For researchers

Is your paper here?

2,673 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.

71 matches for Sanna S, showing the first 20.

Genome-wide association study identifies eight loci associated with blood pressure
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · open access
4 pages
rs12946454 rs1530440 rs16948048 rs17367504
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
Identification of ten loci associated with height highlights new biological pathways in human growth
Diabetes Genetics Initiative · FUSION and 4 more consortia
Nature genetics · 2008 · PMID 18391950
3 pages
rs4896582 rs1492820 rs10946808
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations
EUROSPAN Consortium · ENGAGE Consortium and 3 more consortia
PLoS genetics · 2009 · PMID 19503597 · open access
3 pages
rs12356193 rs742132 rs780094
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Wellcome Trust Case Control Consortium · Procardis Consortia and 1 more consortia
PLoS genetics · 2009 · PMID 19557161 · open access
3 pages
rs987237 rs7826222 rs2605100
Genetic variants influencing circulating lipid levels and risk of coronary artery disease
Wellcome Trust Case Control Consortium
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20864672
3 pages
rs964184 rs2304130 rs10105606
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
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
PLoS genetics · 2014 · PMID 24586183 · open access
3 pages
rs1230666 rs10944479 Thyroid Autoimmunity (TPO Antibodies)
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia
LifeLines Cohort Study
American journal of human genetics · 2014 · PMID 24954895
3 pages
rs12416687 rs16833934 rs4842666
Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease
Consortium for the study of genetic associations of celiac disease in Latin-America
European journal of human genetics : EJHG · 2020 · PMID 31591516
3 pages
rs6806528 rs9610686 Celiac Disease
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 scan shows genetic variants in the FTO gene are associated with obesity-related traits
PLoS genetics · 2007 · PMID 17658951 · open access
2 pages
rs9930506 Obesity and Body Weight
The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts
PLoS genetics · 2007 · PMID 17997608 · open access
2 pages
rs6855911 Gout
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia
Proceedings of the National Academy of Sciences of the United States of America · 2008 · PMID 18245381
2 pages
rs11886868 Blood Cell Counts
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
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
rs2121279 rs16851483
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels
Nature genetics · 2015 · PMID 26366553 · open access
2 pages
rs570013781 rs5030868
Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project
LifeLines Cohort Study
Nature genetics · 2022 · PMID 35115690
2 pages
rs73344869 rs2282037
DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
Proceedings of the National Academy of Sciences of the United States of America · 2008 · PMID 18667698
1 page
Blood Cell Counts

Showing 20 of 71 · page 3 of 4

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.