For researchers

Is your paper here?

2,665 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.

25 matches for Lee Y, showing the first 20.

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Australian Asthma Genetics Consortium (AAGC) collaborators
Nature genetics · 2018 · PMID 29273806 · open access
12 pages+
rs2952156 rs17806299 rs4988958 rs2596464 rs6893213 rs1663687
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis
23andMe Research Team · AAGC collaborators
Nature genetics · 2018 · PMID 30013184
12 pages+
rs9282864 rs12657787 rs2164068 rs3787184 rs7717955 rs28361986
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
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
23andMe Research Team · Estonian Biobank Research Team
Nature communications · 2023 · PMID 37794016 · open access
12 pages+
rs12138773 rs4705908 rs10988863 rs4312054 rs6023002 rs705699
Genome-wide association study and fine-mapping on Korean biobank to discover renal trait-associated variants
Kidney research and clinical practice · 2024 · PMID 37919891 · open access
12 pages+
rs72941839 rs77366165 rs1058004 rs34446110 rs1919127 rs74175068
Large-scale cross-ancestry genome-wide meta-analysis of serum urate
Nature communications · 2024 · PMID 38658550 · open access
12 pages+
rs12364994 rs2236270 rs76227013 rs36163299 rs2770807 rs62585352
Genetic Architecture of Trans-Laminar Cribrosa Pressure Difference and Primary Open-Angle Glaucoma
Investigative ophthalmology & visual science · 2026 · PMID 42017308 · open access
12 pages+
rs1423422 rs2478873 rs9573609 rs68192516 rs407314 rs35385507
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
11 pages
rs112111458 rs10214237 rs6473227 rs6602364 rs7127307 rs2143950
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
23andMe Research Team · AAGC collaborators and 2 more consortia
Nature genetics · 2017 · PMID 29083406 · open access
10 pages
rs7130753 rs17607589 rs11236814 rs11204896 rs35469349 rs16922576
Age-of-onset information helps identify 76 genetic variants associated with allergic disease
23andMe Research Team · collaborators of the SHARE study
PLoS genetics · 2020 · PMID 32603359 · open access
7 pages
rs7559046 rs7521390 rs73739621 rs2918302 rs3017289 rs61907712
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4
Australian Asthma Genetics Consortium (AAGC)
Nature communications · 2021 · PMID 34785669 · open access
6 pages
rs2844594 rs3848669 rs13208697 rs4372325 rs12334935 rs2918299
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms
Psoriasis Association Genetics Extension
American journal of human genetics · 2015 · PMID 25574825 · open access
5 pages
rs17716942 rs465969 rs11795343 rs41268896 Atopic Dermatitis
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index
Human molecular genetics · 2014 · PMID 24861553
4 pages
rs2535633 rs11030104 rs574367 rs591166
Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2C19 Genotype and Clopidogrel Therapy: 2022 Update
Clinical pharmacology and therapeutics · 2022 · PMID 35034351
4 pages
rs4244285 rs4986893 rs12248560 Coronary Artery Disease
Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations
Gut · 2014 · PMID 23850713
3 pages
rs11235667 rs10947261 rs6856616
Meta-analysis identifies seven susceptibility loci involved in the atopic march
Nature communications · 2015 · PMID 26542096 · open access
3 pages
rs993226 rs9357733 rs17690965
GWAS identifying HLA-DPB1 gene variants associated with responsiveness to hepatitis B virus vaccination in Koreans: Independent association of HLA-DPB1*04:02 possessing rs1042169 G - rs9277355 C - rs9277356 A
Journal of viral hepatitis · 2019 · PMID 31243853
2 pages
rs9277356 Response to Hepatitis B Vaccine
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus
Human molecular genetics · 2022 · PMID 34850884
2 pages
rs145720245 rs7911501
Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits
PloS one · 2013 · PMID 24204828 · open access
1 page
rs2421332
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
rs60780116

Showing 20 of 25 · page 1 of 2

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.