For researchers

Is your paper here?

2,676 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.

84 matches for Liu C, showing the first 20.

Shared genetic and experimental links between obesity-related traits and asthma subtypes in UK Biobank
The Journal of allergy and clinical immunology · 2020 · PMID 31669095
7 pages
rs112104755 rs12493005 rs73086541 rs73084574 rs1787663 rs9275570
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
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations
The Journal of clinical endocrinology and metabolism · 2018 · PMID 29325163
6 pages
rs1526692 rs719700 rs1410656 rs13107347 rs17767445 Vitamin D Deficiency and the GC Gene
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
Genome-wide association study identifies 30 loci associated with bipolar disorder
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature genetics · 2019 · PMID 31043756 · open access
6 pages
rs111444407 rs10950456 rs57957974 rs17183814 rs10896090 rs10035291
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
rs3784634 rs5400 rs17853166 rs75619922 rs7225887 rs56381411
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program
VA Million Veteran Program
PLoS genetics · 2022 · PMID 35653334 · open access
5 pages
rs12143563 rs139405583 rs2197973 rs1840086 rs3812813
Trans-ancestry meta-analysis of genome-wide association study identifies eight novel genetic loci in type 1 diabetes: A multi-population study
Diabetic medicine : a journal of the British Diabetic Association · 2026 · PMID 42594184
5 pages
rs28464459 rs117520198 rs9981704 rs9934969 rs2395639
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium
Human molecular genetics · 2014 · PMID 24430505
4 pages
rs3020331 rs2982552 rs10416265 rs7902708
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Genome biology · 2018 · PMID 30012220 · open access
4 pages
rs11588271 rs116202356 rs3746435 rs11848785
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
4 pages
rs9308788 rs141962517 rs75535814 rs113809930
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
rs12599112 rs11940694 Alcohol Consumption
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Regeneron Genetics Center
Nature communications · 2022 · PMID 36376295 · open access
3 pages
rs981150 rs17513625 rs10738604
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure
VA Million Veteran Program
Nature communications · 2023 · PMID 37429843 · open access
3 pages
rs2832275 rs7795282 rs34163229
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
rs150607032 rs190975828 rs192018195
Genome-wide association study of Tourette's syndrome
North American Brain Expression Consortium · UK Human Brain Expression Database
Molecular psychiatry · 2013 · PMID 22889924 · open access
2 pages
rs7868992 Tourette Syndrome
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Nature genetics · 2013 · PMID 23817570
2 pages
rs13117307 Cervical Cancer
Genome-wide association of body fat distribution in African ancestry populations suggests new loci
PLoS genetics · 2013 · PMID 23966867 · open access
2 pages
rs6931262 rs2075064
Genome-wide analysis links NFATC2 with asparaginase hypersensitivity
Blood · 2015 · PMID 25987655
2 pages
rs6021191 Acute Lymphoblastic Leukemia

Showing 20 of 84 · page 3 of 5

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.