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.

38 matches for Wild SH, showing the first 18.

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Nature genetics · 2010 · PMID 21076409 · open access
5 pages
rs17391905 rs1886512 rs17608766 rs1733724 Cardiac Conduction Intervals (PR Interval and QRS Duration)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Nature genetics · 2010 · PMID 20081858 · open access
4 pages
rs11920090 rs7944584 rs11605924 Fasting Blood Glucose
New loci associated with kidney function and chronic kidney disease
Nature genetics · 2010 · PMID 20383146
4 pages
rs267734 rs10774021 rs7805747 rs6465825
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
International Lung Cancer Consortium · GIANT consortium
Nature genetics · 2011 · PMID 21946350 · open access
4 pages
rs1036429 rs2798641 rs12447804 rs6903823
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Nature genetics · 2014 · PMID 24929828
4 pages
rs1430193 rs6923462 rs2863171 rs6501431
Genome-wide association study identifies five loci associated with lung function
Wellcome Trust Case Control Consortium · NSHD Respiratory Study Team
Nature genetics · 2010 · PMID 20010834
3 pages
rs12899618 rs10516526 rs12504628
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
rs1055144 rs6784615 rs6861681
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
LifeLines Cohort Study · CARDIoGRAM Consortium and 3 more consortia
Nature genetics · 2013 · PMID 23263486
3 pages
rs1481012 rs4475146 Gout
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
Genetic determinants of circulating sphingolipid concentrations in European populations
PLoS genetics · 2009 · PMID 19798445 · open access
2 pages
rs10938494 rs7258249
Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation
PLoS genetics · 2010 · PMID 21203500 · open access
2 pages
rs3760776 rs10483776
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 association analysis identifies multiple loci related to resting heart rate
Human molecular genetics · 2010 · PMID 20639392
1 page
rs9398652
Genetic predictors of fibrin D-dimer levels in healthy adults
Circulation · 2011 · PMID 21502573
1 page
rs12029080
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
Modulation of genetic associations with serum urate levels by body-mass-index in humans
PloS one · 2015 · PMID 25811787 · open access
1 page
rs898534

Showing 18 of 38 · 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.