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83 matches for
To K,
showing the first 20.
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
Hartiala JA,
Han Y,
Jia Q,
Hilser JR,
Huang P,
Gukasyan J,
Schwartzman WS,
Cai Z,
Biswas S,
Trégouët DA,
Smith NL,
Seldin M
and 47 more — show all
Pan C,
Mehrabian M,
Lusis AJ,
Bazeley P,
Sun YV,
Liu C,
Quyyumi AA,
Scholz M,
Thiery J,
Delgado GE,
Kleber ME,
März W,
Howe LJ,
Asselbergs FW,
van Vugt M,
Vlachojannis GJ,
Patel RS,
Lyytikäinen LP,
Kähönen M,
Lehtimäki T,
Nieminen TVM,
Kuukasjärvi P,
Laurikka JO,
Chang X,
Heng CK,
Jiang R,
Kraus WE,
Hauser ER,
Ferguson JF,
Reilly MP,
Ito K,
Koyama S,
Kamatani Y,
Komuro I,
Stolze LK,
Romanoski CE,
Khan MD,
Turner AW,
Miller CL,
Aherrahrou R,
Civelek M,
Ma L,
Björkegren JLM,
Kumar SR,
Tang WHW,
Hazen SL,
Allayee H
INVENT Consortium · CHARGE Consortium Hemostasis Working Group and 2 more consortia
European heart journal · 2021 · PMID 33532862
2 pages
Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease
Hoggart C,
Shimizu C,
Galassini R,
Wright VJ,
Shailes H,
Bellos E,
Herberg JA,
Pollard AJ,
O'Connor D,
Choi SW,
Seaby EG,
Menikou S
and 12 more — show all
Hibberd M,
Sallah N,
Burgner D,
Brogan P,
Patel H,
Kim J,
Tremoulet AH,
Salo E,
van Stijn D,
Kuijpers T,
Burns JC,
Levin M
International Kawasaki Disease Genetics Consortium · UK Kawasaki Disease Genetics Consortium and 1 more consortia
European journal of human genetics : EJHG · 2021 · PMID 33772158 · open access
2 pages
Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population
Flanagan J,
Liu X,
Ortega-Reyes D,
Tomizuka K,
Matoba N,
Akiyama M,
Koido M,
Ishigaki K,
Ashikawa K,
Takata S,
Shi M,
Aoi T
and 8 more — show all
Biobank Japan Project
Communications biology · 2024 · PMID 39702642 · open access
2 pages
A cross-population compendium of gene-environment interactions
Namba S,
Sonehara K,
Koyanagi YN,
Kikuchi T,
Ojima T,
Edahiro R,
Sato G,
Yamaji T,
Tomofuji Y,
Ueda H,
Yamamoto K,
Ogawa Y
and 26 more — show all
Suzuki K,
Kanai A,
Higashiue S,
Kobayashi S,
Yamaguchi H,
Nagata Y,
Okazaki Y,
Matsumoto N,
Motomura K,
Koga H,
Hishida A,
Ikezaki H,
Hara M,
Nagayoshi M,
Oze I,
Nakano S,
Oda Y,
Suzuki Y,
Iwasaki M,
Sawada N,
Matsuo K,
Morisaki T,
Yamauchi T,
Kadowaki T,
Matsuda K,
Okada Y
BioBank Japan Project
Nature · 2026 · PMID 41606330 · open access
2 pages
Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population
Takeuchi F,
Serizawa M,
Yamamoto K,
Fujisawa T,
Nakashima E,
Ohnaka K,
Ikegami H,
Sugiyama T,
Katsuya T,
Miyagishi M,
Nakashima N,
Nawata H
and 4 more — show all
Diabetes · 2009 · PMID 19401414 · open access
1 page
Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count
Okada Y,
Kamatani Y,
Takahashi A,
Matsuda K,
Hosono N,
Ohmiya H,
Daigo Y,
Yamamoto K,
Kubo M,
Nakamura Y,
Kamatani N
Human molecular genetics · 2010 · PMID 20172861
1 page
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus
Okada Y,
Takahashi A,
Ohmiya H,
Kumasaka N,
Kamatani Y,
Hosono N,
Tsunoda T,
Matsuda K,
Tanaka T,
Kubo M,
Nakamura Y,
Yamamoto K
and 1 more — show all
Human molecular genetics · 2011 · PMID 21196492
1 page
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population
Terao C,
Yamada R,
Ohmura K,
Takahashi M,
Kawaguchi T,
Kochi Y,
Okada Y,
Nakamura Y,
Yamamoto K,
Melchers I,
Lathrop M,
Mimori T
and 1 more — show all
Human Disease Genomics Working Group · RA Clinical and Genetic Study Consortium
Human molecular genetics · 2011 · PMID 21505073
1 page
HLA-Cw*1202-B*5201-DRB1*1502 haplotype increases risk for ulcerative colitis but reduces risk for Crohn's disease
