Publication List of Gen Tamiya
(gtamiya@genetix-h.com)
Current h-index (Scopus): 38
Total Citation (Scopus): 6452
Other Source (less-reliable)
No Title Authors Journal Year Vol: Page Impact Factor 2021 Citation 2022/7
163 2023 -
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162 2023 -
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161 2023 -
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160 2023 -
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159 2023 -
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158 2023 -
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157 Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorder. Nishioka M, Takayama J, Sakai N, Kazuno AA, Ishiwata M, Ueda J, Hayama T, Fujii K, Someya T, Kuriyama S, Tamiya G, Takata A, Kato T. Mol Psychiatry. 2023 online ahead of print -
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156 Familial Paget's disease of bone with ocular manifestations and a novel TNFRSF11A duplication variant (72dup27). Saito-Hakoda A, Kikuchi A, Takahashi T, Yokoyama Y, Himori N, Adachi M, Ikeda R, Nomura Y, Takayama J, Kawashima J, Katsuoka F, Fujishima F, Yamaguchi T, Ito A, Hanita T, Kanno J, Aizawa T, Nakazawa T, Kawase T, Tamiya G, Yamamoto M, Fujiwara I, Kure S. J Bone Miner Metab. 2023 41(2):193-202. -
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155 Genome-wide association study of the risk of chronic kidney disease and kidney-related traits in the Japanese population: J-Kidney-Biobank. Sugawara Y, Hirakawa Y, Nagasu H, Narita A, Katayama A, Wada J, Shimizu M, Wada T, Kitamura H, Nakano T, Yokoi H, Yanagita M, Goto S, Narita I, Koshiba S, Tamiya G, Nangaku M, Yamamoto M, Kashihara N. J Hum Genet. 2023 68(2):55-64. -
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154 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Kanoni S, (Tamiya G; 496 in 539 authors) Genome Biol. 2022 23(1):268. -
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153 Pathological variants in genes associated with disorders of sex development and central causes of hypogonadism in a whole-genome reference panel of 8380 Japanese individuals. Shiga N, Yamaguchi-Kabata Y, Igeta S, Yasuda J, Tadaka S, Minato T, Watanabe Z, Kanno J, Tamiya G, Fuse N, Kinoshita K, Kure S, Kondo A, Tachibana M, Yamamoto M, Yaegashi N, Sugawara J. Hum Genome Var. 2022 28;9(1):34. -
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152 Construction of a trio-based structural variation panel utilizing activated T lymphocytes and long-read sequencing technology. Otsuki A, Okamura Y, Ishida N, Tadaka S, Takayama J, Kumada K, Kawashima J, Taguchi K, Minegishi N, Kuriyama S,Tamiya G, Kinoshita K, Katsuoka F, Yamamoto M. Commun Biol. 2022 5(1):991 -
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151 A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids. Ramdas S, et al (Tamiya G; 494 in 540 authors) Am J Hum Genet 2022 Online ahead of print 11.043
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150 Development of a prognostic prediction support system for cervical intraepithelial neoplasia using artificial intelligence-based diagnosis. Takahashi T, Matsuoka H, Sakurai R, Akatsuka J, Kobayashi Y, Nakamura M, Iwata T, Banno K, Matsuzaki M, Takayama J, Aoki D, Yamamoto Y, Tamiya G. J Gynecol Oncol 2022 Online ahead of print 4.756
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149 Two Siblings with Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome 4 and a Novel Variant of ATP8A2. Narishige Y, Yaoita H, Shibuya M, Ikeda M, Kodama K, Kawashima A, Okubo Y, Endo W, Inui T, Togashi N, Tanaka S, Kobayashi Y, Onuma A, Takayama J, Tamiya G, Kikuchi A, Kure S, Haginoya K. Tohoku J Exp Med 2022 256(4):321-326 2.547
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148 Heart Rate Information-Based Machine Learning Prediction of Emotions Among Pregnant Women. Li X, Ono C, Warita N, Shoji T, Nakagawa T, Usukura H, Yu Z, Takahashi Y, Ichiji K, Sugita N, Kobayashi N, Kikuchi S, Kunii Y, Murakami K, Ishikuro M, Obara T, Nakamura T, Nagami F, Takai T, Ogishima S, Sugawara J, Hoshiai T, Saito M, Tamiya G, Fuse N, Kuriyama S, Yamamoto M, Yaegashi N, Homma N, Tomita H. Front Psychiatry 2022 12:799029 5.435
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147 Heterozygous calcyclin-binding protein/Siah1-interacting protein (CACYBP/SIP) gene pathogenic variant linked to a dominant family with paucity of interlobular bile duct. Kanno M, Suzuki M, Tanikawa K, Numakura C, Matsuzawa SI, Niihori T, Aoki Y, Matsubara Y, Makino S, Tamiya G, Nakano S, Funayama R, Shirota M, Nakayama K, Mitsui T, Hayasaka K. J Hum Genet 2022 67(7):393-397 3.773
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146 The longest reported sibling survivors of a severe form of congenital myasthenic syndrome with the ALG14 pathogenic variant. Katata Y, Uneoka S, Saijyo N, Aihara Y, Miyazoe T, Koyamaishi S, Oikawa Y, Ito Y, Abe Y, Numata-Uematsu Y, Takayama J, Kikuchi A, Tamiya G, Uematsu M, Kure S. Am J Med Genet A 2022 188(4):1293-1298 2.578
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145 The power of genetic diversity in genome-wide association studies of lipids. Graham SE, et al. (Tamiya G; 513th in 530 authors). Nature 2021 600(7890):675-679 69.504
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144 dbTMM: an integrated database of large-scale cohort, genome and clinical data for the Tohoku Medical Megabank Project. Ogishima S, Nagaie S, Mizuno S, Ishiwata R, Iida K, Shimokawa K, Takai-Igarashi T, Nakamura N, Nagase S, Nakamura T, Tsuchiya N, Nakaya N, Murakami K, Ueno F, Onuma T, Ishikuro M, Obara T, Mugikura S, Tomita H, Uruno A, Kobayashi T, Tsuboi A, Tadaka S, Katsuoka F, Narita A, Sakurai M, Makino S, Tamiya G, Aoki Y, Shimizu R, Motoike IN, Koshiba S, Minegishi N, Kumada K, Nobukuni T, Suzuki K, Danjoh I, Nagami F, Tanno K, Ohmomo H, Asahi K, Shimizu A, Hozawa A, Kuriyama S; Tohoku Medical Megabank Project Study Group, Fuse N, Tominaga T, Kure S, Yaegashi N, Kinoshita K, Sasaki M, Tanaka H, Yamamoto M. Hum Genome Var 2021 8(1):44 -
