For researchers

Is your paper here?

2,675 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.

36 matches for Ford I, showing the first 16.

Exome-wide association study of plasma lipids in >300,000 individuals
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
rs201596848 rs900399 rs7157785 rs3927680 rs7946 rs3947
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
PLoS genetics · 2013 · PMID 23408906 · open access
10 pages
rs9497965 rs7860634 rs7240777 rs10799824 rs9472138 rs11755845
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Multiple Tissue Human Expression Resource (MUTHER) Consortium
Nature genetics · 2012 · PMID 22581228
8 pages
rs35747 rs4691380 rs2785980 rs1371614 rs13179048 rs6048205
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
rs7953528 rs163879 rs1864325 rs344081 rs3905706 rs1566045
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
BioBank Japan Project
American journal of human genetics · 2017 · PMID 28017375
5 pages
rs10929547 rs6430549 rs2060597 rs592423 rs4535497
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Nature communications · 2017 · PMID 29030599 · open access
3 pages
rs34831921 rs55730499 Human Lifespan and Longevity
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
3 pages
rs3783347 rs6072275 rs4869272
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 association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
Human molecular genetics · 2014 · PMID 24688116 · open access
2 pages
rs2149954 Human Lifespan and Longevity
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)
Genetic predictors of fibrin D-dimer levels in healthy adults
Circulation · 2011 · PMID 21502573
1 page
rs12029080
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group
American journal of hypertension · 2019 · PMID 31545351
1 page
rs12046278
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
Molecular psychiatry · 2022 · PMID 35974141 · open access
1 page
rs11711421

Showing 16 of 36 · page 2 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.