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.

43 matches for Kim J, showing the first 20.

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
rs2004038 rs34878803 rs13213986 rs7383287 rs11632038 rs17400427
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Profile Study · Australian Prostate Cancer BioResource (APCB) and 7 more consortia
Nature genetics · 2018 · PMID 29892016
12 pages+
rs4962416 rs684232 rs182314334 rs2121875 rs17021918 rs11859370
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
rs73909841 rs10788167 rs3787099 rs371707439 rs12701838 rs565189650
Genetic determinants of daytime napping and effects on cardiometabolic health
23andMe Research Team
Nature communications · 2021 · PMID 33568662 · open access
12 pages+
rs11224896 rs2417268 rs35011311 rs60222088 rs11615756 rs2786547
Leveraging deep phenotyping from health check-up cohort with 10,000 Korean individuals for phenome-wide association study of 136 traits
Scientific reports · 2022 · PMID 35121771 · open access
12 pages+
rs72810954 rs192385957 rs79945097 rs182483569 rs76731854 rs77162552
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature genetics · 2023 · PMID 36539618
12 pages+
rs6434979 rs4236382 rs10751097 rs10978941 rs62042090 rs17686932
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs10886810 rs1037137 rs11892008 rs6151589 rs4713343 rs78416326
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease
23andMe Research Team · Global Parkinson’s Genetics Program (GP2)
Nature genetics · 2024 · PMID 38155330 · open access
12 pages+
rs8018800 rs35161831 rs1442190 rs4421827 rs78327649 rs246815
Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groups
Nature communications · 2025 · PMID 40050615 · open access
12 pages+
rs62112863 rs117424499 rs143479908 rs10751644 rs2145763 rs60702155
Genome-wide association study identifies novel susceptibilities to adult moyamoya disease
Journal of human genetics · 2023 · PMID 37365321
8 pages
rs74790219 rs117343774 rs7211327 rs2887022 rs41301888 rs7525578
Central Adiposity Increases Risk of Kidney Stone Disease through Effects on Serum Calcium Concentrations
Journal of the American Society of Nephrology : JASN · 2023 · PMID 37787550 · open access
8 pages
rs9533022 rs12921916 rs10807202 rs4252512 rs9472142 rs115239632
Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer
Gastroenterology · 2019 · PMID 30529582
6 pages
rs7542665 rs201395236 rs113569514 rs3830041 rs77969132 rs1886450
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs71467682 rs75031349 rs137884934 rs682888 rs10901793
Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits
Nature human behaviour · 2022 · PMID 34426670
4 pages
rs199535 rs1971631 rs62132801 rs9964229
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
Nature genetics · 2009 · PMID 19396169
3 pages
rs6918981 rs13273123 Height
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits
MAGIC consortium
Nature genetics · 2011 · PMID 21909109
3 pages
rs7232775 rs11216126 rs2286276
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease
Human molecular genetics · 2016 · PMID 27702942
3 pages
rs80227144 rs7005606 Hirschsprung Disease
Genome-wide association study of occupational attainment as a proxy for cognitive reserve
Brain : a journal of neurology · 2022 · PMID 34613391
3 pages
rs55769536 rs448809 rs3741368
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease
Molecular psychiatry · 2023 · PMID 37198259 · open access
3 pages
rs9394766 rs74825460 rs117807585
Genome-wide association analyses using machine learning-based phenotyping reveal genetic architecture of occupational creativity and overlap with psychiatric disorders
Psychiatry research · 2024 · PMID 38335777
3 pages
rs35800293 rs73079014 rs34427167

Showing 20 of 43 · page 1 of 3

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.