Asanomi Y - Search Results

1

Whole-genome sequencing reveals novel ethnicity-specific rare variants associated with Alzheimer's disease.

Shigemizu D, Asanomi Y, Akiyama S, Mitsumori R, Niida S, Ozaki K. Shigemizu D, et al. Among authors: asanomi y. Mol Psychiatry. 2022 May;27(5):2554-2562. doi: 10.1038/s41380-022-01483-0. Epub 2022 Mar 10. Mol Psychiatry. 2022. PMID: 35264725 Free PMC article.

2

Risk prediction models for dementia constructed by supervised principal component analysis using miRNA expression data.

Shigemizu D, Akiyama S, Asanomi Y, Boroevich KA, Sharma A, Tsunoda T, Matsukuma K, Ichikawa M, Sudo H, Takizawa S, Sakurai T, Ozaki K, Ochiya T, Niida S. Shigemizu D, et al. Among authors: asanomi y. Commun Biol. 2019 Feb 25;2:77. doi: 10.1038/s42003-019-0324-7. eCollection 2019. Commun Biol. 2019. PMID: 30820472 Free PMC article.

3

A rare functional variant of SHARPIN attenuates the inflammatory response and associates with increased risk of late-onset Alzheimer's disease.

Asanomi Y, Shigemizu D, Miyashita A, Mitsumori R, Mori T, Hara N, Ito K, Niida S, Ikeuchi T, Ozaki K. Asanomi Y, et al. Mol Med. 2019 Jun 20;25(1):20. doi: 10.1186/s10020-019-0090-5. Mol Med. 2019. PMID: 31216982 Free PMC article.

4

A comparison of machine learning classifiers for dementia with Lewy bodies using miRNA expression data.

Shigemizu D, Akiyama S, Asanomi Y, Boroevich KA, Sharma A, Tsunoda T, Sakurai T, Ozaki K, Ochiya T, Niida S. Shigemizu D, et al. Among authors: asanomi y. BMC Med Genomics. 2019 Oct 30;12(1):150. doi: 10.1186/s12920-019-0607-3. BMC Med Genomics. 2019. PMID: 31666070 Free PMC article.

5

Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk.

Shigemizu D, Mitsumori R, Akiyama S, Miyashita A, Morizono T, Higaki S, Asanomi Y, Hara N, Tamiya G, Kinoshita K, Ikeuchi T, Niida S, Ozaki K. Shigemizu D, et al. Among authors: asanomi y. Transl Psychiatry. 2021 Mar 3;11(1):151. doi: 10.1038/s41398-021-01272-3. Transl Psychiatry. 2021. PMID: 33654092 Free PMC article.

6

Dementia subtype prediction models constructed by penalized regression methods for multiclass classification using serum microRNA expression data.

Asanomi Y, Shigemizu D, Akiyama S, Sakurai T, Ozaki K, Ochiya T, Niida S. Asanomi Y, et al. Sci Rep. 2021 Oct 22;11(1):20947. doi: 10.1038/s41598-021-00424-1. Sci Rep. 2021. PMID: 34686734 Free PMC article.

7

A functional variant of SHARPIN confers increased risk of late-onset Alzheimer's disease.

Asanomi Y, Shigemizu D, Akiyama S, Miyashita A, Mitsumori R, Hara N, Ikeuchi T, Niida S, Ozaki K. Asanomi Y, et al. J Hum Genet. 2022 Apr;67(4):203-208. doi: 10.1038/s10038-021-00987-x. Epub 2021 Nov 5. J Hum Genet. 2022. PMID: 34737388 Free PMC article.

8

Network-based meta-analysis and the candidate gene association studies reveal novel ethnicity-specific variants in MFSD3 and MRPL43 associated with dementia with Lewy bodies.

Shigemizu D, Asanomi Y, Akiyama S, Higaki S, Sakurai T, Ito K, Niida S, Ozaki K. Shigemizu D, et al. Among authors: asanomi y. Am J Med Genet B Neuropsychiatr Genet. 2022 Jul;189(5):139-150. doi: 10.1002/ajmg.b.32908. Epub 2022 Jun 28. Am J Med Genet B Neuropsychiatr Genet. 2022. PMID: 35765761 Free PMC article.

9

Early-onset Alzheimer Disease Associated With Neuromyelitis Optica Spectrum Disorder.

Fujisawa C, Saji N, Takeda A, Kato T, Nakamura A, Sakurai K, Asanomi Y, Ozaki K, Takada K, Umegaki H, Kuzuya M, Sakurai T. Fujisawa C, et al. Among authors: asanomi y. Alzheimer Dis Assoc Disord. 2023 Jan-Mar 01;37(1):85-87. doi: 10.1097/WAD.0000000000000517. Epub 2022 Jul 18. Alzheimer Dis Assoc Disord. 2023. PMID: 35838179

10

CRISPR/Cas9-mediated knock-in cells of the late-onset Alzheimer's disease-risk variant, SHARPIN G186R, reveal reduced NF-κB pathway and accelerated Aβ secretion.

Asanomi Y, Kimura T, Shimoda N, Shigemizu D, Niida S, Ozaki K. Asanomi Y, et al. J Hum Genet. 2024 May;69(5):171-176. doi: 10.1038/s10038-024-01224-x. Epub 2024 Feb 13. J Hum Genet. 2024. PMID: 38351238 Free PMC article. No abstract available.

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