Deafness gene discovery in the genomic era

Keyphrases

• Deafness 100%
• Deafness Gene 100%
• Genomic Era 100%
• Gene Discovery 100%
• Auditory Pathway 40%
• Deep Sequencing 40%
• Non-syndromic Hearing Loss 40%
• New mutation 40%
• Vestibular Pathways 40%
• Bioinformatics Tools 20%
• Age of Onset 20%
• Normal Hearing 20%
• Deaf children 20%
• Early Diagnosis 20%
• Hearing Threshold 20%
• Gene mutation 20%
• Massively Parallel Sequencing 20%
• Heterogeneous Disease 20%
• Specific mutation 20%
• High-throughput 20%
• Computational Analysis 20%
• Linkage Analysis 20%
• Inner Ear 20%
• Pathogenic mutations 20%
• Clinical Symptoms 20%
• Next-generation Sequencing 20%
• Genomic Analysis 20%
• Hereditary Deafness 20%
• Inner Ear Function 20%
• Positional Cloning 20%
• Human Genome Project 20%
• Carrier Screening 20%
• Ethnic Populations 20%
• Small Families 20%
• Computational Validation 20%
• Deep Sequencing Technology 20%
• Onset Frequency 20%
• Abnormal Phenotype 20%
• Subsequent Therapy 20%
• Sensory Loss 20%
• Rare Forms 20%
• Large Pedigree 20%

Biochemistry, Genetics and Molecular Biology

• Deep Sequencing 100%
• Gene Discovery 100%
• Genomics 100%
• Genotyping 25%
• Human Genome 25%
• Linkage Analysis 25%
• Next Generation Sequencing 25%
• Pedigree 25%
• Auditory Threshold 25%
• Bioinformatics 25%

Neuroscience

• Deep Sequencing 100%
• Sensation of Hearing 50%
• Human Genome Project 25%