For researchers

Is your paper here?

2,690 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+
rs672769 rs10071837 rs4899520 rs75823898 rs112226333 rs2553033
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+
rs118164457 rs182859029 rs7063597 rs3752435 rs4317621 rs4731113
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+
rs11196296 rs3825801 rs79495865 rs1871045 rs80102379 rs7819706
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs1136774 rs1662340 rs10028665 rs57882498 rs73373266 rs6699943
Genetic basis of pregnancy-associated decreased platelet counts and gestational thrombocytopenia
Blood · 2024 · PMID 38064665 · open access
12 pages+
rs10229569 rs401826 rs28524998 rs11588057 rs12379622 rs3013440
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs183862911 rs61939481 rs12200517 rs7232699 rs10416539 rs11514133
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+
rs61515378 rs9398215 rs17100242 rs191358938 rs231770 rs1348003
Genetic architecture and risk prediction of gestational diabetes mellitus in Chinese pregnancies
Nature communications · 2025 · PMID 40325049 · open access
12 pages+
rs72554664 rs182573065 rs61160304 rs146844151 rs2971667 rs732360
Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Nature genetics · 2026 · PMID 42509370
12 pages+
rs12534879 rs11898263 rs78110695 rs7845824 rs1044327 rs2174208
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
rs434943 rs2106854 rs7968440 rs1938492 rs1019670 rs4817986
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
rs6067293 rs6457109 rs74817271 rs62401434 rs2596546 rs9468487
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
rs72964564 rs77864822 rs7933420 rs10036439 rs613937
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
rs1573036 rs17496332
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.