Keyphrases
Fanconi Anemia
100%
FANCD2
21%
FANCM
20%
BRCA2
19%
FANCA
17%
DNA Repair
16%
TP53 mutation
15%
ERCC4
14%
8-oxoguanine
13%
Bone Marrow Failure
13%
Fanconi Anemia Genes
13%
Breast Cancer Risk
12%
DNA Base Excision Repair
10%
Base Excision Repair
10%
Human Genetics
10%
Hematopoietic Stem Cells
10%
Chromosome Fragility
10%
Bloom Syndrome
9%
TOP3A
9%
Atherosclerotic Lesions
9%
Drosophilidae
9%
Breast Cancer Susceptibility Gene 1 (BRCA1)
9%
Biallelic
8%
Functional Studies
8%
Genome Stability
8%
DNA Damage
8%
Ionizing Radiation
8%
Biallelic mutations
8%
Endonuclease
8%
Mammalian Cells
8%
Cell-free Extract
7%
Fanconi Anemia Pathway
7%
Ovarian Cancer Risk
7%
Tumor Suppressor
7%
Familial Breast Cancer
6%
Human Cells
6%
Gene Therapy
6%
DNA Repair Capacity
6%
Breast Cancer
6%
Interstrand Crosslink Repair
6%
Aneuploidy
6%
DNA Interstrand Crosslinks
6%
High Risk
6%
Rare Variants
6%
Nonsense mutation
6%
Missense mutation
6%
Glycoside Hydrolase
6%
Denaturing Gradient Gel Electrophoresis
5%
Phenocopy
5%
Mouse Cells
5%
Biochemistry, Genetics and Molecular Biology
DNA Repair
31%
FANCD2
30%
FANCA
25%
FANCM
24%
BRCA2
24%
Base Excision Repair
22%
P53
20%
Bone Marrow Failure
19%
Genome Instability
18%
Cross-Link
18%
BRCA1
17%
Gene Therapy
14%
Exon
13%
Allele
13%
Hematopoietic Cell
12%
Human Genetics
12%
Genetics
11%
Homologous Recombination
9%
Bloom Syndrome
9%
Exome Sequencing
9%
Nuclease
9%
Mosaicism
9%
DNA Damage
8%
Cell Extract
8%
Endonuclease
8%
S Phase
7%
Crosslinking of DNA
7%
Chromosome Instability
7%
Mammalian Cell
7%
DNA Damage Response
7%
Aneuploidy
7%
Next Generation Sequencing
7%
Nucleotide Excision Repair
7%
Tumor Suppressor Protein
7%
Gene Mutation
6%
Metabolic Pathway
6%
Mitochondrial DNA
6%
Missense Mutation
6%
Phenocopy
6%
Nonsense Mutation
6%
Erethism
6%
Chromosome Breakage
5%
Gel Electrophoresis
5%
Fibroblast
5%
Codon
5%
Xeroderma pigmentosum
5%
Cytogenetics
5%
