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.

37 matches for Jiang Y, showing the first 17.

Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies
Gut · 2017 · PMID 26701879 · open access
3 pages
rs80142782 rs13361707 Non-Cardia Gastric Cancer
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
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese
American journal of human genetics · 2012 · PMID 23103227
2 pages
rs2494938 rs2285947
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese
PLoS genetics · 2013 · PMID 23341777 · open access
2 pages
rs12296850 Lung Squamous Cell Carcinoma
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
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
Genetic Factors Associated with Prostate Cancer Conversion from Active Surveillance to Treatment
HGG advances · 2022 · PMID 34993496 · open access
2 pages
rs1404610 rs3750827
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
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Nature genetics · 2011 · PMID 21725308
1 page
rs753955
NCK2 is significantly associated with opiates addiction in African-origin men
TheScientificWorldJournal · 2013 · PMID 23533358 · open access
1 page
rs2377339
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23
Nature genetics · 2013 · PMID 24097066
1 page
rs4282438
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 Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis
Hepatology (Baltimore, Md.) · 2019 · PMID 30854688 · open access
1 page
rs1794280
Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study
Diabetes care · 2019 · PMID 31152121
1 page
rs4320356
Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations
Gut · 2020 · PMID 31383772
1 page
rs10029005
Genetic risk, incident gastric cancer, and healthy lifestyle: a meta-analysis of genome-wide association studies and prospective cohort study
The Lancet. Oncology · 2020 · PMID 33002439
1 page
rs10074991
Convergent imaging and genetic signatures of gray matter atrophy in Parkinson's disease
NeuroImage · 2026 · PMID 42336304
1 page
rs470934

Showing 17 of 37 · page 2 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.