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143 A cross-population atlas of genetic associations for 220 human phenotypes. Sakaue S, Kanai M, Tanigawa Y, Karjalainen J, Kurki M, Koshiba S, Narita A, Konuma T, Yamamoto K, Akiyama M, Ishigaki K, Suzuki A, Suzuki K, Obara W, Yamaji K, Takahashi K, Asai S, Takahashi Y, Suzuki T, Shinozaki N, Yamaguchi H, Minami S, Murayama S, Yoshimori K, Nagayama S, Obata D, Higashiyama M, Masumoto A, Koretsune Y; FinnGen, Ito K, Terao C, Yamauchi T, Komuro I, Kadowaki T, Tamiya G, Yamamoto M, Nakamura Y, Kubo M, Murakami Y, Yamamoto K, Kamatani Y, Palotie A, Rivas MA, Daly MJ, Matsuda K, Okada Y. Nature Genetics 2021 53(10):1415?1424 41.379
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142 Smooth-threshold multivariate genetic prediction incorporating gene-environment interactions. Ueki M, Tamiya G G3 Genes|Genomes|Genetics 2021 11(12):jkab278 3.542
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141 A patient with early-onset SMAX3 and a novel variant of ATP7A. Shibuya M, Yaoita H, Kodama K, Okubo Y, Endo W, Inui T, Togashi N, Takayama J, Tamiya G, Kikuchi A, Kure S, Haginoya K. Brain Dev 2022 44(1):63?67 2.272
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140 Japonica Array NEO with increased genome-wide coverage and abundant disease risk SNPs Sakurai-Yageta M, Kumada K, Gocho C, Makino S, Uruno A, Tadaka S, Motoike I N, Kimura M, Ito S, Otsuki A, Narita A, Kudo H, Aoki Y, Danjoh I, Yasuda J, Kawame H, Minegishi N, Koshiba S, Fuse N, Tamiya G, Yamamoto M, Kinoshita K J Biochem 2021 170(3):399?410 3.241
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139 GWAS Identified IL4R and the Major Histocompatibility Complex Region as the Associated Loci of Total Serum IgE Levels in 9,260 Japanese Individuals Shido K, Kojima K, Shirota M, Yamasaki K, Motoike I N, Hozawa A, Ogishima S, Minegishi N, Tanno K, Katsuoka F, Tamiya G, Aiba S, Yamamoto M, Kinoshita K J Invest Dermatol 2021 141(11):2749?2752 7.59
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138 Identification and Validation of Combination Plasma Biomarker of Afamin, Fibronectin and Sex Hormone-Binding Globulin to Predict Pre-eclampsia Uchida Y, Higuchi T, Shirota M, Kagami S, Saigusa D, Koshiba S, Yasuda J, Tamiya G, Kuriyama S, Kinoshita K, Yaegashi N, Yamamoto M, Terasaki T, J Sugawara Biol Pharm Bull 2021 44(6):804-815 2.264
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137 Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk. Shigemizu D, Mitsumori R, Akiyama S, Miyashita A, Morizono T, Higaki S, Asanomi Y, Hara N, Tamiya G, Kinoshita K, Ikeuchi T, Niida S, Ozaki K Transl Psychiatry 2021 11(1):151 7.989
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136 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Gharahkhani P, et al. ( Tamiya G ; 44th in 86 authors) Nature Communications 2021 12(1):1258 17.694
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135 ALOX12 mutation in a family with dominantly inherited bleeding diathesis. Mitsui T, Makino S, Tamiya G, Sato H, Kawakami Y, Takahashi Y, Meguro T, Izumino H, Sudo Y, Norota I, Ishii K, Hayasaka K. J Hum Genet 2021 66:753-759 3.773
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134 Body mass index and colorectal cancer risk: A Mendelian randomization study. Suzuki S, Goto A, Nakatochi M, Narita A, Yamaji T, Sawada N, Katagiri R, Iwagami M, Hanyuda A, Hachiya T, Sutoh Y, Oze I, Koyanagi YN, Kasugai Y, Taniyama Y, Ito H, Ikezaki H, Nishida Y, Tamura T, Mikami H, Takezaki T, Suzuki S, Ozaki E, Kuriki K, Takashima N, Arisawa K, Takeuchi K, Tanno K, Shimizu A, Tamiya G, Hozawa A, Kinoshita K, Wakai K, Sasaki M, Yamamoto M, Matsuo K, Tsugane S, Iwasaki M. Cancer Sci 2021 112(4):1579-1588 6.518
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133 Estimation of the carrier frequencies and proportions of potential patients by detecting causative gene variants associated with autosomal recessive bone dysplasia using a whole-genome reference panel of Japanese individuals. Nagaoka S, Yamaguchi-Kabata Y, Shiga N, Tachibana M, Yasuda J, Tadaka S, Tamiya G, Fuse N, Kinoshita K, Kure S, Murotsuki J, Yamamoto M, Yaegashi N, Sugawara J. Hum Genome Var 2021 8(1):2 -
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132 Facial UV photo imaging for skin pigmentation assessment using conditional generative adversarial networks. Kojima K, Shido K, Tamiya G, Yamasaki K, Kinoshita K, Aiba S. Sci Rep 2021 11(1):1213 4.996
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131 Construction and integration of assemblies toward a population-specific reference. Takayama J, Tadaka S, Yano K, Katsuoka K, Gocho C, Funayama T, Makino S, Okamura Y, Kikuchi A, Sugimoto S, Kawashima J, Otsuki A, Sakurai-Yageta M, Yasuda J, Kure S, Kinoshita K, Yamamoto M & Tamiya G. Nature Communications 2021 12(1):226 17.694
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130 Machine learning to reveal hidden risk combinations for the trajectory of posttraumatic stress disorder symptoms. Takahashi Y, Yoshizoe K, Ueki M, Tamiya G, Zhiqian Y, Utsumi Y, Sakuma A, Tsuda K, Hozawa A, Tsuji I, Tomita H. Sci Rep 2020 10:21726 4.996
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129 jMorp updates in 2020: large enhancement of multi-omics data resources on the general Japanese population. Tadaka S, Hishinuma E, Komaki S, Motoike IN, Kawashima J, Saigusa D, Inoue J, Takayama J, Okamura Y, Aoki Y, Shirota M, Otsuki A, Katsuoka F, Shimizu A, Tamiya G, Koshiba S, Sasaki M, Yamamoto M, Kinoshita K. Nucleic Acids Res 2020 49(D1):D536-544 19.16
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128 Identification of critical genetic variants associated with metabolic phenotypes of the Japanese population. Koshiba S, Motoike IN, Saigusa D, Inoue J, Aoki Y, Tadaka S, Shirota M, Katsuoka F, Tamiya G, Minegishi N, Fuse N, Kinoshita K, Yamamoto M. Commun Biol 2020 3(1):662 6.548
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127 Maternal Baseline Characteristics and Perinatal Outcomes: the Tohoku Medical Megabank Project Birth and Three-Generation Cohort Study. Sugawara J, Ishikuro M, Obara T, Onuma T, Murakami K, Kikuya M, Ueno F, Noda A, Mizuno S, Kobayashi T, Hamanaka Y, Suzuki K, Kodama E, Tsuchiya N, Uruno A, Suzuki Y, Tanabe O, Kiyomoto H, Tsuboi A, Shimizu A, Koshiba S, Minegishi N, Ogishima S, Tamiya G, Metoki H, Hozawa A, Fuse N, Kinoshita K, Kure S, Yaegashi N, Kuriyama S, Yamamoto M. J Epidemiol 2022 32(2):69?79 3.809
