| Altered cortical glutamatergic and GABAergic signal transmission with glial involvement in depression PV Choudary, M Molnar, SJ Evans, H Tomita, JZ Li, MP Vawter, RM Myers, ... Proceedings of the National Academy of Sciences 102 (43), 15653-15658, 2005 | 790 | 2005 |
| Haploinsufficiency of NSD1 causes Sotos syndrome N Kurotaki, K Imaizumi, N Harada, M Masuno, T Kondoh, T Nagai, ... Nature genetics 30 (4), 365-366, 2002 | 683 | 2002 |
| Dysregulation of the fibroblast growth factor system in major depression SJ Evans, PV Choudary, CR Neal, JZ Li, MP Vawter, H Tomita, JF Lopez, ... Proceedings of the National Academy of Sciences 101 (43), 15506-15511, 2004 | 480 | 2004 |
| Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals M Nagasaki, J Yasuda, F Katsuoka, N Nariai, K Kojima, Y Kawai, ... Nature communications 6 (1), 8018, 2015 | 432 | 2015 |
| A SNP in the ABCC11 gene is the determinant of human earwax type K Yoshiura, A Kinoshita, T Ishida, A Ninokata, T Ishikawa, T Kaname, ... Nature genetics 38 (3), 324-330, 2006 | 360 | 2006 |
| Effect of agonal and postmortem factors on gene expression profile: quality control in microarray analyses of postmortem human brain H Tomita, MP Vawter, DM Walsh, SJ Evans, PV Choudary, J Li, ... Biological psychiatry 55 (4), 346-352, 2004 | 360 | 2004 |
| The Tohoku medical megabank project: design and mission S Kuriyama, N Yaegashi, F Nagami, T Arai, Y Kawaguchi, N Osumi, ... Journal of epidemiology 26 (9), 493-511, 2016 | 307 | 2016 |
| Systematic changes in gene expression in postmortem human brains associated with tissue pH and terminal medical conditions JZ Li, MP Vawter, DM Walsh, H Tomita, SJ Evans, PV Choudary, JF Lopez, ... Human molecular genetics 13 (6), 609-616, 2004 | 290 | 2004 |
| Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease A Kinoshita, T Saito, H Tomita, Y Makita, K Yoshida, M Ghadami, ... Nature genetics 26 (1), 19-20, 2000 | 287 | 2000 |
| Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11. 2-q12. 1 H Tomita, S Nagamitsu, K Wakui, Y Fukushima, K Yamada, M Sadamatsu, ... The American Journal of Human Genetics 65 (6), 1688-1697, 1999 | 261 | 1999 |
| Gender-specific gene expression in post-mortem human brain: localization to sex chromosomes MP Vawter, S Evans, P Choudary, H Tomita, J Meador-Woodruff, ... Neuropsychopharmacology 29 (2), 373-384, 2004 | 240 | 2004 |
| Mitochondrial-related gene expression changes are sensitive to agonal-pH state: implications for brain disorders MP Vawter, H Tomita, F Meng, B Bolstad, J Li, S Evans, P Choudary, ... Molecular psychiatry 11 (7), 663-679, 2006 | 212 | 2006 |
| Microarray technology: a review of new strategies to discover candidate vulnerability genes in psychiatric disorders WE Bunney, BG Bunney, MP Vawter, H Tomita, J Li, SJ Evans, ... American Journal of Psychiatry 160 (4), 657-666, 2003 | 194 | 2003 |
| Cohort profile: Tohoku medical megabank project birth and three-generation cohort study (TMM BirThree cohort study): rationale, progress and perspective S Kuriyama, H Metoki, M Kikuya, T Obara, M Ishikuro, C Yamanaka, ... International journal of epidemiology 49 (1), 18-19m, 2020 | 146 | 2020 |
| Methodological considerations for gene expression profiling of human brain M Atz, D Walsh, P Cartagena, J Li, S Evans, P Choudary, K Overman, ... Journal of neuroscience methods 163 (2), 295-309, 2007 | 136 | 2007 |
| Design and characterization of a highly selective peptide inhibitor of the small conductance calcium-activated K+ channel, SkCa2 VG Shakkottai, I Regaya, H Wulff, Z Fajloun, H Tomita, M Fathallah, ... Journal of Biological Chemistry 276 (46), 43145-43151, 2001 | 130 | 2001 |
| Study profile of the Tohoku medical megabank community-based cohort study A Hozawa, K Tanno, N Nakaya, T Nakamura, N Tsuchiya, T Hirata, ... Journal of epidemiology 31 (1), 65-76, 2021 | 120 | 2021 |
| Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions S Ono, K Yoshiura, A Kinoshita, T Kikuchi, Y Nakane, N Kato, ... Journal of human genetics 57 (5), 338-341, 2012 | 103 | 2012 |
| Novel truncated isoform of SK3 potassium channel is a potent dominant-negative regulator of SK currents: implications in schizophrenia H Tomita, VG Shakkottai, GA Gutman, G Sun, WE Bunney, MD Cahalan, ... Molecular psychiatry 8 (5), 524-535, 2003 | 100 | 2003 |
| Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13. 1-q13. 3 M Ghadami, Y Makita, K Yoshida, G Nishimura, Y Fukushima, K Wakui, ... The American Journal of Human Genetics 66 (1), 143-147, 2000 | 91 | 2000 |