Investigating copy number variants in schizophrenia pedigrees using a new consensus pipeline called PECAN
Author:
Funder
National Institutes of Health
Science Foundation Ireland
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41598-024-66021-0.pdf
Reference51 articles.
1. Shaikh, T. H. Copy number variation disorders. Curr. Genet. Med. Rep. 5(4), 183–190 (2017).
2. Zarrei, M., MacDonald, J. R., Merico, D. & Scherer, S. W. A copy number variation map of the human genome. Nat. Rev. Genet. 16(3), 172–183 (2015).
3. Girirajan, S., Campbell, C. D. & Eichler, E. E. Human copy number variation and complex genetic disease. Annu. Rev. Genet. 45(45), 203–226 (2011).
4. Stankiewicz, P. & Lupski, J. R. Structural variation in the human genome and its role in disease. Annu. Rev. Med. 61, 437–455 (2010).
5. Weischenfeldt, J., Symmons, O., Spitz, F. & Korbel, J. O. Phenotypic impact of genomic structural variation: Insights from and for human disease. Nat. Rev. Genet. 14(2), 125–138 (2013).
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