| No | Title | Authors | Journal | Year | Vol: Page | |
|---|---|---|---|---|---|---|
| 173 | Body mass index stratification optimizes polygenic prediction of type 2 diabetes in cross-biobank analyses. | Ojima T, Namba S, Suzuki K, Yamamoto K, Sonehara K, Narita A; Tohoku Medical Megabank Project Study Group; Biobank Japan Project; Kamatani Y, Tamiya G, Yamamoto M, Yamauchi T, Kadowaki T, Okada Y. | Nat Genet. | 2024 | 56(6):1100-1109 | |
| 172 | Long-term clinical observation of patients with heterozygous KIF1A variants. | Kawashima A, Kodama K, Okubo Y, Endo W, Inui T, Ikeda M, Katata Y, Togashi N, Ohba C, Imagawa E, Iwama K, Mizuguchi T, Kitami M, Aihara Y, Takayama J, Tamiya G, Kikuchi A, Kure S, Saitsu H, Matsumoto N, Haginoya K. | Am J Med Genet A. | 2024 | Online ahead of print. | |
| 171 | A fine-scale genetic map of the Japanese population. | Takayama J, Makino S, Funayama T, Ueki M, Narita A, Murakami K, Orui M, Ishikuro M, Obara T; Tohoku Medical Megabank Project Study Group; Kuriyama S, Yamamoto M, Tamiya G. | Clin Genet. | 2024 | Online ahead of print. | |
| 170 | Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities. | Narumi S, Nagasaki K, Kiriya M, Uehara E, Akiba K, Tanase-Nakao K, Shimura K, Abe K, Sugisawa C, Ishii T, Miyako K, Hasegawa Y, Maruo Y, Muroya K, Watanabe N, Nishihara E, Ito Y, Kogai T, Kameyama K, Nakabayashi K, Hata K, Fukami M, Shima H, Kikuchi A, Takayama J, Tamiya G, Hasegawa T. | Nat Genet. | 2024 | Online ahead of print. | |
| 169 | Evaluation of AI-assisted colposcopy for detecting high-risk subtypes of human papillomavirus in CIN2 | Takahashi T, Matsuoka H, Kobayashi Y, Iwata T, Banno K, Yamagami W, Tamiya G. | Eur J Gynaecol Oncol. | 2024 | 143-146 | |
| 168 | Case Report: Identification of a CARD8 variant in all three patients with PFAPA syndrome complicated with Kawasaki disease. | Nakamura H, Kikuchi A, Sakai H, Kamimura M, Watanabe Y, Onuma R, Takayama J, Tamiya G, Mashimo Y, Ebata R, Hamada H, Suenaga T, Onouchi Y, Kumaki S. | Front Pediatr. | 2024 | 12:1340263 | |
| 167 | Development of phenotyping algorithms for hypertensive disorders of pregnancy (HDP) and their application in more than 22,000 pregnant women. | Mizuno S, Wagata M, Nagaie S, Ishikuro M, Obara T, Tamiya G, Kuriyama S, Tanaka H, Yaegashi N, Yamamoto M, Sugawara J, Ogishima S. | Sci Rep. | 2024 | 14(1):6292 | |
| 166 | Genetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population. | Yaoita H, Kawai E, Takayama J, Iwasawa S, Saijo N, Abiko M, Suzuki K, Kimura M, Ozawa A, Tamiya G, Kure S, Kikuchi A. | J Hum Genet. | 2024 | 69(5):177-183 | |
| 165 | Treatment of ZC4H2 Variant-Associated Spastic Paraplegia with Selective Dorsal Rhizotomy and Intensive Postoperative Rehabilitation: A Case Report. | Inotani T, Horaguchi A, Morishita Y, Yoshida A, Otomo M, Suzuki M, Inui T, Okubo Y, Komatsu S, Mizuno C, Takahashi Y, Ochiai T, Kinjo T, Asato T, Takayama J, Tamiya G, Saijo N, Kikuchi A, Haginoya K. | Tohoku J Exp Med. | 2024 | 262(4):239-244 | |
| 164 | Study Profile of the Tsuruoka Metabolomics Cohort Study (TMCS). | Harada S, Iida M, Miyagawa N, Hirata A, Kuwabara K, Matsumoto M, Okamura T, Edagawa S, Kawada Y, Miyake A, Toki R, Akiyama M, Kawai A, Sugiyama D, Sato Y, Takemura R, Fukai K, Ishibashi Y, Kato S, Kurihara A, Sata M, Shibuki T, Takeuchi A, Kohsaka S, Sawano M, Shoji S, Izawa Y, Katsumata M, Oki K, Takahashi S, Takizawa T, Maruya H, Nishiwaki Y, Kawasaki R, Hirayama A, Ishikawa T, Saito R, Sato A, Soga T, Sugimoto M, Tomita M, Komaki S, Ohmomo H, Ono K, Otsuka-Yamasaki Y, Shimizu A, Sutoh Y, Hozawa A, Kinoshita K, Koshiba S, Kumada K, Ogishima S, Sakurai-Yageta M, Tamiya G, Takebayashi T. | J Epidemiol. | 2024 | Online ahead of print. | |
| 163 | Machine Learning of Histopathological Images Predicts Recurrences of Resected Pancreatic Ductal Adenocarcinoma With Adjuvant Treatment. | Yamaguchi R, Morikawa H, Akatsuka J, Numata Y, Noguchi A, Kokumai T, Ishida M, Mizuma M, Nakagawa K, Unno M, Miyake A, Tamiya G, Yamamoto Y, Furukawa T. | Pancreas. | 2024 | 53(2):e199-e204. | |
