| Year |
Citation |
Score |
| 2022 |
Kushima I, Nakatochi M, Aleksic B, Okada T, Kimura H, Kato H, Morikawa M, Inada T, Ishizuka K, Torii Y, Nakamura Y, Tanaka S, Imaeda M, Takahashi N, Yamamoto M, ... ... Yoshikawa T, et al. Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder. Biological Psychiatry. PMID 35667888 DOI: 10.1016/j.biopsych.2022.04.003 |
0.35 |
|
| 2022 |
Uezato A, Jitoku D, Shimazu D, Yamamoto N, Kurumaji A, Iwayama Y, Toyota T, Yoshikawa T, Haroutunian V, Bentea E, Meller J, Sullivan CR, Meador-Woodruff JH, McCullumsmith RE, Nishikawa T. Differential genetic associations and expression of PAPST1/SLC35B2 in bipolar disorder and schizophrenia. Journal of Neural Transmission (Vienna, Austria : 1996). PMID 35501530 DOI: 10.1007/s00702-022-02503-7 |
0.369 |
|
| 2021 |
Balan S, Iwayama Y, Ohnishi T, Fukuda M, Shirai A, Yamada A, Weirich S, Schuhmacher MK, Dileep KV, Endo T, Hisano Y, Kotoshiba K, Toyota T, Otowa T, Kuwabara H, ... ... Yoshikawa T, et al. A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brain. Molecular Psychiatry. PMID 34262135 DOI: 10.1038/s41380-021-01199-7 |
0.806 |
|
| 2021 |
Hara T, Toyoshima M, Hisano Y, Balan S, Iwayama Y, Aono H, Futamura Y, Osada H, Owada Y, Yoshikawa T. Glyoxalase I disruption and external carbonyl stress impair mitochondrial function in human induced pluripotent stem cells and derived neurons. Translational Psychiatry. 11: 275. PMID 33966051 DOI: 10.1038/s41398-021-01392-w |
0.663 |
|
| 2021 |
Ohnishi T, Kiyama Y, Arima-Yoshida F, Kadota M, Ichikawa T, Yamada K, Watanabe A, Ohba H, Tanaka K, Nakaya A, Horiuchi Y, Iwayama Y, Toyoshima M, Ogawa I, Shimamoto-Mitsuyama C, ... ... Yoshikawa T, et al. Cooperation of LIM domain-binding 2 (LDB2) with EGR in the pathogenesis of schizophrenia. Embo Molecular Medicine. e12574. PMID 33656268 DOI: 10.15252/emmm.202012574 |
0.836 |
|
| 2021 |
Balan S, Ohnishi T, Watanabe A, Ohba H, Iwayama Y, Toyoshima M, Hara T, Hisano Y, Miyasaka Y, Toyota T, Shimamoto-Mitsuyama C, Maekawa M, Numata S, Ohmori T, Shimogori T, ... ... Yoshikawa T, et al. Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia. Schizophrenia Bulletin. PMID 33595068 DOI: 10.1093/schbul/sbab007 |
0.824 |
|
| 2021 |
Ogata S, Hashizume K, Hayase Y, Kanno Y, Hori K, Balan S, Yoshikawa T, Takahashi H, Taya S, Hoshino M. Potential involvement of DSCAML1 mutations in neurodevelopmental disorders. Genes to Cells : Devoted to Molecular & Cellular Mechanisms. PMID 33501714 DOI: 10.1111/gtc.12831 |
0.704 |
|
| 2021 |
Oishi K, Niitsu T, Kanahara N, Sato Y, Iwayama Y, Toyota T, Hashimoto T, Sasaki T, Takase M, Shiina A, Yoshikawa T, Iyo M. Genetic risks of schizophrenia identified in a matched case-control study. European Archives of Psychiatry and Clinical Neuroscience. 271: 775-781. PMID 32623490 DOI: 10.1007/s00406-020-01158-3 |
0.338 |
|
| 2020 |
Wada Y, Maekawa M, Ohnishi T, Balan S, Matsuoka S, Iwamoto K, Iwayama Y, Ohba H, Watanabe A, Hisano Y, Nozaki Y, Toyota T, Shimogori T, Itokawa M, Kobayashi T, ... Yoshikawa T, et al. Peroxisome proliferator-activated receptor α as a novel therapeutic target for schizophrenia. Ebiomedicine. 103130. PMID 33279456 DOI: 10.1016/j.ebiom.2020.103130 |
0.805 |
|
| 2020 |
Hayase Y, Amano S, Hashizume K, Tominaga T, Miyamoto H, Kanno Y, Ueno-Inoue Y, Inoue T, Yamada M, Ogata S, Balan S, Hayashi K, Miura Y, Tokudome K, Ohno Y, ... ... Yoshikawa T, et al. Down syndrome cell adhesion molecule like-1 (DSCAML1) links the GABA system and seizure susceptibility. Acta Neuropathologica Communications. 8: 206. PMID 33256836 DOI: 10.1186/s40478-020-01082-6 |
0.655 |
|
| 2020 |
Maekawa M, Ohnishi T, Toyoshima M, Shimamoto-Mitsuyama C, Hamazaki K, Balan S, Wada Y, Esaki K, Takagai S, Tsuchiya KJ, Nakamura K, Iwata Y, Nara T, Iwayama Y, Toyota T, ... ... Yoshikawa T, et al. A potential role of fatty acid binding protein 4 in the pathophysiology of autism spectrum disorder. Brain Communications. 2: fcaa145. PMID 33225276 DOI: 10.1093/braincomms/fcaa145 |
0.797 |
|
| 2020 |
Horiuchi Y, Ichikawa T, Ohnishi T, Iwayama Y, Toriumi K, Miyashita M, Nohara I, Obata N, Toyota T, Yoshikawa T, Itokawa M, Arai M. locus disruption on 4p16.1 as a risk factor for schizophrenia and bipolar disorder. Human Genome Variation. 7: 31. PMID 33082982 DOI: 10.1038/s41439-020-00117-7 |
0.714 |
|
| 2020 |
Shimamoto-Mitsuyama C, Nakaya A, Esaki K, Balan S, Iwayama Y, Ohnishi T, Maekawa M, Toyota T, Dean B, Yoshikawa T. Lipid Pathology of the Corpus Callosum in Schizophrenia and the Potential Role of Abnormal Gene Regulatory Networks with Reduced Microglial Marker Expression. Cerebral Cortex (New York, N.Y. : 1991). PMID 32924060 DOI: 10.1093/cercor/bhaa236 |
0.828 |
|
| 2020 |
Usui N, Iwata K, Miyachi T, Takagai S, Wakusawa K, Nara T, Tsuchiya KJ, Matsumoto K, Kurita D, Kameno Y, Wakuda T, Takebayashi K, Iwata Y, Fujioka T, Hirai T, ... ... Yoshikawa T, et al. VLDL-specific increases of fatty acids in autism spectrum disorder correlate with social interaction. Ebiomedicine. 58: 102917. PMID 32739868 DOI: 10.1016/j.ebiom.2020.102917 |
0.748 |
|
| 2020 |
Qu Y, Zhang K, Pu Y, Chang L, Wang S, Tan Y, Wang X, Zhang J, Ohnishi T, Yoshikawa T, Hashimoto K. Betaine supplementation is associated with the resilience in mice after chronic social defeat stress: a role of brain-gut-microbiota axis. Journal of Affective Disorders. 272: 66-76. PMID 32379622 DOI: 10.1016/j.jad.2020.03.095 |
0.629 |
|
| 2020 |
Esaki K, Balan S, Iwayama Y, Shimamoto-Mitsuyama C, Hirabayashi Y, Dean B, Yoshikawa T. Evidence for Altered Metabolism of Sphingosine-1-Phosphate in the Corpus Callosum of Patients with Schizophrenia. Schizophrenia Bulletin. PMID 32346731 DOI: 10.1093/schbul/sbaa052 |
0.743 |
|
| 2019 |
Ide M, Ohnishi T, Toyoshima M, Balan S, Maekawa M, Shimamoto-Mitsuyama C, Iwayama Y, Ohba H, Watanabe A, Ishii T, Shibuya N, Kimura Y, Hisano Y, Murata Y, Hara T, ... ... Yoshikawa T, et al. Excess hydrogen sulfide and polysulfides production underlies a schizophrenia pathophysiology. Embo Molecular Medicine. e10695. PMID 31657521 DOI: 10.15252/Emmm.201910695 |
0.817 |
|
| 2019 |
Toyoshima M, Jiang X, Ogawa T, Ohnishi T, Yoshihara S, Balan S, Yoshikawa T, Hirokawa N. Enhanced carbonyl stress induces irreversible multimerization of CRMP2 in schizophrenia pathogenesis. Life Science Alliance. 2. PMID 31591136 DOI: 10.26508/lsa.201900478 |
