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Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes
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The TMEM106B risk allele is associated with lower cortical volumes in a clinically diagnosed frontotemporal dementia cohort.
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In: J Neurol Neurosurg Psychiatry (2017) (2017)
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Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.
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In: J Neurol Neurosurg Psychiatry , 84 (12) pp. 1411-1412. (2013) (2013)
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Progressive logopenic/phonological aphasia: Erosion of the language network
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In: NEUROIMAGE , 49 (1) 984 - 993. (2010) (2010)
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The heritability and genetics of frontotemporal lobar degeneration
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In: NEUROLOGY , 73 (18) 1451 - 1456. (2009) (2009)
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A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
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In: BRAIN , 131 706 - 720. (2008) (2008)
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Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene
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In: ARCH NEUROL-CHICAGO , 65 (4) 506 - 513. (2008) (2008)
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Mapping the progression of progranulin-associated frontotemporal lobar degeneration
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In: NAT CLIN PRACT NEURO , 4 (8) 455 - 460. (2008) (2008)
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Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice
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In: P NATL ACAD SCI USA , 105 (10) 3885 - 3890. (2008) (2008)
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Genetic susceptibility, evolution and the kuru epidemic
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In: PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES , 363 (1510) 3741 - 3746. (2008) (2008)
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Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics
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In: Science , 300 (5619) pp. 640-643. (2003) (2003)
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Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics
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In: SCIENCE , 300 (5619) 640 - 643. (2003) (2003)
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