For researchers
Is your paper here?
2,657 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.
6 matches for
Kim DS.
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+
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
Fingerlin TE,
Murphy E,
Zhang W,
Peljto AL,
Brown KK,
Steele MP,
Loyd JE,
Cosgrove GP,
Lynch D,
Groshong S,
Collard HR,
Wolters PJ
and 38 more — show all
Bradford WZ,
Kossen K,
Seiwert SD,
du Bois RM,
Garcia CK,
Devine MS,
Gudmundsson G,
Isaksson HJ,
Kaminski N,
Zhang Y,
Gibson KF,
Lancaster LH,
Cogan JD,
Mason WR,
Maher TM,
Molyneaux PL,
Wells AU,
Moffatt MF,
Selman M,
Pardo A,
Kim DS,
Crapo JD,
Make BJ,
Regan EA,
Walek DS,
Daniel JJ,
Kamatani Y,
Zelenika D,
Smith K,
McKean D,
Pedersen BS,
Talbert J,
Kidd RN,
Markin CR,
Beckman KB,
Lathrop M,
Schwarz MI,
Schwartz DA
Nature genetics · 2013 · PMID 23583980 · open access
5 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
Mapping and annotating genomic loci to prioritize genes and implicate distinct polygenic adaptations for skin color
Kim B,
Kim DS,
Shin JG,
Leem S,
Cho M,
Kim H,
Gu KN,
Seo JY,
You SW,
Martin AR,
Park SG,
Kim Y
and 3 more — show all
Nature communications · 2024 · PMID 38849341 · open access
3 pages
Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network
Palmer MR,
Kim DS,
Crosslin DR,
Stanaway IB,
Rosenthal EA,
Carrell DS,
Cronkite DJ,
Gordon A,
Du X,
Li YK,
Williams MS,
Weng C
and 12 more — show all
Feng Q,
Li R,
Pendergrass SA,
Hakonarson H,
Fasel D,
Sohn S,
Sleiman P,
Handelman SK,
Speliotes E,
Kullo IJ,
Larson EB,
Jarvik GP
eMERGE Consortium
Genetic epidemiology · 2021 · PMID 32964493 · open access
2 pages
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.