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 Li S, showing the first 20.

Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms
Nature communications · 2015 · PMID 25849990 · open access
2 pages
rs12339666 Myeloproliferative Neoplasms
Identification of new susceptibility loci for IgA nephropathy in Han Chinese
Nature communications · 2015 · PMID 26028593 · open access
2 pages
rs2074038 IgA Nephropathy
Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome
Scientific reports · 2015 · PMID 26190474 · open access
2 pages
rs2857281 Trichloroethylene-Induced Hypersensitivity Syndrome
Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection
Human molecular genetics · 2019 · PMID 30412241
2 pages
rs59661306 rs7457728
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Stroke · 2020 · PMID 32517579
2 pages
rs2598420 rs3758575
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
The Lancet. Neurology · 2020 · PMID 32949544
2 pages
rs3747957 Sporadic Creutzfeldt-Jakob Disease
Genome-wide association study of HBV-related hepatocellular carcinoma identifies a functional variant at the FAM114A1 locus
Journal of genetics and genomics = Yi chuan xue bao · 2026 · PMID 41241147
2 pages
rs55718051 HBV-Related Hepatocellular Carcinoma
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
Nature genetics · 2009 · PMID 19079261
1 page
rs10838738
Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study
American journal of human genetics · 2009 · PMID 19185284
1 page
rs12272004
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Nature genetics · 2009 · PMID 19915575 · open access
1 page
rs393152
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population
American journal of human genetics · 2011 · PMID 21640322
1 page
rs9318086
New loci associated with chronic hepatitis B virus infection in Han Chinese
Nature genetics · 2013 · PMID 24162738
1 page
rs3130542
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study
Molecular psychiatry · 2015 · PMID 25469926 · open access
1 page
rs1823125
Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study
Arthritis & rheumatology (Hoboken, N.J.) · 2015 · PMID 25604533
1 page
rs4410768
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Human molecular genetics · 2016 · PMID 26732429
1 page
rs7741164
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 identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese
Nature communications · 2016 · PMID 27244555 · open access
1 page
rs7000921
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations
Journal of lipid research · 2017 · PMID 28298293 · open access
1 page
rs10883511
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
Age at Menarche
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
rs139967528

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.