Yo Niida

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 23

Top Topics

Dna Methylation

Polycystic Kidney Disease

Top Venues

International journal of molecular sciences

American journal of medical genetics. Part A

Human genome variation

This page only lists publications with an associated author ORCID identifier.

Publications

Marin Ishikawa, Kohei Nakamura, Ryutaro Kawano, Hideyuki Hayashi, Tatsuru Ikeda, Makoto Saito, Yo Niida, Jiichiro Sasaki, Hiroyuki Okuda, Satoshi Ishihara, Masatoshi Yamaguchi, Hideaki Shimada, Takeshi Isobe, Yuki Yuza, Akinobu Yoshimura, Hajime Kuroda, Seigo Yukisawa, Takuya Aoki, Kei Takeshita, Shinichi Ueno, Junichi Nakazawa, Yu Sunakawa, Sachio Nohara, Chihiro Okada, Ko Nishimiya, Shigeki Tanishima, Hiroshi Nishihara
Clinical and Diagnostic Utility of Genomic Profiling for Digestive Cancers: Real-World Evidence from Japan. Cancers 16 (8) (2024)
Sumihito Togi, Hiroki Ura, Yo Niida
Qualitative and quantitative analysis of MED12 c.887G>A causing both missense and splicing variants in X-linked Ohdo syndrome. American journal of medical genetics. Part A 194 (9) (2024)
Hiroki Ura, Yo Niida
Comparison of RNA-Sequencing Methods for Degraded RNA. International journal of molecular sciences 25 (11) (2024)
Sumihito Togi, Hiroki Ura, Yo Niida
Qualitative and quantitative analysis of MED12 c.887G>A causing both missense and splicing variants in X-linked Ohdo syndrome. American journal of medical genetics. Part A (2024)
Yo Niida, Wataru Fujita, Sumihito Togi, Hiroki Ura
Investigation of a novel PROS1 splicing variant in a patient with protein S deficiency. Human genome variation 11 (1) (2024)
Sumihito Togi, Hiroki Ura, Yo Niida
Qualitative and quantitative analysis of MED12 c.887G>A causing both missense and splicing variants in X-linked Ohdo syndrome. American journal of medical genetics. Part A 194 (9) (2024)
Hiroki Ura, Yo Niida
Comparison of RNA-Sequencing Methods for Degraded RNA. International journal of molecular sciences 25 (11) (2024)
Marin Ishikawa, Kohei Nakamura, Ryutaro Kawano, Hideyuki Hayashi, Tatsuru Ikeda, Makoto Saito, Yo Niida, Jiichiro Sasaki, Hiroyuki Okuda, Satoshi Ishihara, Masatoshi Yamaguchi, Hideaki Shimada, Takeshi Isobe, Yuki Yuza, Akinobu Yoshimura, Hajime Kuroda, Seigo Yukisawa, Takuya Aoki, Kei Takeshita, Shinichi Ueno, Junichi Nakazawa, Yu Sunakawa, Sachio Nohara, Chihiro Okada, Ko Nishimiya, Shigeki Tanishima, Hiroshi Nishihara
Clinical and Diagnostic Utility of Genomic Profiling for Digestive Cancers: Real-World Evidence from Japan. Cancers 16 (8) (2024)
Sumihito Togi, Hiroki Ura, Yo Niida
Qualitative and quantitative analysis of MED12 c.887G>A causing both missense and splicing variants in X-linked Ohdo syndrome. American journal of medical genetics. Part A 194 (9) (2024)
Yo Niida, Wataru Fujita, Sumihito Togi, Hiroki Ura
Investigation of a novel PROS1 splicing variant in a patient with protein S deficiency. Human genome variation 11 (1) (2024)
Yo Niida, Wataru Fujita, Sumihito Togi, Hiroki Ura
Investigation of a novel PROS1 splicing variant in a patient with protein S deficiency. Human genome variation 11 (1) (2024)
Fumie Nomura, Akira Shimizu, Sumihito Togi, Hiroki Ura, Yo Niida
