Missing heritability and strategies for finding the underlying causes of complex disease-Reference-Cited by-同舟云学术

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Missing heritability and strategies for finding the underlying causes of complex disease

Published:2010-06 Issue:6 Volume:11 Page:446-450
ISSN:1471-0056
Container-title:Nature Reviews Genetics
language:en
Short-container-title:Nat Rev Genet

Author:

Eichler Evan E.,Flint Jonathan,Gibson Greg,Kong Augustine,Leal Suzanne M.,Moore Jason H.,Nadeau Joseph H.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

http://www.nature.com/articles/nrg2809.pdf

Reference61 articles.

1. Cooper, G. M., Zerr, T., Kidd, J. M., Eichler, E. E. & Nickerson, D. A. Systematic assessment of copy number variant detection via genome-wide SNP genotyping. Nature Genet. 40, 1199–1203 (2008).

2. McCarroll, S. A. et al. Integrated detection and population-genetic analysis of SNPs and copy number variation. Nature Genet. 40, 1166–1174 (2008).

3. Redon, R. et al. Global variation in copy number in the human genome. Nature 444, 444–454 (2006).

4. Kidd, J. M. et al. Mapping and sequencing of structural variation from eight human genomes. Nature 453, 56–64 (2008).

5. Conrad, D. F. et al. Origins and functional impact of copy number variation in the human genome. Nature 464, 704–712 (2010).

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