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.
8 matches for
Jung SH.
Large-scale cross-ancestry genome-wide meta-analysis of serum urate
Cho C,
Kim B,
Kim DS,
Hwang MY,
Shim I,
Song M,
Lee YC,
Jung SH,
Cho SK,
Park WY,
Myung W,
Kim BJ
and 5 more — show all
Nature communications · 2024 · PMID 38658550 · open access
12 pages+
Genetic Architecture of Trans-Laminar Cribrosa Pressure Difference and Primary Open-Angle Glaucoma
Hong IS,
Cho C,
Kim B,
Shim I,
Lee YC,
Jung SH,
Song M,
Park S,
Hong S,
Jo H,
Kim H,
Seo JH
and 1 more — show all
Investigative ophthalmology & visual science · 2026 · PMID 42017308 · open access
12 pages+
Genome-wide association study of occupational attainment as a proxy for cognitive reserve
Ko H,
Kim S,
Kim K,
Jung SH,
Shim I,
Cha S,
Lee H,
Kim B,
Yoon J,
Ha TH,
Kwak S,
Kang JM
and 7 more — show all
Brain : a journal of neurology · 2022 · PMID 34613391
3 pages
Genome-wide association analyses using machine learning-based phenotyping reveal genetic architecture of occupational creativity and overlap with psychiatric disorders
Kim H,
Ahn Y,
Yoon J,
Jung K,
Kim S,
Shim I,
Park TH,
Ko H,
Jung SH,
Kim J,
Park S,
Lee DJ
and 15 more — show all
Choi S,
Cha S,
Kim B,
Cho MY,
Cho H,
Kim DS,
Jang Y,
Ihm HK,
Park WY,
Bakhshi H,
O Connell KS,
Andreassen OA,
Kendler KS,
Myung W,
Won HH
Psychiatry research · 2024 · PMID 38335777
3 pages
Shared genetic architectures of subjective well-being in East Asian and European ancestry populations
Kim S,
Kim K,
Hwang MY,
Ko H,
Jung SH,
Shim I,
Cha S,
Lee H,
Kim B,
Yoon J,
Ha TH,
Kim DK
and 7 more — show all
Nature human behaviour · 2022 · PMID 35589828
1 page
Cross-ancestry genome-wide association study identifies implications of SORL1 in cerebral beta-amyloid deposition
Kim JP,
Jung SH,
Jang B,
Cho M,
Song M,
Kim J,
Kim B,
Lee H,
Shin D,
Lee EH,
Jang H,
Kim BH
and 8 more — show all
Nature communications · 2025 · PMID 40175353 · open access
1 page
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.