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126 A genotype imputation method for de-identified haplotype reference information by using recurrent neural network. Kojima K, Tadaka S, Katsuoka F, Tamiya G, Yamamoto M, Kinoshita K. PLoS Comput Biol 2020 16(10):e1008207 4.779
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125 Machine learning for effectively avoiding overfitting is a crucial strategy for the genetic prediction of polygenic psychiatric phenotypes. Takahashi Y, Ueki M, Tamiya G, Ogishima S, Kinoshita K, Hozawa A, Minegishi N, Nagami F, Fukumoto K, Otsuka K, Tanno K, Sakata K, Shimizu A, Sasaki M, Sobue K, Kure S, Yamamoto M, Tomita H. Transl Psychiatry 2020 10(1):294 7.989
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124 Clustering by phenotype and genome-wide association study in autism. Narita A, Nagai M, Mizuno S, Ogishima S, Tamiya G, Ueki M, Sakurai R, Makino S, Obara T, Ishikuro M, Yamanaka C, Matsubara H, Kuniyoshi Y, Murakami K, Ueno F, Noda A, Kobayashi T, Kobayashi M, Usuzaki T, Ohseto H, Hozawa A, Kikuya M, Metoki H, Kure S, Kuriyama S. Transl Psychiatry 2020 10(1):290 7.989
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123 Artificial intelligence powered statistical genetics in biobanks. Narita A, Ueki M, Tamiya G. J Hum Genet 2020 66:61-65 3.773
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122 Endogenization and excision of human herpesvirus 6 in human genomes. Liu X, Kosugi S, Koide R, Kawamura Y, Ito J, Miura H, Matoba N, Matsuzaki M, Fujita M, Kamada AJ, Nakagawa H, Tamiya G, Matsuda K, Murakami Y, Kubo M, Aswad A, Sato K, Momozawa Y, Ohashi J, Terao C, Yoshikawa T, Parrish NF, Kamatani Y. PLoS Genet 2020 16(8):e1008915 6.02
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121 Design and Progress of Oral Health Examinations in the Tohoku Medical Megabank Project. Tsuboi A, Matsui H, Shiraishi N, Murakami T, Otsuki A, Kawashima J, Kiyama T, Tamahara T, Goto M, Koyama S, Sugawara J, Kodama EN, Metoki H, Hozawa A, Kuriyama S, Tomita H, Kikuya M, Minegishi N, Suzuki K, Koshiba S, Tamiya G, Fuse N, Aoki Y, Takai-Igarashi T, Ogishima S, Nakamura T, Sakurai-Yageta M, Nagami F, Kinoshita K, Kure S, Shimizu R, Sasaki K, Yamamoto M. Tohoku J Exp Med 2020 251(2):97-115 2.547
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120 Improved metabolomic data-based prediction of depressive symptoms using nonlinear machine learning with feature selection. Takahashi Y, Ueki M, Yamada M, Tamiya G, Motoike IN, Saigusa D, Sakurai M, Nagami F, Ogishima S, Koshiba S, Kinoshita K, Yamamoto M, Tomita H. Transl Psychiatry 2020 10(1):157 7.989
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119 Genome-wide association study identifies new loci for albuminuria in the Japanese population. Okuda H, Okamoto K, Abe M, Ishizawa K, Makino S, Tanabe O, Sugawara J, Hozawa A, Tanno K, Sasaki M, Tamiya G, Yamamoto M, Ito S, Ishii T. Clin Exp Nephrol 2020 24(8):1-9 2.624
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118 Study profile of The Tohoku Medical Megabank Community-Based Cohort Study. Hozawa A, Tanno K, (Tamiya G; 47 in 84 authors). J Epidemiol 2021 31(1):65-76 3.809
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117 Cohort Profile: Tohoku Medical Megabank Project Birth and Three-Generation Cohort Study (TMM BirThree Cohort Study): Rationale, Progress and Perspective Kuriyama S, Metoki H, Tamiya G ( 6th in 65 authors) Int J Epidemiol 2020 49(1):18-19M 9.685
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116 Automated acquisition of explainable knowledge from unannotated histopathology images. Yamamoto Y, Tsuzuki T, Akatsuka J, Ueki M, Morikawa H, Numata Y, Takahara T, Tsuyuki T, Tsutsumi K, Nakazawa R, Shimizu A, Maeda I, Tsuchiya S, Kanno H, Kondo Y, Fukumoto M, Tamiya G, Ueda N, Kimura G. Nature Communications 2019 10(1):5642 17.694
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115 Illuminating Clues of Cancer Buried in Prostate MR Image: Deep Learning and Expert Approaches. Akatsuka J, Yamamoto Y, Sekine T, Numata Y, Morikawa H, Tsutsumi K, Yanagi M, Endo Y, Takeda H, Hayashi T, Ueki M, Tamiya G, Maeda I, Fukumoto M, Shimizu A, Tsuzuki T, Kimura G, Kondo Y. Biomolecules 2019 9(11):673 6.064
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114 Establishment of Integrated Biobank for Precision Medicine and Personalized Healthcare: The Tohoku Medical Megabank Project. Fuse N, Sakurai-YagetaM, Katsuoka F, Danjoh I, Shimizu R, Tamiya G, Nagami F, Kawame H, Higuchi S, Kinoshita K, Kure S, Yamamoto M. JMA Journal 2019 2(2):113-122 -
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113 GWAS with principal component analysis identifies a gene comprehensively controlling rice architecture. Yano K, Morinaka Y, Wang F, Huang P, Takehara S, Hirai T, Ito A, Koketsu E, Kawamura M, Kotake K, Yoshida S, Endo M, Tamiya G, Kitano H, Ueguchi-Tanaka M, Hirano K, Matsuoka M. Proc Natl Acad Sci USA 2019 116(42):21262-21267 12.779
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112 In Vivo Expression of NUP93 and Its Alteration by NUP93 Mutations Causing Focal Segmental Glomerulosclerosis. Hashimoto T, Harita Y, Takizawa K, Urae S, Ishizuka K, Miura K, Horita S, Ogino D, Tamiya G, Ishida H, Mitsui T, Hayasaka K, Hattori M. Kidney Int Rep 2019 4(9):1312-1322 6.234
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111 Quick assessment for systematic test statistic inflation/deflation due to null model misspecifications in genome-wide environment interaction studies. Ueki M, Fujii M, Tamiya G, for Alzheimer¡Çs Disease Neuroimaging Initiative and the Alzheimer¡Çs Disease Metabolomics Consortium. PLoS ONE 2019 14(7):e0219825 3.752
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110 3.5KJPNv2: an allele frequency panel of 3552 Japanese individuals including the X chromosome. Tadaka S, Katsuoka F, Ueki M, Kojima K, Makino S, Saito S, Otsuki A, Gocho C, Sakurai-Yageta M, Danjoh I, Motoike IN, Yamaguchi-Kabata Y, Shirota M, Koshiba S, Nagasaki M, Minegishi N, Hozawa A, Kuriyama S, Shimizu A, Yasuda J, Fuse N, Tohoku Medical Megabank Project Study Group, Tamiya G, Yamamoto M, Kinoshita K. Hum Genome Var 2019 6(1):28 -
