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.
8 matches for
Nakamura T.
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
Genome-wide Association Study of Axial Length in Population-based Cohorts in Japan: The Tohoku Medical Megabank Organization Eye Study
Fuse N,
Sakurai M,
Motoike IN,
Kojima K,
Takai-Igarashi T,
Nakaya N,
Tsuchiya N,
Nakamura T,
Ishikuro M,
Obara T,
Miyazawa A,
Homma K
and 21 more — show all
Ido K,
Taira M,
Kobayashi T,
Shimizu R,
Uruno A,
Kodama EN,
Suzuki K,
Hamanaka Y,
Tomita H,
Sugawara J,
Suzuki Y,
Nagami F,
Ogishima S,
Katsuoka F,
Minegishi N,
Hozawa A,
Kuriyama S,
Yaegashi N,
Kure S,
Kinoshita K,
Yamamoto M
Ophthalmology science · 2022 · PMID 36246171 · open access
7 pages
Subtype-specific gout susceptibility loci and enrichment of selection pressure on <i>ABCG2</i> and <i>ALDH2</i> identified by subtype genome-wide meta-analyses of clinically defined gout patients
Nakayama A,
Nakatochi M,
Kawamura Y,
Yamamoto K,
Nakaoka H,
Shimizu S,
Higashino T,
Koyama T,
Hishida A,
Kuriki K,
Watanabe M,
Shimizu T
and 42 more — show all
Ooyama K,
Ooyama H,
Nagase M,
Hidaka Y,
Matsui D,
Tamura T,
Nishiyama T,
Shimanoe C,
Katsuura-Kamano S,
Takashima N,
Shirai Y,
Kawaguchi M,
Takao M,
Sugiyama R,
Takada Y,
Nakamura T,
Nakashima H,
Tsunoda M,
Danjoh I,
Hozawa A,
Hosomichi K,
Toyoda Y,
Kubota Y,
Takada T,
Suzuki H,
Stiburkova B,
Major TJ,
Merriman TR,
Kuriyama N,
Mikami H,
Takezaki T,
Matsuo K,
Suzuki S,
Hosoya T,
Kamatani Y,
Kubo M,
Ichida K,
Wakai K,
Inoue I,
Okada Y,
Shinomiya N,
Matsuo H
Japan Gout Genomics Consortium (Japan Gout)
Annals of the rheumatic diseases · 2020 · PMID 32238385 · open access
6 pages
Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals
Nakatochi M,
Kanai M,
Nakayama A,
Hishida A,
Kawamura Y,
Ichihara S,
Akiyama M,
Ikezaki H,
Furusyo N,
Shimizu S,
Yamamoto K,
Hirata M
and 38 more — show all
Okada R,
Kawai S,
Kawaguchi M,
Nishida Y,
Shimanoe C,
Ibusuki R,
Takezaki T,
Nakajima M,
Takao M,
Ozaki E,
Matsui D,
Nishiyama T,
Suzuki S,
Takashima N,
Kita Y,
Endoh K,
Kuriki K,
Uemura H,
Arisawa K,
Oze I,
Matsuo K,
Nakamura Y,
Mikami H,
Tamura T,
Nakashima H,
Nakamura T,
Kato N,
Matsuda K,
Murakami Y,
Matsubara T,
Naito M,
Kubo M,
Kamatani Y,
Shinomiya N,
Yokota M,
Wakai K,
Okada Y,
Matsuo H
Communications biology · 2019 · PMID 30993211 · open access
4 pages
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes
Nakayama A,
Nakaoka H,
Yamamoto K,
Sakiyama M,
Shaukat A,
Toyoda Y,
Okada Y,
Kamatani Y,
Nakamura T,
Takada T,
Inoue K,
Yasujima T
and 34 more — show all
Yuasa H,
Shirahama Y,
Nakashima H,
Shimizu S,
Higashino T,
Kawamura Y,
Ogata H,
Kawaguchi M,
Ohkawa Y,
Danjoh I,
Tokumasu A,
Ooyama K,
Ito T,
Kondo T,
Wakai K,
Stiburkova B,
Pavelka K,
Stamp LK,
Dalbeth N,
Sakurai Y,
Suzuki H,
Hosoyamada M,
Fujimori S,
Yokoo T,
Hosoya T,
Inoue I,
Takahashi A,
Kubo M,
Ooyama H,
Shimizu T,
Ichida K,
Shinomiya N,
Merriman TR,
Matsuo H
Eurogout Consortium · Eurogout Consortium
Annals of the rheumatic diseases · 2017 · PMID 27899376 · open access
3 pages
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
Genetic loci for lung function in Japanese adults with adjustment for exhaled nitric oxide levels as airway inflammation indicator
Yamada M,
Motoike IN,
Kojima K,
Fuse N,
Hozawa A,
Kuriyama S,
Katsuoka F,
Tadaka S,
Shirota M,
Sakurai M,
Nakamura T,
Hamanaka Y
and 14 more — show all
Suzuki K,
Sugawara J,
Ogishima S,
Uruno A,
Kodama EN,
Fujino N,
Numakura T,
Ichikawa T,
Mitsune A,
Ohe T,
Kinoshita K,
Ichinose M,
Sugiura H,
Yamamoto M
Communications biology · 2021 · PMID 34782693 · open access
1 page
A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations
Morii W,
Kasai K,
Nakamura T,
Hayashi D,
Hara M,
Naito T,
Sonehara K,
Fukuie T,
Saito-Abe M,
Yang L,
Yamamoto-Hanada K,
Narita M
and 4 more — show all
The journal of allergy and clinical immunology. Global · 2023 · PMID 37780799 · 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.