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- 2024
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Mark
The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1
(
- Contribution to journal › Article
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Mark
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia
(
- Contribution to journal › Article
- 2021
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Mark
Genetic influence during the early phases of Alzheimer's disease on longitudinal cognitive impairment
(
- Contribution to journal › Article
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Mark
Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease
(
- Contribution to journal › Article
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Mark
Genetic interaction study of Alzheimer's disease quantitative biomarkers : A polygenic risk score analysis and evaluation
(
- Contribution to journal › Article
- 2020
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Mark
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
2020) In Neuron(
- Contribution to journal › Article
- 2019
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Mark
Endo-lysosomal proteins and ubiquitin CSF concentrations in Alzheimer's and Parkinson's disease
(
- Contribution to journal › Article
- 2018
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Mark
Investigating the genetic architecture of dementia with Lewy bodies : a two-stage genome-wide association study
(
- Contribution to journal › Article
- 2016
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Mark
Selective vulnerability in neurodegeneration: insights from clinical variants of Alzheimer's disease.
(
- Contribution to journal › Scientific review
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Mark
Increased cerebrospinal fluid soluble TREM2 concentration in Alzheimer's disease
(
- Contribution to journal › Article
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Mark
Vascular disease and vascular risk factors in relation to motor features and cognition in early Parkinson's disease
(
- Contribution to journal › Article
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Mark
Variation in Recent Onset Parkinson's Disease : Implications for Prodromal Detection
(
- Contribution to journal › Article
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Mark
Deletions at 22q11.2 in idiopathic Parkinson's disease : a combined analysis of genome-wide association data
(
- Contribution to journal › Article
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Mark
Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases.
(
- Contribution to journal › Article
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Mark
A genome-wide association study in multiple system atrophy
(
- Contribution to journal › Article
- 2015
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Mark
Tracking Parkinson's : Study Design and Baseline Patient Data
(
- Contribution to journal › Article
- 2014
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Mark
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of Dementia with Lewy Bodies.
(
- Contribution to journal › Article
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Mark
Frontotemporal dementia and its subtypes: a genome-wide association study.
(
- Contribution to journal › Article
- 2012
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Mark
Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.
2012) In Neurobiology of Aging(
- Contribution to journal › Article
-
Mark
Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research
(
- Contribution to journal › Article
-
Mark
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
(
- Contribution to journal › Article