Associated Papers
Genome-wide association meta-analysis and rare copy number variant analysis of treatment-resistant depression.
Xiong Y et al.
Molecular Psychiatry, 2025
40571737 (PubMed )
Supplement: 41380_2025_3084_MOESM2_ESM.xlsx › Supplementary_Table_15
Rare copy number variation in posttraumatic stress disorder.
Maihofer AX et al.
Molecular Psychiatry, 2022
36131047 (PubMed )
Supplement: NIHMS1853619-supplement-Supplementary_Table_4.xlsx › ST4._Neurodevelopmental_CNV
Analysis of Diffusion Tensor Imaging Data From the UK Biobank Confirms Dosage Effect of 15q11.2 Copy Number Variation on White Matter and Shows Association With Cognition.
Silva AI et al.
Biological Psychiatry, 2021
33931204 (PubMed )
Supplement: mmc2.xlsx › TableS2
The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.
Curry CJ et al.
American Journal of Medical Genetics. Part A, 2013
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