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Yosuke Kawai
Yosuke Kawai
Deputy Project Manager, National Center for Global Health and Medicine
Verified email at ri.ncgm.go.jp
Title
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Cited by
Year
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
11402017
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
4352015
Evolution and diversity of the 2–oxoglutarate]dependent dioxygenase superfamily in plants
Y Kawai, E Ono, M Mizutani
The Plant Journal 78 (2), 328-343, 2014
3752014
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
1972010
Japonica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individuals
Y Kawai, T Mimori, K Kojima, N Nariai, I Danjoh, R Saito, J Yasuda, ...
Journal of human genetics 60 (10), 581-587, 2015
1562015
NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter c
Y Kakuta, Y Kawai, D Okamoto, T Takagawa, K Ikeya, H Sakuraba, ...
Journal of gastroenterology 53, 1065-1078, 2018
1202018
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
1192021
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
1152017
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
1132015
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
1042020
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
1002015
Genetic architecture of the inflammatory bowel diseases across East Asian and European ancestries
Z Liu, R Liu, H Gao, S Jung, X Gao, R Sun, X Liu, Y Kim, HS Lee, Y Kawai, ...
Nature genetics 55 (5), 796-806, 2023
892023
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
842019
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
802017
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
722018
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
702018
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
692019
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
672020
LRRK2 but not ATG16L1 is associated with Paneth cell defect in Japanese Crohnfs disease patients
TC Liu, T Naito, Z Liu, KL VanDussen, T Haritunians, D Li, K Endo, ...
JCI insight 2 (6), 2017
642017
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
642015
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