For researchers

Is your paper here?

2,677 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.

59 matches for Fox C, showing the first 19.

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 for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women
GIANT Consortium · MAGIC Consortium and 1 more consortia
PLoS genetics · 2012 · PMID 22589738 · open access
2 pages
rs11118316 rs1659258
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
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
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
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis
Journal of the American Society of Nephrology : JASN · 2014 · PMID 24578125
2 pages
rs12446492 rs4494548
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
Variants in MTNR1B influence fasting glucose levels
Nature genetics · 2009 · PMID 19060907
1 page
rs560887
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
Common genetic variants associate with serum phosphorus concentration
Journal of the American Society of Nephrology : JASN · 2010 · PMID 20558539
1 page
rs947583
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
CUBN is a gene locus for albuminuria
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
1 page
Kidney Function
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
FTO genotype is associated with phenotypic variability of body mass index
Nature · 2012 · PMID 22982992
1 page
rs7202116
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
Genome-wide association analysis of plasma B-type natriuretic peptide in blacks: the Jackson Heart Study
Circulation. Cardiovascular genetics · 2015 · PMID 25561047
1 page
rs198389
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

Showing 19 of 59 · page 3 of 3

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.