For researchers

Is your paper here?

2,671 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.

8 matches for Wan B.

Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals
VA Million Veteran Program
Nature communications · 2021 · PMID 34272381 · open access
12 pages+
rs57445665 rs17713396 rs59646751 rs2250067 rs148635648 rs2034899
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs76181804 rs9290877 rs9594366 rs16856530 rs62283809 rs10854002
Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B
Hepatology (Baltimore, Md.) · 2015 · PMID 25802187
2 pages
rs2853953 rs2856718
Lifestyle Factors and Genetic Variants on 2 Biological Age Measures: Evidence From 94 443 Taiwan Biobank Participants
The journals of gerontology. Series A, Biological sciences and medical sciences · 2022 · PMID 34427645
2 pages
rs966965120 rs1057209
Gene-Environment Interactions and Gene-Gene Interactions on Two Biological Age Measures: Evidence from Taiwan Biobank Participants
Advanced biology · 2024 · PMID 38684452
2 pages
rs76038336 rs35276921
Genome-wide association study of primary dysmenorrhea in the Taiwan Biobank validates associations near the NGF and IL1 gene loci
National Taiwan University Hospital, Health Data Science Research Group
Journal of human genetics · 2022 · PMID 35351958
1 page
rs11676014
Genome-Wide Association Study of CKD Progression
Journal of the American Society of Nephrology : JASN · 2023 · PMID 37261792
1 page
rs16996674
Colorectal Polyp Occurrence Associated With the ZMIZ1-AS1 rs704017 Variant and Hypertension Among Taiwan Biobank Participants
Cancer medicine · 2026 · PMID 42706660
1 page
Research roundup — September 2026

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.