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.

13 matches for Yoon K.

Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs61342118 rs7656416 rs12907887 rs73085586 rs13086331 rs117737118
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus
Japanese Research Committee on Idiopathic Osteonecrosis of the Femoral Head
Annals of the rheumatic diseases · 2021 · PMID 33272962 · open access
12 pages+
rs116785379 rs12120358 rs76107698 rs2039982 rs4143303 rs218174
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs11207980 rs598253 rs57825321 rs12603290 rs186793936 rs9844432
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs12669223 rs3768301 rs72830009 rs7100404 rs7076754 rs835576
The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians
Nature communications · 2022 · PMID 36333282 · open access
12 pages+
rs12035737 rs61855849 rs4487569 rs35950463 rs12053049 rs7032795
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1475655 rs67269808 rs7304270 rs2658746 rs75417759 rs12746673
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs151113194 rs762517 rs12012576 rs139120857 rs5942972 rs7063103
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits
Scientific reports · 2019 · PMID 30718733 · open access
6 pages
rs77768175 rs2303790 rs66626994 rs151193009 rs2980888 Cholesterol (LDL, HDL and Total)
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs12415501 rs60401382 rs72934589 rs76110445 Cardioembolic Stroke
Genome-wide association study using the ethnicity-specific Japonica array: identification of new susceptibility loci for cold medicine-related Stevens-Johnson syndrome with severe ocular complications
Journal of human genetics · 2017 · PMID 28100913
2 pages
rs16957893 Cold Medicine-Related SJS/TEN with Severe Ocular Complications
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations
Nature genetics · 2010 · PMID 20871597
1 page
rs2736100
A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population
Human molecular genetics · 2010 · PMID 20876614
1 page
rs2131877
Variants in NEB and RIF1 genes on chr2q23 are associated with skeletal muscle index in Koreans: genome-wide association study
Scientific reports · 2021 · PMID 33674626 · open access
1 page
rs138684936

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.