Որոնման արդյունքները - Daichi Shigemizu
- Ցուցադրվում են 1 - 18 արդյունքները 18
-
1
-
2
-
3
-
4
-
5
Identification of potential blood biomarkers for early diagnosis of Alzheimer’s disease through RNA sequencing analysis Daichi Shigemizu, Taiki Mori, Shintaro Akiyama, Sayuri Higaki, Hiroshi Watanabe, Takashi Sakurai, Shumpei Niida, Kouichi Ozaki
Հրապարակվել է 2020Revisão -
6
Classification and deep-learning–based prediction of Alzheimer disease subtypes by using genomic data Daichi Shigemizu, Shintaro Akiyama, Mutsumi Suganuma, Motoki Furutani, Akiko Yamakawa, Yukiko Nakano, Kouichi Ozaki, Shumpei Niida
Հրապարակվել է 2023Artigo -
7
Performance comparison of four commercial human whole-exome capture platforms Daichi Shigemizu, Yukihide Momozawa, Testuo Abe, Takashi Morizono, Keith A. Boroevich, Sadaaki Takata, Kyota Ashikawa, Michiaki Kubo, Tatsuhiko Tsunoda
Հրապարակվել է 2015Artigo -
8
Chromothripsis-like chromosomal rearrangements induced by ionizing radiation using proton microbeam irradiation system Maki Morishita, Tomoki Muramatsu, Yumiko Suto, Momoki Hirai, Teruaki Konishi, Shin Hayashi, Daichi Shigemizu, Tatsuhiko Tsunoda, Keiji Moriyama, Johji Inazawa
Հրապարակվել է 2016Artigo -
9
A rare functional variant of SHARPIN attenuates the inflammatory response and associates with increased risk of late-onset Alzheimer’s disease Yuya Asanomi, Daichi Shigemizu, Akinori Miyashita, Risa Mitsumori, Taiki Mori, Norikazu Hara, Kaoru Ito, Shumpei Niida, Takeshi Ikeuchi, Kouichi Ozaki
Հրապարակվել է 2019Artigo -
10
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer Akihiro Fujimoto, Jing Hao Wong, Yukiko Yoshii, Shintaro Akiyama, Azusa Tanaka, Hitomi Yagi, Daichi Shigemizu, Hidewaki Nakagawa, Masashi Mizokami, Mihoko Shimada
Հրապարակվել է 2021Artigo -
11
A practical method to detect SNVs and indels from whole genome and exome sequencing data Daichi Shigemizu, Akihiro Fujimoto, Shintaro Akiyama, Tetsuo Abe, Kaoru Nakano, Keith A. Boroevich, Yujiro Yamamoto, Mayuko Furuta, Michiaki Kubo, Hidewaki Nakagawa, Tatsuhiko Tsunoda
Հրապարակվել է 2013Artigo -
12
Prognosis prediction model for conversion from mild cognitive impairment to Alzheimer’s disease created by integrative analysis of multi-omics data Daichi Shigemizu, Shintaro Akiyama, Sayuri Higaki, Taiki Sugimoto, Takashi Sakurai, Keith A. Boroevich, Alok Sharma, Tatsuhiko Tsunoda, Takahiro Ochiya, Shumpei Niida, Kouichi Ozaki
Հրապարակվել է 2020Revisão -
13
Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer’s disease risk Daichi Shigemizu, Risa Mitsumori, Shintaro Akiyama, Akinori Miyashita, Takashi Morizono, Sayuri Higaki, Yuya Asanomi, Norikazu Hara, Gen Tamiya, Kengo Kinoshita, Takeshi Ikeuchi, Shumpei Niida, Kouichi Ozaki
Հրապարակվել է 2021Revisão -
14
Risk prediction models for dementia constructed by supervised principal component analysis using miRNA expression data Daichi Shigemizu, Shintaro Akiyama, Yuya Asanomi, Keith A. Boroevich, Alok Sharma, Tatsuhiko Tsunoda, Kana Matsukuma, Makiko Ichikawa, Hiroko Sudo, Satoko Takizawa, Takashi Sakurai, Kouichi Ozaki, Takahiro Ochiya, Shumpei Niida