0.793 |
|
| 2019 |
Ohnishi T, Balan S, Toyoshima M, Maekawa M, Ohba H, Watanabe A, Iwayama Y, Fujita Y, Tan Y, Hisano Y, Shimamoto-Mitsuyama C, Nozaki Y, Esaki K, Nagaoka A, Matsumoto J, ... ... Yoshikawa T, et al. Investigation of betaine as a novel psychotherapeutic for schizophrenia. Ebiomedicine. PMID 31255657 DOI: 10.1016/j.ebiom.2019.05.062 |
0.817 |
|
| 2019 |
Ma M, Ren Q, Yang J, Zhang K, Xiong Z, Ishima T, Pu Y, Hwang SH, Toyoshima M, Iwayama Y, Hisano Y, Yoshikawa T, Hammock BD, Hashimoto K. Key role of soluble epoxide hydrolase in the neurodevelopmental disorders of offspring after maternal immune activation. Proceedings of the National Academy of Sciences of the United States of America. PMID 30890645 DOI: 10.1073/Pnas.1819234116 |
0.34 |
|
| 2019 |
Vadgama N, Pittman A, Simpson M, Nirmalananthan N, Murray R, Yoshikawa T, De Rijk P, Rees E, Kirov G, Hughes D, Fitzgerald T, Kristiansen M, Pearce K, Cerveira E, Zhu Q, et al. De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes. European Journal of Human Genetics : Ejhg. PMID 30886340 DOI: 10.1038/S41431-019-0376-7 |
0.334 |
|
| 2019 |
Shimamoto-Mitsuyama C, Ohnishi T, Balan S, Ohba H, Watanabe A, Maekawa M, Hisano Y, Iwayama Y, Owada Y, Yoshikawa T. Evaluation of the role of fatty acid-binding protein 7 in controlling schizophrenia-relevant phenotypes using newly established knockout mice. Schizophrenia Research. PMID 30765249 DOI: 10.1016/j.schres.2019.02.002 |
0.831 |
|
| 2018 |
Nakamura T, Nakajima K, Ohnishi T, Yoshikawa T, Nakanishi M, Takumi T, Tsuboi T, Kato T. Quantitative evaluation of incomplete preweaning lethality in mice by using the CRISPR/Cas9 system. Scientific Reports. 8: 16025. PMID 30375401 DOI: 10.1038/s41598-018-34270-5 |
0.65 |
|
| 2018 |
Ikeda M, Takahashi A, Kamatani Y, Momozawa Y, Saito T, Kondo K, Shimasaki A, Kawase K, Sakusabe T, Iwayama Y, Toyota T, Wakuda T, Kikuchi M, Kanahara N, Yamamori H, ... ... Yoshikawa T, et al. Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. Schizophrenia Bulletin. PMID 30285260 DOI: 10.1093/Schbul/Sby140 |
0.316 |
|
| 2018 |
Kushima I, Aleksic B, Nakatochi M, Shimamura T, Okada T, Uno Y, Morikawa M, Ishizuka K, Shiino T, Kimura H, Arioka Y, Yoshimi A, Takasaki Y, Yu Y, Nakamura Y, ... ... Yoshikawa T, ... ... Yoshikawa T, et al. Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights. Cell Reports. 24: 2838-2856. PMID 30208311 DOI: 10.1016/J.Celrep.2018.08.022 |
0.388 |
|
| 2018 |
Maekawa M, Ohnishi T, Balan S, Hisano Y, Nozaki Y, Ohba H, Toyoshima M, Shimamoto C, Tabata C, Wada Y, Yoshikawa T. Thiosulfate promotes hair growth in mouse model. Bioscience, Biotechnology, and Biochemistry. 1-9. PMID 30200826 DOI: 10.1080/09168451.2018.1518705 |
0.749 |
|
| 2018 |
Balan S, Toyoshima M, Yoshikawa T. Contribution of induced pluripotent stem cell technologies to the understanding of cellular phenotypes in schizophrenia. Neurobiology of Disease. PMID 29729395 DOI: 10.1016/j.nbd.2018.04.021 |
0.733 |
|
| 2018 |
Tomioka Y, Numata S, Kinoshita M, Umehara H, Watanabe SY, Nakataki M, Iwayama Y, Toyota T, Ikeda M, Yamamori H, Shimodera S, Tajima A, Hashimoto R, Iwata N, Yoshikawa T, et al. Decreased serum pyridoxal levels in schizophrenia: meta-analysis and Mendelian randomization analysis. Journal of Psychiatry & Neuroscience : Jpn. 43: 194-200. PMID 29688875 DOI: 10.1503/jpn.170053 |
0.304 |
|
| 2018 |
Tomioka Y, Numata S, Kinoshita M, Umehara H, Watanabe SY, Nakataki M, Iwayama Y, Toyota T, Ikeda M, Yamamori H, Shimodera S, Tajima A, Hashimoto R, Iwata N, Yoshikawa T, et al. Decreased serum pyridoxal levels in schizophrenia: meta-analysis and Mendelian randomization analysis. Journal of Psychiatry & Neuroscience : Jpn. 43: 170053. PMID 29402374 DOI: 10.1503/jpn.170053 |
0.304 |
|
| 2018 |
Matsuura A, Ishima T, Fujita Y, Iwayama Y, Hasegawa S, Kawahara-Miki R, Maekawa M, Toyoshima M, Ushida Y, Suganuma H, Kida S, Yoshikawa T, Iyo M, Hashimoto K. Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation. Scientific Reports. 8: 2158. PMID 29391571 DOI: 10.1038/S41598-018-20538-3 |
0.659 |
|
| 2018 |
Shimazu T, Furuse T, Balan S, Yamada I, Okuno S, Iwanari H, Suzuki T, Hamakubo T, Dohmae N, Yoshikawa T, Wakana S, Shinkai Y. Role of METTL20 in regulating β-oxidation and heat production in mice under fasting or ketogenic conditions. Scientific Reports. 8: 1179. PMID 29352221 DOI: 10.1038/s41598-018-19615-4 |
0.644 |
|
| 2018 |
Kobayashi M, Jitoku D, Iwayama Y, Yamamoto N, Toyota T, Suzuki K, Kikuchi M, Hashimoto T, Kanahara N, Kurumaji A, Yoshikawa T, Nishikawa T. Association studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population. Plos One. 13: e0190991. PMID 29309433 DOI: 10.1371/journal.pone.0190991 |
0.412 |
|
| 2017 |
Uezato A, Yamamoto N, Jitoku D, Haramo E, Hiraaki E, Iwayama Y, Toyota T, Umino M, Umino A, Iwata Y, Suzuki K, Kikuchi M, Hashimoto T, Kanahara N, Kurumaji A, ... Yoshikawa T, et al. Genetic and molecular risk factors within the newly identified primate-specific exon of the SAP97/DLG1 gene in the 3q29 schizophrenia-associated locus. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 28990294 DOI: 10.1002/ajmg.b.32595 |
0.457 |
|
| 2017 |
Morimura N, Yasuda H, Yamaguchi K, Katayama KI, Hatayama M, Tomioka NH, Odagawa M, Kamiya A, Iwayama Y, Maekawa M, Nakamura K, Matsuzaki H, Tsujii M, Yamada K, Yoshikawa T, et al. Autism-like behaviours and enhanced memory formation and synaptic plasticity in Lrfn2/SALM1-deficient mice. Nature Communications. 8: 15800. PMID 28604739 DOI: 10.1038/ncomms15800 |
0.615 |
|
| 2017 |
Balan S, Yamada K, Iwayama Y, Hashimoto T, Toyota T, Shimamoto C, Maekawa M, Takagai S, Wakuda T, Kameno Y, Kurita D, Yamada K, Kikuchi M, Hashimoto T, Kanahara N, ... Yoshikawa T, et al. Comprehensive association analysis of 27 genes from the GABAergic system in Japanese individuals affected with schizophrenia. Schizophrenia Research. PMID 28073605 DOI: 10.1016/J.Schres.2017.01.003 |
0.826 |
|
| 2016 |
Ohnishi T, Miura I, Ohba H, Shimamoto C, Iwayama Y, Wakana S, Yoshikawa T. A spontaneous and novel Pax3 mutant mouse that models Waardenburg syndrome and neural tube defects. Gene. PMID 28043919 DOI: 10.1016/j.gene.2016.12.037 |
0.624 |
|
| 2016 |
