Biochemistry, Genetics and Molecular Biology
Proband
100%
Gene Discovery
100%
Pedigree
100%
Genetics
100%
Allele
100%
Genomics
100%
Sample Size
50%
Exome Sequencing
50%
RNA
50%
Genome-Wide Association Study
50%
Prevalence
50%
Genetic Heterogeneity
50%
Phenotypic Heterogeneity
50%
Copy-Number Variation
50%
Genotyping
50%
Transcriptome
50%
Comorbidity
50%
Neuroscience
Transcriptome
100%
Attention Deficit Hyperactivity Disorder
100%
Cell Line
100%
Genome-Wide Association Study
100%
Obsessive-Compulsive Disorder
100%
Copy Number Variation
100%
Complementary DNA
100%
Psychiatric Co-Morbidity
100%
Exome Sequencing
100%
Keyphrases
Genomic Studies
100%
Tourette Syndrome
100%
Specific Intent
33%
Gene Discovery
16%
Pedigree
16%
Proband
16%
Genome-wide Association Study
8%
Complex Allele
8%
Structural Variants
8%
Family Members
8%
Genetic Contribution
8%
Sequence Variation
8%
Cis-trans Isomerization
8%
Biomaterials
8%
Collaborative Study
8%
Rate Limiting
8%
Neuropsychiatric Syndromes
8%
Geneticists
8%
Genetic Heterogeneity
8%
Family-centered
8%
Phenotypic Data
8%
Genetic Etiology
8%
Key Rate
8%
Neuropsychiatric Disorders
8%
Genotype
8%
Risk Allele
8%
Obsessive-compulsive Disorder
8%
Potential Contribution
8%
Sequence Method
8%
Quad
8%
Attention Deficit Hyperactivity Disorder
8%
Complementary DNA (cDNA)
8%
Transcriptome
8%
Rare Variants
8%
Expert Clinician
8%
Parent-child Trios
8%
Scientific Community
8%
Whole Exome Sequencing
8%
Motor Tics
8%
Psychiatric Comorbidity
8%
PAXgene
8%
Genome-wide Expression
8%
Effective Approach
8%
Structural Variation
8%
Phonic Tic
8%
Public Health Risk
8%
Paucity
8%
Phenotypic Heterogeneity
8%
Illumina
8%
Publicly Available
8%
Public Health Benefit
8%
Large Sample Size
8%
State-of-the-art Techniques
8%
Sequence Variants
8%
Copy number Analysis
8%
Complex Inheritance
8%
Complex Disorders
8%
Rare Allele
8%
Common Variants
8%
BeadChip
8%