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.

79 matches for Frayling T, showing the first 20.

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs4267865 rs57634870 rs11196296 rs3825801 rs79495865 rs1871045
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs12441639 rs16944691 rs17079512 rs17138668 rs17277029 rs17301221
Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood
Diabetologia · 2023 · PMID 37280435 · open access
12 pages+
rs973526 rs1453059 rs6014536 rs2922790 rs116631513 rs71324800
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs3742636 rs74387263 rs10758321 rs11023938 rs116257126 rs144589448
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
11 pages
rs543874 rs10150332 rs2241423 rs2287019 rs12444979 rs206936
Exome-wide association study of plasma lipids in >300,000 individuals
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
rs10861661 rs201596848 rs900399 rs7157785 rs3927680 rs7946
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Wellcome Trust Case Control Consortium · Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators and 4 more consortia
Nature genetics · 2012 · PMID 22885922 · open access
10 pages
rs2075423 rs10203174 rs1496653 rs7955901 rs7177055 rs7640539
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
PLoS genetics · 2013 · PMID 23408906 · open access
10 pages
rs9497965 rs7860634 rs7240777 rs10799824 rs9472138 rs11755845
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
rs6813195 rs17106184 rs849135 rs2261181 rs9936385 rs4458523
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
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Multiple Tissue Human Expression Resource (MUTHER) Consortium
Nature genetics · 2012 · PMID 22581228
8 pages
rs35747 rs4691380 rs2785980 rs1371614 rs13179048 rs6048205
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Genetic predictors of participation in optional components of UK Biobank
Nature communications · 2021 · PMID 33563987 · open access
7 pages
rs12189679 rs2622102 rs11134465 rs1565440 rs1261078 rs2049604
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
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
Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci
Diabetes · 2016 · PMID 27416945
6 pages
rs13422522 rs7578326 rs6027072 rs12583553 rs10483182 rs6013915
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
Biological and clinical insights from genetics of insomnia symptoms
HUNT All In Sleep
Nature genetics · 2019 · PMID 30804566 · open access
6 pages
rs7711696 rs11184946 rs2062113 rs11651809 rs2296580 rs17669584
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
Wellcome Trust Case Control Consortium
Nature genetics · 2008 · PMID 18372903
5 pages
rs12779790 rs864745 rs7961581 rs7578597 rs10923931
Genome-wide association analysis identifies 20 loci that influence adult height
Diabetes Genetics Initiative · Wellcome Trust Case Control Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18391952
5 pages
rs6060373 rs1390401 rs6724465 rs2814993 rs2282978

Showing 20 of 79 · page 2 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.