Miyashita M, Watanabe T, Ichikawa T, Toriumi K, Horiuchi Y, Kobori A, Kushima I, Hashimoto R, Fukumoto M, Koike S, Ujike H, Arinami T, Tatebayashi Y, Kasai K, Takeda M, ... ... Yoshikawa T, et al. The regulation of soluble receptor for AGEs contributes to carbonyl stress in schizophrenia. Biochemical and Biophysical Research Communications. PMID 27641663 DOI: 10.1016/J.Bbrc.2016.09.074 |
0.337 |
|
| 2016 |
Maekawa M, Iwayama Y, Ohnishi T, Toyoshima M, Shimamoto C, Hisano Y, Toyota T, Balan S, Matsuzaki H, Iwata Y, Takagai S, Yamada K, Ota M, Fukuchi S, Okada Y, ... ... Yoshikawa T, et al. Erratum: Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism. Scientific Reports. 6: 20268. PMID 26822806 DOI: 10.1038/Srep20268 |
0.778 |
|
| 2016 |
Hamazaki K, Maekawa M, Toyota T, Iwayama Y, Dean B, Hamazaki T, Yoshikawa T. Fatty acid composition and fatty acid binding protein expression in the postmortem frontal cortex of patients with schizophrenia: A case-control study. Schizophrenia Research. PMID 26792082 DOI: 10.1016/j.schres.2016.01.014 |
0.636 |
|
| 2015 |
Maekawa M, Iwayama Y, Ohnishi T, Toyoshima M, Shimamoto C, Hisano Y, Toyota T, Balan S, Matsuzaki H, Iwata Y, Takagai S, Yamada K, Ota M, Fukuchi S, Okada Y, ... ... Yoshikawa T, et al. Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism. Scientific Reports. 5: 16239. PMID 26548558 DOI: 10.1038/Srep16239 |
0.811 |
|
| 2015 |
Yamada K, Hattori E, Iwayama Y, Toyota T, Iwata Y, Suzuki K, Kikuchi M, Hashimoto T, Kanahara N, Mori N, Yoshikawa T. Population-dependent contribution of the major histocompatibility complex region to schizophrenia susceptibility. Schizophrenia Research. 168: 444-9. PMID 26324334 DOI: 10.1016/j.schres.2015.08.018 |
0.385 |
|
| 2015 |
Liu X, Shimada T, Otowa T, Wu YY, Kawamura Y, Tochigi M, Iwata Y, Umekage T, Toyota T, Maekawa M, Iwayama Y, Suzuki K, Kakiuchi C, Kuwabara H, Kano Y, ... ... Yoshikawa T, et al. Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations. Autism Research : Official Journal of the International Society For Autism Research. PMID 26314684 DOI: 10.1002/Aur.1536 |
0.675 |
|
| 2015 |
Ebrahimi M, Yamamoto Y, Sharifi K, Kida H, Kagawa Y, Yasumoto Y, Islam A, Miyazaki H, Shimamoto C, Maekawa M, Mitsushima D, Yoshikawa T, Owada Y. Astrocyte-expressed FABP7 regulates dendritic morphology and excitatory synaptic function of cortical neurons. Glia. PMID 26296243 DOI: 10.1002/glia.22902 |
0.618 |
|
| 2015 |
Hamazaki K, Maekawa M, Toyota T, Dean B, Hamazaki T, Yoshikawa T. Fatty acid composition of the postmortem prefrontal cortex of patients with schizophrenia, bipolar disorder, and major depressive disorder. Psychiatry Research. 227: 353-9. PMID 25858798 DOI: 10.1016/j.psychres.2015.01.004 |
0.664 |
|
| 2015 |
Shimamoto C, Ohnishi T, Maekawa M, Watanabe A, Ohba H, Arai R, Iwayama Y, Hisano Y, Toyota T, Toyoshima M, Suzuki K, Shirayama Y, Nakamura K, Mori N, Owada Y, ... ... Yoshikawa T, et al. Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies. Human Molecular Genetics. 24: 2409. PMID 25655139 DOI: 10.1093/hmg/ddv011 |
0.817 |
|
| 2015 |
Bangel FN, Yamada K, Arai M, Iwayama Y, Balan S, Toyota T, Iwata Y, Suzuki K, Kikuchi M, Hashimoto T, Kanahara N, Mori N, Itokawa M, Stork O, Yoshikawa T. Genetic analysis of the glyoxalase system in schizophrenia. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 59: 105-10. PMID 25645869 DOI: 10.1016/J.Pnpbp.2015.01.014 |
0.757 |
|
| 2015 |
Kagawa Y, Yasumoto Y, Sharifi K, Ebrahimi M, Islam A, Miyazaki H, Yamamoto Y, Sawada T, Kishi H, Kobayashi S, Maekawa M, Yoshikawa T, Takaki E, Nakai A, Kogo H, et al. Fatty acid-binding protein 7 regulates function of caveolae in astrocytes through expression of caveolin-1. Glia. 63: 780-94. PMID 25601031 DOI: 10.1002/Glia.22784 |
0.587 |
|
| 2015 |
Maekawa M, Yamada K, Toyoshima M, Ohnishi T, Iwayama Y, Shimamoto C, Toyota T, Nozaki Y, Balan S, Matsuzaki H, Iwata Y, Suzuki K, Miyashita M, Kikuchi M, Kato M, ... ... Yoshikawa T, et al. Utility of Scalp Hair Follicles as a Novel Source of Biomarker Genes for Psychiatric Illnesses. Biological Psychiatry. 78: 116-25. PMID 25444170 DOI: 10.1016/J.Biopsych.2014.07.025 |
0.803 |
|
| 2015 |
Jitoku D, Yamamoto N, Iwayama Y, Toyota T, Miyagi M, Enokida T, Tasaka Y, Umino M, Umino A, Uezato A, Iwata Y, Suzuki K, Kikuchi M, Hashimoto T, Kanahara N, ... ... Yoshikawa T, et al. Association study of H2AFZ with schizophrenia in a Japanese case-control sample. Journal of Neural Transmission (Vienna, Austria : 1996). 122: 915-23. PMID 25392085 DOI: 10.1007/s00702-014-1332-x |
0.392 |
|
| 2015 |
Kimura H, Tsuboi D, Wang C, Kushima I, Koide T, Ikeda M, Iwayama Y, Toyota T, Yamamoto N, Kunimoto S, Nakamura Y, Yoshimi A, Banno M, Xing J, Takasaki Y, ... ... Yoshikawa T, et al. Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility. Schizophrenia Bulletin. 41: 744-53. PMID 25332407 DOI: 10.1093/Schbul/Sbu147 |
0.37 |
|
| 2015 |
Balan S, Iwayama Y, Yamada K, Toyota T, Ohnishi T, Toyoshima M, Shimamoto C, Ide M, Iwata Y, Suzuki K, Kikuchi M, Hashimoto T, Kanahara N, Yoshikawa T, Maekawa M. Sequencing and expression analyses of the synaptic lipid raft adapter gene PAG1 in schizophrenia. Journal of Neural Transmission (Vienna, Austria : 1996). 122: 477-85. PMID 25005592 DOI: 10.1007/s00702-014-1269-0 |
0.827 |
|
| 2014 |
Balan S, Iwayama Y, Maekawa M, Toyota T, Ohnishi T, Toyoshima M, Shimamoto C, Esaki K, Yamada K, Iwata Y, Suzuki K, Ide M, Ota M, Fukuchi S, Tsujii M, ... ... Yoshikawa T, et al. Exon resequencing of H3K9 methyltransferase complex genes, EHMT1, EHTM2 and WIZ, in Japanese autism subjects. Molecular Autism. 5: 49. PMID 25400900 DOI: 10.1186/2040-2392-5-49 |
0.81 |
|
| 2014 |
Shimamoto C, Ohnishi T, Maekawa M, Watanabe A, Ohba H, Arai R, Iwayama Y, Hisano Y, Toyota T, Toyoshima M, Suzuki K, Shirayama Y, Nakamura K, Mori N, Owada Y, ... ... Yoshikawa T, et al. Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies. Human Molecular Genetics. 23: 6495-511. PMID 25027319 DOI: 10.1093/hmg/ddu369 |
0.833 |
|
| 2014 |
Saito T, Kondo K, Iwayama Y, Shimasaki A, Aleksic B, Yamada K, Toyota T, Hattori E, Esaki K, Ujike H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ozaki N, et al. Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 421-7. PMID 24888570 DOI: 10.1002/Ajmg.B.32246 |
0.301 |
|
| 2014 |
