For researchers

Is your paper here?

2,692 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.

31 matches for Liu S, 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+
rs12332985 rs146576224 rs10180829 rs672769 rs10071837 rs4899520
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs146474788 rs17256082 rs12784552 rs142484519 rs118164457 rs182859029
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
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+
rs10052346 rs139027698 rs12669223 rs3768301 rs72830009 rs7100404
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs1151285 rs183347579 rs3738685 rs73068914 rs74552897 rs34411702
Genetic basis of pregnancy-associated decreased platelet counts and gestational thrombocytopenia
Blood · 2024 · PMID 38064665 · open access
12 pages+
rs59900889 rs692503 rs143079295 rs6828754 rs2292765 rs111800900
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs16849467 rs36090640 rs58090211 rs1475655 rs67269808 rs7304270
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+
rs1348003 rs9393917 rs2234036 rs1051365311 rs2288187 rs145816106
Genetic architecture and risk prediction of gestational diabetes mellitus in Chinese pregnancies
Nature communications · 2025 · PMID 40325049 · open access
12 pages+
rs732360 rs1337919 rs968919 rs188561366 rs12118238 rs36115340
Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Nature genetics · 2026 · PMID 42509370
12 pages+
rs73037761 rs56169464 rs7471612 rs6048202 rs6723506 rs77001541
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
VTE Consortium · STROKE Consortium and 3 more consortia
Circulation · 2013 · PMID 23969696
9 pages
rs7968440 rs1938492 rs1019670 rs4817986 rs6010044 rs10226084
Novel genetic insight for psoriasis: integrative genome-wide analyses in 863 080 individuals and proteome-wide Mendelian randomization
Briefings in bioinformatics · 2024 · PMID 39883516 · open access
8 pages
rs6457109 rs74817271 rs62401434 rs2596546 rs9468487 rs1306395
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study
Stroke · 2018 · PMID 29273593
6 pages
rs9614159 rs74388387 rs9907978 rs10782008 rs117353193 Moyamoya Disease
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2026 · PMID 42225636 · open access
5 pages
rs77864822 rs7933420 rs10036439 rs613937 rs72964564
The STROMICS genome study: deep whole-genome sequencing and analysis of 10K Chinese patients with ischemic stroke reveal complex genetic and phenotypic interplay
Cell discovery · 2023 · PMID 37479695 · open access
3 pages
rs12718465 rs12081480 rs866262287
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis
PLoS genetics · 2010 · PMID 20072603 · open access
2 pages
rs13182402 Osteoporosis
Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population
Nature genetics · 2011 · PMID 21666691
2 pages
rs3126085 Atopic Dermatitis
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
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation
PLoS genetics · 2012 · PMID 22829776 · open access
2 pages
rs17496332 rs1573036
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

Showing 20 of 31 · page 1 of 2

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.