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.
4 matches for
Toh T.
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Schumann G,
Liu C,
O'Reilly P,
Gao H,
Song P,
Xu B,
Ruggeri B,
Amin N,
Jia T,
Preis S,
Segura Lepe M,
Akira S
and 115 more — show all
Barbieri C,
Baumeister S,
Cauchi S,
Clarke TK,
Enroth S,
Fischer K,
Hällfors J,
Harris SE,
Hieber S,
Hofer E,
Hottenga JJ,
Johansson Å,
Joshi PK,
Kaartinen N,
Laitinen J,
Lemaitre R,
Loukola A,
Luan J,
Lyytikäinen LP,
Mangino M,
Manichaikul A,
Mbarek H,
Milaneschi Y,
Moayyeri A,
Mukamal K,
Nelson C,
Nettleton J,
Partinen E,
Rawal R,
Robino A,
Rose L,
Sala C,
Satoh T,
Schmidt R,
Schraut K,
Scott R,
Smith AV,
Starr JM,
Teumer A,
Trompet S,
Uitterlinden AG,
Venturini C,
Vergnaud AC,
Verweij N,
Vitart V,
Vuckovic D,
Wedenoja J,
Yengo L,
Yu B,
Zhang W,
Zhao JH,
Boomsma DI,
Chambers J,
Chasman DI,
Daniela T,
de Geus E,
Deary I,
Eriksson JG,
Esko T,
Eulenburg V,
Franco OH,
Froguel P,
Gieger C,
Grabe HJ,
Gudnason V,
Gyllensten U,
Harris TB,
Hartikainen AL,
Heath AC,
Hocking L,
Hofman A,
Huth C,
Jarvelin MR,
Jukema JW,
Kaprio J,
Kooner JS,
Kutalik Z,
Lahti J,
Langenberg C,
Lehtimäki T,
Liu Y,
Madden PA,
Martin N,
Morrison A,
Penninx B,
Pirastu N,
Psaty B,
Raitakari O,
Ridker P,
Rose R,
Rotter JI,
Samani NJ,
Schmidt H,
Spector TD,
Stott D,
Strachan D,
Tzoulaki I,
van der Harst P,
van Duijn CM,
Marques-Vidal P,
Vollenweider P,
Wareham NJ,
Whitfield JB,
Wilson J,
Wolffenbuttel B,
Bakalkin G,
Evangelou E,
Liu Y,
Rice KM,
Desrivières S,
Kliewer SA,
Mangelsdorf DJ,
Müller CP,
Levy D,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
Whole-genome sequencing reveals rare and structural variants contributing to psoriasis and identifies CERCAM as a risk gene
Sonehara K,
Watanabe R,
Matsumura Y,
Mitsui Y,
Ogawa Y,
Odomari K,
Sakaue S,
Namba S,
Komuro M,
Edamoto M,
Watanabe J,
Hirota T
and 59 more — show all
Arase N,
Nakamura Y,
Nakajima K,
Okamoto T,
Nishikawa R,
Yamamoto K,
Suzuki K,
Kishikawa T,
Edahiro R,
Shirai Y,
Naito T,
Sasa N,
Ishitsuka Y,
Furuta J,
Kunimoto K,
Kajihara I,
Fukushima S,
Miyachi H,
Matsue H,
Kamata M,
Momose M,
Miyagawa I,
Tanaka H,
Ueno M,
Bito T,
Nagai H,
Ikeda T,
Horikawa T,
Adachi A,
Matsubara T,
Nishida E,
Matsuda K,
Shojima N,
Nakagawa I,
Asano Y,
Sato S,
Imafuku S,
Tada Y,
Nishigori C,
Jinnin M,
Ihn H,
Asahina A,
Saeki H,
Yamauchi T,
Kadowaki T,
Kawamura T,
Shimada S,
Katayama I,
Higasa K,
Noguchi E,
Sano S,
Tanaka Y,
Matsuda F,
Kumanogoh A,
Tamari M,
Satoh T,
Fujimoto M,
Morita A,
Okada Y
Biobank Japan Project
Cell genomics · 2025 · PMID 40848718 · open access
3 pages
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness
Lu Y,
Dimasi DP,
Hysi PG,
Hewitt AW,
Burdon KP,
Toh T,
Ruddle JB,
Li YJ,
Mitchell P,
Healey PR,
Montgomery GW,
Hansell N
and 7 more — show all
PLoS genetics · 2010 · PMID 20485516 · open access
1 page
Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout
Kawamura Y,
Nakaoka H,
Nakayama A,
Okada Y,
Yamamoto K,
Higashino T,
Sakiyama M,
Shimizu T,
Ooyama H,
Ooyama K,
Nagase M,
Hidaka Y
and 38 more — show all
Shirahama Y,
Hosomichi K,
Nishida Y,
Shimoshikiryo I,
Hishida A,
Katsuura-Kamano S,
Shimizu S,
Kawaguchi M,
Uemura H,
Ibusuki R,
Hara M,
Naito M,
Takao M,
Nakajima M,
Iwasawa S,
Nakashima H,
Ohnaka K,
Nakamura T,
Stiburkova B,
Merriman TR,
Nakatochi M,
Ichihara S,
Yokota M,
Takada T,
Saitoh T,
Kamatani Y,
Takahashi A,
Arisawa K,
Takezaki T,
Tanaka K,
Wakai K,
Kubo M,
Hosoya T,
Ichida K,
Inoue I,
Shinomiya N,
Matsuo H,
Matsuo H
Annals of the rheumatic diseases · 2019 · PMID 31289104 · 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.