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.

76 matches for Lind L, showing the first 20.

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
UK BiLEVE
Nature communications · 2015 · PMID 26635082 · open access
8 pages
rs6681426 rs61067109 rs6441207 rs6856422 rs148274477 rs12149828
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
SUMMIT Consortium · BioBank Japan Project
American journal of human genetics · 2016 · PMID 27588450 · open access
8 pages
rs35716097 rs5020545 rs62435145 rs57989581 rs8096658 rs1511299
Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior
Swiss Kidney Project on Genes in Hypertension (SKIPOGH) team
Human molecular genetics · 2016 · PMID 27702941
7 pages
rs10275488 rs12909047 rs35107470 rs2892838 rs2470893 rs66500423
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation
Nature genetics · 2017 · PMID 27918534
7 pages
rs2434264 rs7374732 rs6689335 rs912056 rs10060123 rs2123685
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
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
Nature communications · 2017 · PMID 28613276 · open access
6 pages
rs12980262 rs1812835 rs2529471 rs4899412 rs12974991 rs12974440
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
Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank
Metabolic syndrome and related disorders · 2020 · PMID 31928498
6 pages
rs2678204 rs9689096 rs60683614 rs73222243 rs111297471 rs30351
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
6 pages
rs56381411 rs3784634 rs5400 rs17853166 rs75619922 rs7225887
Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels
Circulation research · 2011 · PMID 21757650
5 pages
rs4513773 rs6993770 rs10738760 rs9472155 Serum VEGF Levels
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
The Journal of clinical investigation · 2017 · PMID 28394258
5 pages
rs6702619 rs17696696 rs7127129 rs2649 rs11207426
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
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 identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Diabetes · 2011 · PMID 21873549 · open access
3 pages
rs6235 rs11558471 rs1549318
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
MEGASTROKE Consortium
Nature communications · 2018 · PMID 30510157 · open access
3 pages
rs11196033 rs2912063 rs844396
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
Clinical and genetic correlates of growth differentiation factor 15 in the community
Clinical chemistry · 2012 · PMID 22997280
2 pages
rs888663 rs1054564

Showing 20 of 76 · 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.