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Year Number of Results
1998 1
1999 3
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2001 1
2004 3
2005 2
2007 1
2008 4
2009 1
2010 2
2011 2
2012 3
2013 2
2014 6
2015 4
2016 3
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52 results

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Page 1
The structural origin of metabolic quantitative diversity.
Koshiba S, Motoike I, Kojima K, Hasegawa T, Shirota M, Saito T, Saigusa D, Danjoh I, Katsuoka F, Ogishima S, Kawai Y, Yamaguchi-Kabata Y, Sakurai M, Hirano S, Nakata J, Motohashi H, Hozawa A, Kuriyama S, Minegishi N, Nagasaki M, Takai-Igarashi T, Fuse N, Kiyomoto H, Sugawara J, Suzuki Y, Kure S, Yaegashi N, Tanabe O, Kinoshita K, Yasuda J, Yamamoto M. Koshiba S, et al. Among authors: yamaguchi kabata y. Sci Rep. 2016 Aug 16;6:31463. doi: 10.1038/srep31463. Sci Rep. 2016. PMID: 27528366 Free PMC article.
Trans-ethnic meta-analysis of white blood cell phenotypes.
Keller MF, Reiner AP, Okada Y, van Rooij FJ, Johnson AD, Chen MH, Smith AV, Morris AP, Tanaka T, Ferrucci L, Zonderman AB, Lettre G, Harris T, Garcia M, Bandinelli S, Qayyum R, Yanek LR, Becker DM, Becker LC, Kooperberg C, Keating B, Reis J, Tang H, Boerwinkle E, Kamatani Y, Matsuda K, Kamatani N, Nakamura Y, Kubo M, Liu S, Dehghan A, Felix JF, Hofman A, Uitterlinden AG, van Duijn CM, Franco OH, Longo DL, Singleton AB, Psaty BM, Evans MK, Cupples LA, Rotter JI, O'Donnell CJ, Takahashi A, Wilson JG, Ganesh SK, Nalls MA; CHARGE Hematology; COGENT; BioBank Japan Project (RIKEN) Working Groups. Keller MF, et al. Hum Mol Genet. 2014 Dec 20;23(25):6944-60. doi: 10.1093/hmg/ddu401. Epub 2014 Aug 5. Hum Mol Genet. 2014. PMID: 25096241 Free PMC article.
A Pilot Study for Return of Individual Pharmacogenomic Results to Population-Based Cohort Study Participants.
Ohneda K, Hiratsuka M, Kawame H, Nagami F, Suzuki Y, Suzuki K, Uruno A, Sakurai-Yageta M, Hamanaka Y, Taira M, Ogishima S, Kuriyama S, Hozawa A, Tomita H, Minegishi N, Sugawara J, Danjoh I, Nakamura T, Kobayashi T, Yamaguchi-Kabata Y, Tadaka S, Obara T, Hishimuma E, Mano N, Matsuura M, Sato Y, Nakasone M, Honkura Y, Suzuki J, Katori Y, Kakuta Y, Masamune A, Aoki Y, Nakayama M, Kure S, Kinoshita K, Fuse N, Yamamoto M. Ohneda K, et al. Among authors: yamaguchi kabata y. JMA J. 2022 Apr 15;5(2):177-189. doi: 10.31662/jmaj.2021-0156. Epub 2022 Mar 11. JMA J. 2022. PMID: 35611229 Free PMC article.
Progress Report of the Tohoku Medical Megabank Community-based Cohort Study: Study Profile of the Repeated Center-based Survey During Second Period in Miyagi Prefecture.
Hozawa A, Nakaya K, Nakaya N, Nakamura T, Kogure M, Hatanaka R, Chiba I, Kanno I, Sugawara J, Kodama E, Hamanaka Y, Kobayashi T, Uruno A, Tsuchiya N, Hirata T, Narita A, Tsuboi A, Tamahara T, Otsuki A, Goto M, Taira M, Shimizu R, Suzuki K, Obara T, Kikuya M, Metoki H, Ishikuro M, Danjoh I, Ogishima S, Nagaie S, Minegishi N, Hiratsuka M, Kumada K, Nishijima I, Nobukuni T, Yamaguchi-Kabata Y, Nagami F, Kure S, Fuse N, Kinoshita K, Izumi Y, Kuriyama S, Yamamoto M. Hozawa A, et al. Among authors: yamaguchi kabata y. J Epidemiol. 2024 Sep 5;34(9):434-443. doi: 10.2188/jea.JE20230241. Epub 2024 Jul 31. J Epidemiol. 2024. PMID: 38403692 Free PMC article.
Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals.
Nagasaki M, Yasuda J, Katsuoka F, Nariai N, Kojima K, Kawai Y, Yamaguchi-Kabata Y, Yokozawa J, Danjoh I, Saito S, Sato Y, Mimori T, Tsuda K, Saito R, Pan X, Nishikawa S, Ito S, Kuroki Y, Tanabe O, Fuse N, Kuriyama S, Kiyomoto H, Hozawa A, Minegishi N, Douglas Engel J, Kinoshita K, Kure S, Yaegashi N; ToMMo Japanese Reference Panel Project; Yamamoto M. Nagasaki M, et al. Among authors: yamaguchi kabata y. Nat Commun. 2015 Aug 21;6:8018. doi: 10.1038/ncomms9018. Nat Commun. 2015. PMID: 26292667 Free PMC article.
Corticotropin-Releasing Hormone Receptor 2 Gene Variants in Irritable Bowel Syndrome.
Komuro H, Sato N, Sasaki A, Suzuki N, Kano M, Tanaka Y, Yamaguchi-Kabata Y, Kanazawa M, Warita H, Aoki M, Fukudo S. Komuro H, et al. Among authors: yamaguchi kabata y. PLoS One. 2016 Jan 25;11(1):e0147817. doi: 10.1371/journal.pone.0147817. eCollection 2016. PLoS One. 2016. PMID: 26808377 Free PMC article.
Pathological variants in genes associated with disorders of sex development and central causes of hypogonadism in a whole-genome reference panel of 8380 Japanese individuals.
Shiga N, Yamaguchi-Kabata Y, Igeta S, Yasuda J, Tadaka S, Minato T, Watanabe Z, Kanno J, Tamiya G, Fuse N, Kinoshita K, Kure S, Kondo A, Tachibana M, Yamamoto M, Yaegashi N, Sugawara J. Shiga N, et al. Among authors: yamaguchi kabata y. Hum Genome Var. 2022 Sep 28;9(1):34. doi: 10.1038/s41439-022-00213-w. Hum Genome Var. 2022. PMID: 36171209 Free PMC article.
52 results