For researchers

Is your paper here?

2,663 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.

18 matches for Jiang X.

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
rs67340775 rs2004038 rs34878803 rs13213986 rs7383287 rs11632038
Association analysis identifies 65 new breast cancer risk loci
NBCS Collaborators · ABCTB Investigators and 1 more consortia
Nature · 2017 · PMID 29059683 · open access
12 pages+
rs1268974 rs34507830 rs62235635 rs55821517 rs217727 rs117618124
Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants
Communications biology · 2020 · PMID 33311554 · open access
12 pages+
rs35819343 rs7235583 rs113391921 rs13065564 rs6816503 rs62014489
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
Lifelines Cohort Study · VA Million Veteran Program
Nature communications · 2021 · PMID 33972514 · open access
12 pages+
rs6684154 rs8046061 rs4712253 rs7450517 rs2465956 rs11582968
GWAS on retinal vasculometry phenotypes
UK Biobank Eye and Vision Consortium
PLoS genetics · 2023 · PMID 36757925 · open access
12 pages+
rs10415219 rs115456027 rs4950743 rs9900613 rs11727963 rs187691758
A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses
Osteoarthritis and cartilage · 2023 · PMID 36889626
12 pages+
rs2681781 rs4858223 rs11753081 rs10846921 rs3731695 rs12200892
Using human genetics to understand the phenotypic association between chronotype and breast cancer
Journal of sleep research · 2024 · PMID 37380357
12 pages+
rs61863443 rs7907439 rs1242507 rs2413624 rs4321976 rs2737250
Investigating the shared genetic architecture of uterine leiomyoma and breast cancer: A genome-wide cross-trait analysis
American journal of human genetics · 2022 · PMID 35803233
8 pages
rs851982 rs9611271 rs12217370 rs851984 rs10789665 rs12555322
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
AOGC Consortium · UK10K Consortium
Nature · 2015 · PMID 26367794
7 pages
rs188303909 rs11024028 rs148771817 rs11692564 rs6542457 Spine Bone Mineral Density
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
Genetic contribution of reproductive traits to risk of uterine leiomyomata: a large-scale, genome-wide, cross-trait analysis
American journal of obstetrics and gynecology · 2024 · PMID 38191017
4 pages
rs56186913 rs1717777 rs6430580 rs12599260
Epidemiological and Genetic Analyses of Schizophrenia and Breast Cancer
Schizophrenia bulletin · 2024 · PMID 37467357
3 pages
rs2905432 rs2532363 rs7447717
Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder
BiGS
Molecular psychiatry · 2013 · PMID 22182935
2 pages
rs9834970 rs4948418
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 study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
Nature communications · 2018 · PMID 29343764 · open access
2 pages
rs10745742 Vitamin D Deficiency and the GC Gene
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
kConFab Investigators · ABCTB Investigators and 2 more consortia
Nature genetics · 2020 · PMID 32424353 · open access
2 pages
rs11065822 rs17743054
A genome-wide cross-trait analysis identifies shared loci and causal relationships of type 2 diabetes and glycaemic traits with polycystic ovary syndrome
Diabetologia · 2022 · PMID 35771237 · open access
2 pages
rs9930501 rs9844212
A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers
iScience · 2023 · PMID 37636041 · open access
2 pages
rs71238846 rs9620778

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.