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109 The prevalence of GALM mutations that cause galactosemia: A database of functionally evaluated variants. Iwasawa S, Kikuchi A, Wada Y, Arai-Ichinoi N, Sakamoto O, Tamiya G, Kure S. Mol Genet Metab 2019 126(4):362-367 4.204
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108 Estimating carrier frequencies of newborn screening disorders using a whole-genome reference panel of 3552 Japanese individuals. Yamaguchi-Kabata Y, Yasuda J, Uruno A, Shimokawa K, Koshiba S, Suzuki Y, Fuse N, Kawame H, Tadaka S, Nagasaki M, Kojima K, Katsuoka F, Kumada K, Tanabe O, Tamiya G, Yaegashi N, Kinoshita K, Yamamoto M, Kure S, Tohoku Medical Megabank Project Study Group. Hum Genet 2019 138(4):389-409 5.881
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107 Outlier detection for questionnaire data in biobanks. Sakurai R, Ueki M, Makino S, Hozawa A, Kuriyama S, Takai-Igarashi T, Kinoshita K, Yamamoto M, Tamiya G. Int J Epidemiol 2019 48(4):1305-1315 9.685
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106 Respiratory resistance among adults in a population-based cohort study in Northern Japan. Miura E, Tsuchiya N, Igarashi Y, Arakawa R, Nikkuni E, Tamai T, Tabata M, Ohkouchi S, Irokawa T, Ogawa H, Takai-Igarashi T, Suzuki Y, Kuriyama S, Tamiya G, Hozawa A, Yamamoto M, Kurosawa H. Respir Investig 2019 57(3):274-281 -
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105 Growth impairment in individuals with citrin deficiency. Numakura C, Tamiya G, Ueki M, Okada T, Maisawa SI, Kojima-Ishii K, Murakami J, Horikawa R, Tokuhara D, Ito K, Adachi M, Abiko T, Mitsui T, Hayasaka K. J Inherit Metab Dis 2019 42(3):501-508 4.75
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104 Susceptibility loci for tanning ability in Japanese population identified by genome-wide association study from Tohoku Medical Megabank Project cohort study. Shido K, Kojima K, Yamasaki K, Hozawa A, Tamiya G, Ogishima S, Minegishi N, Kawai Y, Tanno K, Suzuki Y, Nagasaki M, Aiba S. J Invest Dermatol 2019 139(7):1605-1608 7.59
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103 Genome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcare. Yasuda J, Kinoshita K, Katsuoka F, Danjoh I, Sakurai-Yageta M, Motoike IN, Kuroki Y, Saito S, Kojima K, Shirota M, Saigusa D, Otsuki A, Kawashima J, Yamaguchi-Kabata Y, Tadaka S, Aoki Y, Mimori T, Kumada K, Inoue J, Makino S, Kuriki M, Fuse N, Koshiba S, Tanabe O, Nagasaki M, Tamiya G, Shimizu R, Takai-Igarashi T, Ogishima S, Hozawa A, Kuriyama S, Sugawara J, Tsuboi A, Kiyomoto H, Ishii T, Tomita H, Minegishi N, Suzuki Y, Suzuki K, Kawame H, Tanaka H, Taki Y, Yaegashi N, Kure S, Nagami F; Tohoku Medical Megabank Project Study Group, Kosaki K, Sutoh Y, Hachiya T, Shimizu A, Sasaki M, Yamamoto M. J Biochem 2018 65(2):139-158 3.241
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102 Potential identification of vitamin B6 responsiveness in autism spectrum disorder utilizing phenotype variables and machine learning methods. Obara T, Ishikuro M, Tamiya G, Ueki M, Yamanaka C, Mizuno S, Kikuya M, Metoki H, Matsubara H, Nagai M, Kobayashi T, Kamiyama M, Watanabe M, Kakuta K, Ouchi M, Kurihara A, Fukuchi N, Yasuhara A, Inagaki M, Kaga M, Kure S, Kuriyama S. Sci Rep 2018 8(1):14840 4.996
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101 Regional genetic differences among Japanese populations and performance of genotype imputation using whole-genome reference panel of the Tohoku Medical Megabank Project. Yasuda J, Katsuoka F, Danjoh I, Kawai Y, Kojima K, Nagasaki M, Saito S, Yamaguchi-Kabata Y, Tadaka S, Motoike IN, Kumada K, Sakurai-Yageta M, Tanabe O, Fuse N, Tamiya G, Higasa K, Matsuda F, Yasuda N, Iwasaki M, Sasaki M, Shimizu A, Kinoshita K, Yamamoto M. BMC Genomics 2018 9(1):551 4.56
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100 Ethylene-gibberellin signaling underlies adaptation of rice to periodic flooding. Kuroha T, Nagai K, Gamuyao R, Wang DR, Furuta T, Nakamori M, Kitaoka T, Adachi K, Minami A, Mori Y, Mashiguchi K, Seto Y, Yamaguchi S, Kojima M, Sakakibara H, Wu J, Ebana K, Mitsuda N, Ohme-Takagi M, Yanagisawa S, Yamasaki M, Yokoyama R, Nishitani K, Mochizuki T, Tamiya G, McCouch SR, Ashikari M. Science 2018 361(6398):181-186 63.798
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99 Female Japanese quail visually differentiate testosterone-dependent male attractiveness for mating preferences. Hiyama G, Mizushima S, Matsuzaki M, Tobari Y, Choi JH, Ono T, Tsudzuki M, Makino S, Tamiya G, Tsukahara N, Sugita S, Sasanami T. Sci Rep 2018 8(1):10012 4.996
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98 Omics research project on prospective cohort studies from the Tohoku Medical Megabank Project. Koshiba S, Motoike I, Saigusa D, Inoue J, Shirota M, Katoh Y, Katsuoka F, Danjoh I, Hozawa A, Kuriyama S, Minegishi N, Nagasaki M, Takai-Igarashi T, Ogishima S, Fuse N, Kure S, Tamiya G, Tanabe O, Yasuda J, Kinoshita K, Yamamoto M. Genes Cells 2018 23(6):406-417 2.3
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97 Evaluation of reported pathogenic variants and their frequencies in a Japanese population based on a whole-genome reference panel of 2049 individuals. Yamaguchi-Kabata Y, Yasuda J, Tanabe O, Suzuki Y, Kawame H, Fuse N, Nagasaki M, Kawai Y, Kojima K, Katsuoka F, Saito S, Danjoh I, Motoike IN, Yamashita R, Koshiba S, Saigusa D, Tamiya G, Kure S, Yaegashi N, Kawaguchi Y, Nagami F, Kuriyama S, Sugawara J, Minegishi N, Hozawa A, Ogishima S, Kiyomoto H, Takai-Igarashi T; ToMMo Study Group, Kinoshita K, Yamamoto M. J Hum Genet 2018 63(2):213-230 3.773
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96 Genome-wide meta-analysis in Japanese populations identifies novel variants at the TMC6-TMC8 and SIX3-SIX2 loci associated with HbA1c. Hachiya T, Komaki S, Hasegawa Y, Ohmomo H, Tanno K, Hozawa A, Tamiya G, Yamamoto M, Ogasawara K, Nakamura M, Hitomi J, Ishigaki Y, Sasaki M, Shimizu A. Sci Rep 2017 7(1):16147 4.996
