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