Okahara K, Kizuka Y, Kitazume S, Ota F, Nakajima K, Hirabayashi Y, Maekawa M, Yoshikawa T, Taniguchi N. Ceramide galactosyltransferase expression is regulated positively by Nkx2.2 and negatively by OLIG2. Glycobiology. 24: 926-34. PMID 24821492 DOI: 10.1093/glycob/cwu042 |
0.588 |
|
| 2014 |
Ohnishi T, Murata T, Watanabe A, Hida A, Ohba H, Iwayama Y, Mishima K, Gondo Y, Yoshikawa T. Defective craniofacial development and brain function in a mouse model for depletion of intracellular inositol synthesis. The Journal of Biological Chemistry. 289: 10785-96. PMID 24554717 DOI: 10.1074/Jbc.M113.536706 |
0.663 |
|
| 2014 |
Nishimura Y, Takizawa R, Koike S, Kinoshita A, Satomura Y, Kawasaki S, Yamasue H, Tochigi M, Kakiuchi C, Sasaki T, Iwayama Y, Yamada K, Yoshikawa T, Kasai K. Association of decreased prefrontal hemodynamic response during a verbal fluency task with EGR3 gene polymorphism in patients with schizophrenia and in healthy individuals. Neuroimage. 85: 527-34. PMID 23962955 DOI: 10.1016/J.Neuroimage.2013.08.021 |
0.348 |
|
| 2013 |
Kondo K, Ikeda M, Kajio Y, Saito T, Iwayama Y, Aleksic B, Yamada K, Toyota T, Hattori E, Ujike H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ozaki N, et al. Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study. Plos One. 8: e70964. PMID 23967141 DOI: 10.1371/Journal.Pone.0070964 |
0.313 |
|
| 2013 |
Balan S, Yamada K, Hattori E, Iwayama Y, Toyota T, Ohnishi T, Maekawa M, Toyoshima M, Iwata Y, Suzuki K, Kikuchi M, Yoshikawa T. Population-specific haplotype association of the postsynaptic density gene DLG4 with schizophrenia, in family-based association studies. Plos One. 8: e70302. PMID 23936182 DOI: 10.1371/journal.pone.0070302 |
0.832 |
|
| 2013 |
Balan S, Yamada K, Iwayama Y, Toyota T, Ohnishi T, Maekawa M, Toyoshima M, Iwata Y, Suzuki K, Kikuchi M, Ujike H, Inada T, Kunugi H, Ozaki N, Iwata N, ... ... Yoshikawa T, et al. Lack of association of EGR2 variants with bipolar disorder in Japanese population. Gene. 526: 246-50. PMID 23747400 DOI: 10.1016/j.gene.2013.05.055 |
0.812 |
|
| 2013 |
Jitoku D, Yoshikawa T. [Genetics of schizophrenia]. Nihon Rinsho. Japanese Journal of Clinical Medicine. 71: 599-604. PMID 23678585 |
0.334 |
|
| 2013 |
Takata A, Iwayama Y, Fukuo Y, Ikeda M, Okochi T, Maekawa M, Toyota T, Yamada K, Hattori E, Ohnishi T, Toyoshima M, Ujike H, Inada T, Kunugi H, Ozaki N, ... ... Yoshikawa T, et al. A population-specific uncommon variant in GRIN3A associated with schizophrenia. Biological Psychiatry. 73: 532-9. PMID 23237318 DOI: 10.1016/j.biopsych.2012.10.024 |
0.789 |
|
| 2013 |
Ohnishi T, Tanizawa Y, Watanabe A, Nakamura T, Ohba H, Hirata H, Kaneda C, Iwayama Y, Arimoto T, Watanabe K, Mori I, Yoshikawa T. Human myo-inositol monophosphatase 2 rescues the nematode thermotaxis mutant ttx-7 more efficiently than IMPA1: functional and evolutionary considerations of the two mammalian myo-inositol monophosphatase genes. Journal of Neurochemistry. 124: 685-94. PMID 23205734 DOI: 10.1111/Jnc.12112 |
0.676 |
|
| 2012 |
Matsunaga S, Ikeda M, Kishi T, Fukuo Y, Aleksic B, Yoshimura R, Okochi T, Yamanouchi Y, Kinoshita Y, Kawashima K, Umene-Nakano W, Inada T, Kunugi H, Kato T, Yoshikawa T, et al. An evaluation of polymorphisms in casein kinase 1 delta and epsilon genes in major psychiatric disorders. Neuroscience Letters. 529: 66-9. PMID 22981886 DOI: 10.1016/J.Neulet.2012.08.070 |
0.35 |
|
| 2012 |
Doi N, Hoshi Y, Itokawa M, Yoshikawa T, Ichikawa T, Arai M, Usui C, Tachikawa H. Paradox of schizophrenia genetics: is a paradigm shift occurring? Behavioral and Brain Functions : Bbf. 8: 28. PMID 22650965 DOI: 10.1186/1744-9081-8-28 |
0.318 |
|
| 2012 |
Matsumata M, Sakayori N, Maekawa M, Owada Y, Yoshikawa T, Osumi N. The effects of Fabp7 and Fabp5 on postnatal hippocampal neurogenesis in the mouse. Stem Cells (Dayton, Ohio). 30: 1532-43. PMID 22581784 DOI: 10.1002/Stem.1124 |
0.615 |
|
| 2012 |
Yamada K, Iwayama Y, Toyota T, Ohnishi T, Ohba H, Maekawa M, Yoshikawa T. Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population. Human Genetics. 131: 443-51. PMID 21927946 DOI: 10.1007/s00439-011-1089-3 |
0.812 |
|
| 2011 |
Hatayama M, Ishiguro A, Iwayama Y, Takashima N, Sakoori K, Toyota T, Nozaki Y, Odaka YS, Yamada K, Yoshikawa T, Aruga J. Zic2 hypomorphic mutant mice as a schizophrenia model and ZIC2 mutations identified in schizophrenia patients. Scientific Reports. 1: 16. PMID 22355535 DOI: 10.1038/srep00016 |
0.401 |
|
| 2011 |
Ohnishi T, Yamada K, Watanabe A, Ohba H, Sakaguchi T, Honma Y, Iwayama Y, Toyota T, Maekawa M, Watanabe K, Detera-Wadleigh SD, Wakana S, Yoshikawa T. Ablation of Mrds1/Ofcc1 induces hyper-γ-glutamyl transpeptidasemia without abnormal head development and schizophrenia-relevant behaviors in mice. Plos One. 6: e29499. PMID 22242126 DOI: 10.1371/journal.pone.0029499 |
0.834 |
|
| 2011 |
Sharifi K, Morihiro Y, Maekawa M, Yasumoto Y, Hoshi H, Adachi Y, Sawada T, Tokuda N, Kondo H, Yoshikawa T, Suzuki M, Owada Y. FABP7 expression in normal and stab-injured brain cortex and its role in astrocyte proliferation. Histochemistry and Cell Biology. 136: 501-13. PMID 21938553 DOI: 10.1007/s00418-011-0865-4 |
0.6 |
|
| 2011 |
Itokawa M, Arai M, Ichikawa T, Miyashita M, Yoshikawa T, Okazaki Y, Miyata T. [Molecular pathophysiology of schizophrenia and preventive strategy in pubertal period]. Seishin Shinkeigaku Zasshi = Psychiatria Et Neurologia Japonica. 113: 672-8. PMID 21882541 |
0.333 |
|
| 2011 |
Kato T, Hayashi-Takagi A, Toyota T, Yoshikawa T, Iwamoto K. Gene expression analysis in lymphoblastoid cells as a potential biomarker of bipolar disorder. Journal of Human Genetics. 56: 779-83. PMID 21866111 DOI: 10.1038/jhg.2011.101 |
0.304 |
|
| 2011 |
Yamada K, Iwayama Y, Hattori E, Iwamoto K, Toyota T, Ohnishi T, Ohba H, Maekawa M, Kato T, Yoshikawa T. Genome-wide association study of schizophrenia in Japanese population. Plos One. 6: e20468. PMID 21674006 DOI: 10.1371/journal.pone.0020468 |
0.807 |
|
| 2011 |
Jitoku D, Hattori E, Iwayama Y, Yamada K, Toyota T, Kikuchi M, Maekawa M, Nishikawa T, Yoshikawa T. Association study of Nogo-related genes with schizophrenia in a Japanese case-control sample. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 581-92. PMID 21563301 DOI: 10.1002/ajmg.b.31199 |
0.669 |
|
| 2011 |
Maekawa M, Owada Y, Yoshikawa T. Role of polyunsaturated fatty acids and fatty acid binding protein in the pathogenesis of schizophrenia. Current Pharmaceutical Design. 17: 168-75. PMID 21355837 DOI: 10.2174/138161211795049615 |
