For researchers

Is your paper here?

2,681 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.

17 matches for Pang C.

Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
NEIGHBORHOOD consortium · ANZRAG consortium and 5 more consortia
Nature communications · 2021 · PMID 33627673 · open access
12 pages+
rs62391632 rs66819623 rs8141610 rs56233426 rs11710845 rs1412829
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
NEIGHBOR Consortium
Nature genetics · 2013 · PMID 23291589
10 pages
rs2307121 rs1007000 rs1536482 rs11145951 rs4938174 rs1564892
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
rs10853531 rs11145488 rs12511037 rs1649081 rs16949788 rs10089517
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Consortium for Refractive Error and Myopia (CREAM) · Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and 2 more consortia
Nature genetics · 2013 · PMID 23396134
6 pages
rs1656404 rs4793501 rs10882165 rs17183295 rs11145465 Myopia
Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Science China. Life sciences · 2019 · PMID 30591961
6 pages
rs17737857 rs4467035 rs201143466 rs12504231 rs7047871 rs11078446
Genome-wide association study identified novel loci and gene-environment interaction for refractive error in children
NPJ genomic medicine · 2025 · PMID 40410244 · open access
3 pages
rs17074027 rs6925312 rs4609227
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
2 pages
rs9811920 rs12193446
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3
Nature genetics · 2014 · PMID 25108386
2 pages
rs117633859 Vogt-Koyanagi-Harada Syndrome
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes
Nature communications · 2023 · PMID 37696869 · open access
2 pages
rs4769312 rs6121609
Association of Novel Loci With Keratoconus Susceptibility in a Chinese Genome-Wide Association Study
Investigative ophthalmology & visual science · 2024 · PMID 38767907 · open access
2 pages
rs2300163 rs3743680
GWAS for primary angle-closure glaucoma identifies loci related to ocular biometry and morphology
Nature communications · 2025 · PMID 41238566 · open access
2 pages
rs134545 rs11984688
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
Nature genetics · 2010 · PMID 20835238
1 page
rs4236601
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population
American journal of human genetics · 2011 · PMID 21640322
1 page
rs9318086
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population
Human molecular genetics · 2013 · PMID 23406873
1 page
rs4455882
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
Nagahama Study Group
Human molecular genetics · 2013 · PMID 23933737
1 page
rs6469937
ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma
PLoS genetics · 2014 · PMID 24603532 · open access
1 page
rs1401999
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Nature genetics · 2016 · PMID 27064256
1 page
rs3739821

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.