rs9902453 rs7800944
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
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium
PloS one · 2016 · PMID 26950853 · open access
2 pages
rs6941513 Myocardial Infarction
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
2 pages
rs60839105 rs116843064
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Journal of medical genetics · 2016 · PMID 27587472
2 pages
rs247616 Cholesterol (LDL, HDL and Total)
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
Nature communications · 2018 · PMID 29343764 · open access
2 pages
rs10745742 Vitamin D Deficiency and the GC Gene
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Nature genetics · 2023 · PMID 37770635
2 pages
rs10899970 rs62555371
Variants in MTNR1B influence fasting glucose levels
Nature genetics · 2009 · PMID 19060907
1 page
rs560887
Genome-wide association meta-analysis for total serum bilirubin levels
Human molecular genetics · 2009 · PMID 19414484
1 page
rs6742078
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium
PLoS genetics · 2009 · PMID 19557197 · open access
1 page
rs10146997
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits
PLoS genetics · 2010 · PMID 20548944 · open access
1 page
rs494453
CUBN is a gene locus for albuminuria
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
1 page
Kidney Function
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)
FTO genotype is associated with phenotypic variability of body mass index
Nature · 2012 · PMID 22982992
1 page
rs7202116
Genome-wide association study of age at menarche in African-American women
Human molecular genetics · 2013 · PMID 23599027
1 page
rs10441737
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course
GIANT Consortium
Human molecular genetics · 2013 · PMID 23669352
1 page
rs1561288
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)
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
rs139967528

Showing 20 of 66 · page 3 of 4

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.