0.698 |
|
| 2011 |
Fujita S, Ohnishi T, Okuda S, Kobayashi R, Fukuno S, Furuta D, Kikuchi T, Yoshikawa T, Fujita N. In silico study on the substrate binding manner in human myo-inositol monophosphatase 2. Journal of Molecular Modeling. 17: 2559-67. PMID 21213002 DOI: 10.1007/s00894-010-0937-8 |
0.592 |
|
| 2011 |
Kishi T, Okochi T, Tsunoka T, Okumura T, Kitajima T, Kawashima K, Yamanouchi Y, Kinoshita Y, Naitoh H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ujike H, Ozaki N, et al. Serotonin 1A receptor gene, schizophrenia and bipolar disorder: An association study and meta-analysis Psychiatry Research. 185: 20-26. PMID 20594600 DOI: 10.1016/j.psychres.2010.06.003 |
0.389 |
|
| 2010 |
Yoshikawa T, Maekawa M, Ohnishi T, Hashimoto K, Watanabe A. [Analysis of mouse strain-dependent prepulse inhibition points to a role for Shmt1 (SHMT1) in mice and in schizophrenia]. Nihon Shinkei Seishin Yakurigaku Zasshi = Japanese Journal of Psychopharmacology. 30: 197-200. PMID 21226315 |
0.807 |
|
| 2010 |
Umeda T, Takashima N, Nakagawa R, Maekawa M, Ikegami S, Yoshikawa T, Kobayashi K, Okanoya K, Inokuchi K, Osumi N. Evaluation of Pax6 mutant rat as a model for autism. Plos One. 5: e15500. PMID 21203536 DOI: 10.1371/Journal.Pone.0015500 |
0.619 |
|
| 2010 |
Maekawa M, Ohnishi T, Hashimoto K, Watanabe A, Iwayama Y, Ohba H, Hattori E, Yamada K, Yoshikawa T. Analysis of strain-dependent prepulse inhibition points to a role for Shmt1 (SHMT1) in mice and in schizophrenia. Journal of Neurochemistry. 115: 1374-85. PMID 20977478 DOI: 10.1111/j.1471-4159.2010.07039.x |
0.823 |
|
| 2010 |
Maekawa M, Iwayama Y, Watanabe A, Nozaki Y, Ohnishi T, Ohba H, Toyoshima M, Hamazaki K, Osumi N, Aruga J, Yoshikawa T. Excessive ingestion of long-chain polyunsaturated fatty acids during developmental stage causes strain- and sex-dependent eye abnormalities in mice. Biochemical and Biophysical Research Communications. 402: 431-7. PMID 20951676 DOI: 10.1016/J.Bbrc.2010.10.051 |
0.728 |
|
| 2010 |
Arai M, Yuzawa H, Nohara I, Ohnishi T, Obata N, Iwayama Y, Haga S, Toyota T, Ujike H, Arai M, Ichikawa T, Nishida A, Tanaka Y, Furukawa A, Aikawa Y, ... ... Yoshikawa T, et al. Enhanced carbonyl stress in a subpopulation of schizophrenia. Archives of General Psychiatry. 67: 589-97. PMID 20530008 DOI: 10.1001/archgenpsychiatry.2010.62 |
0.665 |
|
| 2010 |
Maekawa M, Fujisawa H, Iwayama Y, Tamase A, Toyota T, Osumi N, Yoshikawa T. Giant subependymoma developed in a patient with aniridia: analyses of PAX6 and tumor-relevant genes. Brain Pathology (Zurich, Switzerland). 20: 1033-41. PMID 20500513 DOI: 10.1111/J.1750-3639.2010.00406.X |
0.612 |
|
| 2010 |
Iwata Y, Yamada K, Iwayama Y, Anitha A, Thanseem I, Toyota T, Hattori E, Ohnishi T, Maekawa M, Nakamura K, Suzuki K, Matsuzaki H, Tsuchiya KJ, Suda S, Sugihara G, ... ... Yoshikawa T, et al. Failure to confirm genetic association of the FXYD6 gene with schizophrenia: the Japanese population and meta-analysis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1221-7. PMID 20468077 DOI: 10.1002/ajmg.b.31095 |
0.815 |
|
| 2010 |
Schulze TG, Alda M, Adli M, Akula N, Ardau R, Bui ET, Chillotti C, Cichon S, Czerski P, Del Zompo M, Detera-Wadleigh SD, Grof P, Gruber O, Hashimoto R, Hauser J, ... ... Yoshikawa T, et al. The International Consortium on Lithium Genetics (ConLiGen): an initiative by the NIMH and IGSLI to study the genetic basis of response to lithium treatment. Neuropsychobiology. 62: 72-8. PMID 20453537 DOI: 10.1159/000314708 |
0.581 |
|
| 2010 |
Ohnishi T, Watanabe A, Ohba H, Iwayama Y, Maekawa M, Yoshikawa T. Behavioral analyses of transgenic mice harboring bipolar disorder candidate genes, IMPA1 and IMPA2. Neuroscience Research. 67: 86-94. PMID 20153384 DOI: 10.1016/j.neures.2010.02.003 |
0.785 |
|
| 2010 |
Kushima I, Aleksic B, Ito Y, Nakamura Y, Nakamura K, Mori N, Kikuchi M, Inada T, Kunugi H, Nanko S, Kato T, Yoshikawa T, Ujike H, Suzuki M, Iwata N, et al. Association study of ubiquitin-specific peptidase 46 (USP46) with bipolar disorder and schizophrenia in a Japanese population. Journal of Human Genetics. 55: 133-6. PMID 20111060 DOI: 10.1038/Jhg.2009.139 |
0.444 |
|
| 2010 |
Maekawa M, Iwayama Y, Arai R, Nakamura K, Ohnishi T, Toyota T, Tsujii M, Okazaki Y, Osumi N, Owada Y, Mori N, Yoshikawa T. Polymorphism screening of brain-expressed FABP7, 5 and 3 genes and association studies in autism and schizophrenia in Japanese subjects. Journal of Human Genetics. 55: 127-30. PMID 20057506 DOI: 10.1038/Jhg.2009.133 |
0.813 |
|
| 2010 |
Ohi K, Hashimoto R, Yasuda Y, Yoshida T, Takahashi H, Iike N, Iwase M, Kamino K, Ishii R, Kazui H, Fukumoto M, Takamura H, Yamamori H, Azechi M, Ikezawa K, ... ... Yoshikawa T, et al. The chitinase 3-like 1 gene and schizophrenia: evidence from a multi-center case-control study and meta-analysis. Schizophrenia Research. 116: 126-32. PMID 20051317 DOI: 10.1016/j.schres.2009.12.002 |
0.391 |
|
| 2010 |
Iwayama Y, Hattori E, Maekawa M, Yamada K, Toyota T, Ohnishi T, Iwata Y, Tsuchiya KJ, Sugihara G, Kikuchi M, Hashimoto K, Iyo M, Inada T, Kunugi H, Ozaki N, ... ... Yoshikawa T, et al. Association analyses between brain-expressed Fatty-Acid Binding Protein (FABP) genes and schizophrenia and bipolar disorder American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153: 484-493. PMID 19554614 DOI: 10.1002/ajmg.b.31004 |
0.832 |
|
| 2009 |
Doi N, Hoshi Y, Itokawa M, Usui C, Yoshikawa T, Tachikawa H. Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint. Plos One. 4: e7799. PMID 19911060 DOI: 10.1371/journal.pone.0007799 |
0.386 |
|
| 2009 |
Vijayan NN, Iwayama Y, Koshy LV, Natarajan C, Nair C, Allencherry PM, Yoshikawa T, Banerjee M. Evidence of association of serotonin transporter gene polymorphisms with schizophrenia in a South Indian population. Journal of Human Genetics. 54: 538-42. PMID 19713975 DOI: 10.1038/jhg.2009.76 |
0.303 |
|
| 2009 |
Maekawa M, Iwayama Y, Nakamura K, Sato M, Toyota T, Ohnishi T, Yamada K, Miyachi T, Tsujii M, Hattori E, Maekawa N, Osumi N, Mori N, Yoshikawa T. A novel missense mutation (Leu46Val) of PAX6 found in an autistic patient. Neuroscience Letters. 462: 267-71. PMID 19607881 DOI: 10.1016/J.Neulet.2009.07.021 |
0.743 |
|
| 2009 |
