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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 | 435 | 2015 |
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 | 375 | 2014 |
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 | 197 | 2010 |
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 | 156 | 2015 |
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 | 120 | 2018 |
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 | 119 | 2021 |
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 | 115 | 2017 |
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 | 113 | 2015 |
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 | 104 | 2020 |
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 | 100 | 2015 |
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 | 89 | 2023 |
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 | 84 | 2019 |
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 | 80 | 2017 |
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 | 72 | 2018 |
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 | 70 | 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 | 69 | 2019 |
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 | 67 | 2020 |
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 | 64 | 2017 |
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 | 64 | 2015 |