For researchers

Is your paper here?

2,676 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.

53 matches for Chen S, showing the first 20.

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
6 pages
rs3784634 rs5400 rs17853166 rs75619922 rs7225887 rs56381411
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension
Human molecular genetics · 2015 · PMID 25249183
5 pages
rs9810888 rs2021783 rs1902859 rs13143871 rs4409766
Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy
Nature genetics · 2015 · PMID 25642632
5 pages
rs13220141 rs10817758 rs58600253 rs10414149 Leprosy
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Gut · 2021 · PMID 33632709 · open access
5 pages
rs73161913 rs62131228 rs6014965 rs61975764 rs80158569
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
COVICAT study group, Aachen Study (COVAS) · Norwegian SARS-CoV-2 Study group and 2 more consortia
Human molecular genetics · 2022 · PMID 35848942 · open access
5 pages
rs77534576 rs143334143 rs35731912 rs2269899 COVID-19 with Respiratory Failure Requiring Mechanical Ventilation
Genomewide association study of leprosy
The New England journal of medicine · 2009 · PMID 20018961
4 pages
rs602875 rs40457 rs42490 Leprosy
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Nature genetics · 2011 · PMID 21151128
4 pages
rs13429458 rs10818854 rs12478601 Polycystic Ovary Syndrome
Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy
Nature genetics · 2011 · PMID 22019778
4 pages
rs16948876 rs2275606 rs3762318 Leprosy
Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations
Circulation. Cardiovascular genetics · 2016 · PMID 26582766
4 pages
rs1260333 rs2575876 rs7525649 rs9357121
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
DBDS Consortium · 23andMe Research Team
Gut · 2021 · PMID 33888516 · open access
4 pages
rs11585073 rs11176001 rs722587 Haemorrhoidal Disease
Genome-wide meta-analysis identifies ancestry-specific loci for Alzheimer's disease
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024 · PMID 39023044 · open access
4 pages
rs10806784 rs6140401 rs79872316 rs3804082
Genome-wide association study of diabetic retinopathy in a Taiwanese population
Ophthalmology · 2011 · PMID 21310492
3 pages
rs17376456 rs12219125 Diabetic Retinopathy
A genome-wide association study identifies novel loci of vertigo in an Asian population-based cohort
Communications biology · 2024 · PMID 39174713 · open access
3 pages
rs10862089 rs428549 rs612969
Genome-wide analysis implicates inner ear development in Ménière disease
American journal of human genetics · 2026 · PMID 42302782 · open access
3 pages
rs61861121 rs3777811 Meniere's Disease
Genome-wide association study in Han Chinese identifies three novel loci for human height
Human genetics · 2013 · PMID 23456168
2 pages
rs3816804 rs3751599
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Nature genetics · 2013 · PMID 23817570
2 pages
rs13117307 Cervical Cancer
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
Nature communications · 2015 · PMID 26151496 · open access
2 pages
rs9263688 rs7768644
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Nature communications · 2017 · PMID 28425483 · open access
2 pages
rs9501251 Primary Biliary Cholangitis
Genome-Wide Association and Functional Studies Identify <i>SCML4</i> and <i>THSD7A</i> as Novel Susceptibility Genes for Coronary Artery Disease
Arteriosclerosis, thrombosis, and vascular biology · 2018 · PMID 29472232
2 pages
rs852787 rs17165136
Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population
The Journal of investigative dermatology · 2018 · PMID 29857070
2 pages
rs11218708 Pemphigus Vulgaris

Showing 20 of 53 · page 2 of 3

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.