Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis
- 30 April 2011
- journal article
- Published by Elsevier BV in Neurobiology of Aging
- Vol. 32 (4), 758.e1-758.e7
- https://doi.org/10.1016/j.neurobiolaging.2010.12.005
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyThe Lancet Neurology, 2010
- Identification of 2 Loci at Chromosomes 9 and 14 in a Multiplex Family With Frontotemporal Lobar Degeneration and Amyotrophic Lateral SclerosisArchives of Neurology, 2010
- Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron diseaseNeurology, 2009
- Genomewide Association Studies and Human DiseaseThe New England Journal of Medicine, 2009
- Pedigree with frontotemporal lobar degeneration – motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9BMC Neurology, 2008
- Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Nature, 2006
- Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21Nature, 2006
- CHMP2B mutations are not a common cause of frontotemporal lobar degenerationNeuroscience Letters, 2006
- The Structure of Haplotype Blocks in the Human GenomeScience, 2002
- Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17Nature, 1998