Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics,Molecular Biology,Biochemistry,General Medicine
Link
http://academic.oup.com/bfg/article-pdf/14/5/315/5039028/elv018.pdf
Reference170 articles.
1. Human Copy Number Variation and Complex Genetic Disease
2. Genomic rearrangements and sporadic disease
3. Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease
4. Genome structural variation discovery and genotyping
5. A Human Genome Structural Variation Sequencing Resource Reveals Insights into Mutational Mechanisms
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1. The gene dose makes the disease;Cell;2022-08
2. Neurodevelopmental copy-number variants: A roadmap to improving outcomes by uniting patient advocates, researchers, and clinicians for collective impact;The American Journal of Human Genetics;2022-08
3. The role of ROH in the etiopathogenesis of complex diseases;South of Russia: ecology, development;2022-07-15
4. Advances in Next-Generation Sequencing Technologies and Functional Investigation of Candidate Variants in Neurological and Behavioral Disorders;Encyclopedia of Behavioral Neuroscience, 2nd edition;2022
5. Quantitative neurogenetics: applications in understanding disease;Biochemical Society Transactions;2021-07-20
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