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95 Security controls in an integrated Biobank to protect privacy in data sharing: rationale and study design Takai-Igarashi T, Kinoshita K, Nagasaki M, Ogishima S, Nakamura N, Nagase S, Nagaie S, Saito T, Nagami F, Minegishi N, Suzuki Y, Suzuki K, Hashizume H, Kuriyama S, Hozawa A, Yaegashi N, Kure S, Tamiya G, Kawaguchi Y, Tanaka H, Yamamoto M BMC Med Inform Decis Mak 2017 17(1):100 3.298
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94 Detecting genetic association through shortest paths in a bi-directed graph Ueki M, Kawasaki Y, Tamiya G Genet Epidemiol 2017 41(6):481-497 2.344
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93 Whole-exome sequencing confirmation of multiple MC1R variants associated with extensive freckles and red hair: Analysis of a Mongolian family. Araki Y, Okamura K, Munkhbat B, Tamiya G. Erdene-Ochir B, Nemekhbaatar L, Hozumi Y, Suzuki T. J Dermatol Sci 2016 84(2):216-219 5.408
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92 The Tohoku Medical Megabank Project: Design and Mission. Kuriyama S, Yaegashi N, et al. (Tamiya G; 11th in 58 authors)) J Epidemiol 2016 26(9):493-511 3.809
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91 Smooth-threshold multivariate genetic prediction with unbiased model selection. Ueki M, Tamiya G Genet Epidemiol 2016 40(3): 233-43 2.344
8
90 Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole exome sequencing analysis. Ogino D, Hashimoto T,Hattori M, Sugawara N, Akioka Y, Tamiya G, Makino S, Toyota K, Mitsui T, Hayasaka K J Hum Genet 2016 61(2):137-41 3.773
21
89 Waardenburg syndrome type IIE in a Japanese patient caused by a novel missense mutation in the SOX10 gene. Okamura K, Oiso N, Tamiya G, Makino S, Tsujioka D, Abe Y, Kawaguchi M, Hozumi Y, Shimomura Y, Suzuki T. J Dermatol 2015 42(12):1211-2 3.468
5
88 Immunohistopathological analysis of frizzled-4-positive immature melanocytes from hair follicles of patients with Rhododenol-induced leukoderma. Okamura K, Ohe R, Abe Y, Ueki M, Hozumi Y, Tamiya G, Matsunaga K, Yamakawa M, Suzuki T. J Dermatol Sci 2015 80(2):156-8 5.408
7
87 Positive selection with diversity in oculocutaneous albinisms type 2 gene (OCA2) among Japanese. Shimanuki M, Abe Y, Tamiya G, Ueki M, Hozumi Y, Suzuki T. Pigment Cell Melanoma Res 2015 28(2):233-5 4.159
2
86 Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms. Sato H, Uchida T, Toyota K, Nakamura T, Tamiya G, Kanno M, Hashimoto T, Watanabe M, Aoki K, Hayasaka K. J Hum Genet 2015 60(1):35-40 3.773
11
85 A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease. Tamiya G (Corresponding author), Makino S, Hayashi M, Abe A, Numakura C, Ueki M, Tanaka A, Ito C, Toshimori K, Ogawa N, Terashima T, Maegawa H, Yanagisawa D, Tooyama I, Tada M, Onodera O, Hayasaka K. Am J Hum Genet 2014 95(3):294-300 11.043
54
84 Likelihood ratio-based integrated personal risk assessment of type 2 diabetes. Sato N, Htun NC, Daimon M, Tamiya G, Kato T, Kubota I, Ueno Y, Yamashita H, Fukao A, Kayama T, Muramatsu M. Endocr J 2014 61(10):967-88 2.86
1
83 Whole-exome sequencing confirmation of a novel heterozygous mutation in RUNX1 in a pregnant woman with platelet disorder Obata M, Tsutsumi S, Makino S, Takahashi K, Watanabe N, Yoshida T, Tamiya G, Kurachi H. Platelets 2015 26(4):364-369 4.236
5
82 Divergence of East Asians and Europeans estimated using male- and female-specific genetic markers. Tateno Y, Komiyama T, Katoh T, Munkhbat B, Haida Y,Kobayashi H, Tamiya G, Inoko H. Genome Biol Evol 2014 6(3):466-73 4.065
5
81 A pollen coat-inducible autoinhibited Ca2+-ATPase expressed in stigmatic papilla cell is required for compatible pollination in the Brassicaceae. Iwano M, Igarashi M, Tarutani Y, Kaothien-Nakayama P, Nakayama H, Moriyama H, Yakabe R, Entani T, Shimosato-Asano H, Ueki M, Tamiya G, Takayama S Plant Cell 2014 26(2):636-49 12.085
49
80 Pleiotropic Effect of Common Variants at ABO Glycosyltranferase Locus in 9q32 on Plasma Levels of Pancreatic Lipase and Angiotensin Converting Enzyme. Yamagata University Genomic Cohort Consortium (Tamiya G; Corresponding author) PLoS ONE 2014 9(2):e55903 3.752
10
79 Variants in melanogenesis-related genes associate with skin cancer risk among Japanese populations. Yoshizawa J, Abe Y, Oiso N, Fukai K, Hozumi Y, Nakamura T, Narita T, Motokawa T, Wakamatsu K, Ito S, Kawada A, Tamiya G, Suzuki T J Dermatol 2014 41(4):296-302 3.468
11
78 Gamete Attachment Requires GEX2 for Successful Fertilization in Arabidopsis. Mori T, Igawa T, Tamiya G, Miyagishima SY, Berger F. Curr Biol 2014 24(2):170-5 10.9
73
77 Case of a Mongolian child with extensive Mongolian spots in Mucopolysaccharidosis type VI: Identification of a novel mutation in the arylsulfatase B gene. Okamura K, Munkhbat B, Bachimeg B, Tamiya G, Hozumi Y, Suzuki T. J Dermatol 2013 40(9):758-9 3.468
0
76 Comparison of caregiver strain in Parkinson's disease between Yamagata, Japan, and Maryland, The United States. Tanji H, Koyama S, Wada M, Kawanami T, Kurita K, Tamiya G, Saito N, Suzuki K, Kato T, Anderson KE, Gruber-Baldini AL, Fishman PS, Reich SG, Weiner WJ, Shulman LM. Parkinsonism Relat Disord 2013 19(6):628-33 4.402
9
75 The confounding effect of cryptic relatedness for environmental risks of systolic blood pressure on cohort studies. Shibata K, Hozawa A, Tamiya G, Ueki M, Nakamura T, et al. Mol Genet Genomic Med 2013 1(1):45-53 2.473
1
74 A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy. Toyota K, Hashimoto T, Ogino D, Matsunaga A, Ito M, Masakane I, Degawa N, Sato H, Shirai S, Umetsu K, Tamiya G, Saito T, Hayasaka K. J Hum Genet 2013 58(5):254-8 3.773
14
73 Generation of a Monoclonal Antibody Specifically Reacting with Neuron-specific TATA-Box Binding Protein-Associated Factor 1 (N-TAF1). Makino S, Masuda C, Ando S, Tamiya G and Tooyama I. Antibodies 2013 2(1):1-8 -
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72 Association of melanogenesis genes with skin color variation among Japanese females. Abe Y, Tamiya G, Nakamura T, Hozumi Y, and Suzuki T. J Dermatol Sci 2013 69(2):167-72 5.408
25
71 Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G4A (G71R) mutation becomes a risk factor under inadequate feeding Sato H, Uchida T, Toyota K, Kanno M, Hashimoto T, Watanabe M, Nakamura T, Tamiya G, Aoki K, Hayasaka K. J Hum Genet 2013 58:7-10 3.773
26