SNP Array Screening and Long Range PCR-Based Targeted Next Generation Sequencing for Autosomal Recessive Disease with Consanguinity: Insight from a Case of Xeroderma Pigmentosum Group C. Genes 14 (11) (2023)
Terutsugu Koya, Kenichi Yoshida, Misa Togi, Yo Niida, Sumihito Togi, Hiroki Ura, Shuichi Mizuta, Tomohisa Kato, Sohsuke Yamada, Takeo Shibata, Yi-Chang Liu, Shyng-Shiou F Yuan, Deng-Chyang Wu, Hirohito Kobayashi, Taiju Utsugisawa, Hitoshi Kanno, Shigetaka Shimodaira
Clinical Trial on the Safety and Tolerability of Personalized Cancer Vaccines Using Human Platelet Lysate-Induced Antigen-Presenting Cells. Cancers 15 (14) (2023)
Yo Niida, Azusa Kobayashi, Sumihito Togi, Hiroki Ura
Recessive dystrophic epidermolysis bullosa caused by a novel COL7A1 variant with isodisomy. Human genome variation 10 (1) (2023)
Terutsugu Koya, Yo Niida, Misa Togi, Kenichi Yoshida, Takuya Sakamoto, Hiroki Ura, Sumihito Togi, Tomohisa Kato, Sohsuke Yamada, Haruo Sugiyama, Shigeo Koido, Shigetaka Shimodaira
The Detection of Immunity against WT1 and SMAD4 P130L of EpCAM + Cancer Cells in Malignant Pleural Effusion. International journal of molecular sciences 23 (20) (2022)
Sumihito Togi, Hiroki Ura, Hisayo Hatanaka, Yo Niida
Genotype and Phenotype Landscape of 283 Japanese Patients with Tuberous Sclerosis Complex. International journal of molecular sciences 23 (19) (2022)
Seiko Miura, Yo Niida, Chieko Hashizume, Ai Fujii, Yuta Takagaki, Kahoru Kusama, Sumiyo Akazawa, Tetsuya Minami, Tsuyoshi Mukai, Kengo Furuichi, Mutsumi Tsuchishima, Nobuhiko Ueda, Hiroyuki Takamura, Daisuke Koya, Tohru Ito
Novel PKD2 Missense Mutation p.Ile424Ser in an Individual with Multiple Hepatic Cysts: A Case Report. Medicines (Basel, Switzerland) 9 (4) (2022)
Hajime Kato, Anenya J Ansh, Ethan R Lester, Yuka Kinoshita, Naoko Hidaka, Yoshitomo Hoshino, Minae Koga, Yuki Taniguchi, Taisuke Uchida, Hideki Yamaguchi, Yo Niida, Masamitsu Nakazato, Masaomi Nangaku, Noriko Makita, Toshinari Takamura, Taku Saito, Demetrios T Braddock, Nobuaki Ito
Identification of ENPP1 Haploinsufficiency in Patients With Diffuse Idiopathic Skeletal Hyperostosis and Early-Onset Osteoporosis. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 37 (6) (2022)
Hiroki Ura, Sumihito Togi, Yo Niida
Targeted Double-Stranded cDNA Sequencing-Based Phase Analysis to Identify Compound Heterozygous Mutations and Differential Allelic Expression. Biology 10 (4) (2021)
Yo Niida, Sumihito Togi, Hiroki Ura
Molecular Bases of Human Malformation Syndromes Involving the SHH Pathway: GLIA/R Balance and Cardinal Phenotypes. International journal of molecular sciences 22 (23) (2021)
Hiroki Ura, Sumihito Togi, Yo Niida
Target-capture full-length double-strand cDNA sequencing for alternative splicing analysis. RNA biology 18 (11) (2021)
Sumihito Togi, Hiroki Ura, Yo Niida
Application of Combined Long Amplicon Sequencing (CoLAS) for Genetic Analysis of Neurofibromatosis Type 1: A Pilot Study. Current issues in molecular biology 43 (2) (2021)
Hiroki Ura, Sumihito Togi, Yo Niida
Dual Deep Sequencing Improves the Accuracy of Low-Frequency Somatic Mutation Detection in Cancer Gene Panel Testing. International journal of molecular sciences 21 (10) (2020)