A genome-wide association study has identified a new genetic susceptibility factor for a subtype of frontotemporal lobar dementia characterized by TDP-43 inclusions. The work illustrates how high-quality phenotyping can increase power to detect risk alleles for rare heterogeneous diseases.
References
Lambert, J.C. et al. Nat. Genet. 41, 1094–1099 (2009).
Harold, D. et al. Nat. Genet. 41, 1088–1093 (2009).
Satake, W. et al. Nat. Genet. 41, 1303–1307 (2009).
Simón-Sánchez, J. et al. Nat. Genet. 41, 1308–1312 (2009).
Van Deerlin, V.M. et al. Nat. Genet. 42, 234–239 (2010).
Rosso, S.M. et al. Brain 126, 2016–2022 (2003).
Snowden, J., Neary, D. & Mann, D. Acta Neuropathol. 114, 31–38 (2007).
Le Ber, I. et al. Brain 131, 732–746 (2008).
Hutton, M. et al. Nature 393, 702–705 (1998).
Cruts, M. et al. Nature 442, 920–924 (2006).
Baker, M. et al. Nature 442, 916–919 (2006).
Le Ber, I. et al. Hum. Mutat. 28, 846–855 (2007).
Watts, G.D. et al. Nat. Genet. 36, 377–381 (2004).
Skibinski, G. et al. Nat. Genet. 37, 806–808 (2005).
Neumann, M. et al. Science 314, 130–133 (2006).
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Lambert, JC., Amouyel, P. Deciphering genetic susceptibility to frontotemporal lobar dementia. Nat Genet 42, 189–190 (2010). https://doi.org/10.1038/ng0310-189
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DOI: https://doi.org/10.1038/ng0310-189
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