70 Constructing a contemporary gene-environmental cohort : Study design of the Yamagata Molecular Epidemiological Cohort Study. Yamagata University Genomic Cohort Consortium J Hum Genet 2013 58:54-6 3.773
10
69 UBR5 Gene Mutation Is Associated with Familial Adult Myoclonic Epilepsy in a Japanese Family. Kato T, Tamiya G, Koyama S, Nakamura T, Makino S, Arawaka S, Kawanami T, Tooyama I. ISRN Neurol 2012 2012:508308 -
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68 Sustained expression of a neuron-specific isoform of the Taf1 gene in development stages and aging in mice. Jambaldorj J, Makino S, Munkhbat B, Tamiya G. Biochem Biophys Res Commun 2012 425(2):273-277 3.322
13
67 HLA-A*0206 with TLR3 Polymorphisms Exerts more than Additive Effects in Stevens-Johnson Syndrome with Severe Ocular Surface Complications. Ueta M, Tokunaga K, Sotozono C, Sawai H, Tamiya G, Inatomi T, Kinoshita S. PLoS ONE 2012 7(8):e43650 3.752
32
66 Ultrahigh-dimensional variable selection method for whole-genome gene-gene interaction analysis. Ueki M, Tamiya G. BMC Bioinformatics 2012 13(1):72 3.328
28
65 Epistatic interaction between TLR3 and PTGER3 genes. Ueta M, Tamiya G, Tokunaga K, Sotozono C, Ueki M, Sawai H, Inatomi T, Matsuoka T, Akira S, Narumiya S, Tashiro K, Kinoshita S. J Allergy Clin Immunol 2012 129(5):1413-1416 11.022
25
64 Impaired Glucose Metabolism Slows Executive Function Independent of Cerebral Ischemic Lesions in Japanese Elderly: The Takahata Study. Takahashi Y, Iseki C, Wada M, Momma T, Ueki M, Kawanami T, Daimon M, Suzuki K, Tamiya G, Kato T. Internal Med 2011 50(16):1671-8 1.282
6
63 Polymorphism of proinflammatory cytokine genes and albuminuria in the Japanese general population: the Takahata study. Mashima Y, Konta T, Kudo K, Suzuki K, Ikeda A, Ichikawa K, Shibata Y, Watanabe T, Tamiya G, Kato T, Kawata S, Kubota I. Nephrol Dial Transplant 2011 26(12):3902-7 7.186
3
62 Transcriptional dysregulation: a cause of dystonia? Tamiya G (Corresponding author). Lancet Neurol 2009 8(5):416-8 59.935
8
61 Identification of MICA as a susceptibility gene for pulmonary Mycobacterium avium complex infection. Shojima J, Tanaka G, Keicho N, Tamiya G, et al. J Infect Dis 2009 199(11):1707-15 7.759
19
60 Hepatic AdipoR2 signaling plays a protective role against progression of nonalcoholic steatohepatitis in mice. Tomita K, Oike Y, Teratani T, Taguchi T, Noguchi M, Suzuki T, Mizutani A, Yokoyama H, Irie R, Sumimoto H, Takayanagi A, Miyashita K, Akao M, Tabata M, Tamiya G, Ohkura T, Hibi T. Hepatology 2008 48(2):458-73 17.298
106
59 Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity. Maeda K, Kaji R, Yasuno K, Jambaldorj J, Nodera H, Takashima H, Nakagawa M, Makino S, Tamiya G (Corresponding author). J Hum Genet 2007 52(11):907-14 3.773
20
58 TAF1 as the most plausible disease gene of XDP/DYT3. (Contribution) Tamiya G (Corresponding author), Makino S, Kaji R. Am J Hum Genet 2007 81(2):417-8 11.043
6
57 Genetic Analysis of Craniofacial Traits in the Medaka. Kimura T, Shimada A, Sakai N, Mitani H, Naruse K, Takeda H, Inoko H, Tamiya G, Shinya M. Genetics 2007 177(4):2379-88 4.402
20
56 Synergistic association of mitochondrial Uncoupling Protein (UCP) genes with schizophrenia. Yasuno K, Ando S, Misumi S, Makino S, Kulski JK, Muratake T, Kaneko N, Amagane H, Someya T, Inoko H, Suga H, Kanemoto K, Tamiya G (Corresponding author). Neuropsychiatr Genet (Am J Med Genet B) 2007 144(2):250-3 3.358
35
55 Reduced Neuron-specific Expression of the TAF1 Gene Is Associated with X-linked Dystonia-Parkinsonism. Makino S, Kaji R, Ando S, Tomizawa M, Yasuno K, Goto S, Matsumoto S, Tabuena D, Maranon E, Dantes M, Lee LV, Ogasawara K, Tooyama I, Akatsu H, Nishimura M, Tamiya G (Corresponding author). Am J Hum Genet 2007 80(3):393-406 11.043
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54 Genome-wide association analysis of human narcolepsy and a new resistance gene. Kawashima M, Tamiya G, Oka A, Hohjoh H, Juji T, Ebisawa T, Honda Y, Inoko H, Tokunaga K. Am J Hum Genet 2006 79(2):252-63 11.043
57
53 Tumor necrosis factor-alpha signaling through activation of Kupffer cells plays an essential role in liver fibrosis of nonalcoholic steatohepatitis in mice. Tomita K, Tamiya G, Ando A, Ohsumi K, Chiyo T, Mizutani A, Kitamura N, Toda K, Kaneko T, Horie Y, Han JY, Kato S, Shimoda M, Oike Y, Tomizawa M, Makino S, Ohkura T, Saito H, Kumagai N, Nagata H, Ishii H, and Hibi T. Gut 2006 55(3):415-24 31.84
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52 AICAR, an AMPK activator, has protective effects on alcohol-induced fatty liver in rats. Tomita K, Tamiya G, Ando S, Kitamura N, Koizumi H, Kato S, Horie Y, Kaneko T, Azuma T, Nagata H, Ishii H, Hibi T. Alcohol Clin Exp Res 2005 29(12 Suppl):240S-5S 3.928
85
51 Gene expression profiling of Japanese psoriatic skin reveals an increased activity in molecular stress and immune-response signals. Kulski JK, Kenworthy W, Bellgard M, Taplin R, Okamoto K, Oka A, Mabuchi T, Ozawa A, Tamiya G, Inoko H. J Mol Med 2005 83(12):964-75 5.606
54
50 Immunohistochemical study of TAFII250 in the rat laryngeal nervous system. Okano H, Bamba H, Hisa Y, Makino S, Ando S, Tamiya G, Goto S, Kaji R, Kimura H, Tooyama I. Histol Histopathol 2005 20(4):1029-35 2.13
6
49 Molecular dissection and anatomical basis of dystonia: X-linked recessive dystonia-parkinsonism (DYT3). Kaji R, Goto S, Tamiya G, Ando S, Makino S, Lee LV. J Med Invest 2005 52 Suppl:280-3 -
10
48 Genetic linkage map of medaka with polymerase chain reaction length polymorphisms. Kimura T, Yoshida K, Shimada A, Jindo T, Mitani H, Naruse K, Takeda H, Inoko H, Tamiya G, Shinya M. Gene 2005 363:24-31 3.913
21
47 Genetic features of Khoton Mongolians revealed by SNP analysis of the X chromosome. Katoh T, Mano S, Munkhbat B, Tounai K, Oyungerel G, Chae GT, Han H, Jia GJ, Tokunaga K, Munkhtuvshin N, Tamiya G, Inoko H. Gene 2005 357(2):95-102 3.913
2
46 Whole Genome Association Study of Rheumatoid Arthritis Using 27,039 Microsatellites. Tamiya G, Shinya M, Imanishi T, Ikuta T, Makino S, Okamoto K, Furugaki K, Matsumoto T, Mano S, Ando S, Nozaki Y, Yukawa W, Nakashige R, Yamaguchi D, Ishibashi H, Yonekura M, Nakami Y, Takayama S, Endo T, Saruwatari T, Yagura M, Yoshikawa Y, Fujimoto K, Oka A, Chiku S, Linsen S.E.V, Giphart M.J, Kulski J.K, Fukazawa T, Hashimoto H, Kimura K, Hoshina Y, Suzuki Y, Hotta T, Mochida J, Minezaki T, Komai K, Shiozawa S, Taniguchi A, Yamanaka H, Kamatani N, Gojobori T, Bahram S, Inoko H. Hum Mol Genet 2005 14(16):2305-21 5.121
