Keyphrases
Multiple Endocrine Neoplasia Type 1 (MEN1)
100%
Genetic Testing
71%
Primary Hyperparathyroidism (pHPT)
61%
Monogenic
55%
Tumor
47%
Germ Cells
37%
Prolactin Receptor
34%
Endocrine Disorders
31%
Pheochromocytoma
31%
Parathyroid Tumors
29%
Scotland
29%
Hyperprolactinemia
28%
Sequencing Studies
26%
Receptor Subtypes
26%
Endocrinology
26%
Whole Exome Sequencing
26%
Skeletal Disorders
21%
Cell Division Cycle
20%
Hyperparathyroidism-jaw Tumor Syndrome (HPT-JT)
20%
Tumor Development
19%
Pituitary
19%
Autosomal Dominant Disorder
18%
Polygenic Disorder
18%
Oligogenic Disease
18%
Clinical Features
18%
Pancreatic Neuroendocrine Tumors (pNETs)
18%
Population-based Study
17%
Nonfunctional Pancreatic Neuroendocrine Tumor
17%
Receptor Signaling
17%
Genetic Basis
16%
Penetrance
15%
Menin
15%
Family Members
15%
Pituitary Tumor
15%
Variants of Uncertain Significance
15%
Paraganglioma
15%
Pathogenicity
14%
Parafibromin
13%
DNA Sequencing
13%
MEN1 Gene
13%
Mendelian Disease
13%
Missense
12%
Tayside
12%
Disease Risk
12%
Prolactin
12%
Clinical Management
11%
Genetic Diagnosis
11%
Single-point mutation
11%
Appropriate Management
11%
McCune-Albright Syndrome
11%
Biochemistry, Genetics and Molecular Biology
Genetics
99%
Genetic Screening
67%
Germ Cell
44%
Germline
44%
Single-Nucleotide Polymorphism
33%
Missense
32%
Penetrance
26%
Prolactin Receptor
26%
Exome Sequencing
26%
Gene Mutation
24%
Autosomal Dominant Inheritance
23%
MEN1
21%
Genetic Test
19%
DNA Sequence
17%
GNA11
17%
Tumor Suppressor Protein
14%
Carcinogenesis
13%
Molecular Genetics
13%
Exome
13%
Cyclin D1
13%
Methionine
12%
Protein Sequencing
11%
Leukocyte
11%
Genetic Divergence
10%
Gene Expression
10%
Clinical Trial
10%
Nuclear Protein
9%
Allele
9%
Hypercalcaemia
8%
Disorders of Calcium Metabolism
8%
Genetic Approach
8%
Hypocalcaemia
8%
Homeostasis
8%
Von Hippel-Lindau Disease
8%
Metabolite
8%
Gene Function
8%
SDHA
8%
Genome-Wide Association Study
8%
Vitamin D
8%
Induced Pluripotent Stem Cell
8%
Cell Cycle Protein
8%
Genetic Variation
8%
Cell Growth
8%
Cell Survival
8%
Embryogenesis
8%
Histone Modification
8%
APOBEC
8%
Preprotachykinin
8%
Vitamin D Analog
8%
Cell Invasion
8%
Medicine and Dentistry
Multiple Endocrine Neoplasia Type I
65%
Neoplasm
64%
Disease
45%
Primary Hyperparathyroidism
44%
Genetic Screening
42%
Pancreas Islet Cell Tumor
33%
Parathyroid Tumor
27%
Multiple Endocrine Neoplasia
26%
Hyperparathyroidism
23%
Cancer Syndrome
22%
Endocrine Disease
20%
Jaw Tumor
19%
Endocrinology
17%
Prolactin Receptor
17%
Parathyroid Hormone
16%
Autosomal Dominant Disorder
16%
Isotopes of Calcium
16%
Monogenic Disorder
16%
Germ Cell
15%
Pheochromocytoma
14%
Prevalence
13%
Clinician
12%
Prolactinoma
11%
Clinical Feature
11%
Autosomal Dominant Inheritance
11%
Pituitary Tumour
10%
Clinical Genetics
10%
Methionine
10%
Bone Disease
10%
Somatics
10%
Parathyroid
9%
Mutational Analysis
9%
Diagnosis
9%
Endocrine Tumor
8%
Quality of Life
8%
Genetic Background
8%
Hypocalcaemia
8%
Disorders of Calcium Metabolism
8%
C57BL/6
8%
Vitamin D Analog
8%
Patient Referral
8%
Endocrine Tumor Syndromes
8%
Metabolic Bone Disease
8%
Paraganglioma
8%
Single Nucleotide Polymorphism
8%
Receptor
8%
Induced Pluripotent Stem Cell
8%
Cell Cycle Protein
8%
Bone Remodeling
8%
Gene Function
8%
