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.

165 matches for Liu Y, showing the first 20.

Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs10180829 rs672769 rs10071837 rs4899520 rs75823898 rs112226333
Genetic Evidence for Different Adiposity Phenotypes and Their Opposing Influences on Ectopic Fat and Risk of Cardiometabolic Disease
Diabetes · 2021 · PMID 33980691
12 pages+
rs12130231 rs441792 rs987469 rs7258937 rs9764678 rs10172678
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort
Nature genetics · 2022 · PMID 35115689
12 pages+
rs187309577 rs143507801 rs113594963 rs11153022 rs138925568 rs151169359
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
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
NHLBI Trans-Omics for Precision Medicine 1 Consortium
Nature communications · 2022 · PMID 35995766 · open access
12 pages+
rs7523082 rs2901260 rs5999721 rs112166402 rs11893881 rs116471547
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs4346013 rs7540968 rs1034809 rs10028613 rs17538230 rs72912375
A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses
Osteoarthritis and cartilage · 2023 · PMID 36889626
12 pages+
rs12200892 rs2303220 rs56103247 rs11738728 rs12191751 rs6029202
Genetic basis of pregnancy-associated decreased platelet counts and gestational thrombocytopenia
Blood · 2024 · PMID 38064665 · open access
12 pages+
rs145450404 rs4741744 rs77649000 rs2040571 rs79647915 rs394772
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
rs324901 rs534415 rs1526193 rs7415357 rs72786643 rs3091404
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
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Million Veteran Program · Lifelines Cohort Study and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
rs11639335 rs2374457 rs35745897 rs57244721 rs75488436 rs73022874
Developing an optimal stratification model for colorectal cancer screening and reducing racial disparities in multi-center population-based studies
Genome medicine · 2024 · PMID 38872215 · open access
12 pages+
rs1562871 rs11169484 rs12822984 rs7494781 rs1961622 rs6510329
Genome-wide association studies of thyroid-related hormones, dysfunction, and autoimmunity among 85,421 Chinese pregnancies
Nature communications · 2024 · PMID 39266554 · open access
12 pages+
rs10901251 rs9378805 rs12321067 rs74868707 rs76569227 rs17020123
Genetic architecture and risk prediction of gestational diabetes mellitus in Chinese pregnancies
Nature communications · 2025 · PMID 40325049 · open access
12 pages+
rs4716672 rs76154673 rs72554664 rs182573065 rs61160304 rs146844151
Genome-wide analyses of variance in blood cell phenotypes provide new insights into complex trait biology and prediction
Nature communications · 2025 · PMID 40335489 · open access
12 pages+
rs773179297 rs574074185 rs9605219 rs35506206 rs143225269 rs149875532
Genome-wide meta-analyses of cross substance use disorders in diverse populations
Molecular psychiatry · 2026 · PMID 41057643 · open access
12 pages+
rs2509377 rs13196692 rs11591603 rs34185469 rs12785533 rs6804453
Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Nature genetics · 2026 · PMID 42509370
12 pages+
rs544856801 rs2961667 rs2965188 rs142065151 rs75633704 rs9654412
Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci
Clinical and translational medicine · 2021 · PMID 33634981 · open access
11 pages
rs9530695 rs73365860 rs117445861 rs6497488 rs74716564 rs8073361
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors
GliomaScan Consortium
Nature genetics · 2017 · PMID 28346443
10 pages
rs12752552 rs3751667 rs11233250 rs2235573 rs4252707 rs12076373

Showing 20 of 165 · page 2 of 9

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.