Biochemistry, Genetics and Molecular Biology
BRCA2
100%
Blood Clot Lysis
66%
BRCA1
66%
Intron
42%
DNA Repair
41%
Allele
37%
Mammalian Target of Rapamycin
33%
CRISPR Activation
33%
Mental Retardation
33%
Population
33%
Prospective Cohort Study
33%
Polypyrimidine Tract
33%
Homologous Recombination
33%
Morbidity
33%
Pedigree
33%
STK11
33%
Cohort Study
33%
Mouse
33%
Genetic Screening
33%
mTOR Signaling
33%
Hailey-Hailey
33%
Bone Morphogenetic Protein 5
33%
Double-Strand DNA Break
33%
CRISPR/Cas9
33%
Messenger RNA
32%
Genetics
28%
Germline
28%
Germ Cell
28%
RNA Sequencing
26%
Genetic Divergence
25%
K562 Cells
25%
RAD51C
16%
Fibroblast
16%
Myelin Protein Zero
16%
Spastin
16%
Next Generation Sequencing
14%
Nonsense-Mediated Decay
13%
Stem Cell
11%
Heterozygote
11%
Genetic Carrier
11%
Mouse Model
11%
Signal Transduction
11%
Haploinsufficiency
11%
Animal Model
11%
N6-Methyladenosine
11%
Development
11%
mRNA Stability
11%
Cell Count
11%
Induced Pluripotent Stem Cell
11%
Cognition
11%
Medicine and Dentistry
Genetic Screening
44%
Intron
42%
Prospective Cohort Study
38%
Apoplexy
33%
Preventive Mastectomy
33%
Genetic Counseling
33%
Contralateral
33%
Breast Cancer
33%
Multiple Sclerosis
33%
Retroviridae
33%
RNA Sequencing
33%
Bone Morphogenetic Protein 5
33%
Hailey-Hailey Disease
33%
Disease
25%
Peutz Jeghers Syndrome
25%
Hazard Ratio
22%
Diagnosis
18%
Medicine
16%
Secondary Prevention
16%
Heritability
16%
Primary Prevention
16%
Nonsense Mediated mRNA Decay
16%
Disease Predisposition
16%
Risk Stratification
11%
Decision Making
11%
Onset Age
11%
Genetic Risk
11%
Exon
9%
Central Nervous System Disease
8%
Cancer Susceptibility
8%
Epstein Barr Virus
8%
Polyposis
8%
Genetic Epidemiology
8%
Ex Vivo
8%
Lymphocyte
8%
Pigmentation
8%
Cycloheximide
8%
Familial Cancer
8%
Next Generation Sequencing
8%
Malignant Neoplasm
8%
Autosomal Dominant Disorder
8%
Base
8%
Outpatient
7%
Bone Disease
6%
Proportional Hazards Model
5%
Quadrantectomy
5%
Cumulative Incidence
5%
Cancer Risk Assessment
5%
Pedigree
5%
Family History
5%
Keyphrases
Double-strand Breaks
33%
Structural Variation
33%
Cas9 Protein
33%
Dysostosis
33%
Atrioventricular Septal Defect
33%
BMP5
33%
Spatial Proximity
33%
DNA Double-strand Breaks
33%
Hailey-Hailey Disease
33%
Deep Intronic Variant
33%
ATP2C1
33%
BOADICEA
33%
K562 Cells
12%
Deep-intronic
8%
Donor Splice Site
8%
Tracheobronchomalacia
5%
Skeletal Malformations
5%
Genetic Skeletal Disorders
5%
Developmental Anomalies
5%
Syndromic Phenotypes
5%
New Association
5%
Dysmorphic Features
5%
