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Shabeesh Balan - Publications

Affiliations: 
2012-2021 Laboratory for Molecular Psychiatry RIKEN Center for Brain Science 
Area:
Molecular Psychiatry
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30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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, 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  0.524
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  0.477
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, ... ... Balan S, 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  0.595
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, 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  0.567
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  0.511
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, 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  0.536
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, 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  0.439
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, 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  0.493
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  0.591
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  0.585
2020 Balan S, Ohnishi T, Watanabe A, Ohba H, Iwayama Y, Hisano Y, Toyota T, Toyoshima M, Shimogori T, Hayashi T, Kikkawa Y, Yoshikawa T. Genetic Deciphering of Prepulse Inhibition Reveals the Putative Role of an Atypical Cadherin in Schizophrenia Pathogenesis Biological Psychiatry. 87: S398. DOI: 10.1016/j.biopsych.2020.02.1017  0.375
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, et al. Excess hydrogen sulfide and polysulfides production underlies a schizophrenia pathophysiology. Embo Molecular Medicine. e10695. PMID 31657521 DOI: 10.15252/Emmm.201910695  0.562
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  0.537
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, et al. Investigation of betaine as a novel psychotherapeutic for schizophrenia. Ebiomedicine. PMID 31255657 DOI: 10.1016/j.ebiom.2019.05.062  0.578
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  0.584
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  0.391
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  0.579
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  0.415
2017 Maekawa M, Watanabe A, Iwayama Y, Kimura T, Hamazaki K, Balan S, Ohba H, Hisano Y, Nozaki Y, Ohnishi T, Toyoshima M, Shimamoto C, Iwamoto K, Bundo M, Osumi N, et al. Polyunsaturated fatty acid deficiency during neurodevelopment in mice models the prodromal state of schizophrenia through epigenetic changes in nuclear receptor genes. Translational Psychiatry. 7: e1229. PMID 28872641 DOI: 10.1038/Tp.2017.182  0.406
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, 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  0.597
2016 Toyoshima M, Akamatsu W, Okada Y, Ohnishi T, Balan S, Hisano Y, Iwayama Y, Toyota T, Matsumoto T, Itasaka N, Sugiyama S, Tanaka M, Yano M, Dean B, Okano H, et al. Analysis of induced pluripotent stem cells carrying 22q11.2 deletion. Translational Psychiatry. 6: e934. PMID 27801899 DOI: 10.1038/Tp.2016.206  0.317
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, 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  0.439
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, 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  0.527
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  0.597
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, 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  0.504
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  0.593
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, 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  0.535
2014 Balan S, Iwayama Y, Toyota T, Toyoshima M, Maekawa M, Yoshikawa T. 22q11.2 deletion carriers and schizophrenia-associated novel variants. The British Journal of Psychiatry : the Journal of Mental Science. 204: 398-9. PMID 24482440 DOI: 10.1192/bjp.bp.113.138420  0.377
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  0.59
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, 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  0.518
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