For researchers

Is your paper here?

2,662 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.

35 matches for Pankow JS, showing the first 15.

Identification of Genetic Variants Linking Protein C and Lipoprotein Metabolism: The ARIC Study (Atherosclerosis Risk in Communities)
Arteriosclerosis, thrombosis, and vascular biology · 2017 · PMID 28082259
4 pages
rs1178979 rs140608390 rs6120848 rs148639156
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
DBDS Consortium · Regeneron Genetics Center
The Journal of clinical investigation · 2022 · PMID 36194491 · open access
4 pages
rs2633321 rs925411 rs9704688 rs2633313
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease
American journal of human genetics · 2012 · PMID 22703881
3 pages
rs2295888 rs6028 rs2289252
Genetic Variants Associated with Circulating Parathyroid Hormone
Journal of the American Society of Nephrology : JASN · 2017 · PMID 27927781
3 pages
rs4443100 rs35194449 rs4074995
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
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism
Million Veteran Program · CHARGE Hemostasis Working Group
Blood · 2019 · PMID 31420334
2 pages
rs4524 rs191945075
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study
Diabetologia · 2022 · PMID 34951656
2 pages
rs10887773 rs6975024
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
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 identifies novel loci for plasma levels of protein C: the ARIC study
Blood · 2010 · PMID 20802025
1 page
rs6120849
A genome-wide association search for type 2 diabetes genes in African Americans
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
1 page
rs7560163
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
Genetic epidemiology · 2013 · PMID 23650146
1 page
rs4253399
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
rs60780116
Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism
Scientific reports · 2017 · PMID 28588231 · open access
1 page
rs117086479
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
1 page
rs62033408

Showing 15 of 35 · 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.