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.

269 matches for Ng M, showing the first 9.

Associations between a polygenic risk score and the risk of gestational diabetes mellitus in a Chinese population: a case-control study
Endocrine journal · 2023 · PMID 37779084
1 page
rs7925879
Comprehensive Association Analyses of Extraintestinal Manifestations in Inflammatory Bowel Disease
Gastroenterology · 2024 · PMID 38490347
1 page
rs9276456
Genetic risk factors for COVID-19 and influenza are largely distinct
Colorado Center for Precision Medicine · Mayo Clinic Project Generation and 2 more consortia
Nature genetics · 2024 · PMID 39103650 · open access
1 page
rs2837112
Identification of susceptibility loci and relevant cell type for IgA nephropathy in Han Chinese by integrative genome-wide analysis
Frontiers of medicine · 2024 · PMID 39343836
1 page
rs13332545
Cross-ancestry genome-wide association study identifies implications of SORL1 in cerebral beta-amyloid deposition
Nature communications · 2025 · PMID 40175353 · open access
1 page
rs76490923
Genome-wide association study identified novel loci and gene-environment interaction for refractive error in children
NPJ genomic medicine · 2025 · PMID 40410244 · open access
1 page
rs17074027
Omitting post-alignment processing and merging batch-based imputation: an efficient workflow for NIPT data imputation and its application in maternal folate metabolism genotyping
Journal of human genetics · 2026 · PMID 42581209
1 page
Research roundup — September 2026
A preeclampsia prediction model incorporating methylenetetrahydrofolate reductase, vitamin D receptor, and uterine artery pulsatility index
Hypertension in pregnancy · 2026 · PMID 42723529
1 page
Research roundup — September 2026
Resistance to HIV-1 infection in caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene
Nature · 1996 · PMID 8751444
1 page
rs333

Showing 9 of 269 · page 14 of 14

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.