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Robert Hufnagel
Concepts (478)
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Concepts are derived automatically from a person's publications.
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Categories
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Details
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.
Abnormalities, Multiple
Acetyltransferases
Acyltransferases
Adaptor Proteins, Signal Transducing
Adolescent
ADP-Ribosylation Factors
Adult
Age Factors
Age of Onset
Aged
Aged, 80 and over
Alagille Syndrome
Albinism
Algorithms
Alleles
Alopecia
Amelogenesis Imperfecta
Amino Acid Sequence
Amino Acid Substitution
AMP-Activated Protein Kinases
Amyloidosis
Angiogenesis Inhibitors
Angiography
Animals
Animals, Genetically Modified
Aniridia
Anophthalmos
Anterior Eye Segment
Antibodies, Monoclonal, Humanized
Aortic Stenosis, Supravalvular
Arabs
Arthrogryposis
Arylsulfatases
Ataxia
ATPases Associated with Diverse Cellular Activities
ATP-Binding Cassette Transporters
Atrophy
Auditory Pathways
Auditory Threshold
Autistic Disorder
Basal Bodies
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
Bestrophins
beta-Galactosidase
Bevacizumab
Blepharoptosis
Blindness
Body Size
Bone Diseases, Developmental
Bone Morphogenetic Protein Receptors, Type I
Brain
Bromodeoxyuridine
Cadherin Related Proteins
Cadherins
Calcium-Binding Proteins
Carboxylic Ester Hydrolases
Cartilage
Case-Control Studies
Cataract
Cation Transport Proteins
Cell Cycle
Cell Death
Cell Division
Cell Lineage
Cell Movement
Cell Polarity
Cell Survival
Central Nervous System
Cerebellum
Cerebral Palsy
Charcot-Marie-Tooth Disease
Child
Child, Preschool
Choroid
Choroidal Neovascularization
Choroideremia
Chromosome Aberrations
Chromosome Disorders
Chromosomes, Human, Pair 15
Ciliary Body
cis-trans-Isomerases
Cleft Lip
Cleft Palate
Clinical Trials as Topic
Cochlear Nucleus
Codon, Nonsense
Cohort Studies
Collagen Type XI
Coloboma
Color Vision Defects
Coloring Agents
Comorbidity
Computational Biology
Cone-Rod Dystrophies
Consanguinity
Conserved Sequence
Cornea
COS Cells
Craniofacial Abnormalities
Cross-Sectional Studies
Cyclic Nucleotide Phosphodiesterases, Type 6
Cyclic Nucleotide-Gated Cation Channels
Databases, Factual
DEAD Box Protein 58
DEAD-box RNA Helicases
Deafness
Dependovirus
Developmental Disabilities
Diabetes Complications
Diabetes Mellitus
Diagnosis, Differential
Disease Models, Animal
Disease Progression
DNA
DNA Helicases
DNA Mutational Analysis
DNA, Neoplasm
DNA-Binding Proteins
Down-Regulation
Drosophila
Drosophila Proteins
Dwarfism
Dysbindin
Dysostoses
Dystonia
Dystonic Disorders
Dystrophin-Associated Proteins
E-Box Elements
Ectoderm
Ectodermal Dysplasia
Edema
Elastin
Electrooculography
Electroretinography
Embryo, Mammalian
Embryo, Nonmammalian
Embryonic Development
Endoplasmic Reticulum
Endothelin-1
Epilepsy
Epiphyses
Epithelial Cells
Evoked Potentials, Auditory, Brain Stem
Evoked Potentials, Visual
Exanthema
Exome
Exons
Extracellular Matrix Proteins
Eye
Eye Abnormalities
Eye Diseases
Eye Diseases, Hereditary
Eye Proteins
Face
Facies
Family
Female
Fibroblast Growth Factors
Fibroblasts
Fluorescein Angiography
Fluorescent Antibody Technique
Follow-Up Studies
Forkhead Transcription Factors
Founder Effect
Fovea Centralis
Frameshift Mutation
Fundus Oculi
Gain of Function Mutation
Gastrointestinal Diseases
Gene Deletion
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Expression Regulation, Neoplastic
Gene Frequency
Gene Transfer Techniques
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Counseling
Genetic Diseases, X-Linked
Genetic Loci
Genetic Predisposition to Disease
Genetic Testing
Genetic Therapy
Genetic Variation
Genetic Vectors
Genetics
Genetics, Population
Genome
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Glaucoma, Angle-Closure
Glaucoma, Open-Angle
Green Fluorescent Proteins
Growth Cones
GTP Phosphohydrolases
Hair Cells, Auditory, Outer
Hand Deformities, Congenital
Headache
Hearing Loss
Hearing Loss, Bilateral
Hearing Loss, Sensorineural
Heart Defects, Congenital
Heart Valve Diseases
HEK293 Cells
HeLa Cells
Hereditary Autoinflammatory Diseases
Hermanski-Pudlak Syndrome
Heterozygote
Hexokinase
High-Throughput Nucleotide Sequencing
Histone Acetyltransferases
Holoprosencephaly
Homeodomain Proteins
Homozygote
Humans
Hyperglycemia
Hyperopia
Hypertrichosis
Hypogonadism
Hypohidrosis
Ichthyosis
Image Processing, Computer-Assisted
Immunohistochemistry
In Situ Hybridization
Indocyanine Green
Infant
Infant, Newborn
Inflammation
Inheritance Patterns
Insulin
Intellectual Disability
Interferons
Intestinal Polyposis
Intestines
Intracellular Signaling Peptides and Proteins
Intravitreal Injections
Introns
