For researchers

Is your paper here?

2,665 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.

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
rs348495 rs10261878
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 association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
2 pages
rs17428471 rs17080102
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations
SUNLIGHT Consortium · GEFOS Consortium
PLoS genetics · 2013 · PMID 24068962 · open access
2 pages
rs7481584 rs7336933
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
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
Aging cell · 2016 · PMID 27325353 · open access
2 pages
rs752045 Hand Grip Strength
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)
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
American journal of human genetics · 2019 · PMID 31178129
2 pages
rs145119400 rs11646213
Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene
PLoS genetics · 2009 · PMID 19180233 · open access
1 page
Duffy-Null Phenotype and Benign Ethnic Neutropenia
Genome-wide association meta-analysis for total serum bilirubin levels
Human molecular genetics · 2009 · PMID 19414484
1 page
rs6742078
Multiple loci associated with indices of renal function and chronic kidney disease
Nature genetics · 2009 · PMID 19430482
1 page
rs17319721
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
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Nature genetics · 2009 · PMID 19597492 · open access
1 page
rs17042171
Common variants in KCNN3 are associated with lone atrial fibrillation
Nature genetics · 2010 · PMID 20173747 · open access
1 page
rs13376333
Genome-wide association analysis identifies multiple loci related to resting heart rate
Human molecular genetics · 2010 · PMID 20639392
1 page
rs9398652
Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels
GEFOS Consortium
Human molecular genetics · 2010 · PMID 20705733
1 page
rs17251221
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

Showing 20 of 135 · page 6 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.