Mutation screening in Chinese patients with familial Alzheimer&#39;s disease by whole-exome sequencing

Mutation screening in Chinese patients with familial Alzheimer's disease by whole-exome sequencing

IBRO Reports ◽

10.1016/j.ibror.2019.07.1490 ◽

2019 ◽

Vol 6 ◽

pp. S473

Author(s):

Qing-Qing Tao ◽

Bin Jiang ◽

Zhi-Ying Wu

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Exome Sequencing ◽

Whole Exome Sequencing ◽

Mutation Screening ◽

Chinese Patients ◽

Familial Alzheimer’S Disease ◽

Whole Exome ◽

Familial Alzheimer's Disease

Mutation and association analyses of dementia-causal genes in Han Chinese patients with early-onset and familial Alzheimer's disease

Journal of Psychiatric Research ◽

10.1016/j.jpsychires.2019.03.026 ◽

2019 ◽

Vol 113 ◽

pp. 141-147 ◽

Cited By ~ 3

Author(s):

Guihong Wang ◽

Deng-Feng Zhang ◽

Hong-Yan Jiang ◽

Yu Fan ◽

Lingyan Ma ◽

...

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Early Onset ◽

Han Chinese ◽

Chinese Patients ◽

Familial Alzheimer’S Disease ◽

Association Analyses ◽

Causal Genes ◽

Familial Alzheimer's Disease

P1-170: WHOLE-EXOME SEQUENCING IN 20,197 INDIVIDUALS IDENTIFIES ULTRA-RARE SORL1 LOSS-OF-FUNCTION VARIANTS IN LATE-ONSET ALZHEIMER'S DISEASE

10.1016/j.jalz.2018.06.174 ◽

2006 ◽

Vol 14 (7S_Part_6) ◽

pp. P344-P344

Author(s):

Neha S. Raghavan ◽

Adam M. Brickman ◽

Howard Andrews ◽

Jennifer J. Manly ◽

Nicole Schupf ◽

...

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Exome Sequencing ◽

Whole Exome Sequencing ◽

Late Onset ◽

Loss Of Function ◽

Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease

Annals of Clinical and Translational Neurology ◽

10.1002/acn3.582 ◽

2018 ◽

Vol 5 (7) ◽

pp. 832-842 ◽

Cited By ~ 33

Author(s):

Neha S. Raghavan ◽

Adam M. Brickman ◽

Howard Andrews ◽

Jennifer J. Manly ◽

Nicole Schupf ◽

...

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Exome Sequencing ◽

Whole Exome Sequencing ◽

Rare Variants ◽

P1-146: WHOLE EXOME SEQUENCING IN PATIENTS WITH EARLY-ONSET ALZHEIMER'S DISEASE AND FRONTOTEMPORAL DEMENTIA: MUTATION DETECTION IN CAUSAL AND RISK GENES FOR DEMENTIA

10.1016/j.jalz.2018.06.149 ◽

2006 ◽

Vol 14 (7S_Part_6) ◽

pp. P332-P332

Author(s):

Albert Lladó ◽

Raquel Sanchez-Valle ◽

Neus Falgas ◽

Mircea Balasa ◽

Benjamin Rodríguez-Santiago ◽

...

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Exome Sequencing ◽

Frontotemporal Dementia ◽

Whole Exome Sequencing ◽

Early Onset ◽

Mutation Detection ◽

Risk Genes ◽

Whole Exome ◽

Early Onset Alzheimer’S Disease

Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease

Annals of Clinical and Translational Neurology ◽

10.1002/acn3.742 ◽

2019 ◽

Vol 6 (2) ◽

pp. 416-416

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Exome Sequencing ◽

Whole Exome Sequencing ◽

Rare Variants ◽

P2-024: Whole-exome sequencing in dutch families with Alzheimer's disease

10.1016/j.jalz.2015.06.560 ◽

2015 ◽

Vol 11 (7S_Part_10) ◽

pp. P490-P490

Author(s):

Tsz Hang Wong ◽

Sven J. van der Lee ◽

Lieke H.H. Meeter ◽

Jeroen G.J. van Rooij ◽

M. Arfan Ikram ◽

...

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Exome Sequencing ◽

Whole Exome Sequencing ◽

O1-09-02: Whole Exome Sequencing of Late Onset Multiplex Families Identifies Rare Coding Variants in Known and Novel Alzheimer’s Disease Genes

10.1016/j.jalz.2016.06.342 ◽

2016 ◽

Vol 12 ◽

pp. P196-P197

Author(s):

Holly N. Cukier ◽

Brian W. Kunkle ◽

Sophie Rolati ◽

Patrice L. Whitehead ◽

Jeffery M. Vance ◽

...

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Exome Sequencing ◽

Whole Exome Sequencing ◽

Late Onset ◽

Disease Genes ◽

Whole Exome ◽

Multiplex Families ◽

Coding Variants

O1-03-04: Whole Exome Sequencing in Healthy Elderly APOE E44 Subjects to Identify Protective Variants in Alzheimer’s Disease

10.1016/j.jalz.2016.06.307 ◽

2016 ◽

Vol 12 ◽

pp. P178-P178

Author(s):

Badri N. Vardarajan ◽

Alexander H. Li ◽

Eric Boerwinkle ◽

Richard Mayeux

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Exome Sequencing ◽

Whole Exome Sequencing ◽

Healthy Elderly ◽

Whole Exome ◽

Protective Variants

O1-03-03: Identification of Novel Candidate Genes for Early-Onset Alzheimer's Disease Through Integrated Whole-Exome Sequencing and Exome Chip Array Association Analysis

10.1016/j.jalz.2016.06.306 ◽

2016 ◽

Vol 12 ◽

pp. P177-P178 ◽

Cited By ~ 1

Author(s):

Brian W. Kunkle ◽

Badri N. Vardarajan ◽

Adam C. Naj ◽

Holly N. Cukier ◽

Derek M. Dykxhoorn ◽

...

Keyword(s):

Alzheimer’S Disease ◽

Alzheimer's Disease ◽

Exome Sequencing ◽

Candidate Genes ◽

Whole Exome Sequencing ◽

Association Analysis ◽

Early Onset ◽

Whole Exome ◽

Early Onset Alzheimer’S Disease ◽

Exome Chip