INIS
genetics
100%
mutations
72%
genes
60%
patients
52%
testing
42%
risks
36%
carriers
30%
humans
30%
diseases
28%
cancer
22%
dna
22%
birth
18%
detection
16%
data
16%
embryos
15%
drugs
15%
pregnancy
15%
spectra
14%
erythrocytes
14%
control
13%
congenital diseases
13%
nucleotides
12%
ovaries
12%
inosine
12%
levels
12%
screening
12%
weight
11%
mitochondria
11%
in vitro
11%
therapy
10%
Biochemistry, Genetics and Molecular Biology
Genetics
29%
Genetic Screening
25%
Preimplantation
23%
Preimplantation Genetic Diagnosis
19%
Long QT Syndrome
15%
Inosine Triphosphatase
12%
Mitochondrial DNA
10%
Birth Weight
10%
Inosine
9%
Human Ether A Go Go Related Gene
9%
Human Immunodeficiency Virus
9%
Mosaicism
9%
Genotyping
9%
Leptin
8%
Exome Sequencing
8%
Gene Linkage
7%
ITPA
7%
Penetrance
7%
Single-Nucleotide Polymorphism
7%
DNA Mutation
6%
BRCA1
6%
Candidate Gene
6%
Exome
6%
Lipid Metabolism
6%
Carbohydrate Metabolism
6%
ZIC2
6%
PTCH1
6%
Autosomal Recessive Disorder
6%
Whole Genome Sequencing
6%
Inorganic Pyrophosphatase
6%
Keyphrases
Preimplantation Genetic Diagnosis
52%
Birth Weight
14%
Long QT Syndrome
13%
Inosine Triphosphatase
12%
Holoprosencephaly
12%
Erythrocytes
11%
Flanders
10%
Consanguineous
9%
Netherlands
9%
Basal Cell Nevus Syndrome
9%
Polymorphism
8%
Haplarithmisis
7%
Novel mutation
7%
KCNH2
7%
Metabolic Risk Factors
7%
Preimplantation Genetic Testing for Monogenic Disorders (PGT-M)
7%
Mitochondrial DNA mutation
6%
Heritability
6%
Genetic Diagnosis
6%
Hereditary Breast Cancer
6%
Mutation Carriers
6%
Hereditary Ovarian Cancer
6%
SCN5A
6%
Neurofibromatosis Type I
6%
Bladder Cancer
6%
PTCH1
6%
Belgian
6%
Leptin
6%
Exome
6%
Bladder Cancer Risk
6%
