Epidemiología y Salud Pública
German Center for Neurodegenerative Diseases
Bonn, AlemaniaPublikationen in Zusammenarbeit mit Forschern von German Center for Neurodegenerative Diseases (13)
2020
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Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (Acta Neuropathologica, (2019), 138, 2, (237-250), 10.1007/s00401-019-02026-8)
Acta Neuropathologica
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Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis
Scientific Reports, Vol. 10, Núm. 1
2019
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Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
Scientific Reports, Vol. 9, Núm. 1
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Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia
Nature Medicine, Vol. 25, Núm. 1, pp. 152-164
2018
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CXCR4 involvement in neurodegenerative diseases
Translational Psychiatry, Vol. 8, Núm. 1
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Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies
PLoS Medicine, Vol. 15, Núm. 1
2017
2015
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Convergent genetic and expression data implicate immunity in Alzheimer's disease
Alzheimer's and Dementia, Vol. 11, Núm. 6, pp. 658-671
2014
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Frontotemporal dementia and its subtypes: A genome-wide association study
The Lancet Neurology, Vol. 13, Núm. 7, pp. 686-699
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Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease
PLoS ONE, Vol. 9, Núm. 6
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Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes
Neurobiology of Aging, Vol. 35, Núm. 11, pp. 2657.e13-2657.e19
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
Acta Neuropathologica, Vol. 128, Núm. 3, pp. 397-410
2013
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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Nature Genetics, Vol. 45, Núm. 12, pp. 1452-1458