Mendelian disorders and multifactorial traits: the big divide or one for all?-Reference-Cited by-同舟云学术

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Mendelian disorders and multifactorial traits: the big divide or one for all?

Published:2010-05 Issue:5 Volume:11 Page:380-384
ISSN:1471-0056
Container-title:Nature Reviews Genetics
language:en
Short-container-title:Nat Rev Genet

Author:

Antonarakis Stylianos E.,Chakravarti Aravinda,Cohen Jonathan C.,Hardy John

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

http://www.nature.com/articles/nrg2793.pdf

Reference21 articles.

1. Gibbs, J. R. & Singleton, A. Application of genome-wide single nucleotide polymorphism typing: simple association and beyond. PLoS Genet. 2, e150 (2006).

2. van de Leemput, J. & Chandran, J. et al. Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans. PLoS Genet. 3, e108 (2007).

3. Ng, S. B. et al. Targeted capture and massively parallel sequencing of 12 human exomes. Nature 461, 272–276 (2009).

4. Singleton, A., Myers, A. & Hardy, J. The law of mass action applied to neurodegenerative disease: a hypothesis concerning the etiology and pathogenesis of complex diseases. Hum. Mol. Genet. 13, R123–R126 (2004).

5. Hutton, M. et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 393, 702–705 (1998).

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