Keyphrases
Schizophrenia
100%
Copy number Variation
38%
Duplication
33%
Polymorphism
31%
Angiotensin-converting Enzyme Inhibitor (ACEi)
31%
Replication Study
31%
Meta-analysis
31%
Confidence Interval
19%
Schizophrenia Risk
19%
Cytochrome P450 2D6 (CYP2D6)
19%
Mental Disorders
18%
Risk Factors
18%
Clinical High Risk for Psychosis (CHR-P)
18%
High Risk
18%
Age of Onset
17%
Comorbidity
17%
Single nucleotide Polymorphism
17%
Patients with Schizophrenia
15%
Human Endogenous Retrovirus
15%
Multiple Sclerosis Genetics
15%
Cyclophosphamide
15%
Pharmacogenetics
15%
Multiple Chemical Sensitivity
15%
Missense mutation
15%
Multiple Myeloma
15%
Retrospective Cohort Study
15%
NsSNPs
15%
CYP2D6 Genotype
15%
Imprinted Genes
15%
Type 2 Diabetes Mellitus (T2DM)
15%
15q11-q13
15%
Angiotensin Receptor Blockers
15%
ZNF804A
15%
CYP2C19
15%
Carboxylesterase 1 (CES1)
15%
Methylenetetrahydrofolate Reductase Polymorphism
15%
Thalidomide
15%
Suicidal Behavior
15%
At-risk
15%
Dopamine Transporter Gene
15%
Integration Site
15%
Tryptophan Hydroxylase
15%
Microduplication
15%
Psychiatric Disorders
15%
Runs of Homozygosity
15%
Whole Genome Sequencing
15%
Mucocutaneous
15%
Erythema multiforme
15%
In Silico
15%
MEF2A
15%
Biochemistry, Genetics and Molecular Biology
Single-Nucleotide Polymorphism
32%
Gene Linkage
31%
Allele
24%
Genomics
21%
Methylenetetrahydrofolate Reductase
19%
Pharmacogenetics
15%
Gene Locus
15%
Low Copy Repeat
15%
Genetic Susceptibility
15%
Gene Linkage Disequilibrium
15%
Dopamine Transporter
15%
Missense Mutation
15%
Genetics
15%
Carboxylesterase 1
15%
Copy-Number Variation
15%
Haplotype
15%
Angiotensin-Converting Enzyme
15%
Whole Genome Sequencing
15%
Angelman Syndrome
15%
Transporter Genes
15%
Cohort Study
15%
Runs Of Homozygosity
15%
Enzyme Inhibitor
15%
Phosphodiesterase
15%
Candidate Gene
15%
Neuroscience
Single-Nucleotide Polymorphism
59%
Mental Disorder
52%
Meta-Analysis
31%
Copy Number Variation
31%
Genome-Wide Association Study
23%
Intron
21%
Bipolar Disorder
18%
Dopamine Transporter
15%
Solute Carrier Protein
15%
Missense Mutation
15%
Autism
15%
Multiple Sclerosis
15%
Major Histocompatibility Complex
15%
Whole Genome Sequencing
15%
Carboxylesterase
15%
Etiology of Multiple Sclerosis
15%
Comorbidity
15%
TCF7L2
15%
5,10 Methylenetetrahydrofolate Reductase (FADH2)
15%
Tryptophan Hydroxylase
15%
