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.

44 matches for Chen X, showing the first 20.

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
ABCTB Investigators · EMBRACE and 4 more consortia
Nature genetics · 2017 · PMID 29058716
5 pages
rs10995201 rs9397437 rs6562760 rs6678914 rs67397200
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
4 pages
rs9308788 rs141962517 rs75535814 rs113809930
Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis
GeseDNA Research Team
JAMA psychiatry · 2021 · PMID 33263727
4 pages
rs3804640 rs6130764 rs11557713 rs11647445
GWAS of Chronic Spontaneous Urticaria Reveals Genetic Overlap with Autoimmune Diseases, Not Atopic Diseases
The Journal of investigative dermatology · 2023 · PMID 35933036
4 pages
rs117754460 rs434124 rs61986182 rs73075571
Genetic signatures of high-altitude adaptation in Tibetans
Proceedings of the National Academy of Sciences of the United States of America · 2017 · PMID 28373541
3 pages
rs71673426 rs78720557 rs2584462
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 identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Nature genetics · 2013 · PMID 23817570
2 pages
rs13117307 Cervical Cancer
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth
The New England journal of medicine · 2017 · PMID 28877031 · open access
2 pages
rs2955117 rs56318008
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese
Nature communications · 2018 · PMID 30287856 · open access
2 pages
rs6114027 Tuberculosis
Exome-Wide Association Analysis Suggests LRP2BP as a Susceptibility Gene for Endothelial Injury in Systemic Sclerosis in the Han Chinese Population
The Journal of investigative dermatology · 2021 · PMID 33069728
2 pages
rs76285340 rs45471499
Genome-wide association study identifies novel breast cancer susceptibility loci
SEARCH collaborators · kConFab and 1 more consortia
Nature · 2007 · PMID 17529967
1 page
rs3817198
Genome-wide association and replication studies identified TRHR as an important gene for lean body mass
American journal of human genetics · 2009 · PMID 19268274
1 page
rs7832552
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Nature genetics · 2016 · PMID 27064256
1 page
rs3739821
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
Alcohol Intake Interacts with Functional Genetic Polymorphisms of Aldehyde Dehydrogenase (ALDH2) and Alcohol Dehydrogenase (ADH) to Increase Esophageal Squamous Cell Cancer Risk
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2019 · PMID 30639619
1 page
ALDH2 Deficiency (Alcohol Flush Reaction)
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
rs492571
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study
China Consortium for the Genetics of Autoimmune Thyroid Disease
JAMA network open · 2019 · PMID 31050781 · open access
1 page
rs12451295
Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes
Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2020 · PMID 31294817
1 page
rs16969968

Showing 20 of 44 · 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.