For researchers
Is your paper here?
2,661 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.
1 match for
Antwi SO.
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
Purdue MP,
Dutta D,
Machiela MJ,
Gorman BR,
Winter T,
Okuhara D,
Cleland S,
Ferreiro-Iglesias A,
Scheet P,
Liu A,
Wu C,
Antwi SO
and 120 more — show all
Larkin J,
Zequi SC,
Sun M,
Hikino K,
Hajiran A,
Lawson KA,
Cárcano F,
Blanchet O,
Shuch B,
Nepple KG,
Margue G,
Sundi D,
Diver WR,
Folgueira MAAK,
van Bokhoven A,
Neffa F,
Brown KM,
Hofmann JN,
Rhee J,
Yeager M,
Cole NR,
Hicks BD,
Manning MR,
Hutchinson AA,
Rothman N,
Huang WY,
Linehan WM,
Lori A,
Ferragu M,
Zidane-Marinnes M,
Serrano SV,
Magnabosco WJ,
Vilas A,
Decia R,
Carusso F,
Graham LS,
Anderson K,
Bilen MA,
Arciero C,
Pellegrin I,
Ricard S,
Scelo G,
Banks RE,
Vasudev NS,
Soomro N,
Stewart GD,
Adeyoju A,
Bromage S,
Hrouda D,
Gibbons N,
Patel P,
Sullivan M,
Protheroe A,
Nugent FI,
Fournier MJ,
Zhang X,
Martin LJ,
Komisarenko M,
Eisen T,
Cunningham SA,
Connolly DC,
Uzzo RG,
Zaridze D,
Mukeria A,
Holcatova I,
Hornakova A,
Foretova L,
Janout V,
Mates D,
Jinga V,
Rascu S,
Mijuskovic M,
Savic S,
Milosavljevic S,
Gaborieau V,
Abedi-Ardekani B,
McKay J,
Johansson M,
Phouthavongsy L,
Hayman L,
Li J,
Lungu I,
Bezerra SM,
Souza AG,
Sares CTG,
Reis RB,
Gallucci FP,
Cordeiro MD,
Pomerantz M,
Lee GM,
Freedman ML,
Jeong A,
Greenberg SE,
Sanchez A,
Thompson RH,
Sharma V,
Thiel DD,
Ball CT,
Abreu D,
Lam ET,
Nahas WC,
Master VA,
Patel AV,
Bernhard JC,
Freedman ND,
Bigot P,
Reis RM,
Colli LM,
Finelli A,
Manley BJ,
Terao C,
Choueiri TK,
Carraro DM,
Houlston R,
Eckel-Passow JE,
Abbosh PH,
Ganna A,
Brennan P,
Gu J,
Chanock SJ
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 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.