For researchers

Is your paper here?

2,663 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.

20 matches for Yu B.

A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos
American journal of human genetics · 2020 · PMID 33031748
12 pages+
rs74353024 rs77654326 rs7964228 rs74882993 rs11607853 rs363334
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs11718848 rs11537816 rs16859180 rs1449592 rs13196885 rs576629818
A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic aetiology with obesity
The European respiratory journal · 2021 · PMID 33766948
12 pages+
rs16828537 rs73995038 rs801170 rs6696174 rs1482675 rs78732306
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs56372821 rs540508277 rs6430080 rs28673808 rs78875955 rs739447
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
rs811689 rs1076135 rs980896 rs75128958 rs947350 rs1528683
Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations
NHLBI Trans-Omics for Precision Medicine (TOPMed)
Nature communications · 2023 · PMID 37253714 · open access
12 pages+
rs59667296 rs2289329 rs233066 rs56660645 rs11038172 rs114080902
Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine
GCKD Investigators
Nature genetics · 2023 · PMID 37277652 · open access
12 pages+
rs2460451 rs7557590 rs114488830 rs61886489 rs2433228 rs7549167
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Genes & Health Research Team · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2025 · PMID 40038546 · open access
12 pages+
rs149780392 rs3794752 rs62233286 rs7095308 rs73048654 rs143445113
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders
Nature human behaviour · 2019 · PMID 31358974
9 pages
rs2277499 rs10496076 rs71414193 rs57281063 rs227179 rs4794015
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
8 pages
rs11230661 rs2050058 rs79624003 rs55809639 rs4847240 rs4660303
Genetic determinants influencing human serum metabolome among African Americans
PLoS genetics · 2014 · PMID 24625756 · open access
6 pages
rs2433610 rs12288023 rs7499271 rs12282107 rs555044 rs507080
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
A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease
American journal of physiology. Lung cellular and molecular physiology · 2021 · PMID 33909500
4 pages
rs11155242 rs2523989 rs11938093 rs13195509
Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases
JCI insight · 2022 · PMID 35446786 · open access
4 pages
rs9646256 rs7224888 rs73338360 rs10738906
Genetic loci of beta-aminoisobutyric acid are associated with aging-related mild cognitive impairment
Translational psychiatry · 2023 · PMID 37120436 · open access
4 pages
rs13174311 rs344515 rs140156063 rs183958240
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
A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis
Nature genetics · 2011 · PMID 22138694
2 pages
rs17095830 Ankylosing Spondylitis
Characterizing Common and Rare Variations in Nontraditional Glycemic Biomarkers Using Multivariate Approaches on Multiancestry ARIC Study
Diabetes · 2024 · PMID 38869630
2 pages
rs59443763 rs116714277
Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies
CARDIoGRAM Consortium
Circulation. Cardiovascular genetics · 2013 · PMID 23247143
1 page
rs12564445
Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study
Genetic epidemiology · 2013 · PMID 23934736
1 page
rs12251332

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.