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 Wu X, showing the first 20.

Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542
Epidemiological and Genetic Analyses of Schizophrenia and Breast Cancer
Schizophrenia bulletin · 2024 · PMID 37467357
3 pages
rs7447717 rs2905432 rs2532363
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
Nature genetics · 2009 · PMID 19648920
2 pages
rs2294008 Bladder Cancer
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2
Human molecular genetics · 2010 · PMID 20460270
2 pages
rs17095355 Biliary Atresia
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Nature genetics · 2010 · PMID 20972438 · open access
2 pages
rs8102137 rs798766
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
rs348495 rs10261878
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
2 pages
rs12525220 rs1854853
Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort
Circulation. Cardiovascular genetics · 2014 · PMID 24795349
2 pages
rs74019828 Telomere Length and Epigenetic Age Acceleration
Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B
Hepatology (Baltimore, Md.) · 2015 · PMID 25802187
2 pages
rs2856718 rs2853953
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia
Nature communications · 2016 · PMID 26956414 · open access
2 pages
rs9270750 rs72742684
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 identifies two risk loci for tuberculosis in Han Chinese
Nature communications · 2018 · PMID 30287856 · open access
2 pages
rs6114027 Tuberculosis
Identification of new susceptibility loci associated with rheumatoid arthritis
Annals of the rheumatic diseases · 2020 · PMID 32868391
2 pages
rs770667 rs2201584
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
Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism
Nature communications · 2024 · PMID 39214992 · open access
2 pages
rs149247216 rs5942980
A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity
Human molecular genetics · 2011 · PMID 21106707
1 page
rs8093763
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium
Nature genetics · 2012 · PMID 22751097
1 page
rs9268402
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Nature genetics · 2014 · PMID 24880342 · open access
1 page
rs13314271
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
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis
Hepatology (Baltimore, Md.) · 2019 · PMID 30854688 · open access
1 page
rs1794280

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.