Genetic variations in medical research in the past, at present and in the future

por KAMATANI, Yoichiro, NAKAMURA, Yusuke
Publicado 2021

Efficient prediction of a spatial transcriptomics profile better characterizes breast cancer tissue sections without costly experimentation

por Monjo, Taku, Koido, Masaru, Nagasawa, Satoi, Suzuki, Yutaka, Kamatani, Yoichiro
Publicado 2022

Association of Common Variants in TNFRSF13B, TNFSF13, and ANXA3 with Serum Levels of Non-Albumin Protein and Immunoglobulin Isotypes in Japanese

por Osman, Wael, Okada, Yukinori, Kamatani, Yoichiro, Kubo, Michiaki, Matsuda, Koichi, Nakamura, Yusuke
Publicado 2012

Re-evaluating classical body type theories: genetic correlation between psychiatric disorders and body mass index

por Ikeda, Masashi, Tanaka, Satoshi, Saito, Takeo, Ozaki, Norio, Kamatani, Yoichiro, Iwata, Nakao
Publicado 2018

Comprehensive evaluation of structural variation detection algorithms for whole genome sequencing

por Kosugi, Shunichi, Momozawa, Yukihide, Liu, Xiaoxi, Terao, Chikashi, Kubo, Michiaki, Kamatani, Yoichiro
Publicado 2019

A Mendelian randomization study identified obesity as a causal risk factor of uterine endometrial cancer in Japanese

por Masuda, Tatsuo, Ogawa, Kotaro, Kamatani, Yoichiro, Murakami, Yoshinori, Kimura, Tadashi, Okada, Yukinori
Publicado 2020

A genome-wide association study identifies a novel candidate locus at the DLGAP1 gene with susceptibility to resistant hypertension in the Japanese population

por Takahashi, Yasuo, Yamazaki, Keiko, Kamatani, Yoichiro, Kubo, Michiaki, Matsuda, Koichi, Asai, Satoshi
Publicado 2021

Editorial: Current Status and Future Challenges of Biobank Data Analysis

por Lu, Tzu-Pin, Kamatani, Yoichiro, Belbin, Gillian, Park, Taesung, Hsiao, Chuhsing Kate
Publicado 2022

Detection of trait-associated structural variations using short-read sequencing

por Kosugi, Shunichi, Kamatani, Yoichiro, Harada, Katsutoshi, Tomizuka, Kohei, Momozawa, Yukihide, Morisaki, Takayuki, Terao, Chikashi
Publicado 2023

Using spatio-temporal surveillance data to test the infectious environment of children before type 1 diabetes diagnosis

por Bougnères, Pierre, Le Fur, Sophie, Valtat, Sophie, Kamatani, Yoichiro, Lathrop, Mark, Valleron, Alain-Jacques
Publicado 2017

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

por Naito, Tatsuhiko, Suzuki, Ken, Hirata, Jun, Kamatani, Yoichiro, Matsuda, Koichi, Toda, Tatsushi, Okada, Yukinori
Publicado 2021

Stepwise iterative maximum likelihood clustering approach

por Sharma, Alok, Shigemizu, Daichi, Boroevich, Keith A., López, Yosvany, Kamatani, Yoichiro, Kubo, Michiaki, Tsunoda, Tatsuhiko
Publicado 2016

Empirical evaluation of variant calling accuracy using ultra-deep whole-genome sequencing data

por Kishikawa, Toshihiro, Momozawa, Yukihide, Ozeki, Takeshi, Mushiroda, Taisei, Inohara, Hidenori, Kamatani, Yoichiro, Kubo, Michiaki, Okada, Yukinori
Publicado 2019

Functional variants in ADH1B and ALDH2 are non-additively associated with all-cause mortality in Japanese population

por Sakaue, Saori, Akiyama, Masato, Hirata, Makoto, Matsuda, Koichi, Murakami, Yoshinori, Kubo, Michiaki, Kamatani, Yoichiro, Okada, Yukinori
Publicado 2019

Genetic and phenotypic landscape of the mitochondrial genome in the Japanese population

por Yamamoto, Kenichi, Sakaue, Saori, Matsuda, Koichi, Murakami, Yoshinori, Kamatani, Yoichiro, Ozono, Keiichi, Momozawa, Yukihide, Okada, Yukinori
Publicado 2020

Genome-wide SNP data of Izumo and Makurazaki populations support inner-dual structure model for origin of Yamato people

por Jinam, Timothy, Kawai, Yosuke, Kamatani, Yoichiro, Sonoda, Shunro, Makisumi, Kanro, Sameshima, Hideya, Tokunaga, Katsushi, Saitou, Naruya
Publicado 2021

Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes

por Mutai, Hideki, Momozawa, Yukihide, Kamatani, Yoichiro, Nakano, Atsuko, Sakamoto, Hirokazu, Takiguchi, Tetsuya, Nara, Kiyomitsu, Kubo, Michiaki, Matsunaga, Tatsuo
Publicado 2022

Genetic influences on human blood metabolites in the Japanese population

por Iwasaki, Takeshi, Kamatani, Yoichiro, Sonomura, Kazuhiro, Kawaguchi, Shuji, Kawaguchi, Takahisa, Takahashi, Meiko, Ohmura, Koichiro, Sato, Taka-Aki, Matsuda, Fumihiko
Publicado 2022

Genetically proxied HTRA1 protease activity and circulating levels independently predict risk of ischemic stroke and coronary artery disease

por Dichgans, Martin, Malik, Rainer, Beaufort, Nathalie, Tanaka, Koki, Georgakis, Marios, He, Yunye, Koido, Masaru, Terao, Chikashi, Anderson, Christopher, Kamatani, Yoichiro
Publicado 2023

A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation

por Iida, Aritoshi, Takeshita, Eri, Kosugi, Shunichi, Kamatani, Yoichiro, Momozawa, Yukihide, Kubo, Michiaki, Nakagawa, Eiji, Kurosawa, Kenji, Inoue, Ken, Goto, Yu-ichi
Publicado 2018