Keywords

You will be asked to enter up to five (5) keyword codes in order of importance. Keyword codes aid in the review process and placement of the abstract in a session, if applicable. Keywords also help identify the themes of your abstract.

 

  1. Alternative splicing
  2. Alzheimer’s disease
  3. Amino acidemias
  4. Ancient DNA
  5. Aneuploidy
  6. Anxiety
  7. Assisted reproduction
  8. Asthma
  9. Ataxia
  10. Auditory system
  11. Autism
  12. Autoimmune disorder
  13. Behavior
  14. Biochemical pathology
  15. Bioinformatics
  16. Bone marrow transplantation
  17. Bone/joint abnormalities
  18. Brain/nervous system
  19. Cancer
  20. Cancer cytogenetics
  21. Cancer syndromes
  22. Candidate gene
  23. Cardiovascular system
  24. Cell-free DNA
  25. Cellular metabolism
  26. Centromere structure/function
  27. Channelopathies
  28. Characterization of disorders
  29. Characterization of syndromes
  30. Chromatin
  31. Chromosomal abnormalities
  32. Chromosomal deletions
  33. Chromosomal structure/function
  34. Ciliopathies
  35. Clinical cytogenetics
  36. Clinical history
  37. Clinical testing
  38. Comparative mapping
  39. Complex traits
  40. Computational tools
  41. Consanguinity
  42. Copy number/structural variation
  43. COVID-19
  44. Databases
  45. Delineation of diseases
  46. Depression
  47. Development
  48. Diabetes
  49. Diagnostics
  50. Differentiation
  51. Digital gene expression
  52. Dysmorphology
  53. Education
  54. Electronic health records (EHRs)
  55. Embryonic stem cells
  56. Endocrine system
  57. Enzyme replacement therapy
  58. Epidemiology
  59. Epigenetics
  60. Epigenome-wide association
  61. Epilepsy
  62. Ethical, legal and social issues
  63. Etiology
  64. Evolution
  65. Evolutionary genetics
  66. Exome sequencing
  67. Expression quantitative trait loci (eQTL)
  68. Family history
  69. Family linkage analysis
  70. Fetal pathology
  71. Fetal therapy
  1. FISH
  2. Fragile X syndrome and FXTAS
  3. Functional motifs
  4. Gastrointestinal system
  5. Gene environment interaction
  6. Gene families
  7. Gene localization
  8. Gene regulation
  9. Gene therapy
  10. Gene transfer
  11. Genetic counseling
  12. Genetic diversity
  13. Genetic epidemiology
  14. Genetic instability
  15. Genetic mapping
  16. Genetic testing
  17. Genitourinary system
  18. Genome editing/CRISPR
  19. Genome sequencing
  20. Genome-wide association
  21. Genomic structure
  22. Genomics
  23. Genotype-phenotype correlations
  24. Haplotype
  25. Hematopoietic system
  26. Heritability
  27. Identification of disease genes
  28. Immune system
  29. Imprinting
  30. Infectious disease
  31. Infertility
  32. Inheritance modeling
  33. Inheritance patterns
  34. Intellectual and developmental disability
  35. Limb
  36. Linkage disequilibrium
  37. Linkage mapping
  38. Linkage methods
  39. Lymphatic system
  40. Lysosomal diseases
  41. Malformation
  42. Massively parallel sequencing
  43. Maternal serum screening
  44. Mathematical modeling
  45. Meiosis
  46. Mendelian disorder
  47. Mendelian randomization
  48. Metabolic disorder
  49. Metabolomics
  50. Methodology
  51. Methylation
  52. Microarrays
  53. Microbiome
  54. MicroRNA
  55. Mitochondria
  56. Model organisms
  57. Molecular cytogenetics
  58. Molecular pathophysiology
  59. Morphogenesis
  60. Mosaicism
  61. Muscular abnormalities
  62. Mutation detection
  63. Myotonic dystrophies
  64. Natural history
  65. Natural selection
  66. Nervous system
  67. Neurodegeneration
  68. Neurogenetics
  1. Newborn screening
  2. NIPT
  3. Noncoding RNA
  4. Obesity
  5. Oncogenesis
  6. Organic acidurias
  7. Pathogenesis
  8. Peroxisomal diseases
  9. Pharmacodynamics
  10. Pharmacogenomics
  11. Pharmacokinetics
  12. Pharmacologic therapy
  13. Phenome-wide association
  14. Phenotype
  15. Policy issues
  16. Polyalanine disorders
  17. Polyglutamine diseases
  18. Polymorphism
  19. Population genetics
  20. Population structure
  21. Precision medicine
  22. Preclinical trial
  23. Preimplantation diagnosis
  24. Prenatal diagnosis
  25. Protein structure
  26. Proteomics
  27. Psychiatric genetics
  28. Psychosocial issues
  29. Public health
  30. Quantitative trait
  31. Rare variants
  32. Regulation of transcription
  33. Reproductive genetics
  34. Respiratory system
  35. Risk assessment
  36. RNA
  37. RNA pathology
  38. RNA-seq
  39. RNAi
  40. Single-cell
  41. Skeletal system
  42. SNP analysis/discovery
  43. Somatic Variants
  44. Splicing mechanisms
  45. Statistical genetics
  46. Stem cell(s)
  47. Susceptibility locus
  48. Systems biology
  49. Tandem mass spectroscopy
  50. Targeted sequencing
  51. Telomere structure/function
  52. Teratogens
  53. Transcription
  54. Transcription factor
  55. Transcriptome
  56. Transgenic model
  57. Translational studies and preclinical trials
  58. Transplantation
  59. Transposable elements
  60. Triplet and other repeats
  61. Ultrasound diagnosis
  62. Uniparental disomy
  63. Variant calling
  64. Viral vectors
  65. Visual systems
  66. X-inactivation
  67. X-linked disease

 

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