Jagged-1 Protein
Kearns-Sayre Syndrome
Klinefelter Syndrome
Laser Coagulation
Laurence-Moon Syndrome
Leber Congenital Amaurosis
Leukocytes
Limb Deformities, Congenital
Live Birth
Longitudinal Studies
Loss of Function Mutation
Low Density Lipoprotein Receptor-Related Protein-2
Low Density Lipoprotein Receptor-Related Protein-5
Macaca fascicularis
Macaca mulatta
Macula Lutea
Macular Degeneration
Macular Edema
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Mandibulofacial Dysostosis
MAP Kinase Kinase Kinase 1
Medical Records
Megalencephaly
Melanins
Membrane Proteins
Meta-Analysis as Topic
Metacarpus
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Mice, Inbred ICR
Mice, Knockout
Mice, Mutant Strains
Mice, Transgenic
Microcephaly
Micrognathism
Microphthalmia-Associated Transcription Factor
Microphthalmos
Microscopy, Confocal
Microscopy, Electron, Transmission
Middle Aged
Mitochondria
Mitochondrial Dynamics
Mitochondrial Membranes
Mitochondrial Proteins
Mitosis
Models, Biological
Models, Molecular
Molecular Sequence Data
Morpholinos
Mosaicism
Mucopolysaccharidosis III
Muscle Proteins
Muscle Spasticity
Muscular Atrophy
Musculoskeletal Abnormalities
Mutation
Mutation, Missense
Myopia
Myopia, Degenerative
Nails, Malformed
Neck
Neoplastic Syndromes, Hereditary
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Neural Crest
Neural Stem Cells
Neural Tube
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neuroectodermal Tumors, Primitive
Neurofibromatosis 1
Neurogenesis
Neuroglia
Neurons
Neuropeptides
Neuropsychological Tests
NF-kappa B
Nuclear Proteins
Odontodysplasia
Oligonucleotides, Antisense
Ophthalmology
Ophthalmoscopy
Optic Atrophy, Autosomal Dominant
Optic Disk
Optic Nerve
Optic Nerve Glioma
Optic Nerve Neoplasms
Optical Imaging
Optics and Photonics
Organ Specificity
Osteochondrodysplasias
Osteopetrosis
Paired Box Transcription Factors
Paraplegia
PAX6 Transcription Factor
Pediatricians
Pedigree
Penetrance
Peripherins
Peroxisomal Disorders
Phenotype
Phosphate Transport Proteins
Phosphatidylinositol 3-Kinases
Phospholipases
Phosphoprotein Phosphatases
Photoreceptor Cells
Photoreceptor Cells, Vertebrate
Point Mutation
Polymorphism, Single Nucleotide
Posterior Eye Segment
Precision Medicine
Pregnancy
Premature Birth
Prevalence
Prognosis
Prospective Studies
Protein Binding
Protein Interaction Domains and Motifs
Protein Kinases
Protein Precursors
Protein Sorting Signals
Protein Structure, Tertiary
Protein Transport
Proteoglycans
Proto-Oncogene Proteins
Pseudogenes
Quality of Life
Rabbits
Radiography
Rare Diseases
Rats
Real-Time Polymerase Chain Reaction
Receptor, Endothelin A
Receptors, Immunologic
Receptors, Retinoic Acid
Refractive Errors
Registries
Regulatory Elements, Transcriptional
Renal Insufficiency
Repressor Proteins
Reproducibility of Results
Research Design
Retina
Retinal Cone Photoreceptor Cells
Retinal Degeneration
Retinal Detachment
Retinal Diseases
Retinal Dystrophies
Retinal Ganglion Cells
Retinal Hemorrhage
Retinal Neovascularization
Retinal Pigment Epithelium
Retinal Pigments
Retinal Rod Photoreceptor Cells
Retinitis Pigmentosa
Retinoschisis
Retrospective Studies
Rhombencephalon
Ribonuclease III
Ribosomes
RNA
RNA Interference
RNA Polymerase I
RNA Splice Sites
RNA Splicing
RNA, Messenger
RNA-Binding Proteins
Rod Cell Outer Segment
Rod Opsins
Saccharomyces cerevisiae Proteins
Sequence Analysis, DNA
Serine Proteases
Serum Amyloid A Protein
Severity of Illness Index
Sex Chromosome Disorders
Siblings
Signal Transduction
Skin Abnormalities
Slit Lamp Microscopy
Smell
Smoothened Receptor
South America
SOXB1 Transcription Factors
Spasms, Infantile
Spastic Paraplegia, Hereditary
Sphingomyelin Phosphodiesterase
Spinal Cord
Spinocerebellar Ataxias
Spiral Ganglion
Splenomegaly
Stilbamidines
Structure-Activity Relationship
Sulfotransferases
Synapses
Synaptic Transmission
Syndactyly
Syndrome
TATA-Binding Protein Associated Factors
Telemedicine
Telencephalon
Tetraspanins
Texas
Tissue Inhibitor of Metalloproteinase-3
Tomography, Optical Coherence
Tomography, X-Ray Computed
Transcription Factor TFIID
Transcription Factors
Transcriptome
Transfection
Transgenes
Trisomy
Ubiquitin-Activating Enzymes
Ultrasonography, Prenatal
Uniparental Disomy
United States
Usher Syndromes
Uvea
Uveal Neoplasms
Vascular Endothelial Growth Factor A
Vestibular Nucleus, Lateral
Vision Disorders
Vision, Ocular
Visual Acuity
Visual Field Tests
Visual Fields
Vitelliform Macular Dystrophy
Williams Syndrome
Wnt Signaling Pathway
Young Adult
Zebrafish
Zebrafish Proteins
Zygoma
Concepts (478)
Derived automatically from this person's publications.
Mutation
Retinitis Pigmentosa
Phenotype
Eye Diseases, Hereditary
Retina
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