| Tubastatin A, an HDAC6 inhibitor, alleviates stroke-induced brain infarction and functional deficits: potential roles of α-tubulin acetylation and FGF-21 up-regulation Z Wang, Y Leng, J Wang, HM Liao, J Bergman, P Leeds, A Kozikowski, ... Scientific reports 6 (1), 19626, 2016 | 118 | 2016 |
| Autism-associated gene Dlgap2 mutant mice demonstrate exacerbated aggressive behaviors and orbitofrontal cortex deficits LF Jiang-Xie, HM Liao, CH Chen, YT Chen, SY Ho, DH Lu, LJ Lee, ... Molecular autism 5, 1-13, 2014 | 84 | 2014 |
| Antidepressant mechanism of ketamine: perspective from preclinical studies L Scheuing, CT Chiu, HM Liao, DM Chuang Frontiers in neuroscience 9, 152745, 2015 | 81 | 2015 |
| Preconditioning mesenchymal stem cells with the mood stabilizers lithium and valproic acid enhances therapeutic efficacy in a mouse model of Huntington's disease GR Linares, CT Chiu, L Scheuing, Y Leng, HM Liao, D Maric, DM Chuang Experimental neurology 281, 81-92, 2016 | 72 | 2016 |
| The mood stabilizer lithium potentiates the antidepressant-like effects and ameliorates oxidative stress induced by acute ketamine in a mouse model of stress CT Chiu, L Scheuing, G Liu, HM Liao, GR Linares, D Lin, DM Chuang International Journal of Neuropsychopharmacology 18 (6), pyu102, 2015 | 69 | 2015 |
| Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder CL Yin, HI Chen, LH Li, YL Chien, HM Liao, MC Chou, WJ Chou, WC Tsai, ... Molecular autism 7, 1-13, 2016 | 63 | 2016 |
| Preclinical and clinical investigations of mood stabilizers for Huntington's disease: what have we learned? L Scheuing, CT Chiu, HM Liao, GR Linares, DM Chuang International journal of biological sciences 10 (9), 1024, 2014 | 56 | 2014 |
| Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders WH Chien, SSF Gau, HM Liao, YN Chiu, YY Wu, YS Huang, WC Tsai, ... Molecular Autism 4, 1-12, 2013 | 56 | 2013 |
| Identification and characterization of three inherited genomic copy number variations associated with familial schizophrenia HM Liao, YL Chao, AL Huang, MC Cheng, YJ Chen, KF Lee, JS Fang, ... Schizophrenia research 139 (1-3), 229-236, 2012 | 48 | 2012 |
| Valproic acid and other HDAC inhibitors upregulate FGF21 gene expression and promote process elongation in glia by inhibiting HDAC2 and 3 Y Leng, J Wang, Z Wang, HM Liao, M Wei, P Leeds, DM Chuang International Journal of Neuropsychopharmacology 19 (8), pyw035, 2016 | 39 | 2016 |
| Identification of two inherited copy number variants in a male with autism supports two‐hit and compound heterozygosity models of autism SSF Gau, HM Liao, CC Hong, WH Chien, CH Chen American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159 …, 2012 | 38 | 2012 |
| Identification of a microdeletion at Xp22. 13 in a Taiwanese family presenting with Nance-Horan syndrome HM Liao, DM Niu, YJ Chen, JS Fang, SJ Chen, CH Chen Journal of human genetics 56 (1), 8-11, 2011 | 32 | 2011 |
| Neuroligin 2 R215H mutant mice manifest anxiety, increased prepulse inhibition, and impaired spatial learning and memory CH Chen, PW Lee, HM Liao, PK Chang Frontiers in Psychiatry 8, 257, 2017 | 30 | 2017 |
| Mutation analysis of the human dystrobrevin-binding protein 1 gene in schizophrenic patients HM Liao, CH Chen Schizophrenia research 71 (1), 185-189, 2004 | 27 | 2004 |
| Impairment of social behaviors in Arhgef10 knockout mice DH Lu, HM Liao, CH Chen, HJ Tu, HC Liou, SSF Gau, WM Fu Molecular Autism 9, 1-14, 2018 | 24 | 2018 |
| Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13. 3 associated with autism spectrum disorder CH Chen, HI Chen, HM Liao, YJ Chen, JS Fang, KF Lee, SSF Gau Psychiatric Genetics 27 (1), 23-33, 2017 | 24 | 2017 |
| Chromosomal abnormalities in patients with autism spectrum disorders from Taiwan HM Liao, SSF Gau, WC Tsai, JS Fang, YC Su, MC Chou, SK Liu, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 …, 2013 | 24 | 2013 |
| A novel microdeletion at chromosome 2q31. 1‐31.2 in a three‐generation family presenting duplication of great toes with clinodactyly LP Tsai, HM Liao, YJ Chen, JS Fang, CH Chen Clinical genetics 75 (5), 449-456, 2009 | 23 | 2009 |
| Mutation analysis of DARPP-32 as a candidate gene for schizophrenia CH Li, HM Liao, TW Hung, CH Chen Schizophrenia research 87 (1-3), 1-5, 2006 | 23 | 2006 |
| Identification of molecular variants at the promoter region of the human α7 neuronal nicotinic acetylcholine receptor subunit gene but lack of association with schizophrenia CH Li, HM Liao, CH Chen Neuroscience letters 372 (1-2), 1-5, 2004 | 21 | 2004 |
De-Maw ChuangNational Institute of Mental HealthVerified email at mail.nih.gov
