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Abstract Topics and Keywords

Submission Deadline: June 2, 2011 (8:00 pm U.S. east coast time)

 

 

Topic Categories

 

  1. Cancer Cytogenetics
  2. Cancer Genetics

  3. Cardiovascular Genetics

  4. Clinical Genetics and Dysmorphology

  5. Complex Traits: Theory and Methods

  6. Cytogenetics

  7. Developmental Biology

  8. Epigenetics

  9. Ethical, Legal, Social and Policy Issues in Genetics

  10. Evolutionary and Population Genetics

  11. Gene Structure and Gene Product Function

  12. Genetic Counseling and Clinical Testing

  13. Genetics Education

  14. Genomics

  15. Health Services Research

  16. Metabolic Disorders

  17. Molecular Basis of Mendelian Disorders

  18. Pharmacogenetics

  19. Prenatal and Perinatal Genetics

  20. Psychiatric Genetics, Neurogenetics and Neurodegeneration

  21. Reproductive Genetics

  22. Statistical Genetics and Genetic Epidemiology

  23. Therapy for Genetic Disorders

  24. Technology Advancement

 


 

Keywords

 

  1. amino acidemias
  2. assisted reproduction
  3. ataxia
  4. alternative splicing
  5. auditory system
  6. biochemical pathology
  7. biogenesis
  8. bioinformatics
  9. bone marrow transplantation
  10. bone/joint abnormalities
  11. brain/nervous system
  12. cancer
  13. cancer cytogenetics
  14. cancer syndromes
  15. candidate gene
  16. cardiovascular system
  17. cellular metabolism
  18. centromere structure/function
  19. channelopathies
  20. characterization of disorders
  21. characterization of syndromes
  22. chromatin immunoprecipitation
  23. chromosomal abnormalities
  24. chromosomal deletions
  25. chromosomal structure/function
  26. ciliopathies
  27. clinical applications of molecular cytogenetics
  28. clinical cytogenetics
  29. clinical history
  30. comparative mapping
  31. computational tools
  32. congenital anomaly
  33. contigs
  34. copy number/structural variation
  35. counseling
  36. CVD
  37. databases
  38. deformation
  39. delineation of diseases
  40. development
  41. diabetes
  42. diagnostics
  43. differentiation
  44. digital gene expression
  45. disruption
  46. dysmorphology
  47. education
  48. embryonic stem cells
  49. epidemiology
  50. endocrine system
  51. enzyme replacement therapy
  52. epilepsy
  53. expressed sequence tags
  54. ethical, legal and social issues
  55. etiology
  56. evolution
  57. evolutionary genetics
  58. expansion
  59. family linkage analysis
  60. fetal pathology
  61. fetal therapy
  62. FISH
  63. fragile X syndrome and FXTAS
  64. functional motifs
  65. gastrointestinal system
  66. gene environment interaction
  67. gene families
  68. gene localization
  69. gene therapy
  70. gene transfer methodologies
  71. genes in development
  72. genetic diversity
  73. genetic epidemiology
  74. genetic instability
  75. genetic mapping
  76. genetic testing
  77. genitourinary system
  78. genome scan
  79. genome sequencing
  80. genome-wide association
  81. genomic methodologies
  82. genomic structure
  83. genotype-phenotype correlations
  84. haplotype
  85. hematopoietic system
  86. identification of disease genes
  87. immune system
  88. imprinting
  89. infectious disease
  90. infertility
  91. inheritance modeling

     
  1. inheritance patterns
  2. limb
  3. linkage disequilibrium
  4. linkage mapping
  5. linkage methodology
  6. lymphatic system
  7. lysosomal diseases
  8. malformation
  9. mapping complex traits
  10. maps
  11. massively parallel sequencing
  12. maternal genetic disease
  13. maternal serum screening
  14. mathematical modeling
  15. mental retardation
  16. metabolic disorder
  17. methodology
  18. methylation
  19. microarrays
  20. micro RNA
  21. mitochondria
  22. model organisms
  23. molecular pathophysiology
  24. morphogenesis
  25. muscular abnormalities
  26. mutation detection
  27. myotonic dystrophies
  28. natural history
  29. natural selection
  30. newborn screening
  31. neurodegeneration
  32. neurogenetics
  33. nervous system
  34. noncoding RNA
  35. oncogenesis
  36. organic acidurias
  37. pathogenesis
  38. peroxisomal diseases
  39. pharmacodynamics
  40. pharmacogenetics
  41. pharmacokinetics
  42. pharmacologic therapy
  43. phenotype
  44. physical mapping
  45. policy issues
  46. polyalanine disorders
  47. polyglutamine diseases
  48. polymorphism
  49. population genetics
  50. population structure
  51. preclinical trial
  52. predictive testing
  53. preimplantation diagnosis
  54. prenatal diagnosis
  55. proteomics
  56. psychosocial counseling issues
  57. psychosocial issues
  58. public health
  59. public, patient and professional education
  60. regulation of transcription
  61. reproductive genetics
  62. respiratory system
  63. risk assessment
  64. RNA
  65. RNAi
  66. RNA pathology
  67. skeletal system
  68. SNP analysis/discovery
  69. splicing mechanisms
  70. stem cell(s)
  71. structure/function
  72. susceptibility locus
  73. systems biology
  74. tandem mass spectroscopy
  75. telomere structure/function
  76. teratogens
  77. therapy
  78. transcription
  79. transcription factor
  80. transgenic model
  81. translational studies and preclinical trials
  82. transplantation
  83. transposable elements
  84. triplet and other repeats
  85. ultrasound diagnosis
  86. uniparental disomy
  87. visual systems
  88. viral vectors
  89. X-inactivation
  90. X-linked disease