Yosuke Kawai
Yosuke Kawai
Deputy Project Manager, National Center for Global Health and Medicine
Verified email at
Cited by
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Insights into land plant evolution garnered from the Marchantia polymorpha genome
JL Bowman, T Kohchi, KT Yamato, J Jenkins, S Shu, K Ishizaki, ...
Cell 171 (2), 287-304. e15, 2017
Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals
M Nagasaki, J Yasuda, F Katsuoka, N Nariai, K Kojima, Y Kawai, ...
Nature communications 6 (1), 8018, 2015
Functional Differentiation of the Glycosyltransferases That Contribute to the Chemical Diversity of Bioactive Flavonol Glycosides in Grapevines (Vitis vinifera)
E Ono, Y Homma, M Horikawa, S Kunikane-Doi, H Imai, S Takahashi, ...
The Plant Cell 22 (8), 2856-2871, 2010
iJGVD: an integrative Japanese genome variation database based on whole-genome sequencing
Y Yamaguchi-Kabata, N Nariai, Y Kawai, Y Sato, K Kojima, M Tateno, ...
Human genome variation 2 (1), 1-4, 2015
Genome-wide association study identifies TLL1 variant associated with development of hepatocellular carcinoma after eradication of hepatitis C virus infection
K Matsuura, H Sawai, K Ikeo, S Ogawa, E Iio, M Isogawa, N Shimada, ...
Gastroenterology 152 (6), 1383-1394, 2017
HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data
N Nariai, K Kojima, S Saito, T Mimori, Y Sato, Y Kawai, ...
BMC genomics 16, 1-6, 2015
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
HJ Cordell, JJ Fryett, K Ueno, R Darlay, Y Aiba, Y Hitomi, M Kawashima, ...
Journal of hepatology 75 (3), 572-581, 2021
A conserved strategy of chalcone isomerase-like protein to rectify promiscuous chalcone synthase specificity
T Waki, R Mameda, T Nakano, S Yamada, M Terashita, K Ito, N Tenma, ...
Nature communications 11 (1), 870, 2020
Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population
M Kawashima, Y Hitomi, Y Aiba, N Nishida, K Kojima, Y Kawai, ...
Human molecular genetics 26 (3), 650-659, 2017
Late Jomon male and female genome sequences from the Funadomari site in Hokkaido, Japan
H Kanzawa-Kiriyama, TA Jinam, Y Kawai, T Sato, K Hosomichi, A Tajima, ...
Anthropological Science 127 (2), 83-108, 2019
Involvement of chalcone reductase in the soybean isoflavone metabolon: identification of Gm CHR 5, which interacts with 2]hydroxyisoflavanone synthase
R Mameda, T Waki, Y Kawai, S Takahashi, T Nakayama
The Plant Journal 96 (1), 56-74, 2018
Strong association of the HLA-DR/DQ locus with childhood steroid-sensitive nephrotic syndrome in the Japanese population
X Jia, T Horinouchi, Y Hitomi, A Shono, SS Khor, Y Omae, K Kojima, ...
Journal of the American Society of Nephrology 29 (8), 2189-2199, 2018
A 12-kb structural variation in progressive myoclonic epilepsy was newly identified by long-read whole-genome sequencing
T Mizuguchi, T Suzuki, C Abe, A Umemura, K Tokunaga, Y Kawai, ...
Journal of human genetics 64 (5), 359-368, 2019
Identification of a Highly Specific Isoflavone 7-O-glucosyltransferase in the soybean (Glycine max (L.) Merr.)
A Funaki, T Waki, A Noguchi, Y Kawai, S Yamashita, S Takahashi, ...
Plant and Cell Physiology 56 (8), 1512-1520, 2015
LRRK2 but not ATG16L1 is associated with Paneth cell defect in Japanese Crohnfs disease patients
TC Liu, T Naito, Z Liu, KL VanDussen, T Haritunians, D Li, K Endo, ...
JCI insight 2 (6), 2017
Digenic mutations in ALDH2 and ADH5 impair formaldehyde clearance and cause a multisystem disorder, AMeD syndrome
Y Oka, M Hamada, Y Nakazawa, H Muramatsu, Y Okuno, K Higasa, ...
Science Advances 6 (51), eabd7197, 2020
TIGAR2: sensitive and accurate estimation of transcript isoform expression with longer RNA-Seq reads
N Nariai, K Kojima, T Mimori, Y Sato, Y Kawai, Y Yamaguchi-Kabata, ...
BMC genomics 15, 1-9, 2014
Practical guide for managing large-scale human genome data in research
T Tanjo, Y Kawai, K Tokunaga, O Ogasawara, M Nagasaki
Journal of Human Genetics 66 (1), 39-52, 2021
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome
X Jia, T Yamamura, R Gbadegesin, MT McNulty, K Song, Y Hitomi, D Lee, ...
Kidney international 98 (5), 1308-1322, 2020
Evaluation of reported pathogenic variants and their frequencies in a Japanese population based on a whole-genome reference panel of 2049 individuals
Y Yamaguchi-Kabata, J Yasuda, O Tanabe, Y Suzuki, H Kawame, N Fuse, ...
Journal of human genetics 63 (2), 213-230, 2018
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