Meerabux JM, Ohba H, Iwayama Y, Maekawa M, Detera-Wadleigh SD, DeLisi LE, Yoshikawa T. Analysis of a t(18;21)(p11.1;p11.1) translocation in a family with schizophrenia. Journal of Human Genetics. 54: 386-91. PMID 19461657 DOI: 10.1038/jhg.2009.47 |
0.764 |
|
| 2009 |
Maekawa M, Takashima N, Matsumata M, Ikegami S, Kontani M, Hara Y, Kawashima H, Owada Y, Kiso Y, Yoshikawa T, Inokuchi K, Osumi N. Arachidonic acid drives postnatal neurogenesis and elicits a beneficial effect on prepulse inhibition, a biological trait of psychiatric illnesses. Plos One. 4: e5085. PMID 19352438 DOI: 10.1371/Journal.Pone.0005085 |
0.685 |
|
| 2009 |
Anitha A, Nakamura K, Yamada K, Iwayama Y, Toyota T, Takei N, Iwata Y, Suzuki K, Sekine Y, Matsuzaki H, Kawai M, Thanseem I, Miyoshi K, Katayama T, Matsuzaki S, ... ... Yoshikawa T, et al. Association studies and gene expression analyses of the DISC1-interacting molecules, pericentrin 2 (PCNT2) and DISC1-binding zinc finger protein (DBZ), with schizophrenia and with bipolar disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 967-76. PMID 19191256 DOI: 10.1002/ajmg.b.30926 |
0.439 |
|
| 2009 |
Hattori E, Nakajima M, Yamada K, Iwayama Y, Toyota T, Saitou N, Yoshikawa T. Variable number of tandem repeat polymorphisms of DRD4: Re-evaluation of selection hypothesis and analysis of association with schizophrenia European Journal of Human Genetics. 17: 793-801. PMID 19092778 DOI: 10.1038/ejhg.2008.247 |
0.339 |
|
| 2009 |
Yamada K, Hattori E, Iwayama Y, Toyota T, Ohnishi T, Iwata Y, Tsuchiya KJ, Sugihara G, Kikuchi M, Okazaki Y, Yoshikawa T. Failure to confirm genetic association of the CHI3L1 gene with schizophrenia in Japanese and Chinese populations American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 150: 508-514. PMID 18767121 DOI: 10.1002/ajmg.b.30847 |
0.723 |
|
| 2008 |
Ikeda Y, Yahata N, Ito I, Nagano M, Toyota T, Yoshikawa T, Okubo Y, Suzuki H. Low serum levels of brain-derived neurotrophic factor and epidermal growth factor in patients with chronic schizophrenia. Schizophrenia Research. 101: 58-66. PMID 18289832 DOI: 10.1016/j.schres.2008.01.017 |
0.306 |
|
| 2008 |
Amano K, Yamada K, Iwayama Y, Detera-Wadleigh SD, Hattori E, Toyota T, Tokunaga K, Yoshikawa T, Yamakawa K. Association study between the Down syndrome cell adhesion molecule (DSCAM) gene and bipolar disorder. Psychiatric Genetics. 18: 1-10. PMID 18197079 DOI: 10.1097/YPG.0b013e3281ac238e |
0.601 |
|
| 2008 |
Takeshita M, Yamada K, Hattori E, Iwayama Y, Toyota T, Iwata Y, Tsuchiya KJ, Sugihara G, Hashimoto K, Watanabe H, Iyo M, Kikuchi M, Okazaki Y, Yoshikawa T. Genetic examination of the PLXNA2 gene in Japanese and Chinese people with schizophrenia Schizophrenia Research. 99: 359-364. PMID 18065206 DOI: 10.1016/j.schres.2007.11.002 |
0.372 |
|
| 2008 |
Yoshimi A, Takahashi N, Saito S, Ito Y, Aleksic B, Usui H, Kawamura Y, Waki Y, Yoshikawa T, Kato T, Iwata N, Inada T, Noda Y, Ozaki N. Genetic analysis of the gene coding for DARPP-32 (PPP1R1B) in Japanese patients with schizophrenia or bipolar disorder. Schizophrenia Research. 100: 334-41. PMID 18055181 DOI: 10.1016/J.Schres.2007.10.028 |
0.424 |
|
| 2008 |
Anitha A, Nakamura K, Yamada K, Iwayama Y, Toyota T, Takei N, Iwata Y, Suzuki K, Sekine Y, Matsuzaki H, Kawai M, Miyoshi K, Katayama T, Matsuzaki S, Baba K, ... ... Yoshikawa T, et al. Gene and expression analyses reveal enhanced expression of pericentrin 2 (PCNT2) in bipolar disorder. Biological Psychiatry. 63: 678-85. PMID 17884020 DOI: 10.1016/j.biopsych.2007.07.010 |
0.385 |
|
| 2007 |
Watanabe A, Toyota T, Owada Y, Hayashi T, Iwayama Y, Matsumata M, Ishitsuka Y, Nakaya A, Maekawa M, Ohnishi T, Arai R, Sakurai K, Yamada K, Kondo H, Hashimoto K, ... ... Yoshikawa T, et al. Fabp7 maps to a quantitative trait locus for a schizophrenia endophenotype. Plos Biology. 5: e297. PMID 18001149 DOI: 10.1371/Journal.Pbio.0050297 |
0.814 |
|
| 2007 |
Kakiuchi C, Ishiwata M, Nanko S, Kunugi H, Minabe Y, Nakamura K, Mori N, Fujii K, Umekage T, Tochigi M, Kohda K, Sasaki T, Yamada K, Yoshikawa T, Kato T. Association analysis of HSP90B1 with bipolar disorder. Journal of Human Genetics. 52: 794-803. PMID 17805476 DOI: 10.1007/S10038-007-0188-4 |
0.346 |
|
| 2007 |
Sadakata T, Washida M, Iwayama Y, Shoji S, Sato Y, Ohkura T, Katoh-Semba R, Nakajima M, Sekine Y, Tanaka M, Nakamura K, Iwata Y, Tsuchiya KJ, Mori N, Detera-Wadleigh SD, ... ... Yoshikawa T, et al. Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients. The Journal of Clinical Investigation. 117: 931-43. PMID 17380209 DOI: 10.1172/JCI29031 |
0.603 |
|
| 2007 |
Yamada K, Gerber DJ, Iwayama Y, Ohnishi T, Ohba H, Toyota T, Aruga J, Minabe Y, Tonegawa S, Yoshikawa T. Genetic analysis of the calcineurin pathway identifies members of the EGR gene family, specifically EGR3, as potential susceptibility candidates in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America. 104: 2815-20. PMID 17360599 DOI: 10.1073/pnas.0610765104 |
0.75 |
|
| 2007 |
Kakiuchi C, Ishiwata M, Nanko S, Kunugi H, Minabe Y, Nakamura K, Mori N, Fujii K, Yamada K, Yoshikawa T, Kato T. Association analysis of ATF4 and ATF5, genes for interacting-proteins of DISC1, in bipolar disorder. Neuroscience Letters. 417: 316-21. PMID 17346882 DOI: 10.1016/j.neulet.2007.02.054 |
0.424 |
|
| 2007 |
Arai R, Ito K, Ohnishi T, Ohba H, Akasaka R, Bessho Y, Hanawa-Suetsugu K, Yoshikawa T, Shirouzu M, Yokoyama S. Crystal structure of human myo-inositol monophosphatase 2, the product of the putative susceptibility gene for bipolar disorder, schizophrenia, and febrile seizures. Proteins. 67: 732-42. PMID 17340635 DOI: 10.1002/prot.21299 |
0.656 |
|
| 2007 |
Ohnishi T, Yamada K, Ohba H, Iwayama Y, Toyota T, Hattori E, Inada T, Kunugi H, Tatsumi M, Ozaki N, Iwata N, Sakamoto K, Iijima Y, Iwata Y, Tsuchiya KJ, ... ... Yoshikawa T, et al. A promoter haplotype of the inositol monophosphatase 2 gene (IMPA2) at 18p11.2 confers a possible risk for bipolar disorder by enhancing transcription Neuropsychopharmacology. 32: 1727-1737. PMID 17251911 DOI: 10.1038/Sj.Npp.1301307 |
0.773 |
|
| 2007 |
Nakatani N, Ohnishi T, Iwamoto K, Watanabe A, Iwayama Y, Yamashita S, Ishitsuka Y, Moriyama K, Nakajima M, Tatebayashi Y, Akiyama H, Higuchi T, Kato T, Yoshikawa T. Expression analysis of actin-related genes as an underlying mechanism for mood disorders. Biochemical and Biophysical Research Communications. 352: 780-6. PMID 17141188 DOI: 10.1016/j.bbrc.2006.11.101 |
