公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
2017 | ARHGEF10 knockout inhibits platelet aggregation and protects mice from thrombus formation | Lu D.-H.; Hsu C.-C.; Huang S.-W.; Tu H.-J.; TUR-FU HUANG ; Liou H.-C.; Liao H.-M.; Chen C.-H.; WEN-MEI FU ; SUSAN SHUR-FEN GAU | Journal of Thrombosis and Haemostasis | 10 | 10 | |
2017 | Atg9 antagonizes TOR signaling to regulate intestinal cell growth and epithelial homeostasis in Drosophila | Wen J.-K.; Wang Y.-T.; CHIH-CHIANG CHAN ; Hsieh C.-W.; Liao H.-M.; Hung C.-C.; Chen G.-C. | eLife | 37 | 35 | |
2014 | Autism-associated gene Dlgap2 mutant mice demonstrate exacerbated aggressive behaviors and orbitofrontal cortex deficits | Jiang-Xie L.-F.; Liao H.-M.; Chen C.-H.; Chen Y.-T.; Ho S.-Y.; Lu D.-H.; LI-JEN LEE ; HORNG-HUEI LIOU ; WEN-MEI FU ; SUSAN SHUR-FEN GAU | Molecular Autism | 61 | 60 | |
2013 | Chromosomal Abnormalities in Patients With Autism Spectrum Disorders From Taiwan | Liao H.-M.; SUSAN SHUR-FEN GAU ; Tsai W.-C.; Fang J.-S.; Su Y.-C.; Chou M.-C.; Liu S.-K.; Chou W.-J.; Wu Y.-Y.; Chen C.-H. | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 12 | 13 | |
2017 | Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13.3 associated with autism spectrum disorder | Chen C.-H.; Chen H.-I.; Liao H.-M.; Chen Y.-J.; Fang J.-S.; Lee K.-F.; SUSAN SHUR-FEN GAU | Psychiatric Genetics | 20 | 19 | |
2016 | Complex genomic variants contribute toward the genetic architecture of autism spectrum disorder | Chen C.-H.; Liao H.-M.; Chen H.-I.; Fang J.-S.; Chen Y.-J.; Lee K.-F.; SUSAN SHUR-FEN GAU | Psychiatric genetics | 1 | 1 | |
2013 | Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders | Chien W.-H.; SUSAN SHUR-FEN GAU ; Liao H.-M.; YEN-NAN CHIU ; Wu Y.-Y.; Huang Y.-S.; Tsai W.-C.; Tsai H.-M.; Chen C.-H. | Molecular Autism | 39 | 41 | |
2016 | Dosage of copy number variation at 22q11.2 mediates changes in cognition, social function and brain structure in autism spectrum disorder | Chen H.-I.; YI-LING CHIEN ; Liao H.-M.; Chien W.-H.; Chen C.-H.; Chen Y.-C.; SUSAN SHUR-FEN GAU | Journal of the Formosan Medical Association | 7 | 6 | |
2016 | Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder | Yin C.-L.; Chen H.-I.; Li L.-H.; YI-LING CHIEN ; Liao H.-M.; Chou M.C.; Chou W.-J.; WEN-CHE TSAI ; YEN-NAN CHIU ; Wu Y.-Y.; Lo C.-Z.; Wu J.-Y.; Chen Y.-T.; SUSAN SHUR-FEN GAU | Molecular Autism | 46 | 49 | |
2012 | Identification of two inherited copy number variants in a male with autism supports two-hit and compound heterozygosity models of autism | SUSAN SHUR-FEN GAU ; Liao H.-M.; Hong C.-C.; Chien W.-H.; Chen C.-H. | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 28 | 26 | |
2018 | Impairment of social behaviors in Arhgef10 knockout mice | Lu D.-H.; Liao H.-M.; Chen C.-H.; Tu H.-J.; Liou H.-C.; SUSAN SHUR-FEN GAU ; WEN-MEI FU | Molecular Autism | 21 | 20 |