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Lance H Rodan, M.D.
Concepts (403)
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Concepts are derived automatically from a person's publications.
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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
Acid-Base Equilibrium
Acidosis
Actins
Acute Disease
Acyltransferases
Adaptor Proteins, Signal Transducing
Adenosine Triphosphatases
Adenosine Triphosphate
Administration, Oral
Adolescent
Adult
Aged, 80 and over
Algorithms
Alleles
Alopecia
Ambulances
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Transport Systems, Acidic
Amino Acids
Anemia
Animals
Anions
Antibodies
Anticonvulsants
Antiporters
Arginine
Asparagine
Aspartate Carbamoyltransferase
Aspartate-Ammonia Ligase
Ataxia
Atrophy
Attention Deficit Disorder with Hyperactivity
Autistic Disorder
Autoimmune Diseases
Basal Ganglia
beta Catenin
Binding Sites
Biogenic Amines
Body Dysmorphic Disorders
Brain
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Brain Ischemia
Brain Mapping
Calcium Channels, L-Type
Calcium Channels, R-Type
Calpain
Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing)
Carbohydrate Metabolism, Inborn Errors
Carbon Dioxide
Carbon-Nitrogen Ligases
Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor
Carnitine
Carrier Proteins
Case-Control Studies
Casein Kinase II
Cataplexy
Cation Transport Proteins
Ceftriaxone
Cell Adhesion Molecules
Cell Cycle Proteins
Cell Differentiation
Cell Line
Cell Nucleus
Central Nervous System
Cerebellar Diseases
Cerebral Palsy
Cerebrovascular Circulation
Chelating Agents
Chick Embryo
Child
Child, Preschool
Chorea
Chromatin
Chromatin Assembly and Disassembly
Chromatography, High Pressure Liquid
Chromatography, Liquid
Chromosomal Proteins, Non-Histone
Chromosome Deletion
Chromosome Mapping
Chromosomes, Human, Pair 21
Class I Phosphatidylinositol 3-Kinases
Clinical Protocols
Codon, Nonsense
Cohort Studies
Comorbidity
Comparative Genomic Hybridization
Congenital Abnormalities
Consanguinity
Contracture
Corpus Callosum
Craniofacial Abnormalities
Critical Care
Cross-Sectional Studies
Cyclin D
Cyclin D2
Cytoplasmic Dyneins
Cytoskeletal Proteins
Cytoskeleton
Databases, Genetic
DEAD-box RNA Helicases
Deep Brain Stimulation
Dendritic Spines
Developmental Disabilities
Diagnosis, Differential
Diarrhea
Dicarboxylic Acid Transporters
Diffusion Magnetic Resonance Imaging
Dihydroorotase
Disease Management
Disease Progression
Disorders of Sex Development
DNA Copy Number Variations
DNA Helicases
DNA Mutational Analysis
DNA, Complementary
DNA, Mitochondrial
DNA-Binding Proteins
Dopamine
Dose-Response Relationship, Drug
Down Syndrome
Drosophila
Drosophila melanogaster
Drosophila Proteins
Dwarfism
Dyskinesias
Dystonic Disorders
Early Diagnosis
Electroencephalography
Emergency Medical Services
Emergency Medical Technicians
Emergency Medicine
Emergency Service, Hospital
Epigenesis, Genetic
Epilepsies, Myoclonic
Epilepsies, Partial
Epilepsy
Epilepsy, Generalized
Ergometry
Excitatory Amino Acid Transporter 2
Exercise
Extracellular Matrix
Eye Abnormalities
Eye Movements
Face
Facies
Fatigue
Fatty Acids
F-Box Proteins
Female
Fibroblasts
Focal Adhesions
Folate Receptor 1
Follow-Up Studies
Foot Deformities
Frameshift Mutation
GABA Plasma Membrane Transport Proteins
Gas Chromatography-Mass Spectrometry
Gastric Mucosa
Gastroschisis
Gene Expression
Gene Expression Regulation
Gene Expression Regulation, Developmental
Genes, Dominant
Genes, Recessive
Genetic Association Studies
Genetic Heterogeneity
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genitalia
Genome, Human
Genomics
Genotype
Germ Cells
Germ-Line Mutation
Glasgow Coma Scale
Glutamate Decarboxylase
Glutamine
Glycoproteins
Haploinsufficiency
Health Services Accessibility
Hearing Loss
Heart Defects, Congenital
HEK293 Cells
Hemiplegia
Hereditary Central Nervous System Demyelinating Diseases
Heterozygote
High-Throughput Nucleotide Sequencing
Hippocampus
Histone Demethylases
Histones
Homeostasis
Homozygote
Hospitals
Hospitals, Community
Hotlines
Humans
Hydrocephalus
Hyperkinesis
Hypoxia-Ischemia, Brain
In Situ Hybridization, Fluorescence
Incidence
Infant
Infant, Newborn
Interinstitutional Relations
Intestinal Mucosa
Intracellular Signaling Peptides and Proteins
Intracranial Thrombosis
Jumonji Domain-Containing Histone Demethylases
Kinetics
Kv1.1 Potassium Channel
Language Development Disorders
