Hiroaki Tomita
Hiroaki Tomita
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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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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