For researchers

Is your paper here?

2,682 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.

33 matches for Kamatani N, showing the first 13.

Meta-analysis identifies common variants associated with body mass index in east Asians

Wen W, Cho YS, Zheng W, Zheng W, Dorajoo R, Kato N, Qi L, Chen CH, Delahanty RJ, Okada Y, Tabara Y, Gu D

and 52 more — show all

Zhu D, Haiman CA, Mo Z, Gao YT, Saw SM, Go MJ, Takeuchi F, Chang LC, Kokubo Y, Liang J, Hao M, Le Marchand L, Zhang Y, Hu Y, Wong TY, Long J, Han BG, Kubo M, Yamamoto K, Su MH, Miki T, Henderson BE, Song H, Tan A, He J, Ng DP, Cai Q, Tsunoda T, Tsai FJ, Iwai N, Chen GK, Shi J, Xu J, Sim X, Xiang YB, Maeda S, Ong RT, Li C, Nakamura Y, Aung T, Kamatani N, Liu JJ, Lu W, Yokota M, Seielstad M, Fann CS, Wu JY, Lee JY, Hu FB, Tanaka T, Tai ES, Shu XO

Genetic Investigation of ANthropometric Traits (GIANT) Consortium

Nature genetics · 2012 · PMID 22344219 · open access

2 pages

rs9356744 rs261967

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

Kato N, Wu JY, Lu Q, Tsunoda T, Yamamoto K, Nakamura Y, Kamatani N, Tanaka T

GIANT consortium

Nature genetics · 2012 · PMID 22344221

2 pages

rs12149832 rs11671664

Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines for human leukocyte antigen B (HLA-B) genotype and allopurinol dosing: 2015 update

Saito Y, Stamp LK, Caudle KE, Hershfield MS, McDonagh EM, Callaghan JT, Tassaneeyakul W, Mushiroda T, Kamatani N, Goldspiel BR, Phillips EJ, Klein TE

and 1 more — show all

Lee MT

Clinical Pharmacogenetics Implementation Consortium

Clinical pharmacology and therapeutics · 2016 · PMID 26094938

2 pages

Gout Drug-Induced Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis

Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs

Hirata T, Koga K, Johnson TA, Morino R, Nakazono K, Kamitsuji S, Akita M, Kawajiri M, Kami A, Hoshi Y, Tada A, Ishikawa K

and 6 more — show all

Hine M, Kobayashi M, Kurume N, Fujii T, Kamatani N, Osuga Y

Scientific reports · 2018 · PMID 29855537 · open access

2 pages

rs10167914 rs17181171

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

Arimura Y, Shinomura Y, Kiyohara Y, Tsunoda T, Kamatani N, Iida M, Nakamura Y, Kubo M

Nature genetics · 2009 · PMID 19915573

1 page

rs9263739

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

rs2072910

A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese

Uno S, Zembutsu H, Hirasawa A, Takahashi A, Kubo M, Akahane T, Aoki D, Kamatani N, Hirata K, Nakamura Y

Nature genetics · 2010 · PMID 20601957

1 page

rs10965235

A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population

Nakashima M, Chung S, Takahashi A, Kamatani N, Kawaguchi T, Tsunoda T, Hosono N, Kubo M, Nakamura Y, Zembutsu H

Nature genetics · 2010 · PMID 20711176

1 page

rs873549

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

Chayama K, Takahashi T, Inazawa J, Nakamura Y, Daigo Y

Nature genetics · 2010 · PMID 20871597

1 page

rs2736100

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

Kamatani N

Human molecular genetics · 2011 · PMID 21196492

1 page

rs2097677

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

Nakamura Y, Yamamoto K, Kubo M

Gastroenterology · 2011 · PMID 21699788

1 page

rs2006996

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

PLoS genetics · 2012 · PMID 22291604 · open access

1 page

rs340630

Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene

Betcheva ET, Yosifova AG, Mushiroda T, Kubo M, Takahashi A, Karachanak SK, Zaharieva IT, Hadjidekova SP, Dimova II, Vazharova RV, Stoyanov DS, Milanova VK

and 5 more — show all

Tolev T, Kirov G, Kamatani N, Toncheva DI, Nakamura Y

Psychiatric genetics · 2013 · PMID 23142968

1 page

rs7527939

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.