Language Disorders
Leigh Disease
Leukocytosis
Limbic Encephalitis
Lissencephaly
Long QT Syndrome
Longitudinal Studies
Loss of Heterozygosity
Lower Extremity
Lower Extremity Deformities, Congenital
Lupus Erythematosus, Systemic
Lymphangiectasis, Intestinal
Lymphedema
Lysosomes
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Male
Malformations of Cortical Development
Malonates
Manganese
Maple Syrup Urine Disease
Mass Spectrometry
Massachusetts
Medulloblastoma
MELAS Syndrome
Membrane Proteins
Metabolic Diseases
Metabolism, Inborn Errors
Metabolomics
Metal Metabolism, Inborn Errors
Methylation
Methyltransferases
Mi-2 Nucleosome Remodeling and Deacetylase Complex
Mice
Mice, Inbred C57BL
Microcephaly
Microfilament Proteins
Microscopy, Confocal
Microtubule-Associated Proteins
Middle Aged
Mitochondrial Diseases
Mitochondrial Membrane Transport Proteins
Mitochondrial Proteins
Models, Molecular
Molecular Diagnostic Techniques
Monitoring, Physiologic
Monosaccharide Transport Proteins
Movement Disorders
Muscle Hypotonia
Muscle Spasticity
Muscles
Muscular Atrophy, Spinal
Musculoskeletal Abnormalities
Mutation
Mutation, Missense
Myoclonic Epilepsies, Progressive
Myokymia
Nephrosis
Nerve Tissue Proteins
Nervous System Malformations
Neurites
Neuroaxonal Dystrophies
Neurogenesis
Neuroglia
Neurons
Neuropsychological Tests
Neurotransmitter Agents
Nuclear Proteins
Nucleocytoplasmic Transport Proteins
Obesity
Ocular Motility Disorders
Ontario
Open Reading Frames
Optic Atrophy
Organoids
Ornithine
Oxidation-Reduction
Oxidoreductases
Oxygen
Paresis
Parkinsonian Disorders
Patient Care Team
Patient Selection
Patient Transfer
Pedigree
Pelger-Huet Anomaly
Pentose Phosphate Pathway
Phenotype
Phosphatidylinositol 3-Kinases
Phosphatidylinositol Phosphates
Phosphatidylinositols
Phosphocreatine
Phosphoric Monoester Hydrolases
Physicians
Pilot Projects
Polydactyly
Polymorphism, Single Nucleotide
Practice Guidelines as Topic
Procollagen N-Endopeptidase
Propionic Acidemia
Prospective Studies
Proteasome Endopeptidase Complex
Protein Binding
Protein Processing, Post-Translational
Protein Structure, Secondary
Protein-Arginine N-Methyltransferases
Proteins
Proto-Oncogene Proteins c-akt
Psychomotor Disorders
Psychotic Disorders
PTEN Phosphohydrolase
Pupil
Purpura
Pyridoxal Phosphate
Pyridoxaminephosphate Oxidase
Quadriplegia
Rare Diseases
Rats
Receptors, GABA-A
Recovery of Function
Recurrence
Referral and Consultation
Registries
Rest
Retina
Retinal Diseases
Retinitis Pigmentosa
Retrospective Studies
rhoB GTP-Binding Protein
Risk Factors
RNA Splice Sites
RNA Splicing
RNA, Messenger
RNA, Small Nuclear
RNA-Binding Proteins
Seizures
Semaphorins
Sequence Alignment
Sequence Analysis, DNA
Serine
Severity of Illness Index
Siblings
Signal Transduction
SKP Cullin F-Box Protein Ligases
Spasms, Infantile
Spastic Paraplegia, Hereditary
Speech Disorders
Spinocerebellar Ataxias
Spliceosomes
Stem Cell Niche
Stroke
Syndactyly
Syndrome
Temporal Lobe
Tetrahydrofolates
Thiamine Deficiency
Thrombolytic Therapy
Time Factors
Tissue Plasminogen Activator
Toes
Tomography, X-Ray Computed
TOR Serine-Threonine Kinases
Transaldolase
Transcription Factor 7-Like 2 Protein
Transcription Factors
Transketolase
Transportation of Patients
Treatment Outcome
Triage
Tubulin
Tumor Suppressor Proteins
Ubiquitination
Ubiquitin-Protein Ligases
Urea Cycle Disorders, Inborn
Uridine
Uridine Diphosphate Glucose Dehydrogenase
Vacuolar Proton-Translocating ATPases
Valproic Acid
Vasospasm, Intracranial
Vigabatrin
Vision Disorders
Visual Cortex
Wernicke Encephalopathy
Wnt Proteins
Young Adult
Zebrafish
Zebrafish Proteins
Rodan's Networks
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Concepts (403)
Derived automatically from this person's publications.
MELAS Syndrome
Developmental Disabilities
Genetic Variation
Epilepsy
Muscle Hypotonia
Explore
_
Co-Authors (117)
People in Profiles who have published with this person.
Levy, Harvey
Yang, Edward
Berry, Gerard
Picker, Jonathan
Peake, Roy
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_
Similar People (60)
People who share similar concepts with this person.
Kohane, Zak
Walsh, Christopher
Alkuraya, Fowzan
Chung, Wendy
Pearl, Phillip
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_
Same Department
People in same department with this person.
Abu-El-Haija, Aya
Beggs, Alan
Hill, Robert
Kim, Sonia
Kunkel, Louis
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_