For researchers

Is your paper here?

2,661 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.

12 matches for Sladek R.

Seventy-five genetic loci influencing the human red blood cell
Nature · 2012 · PMID 23222517
12 pages+
rs901683 rs10849023 rs3892630 rs4953318 rs243070 rs10207392
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
rs4745982 rs10823343 rs3824065 rs11154792 rs17509001 rs7040409
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
MAGIC investigators · GIANT Consortium
Nature genetics · 2010 · PMID 20581827
8 pages
rs1552224 rs5945326 rs11634397 rs231362 rs7957197 rs1470579
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs16826069 rs1127787 rs7572857 rs2233580 rs56200889 rs35658696
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways
WTCCC
Diabetes · 2010 · PMID 20858683 · open access
5 pages
rs1799884 rs1046896 rs6474359 rs7998202 Type 2 Diabetes
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
5 pages
rs56381411 rs5400 rs17853166 rs75619922 rs7225887
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
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels
GIANT Consortium
PLoS genetics · 2009 · PMID 20011104 · open access
2 pages
rs1648707 Adiponectin Levels
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Broad Genomics Platform · DiscovEHR Collaboration and 8 more consortia
Nature · 2019 · PMID 31118516 · open access
2 pages
rs17737404 rs11257600
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
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases
MAGIC · DIAGRAM Consortium and 1 more consortia
PLoS genetics · 2012 · PMID 22693455 · open access
1 page
rs3802177

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.