Biochemistry, Genetics and Molecular Biology
Genetics
100%
Induced Pluripotent Stem Cell
95%
Stem Cell Line
64%
Intellectual Disability
52%
Allele
47%
Autosomal Dominant Inheritance
41%
Candidate Gene
41%
Proband
39%
Array Comparative Genomic Hybridization
33%
Single-Nucleotide Polymorphism
32%
Genomics
31%
Exon
31%
Prevalence
30%
Genotyping
29%
Tau Protein
28%
Chromosomal Rearrangement
26%
Fluorescence in Situ Hybridization
25%
MicroRNA
25%
Wild Type
24%
CAG Repeat
24%
Karyotype
23%
Cytogenetics
22%
Germ Cell
22%
Exome Sequencing
22%
Haploinsufficiency
20%
Promoter Region
20%
Mouse Model
19%
Next Generation Sequencing
19%
Genome-Wide Association Study
19%
Nonsense Mutation
19%
Haplotype
19%
Insulin Release
19%
Chromothripsis
19%
Multiplex Ligation-Dependent Probe Amplification
18%
Autosomal Recessive Inheritance
18%
Genetic Screening
18%
Huntingtin
18%
Germline
18%
Genetic Variation
16%
Presenilin
16%
Metabolic Pathway
16%
Genetic Divergence
16%
Fibroblast
16%
Linkage Analysis
16%
Gene Mutation
15%
Molecular Genetics
15%
Von Hippel-Lindau Disease
15%
Magnetic Resonance Imaging
15%
Penetrance
15%
Keyphrases
Induced Pluripotent Stem Cells (iPSCs)
83%
Huntington's Disease
73%
Stem Cell Lines
57%
Intellectual Disability
47%
Frontotemporal Dementia
44%
Denmark
43%
Neurodegenerative Diseases
35%
Von Hippel-Lindau Disease
35%
Obesity
31%
Confidence Interval
23%
Alzheimer's Disease Patient
23%
Isogenic
23%
Autosomal Dominant
23%
Polymorphism
22%
MicroRNA
22%
Mate-pair Sequencing
22%
Presenilin
21%
Epilepsy
21%
Novel mutation
21%
Single nucleotide Polymorphism
20%
Mouse Model
20%
Hereditary Spastic Paraplegia
20%
Receptor Binding
19%
Proband
19%
Type 2 Diabetes Mellitus (T2DM)
18%
Disease Genes
18%
Gene Expansion
18%
Family Members
17%
Hearing Impairment
16%
Haploinsufficiency
16%
Duplication
16%
Methylmercury Exposure
16%
Tourette Syndrome
16%
5-hydroxytryptamine
15%
Genetic Testing
15%
Control Cell
15%
5-HT4 Receptor
15%
Germ Cells
15%
Copy number Variation
15%
Next-generation Sequencing
15%
Deafness
15%