Keyphrases
Carboxylesterase 1 (CES1)
100%
Pharmacogenetics
36%
SNP
33%
Congestive Heart Failure
33%
Angiotensin-converting Enzyme Inhibitor (ACEi)
33%
Genetic Analysis
27%
Colorectal Cancer
27%
Methylphenidate
23%
Whole Genome Sequencing
22%
Familial Adenomatous Polyposis
22%
Copy number Variation
20%
Pathogenic Variants
20%
Familial Colorectal Cancer
19%
Genotype
19%
Drug Metabolism
19%
Tool Comparison
16%
Copy number Variation Detection
16%
Genetic Variation
16%
Gene Variants
16%
Colorectal Polyposis
16%
Amplicon-based NGS
16%
Storage Time
16%
Thyroid Neoplasms
16%
Red Blood Cell Storage
16%
NGS Panel
16%
Intensive Care Unit
16%
Prognostic Impact
16%
Caroli Disease
16%
Enzyme Activity
16%
Gastrointestinal Polyposis
16%
Ritalinic Acid
16%
Confidence Interval
16%
Late-onset Colorectal Cancer
16%
Epistasis Network
16%
Germ Cells
16%
Encoding Gene
16%
Risk Stratification
16%
Pathogenic Germline Variant
16%
RPS20
16%
Children with Attention Deficit
16%
Selective Serotonin Reuptake Inhibitors
16%
Colorectal Cancer Patients
16%
Cell-derived
16%
Unknown Etiology
16%
Weight Loss
16%
Genetic Causes
16%
Missense Variants
16%
Target Identification
16%
Retrospective Cohort Study
16%
Attention Deficit Hyperactivity Disorder
16%
Biochemistry, Genetics and Molecular Biology
Carboxylesterase 1
63%
Genetics
58%
Whole Genome Sequencing
41%
Germ Cell
40%
Germline
40%
Pharmacogenetics
36%
Enzyme Inhibitor
33%
Angiotensin-Converting Enzyme
33%
Single Nucleotide Polymorphism
33%
Single-Nucleotide Polymorphism
31%
Genetic Divergence
27%
Genotyping
27%
Next Generation Sequencing
22%
Carboxylesterase
21%
Copy-Number Variation
20%
Drug Metabolism
18%
Exon
18%
Haplotype
18%
Follicular Cell
16%
Genetic Variation
16%
Homozygote
16%
Missense
16%
Enzyme Activity
16%
Cohort Study
16%
MSH6
16%
Selective Serotonin Reuptake Inhibitor
16%
Transcription
16%
Genetic Screening
16%
Gene Polymorphism
16%
Pharmacogenomics
16%
PMS2
16%
MSH2
16%
Exome
16%
Amplicon
16%
Computer Model
14%
Allele
12%
MUTYH
12%
Promoter Region
12%
Mosaicism
11%
Pseudogene
9%
Hydrolase
9%
Medical Record
8%
DNA Mismatch Repair
8%
BUB1
8%
Intron
7%
Untranslated Region
7%
Metabolic Pathway
7%
Polymerase Chain Reaction
7%
Morphology
6%
Somatic Mutation
6%
