Concepts (156)
Concepts are derived automatically from a person's publications.
In this concept 'cloud', the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
- Adenosine Triphosphate
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Alleles
- Alternative Splicing
- Amino Acid Sequence
- Amino Acid Substitution
- Animals
- Apoptosis
- Asian Continental Ancestry Group
- Audiometry
- Audiometry, Pure-Tone
- Auditory Threshold
- Base Sequence
- Behavior, Animal
- Blindness
- Calcium-Binding Proteins
- Carrier Proteins
- Case-Control Studies
- cdc42 GTP-Binding Protein
- Cell Adhesion Molecules
- Cell Membrane
- Cell Survival
- Child
- Child, Preschool
- Chromosome Mapping
- Chromosomes, Human, Pair 10
- Chromosomes, Human, Pair 4
- Cochlea
- Codon, Nonsense
- Collagen Type XI
- Comparative Genomic Hybridization
- Computational Biology
- Connexins
- Consanguinity
- COS Cells
- Databases, Genetic
- Deafness
- Delivery of Health Care
- Developmental Disabilities
- Diagnosis, Differential
- Disease Models, Animal
- DNA Copy Number Variations
- DNA Mutational Analysis
- Ear, Inner
- Electroretinography
- Ethnic Groups
- European Continental Ancestry Group
- Evoked Potentials, Auditory
- Evoked Potentials, Auditory, Brain Stem
- Evolution, Molecular
- Exons
- Extracellular Matrix Proteins
- Eye
- Family
- Female
- Financing, Organized
- Follow-Up Studies
- Founder Effect
- Frameshift Mutation
- Gene Deletion
- Gene Expression
- Gene Expression Regulation
- Gene Frequency
- Gene Knockout Techniques
- Genes, Dominant
- Genes, Recessive
- Genetic Association Studies
- Genetic Heterogeneity
- Genetic Linkage
- Genetic Markers
- Genetic Predisposition to Disease
- Genetic Testing
- Genetic Variation
- Genome, Human
- Genome-Wide Association Study
| - Genomics
- Genotype
- GPI-Linked Proteins
- Hair Cells, Auditory, Inner
- Haplotypes
- Hearing
- Hearing Loss
- Hearing Loss, Sensorineural
- Heart Defects, Congenital
- Heterozygote
- High-Throughput Nucleotide Sequencing
- Homeostasis
- Homozygote
- Humans
- Infant
- Infant, Newborn
- Infertility, Male
- Introns
- Iran
- Japan
- KCNQ Potassium Channels
- Large-Conductance Calcium-Activated Potassium Channels
- Male
- Maze Learning
- Mechanotransduction, Cellular
- MELAS Syndrome
- Membrane Proteins
- Membrane Transport Proteins
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Mice, Mutant Strains
- Middle Aged
- Mitochondria
- Models, Molecular
- Molecular Sequence Data
- Mutation
- Mutation, Missense
- Myopathies, Structural, Congenital
- Myosins
- Nerve Tissue Proteins
- Organoids
- Pedigree
- Peer Review, Research
- Phenotype
- Phosphoric Monoester Hydrolases
- Phylogeny
- Point Mutation
- Polymorphism, Single Nucleotide
- POU Domain Factors
- Prognosis
- Protein Isoforms
- Protein Tyrosine Phosphatases
- Pyrimidines
- Receptor-Like Protein Tyrosine Phosphatases, Class 3
- Receptors, Estrogen
- Receptors, G-Protein-Coupled
- Receptors, Purinergic P2X2
- Reproducibility of Results
- Retina
- Retrospective Studies
- RNA Splicing
- RNA, Messenger
- Sequence Alignment
- Sequence Analysis, DNA
- Sequence Analysis, RNA
- Serine Proteases
- Single-Cell Analysis
- Societies, Medical
- Software
- Spain
- Testis
- Trans-Activators
- United States
- Usher Syndromes
- Young Adult
- Zebrafish
- Zebrafish Proteins
|
Concepts
(156)
Derived automatically from this person's publications.
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Co-Authors
(20)
People in Profiles who have published with this person.
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Similar People
(60)
People who share similar concepts with this person.
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Same Department
People in same department with this person.
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