For researchers
Is your paper here?
2,651 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
Shima Y.
Genetic study identifies novel genes in developmental dysplasia of the hip
Yoshino S,
Chen S,
Yamaguchi R,
Kurakazu T,
Hatzikotoulas K,
Koike Y,
Inoue D,
Kohno Y,
Sasaki K,
Choe H,
Baba S,
Hara T
and 31 more — show all
Ito J,
Okuzu Y,
Shiomoto K,
Nakamura T,
Koyano G,
Shimizu T,
Kinoshita K,
Takahashi E,
Utsunomiya T,
Hara D,
Sato T,
Kawahara S,
Kaneuji A,
Yamamoto T,
Takahashi D,
Jinno T,
Kawano T,
Goto K,
Takagi M,
Mawatari T,
Inaba Y,
Nakamura T,
Kabata T,
Hamai S,
Motomura G,
Southam L,
Wilkinson JM,
Zeggini E,
Ikegawa S,
Nakashima Y,
Terao C
Bone research · 2026 · PMID 41912496 · open access
9 pages
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
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population
Nakabayashi K,
Tajima A,
Yamamoto K,
Takahashi A,
Hata K,
Takashima Y,
Koyanagi M,
Nakaoka H,
Akamizu T,
Ishikawa N,
Kubota S,
Maeda S
and 6 more — show all
Journal of human genetics · 2011 · PMID 21900946
4 pages
Gamma-aminobutyric acid transaminase genetic polymorphism is a candidate locus for responsiveness to opioid analgesics in patients with cancer pain: An exploratory study
Yokoshima Y,
Sumitani M,
Nishizawa D,
Nagashima M,
Ikeda K,
Kato R,
Hozumi J,
Abe H,
Azuma K,
Tsuchida R,
Yamada Y
Japanese TR-Cancer Pain Research Group
Neuropsychopharmacology reports · 2018 · PMID 30277654 · open access
2 pages
Genome-wide scan identifies novel genetic loci regulating salivary metabolite levels
Nag A,
Kurushima Y,
Bowyer RCE,
Wells PM,
Weiss S,
Pietzner M,
Kocher T,
Raffler J,
Völker U,
Mangino M,
Spector TD,
Milburn MV
and 5 more — show all
Human molecular genetics · 2020 · PMID 31960908 · open access
1 page
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome
Jia X,
Yamamura T,
Gbadegesin R,
McNulty MT,
Song K,
Nagano C,
Hitomi Y,
Lee D,
Aiba Y,
Khor SS,
Ueno K,
Kawai Y
and 33 more — show all
Nagasaki M,
Noiri E,
Horinouchi T,
Kaito H,
Hamada R,
Okamoto T,
Kamei K,
Kaku Y,
Fujimaru R,
Tanaka R,
Shima Y,
Baek J,
Kang HG,
Ha IS,
Han KH,
Yang EM,
Abeyagunawardena A,
Lane B,
Chryst-Stangl M,
Esezobor C,
Solarin A,
Dossier C,
Deschênes G,
Vivarelli M,
Debiec H,
Ishikura K,
Matsuo M,
Nozu K,
Ronco P,
Cheong HI,
Sampson MG,
Tokunaga K,
Iijima K
Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan · Korean Consortium of Hereditary Renal Diseases in Children and 2 more consortia
Kidney international · 2020 · PMID 32554042
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.