| 162 | jMorp: Japanese Multi-Omics Reference Panel update report 2023. | Tadaka S, Kawashima J, Hishinuma E, Saito S, Okamura Y, Otsuki A, Kojima K, Komaki S, Aoki Y, Kanno T, Saigusa D, Inoue J, Shirota M, Takayama J, Katsuoka F, Shimizu A, Tamiya G, Shimizu R, Hiratsuka M, Motoike IN, Koshiba S, Sasaki M, Yamamoto M, Kinoshita K. | Nucleic Acids Res. | 2024 | 52(D1):D622-D632 | |
| 161 | Influence of Diabetes Family History on the Associations of Combined Genetic and Lifestyle Risks with Diabetes in the Tohoku Medical Megabank Community-Based Cohort Study. | Takase M, Nakaya N, Nakamura T, Kogure M, Hatanaka R, Nakaya K, Chiba I, Kanno I, Nochioka K, Tsuchiya N, Hirata T, Narita A, Obara T, Ishikuro M, Uruno A, Kobayashi T, N Kodama E, Hamanaka Y, Orui M, Ogishima S, Nagaie S, Fuse N, Sugawara J, Kuriyama S, Tsuji I, Tamiya G, Hozawa A, Yamamoto M. | J Atheroscler Thromb. | 2023 | 30(12):1950-1965 | |
| 160 | Establishment of the early prediction models of low-birth-weight reveals influential genetic and environmental factors: a prospective cohort study. | Mizuno S, Nagaie S, Tamiya G, Kuriyama S, Obara T, Ishikuro M, Tanaka H, Kinoshita K, Sugawara J, Yamamoto M, Yaegashi N, Ogishima S. | BMC Pregnancy Childbirth | 2023 | 23(1):628 | |
| 159 | Comprehensive evaluation of machine learning algorithms for predicting sleep-wake conditions and differentiating between the wake conditions before and after sleep during pregnancy based on heart rate variability. | Li X, Ono C, Warita N, Shoji T, Nakagawa T, Usukura H, Yu Z, Takahashi Y, Ichiji K, Sugita N, Kobayashi N, Kikuchi S, Kimura R, Hamaie Y, Hino M, 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, Fujii S, Nakayama M, Kuriyama S, Yamamoto M, Yaegashi N, Homma N, Tomita H. | Front Psychiatry | 2023 | 14:1104222 | |
| 158 | A Case Series of Patients With MYBPC1 Gene Variants Featuring Undulating Tongue Movements as Myogenic Tremor. | Uneoka S, Kobayashi T, Numata-Uematsu Y, Oikawa Y, Katata Y, Okubo Y, Abe Y, Kikuchi A, Takayama J, Tamiya G, Kure S, Saito K, Uematsu M. | Pediatr Neurol. | 2023 | 146:16-20 | |
| 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 | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 142 | Smooth-threshold multivariate genetic prediction incorporating gene-environment interactions. | Ueki M, Tamiya G | G3 Genes|Genomes|Genetics | 2021 | 11(12):jkab278 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 123 | Artificial intelligence powered statistical genetics in biobanks. | Narita A, Ueki M, Tamiya G. | J Hum Genet | 2020 | 66:61-65 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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｡ﾇs Disease Neuroimaging Initiative and the Alzheimer｡ﾇs Disease Metabolomics Consortium. | PLoS ONE | 2019 | 14(7):e0219825 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 91 | Smooth-threshold multivariate genetic prediction with unbiased model selection. | Ueki M, Tamiya G | Genet Epidemiol | 2016 | 40(3): 233-43 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 66 | Ultrahigh-dimensional variable selection method for whole-genome gene-gene interaction analysis. | Ueki M, Tamiya G. | BMC Bioinformatics | 2012 | 13(1):72 | |
| 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 | |
| 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 | |
| 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 | |
| 62 | Transcriptional dysregulation: a cause of dystonia? | Tamiya G (Corresponding author). | Lancet Neurol | 2009 | 8(5):416-8 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | 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 | 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 | |
| 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 | |
| 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 |