Biochemistry, Genetics and Molecular Biology
Haplotype
100%
Single Nucleotide Polymorphism
99%
Genome-Wide Association Study
94%
Candidate Gene
83%
Genetics
73%
Genotyping
70%
Allele
55%
Gene Linkage
52%
Gene Linkage Disequilibrium
43%
Single-Nucleotide Polymorphism
39%
DSM-IV
36%
Linkage Analysis
30%
Quantitative Trait Locus
28%
Exon
28%
Case-Control Study
27%
Quantitative Trait
25%
Promoter Region
24%
Transporter Genes
24%
Pedigree
24%
Innate Immunity
24%
T Cell
24%
Autoimmunity
24%
Genomics
23%
Proband
23%
Homozygosity
20%
Genetic Architecture
18%
Major Histocompatibility Complex
18%
Intron
17%
Genetic Determinism
17%
Blood Pressure
16%
X Chromosome
15%
HLA-C
15%
Alternative Splicing
15%
Rare Variant
15%
Gene Frequency
12%
Methylation
12%
BTNL2
12%
Calcium Channel
12%
Transcription
12%
RNA Editing
12%
EPAS1
12%
Motor Neuron
12%
Smoking Cessation
12%
Interleukin-1
12%
Missense
12%
Immune-Related Gene
12%
NAD(P)H Oxidase
12%
Natural Selection
12%
Microsatellite
12%
Monoamine Oxidase
12%
Neuroscience
Haplotype
87%
Attention Deficit Hyperactivity Disorder
72%
Single-Nucleotide Polymorphism
41%
Linkage Disequilibrium
41%
Quantitative Trait Locus
39%
Bipolar Disorder
36%
Genome-Wide Association Study
33%
Allele Frequency
32%
Major Depressive Disorder
24%
Promoter Region
23%
Synaptosomal Associated Protein 25
17%
Neurotransmitter
16%
X Chromosome
15%
Primary Generalized Epilepsy
15%
Intron
13%
Nitric Oxide
12%
Behavior (Neuroscience)
12%
Norepinephrine Transporter
12%
Neuroticism
12%
Hypertension
12%
Severe Depression
12%
Chromosome 3
12%
Serotonin Transporter
12%
Immune-Related Gene
12%
CREB1
12%
Synapsin II
12%
Depressive Disorder
12%
Alzheimer's Disease
12%
Meta-Analysis
12%
Inflammatory Bowel Disease
12%
Cerebrovascular Disease
12%
Calcium Channel
12%
Pathological Gambling
12%
Nerve Cell Degeneration
12%
Monoamine Oxidase A
12%
Monoamine Oxidase
12%
Homeobox Protein Nkx 2.1
12%
5,10 Methylenetetrahydrofolate Reductase (FADH2)
12%
MicroRNA
12%
Methylation
12%
Exon
10%
Parkinson's Disease
9%
Lacunar Stroke
9%
Variable Number Tandem Repeat
7%
Endothelial Nitric Oxide Synthase
7%
Microsatellite
6%
Amyotrophic Lateral Sclerosis
6%
Norepinephrine
6%
T Cell
6%
X Chromosome Inactivation
6%