about
ABCA7 rare variants and Alzheimer disease riskScreening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons.Deletion of exons 9 and 10 of the Presenilin 1 gene in a patient with Early-onset Alzheimer Disease generates longer amyloid seeds.17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls.Alzheimer disease: modeling an Aβ-centered biological network.SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's disease.De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease.
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Q36982034-CF2CFA4B-6869-44DB-8253-A231C5EE7C4CQ37058503-57110616-45C1-4C6E-91DC-9976D388EC4BQ38810339-EA60C548-FF42-4F71-BA89-BB275F2724BDQ39107119-87AC85D7-9BD7-4812-827C-07CA450F111AQ40090252-F77724BE-56B2-427F-96C9-E466C99FCED3Q47878052-AD27783D-C329-43D6-A097-7E919AD09CD7Q48142613-2FDBA7E6-A3E5-4E23-B96D-D4B3C99FA788Q50953138-82DC87C8-8EB7-46BD-906B-8D09F97D7176
P50
description
onderzoeker
@nl
researcher, ORCID id # 0000-0002-9332-2281
@en
name
Kilan Le Guennec
@ast
Kilan Le Guennec
@en
Kilan Le Guennec
@nl
type
label
Kilan Le Guennec
@ast
Kilan Le Guennec
@en
Kilan Le Guennec
@nl
prefLabel
Kilan Le Guennec
@ast
Kilan Le Guennec
@en
Kilan Le Guennec
@nl
P106
P31
P496
0000-0002-9332-2281