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.
4 matches for
Cheung K.
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans
Bigdeli TB,
Fanous AH,
Li Y,
Rajeevan N,
Sayward F,
Genovese G,
Gupta R,
Radhakrishnan K,
Malhotra AK,
Sun N,
Lu Q,
Hu Y
and 33 more — show all
Li B,
Chen Q,
Mane S,
Miller P,
Cheung KH,
Gur RE,
Greenwood TA,
Braff DL,
Achtyes ED,
Buckley PF,
Escamilla MA,
Lehrer D,
Malaspina DP,
McCarroll SA,
Rapaport MH,
Vawter MP,
Pato MT,
Pato CN,
Zhao H,
Kosten TR,
Brophy M,
Pyarajan S,
Shi Y,
O'Leary TJ,
Gleason T,
Przygodzki R,
Muralidhar S,
Gaziano JM,
Huang GD,
Concato J,
Siever LJ,
Aslan M,
Harvey PD
Consortium on the Genetics of Schizophrenia (COGS) · Genomic Psychiatry Cohort (GPC) Investigators and 1 more consortia
Schizophrenia bulletin · 2021 · PMID 33169155
4 pages
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease
Garcia-Barcelo MM,
Tang CS,
Ngan ES,
Lui VC,
Chen Y,
So MT,
Leon TY,
Miao XP,
Shum CK,
Liu FQ,
Yeung MY,
Yuan ZW
and 12 more — show all
Guo WH,
Liu L,
Sun XB,
Huang LM,
Tou JF,
Song YQ,
Chan D,
Cheung KM,
Wong KK,
Cherny SS,
Sham PC,
Tam PK
Proceedings of the National Academy of Sciences of the United States of America · 2009 · PMID 19196962
2 pages
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2
Garcia-Barceló MM,
Yeung MY,
Miao XP,
Tang CS,
Cheng G,
So MT,
Ngan ES,
Lui VC,
Chen Y,
Liu XL,
Hui KJ,
Li L
and 13 more — show all
Guo WH,
Sun XB,
Tou JF,
Chan KW,
Wu XZ,
Song YQ,
Chan D,
Cheung K,
Chung PH,
Wong KK,
Sham PC,
Cherny SS,
Tam PK
Human molecular genetics · 2010 · PMID 20460270
2 pages
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis gene
Boer CG,
Yau MS,
Rice SJ,
Coutinho de Almeida R,
Cheung K,
Styrkarsdottir U,
Southam L,
Broer L,
Wilkinson JM,
Uitterlinden AG,
Zeggini E,
Felson D
and 5 more — show all
Annals of the rheumatic diseases · 2021 · PMID 33055079 · 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.