Association of rare variants in neurodegenerative genes with familial Alzheimer’s disease
出版年份 2020 全文链接
标题
Association of rare variants in neurodegenerative genes with familial Alzheimer’s disease
作者
关键词
-
出版物
Annals of Clinical and Translational Neurology
Volume 7, Issue 10, Pages 1985-1995
出版商
Wiley
发表日期
2020-09-18
DOI
10.1002/acn3.51197
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Analysis of 50 Neurodegenerative Genes in Clinically Diagnosed Early-Onset Alzheimer’s Disease
- (2019) Vo Giau et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Rare Variants in PLD3 Increase Risk for Alzheimer’s Disease in Han Chinese
- (2018) Meng-Shan Tan et al. JOURNAL OF ALZHEIMERS DISEASE
- Convergent molecular defects underpin diverse neurodegenerative diseases
- (2018) George K Tofaris et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Genetic risk for neurodegenerative disorders, and its overlap with cognitive ability and physical function
- (2018) Saskia P. Hagenaars et al. PLoS One
- Analysis of neurodegenerative Mendelian genes in clinically diagnosed Alzheimer Disease
- (2017) Maria Victoria Fernández et al. PLoS Genetics
- Clinical heterogeneity of LRRK2 p.I2012T mutation
- (2016) Tian-Sin Fan et al. PARKINSONISM & RELATED DISORDERS
- Coding mutations inSORL1and Alzheimer disease
- (2015) Badri N. Vardarajan et al. ANNALS OF NEUROLOGY
- Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci
- (2015) Badri N. Vardarajan et al. ANNALS OF NEUROLOGY
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study
- (2015) Elise Cuyvers et al. LANCET NEUROLOGY
- PLD3 variants in population studies
- (2015) Sven J. van der Lee et al. NATURE
- A conceptual framework for research on subjective cognitive decline in preclinical Alzheimer's disease
- (2014) Frank Jessen et al. Alzheimers & Dementia
- Structural and functional in silico analysis of LRRK2 missense substitutions
- (2014) Fernando Cardona et al. MOLECULAR BIOLOGY REPORTS
- Investigation of TREM2, PLD3, and UNC5C variants in patients with Alzheimer's disease from mainland China
- (2014) Bin Jiao et al. NEUROBIOLOGY OF AGING
- The global prevalence of dementia: A systematic review and metaanalysis
- (2013) Martin Prince et al. Alzheimers & Dementia
- Epidemiology of Alzheimer's disease and other forms of dementia in China, 1990–2010: a systematic review and analysis
- (2013) Kit Yee Chan et al. LANCET
- Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
- (2013) Carlos Cruchaga et al. NATURE
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
- (2013) Jean-Charles Lambert et al. NATURE GENETICS
- Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor
- (2012) Nancy D. Merner et al. AMERICAN JOURNAL OF HUMAN GENETICS
- High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease
- (2012) C Pottier et al. MOLECULAR PSYCHIATRY
- Variant of TREM2 Associated with the Risk of Alzheimer's Disease
- (2012) Thorlakur Jonsson et al. NEW ENGLAND JOURNAL OF MEDICINE
- Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants
- (2012) Chaodong Wang et al. PARKINSONISM & RELATED DISORDERS
- Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
- (2011) Paul Hollingworth et al. NATURE GENETICS
- Genetic contribution of FUS to frontotemporal lobar degeneration
- (2010) T. Van Langenhove et al. NEUROLOGY
- Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
- (2009) Jean-Charles Lambert et al. NATURE GENETICS
- Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
- (2009) T. J. Kwiatkowski et al. SCIENCE
- Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
- (2008) Daniel G Healy et al. LANCET NEUROLOGY
- Genetics of familial amyotrophic lateral sclerosis
- (2008) P. N. Valdmanis et al. NEUROLOGY
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now