Keywords
You will be asked to select up to five (5) keywords in order of importance that are broad and inclusive. Keywords aid in the review process, help tag presentations, and if applicable, determine placement of the abstract in a session. Keywords also help identify the themes of your abstract.
- Alternative splicing
- Alzheimer’s disease
- Amino acidemias
- Ancient DNA
- Aneuploidy
- Anxiety
- Assisted reproduction
- Asthma
- Ataxia
- Auditory system
- Autism
- Autoimmune disorder
- Behavior
- Biochemical pathology
- Bioinformatics
- Bone marrow transplantation
- Bone/joint abnormalities
- Brain/nervous system
- Cancer
- Cancer cytogenetics
- Cancer syndromes
- Candidate gene
- Cardiovascular system
- Cell-free DNA
- Cellular metabolism
- Centromere structure/function
- Channelopathies
- Characterization of disorders
- Characterization of syndromes
- Chromatin
- Chromosomal abnormalities
- Chromosomal deletions
- Chromosomal structure/function
- Ciliopathies
- Clinical cytogenetics
- Clinical history
- Clinical testing
- Comparative mapping
- Complex traits
- Computational tools
- Consanguinity
- Copy number/structural variation
- COVID-19
- Databases
- Delineation of diseases
- Depression
- Development
- Diabetes
- Diagnostics
- Differentiation
- Digital gene expression
- Dysmorphology
- Education
- Electronic health records (EHRs)
- Embryonic stem cells
- Endocrine system
- Enzyme replacement therapy
- Epidemiology
- Epigenetics
- Epigenome-wide association
- Epilepsy
- Ethical, legal and social issues
- Etiology
- Evolution
- Evolutionary genetics
- Exome sequencing
- Expression quantitative trait loci (eQTL)
- Family history
- Family linkage analysis
- Fetal pathology
- Fetal therapy
- FISH
- Fragile X syndrome and FXTAS
- Functional motifs
- Gastrointestinal system
- Gene environment interaction
- Gene families
- Gene localization
- Gene regulation
- Gene therapy
- Gene transfer
- Genetic counseling
- Genetic diversity
- Genetic epidemiology
- Genetic instability
- Genetic mapping
- Genetic testing
- Genitourinary system
- Genome editing/CRISPR
- Genome sequencing
- Genome-wide association
- Genomic structure
- Genomics
- Genotype-phenotype correlations
- Haplotype
- Hematopoietic system
- Heritability
- Identification of disease genes
- Immune system
- Imprinting
- Infectious disease
- Infertility
- Inheritance modeling
- Inheritance patterns
- Intellectual and developmental disability
- Limb
- Linkage disequilibrium
- Linkage mapping
- Linkage methods
- Lymphatic system
- Lysosomal diseases
- Malformation
- Massively parallel sequencing
- Maternal serum screening
- Mathematical modeling
- Meiosis
- Mendelian disorder
- Mendelian randomization
- Metabolic disorder
- Metabolomics
- Methodology
- Methylation
- Microarrays
- Microbiome
- MicroRNA
- Mitochondria
- Model organisms
- Molecular cytogenetics
- Molecular pathophysiology
- Morphogenesis
- Mosaicism
- Muscular abnormalities
- Mutation detection
- Myotonic dystrophies
- Natural history
- Natural selection
- Nervous system
- Neurodegeneration
- Neurogenetics
- Newborn screening
- NIPT
- Noncoding RNA
- Obesity
- Oncogenesis
- Organic acidurias
- Pathogenesis
- Peroxisomal diseases
- Pharmacodynamics
- Pharmacogenomics
- Pharmacokinetics
- Pharmacologic therapy
- Phenome-wide association
- Phenotype
- Policy issues
- Polyalanine disorders
- Polyglutamine diseases
- Polymorphism
- Population genetics
- Population structure
- Precision medicine
- Preclinical trial
- Preimplantation diagnosis
- Prenatal diagnosis
- Protein structure
- Proteomics
- Psychiatric genetics
- Psychosocial issues
- Public health
- Quantitative trait
- Rare variants
- Regulation of transcription
- Reproductive genetics
- Respiratory system
- Risk assessment
- RNA
- RNA pathology
- RNA-seq
- RNAi
- Single-cell
- Skeletal system
- SNP analysis/discovery
- Somatic Variants
- Splicing mechanisms
- Statistical genetics
- Stem cell(s)
- Susceptibility locus
- Systems biology
- Tandem mass spectroscopy
- Targeted sequencing
- Telomere structure/function
- Teratogens
- Transcription
- Transcription factor
- Transcriptome
- Transgenic model
- Translational studies and preclinical trials
- Transplantation
- Transposable elements
- Triplet and other repeats
- Ultrasound diagnosis
- Uniparental disomy
- Variant calling
- Viral vectors
- Visual systems
- X-inactivation
- X-linked disease