For researchers

Is your paper here?

2,676 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.

16 matches for Kang J.

New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
NEIGHBORHOOD Consortium
Human molecular genetics · 2017 · PMID 28073927
12 pages+
rs6107845 rs2157719 rs114503346 rs10753787 rs72759609 rs8015152
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2018 · PMID 29760442 · open access
12 pages+
rs3808520 rs7026684 rs10980623 rs7040970 rs7308752 rs11553764
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+
rs66819623 rs8141610 rs56233426 rs11710845 rs1412829 rs61870251
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
arcOGEN Consortium · HUNT All-In Pain and 2 more consortia
Cell · 2021 · PMID 34450027 · open access
12 pages+
rs747952496 rs3993110 rs781661531 rs7967762 rs10842226 rs116112221
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
FinnGen
Nature communications · 2022 · PMID 35347128 · open access
12 pages+
rs9516563 rs116382069 rs16902835 rs4838190 rs1247627279 rs189228944
Translational genomics of osteoarthritis in 1,962,069 individuals
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
rs62052494 rs79057214 rs1592795 rs2058744 rs12155373 rs11042731
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
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
BMES GWAS Group · NEIGHBORHOOD Consortium and 1 more consortia
Nature genetics · 2014 · PMID 25173106 · open access
4 pages
rs747782 rs10258482 rs12419342 Glaucoma
Genome-wide association study of occupational attainment as a proxy for cognitive reserve
Brain : a journal of neurology · 2022 · PMID 34613391
3 pages
rs448809 rs3741368 rs55769536
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2014 · PMID 25241763 · open access
2 pages
rs17658229 rs17756712
Identification of five novel genetic loci related to facial morphology by genome-wide association studies
BMC genomics · 2018 · PMID 29921221 · open access
2 pages
rs2206437 rs2193054
Genome-wide association study confirming association of HLA-DP with protection against chronic hepatitis B and viral clearance in Japanese and Korean
PloS one · 2012 · PMID 22737229 · open access
1 page
rs9277535
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
ANZRAG Consortium
Nature genetics · 2016 · PMID 26752265 · open access
1 page
rs1333037
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
NEIGHBORHOOD consortium
Scientific reports · 2018 · PMID 29449654 · open access
1 page
rs72815193
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis
23andMe Research Team
JAMA neurology · 2022 · PMID 34982113 · open access
1 page
rs139378881
Whole exome sequencing identified six novel genes for depressive symptoms
Molecular psychiatry · 2025 · PMID 39472661
1 page
rs7853605

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.