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.
5 matches for
Horita T.
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region
Ishikawa Y,
Tanaka N,
Asano Y,
Kodera M,
Shirai Y,
Akahoshi M,
Hasegawa M,
Matsushita T,
Saito K,
Motegi SI,
Yoshifuji H,
Yoshizaki A
and 60 more — show all
Kohmoto T,
Takagi K,
Oka A,
Kanda M,
Tanaka Y,
Ito Y,
Nakano K,
Kasamatsu H,
Utsunomiya A,
Sekiguchi A,
Niiro H,
Jinnin M,
Makino K,
Makino T,
Ihn H,
Yamamoto M,
Suzuki C,
Takahashi H,
Nishida E,
Morita A,
Yamamoto T,
Fujimoto M,
Kondo Y,
Goto D,
Sumida T,
Ayuzawa N,
Yanagida H,
Horita T,
Atsumi T,
Endo H,
Shima Y,
Kumanogoh A,
Hirata J,
Otomo N,
Suetsugu H,
Koike Y,
Tomizuka K,
Yoshino S,
Liu X,
Ito S,
Hikino K,
Suzuki A,
Momozawa Y,
Ikegawa S,
Tanaka Y,
Ishikawa O,
Takehara K,
Torii T,
Sato S,
Okada Y,
Mimori T,
Matsuda F,
Matsuda K,
Amariuta T,
Imoto I,
Matsuo K,
Kuwana M,
Kawaguchi Y,
Ohmura K,
Terao C
Nature communications · 2024 · PMID 38296975 · open access
7 pages
Genetic determinants and an epistasis of <i>LILRA3</i> and HLA-B*52 in Takayasu arteritis
Terao C,
Yoshifuji H,
Matsumura T,
Naruse TK,
Ishii T,
Nakaoka Y,
Kirino Y,
Matsuo K,
Origuchi T,
Shimizu M,
Maejima Y,
Amiya E
and 29 more — show all
Tamura N,
Kawaguchi T,
Takahashi M,
Setoh K,
Ohmura K,
Watanabe R,
Horita T,
Atsumi T,
Matsukura M,
Miyata T,
Kochi Y,
Suda T,
Tanemoto K,
Meguro A,
Okada Y,
Ogimoto A,
Yamamoto M,
Takahashi H,
Nakayamada S,
Saito K,
Kuwana M,
Mizuki N,
Tabara Y,
Ueda A,
Komuro I,
Kimura A,
Isobe M,
Mimori T,
Matsuda F
Proceedings of the National Academy of Sciences of the United States of America · 2018 · PMID 30498034
3 pages
The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome
Sugiura-Ogasawara M,
Omae Y,
Kawashima M,
Toyo-Oka L,
Khor SS,
Sawai H,
Horita T,
Atsumi T,
Murashima A,
Fujita D,
Fujita T,
Morimoto S
and 6 more — show all
Journal of human genetics · 2017 · PMID 28424481
2 pages
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese
Okada Y,
Shimane K,
Kochi Y,
Tahira T,
Suzuki A,
Higasa K,
Takahashi A,
Horita T,
Atsumi T,
Ishii T,
Okamoto A,
Fujio K
and 32 more — show all
Hirakata M,
Amano H,
Kondo Y,
Ito S,
Takada K,
Mimori A,
Saito K,
Kamachi M,
Kawaguchi Y,
Ikari K,
Mohammed OW,
Matsuda K,
Terao C,
Ohmura K,
Myouzen K,
Hosono N,
Tsunoda T,
Nishimoto N,
Mimori T,
Matsuda F,
Tanaka Y,
Sumida T,
Yamanaka H,
Takasaki Y,
Koike T,
Horiuchi T,
Hayashi K,
Kubo M,
Kamatani N,
Yamada R,
Nakamura Y,
Yamamoto K
PLoS genetics · 2012 · PMID 22291604 · open access
1 page
Splicing variant of <i>WDFY4</i> augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis
Kochi Y,
Kamatani Y,
Kondo Y,
Suzuki A,
Kawakami E,
Hiwa R,
Momozawa Y,
Fujimoto M,
Jinnin M,
Tanaka Y,
Kanda T,
Cooper RG
and 36 more — show all
Chinoy H,
Rothwell S,
Lamb JA,
Vencovský J,
Mann H,
Ohmura K,
Myouzen K,
Ishigaki K,
Nakashima R,
Hosono Y,
Tsuboi H,
Kawasumi H,
Iwasaki Y,
Kajiyama H,
Horita T,
Ogawa-Momohara M,
Takamura A,
Tsunoda S,
Shimizu J,
Fujio K,
Amano H,
Mimori A,
Kawakami A,
Umehara H,
Takeuchi T,
Sano H,
Muro Y,
Atsumi T,
Mimura T,
Kawaguchi Y,
Mimori T,
Takahashi A,
Kubo M,
Kohsaka H,
Sumida T,
Yamamoto K
Annals of the rheumatic diseases · 2018 · PMID 29331962
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.