Biochemistry, Genetics and Molecular Biology
Association
100%
Nested Gene
91%
Genetics
78%
Single-Nucleotide Polymorphism
39%
Genome-Wide Association Study
38%
Genotyping
35%
Aging
35%
Allele
35%
Phenotype
30%
Age
27%
Protein
27%
ABCC9
23%
Genetic Divergence
22%
Tau
22%
Sample
21%
Transactive Response Dna Binding Protein-43
20%
Single Nucleotide Polymorphism
19%
Sequencing
18%
CD33
15%
Amyloid
14%
Lipid
14%
Genetic Risk
14%
Isoform
13%
Proteinopathy
13%
Liquid
13%
Apolipoprotein E
12%
Adjustment
12%
Genome Sequencing
12%
Exon
10%
PICALM
10%
Endophenotype
10%
Time
10%
Pedigree
10%
Genetic Association Study
10%
Quality Control
9%
MicroRNA
9%
Sex Difference
8%
Protein Complexes
8%
Alpha Chain
8%
Thyroid Hormone
8%
Sleep
8%
Genetic Architecture
7%
Genetic Disorder
7%
Memory
7%
Comprehension
7%
Prevalence
7%
Mutation
6%
Experiment
6%
Minor Allele Frequency
6%
TREM2
6%
Medicine and Dentistry
Alzheimer's Disease
94%
Association
59%
Pathology
48%
Age
45%
Dementia
44%
Gene
26%
Aging
25%
Diagnosis
24%
Transactive Response Dna Binding Protein-43
23%
Brain Disease
23%
Genome Wide Association Study
22%
Hippocampal Sclerosis
21%
Allele
21%
Analysis
20%
Patient
20%
Genotype
19%
Neuropathology
19%
Older Adult
17%
Arteriolosclerosis
17%
Diabetes
16%
Person
15%
Apolipoprotein E
14%
TDP 43 Proteinopathy
14%
Life
14%
Family
14%
Cognition
13%
Brain
13%
Memory
13%
Autopsy
13%
Protein
12%
Cerebrovascular Disease
12%
Death
11%
Phenotype
11%
Cognitive Defect
10%
Therapeutic Procedure
10%
Child
9%
Evaluation Study
9%
Diseases
9%
Single Nucleotide Polymorphism
9%
Apolipoprotein
9%
Alcohol Consumption
8%
Hyperhomocysteinemia
8%
Consensus
8%
Brain Tissue
7%
Mild Cognitive Impairment
7%
Assessment
7%
Genetic Risk Factor
7%
Frontotemporal Lobar Degeneration
6%
Prevalence
6%
Infarction
6%
Neuroscience
Brain
72%
Gene
71%
Dementia
69%
Hippocampal Sclerosis
56%
Encephalopathy
37%
Genotype
35%
Protein
34%
Genome-Wide Association Study
29%
Mild Cognitive Impairment
24%
Single-Nucleotide Polymorphism
22%
Phenotype
22%
Cognition
21%
Apolipoprotein E
19%
Cognitive Disorders
18%
Amyloid
18%
Memory
16%
Polymorphism
15%
Diabetes
13%
Neurodegenerative Disorder
13%
Frontotemporal Dementia
11%
Amygdala
9%
Homocysteine
9%
MicroRNA
9%
Cerebrovascular Disease
9%
Endophenotype
9%
Opioid
8%
Protein Complexes
8%
Thyroid Hormone
8%
Alpha Chain
8%
Mucin 6
8%
Gene Expression
7%
Cerebral Amyloid Angiopathy
6%
Apolipoprotein E4
6%
Variable Number Tandem Repeat
6%
Hippocampus
6%
Allele Frequency
5%
Promoter Region
5%
DNA-binding Protein
5%
Synuclein
5%
Adenosine Triphosphate
5%