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.

108 matches for Guo X, showing the first 20.

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
rs348495 rs10261878
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 association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
2 pages
rs17428471 rs17080102
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Journal of medical genetics · 2016 · PMID 27587472
2 pages
rs247616 Cholesterol (LDL, HDL and Total)
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
American journal of human genetics · 2019 · PMID 31178129
2 pages
rs145119400 rs11646213
GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations
PloS one · 2019 · PMID 31251759 · open access
2 pages
rs9856387 rs62241190
A multiethnic genome-wide analysis of 19,420 individuals identifies novel loci associated with axial length and shared genetic influences with refractive error and myopia
Consortium for Refractive Error and Myopia (CREAM)
Frontiers in genetics · 2023 · PMID 37351342 · open access
2 pages
rs2181346 rs869422
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Nature genetics · 2023 · PMID 37770635
2 pages
rs10899970 rs62555371
Genetic determinants of IgG antibody response to COVID-19 vaccination
American journal of human genetics · 2024 · PMID 38181733 · open access
2 pages
rs35986240 rs10947290
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations
Biobank Japan Project · Lifelines Cohort Study,
HGG advances · 2026 · PMID 41520179 · open access
2 pages
rs145132348 rs757194
Genetic predictors of fibrin D-dimer levels in healthy adults
Circulation · 2011 · PMID 21502573
1 page
rs12029080
NCK2 is significantly associated with opiates addiction in African-origin men
TheScientificWorldJournal · 2013 · PMID 23533358 · open access
1 page
rs2377339
Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease
WTCCC+
PloS one · 2013 · PMID 23593153 · open access
1 page
rs6730157
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations
Nature genetics · 2013 · PMID 23708190
1 page
rs1531070
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Scientific reports · 2016 · PMID 26785701 · open access
1 page
rs10051787
Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts
Heart rhythm · 2017 · PMID 28610988
1 page
rs12982903
Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy
Scientific reports · 2018 · PMID 29618737 · open access
1 page
rs7545860
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals
Circulation. Genomic and precision medicine · 2018 · PMID 29874175 · open access
1 page
rs12053903
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
rs492571
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group
American journal of hypertension · 2019 · PMID 31545351
1 page
rs12046278

Showing 20 of 108 · page 5 of 6

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.