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45 Functional Anatomy of the Basal Ganglia in X-Linked Recessive Dystonia-Parkinsonism. Goto S, Lee LV, Dantes MB, Tooyama I, Tamiya G, Makino S, Ando S, Munoz EL, Yamada K, Matsumoto S, Shimazu H, Kuratsu J, Hirano A, Kaji R. Ann Neurol 2005 58(1):7-17 11.274
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44 Genetic features of Mongolian ethnic groups revealed by Y-chromosomal analysis. Katoh T, Munkhbat B, Tounai K, Mano S, Ando H, Oyungerel G, Chae GT, Han H, Jia GJ, Tokunaga K, Munkhtuvshin N, Tamiya G, Inoko H. Gene 2005 346:63-70 3.913
36
43 Identification and characterization of novel variants of the thioredoxin reductase 3 new transcript 1 TXNRD3NT1. Matsuzaka Y, Okamoto K, Mabuchi T, Iizuka M, Ozawa A, Oka A, Tamiya G, Kulski JK, Inoko H. Mamm Genome 2005 16(1):41-9 3.224
5
42 Identification, expression analysis and polymorphism of a novel RLTPR gene encoding a RGD motif, tropomodulin domain and proline/leucine-rich regions. Matsuzaka Y, Okamoto K, Mabuchi T, Iizuka M, Ozawa A, Oka A, Tamiya G, Kulski JK, Inoko H. Gene 2004 343(2):291-304 3.913
26
41 Novel Algorithm for Automated Genotyping of Microsatellites. Matsumoto T, Yukawa W, Nozaki N, Nakashige R, Shinya M, Makino S, Yagura M, Ikuta T, Imanishi T, Inoko H, Tamiya G, Gojobori T. Nucleic Acids Res 2004 32(20):6069-77 19.16
12
40 Leptin deficiency enhances sensitivity of rats to alcoholic steatohepatitis through suppression of metallothionein. Tomita K, Azuma T, Kitamura N, Tamiya G, Ando S, Nagata H, Kato S, Inokuchi S, Nishimura T, Ishii H, Hibi T. Am J Physiol -Gastrointest Liver Physiol 2004 287(5):G1078-85 4.889
28
39 hRDH-E2 gene polymorphisms, variable transcriptional start sites, and psoriasis. Matsuzaka Y, Okamoto K, Yoshikawa Y, Takaki A, Oka A, Mabuchi T, Iizuka M, Ozawa A, Tamiya G, Kulski JK, Inoko H. Mamm Genome 2004 15(8):668-75 3.224
5
38 Integrative annotation of 21,037 human genes validated by full-length cDNA clones. Imanishi T, Itoh T, et al. (Tamiya G ; 122th in 160 authors) PLoS Biol 2004 2(6):e162 9.593
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37 Notes on the maximum likelihood estimation of haplotype frequencies. Mano S, Yasuda N, Katoh T, Tounai K, Inoko H, Imanishi T, Tamiya G, Gojobori T. Ann Hum Genet 2004 68(Pt 3):257-64 2.18
6
36 Natural selection and popualtion history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in worldwide chromosomes. Nakajima T, Wooding S, Sakagami T, Emi M, Tokunaga K, Tamiya G, Ishigami T, Umemura S, Munkhbat B, Jin F, Guan-jun J, Hayasaka I, Ishida T, Saito N, Pavelka K, Lalouel JM, Jorde LB, Inoue I. Am J Hum Genet 2004 74(5):898-916 11.043
106
35 Pioglitazone prevents alcohol-induced fatty liver in rats through up-regulation of c-Met. Tomita K, Azuma T, Kitamura N, Nishida J, Tamiya G, Oka A, Inokuchi S, Nishimura T, Suematsu M, Ishii H. Gastroenterology 2004 126(3):873-85 33.883
115
34 Identification of two new C4 alleles by DNA sequencing and evidence for a historical recombination of serologically defined C4A and C4B alleles. Hui J, Oka A, Tomizawa M, Tay GK, Kulski JK, Penhale WJ, Iaschi SP, Makino S, Tamiya G, Inoko H. Tissue Antigens 2004 63(3):263-9 1.348
2
33 Identification of NAD+-dependent isocitrate dehydrogenase 3 gamma-like (IDH3GL) gene and its genetic polymorphisms. Okamoto K, Matsuzaka Y, Yoshikawa Y, Takaki A, Kulski JK, Tamiya G, Inoko H. Gene 2003 323:141-8 3.913
2
32 Toward identification of susceptibility genes for sporadic Parkinson's disease. Toda T, Momose Y, Murata M, Tamiya G, Yamamoto M, Hattori N, Inoko H. J Neurol 2003 250 Suppl 3:III40-3 6.682
51
31 Corneodesmosin gene: no evidence for PSORS 1 gene in North-eastern Thai psoriasis patients. Romphruk AV, Oka A, Romphruk A, Tomizawa M, Choonhakarn C, Naruse TK, Puapairoj C, Tamiya G, Leelayuwat C, Inoko H. Tissue Antigens 2003 62(3):217-24 1.348
12
30 Localization of a non-melanoma skin cancer susceptibility region within the Major Histocompatibility Complex by association analysis using microsatellite markers. Oka A, Hayashi H, Tomizawa M, Okamoto K, Hui L, Kulski JK, Beilby J, Tamiya G, Inoko H. Tissue Antigens 2003 61(3):203-10 1.348
23
29 SLURP-2, a novel member of the human Ly-6 superfamily that is up-regulated in psoriasis vulgaris. Tsuji H, Okamoto K, Matsuzaka Y, Iizuka H, Tamiya G, Inoko H. Genomics 2003 81(1): 26-33 4.31
76
28 Identification of IkappaBL as the Second Major Histocompatibility Complex-Linked Susceptibility Locus for Rheumatoid Arthritis. Okamoto K, Makino S, Yoshikawa Y, Takaki A, Nagatsuka Y, Ota M, Tamiya G, Kimura A, Bahram S, Inoko H. Am J Hum Genet 2003 72(2):303-12 11.043
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27 Identification of the hRDH-E2 gene, a novel member of the SDR family, and its increased expression in psoriatic lesion. Matsuzaka Y, Okamoto K, Tsuji H, Mabuchi T, Ozawa A, Tamiya G, Inoko H. Biochem Biophys Res Commun 2002 297(5):1171-80 3.322
17
26 Corneodesmosin DNA polymorphisms in MHC haplotypes and Japanese patients with psoriasis. Hui J, Oka A, Tamiya G, Tomizawa M, Kulski JK, Penhale WJ, Tay GK, Iizuka M, Ozawa A, Inoko H. Tissue Antigens 2002 60(1):77-83 1.348
17
25 Susceptibility locus for non-obstructive azoospermia is localized within the HLA-DR/DQ subregion: primary role of DQB1*0604. Matsuzaka Y, Makino S, Okamoto K, Oka A, Tsujimura A, Matsumiya K, Takahara S, Okuyama A, Sada M, Gotoh R, Nakatani T, Ota M, Katsuyama Y, Tamiya G, Inoko H. Tissue Antigens 2002 60(1):53-63 1.348
27
24 Identification of novel candidate genes in the diffuse panbronchiolitis critical region of the class I human MHC. Matsuzaka Y, Tounai K, Denda A, Tomizawa M, Makino S, Okamoto K, Keicho N, Oka A, Kulski JK, Tamiya G, Inoko H. Immunogenetics 2002 54(5):301-9 3.33
27
23 Genetic isolates in East Asia: a study of linkage disequilibrium in the X chromosome. Katoh T, Mano S, Ikuta T, Munkhbat B, Tounai K, Ando H, Munkhtuvshin N, Imanishi T, Inoko H, Tamiya G (Corresponding author). Am J Hum Genet 2002 71(2):395-400 11.043