Հրապարակվել է 2019Artigo -
15
A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese Megumi Hirokawa, Hiroyuki Morita, Tomoyuki Tajima, Atsushi Takahashi, Kyota Ashikawa, Fuyuki Miya, Daichi Shigemizu, Kouichi Ozaki, Yasuhiko Sakata, Daisaku Nakatani, Shinichiro Suna, Yasushi Imai, Toshihiro Tanaka, Tatsuhiko Tsunoda, Koichi Matsuda, Takashi Kadowaki, Yusuke Nakamura, Ryozo Nagai, Issei Komuro, Michiaki Kubo
Հրապարակվել է 2014Artigo -
16
High-Risk Ovarian Cancer Based on 126-Gene Expression Signature Is Uniquely Characterized by Downregulation of Antigen Presentation Pathway Kosuke Yoshihara, Tatsuhiko Tsunoda, Daichi Shigemizu, Hiroyuki Fujiwara, Masayuki Hatae, Hisaya Fujiwara, Hideaki Masuzaki, Hidetaka Katabuchi, Yosuke Kawakami, Aikou Okamoto, Takayoshi Nogawa, Noriomi Matsumura, Yasuhiro Udagawa, Tsuyoshi Saito, Hiroaki Itamochi, Masashi Takano, Etsuko Miyagi, Tamotsu Sudo, Kimio Ushijima, Haruko Iwase, Hiroyuki Seki, Yasuhisa Terao, Takayuki Enomoto, Mikio Mikami, Kohei Akazawa, Hitoshi Tsuda, Takuya Moriya, Atsushi Tajima, Ituro Inoue, Kenichi Tanaka
Հրապարակվել է 2012Artigo -
17
Whole-genome mutational landscape of liver cancers displaying biliary phenotype reveals hepatitis impact and molecular diversity Akihiro Fujimoto, Mayuko Furuta, Yuichi Shiraishi, Kunihito Gotoh, Yoshiiku Kawakami, Koji Arihiro, Toru Nakamura, Masaki Ueno, Shun-ichi Ariizumi, Nguyễn Hải Hà, Daichi Shigemizu, Tetsuo Abe, Keith A. Boroevich, Kaoru Nakano, Aya Sasaki, Rina Kitada, Kazihiro Maejima, Yujiro Yamamoto, Hiroko Tanaka, Tetsuo Shibuya, Tatsuhiro Shibata, Hidenori Ojima, Kazuaki Shimada, Shinya Hayami, Yoshinobu Shigekawa, Hiroshi Aikata, Hideki Ohdan, Shigeru Marubashi, Terumasa Yamada, Michiaki Kubo, Satoshi Hirano, Osamu Ishikawa, Masakazu Yamamoto, Hiroki Yamaue, Kazuaki Chayama, Satoru Miyano, Tatsuhiko Tsunoda, Hidewaki Nakagawa
Հրապարակվել է 2015Artigo -
18
Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility Naomasa Makita, Nobue Yagihara, Lia Crotti, Christopher N. Johnson, Britt Maria Beckmann, Michelle S. Roh, Daichi Shigemizu, Peter Lichtner, Taisuke Ishikawa, Takeshi Aiba, Tessa Homfray, Elijah R. Behr, Didier Klug, Isabelle Denjoy, Elisa Mastantuono, Daniel Theisen, Tatsuhiko Tsunoda, Wataru Satake, Tatsushi Toda, Hidewaki Nakagawa, Yukiomi Tsuji, Takeshi Tsuchiya, Hirokazu Yamamoto, Yoshihiro Miyamoto, Naoto Endo, Akinori Kimura, Kouichi Ozaki, Hideki Motomura, Kenji Suda, Toshihiro Tanaka, Peter J. Schwartz, Thomas Meitinger, Stefan Kääb, Pascale Guicheney, Wataru Shimizu, Zahurul A. Bhuiyan, Hiroshi Watanabe, Walter Chazin, Alfred L. George
Հրապարակվել է 2014Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Gene
Genetics
Medicine
Internal medicine
Genotype
Computational biology
Disease
Single-nucleotide polymorphism
Computer science
Genome
Genome-wide association study
Mutation
Artificial intelligence
Bioinformatics
DNA
DNA sequencing
Dementia
Exome
Exome sequencing
Genetic association
Genotyping
Biochemistry
Botany
Cancer
Cancer research
Cohort
Endocrinology
Environmental health
Gene expression