0.67 |
|
| 2007 |
Iwata Y, Nakajima M, Yamada K, Nakamura K, Sekine Y, Tsuchiya KJ, Sugihara G, Matsuzaki H, Suda S, Suzuki K, Takei N, Mori N, Iwayama Y, Takao H, Yoshikawa T, et al. Linkage disequilibrium analysis of the CHRNA7 gene and its partially duplicated region in schizophrenia. Neuroscience Research. 57: 194-202. PMID 17113175 DOI: 10.1016/j.neures.2006.10.002 |
0.42 |
|
| 2007 |
Ohnishi T, Ohba H, Seo KC, Im J, Sato Y, Iwayama Y, Furuichi T, Chung SK, Yoshikawa T. Spatial expression patterns and biochemical properties distinguish a second myo-inositol monophosphatase IMPA2 from IMPA1. The Journal of Biological Chemistry. 282: 637-46. PMID 17068342 DOI: 10.1074/Jbc.M604474200 |
0.672 |
|
| 2007 |
Doi N, Itokawa M, Hoshi Y, Arai M, Furukawa A, Ujike H, Sora I, Yoshikawa T. A resistance gene in disguise for schizophrenia? American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165-73. PMID 17066479 DOI: 10.1002/ajmg.b.30365 |
0.337 |
|
| 2006 |
Ide M, Ohnishi T, Murayama M, Matsumoto I, Yamada K, Iwayama Y, Dedova I, Toyota T, Asada T, Takashima A, Yoshikawa T. Failure to support a genetic contribution of AKT1 polymorphisms and altered AKT signaling in schizophrenia. Journal of Neurochemistry. 99: 277-87. PMID 16987250 DOI: 10.1111/j.1471-4159.2006.04033.x |
0.682 |
|
| 2006 |
Iwamoto K, Bundo M, Yamada K, Takao H, Iwayama Y, Yoshikawa T, Kato T. A family-based and case-control association study of SOX10 in schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 477-81. PMID 16741945 DOI: 10.1002/ajmg.b.30304 |
0.435 |
|
| 2006 |
Nakatani N, Hattori E, Ohnishi T, Dean B, Iwayama Y, Matsumoto I, Kato T, Osumi N, Higuchi T, Niwa S, Yoshikawa T. Genome-wide expression analysis detects eight genes with robust alterations specific to bipolar I disorder: relevance to neuronal network perturbation Human Molecular Genetics. 15: 1949-1962. PMID 16687443 DOI: 10.1093/Hmg/Ddl118 |
0.711 |
|
| 2006 |
Shimizu H, Iwayama Y, Yamada K, Toyota T, Minabe Y, Nakamura K, Nakajima M, Hattori E, Mori N, Osumi N, Yoshikawa T. Genetic and expression analyses of the STOP (MAP6) gene in schizophrenia Schizophrenia Research. 84: 244-252. PMID 16624526 DOI: 10.1016/J.Schres.2006.03.017 |
0.389 |
|
| 2006 |
Yamada K, Hattori E, Iwayama Y, Ohnishi T, Ohba H, Toyota T, Takao H, Minabe Y, Nakatani N, Higuchi T, Detera-Wadleigh SD, Yoshikawa T. Distinguishable haplotype blocks in the HTR3A and HTR3B region in the Japanese reveal evidence of association of HTR3B with female major depression. Biological Psychiatry. 60: 192-201. PMID 16487942 DOI: 10.1016/j.biopsych.2005.11.008 |
0.764 |
|
| 2006 |
Itokawa M, Yoshikawa T. [Susceptibility genes for schizophrenia]. Nihon Rinsho. Japanese Journal of Clinical Medicine. 437-40. PMID 16416830 |
0.399 |
|
| 2006 |
Iwamoto K, Bundo M, Yamada K, Takao H, Iwayama-Shigeno Y, Yoshikawa T, Kato T. DNA methylation status of SOX10 correlates with its downregulation and oligodendrocyte dysfunction in schizophrenia. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 5376-81. PMID 15930386 DOI: 10.1523/JNEUROSCI.0766-05.2005 |
0.334 |
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| 2005 |
Arinami T, Ohtsuki T, Ishiguro H, Ujike H, Tanaka Y, Morita Y, Mineta M, Takeichi M, Yamada S, Imamura A, Ohara K, Shibuya H, Ohara K, Suzuki Y, Muratake T, ... ... Yoshikawa T, et al. Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p. American Journal of Human Genetics. 77: 937-44. PMID 16380906 DOI: 10.1086/498122 |
0.346 |
|
| 2005 |
Arai M, Yamada K, Toyota T, Obata N, Haga S, Yoshida Y, Nakamura K, Minabe Y, Ujike H, Sora I, Ikeda K, Mori N, Yoshikawa T, Itokawa M. Association between polymorphisms in the promoter region of the sialyltransferase 8B (SIAT8B) gene and schizophrenia. Biological Psychiatry. 59: 652-9. PMID 16229822 DOI: 10.1016/j.biopsych.2005.08.016 |
0.348 |
|
| 2005 |
Kakiuchi C, Ishiwata M, Nanko S, Kunugi H, Minabe Y, Nakamura K, Mori N, Fujii K, Umekage T, Tochigi M, Kohda K, Sasaki T, Yamada K, Yoshikawa T, Kato T. Functional polymorphisms of HSPA5: possible association with bipolar disorder. Biochemical and Biophysical Research Communications. 336: 1136-43. PMID 16168956 DOI: 10.1016/j.bbrc.2005.08.248 |
0.377 |
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| 2005 |
Meerabux J, Iwayama Y, Sakurai T, Ohba H, Toyota T, Yamada K, Nagata R, Irukayama-Tomobe Y, Shimizu H, Yoshitsugu K, Ohta K, Yoshikawa T. Association of An Orexin 1 Receptor 408Val Variant with Polydipsia–Hyponatremia in Schizophrenic Subjects Biological Psychiatry. 58: 401-407. PMID 15978554 DOI: 10.1016/J.Biopsych.2005.04.015 |
0.347 |
|
| 2005 |
Yamada K, Ohnishi T, Hashimoto K, Ohba H, Iwayama-Shigeno Y, Toyoshima M, Okuno A, Takao H, Toyota T, Minabe Y, Nakamura K, Shimizu E, Itokawa M, Mori N, Iyo M, ... Yoshikawa T, et al. Identification of multiple serine racemase (SRR) mRNA isoforms and genetic analyses of SRR and DAO in schizophrenia and D-serine levels. Biological Psychiatry. 57: 1493-503. PMID 15953485 DOI: 10.1016/j.biopsych.2005.03.018 |
0.676 |
|
| 2005 |
Iwayama-Shigeno Y, Yamada K, Itokawa M, Toyota T, Meerabux JM, Minabe Y, Mori N, Inada T, Yoshikawa T. Extended analyses support the association of a functional (GT)n polymorphism in the GRIN2A promoter with Japanese schizophrenia. Neuroscience Letters. 378: 102-5. PMID 15774266 DOI: 10.1016/j.neulet.2004.12.013 |
0.38 |
|
| 2005 |
Yoshikawa T, Ohnishi T. [Molecular genetic approach to depression from animal models]. Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica. 125: 25-32. PMID 15738618 DOI: 10.1254/fpj.125.25 |
0.582 |
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| 2005 |
Aoki-Suzuki M, Yamada K, Meerabux J, Iwayama-Shigeno Y, Ohba H, Iwamoto K, Takao H, Toyota T, Suto Y, Nakatani N, Dean B, Nishimura S, Seki K, Kato T, Itohara S, ... ... Yoshikawa T, et al. A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia. Biological Psychiatry. 57: 382-93. PMID 15705354 DOI: 10.1016/j.biopsych.2004.11.022 |
0.451 |
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| 2004 |
