Keyphrases
African Ancestry
15%
Autosomal Dominant
17%
Benign Thyroid Disease
13%
Breast Cancer Susceptibility Gene 1 (BRCA1)
15%
Cancer Genes
15%
CHEK2
25%
Clinical Impact
15%
Developmental Delay
16%
Dysregulated Genes
13%
Endocrine Neoplasm
17%
Familial Adenomatous Polyposis
29%
Genetic Counseling
22%
Genetic Predisposition
15%
Genetic Test Results
16%
Genetic Testing
28%
Genome-wide Association Study
16%
Genomic Disorders
13%
Germ Cells
25%
Germline mutation
14%
Germline Variants
23%
Iodine-131 (131I)
13%
Knockdown
13%
Likely Pathogenic Variant
24%
Melanoma
18%
Microdeletion
16%
Microdeletion Syndrome
26%
Neurotransmitters
13%
Nonmedullary Thyroid Cancer
40%
Papillary Thyroid Cancer
67%
Papillary Thyroid Carcinoma
100%
Paraganglioma
14%
Pathogenic Variants
26%
Pre-erythrocytic Stages
13%
Quantitative PCR
14%
Risk Factors
14%
Salivary Gland Damage
13%
Segmental Duplication
17%
Sialadenitis
13%
Single nucleotide Polymorphism
20%
Somatic Variants
26%
SPG11
13%
Splice Variant
14%
Thyroid Cancer
69%
Thyroid Cancer Risk
30%
Thyroid Carcinoma
31%
Thyroid Patients
47%
Thyroid Tissue
21%
TINF2
16%
Transcriptome Analysis
13%
Tumor
39%
Biochemistry, Genetics and Molecular Biology
Allele
19%
Array Comparative Genomic Hybridization
18%
Autosomal Dominant Inheritance
18%
BRCA1
16%
BRCA2
13%
Carcinogenesis
18%
CHEK2
22%
Chromatin Immunoprecipitation
17%
Colon
16%
Dideoxynucleotide Sequencing
20%
DNA Repair
15%
Enhancer Region
17%
Gene Expression
14%
Gene Expression Profiling
23%
Gene Fusion
13%
Gene Linkage Disequilibrium
19%
Gene Regulatory Network
13%
Genetic Counseling
13%
Genetic Predisposition
17%
Genetic Test
16%
Genetics
15%
Genome-Wide Association Study
21%
Germ Cell
83%
Germline
70%
Germline Mutation
20%
Haplotype
33%
Homologous Recombination
18%
Isoform
13%
Leucine-Rich Repeat
13%
Locus Control Region
13%
Long Noncoding RNA
13%
Low Copy Repeats
26%
Luciferase
22%
Microdeletion Syndrome
26%
Missense
17%
Myeloid
13%
Newborn Period
13%
Penetrance
27%
Promoter Region
16%
Pyruvate Dehydrogenase
13%
SATB2
13%
Shotgun Sequencing
13%
Single-Nucleotide Polymorphism
28%
Somatic Mutation
17%
Spectrin
13%
Spherocytosis
13%
Telomere
13%
Telomere Homeostasis
13%
TINF2
16%
Whole Genome Sequencing
21%
Medicine and Dentistry
Adrenal Cortex Carcinoma
13%
Adrenal Tumor
13%
Autosomal Dominant Inheritance
12%
BRCA1
15%
BRCA2
13%
Breast Cancer
13%
Cancer
15%
Carcinogenesis
13%
CDKN1B
8%
Cytotechnology
13%
Disease
10%
Diseases
11%
DNA Repair
14%
Endocrine Cancer
10%
Endocrine Tumor
21%
Endocrine Tumor Syndromes
13%
Fanconi Anemia
13%
Genetic Counseling
20%
Genetic Evaluation
13%
Genetic Screening
24%
Germ Cell
40%
Germ Line
13%
Haplotype
13%
Hematopoietic Cell
13%
Iodine 131
13%
Liver Metastasis
10%
Long Untranslated RNA
13%
Malignant Neoplasm
10%
Microsatellite Instability
13%
Multiple Endocrine Neoplasia
19%
Myeloid Malignancy
13%
Neoplasm
39%
Neuroendocrine Tumor
13%
Neurofibromatosis
13%
Neurofibromatosis Type I
13%
Orthopedics
13%
Ovarian Cancer
13%
Papillary Thyroid Cancer
47%
Paraganglioma
11%
Penetrance
13%
Plexiform Neurofibroma
13%
Radioactive Iodine
20%
Recurrent Disease
13%
Salivary Gland
13%
Somatics
14%
Systemic Therapy
9%
Thyroid Cancer
75%
Thyroid Disease
10%
Thyroid Gland
22%
Transplantation
13%
