Biochemistry, Genetics and Molecular Biology
Nested Gene
100%
Mutation
75%
Phenotype
56%
Exome Sequencing
46%
Promoter Region
37%
Protein
35%
Association
34%
Embryonic Stem Cell
27%
Spectrum
25%
Proband
23%
Evolution
21%
RNA
20%
Gain of Function Mutation
20%
Next Generation Sequencing
18%
Structural Protein
18%
Genetics
18%
Exome
16%
Electric Potential
16%
Development
15%
Dysplasia
14%
Protein Interaction
13%
Hearing
12%
Genetic Heterogeneity
12%
Interferon Type I
12%
Loss of Function Mutation
12%
DNA
11%
Transcription Factor
11%
Interactome
11%
Amelogenesis
11%
Heart Rate
11%
Yeast
11%
FLT4
10%
GATA6
10%
Genome Wide Association Study
10%
down Regulation
10%
Genetic Divergence
9%
Candidate Gene
9%
Aptitude
9%
RNase P
9%
Vascularization
9%
Atom
9%
Ceramide
9%
Molecule
9%
Progeny
9%
Life
9%
Biogenesis
9%
Human Genetics
9%
Peroxisome
9%
Allele
9%
Whole Genome Sequencing
9%
Medicine and Dentistry
Gene
52%
Family
33%
Syndrome
30%
Tetralogy of Fallot
28%
Patient
27%
Persistent Truncus Arteriosus
23%
Phenotype
21%
Analysis
19%
Diseases
17%
Exome Sequencing
14%
Base
14%
Sensorineural Hearing Loss
12%
Exome
11%
Transcription Factor GATA 6
10%
Vasculotropin Receptor 2
10%
Heart Failure
10%
Inpatient
10%
Protein Interaction
10%
Interaction Network
10%
Vascularity
9%
Hypoplastic Left Heart Syndrome
9%
Whole Genome Sequencing
9%
Schwannomatosis
9%
Microphthalmia
9%
Dysplasia
9%
Adult
9%
Chronic Obstructive Pulmonary Disease
9%
Peripheral Neuropathy
9%
Retina Disease
9%
Induced Pluripotent Stem Cell
9%
Diagnostics
9%
Genetic Risk
9%
Molecular Diagnosis
9%
Clinical Genetics
9%
Joint
9%
Gain of Function Mutation
9%
Growth Differentiation Factor 15
9%
Protein
8%
Microcephaly
8%
Association
8%
Sibling
7%
Catenin
7%
In Vitro
5%
Developmental Delay
5%
Growth Retardation
5%
Hypertelorism
5%
Vestibular Schwannoma
5%
