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ASHG 2012 Abstract Submission Key Words

 

 

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
92 inheritance patterns
93 limb
94 linkage disequilibrium
95 linkage mapping
96 linkage methodology
97 lymphatic system
98 lysosomal diseases
99 malformation
100 mapping complex traits
101 maps
102 massively parallel sequencing
103 maternal genetic disease
104 maternal serum screening
105 mathematical modeling
106 intellectual and developmental disability
107 metabolic disorder
108 methodology
109 methylation
110 microarrays
111 micro RNA
112 mitochondria
113 model organisms
114 molecular pathophysiology
115 morphogenesis
116 muscular abnormalities
117 mutation detection
118 myotonic dystrophies
119 natural history
120 natural selection
121 newborn screening
122 neurodegeneration
123 neurogenetics
124 nervous system
125 noncoding RNA
126 oncogenesis
127 organic acidurias
128 pathogenesis
129 peroxisomal diseases
130 pharmacodynamics
131 pharmacogenetics
132 pharmacokinetics
133 pharmacologic therapy
134 phenotype
135 physical mapping
136 policy issues
137 polyalanine disorders
138 polyglutamine diseases
139 polymorphism
140 population genetics
141 population structure
142 preclinical trial
143 predictive testing
144 preimplantation diagnosis
145 prenatal diagnosis
146 proteomics
147 psychosocial counseling issues
148 psychosocial issues
149 public health
150 public, patient and professional education
151 regulation of transcription
152 reproductive genetics
153 respiratory system
154 risk assessment
155 RNA
156 RNAi
157 RNA pathology
158 skeletal system
159 SNP analysis/discovery
160 splicing mechanisms
161 stem cell(s)
162 structure/function
163 susceptibility locus
164 systems biology
165 tandem mass spectroscopy
166 telomere structure/function
167 teratogens
168 therapy
169 transcription
170 transcription factor
171 transgenic model
172 translational studies and preclinical trials
173 transplantation
174 transposable elements
175 triplet and other repeats
176 ultrasound diagnosis
177 uniparental disomy
178 visual systems
179 viral vectors
180 X-inactivation
181 X-linked disease

 


 

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