Keyphrases
Autosomal Dominant Disorder
18%
Cell Division Cycle
20%
Clinical Features
18%
Computational Prediction Tools
17%
DNA Sequencing
15%
Endocrine Disorders
40%
Endocrinology
26%
Family Members
15%
Gene-specific
17%
Genetic Basis
16%
Genetic Testing
71%
Germ Cells
39%
GnomAD
13%
Hyperparathyroidism-jaw Tumor Syndrome (HPT-JT)
20%
Hyperprolactinemia
28%
MEN1 Gene
13%
Mendelian Disease
13%
Menin
15%
Missense
19%
Missense Variants
17%
Monogenic
63%
Multiple Endocrine Neoplasia Type 1 (MEN1)
100%
Nonfunctional Pancreatic Neuroendocrine Tumor
17%
Oligogenic Disease
18%
Pancreatic Neuroendocrine Tumors (pNETs)
18%
Parafibromin
13%
Paraganglioma
15%
Parathyroid Tumors
29%
Pathogenicity
19%
Penetrance
15%
Pheochromocytoma
31%
Pituitary
19%
Pituitary Tumor
15%
Polygenic Disorder
18%
Population-based Study
17%
Primary Hyperparathyroidism (pHPT)
61%
Prolactin Receptor
34%
Receptor Signaling
17%
Receptor Subtypes
26%
Scotland
29%
Sequencing Studies
26%
Single nucleotide Variant
18%
Skeletal Disorders
21%
Specific Applications
17%
Tayside
12%
Tumor
47%
Tumor Development
19%
Variant Interpretation
13%
Variants of Uncertain Significance
15%
Whole Exome Sequencing
26%
Biochemistry, Genetics and Molecular Biology
Allele
9%
APOBEC
8%
Autosomal Dominant Inheritance
23%
Carcinogenesis
13%
Cell Cycle Protein
8%
Cell Growth
8%
Cell Invasion
8%
Cell Survival
8%
Clinical Trial
10%
Cyclin D1
13%
Disorders of Calcium Metabolism
8%
DNA Sequence
17%
Embryogenesis
8%
Exome
13%
Exome Sequencing
26%
Gene Expression
10%
Gene Function
8%
Gene Mutation
24%
Genetic Approach
8%
Genetic Divergence
10%
Genetic Screening
67%
Genetic Test
19%
Genetic Variation
8%
Genetics
99%
Genome-Wide Association Study
8%
Germ Cell
44%
Germline
44%
GNA11
17%
Histone Modification
8%
Homeostasis
8%
Hypercalcaemia
8%
Hypocalcaemia
8%
Leukocyte
11%
MEN1
21%
Metabolite
8%
Methionine
12%
Missense
32%
Molecular Genetics
13%
Nuclear Protein
9%
Penetrance
26%
Preprotachykinin
8%
Prolactin Receptor
26%
Protein Sequencing
11%
SDHA
8%
Shotgun Sequencing
11%
Single-Nucleotide Polymorphism
33%
Tumor Suppressor Protein
14%
Vitamin D
8%
Vitamin D Analog
8%
Von Hippel-Lindau Disease
8%
Medicine and Dentistry
Autosomal Dominant Disorder
12%
Autosomal Dominant Inheritance
11%
Bone Disease
10%
Bone Remodeling
8%
C57BL/6
8%
Cancer Syndrome
13%
Cell Cycle Protein
8%
Clinical Feature
9%
Clinical Genetics
10%
Clinician
17%
Disease
24%
Diseases
36%
Disorders of Calcium Metabolism
8%
Endocrine Disease
21%
Endocrine Tumor
8%
Endocrine Tumor Syndromes
8%
Endocrinology
17%
Gene Function
8%
Gene Mutation
11%
Genetic Background
8%
Genetic Screening
41%
Germ Cell
19%
Hyperparathyroidism
14%
Hypocalcaemia
8%
Hypoparathyroidism
8%
Induced Pluripotent Stem Cell
8%
Isotopes of Calcium
11%
Jaw Tumor
10%
Metabolic Bone Disease
8%
Methionine
10%
Monogenic Disorder
21%
Multiple Endocrine Neoplasia
17%
Multiple Endocrine Neoplasia Type I
62%
Mutational Analysis
9%
Neoplasm
52%
Pancreas Islet Cell Tumor
30%
Paraganglioma
8%
Parathyroid Disease
8%
Parathyroid Tumor
16%
Patient Referral
8%
Pheochromocytoma
11%
Pituitary Tumour
10%
Prevalence
13%
Primary Hyperparathyroidism
45%
Prolactin Receptor
17%
Prolactinoma
11%
Receptor
8%
Single Nucleotide Polymorphism
8%
Somatics
12%
Vitamin D Analog
8%
