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Familial acorea, microphthalmia and cataract syndrome.
Kondo H, Tahira T, Yamamoto K, Tawara A. Kondo H, et al. Among authors: yamamoto k. Br J Ophthalmol. 2013 Sep;97(9):1155-60. doi: 10.1136/bjophthalmol-2013-303165. Epub 2013 Jul 5. Br J Ophthalmol. 2013. PMID: 23832966
Submicroscopic deletions at 13q32.1 cause congenital microcoria.
Fares-Taie L, Gerber S, Tawara A, Ramirez-Miranda A, Douet JY, Verdin H, Guilloux A, Zenteno JC, Kondo H, Moisset H, Passet B, Yamamoto K, Iwai M, Tanaka T, Nakamura Y, Kimura W, Bole-Feysot C, Vilotte M, Odent S, Vilotte JL, Munnich A, Regnier A, Chassaing N, De Baere E, Raymond-Letron I, Kaplan J, Calvas P, Roche O, Rozet JM. Fares-Taie L, et al. Among authors: yamamoto k. Am J Hum Genet. 2015 Apr 2;96(4):631-9. doi: 10.1016/j.ajhg.2015.01.014. Epub 2015 Mar 12. Am J Hum Genet. 2015. PMID: 25772937 Free PMC article.
Japanese genome-wide association study identifies a significant colorectal cancer susceptibility locus at chromosome 10p14.
Takahashi Y, Sugimachi K, Yamamoto K, Niida A, Shimamura T, Sato T, Watanabe M, Tanaka J, Kudo S, Sugihara K, Hase K, Kusunoki M, Yamada K, Shimada Y, Moriya Y, Suzuki Y, Miyano S, Mori M, Mimori K. Takahashi Y, et al. Among authors: yamamoto k. Cancer Sci. 2017 Nov;108(11):2239-2247. doi: 10.1111/cas.13391. Epub 2017 Sep 26. Cancer Sci. 2017. PMID: 28869801 Free PMC article.
Genome-wide linkage analysis of type 2 diabetes mellitus reconfirms the susceptibility locus on 11p13-p12 in Japanese.
Nawata H, Shirasawa S, Nakashima N, Araki E, Hashiguchi J, Miyake S, Yamauchi T, Hamaguchi K, Yoshimatsu H, Takeda H, Fukushima H, Sasahara T, Yamaguchi K, Sonoda N, Sonoda T, Matsumoto M, Tanaka Y, Sugimoto H, Tsubouchi H, Inoguchi T, Yanase T, Wake N, Narazaki K, Eto T, Umeda F, Nakazaki M, Ono J, Asano T, Ito Y, Akazawa S, Hazegawa I, Takasu N, Shinohara M, Nishikawa T, Nagafuchi S, Okeda T, Eguchi K, Iwase M, Ishikawa M, Aoki M, Keicho N, Kato N, Yasuda K, Yamamoto K, Sasazuki T. Nawata H, et al. Among authors: yamamoto k. J Hum Genet. 2004;49(11):629-634. doi: 10.1007/s10038-004-0199-3. Epub 2004 Oct 14. J Hum Genet. 2004. PMID: 15490285
A novel missense mutation of RYR1 in familial idiopathic hyper CK-emia.
Sano K, Miura S, Fujiwara T, Fujioka R, Yorita A, Noda K, Kida H, Azuma K, Kaieda S, Yamamoto K, Taniwaki T, Fukumaki Y, Shibata H. Sano K, et al. Among authors: yamamoto k. J Neurol Sci. 2015 Sep 15;356(1-2):142-7. doi: 10.1016/j.jns.2015.06.035. Epub 2015 Jun 19. J Neurol Sci. 2015. PMID: 26119398
Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals.
Nakatochi M, Kanai M, Nakayama A, Hishida A, Kawamura Y, Ichihara S, Akiyama M, Ikezaki H, Furusyo N, Shimizu S, Yamamoto K, Hirata M, Okada R, Kawai S, Kawaguchi M, Nishida Y, Shimanoe C, Ibusuki R, Takezaki T, Nakajima M, Takao M, Ozaki E, Matsui D, Nishiyama T, Suzuki S, Takashima N, Kita Y, Endoh K, Kuriki K, Uemura H, Arisawa K, Oze I, Matsuo K, Nakamura Y, Mikami H, Tamura T, Nakashima H, Nakamura T, Kato N, Matsuda K, Murakami Y, Matsubara T, Naito M, Kubo M, Kamatani Y, Shinomiya N, Yokota M, Wakai K, Okada Y, Matsuo H. Nakatochi M, et al. Among authors: yamamoto k. Commun Biol. 2019 Apr 8;2:115. doi: 10.1038/s42003-019-0339-0. eCollection 2019. Commun Biol. 2019. PMID: 30993211 Free PMC article.
Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population.
Otsuka I, Akiyama M, Shirakawa O, Okazaki S, Momozawa Y, Kamatani Y, Izumi T, Numata S, Takahashi M, Boku S, Sora I, Yamamoto K, Ueno Y, Toda T, Kubo M, Hishimoto A. Otsuka I, et al. Among authors: yamamoto k. Neuropsychopharmacology. 2019 Nov;44(12):2119-2124. doi: 10.1038/s41386-019-0506-5. Epub 2019 Sep 2. Neuropsychopharmacology. 2019. PMID: 31476763 Free PMC article.
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