Associated Papers
Unraveling the enigma of mental disorders: a genetics-first approach and the role of mouse models based on rare disease-susceptible genome variants.
Kondo R et al.
Nagoya Journal of Medical Science, 2025
Copy number variations (CNVs) and karyotyping analysis in males with azoospermia and oligospermia.
Xin X et al.
Bmc Medical Genomics, 2023
Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder.
Kushima I et al.
Biological Psychiatry, 2022
Associations of cognitive impairment in patients with schizophrenia with genetic features and with schizophrenia-related structural and functional brain changes.
Zhuo C et al.
Frontiers in Genetics, 2022
Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.
Crawford K et al.
Journal of Medical Genetics, 2019
Childhood-Onset Schizophrenia: Insights from Induced Pluripotent Stem Cells.
Hoffmann A et al.
International Journal of Molecular Sciences, 2018
Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.
Rees E et al.
Jama Psychiatry, 2016
A pilot study on commonality and specificity of copy number variants in schizophrenia and bipolar disorder.
Chen J et al.
Translational Psychiatry, 2016
Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants.
Duan J et al.
Human Molecular Genetics, 2015
Copy number variation in schizophrenia in Sweden.
Szatkiewicz JP et al.
Molecular Psychiatry, 2014
Evidence that duplications of 22q11.2 protect against schizophrenia.
Rees E et al.
Molecular Psychiatry, 2014
Identification of rare copy number variants in high burden schizophrenia families.
Van Den Bossche MJ et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2013
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