Okada Y,
Yamazaki K,
Umeno J,
Takahashi A,
Kumasaka N,
Ashikawa K,
Aoi T,
Takazoe M,
Matsui T,
Hirano A,
Matsumoto T,
Kamatani N
and 3 more — show all
Gastroenterology · 2011 · PMID 21699788
1 page
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
Cho YS,
Chen CH,
Hu C,
Long J,
Ong RT,
Sim X,
Takeuchi F,
Wu Y,
Go MJ,
Yamauchi T,
Chang YC,
Kwak SH
and 56 more — show all
Ma RC,
Yamamoto K,
Adair LS,
Aung T,
Cai Q,
Chang LC,
Chen YT,
Gao Y,
Hu FB,
Kim HL,
Kim S,
Kim YJ,
Lee JJ,
Lee NR,
Li Y,
Liu JJ,
Lu W,
Nakamura J,
Nakashima E,
Ng DP,
Tay WT,
Tsai FJ,
Wong TY,
Yokota M,
Zheng W,
Zheng W,
Zhang R,
Wang C,
So WY,
Ohnaka K,
Ikegami H,
Hara K,
Cho YM,
Cho NH,
Chang TJ,
Bao Y,
Hedman ÅK,
Morris AP,
McCarthy MI,
Takayanagi R,
Park KS,
Jia W,
Chuang LM,
Chuang LM,
Chan JC,
Maeda S,
Kadowaki T,
Lee JY,
Wu JY,
Teo YY,
Tai ES,
Shu XO,
Mohlke KL,
Kato N,
Han BG,
Seielstad M
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
1 page
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
Common variants at 1p36 are associated with superior frontal gyrus volume
Hashimoto R,
Ikeda M,
Yamashita F,
Ohi K,
Yamamori H,
Yasuda Y,
Fujimoto M,
Fukunaga M,
Nemoto K,
Takahashi T,
Tochigi M,
Onitsuka T
and 8 more — show all
Translational psychiatry · 2014 · PMID 25335168 · open access
1 page
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Wen W,
Kato N,
Hwang JY,
Guo X,
Tabara Y,
Li H,
Dorajoo R,
Yang X,
Tsai FJ,
Li S,
Wu Y,
Wu T
and 64 more — show all
Kim S,
Guo X,
Liang J,
Shungin D,
Adair LS,
Akiyama K,
Allison M,
Cai Q,
Chang LC,
Chen CH,
Chen YT,
Cho YS,
Choi BY,
Gao Y,
Go MJ,
Gu D,
Han BG,
He M,
Hixson JE,
Hu Y,
Huang T,
Isono M,
Jung KJ,
Kang D,
Kim YJ,
Kita Y,
Lee J,
Lee NR,
Lee J,
Wang Y,
Liu JJ,
Long J,
Moon S,
Nakamura Y,
Nakatochi M,
Ohnaka K,
Rao D,
Shi J,
Sull JW,
Tan A,
Ueshima H,
Wu C,
Xiang YB,
Yamamoto K,
Yao J,
Ye X,
Yokota M,
Zhang X,
Zheng Y,
Qi L,
Rotter JI,
Jee SH,
Lin D,
Mohlke KL,
He J,
Mo Z,
Wu JY,
Tai ES,
Lin X,
Miki T,
Kim BJ,
Takeuchi F,
Zheng W,
Shu XO
Scientific reports · 2016 · PMID 26785701 · 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
Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy
Schoeler NE,
Leu C,
Balestrini S,
Mudge JM,
Steward CA,
Frankish A,
Leung MA,
Mackay M,
Scheffer I,
Williams R,
Sander JW,
Cross JH
and 1 more — show all
Epilepsia · 2018 · PMID 30009487
1 page
Genome-Wide Association Study to Identify a New Susceptibility Locus for Central Serous Chorioretinopathy in the Japanese Population
Miki A,
Sakurada Y,
Tanaka K,
Semba K,
Mitamura Y,
Yuzawa M,
Tajima A,
Nakatochi M,
Yamamoto K,
Matsuo K,
Imoto I,
Honda S
Investigative ophthalmology & visual science · 2018 · PMID 30480742
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
A Prospective Analysis of Genetic Variants Associated with Human Lifespan
Wright KM,
Rand KA,
Kermany A,
Noto K,
Curtis D,
Garrigan D,
Slinkov D,
Dorfman I,
Granka JM,
Byrnes J,
Myres N,
Ball CA
and 1 more — show all
G3 (Bethesda, Md.) · 2019 · PMID 31484785 · open access
1 page
Genetic Analysis of Ulcerative Colitis in Japanese Individuals Using Population-specific SNP Array
Okamoto D,
Kawai Y,
Kakuta Y,
Naito T,
Torisu T,
Hirano A,
Umeno J,
Fuyuno Y,
Li D,
Nakano T,
Izumiyama Y,
Ichikawa R
and 13 more — show all
Hiramoto K,
Moroi R,
Kuroha M,
Kanazawa Y,
Shiga H,
Tokunaga K,
Nakamura M,
Esaki M,
Matsumoto T,
McGovern DPB,
Nagasaki M,
Kinouchi Y,
Masamune A
Inflammatory bowel diseases · 2020 · PMID 32072174
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.