Medicine and Dentistry
Patient
100%
Syndrome
55%
Gene
51%
Diagnosis
49%
Hereditary Nonpolyposis Colorectal Cancer
40%
Family
35%
Adult
29%
Genetic Screening
28%
Age
27%
Molar Pregnancy
25%
Malignant Neoplasm
24%
Colorectal Cancer
24%
Rokitansky Syndrome
23%
Phenotype
22%
DNA Mismatch Repair
21%
Diseases
21%
Inpatient
20%
Prevalence
20%
Surveillance
19%
Mitochondrial DNA
19%
Female
18%
Therapeutic Procedure
18%
Exome Sequencing
17%
Association
16%
Case Report
16%
Hereditary Colorectal Cancer
15%
Disorders of Mitochondrial Functions
12%
Pregnancy
11%
BRCA1
11%
Peutz Jeghers Syndrome
11%
BRCA2
11%
DNA Mutation
11%
Girl
11%
Cancer Risk
11%
Hypophosphatasia
10%
Muscle
10%
Tissues
10%
Follow up
10%
Male
10%
Woman
10%
Analysis
9%
Mutational Load
9%
Genotype
9%
Person
9%
Autosomal Dominant Inheritance
9%
Symptom
9%
Penetrance
9%
Colonoscopy
8%
Cross Sectional Study
8%
Survival
8%
Gender
8%
Epilepsy
8%
Trophoblast
8%
Surgery
8%
Cancer Susceptibility
8%
Juvenile Polyposis Syndrome
8%
Clinical Genetics
8%
Polyposis
8%
Cancer Staging
8%
Screening
7%
Development
7%
Salpingooophorectomy
7%
Polycystic Kidney Disease
7%
Maternal Blood
7%
Breast Cancer
7%
Hysterectomy
7%
Cohort Analysis
7%
Whole Genome Sequencing
7%
Gestational Trophoblastic Disease
7%
Diabetes
7%
Child
7%
Blood
7%
Ovarian Cancer
7%
Incidence
7%
Mortality
7%
Etiology
7%
Gene Repair
6%
Hearing Impairment
6%
Hospital
6%
Point Mutation
6%
Sensorineural Hearing Loss
6%
Lactic Acidosis
6%
Death
6%
Bone
6%
Conceptus
6%
Pedigree
6%
Organ
6%
Cancer Incidence
6%
Mosaicism
6%
Kidney
5%
Family History
5%
Fetus
5%
Apoplexy
5%
Genome Sequencing
5%
Complication
5%
Renal Agenesis
5%
Examination
5%
Protein
5%
Maternally Inherited Diabetes and Deafness
5%
Familial Cancer
5%
Biochemistry, Genetics and Molecular Biology
Mutation
44%
Genetic Screening
36%
Phenotype
32%
Nested Gene
31%
Genetics
30%
Association
22%
Hearing
21%
Age
21%
Mole (Insectivora)
19%
Germline
15%
BRCA1
15%
Preimplantation
15%
Exome Sequencing
14%
Genotyping
13%
Pregnancy
13%
Development
12%
DNA
12%
Prevalence
11%
BRCA2
11%
Spectrum
11%
Point Mutation
10%
Screening
8%
Trophoblast
8%
Genetic Disorder
8%
Aneuploidy
7%
Phosphorylase
7%
Kinase
7%
Mitochondrial DNA
7%
Mosaicism
7%
Transfer RNA
7%
Next Generation Sequencing
7%
Mental Retardation
6%
Protein
6%
Sequencing
6%
Lysozyme
6%
Inheritance
5%
Electron Transport Chain
5%
Phosphate
5%
Time
5%
Glucose
5%