Biochemistry, Genetics and Molecular Biology
Genetic Screening
100%
Genetics
70%
Medical Genetics
67%
Medical Genomics
60%
Genome Sequencing
54%
Cystic Fibrosis
49%
Allele
49%
Dystrophin
38%
X Chromosome
31%
Exon
26%
Human Genetics
26%
Molecular Genetics
24%
Exome Sequencing
24%
Genotyping
23%
Mouse
21%
Human Genome
19%
CAG Repeat
18%
Proband
17%
Trinucleotide Repeat Expansion
17%
Decision Making
16%
Genetic Variation
16%
Hepatocyte
15%
Glucagon
15%
Denaturing High Performance Liquid Chromatography
15%
Prevalence
15%
Homozygosity
14%
Mass Screening
14%
Major Histocompatibility Complex
14%
Fluorescence in Situ Hybridization
14%
Fructose
14%
MSH6
14%
Exome Sequencing
14%
Skewed X-Inactivation
14%
Carnitine O-Palmitoyltransferase
14%
Phosphofructokinase
14%
Genetic Test
13%
DNA Sequence
13%
Laboratory Test
13%
Gene Deletion
13%
Quality Control
12%
Lifespan
12%
Oligonucleotide
11%
Next Generation Sequencing
11%
Cytogenetics
11%
Population
10%
Mosaicism
10%
BRCA1
10%
BRCA2
10%
DNA Mismatch Repair
10%
MSH2
9%
Medicine and Dentistry
Genetic Screening
56%
Disease
55%
Cystic Fibrosis
42%
Genome Sequencing
32%
Health Care Cost
28%
Malignant Neoplasm
27%
Health Outcomes
25%
Clinician
24%
Family History
24%
Exome Sequencing
23%
Medicine
21%
Colorectal Cancer
20%
Hereditary Nonpolyposis Colorectal Cancer
19%
Neoplasm
18%
Human Genetics
17%
Decision Making
17%
Carrier Testing
15%
Whole Genome Sequencing
14%
Prenatal Screening
14%
Metastatic Colorectal Cancer
14%
Laboratory Test
13%
Codon
12%
Diagnosis
12%
Pathologist
12%
DNA Sequence
11%
DNA Mismatch Repair
11%
Clinical Genetics
10%
Consumer
10%
Health System
10%
Genetic Disorder
9%
Prevalence
9%
Breast Cancer
9%
Exome
8%
BRCA1
8%
Public Health
8%
Sensitivity and Specificity
8%
Human Genome
8%
Gene Repair
7%
Allele
7%
Neurofibromatosis Type I
7%
Randomized Controlled Trial
7%
Carcinogenicity
7%
Thyroid Medullary Carcinoma
7%
Maturity Onset Diabetes of the Young
7%
Venous Thromboembolism
7%
Mammography
7%
Dystrophin
7%
Epidermal Growth Factor Receptor
7%
Clinical Health
7%
FMR1
7%
Keyphrases
Duchenne muscular Dystrophy
21%
Human Variome Project
21%
Denaturing High-performance Liquid Chromatography (DHPLC)
20%
Exon
20%
American College of Medical Genetics
18%
Clinical Sequencing
18%
Female Carrier
17%
Dystrophin Gene
16%
Dystrophin
15%
X Chromosome
14%
Homozygosity
14%
Hepatocytes
14%
6-P2
14%
Project Meeting
14%
Fluorescence in Situ Hybridization
14%
Cystic Fibrosis
14%
MSH6
14%
Sequence Variation
14%
Fructose
14%
Genomic Applications
14%
Application in Practice
14%
Human Genetics
13%
Medical Genomics
11%
Research Consortium
11%
Genetic Testing
11%
Genome Sequencing
11%
Gene Deletion
10%
Glucagon
10%
X-linked
10%
Hereditary Colorectal Cancer Syndromes
10%
Major Histocompatibility Complex
10%
EGAPP
10%
Analytic Validity
10%
Health Care Costs
9%
Mutation Testing
9%
Practice Method
9%
Genomic Medicine
9%
Isolated Hepatocytes
8%
MSH2
8%
MLH1
8%
Patient Phenotype
8%
Kindred
8%
Becker muscular Dystrophy
8%
Prenatal Diagnosis
8%
Clinical Genetic Testing
8%
Mutation Screening
8%
CAG Repeat Expansion
7%
Clinical Presentation
7%
CAG Repeat
7%
Homozygous mutation
7%
