Toda T - Search Results

1

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: toda t. 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.

2

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.

Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T. Satake W, et al. Among authors: toda t. Nat Genet. 2009 Dec;41(12):1303-7. doi: 10.1038/ng.485. Epub 2009 Nov 15. Nat Genet. 2009. PMID: 19915576

3

[Personal genome research and neurological diseases: overview].

Toda T. Toda T. Brain Nerve. 2013 Mar;65(3):227-34. Brain Nerve. 2013. PMID: 23475514 Review. Japanese.

4

Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes.

Shigemizu D, Aiba T, Nakagawa H, Ozaki K, Miya F, Satake W, Toda T, Miyamoto Y, Fujimoto A, Suzuki Y, Kubo M, Tsunoda T, Shimizu W, Tanaka T. Shigemizu D, et al. Among authors: toda t. PLoS One. 2015 Jul 1;10(7):e0130329. doi: 10.1371/journal.pone.0130329. eCollection 2015. PLoS One. 2015. PMID: 26132555 Free PMC article.

5

Wide distribution of alpha-synuclein oligomers in multiple system atrophy brain detected by proximity ligation.

Sekiya H, Kowa H, Koga H, Takata M, Satake W, Futamura N, Funakawa I, Jinnai K, Takahashi M, Kondo T, Ueno Y, Kanagawa M, Kobayashi K, Toda T. Sekiya H, et al. Among authors: toda t. Acta Neuropathol. 2019 Mar;137(3):455-466. doi: 10.1007/s00401-019-01961-w. Epub 2019 Feb 5. Acta Neuropathol. 2019. PMID: 30721406

6

Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients.

Cha PC, Satake W, Ando-Kanagawa Y, Yamamoto K, Murata M, Toda T. Cha PC, et al. Among authors: toda t. J Hum Genet. 2020 Aug;65(8):693-704. doi: 10.1038/s10038-020-0760-8. Epub 2020 May 1. J Hum Genet. 2020. PMID: 32355309 Free PMC article.

7

Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population.

Naruse H, Ishiura H, Mitsui J, Takahashi Y, Matsukawa T, Yoshimura J, Doi K, Morishita S, Goto J, Toda T, Tsuji S. Naruse H, et al. Among authors: toda t. J Hum Genet. 2021 Mar;66(3):237-241. doi: 10.1038/s10038-020-00830-9. Epub 2020 Sep 12. J Hum Genet. 2021. PMID: 32920598

8

A deep learning method for HLA imputation and trans-ethnic MHC fine-mapping of type 1 diabetes.

Naito T, Suzuki K, Hirata J, Kamatani Y, Matsuda K, Toda T, Okada Y. Naito T, et al. Among authors: toda t. Nat Commun. 2021 Mar 12;12(1):1639. doi: 10.1038/s41467-021-21975-x. Nat Commun. 2021. PMID: 33712626 Free PMC article.

9

A linkage study with DNA markers (D4S95, D4S115, and D4S111) in Japanese Huntington disease families.

Watanabe M, Kondo I, Nissato S, Wakisaka A, Toda T, Ikeda J, Wasmuth JJ, Gusella JF, Kanazawa I. Watanabe M, et al. Among authors: toda t. Jpn J Hum Genet. 1993 Jun;38(2):193-201. doi: 10.1007/BF01883710. Jpn J Hum Genet. 1993. PMID: 8102909

10

Genetic variations on the Y chromosome in the Japanese population and implications for modern human Y chromosome lineage.

Shinka T, Tomita K, Toda T, Kotliarova SE, Lee J, Kuroki Y, Jin DK, Tokunaga K, Nakamura H, Nakahori Y. Shinka T, et al. Among authors: toda t. J Hum Genet. 1999;44(4):240-5. doi: 10.1007/s100380050151. J Hum Genet. 1999. PMID: 10429363

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