Concepts (217)
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.
- Adenine Nucleotide Translocator 1
- Adolescent
- Adult
- Age of Onset
- Aged
- Aged, 80 and over
- Aging
- Alleles
- Alternative Splicing
- Alzheimer Disease
- Amino Acid Sequence
- Amyotrophic Lateral Sclerosis
- Animals
- Arm
- Arrhythmias, Cardiac
- Audiometry, Pure-Tone
- Auditory Threshold
- B7-H1 Antigen
- Base Sequence
- Beckwith-Wiedemann Syndrome
- Biological Variation, Population
- Biomarkers
- Biopsy
- Blotting, Western
- Brazil
- C9orf72 Protein
- Case-Control Studies
- Caveolin 3
- Cell Compartmentation
- Cell Differentiation
- Cell Line
- Cell Line, Tumor
- Cell Nucleus
- Cell Proliferation
- Cells, Cultured
- Child
- Child, Preschool
- Choanal Atresia
- Chromatin
- Chromatin Immunoprecipitation
- Chromosome Deletion
- Chromosome Disorders
- Chromosome Mapping
- Chromosomes, Human, Pair 14
- Chromosomes, Human, Pair 4
- Cochlea
- Cohort Studies
- CpG Islands
- Creatine
- Cross-Sectional Studies
- Delayed Diagnosis
- Delivery of Health Care
- Dental Pulp
- Dependovirus
- Diagnosis, Differential
- Dietary Supplements
- Disease Models, Animal
- Disease Progression
- DNA Methylation
- DNA Mutational Analysis
- DNA Repeat Expansion
- DNA, Mitochondrial
- Echocardiography
- Electromyography
- Electron Transport Complex IV
- Epigenesis, Genetic
- Epigenomics
- Exercise Therapy
- Face
- Facial Muscles
- Family
- Female
- Fibroblasts
- Fibrosis
- Follow-Up Studies
- Frontotemporal Dementia
- Gene Deletion
- Gene Expression
- Gene Expression Regulation
- Gene Frequency
- Gene Rearrangement
- Gene Silencing
- Gene Transfer Techniques
- Genes, Dominant
- Genetic Association Studies
- Genetic Counseling
- Genetic Diseases, Inborn
- Genetic Predisposition to Disease
- Genetic Testing
- Genetic Therapy
- Genetic Variation
- Genetic Vectors
- Genotype
- Hand Strength
- Haplotypes
- Hearing Loss
- Hearing Loss, Sensorineural
- Heat-Shock Proteins
- HEK293 Cells
- HeLa Cells
- Heterozygote
- Homeodomain Proteins
- HSP27 Heat-Shock Proteins
- Humans
- Immunomodulation
- Infant
- Infant, Newborn
- Intercellular Signaling Peptides and Proteins
- Intracellular Signaling Peptides and Proteins
| - Isometric Contraction
- Italy
- Kaplan-Meier Estimate
- Klippel-Trenaunay-Weber Syndrome
- Kyphosis
- Lamin Type A
- LIM Domain Proteins
- Lod Score
- Male
- Methyl-CpG-Binding Protein 2
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Mice, Mutant Strains
- Mice, Transgenic
- Microfilament Proteins
- Microphthalmos
- MicroRNAs
- Microsatellite Repeats
- Middle Aged
- Migraine without Aura
- Mitochondria
- Molecular Diagnostic Techniques
- Molecular Sequence Data
- Motor Activity
- Multiple Sclerosis
- Muscle Development
- Muscle Fatigue
- Muscle Fibers, Fast-Twitch
- Muscle Fibers, Skeletal
- Muscle Proteins
- Muscle Strength
- Muscle Weakness
- Muscle, Skeletal
- Muscles
- Muscular Diseases
- Muscular Dystrophies
- Muscular Dystrophy, Animal
- Muscular Dystrophy, Facioscapulohumeral
- Mutation
- Myoblasts
- Myoclonic Epilepsies, Progressive
- Myogenin
- Myosin Heavy Chains
- Neurologic Examination
- Nose
- Nuclear Proteins
- Nucleic Acid Conformation
- Observer Variation
- Organ Size
- Otoacoustic Emissions, Spontaneous
- Paired Box Transcription Factors
- PAX3 Transcription Factor
- Pedigree
- Phenotype
- Physical Conditioning, Animal
- Physical Endurance
- Physical Exertion
- Poliomyelitis
- Polymorphism, Genetic
- Polymorphism, Restriction Fragment Length
- Precision Medicine
- Prevalence
- Prognosis
- Promoter Regions, Genetic
- Protein Binding
- Protein Isoforms
- Protein Processing, Post-Translational
- Protein Transport
- Proteins
- Pseudogenes
- Rare Diseases
- Recombination, Genetic
- Regeneration
- Registries
- Repressor Proteins
- Reproducibility of Results
- Rett Syndrome
- Reverse Transcriptase Polymerase Chain Reaction
- Risk Factors
- RNA
- RNA Interference
- RNA, Messenger
- RNA, Transfer, Leu
- RNA-Binding Proteins
- ROC Curve
- Ryanodine Receptor Calcium Release Channel
- Satellite Cells, Skeletal Muscle
- Sequence Analysis
- Sequence Analysis, DNA
- Sequence Deletion
- Severity of Illness Index
- Sex Characteristics
- Shoulder
- Stem Cell Transplantation
- Stem Cells
- Tandem Repeat Sequences
- Transcription, Genetic
- Transcriptional Activation
- Transduction, Genetic
- Transgenes
- Treatment Outcome
- Troponin T
- Up-Regulation
- Weight Loss
- Williams Syndrome
- Young Adult
- YY1 Transcription Factor
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Concepts
(217)
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