W. Chen

发表

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

J Sergeant, R Plomin, A Rothenberger, 2006, Molecular Psychiatry.

Efficiency of diagnostic criteria for attention deficit disorder: toward an empirical approach to designing and validating diagnostic algorithms.

S. Faraone, J. Biederman, M. Tsuang, 1993, Journal of the American Academy of Child and Adolescent Psychiatry.

Association evidence of schizophrenia with distal genomic region of NOTCH4 in Taiwanese families

S. Faraone, H. Hwu, M. Tsuang, 2007, Genes, brain, and behavior.

Corpus callosum may be similar in children with ADHD and siblings of children with ADHD

A. Simmons, C. Andrew, E. Taylor, 2000, Developmental medicine and child neurology.

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

B. Franke, M. Gill, R. Anney, 2006, Molecular Psychiatry.

Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth

B. Franke, M. Gill, B. Neale, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Polygenic risk for schizophrenia and neurocognitive performance in patients with schizophrenia

S. Mccarroll, N. Laird, B. Neale, 2018, Genes, brain, and behavior.

Concordance of positive and negative symptoms in coaffected sib-pairs with schizophrenia.

H. Hwu, H. Hsu, W. Chen, 1997, American journal of medical genetics.

Schizotypy in community samples: the three-factor structure and correlation with sustained attention.

C. K. Hsiao, W. Chen, C. C. Lin, 1997, Journal of abnormal psychology.

Neuropsychological functions among adolescents with persistent, subsyndromal and remitted attention deficit hyperactivity disorder

S. Gau, W. Chen, Y. J. Lin, 2013, Psychological Medicine.

Association of older paternal age with earlier onset among co-affected schizophrenia sib-pairs

H. Hwu, C. K. Hsiao, C. M. Liu, 2015, Psychological Medicine.

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

S. Gabriel, N. Craddock, L. DeLisi, 2020, medRxiv.

Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p

Chu-Song Chen, Y. Jou, C. M. Liu, 2009, Genes, brain, and behavior.

Minor physical anomalies and craniofacial measures in patients with treatment-resistant schizophrenia

H. Hwu, W. Chen, Ying-Chieh Peng, 2014, Psychological Medicine.

A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16

Henrik, B. Franke, M. Gill, 2008, Molecular Psychiatry.

Analysis across Taiwan Biobank, Biobank Japan, and UK Biobank identifies hundreds of novel loci for 36 quantitative traits

M. Daly, T. Ge, Hwai I. Yang, 2021, medRxiv.

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia

E. Banks, M. O’Donovan, S. Mccarroll, 2015, Translational Psychiatry.

Replication of a rare protective allele in the noradrenaline transporter gene and ADHD

B. Franke, M. Gill, R. Anney, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic variants in COMT and neurocognitive impairment in families of patients with schizophrenia

H. Hwu, Chih-Min Liu, Wei J. Chen, 2009, Genes, brain, and behavior.

Co-transmission of conduct problems with attention-deficit/hyperactivity disorder: familial evidence for a distinct disorder

B. Franke, M. Gill, R. Ebstein, 2008, Journal of Neural Transmission.

Aberrant expression of microRNAs as biomarker for schizophrenia: from acute state to partial remission, and from peripheral blood to cortical tissue

B. Dean, Ch Lai, E. Scarr, 2016, Translational psychiatry.

Sustained attention deficits as markers of genetic susceptibility to schizophrenia.

S. Faraone, Wei J. Chen, W. Chen, 2000, American journal of medical genetics.

A genome‐wide quantitative trait loci scan of neurocognitive performances in families with schizophrenia

M. Tsuang, S. Faraone, W. Chen, 2010, Genes, brain, and behavior.

More evidence supports the association of PPP3CC with schizophrenia

S. Faraone, H. Hwu, M. Tsuang, 2007, Molecular Psychiatry.

Sustained attention deficit and schizotypal personality features in nonpsychotic relatives of schizophrenic patients.

H. Hwu, Shi K. Liu, W. Chen, 1998, The American journal of psychiatry.

Social Adjustment Inventory for Children and Adolescents: concurrent validity in ADHD children.

S. Faraone, J. Biederman, W. Chen, 1993, Journal of the American Academy of Child and Adolescent Psychiatry.

Evidence for the independent familial transmission of attention deficit hyperactivity disorder and learning disabilities: results from a family genetic study.

S. Faraone, J. Biederman, L. Seidman, 1993, The American journal of psychiatry.

Performance of the Continuous Performance Test among community samples.

C K Hsiao, H. Hwu, L. Hsiao, 1998, Schizophrenia bulletin.

No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder

B. Franke, R. Anney, J. Sergeant, 2009 .

No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder

B. Franke, M. Gill, R. Anney, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Patterns and clinical correlates of neuropsychologic deficits in patients with schizophrenia.

H. Hwu, M. Hua, Wei J. Chen, 2006, Journal of the Formosan Medical Association = Taiwan yi zhi.