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.
16 matches for
Hosono N.
A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci
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 20189936
5 pages
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population
Okada Y,
Hirota T,
Kamatani Y,
Takahashi A,
Ohmiya H,
Kumasaka N,
Higasa K,
Yamaguchi-Kabata Y,
Hosono N,
Nalls MA,
Chen MH,
van Rooij FJ
and 19 more — show all
Smith AV,
Tanaka T,
Couper DJ,
Zakai NA,
Ferrucci L,
Longo DL,
Hernandez DG,
Witteman JC,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Tamari M,
Yamamoto K,
Kamatani N
PLoS genetics · 2011 · PMID 21738478 · open access
5 pages
A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population
Yamazaki K,
Umeno J,
Takahashi A,
Hirano A,
Johnson TA,
Kumasaka N,
Morizono T,
Hosono N,
Kawaguchi T,
Takazoe M,
Yamada T,
Suzuki Y
and 12 more — show all
Tanaka H,
Motoya S,
Hosokawa M,
Arimura Y,
Shinomura Y,
Matsui T,
Matsumoto T,
Iida M,
Tsunoda T,
Nakamura Y,
Kamatani N,
Kubo M
Gastroenterology · 2013 · PMID 23266558
4 pages
Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population
Takata R,
Akamatsu S,
Kubo M,
Takahashi A,
Hosono N,
Kawaguchi T,
Tsunoda T,
Inazawa J,
Kamatani N,
Ogawa O,
Fujioka T,
Nakamura Y
and 1 more — show all
Nature genetics · 2010 · PMID 20676098
2 pages
A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population
Mbarek H,
Ochi H,
Urabe Y,
Kumar V,
Kubo M,
Hosono N,
Takahashi A,
Kamatani Y,
Miki D,
Abe H,
Tsunoda T,
Kamatani N
and 3 more — show all
Human molecular genetics · 2011 · PMID 21750111
2 pages
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations
Okada Y,
Kubo M,
Ohmiya H,
Takahashi A,
Kumasaka N,
Hosono N,
Maeda S,
Wen W,
Dorajoo R,
Go MJ,
Zheng W,
Zheng W
and 8 more — show all
GIANT consortium
Nature genetics · 2012 · PMID 22344221
2 pages
Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3
Miyake A,
Kou I,
Takahashi Y,
Johnson TA,
Ogura Y,
Dai J,
Qiu X,
Takahashi A,
Jiang H,
Yan H,
Kono K,
Kawakami N
and 19 more — show all
Uno K,
Ito M,
Minami S,
Yanagida H,
Taneichi H,
Hosono N,
Tsuji T,
Suzuki T,
Sudo H,
Kotani T,
Yonezawa I,
Kubo M,
Tsunoda T,
Watanabe K,
Chiba K,
Toyama Y,
Qiu Y,
Matsumoto M,
Ikegawa S
PloS one · 2013 · PMID 24023777 · open access
2 pages
A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population
Asano K,
Matsushita T,
Umeno J,
Hosono N,
Takahashi A,
Kawaguchi T,
Matsumoto T,
Matsui T,
Kakuta Y,
Kinouchi Y,
Shimosegawa T,
Hosokawa M
and 8 more — show all
Nature genetics · 2009 · PMID 19915573
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
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations
Miki D,
Kubo M,
Takahashi A,
Yoon KA,
Kim J,
Lee GK,
Zo JI,
Lee JS,
Hosono N,
Morizono T,
Tsunoda T,
Kamatani N
and 5 more — show all
Nature genetics · 2010 · PMID 20871597
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
A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese
Kiyotani K,
Mushiroda T,
Tsunoda T,
Morizono T,
Hosono N,
Kubo M,
Tanigawara Y,
Imamura CK,
Flockhart DA,
Aki F,
Hirata K,
Takatsuka Y
and 6 more — show all
Human molecular genetics · 2012 · PMID 22180457
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
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.