Yamada K, Nakamura K, Minabe Y, Iwayama-Shigeno Y, Takao H, Toyota T, Hattori E, Takei N, Sekine Y, Suzuki K, Iwata Y, Miyoshi K, Honda A, Baba K, Katayama T, ... ... Yoshikawa T, et al. Association analysis of FEZ1 variants with schizophrenia in Japanese cohorts. Biological Psychiatry. 56: 683-90. PMID 15522253 DOI: 10.1016/j.biopsych.2004.08.015 |
0.444 |
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| 2004 |
Fukasawa M, Aoki M, Yamada K, Iwayama-Shigeno Y, Takao H, Meerabux J, Toyota T, Nishikawa T, Yoshikawa T. Case-control association study of human netrin G1 gene in Japanese schizophrenia. Journal of Medical and Dental Sciences. 51: 121-8. PMID 15508520 |
0.4 |
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| 2004 |
Ide M, Muratake T, Yamada K, Iwayama-Shigeno Y, Iwamoto K, Takao H, Toyota T, Kaneko N, Minabe Y, Nakamura K, Kato T, Mori N, Asada T, Someya T, Yoshikawa T. Genetic and expression analyses of FZD3 in schizophrenia. Biological Psychiatry. 56: 462-5. PMID 15364045 DOI: 10.1016/j.biopsych.2004.06.039 |
0.405 |
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| 2004 |
Kockelkorn TT, Arai M, Matsumoto H, Fukuda N, Yamada K, Minabe Y, Toyota T, Ujike H, Sora I, Mori N, Yoshikawa T, Itokawa M. Association study of polymorphisms in the 5' upstream region of human DISC1 gene with schizophrenia. Neuroscience Letters. 368: 41-5. PMID 15342131 DOI: 10.1016/j.neulet.2004.06.048 |
0.401 |
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| 2004 |
Kunugi H, Iijima Y, Tatsumi M, Yoshida M, Hashimoto R, Kato T, Sakamoto K, Fukunaga T, Inada T, Suzuki T, Iwata N, Ozaki N, Yamada K, Yoshikawa T. No association between the Val66Met polymorphism of the brain-derived neurotrophic factor gene and bipolar disorder in a Japanese population: a multicenter study. Biological Psychiatry. 56: 376-8. PMID 15336520 DOI: 10.1016/j.biopsych.2004.06.017 |
0.3 |
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| 2004 |
Itokawa M, Arai M, Ujiie H, Sora I, Yoshikawa T, Ikeda K. [Study on genes involved in pathogenesis of schizophrenia with DNA microarray]. Seishin Shinkeigaku Zasshi = Psychiatria Et Neurologia Japonica. 106: 42-8. PMID 15152654 |
0.347 |
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| 2004 |
Kikuchi M, Yamada K, Toyota T, Yoshikawa T. C18orf1 located on chromosome 18p11.2 may confer susceptibility to schizophrenia. Journal of Medical and Dental Sciences. 50: 225-9. PMID 15074360 |
0.416 |
|
| 2004 |
Itokawa M, Yoshikawa T. [Hypoglutamatergic hypothesis of schizophrenia: evidence from genetic studies]. Seishin Shinkeigaku Zasshi = Psychiatria Et Neurologia Japonica. 105: 1349-62. PMID 14758783 |
0.422 |
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| 2004 |
Toyota T, Yoshitsugu K, Ebihara M, Yamada K, Ohba H, Fukasawa M, Minabe Y, Nakamura K, Sekine Y, Takei N, Suzuki K, Itokawa M, Meerabux JM, Iwayama-Shigeno Y, Tomaru Y, ... ... Yoshikawa T, et al. Association between schizophrenia with ocular misalignment and polyalanine length variation in PMX2B. Human Molecular Genetics. 13: 551-61. PMID 14709596 DOI: 10.1093/hmg/ddh047 |
0.42 |
|
| 2004 |
Horiuchi Y, Nakayama J, Ishiguro H, Ohtsuki T, Detera-Wadleigh SD, Toyota T, Yamada K, Nankai M, Shibuya H, Yoshikawa T, Arinami T. Possible association between a haplotype of the GABA-A receptor alpha 1 subunit gene (GABRA1) and mood disorders. Biological Psychiatry. 55: 40-5. PMID 14706423 DOI: 10.1016/s0006-3223(03)00689-9 |
0.591 |
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| 2004 |
Itokawa M, Yamada K, Yoshitsugu K, Toyota T, Suga T, Ohba H, Watanabe A, Hattori E, Shimizu H, Kumakura T, Ebihara M, Meerabux JM, Toru M, Yoshikawa T. A microsatellite repeat in the promoter of the N-methyl-D-aspartate receptor 2A subunit (GRIN2A) gene suppresses transcriptional activity and correlates with chronic outcome in schizophrenia. Pharmacogenetics. 13: 271-8. PMID 12724619 DOI: 10.1097/00008571-200305000-00006 |
0.402 |
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| 2003 |
Itokawa M, Arai M, Kato S, Ogata Y, Furukawa A, Haga S, Ujike H, Sora I, Ikeda K, Yoshikawa T. Association between a novel polymorphism in the promoter region of the neuropeptide Y gene and schizophrenia in humans. Neuroscience Letters. 347: 202-4. PMID 12875921 DOI: 10.1016/s0304-3940(03)00718-3 |
0.403 |
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| 2003 |
Itokawa M, Yamada K, Iwayama-Shigeno Y, Ishitsuka Y, Detera-Wadleigh S, Yoshikawa T. Genetic analysis of a functional GRIN2A promoter (GT)n repeat in bipolar disorder pedigrees in humans. Neuroscience Letters. 345: 53-6. PMID 12809987 DOI: 10.1016/S0304-3940(03)00501-9 |
0.699 |
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| 2003 |
Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, ... ... Yoshikawa T, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. American Journal of Human Genetics. 73: 49-62. PMID 12802785 DOI: 10.1086/376547 |
0.595 |
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| 2003 |
Iwayama-Shigeno Y, Yamada K, Toyota T, Shimizu H, Hattori E, Yoshitsugu K, Fujisawa T, Yoshida Y, Kobayashi T, Toru M, Kurumaji A, Detera-Wadleigh S, Yoshikawa T. Distribution of haplotypes derived from three common variants of the NR4A2 gene in Japanese patients with schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 20-4. PMID 12627459 DOI: 10.1002/ajmg.b.10053 |
0.689 |
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| 2003 |
Toyota T, Yamada K, Detera-Wadleigh SD, Yoshikawa T. Analysis of a cluster of polymorphisms in AKT1 gene in bipolar pedigrees: a family-based association study. Neuroscience Letters. 339: 5-8. PMID 12618287 DOI: 10.1016/s0304-3940(02)01428-3 |
0.623 |
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| 2002 |
Akanuma N, Saitoh O, Yoshikawa T, Matsuda H, Ishikura N, Kato M, Adachi N, Onuma T. Interictal schizophrenia-like psychosis in a patient with double cortex syndrome. Journal of Neuropsychiatry and Clinical Neurosciences. 14: 210-213. PMID 11983798 DOI: 10.1176/Jnp.14.2.210 |
0.319 |
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| 2002 |
Toyota T, Hattori E, Meerabux J, Yamada K, Saito K, Shibuya H, Nankai M, Yoshikawa T. Molecular analysis, mutation screening, and association study of adenylate cyclase type 9 gene (ADCY9) in mood disorders. American Journal of Medical Genetics. 114: 84-92. PMID 11840511 DOI: 10.1002/ajmg.10117 |
0.329 |
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