For researchers

Is your paper here?

2,661 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.

10 matches for Ma X.

Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia
American journal of human genetics · 2021 · PMID 34469753
12 pages+
rs116141391 rs12219294 rs141800474 rs141951483 rs149524498 rs28724235
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
PBC Consortia · Canadian PBC Consortium and 5 more consortia
Journal of hepatology · 2021 · PMID 34033851 · open access
10 pages
rs12942330 rs4709148 rs34655300 rs589446 rs11742270 rs859767
Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study
Chinese Antipsychotics Pharmacogenomics Consortium
The lancet. Psychiatry · 2018 · PMID 29503163
4 pages
rs16921385 rs17022006 rs72790443 rs1471786
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
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
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
GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21
Nature communications · 2018 · PMID 29348612 · open access
2 pages
rs2290400 rs7089424
Genome-wide association study of childhood B-cell acute lymphoblastic leukemia reveals novel African ancestry-specific susceptibility loci
Nature communications · 2025 · PMID 41125582 · open access
2 pages
rs183221417 rs17133807
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis
Hepatology (Baltimore, Md.) · 2019 · PMID 30854688 · open access
1 page
rs1794280
Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer
Genome medicine · 2022 · PMID 35313970 · open access
1 page
rs732314

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.