Keyphrases
Angelman Syndrome
100%
Prader-Willi Syndrome
55%
Transgenerational Epigenetic Inheritance
50%
Sperm Epigenome
50%
Medical Aspects
50%
Behavioral Aspects
50%
Genetic Diagnosis
50%
Epigenetic Information
37%
Intellectual Disability
33%
Genetic Mechanism
33%
Environmental Factors
25%
Spermatozoa
25%
Epigenetic Mechanisms
25%
Hypotonia
21%
Behavioral Phenotype
21%
Feeding Difficulties
21%
Genomic Imprinting
16%
UBE3A
16%
Tremor
16%
Ataxia
16%
Behavioral Disorders
16%
Hypogonadism
16%
Obesity
16%
Genetic Counseling
16%
Neonatal Period
16%
Hyperactivity
16%
Microcephaly
16%
Chromosome 15
16%
Clinical Diagnosis
16%
Convulsion
16%
Diagnostic Algorithm
16%
15q11-q13
16%
Epigenetic Reprogramming
12%
Cell Totipotency
12%
Changes in Gene Expression
12%
Individual Life
12%
Chromatin Structure
12%
Environmental Information
12%
Heritable Changes
12%
Epimutation
12%
Sperm Epigenetics
12%
Embryo Development
12%
Germ Cells
12%
Three-period
12%
Non-coding RNA (ncRNA)
12%
Sequence-level
12%
Gametes
12%
Cell-type-specific Gene Expression
12%
DNA Sequencing
12%
Epigenome
12%
Biochemistry, Genetics and Molecular Biology
Epigenome
50%
Prader-Willi Syndrome
50%
Genetics
50%
Transgenerational Epigenetics
50%
Angelman Syndrome
50%
Epigenetics
41%
Genetic Mechanism
33%
Reprogramming
33%
Genomic Imprinting
16%
UBE3A
16%
Genetic Counseling
16%
Epigenetic Mechanism
16%
Chromosome 15
16%
Progeny
16%
Cognition
16%
Newborn Period
16%
Gene Expression
16%
Posttranslational Modification
8%
Embryogenesis
8%
Epimutation
8%
Non-Coding RNA
8%
Chromatin Structure
8%
Gamete
8%
DNA Sequence
8%
DNA Methylation
8%
Histone
8%
Neuroscience
Angelman Syndrome
100%
Prader Willi Syndrome
55%
Hypotonia
21%
Behavior (Neuroscience)
16%
Tremor
16%
Microcephaly
16%
Chromosome 15
16%
Hypogonadism
16%
Ataxia
16%
Behavior Disorder
16%
Hyperactivity
16%
Febrile Seizure
5%