40
22 Association of a determinant on mouse chromosome 18 with experimental severe Plasmodium berghei malaria. Nagayasu E, Nagakura K, Akaki M, Tamiya G, Makino S, Nakano Y, Kimura M, Aikawa M. Infect Immun 2002 70(2):512-6 3.621
27
21 New polymorphic microsatellite markers in the human MHC class III region. Matsuzaka Y, Makino S, Nakajima K, Tomizawa M, Oka A, Bahram S, Kulski JK, Tamiya G, Inoko H. Tissue Antigens 2001 57(5):397-404 1.348
27
20 Genomic anatomy of a premier major histocompatibility complex paralogous region on chromosome 1q21-q22. Shiina T, Ando A, Suto Y, Kasai F, Shigenari A, Takishima N, Kikkawa E, Iwata K, Kuwano Y, Kitamura Y, Matsuzawa Y, Sano K, Nogami M, Kawata H, Li S, Fukuzumi Y, Yamazaki M, Tashiro H, Tamiya G, Kohda A, Okumura K, Ikemura T, Soeda E, Mizuki N, Kimura M, Bahram S, Inoko H. Genome Res 2001 11(5):789-802 9.438
29
19 Bioinformatics issues for automating the annotation of genomic sequences. Carter K, Oka A, Tamiya G, Bellgard MI. Genome Inform Ser 2001 12:204-11 -
8
18 New polymorphic microsatellite markers in the human MHC class II region. Matsuzaka Y, Makino S, Nakajima K, Tomizawa M, Oka A, Kimura M, Bahram S, Tamiya G, Inoko H. Tissue Antigens 2000 56(6):492-500 1.348
27
17 Genomic organization, chromosomal localization, and the complete 22 kb DNA sequence of the human GCMa/GCM1, a placenta-specific transcription factor gene. Yamada K, Ogawa H, Tamiya G, Ikeno M, Morita M, Asakawa S, Shimizu N, Okazaki T. Biochem Biophys Res Commun 2000 278(1):134-9 3.322
11
16 Gene structure and promoter for Crad2 encoding mouse cis-retinol/3alpha-hydroxysterol short-chain dehydrogenase isozyme. Tomita K, Sato M, Kajiwara K, Tanaka M, Tamiya G, Makino S, Tomizawa M, Mizutani A, Kuwano Y, Shiina T, Ishii H, Kimura M. Gene 2000 251(2):175-86 3.913
13
15 Fine localization of a major disease-susceptibility locus for diffuse panbronchiolitis. Keicho N, Ohashi J, Tamiya G, Nakata K, Taguchi Y, Azuma A, Ohishi N, Emi M, Park MH, Inoko H, Tokunaga K, Kudoh S. Am J Hum Genet 2000 66(2):501-7 11.043
63
14 Association analysis using refined microsatellite markers localizes a susceptibility locus for psoriasis vulgaris within a 111 kb segment telomeric to the HLA-C gene. Oka A, Tamiya G, Tomizawa M, Ota M, Katsuyama Y, Makino S, Shiina T, Yoshitome M, Iizuka M, Sasao Y, Iwashita K, Kawakubo Y, Sugai J, Ozawa A, Ohkido M, Kimura M, Bahram S, Inoko H. Hum Mol Genet 1999 8(12):2165-70 5.121
149
13 Molecular dynamics of MHC genesis unraveled by sequence analysis of the 1,796,938-bp HLA class I region. Shiina T, Tamiya G, Oka A, Takishima N, Yamagata T, Kikkawa E, Iwata K, Tomizawa M, Okuaki N, Kuwano Y, Watanabe K, Fukuzumi Y, Itakura S, Sugawara C, Ono A, Yamazaki M, Tashiro H, Ando A, Ikemura T, Soeda E, Kimura M, Bahram S, Inoko H. Proc Natl Acad Sci USA 1999 96(23):13282-7 12.779
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12 Complete sequence and gene map of a human major histocompatibility complex. The MHC sequencing consortium. (Consortium members in alphabetical order: Aguado B, Bahram S, Beck S, Campbell RD, Forbes SA, Geraghty D, Guillaudeux T, Hood L, Horton R, Inoko H, Janer M, Jasoni C, Madan A, Milne S, Neville M, Oka A, Qin S, Ribas-Despuig G, Rogers J, Rowen L, Shiina T, Spies T, Tamiya G, Tashiro H, Trowsdale J, Vu Q, Williams L, Yamazaki M.) Nature 1999 401(6756):921-3 69.504
905
11 New polymorphic microsatellite markers in the human MHC class I region. Tamiya G, Shiina T, Oka A, Tomizawa M, Ota M, Katsuyama Y, Yoshitome M, Makino S, Kimura M, Inoko H. Tissue Antigens 1999 54(3):221-8 1.348
35
10 The critical region for Behcet disease in the human major histocompatibility complex is reduced to a 46-kb segment centromeric of HLA-B, by association analysis using refined microsatellite mapping. Ota M, Mizuki N, Katsuyama Y, Tamiya G, Shiina T, Oka A, Ando H, Kimura M, Goto K, Ohno S, Inoko H. Am J Hum Genet 1999 64(5):1406-10 11.043
96
9 Genome sequencing analysis of the 1.8 Mb entire human MHC class I region. Shiina T, Tamiya G, Oka A, Takishima N, Inoko H. Immunol Rev 1999 167:193-9 10.983
57
8 Physical mapping between the S and HLA-E genes in the human MHC class I region: construction of a BAC, PAC, and cosmid contig. Shiina T, Kikkawa E, Saito W, Tamiya G, Oka A, Watanabe K, Yamazaki M, Tashiro H, Okumura K, Ando A, Kimura M, Soeda E, Pontarotti P, Inoko H. Immunogenetics 1998 48(6):402-7 3.33
2
7 Microsatellite polymorphism within the MICB gene among Japanese patients with Behcet's disease. Kimura T, Goto K, Yabuki K, Mizuki N, Tamiya G, Sato M, Kimura M, Inoko H, Ohno S. Hum Immunol 1998 59(8):500-2 2.211
36
6 Twenty-six new polymorphic microsatellite markers around the HLA-B, -C and -E loci in the human MHC class I region. Tamiya G, Ota M, Katsuyama Y, Shiina T, Oka A, Makino S, Kimura M, Inoko H. Tissue Antigens 1998 51(4 Pt 1):337-46 1.348
69
5 Nucleotide sequencing analysis of the 146-kilobase segment around the IkBL and MICA genes at the centromeric end of the HLA class I region. Shiina T, Tamiya G, Oka A, Yamagata T, Yamagata N, Kikkawa E, Goto K, Mizuki N, Watanabe K, Fukuzumi Y, Taguchi S, Sugawara C, Ono A, Chen L, Yamazaki M, Tashiro H, Ando A, Ikemura T, Kimura M, Inoko H. Genomics 1998 47(3):372-82 4.31
74
4 An embryological study of ventralization of dorsal structures in the tail of medaka (Oryzias latipes) Da mutants. Tamiya G, Wakamatsu Y, Ozato K. Dev Growth Differ 1997 39(4):531-8 3.063
12
3 Physical mapping 220 kb centromeric of the human MHC and DNA sequence analysis of the 43-kb segment including the RING1, HKE6, and HKE4 genes. Kikuti YY, Tamiya G, Ando A, Chen L, Kimura M, Ferreira E, Tsuji K, Trowsdale J, Inoko H. Genomics 1997 42(3):422-35 4.31
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2 Genomic structure of the human MHC class I MICB gene. Bahram S, Shiina T, Oka A, Tamiya G, Inoko H. Immunogenetics 1996 45(2):161-2 3.33
32
1 An efficient expression vector for transgenic medaka construction. Takagi S, Sasado T, Tamiya G, Ozato K, Wakamatsu Y, Takeshita A, Kimura M. Mol Mar Biol Biotechnol (Mar Biotechnol) 1994 3(4):192-9 1.625 (discontinued)
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