For researchers

Is your paper here?

2,673 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.

111 matches for Lee J, showing the first 20.

Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs73085586 rs13086331 rs117737118 rs147689733 rs3135911 rs76541615
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
HPAP Consortium · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2020 · PMID 32541925 · open access
12 pages+
rs9370243 rs9900074 rs73121277 rs1470560 rs7538321 rs11114650
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs7178801 rs76480089 rs1634517 rs62193063 rs9807908 rs3742564
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+
rs10928512 rs187479321 rs6493583 rs72729623 rs115726216 rs144242131
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
23andMe Research Team · Social Science Genetic Association Consortium
Nature genetics · 2022 · PMID 35361970 · open access
12 pages+
rs35377646 rs6824923 rs114109036 rs11941559 rs12534982 rs12634802
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs77622099 rs619091 rs12652777 rs12476312 rs79445414 rs10860960
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+
rs9899520 rs75307421 rs3780012 rs4267865 rs57634870 rs11196296
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs1887200 rs11904581 rs6139109 rs1442883 rs973730 rs6020177
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+
rs62133107 rs1013304 rs62473520 rs59757115 rs2251964 rs9787150
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs2296740 rs2371340 rs403407 rs4953150 rs56357145 rs7960340
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
rs62454414 rs6541092 rs661857 rs2967516 rs17160476 rs6667222
A Genome-Wide Association Study of Metabolic Syndrome in the Taiwanese Population
Nutrients · 2023 · PMID 38201907 · open access
12 pages+
rs10892049 rs191655881 rs17440824 rs11601584 rs61905145 rs35732917
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1683935 rs71474196 rs72798545 rs1523539 rs7307263 rs11716527
Genetic architecture of cerebrospinal fluid and brain metabolite levels and the genetic colocalization of metabolites with human traits
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528826
12 pages+
rs7073937 rs12572781 rs9299324 rs291429 rs4774478 rs55878528
Genome-wide association studies in a large Korean cohort identify quantitative trait loci for 36 traits and illuminate their genetic architectures
Nature communications · 2025 · PMID 40436827 · open access
12 pages+
rs4896712 rs10500326 rs13264882 rs11697082 rs7840329 rs191205856
A genome-wide study on gene-nutrient interactions for hyperuricemia in a large Korean cohort (KoGES)
Scientific reports · 2025 · PMID 40835619 · open access
12 pages+
rs576114454 rs183195599 rs2725234 rs9999470 rs138409370 rs75786299
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Colorado Center for Personalized Medicine · DBDS Genomic Consortium and 2 more consortia
Nature genetics · 2026 · PMID 41419686 · open access
12 pages+
rs10219671 rs11001768 rs17161463 rs9674961 rs12188931 rs147558377
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
CHD Exome+ Consortium · EPIC-CVD Consortium and 2 more consortia
Nature genetics · 2017 · PMID 28869590 · open access
11 pages
rs9505118 rs4689388 rs2706785 rs329122 rs2050188 rs12681990
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
LifeLines Cohort Study
Nature genetics · 2016 · PMID 27089181 · open access
10 pages
rs782212 rs12903563 rs12961969 rs35688236 rs2075677 rs4958581
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
rs4745982 rs10823343 rs3824065 rs11154792 rs17509001 rs7040409

Showing 20 of 111 · page 2 of 6

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.