For researchers
Is your paper here?
2,660 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
Ozaki K.
Transethnic Meta-Analysis of Genome-Wide Association Studies Identifies Three New Loci and Characterizes Population-Specific Differences for Coronary Artery Disease
Matsunaga H,
Ito K,
Akiyama M,
Takahashi A,
Koyama S,
Nomura S,
Ieki H,
Ozaki K,
Onouchi Y,
Sakaue S,
Suna S,
Ogishima S
and 24 more — show all
Yamamoto M,
Hozawa A,
Satoh M,
Sasaki M,
Yamaji T,
Sawada N,
Iwasaki M,
Tsugane S,
Tanaka K,
Arisawa K,
Ikezaki H,
Takashima N,
Naito M,
Wakai K,
Tanaka H,
Sakata Y,
Morita H,
Sakata Y,
Matsuda K,
Murakami Y,
Akazawa H,
Kubo M,
Kamatani Y,
Komuro I
Circulation. Genomic and precision medicine · 2020 · PMID 32469254
12 pages+
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Ishigaki K,
Akiyama M,
Kanai M,
Takahashi A,
Kawakami E,
Sugishita H,
Sakaue S,
Matoba N,
Low SK,
Okada Y,
Terao C,
Amariuta T
and 77 more — show all
Gazal S,
Kochi Y,
Horikoshi M,
Suzuki K,
Ito K,
Koyama S,
Ozaki K,
Niida S,
Sakata Y,
Sakata Y,
Kohno T,
Shiraishi K,
Momozawa Y,
Hirata M,
Matsuda K,
Ikeda M,
Iwata N,
Ikegawa S,
Kou I,
Tanaka T,
Nakagawa H,
Suzuki A,
Hirota T,
Tamari M,
Chayama K,
Miki D,
Mori M,
Nagayama S,
Daigo Y,
Miki Y,
Katagiri T,
Ogawa O,
Obara W,
Ito H,
Yoshida T,
Imoto I,
Takahashi T,
Tanikawa C,
Suzuki T,
Sinozaki N,
Minami S,
Yamaguchi H,
Asai S,
Takahashi Y,
Yamaji K,
Takahashi K,
Fujioka T,
Takata R,
Yanai H,
Masumoto A,
Koretsune Y,
Kutsumi H,
Higashiyama M,
Murayama S,
Minegishi N,
Suzuki K,
Tanno K,
Shimizu A,
Yamaji T,
Iwasaki M,
Sawada N,
Uemura H,
Tanaka K,
Naito M,
Sasaki M,
Wakai K,
Tsugane S,
Yamamoto M,
Yamamoto K,
Murakami Y,
Nakamura Y,
Raychaudhuri S,
Inazawa J,
Yamauchi T,
Kadowaki T,
Kubo M,
Kamatani Y
Nature genetics · 2020 · PMID 32514122
12 pages+
Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction
Miyazawa K,
Ito K,
Ito M,
Zou Z,
Kubota M,
Nomura S,
Matsunaga H,
Koyama S,
Ieki H,
Akiyama M,
Koike Y,
Kurosawa R
and 14 more — show all
Yoshida H,
Ozaki K,
Onouchi Y,
Takahashi A,
Matsuda K,
Murakami Y,
Aburatani H,
Kubo M,
Momozawa Y,
Terao C,
Oki S,
Akazawa H,
Kamatani Y,
Komuro I
BioBank Japan Project
Nature genetics · 2023 · PMID 36653681 · open access
12 pages+
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population
Enzan N,
Miyazawa K,
Koyama S,
Kurosawa R,
Ieki H,
Yoshida H,
Takechi F,
Fukuyama M,
Osako R,
Tomizuka K,
Liu X,
Ozaki K
and 18 more — show all
Onouchi Y,
Matsuda K,
Momozawa Y,
Aburatani H,
Kamatani Y,
Yamaguchi T,
Akazawa H,
Node K,
Ellinor PT,
Levin MG,
Damrauer SM,
Voight BF,
Joseph J,
Sun YV,
Terao C,
Ninomiya T,
Komuro I,
Ito K
BioBank Japan Project
Nature communications · 2025 · PMID 41184235 · open access
12 pages+
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population
Low SK,
Takahashi A,
Ebana Y,
Ozaki K,
Christophersen IE,
Ellinor PT,
Ogishima S,
Yamamoto M,
Satoh M,
Sasaki M,
Yamaji T,
Iwasaki M
and 10 more — show all
AFGen Consortium
Nature genetics · 2017 · PMID 28416822
5 pages
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor PT,
Lunetta KL,
Albert CM,
Glazer NL,
Ritchie MD,
Smith AV,
Arking DE,
Müller-Nurasyid M,
Krijthe BP,
Lubitz SA,
Bis JC,
Chung MK
and 77 more — show all
Dörr M,
Ozaki K,
Roberts JD,
Smith JG,
Pfeufer A,
Sinner MF,
Lohman K,
Ding J,
Smith NL,
Smith JD,
Rienstra M,
Rice KM,
Van Wagoner DR,
Magnani JW,
Wakili R,
Clauss S,
Rotter JI,
Steinbeck G,
Launer LJ,
Davies RW,
Borkovich M,
Harris TB,
Lin H,
Völker U,
Völzke H,
Milan DJ,
Hofman A,
Boerwinkle E,
Chen LY,
Soliman EZ,
Voight BF,
Li G,
Chakravarti A,
Kubo M,
Tedrow UB,
Rose LM,
Ridker PM,
Conen D,
Tsunoda T,
Furukawa T,
Sotoodehnia N,
Xu S,
Kamatani N,
Levy D,
Nakamura Y,
Parvez B,
Mahida S,
Furie KL,
Rosand J,
Muhammad R,
Psaty BM,
Meitinger T,
Perz S,
Wichmann HE,
Witteman JC,
Kao WH,
Kathiresan S,
Roden DM,
Uitterlinden AG,
Rivadeneira F,
McKnight B,
Sjögren M,
Newman AB,
Liu Y,
Gollob MH,
Melander O,
Tanaka T,
Stricker BH,
Felix SB,
Alonso A,
Darbar D,
Barnard J,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Gudnason V,
Kääb S
Nature genetics · 2012 · PMID 22544366
3 pages
Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population
Matsukura M,
Ozaki K,
Takahashi A,
Onouchi Y,
Morizono T,
Komai H,
Shigematsu H,
Kudo T,
Inoue Y,
Kimura H,
Hosaka A,
Shigematsu K
and 5 more — show all
PloS one · 2015 · PMID 26488411 · open access
2 pages
Association of an IGHV3-66 gene variant with Kawasaki disease
Johnson TA,
Mashimo Y,
Wu JY,
Yoon D,
Hata A,
Kubo M,
Takahashi A,
Tsunoda T,
Ozaki K,
Tanaka T,
Ito K,
Suzuki H
and 18 more — show all
Hamada H,
Kobayashi T,
Hara T,
Chen CH,
Lee YC,
Liu YM,
Chang LC,
Chang CP,
Hong YM,
Jang GY,
Yun SW,
Yu JJ,
Lee KY,
Kim JJ,
Park T,
Lee JK,
Chen YT,
Onouchi Y
Korean Kawasaki Disease Genetics Consortium, Taiwan Kawasaki Disease Genetics Consortium, Taiwan Pediatric ID Alliance, Japan Kawasaki Disease Genome Consortium
Journal of human genetics · 2021 · PMID 33106546 · 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.