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Irina Anselm, M.D.
Concepts (205)
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Concepts are derived automatically from a person's publications.
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Categories
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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
Acidosis, Lactic
Action Potentials
Acute Disease
Acute Kidney Injury
Acyltransferases
Adenosine Triphosphatases
Adolescent
Adrenal Insufficiency
Adrenoleukodystrophy
Adult
Age of Onset
Alleles
Amino Acid Metabolism, Inborn Errors
Amino Acid Substitution
Amino Acid Transport Systems, Acidic
Angelman Syndrome
Antiporters
Apoptosis Inducing Factor
Aromatic-L-Amino-Acid Decarboxylases
Arrhythmias, Cardiac
ATP-Binding Cassette Transporters
Atrophy
Autistic Disorder
Base Sequence
Betaine
Brain
Brain Chemistry
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Carbon-Nitrogen Ligases
Carboxy-Lyases
Cardiotonic Agents
Carotid Artery, Internal
Carotid Stenosis
Carrier Proteins
Case-Control Studies
Cataract
Cell Adhesion Molecules
Cerebellar Diseases
Cerebral Infarction
Charcot-Marie-Tooth Disease
Child
Child Behavior Disorders
Child, Preschool
Cholestasis, Intrahepatic
Chorea
Chromosome Aberrations
Chromosome Deletion
Chromosomes, Human, Pair 15
Chromosomes, Human, X
Comparative Genomic Hybridization
Consanguinity
Consensus
Craniofacial Abnormalities
Creatine
Cross-Over Studies
Cytochrome Reductases
Data Collection
Deep Brain Stimulation
Deglutition Disorders
Delphi Technique
Developmental Disabilities
Dietary Supplements
Diffusion Magnetic Resonance Imaging
Disease Management
Disease Progression
DNA
DNA Copy Number Variations
DNA Methylation
DNA Mutational Analysis
DNA, Mitochondrial
Dopamine
Double-Blind Method
Drug Combinations
Dystonia
Dystonic Disorders
Electrocardiography, Ambulatory
Electroencephalography
Electron Transport
Epilepsies, Partial
Epilepsy
Evidence-Based Medicine
Exons
Eye
Facies
Family
Fatal Outcome
Female
Fibroblasts
Folate Receptor 1
Folic Acid
Follow-Up Studies
Frameshift Mutation
Gastrointestinal Agents
Gene Deletion
Gene Duplication
Gene Expression Regulation
Genes, X-Linked
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genomic Imprinting
Genotype
Glutaryl-CoA Dehydrogenase
Glycine
Growth Disorders
GTP-Binding Protein alpha Subunits, Gi-Go
Heart Arrest
Hereditary Central Nervous System Demyelinating Diseases
Heterogeneous-Nuclear Ribonucleoproteins
Heterozygote
Humans
Hyperkinesis
Immunohistochemistry
Infant
Infant, Newborn
Inheritance Patterns
Intracranial Arteriosclerosis
Language Development Disorders
Leigh Disease
Leukocytes
Lipotropic Agents
Lissencephaly
Longitudinal Studies
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Male
MELAS Syndrome
Membrane Proteins
Membrane Transport Proteins
Mental Retardation, X-Linked
Metabolic Diseases
Metabolism, Inborn Errors
Microcephaly
Microfilament Proteins
Middle Aged
Mitochondria
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Proteins
Molecular Sequence Data
Morocco
Muscle Hypotonia
Muscle, Skeletal
Muscular Diseases
Mutation
Mutation, Missense
Nerve Tissue Proteins
Nervous System Malformations
Neural Conduction
Neuroaxonal Dystrophies
Neuropsychological Tests
Norepinephrine
North America
Optic Atrophy
Oxidoreductases Acting on Sulfur Group Donors
Oxygen
Parkinson Disease
Parkinsonian Disorders
Pedigree
Peptide Termination Factors
Peripheral Nervous System Diseases
Peroneal Nerve
Phenotype
Phosphorylation
Physicians
Placebos
Plasma Membrane Neurotransmitter Transport Proteins
Polymorphism, Single Nucleotide
Positron-Emission Tomography
Pregnancy
Progeria
Psychometrics
Psychomotor Disorders
Putamen
Radiography
Randomized Controlled Trials as Topic
Retrospective Studies
Rhabdomyolysis
RNA Processing, Post-Transcriptional
Sequence Deletion
Siblings
Single-Cell Analysis
Sodium-Potassium-Exchanging ATPase
Standard of Care
Statistics, Nonparametric
Succinate-CoA Ligases
Sural Nerve
Syndrome
Tetrahydrofolates
Transcription Factors
Treatment Outcome
Tubulin
Twins, Monozygotic
Ubiquitin-Protein Ligases
Vasculitis, Central Nervous System
Vasoconstrictor Agents
Ventricular Premature Complexes
Vitamin B Complex
Young Adult
Anselm's Networks
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Concepts (205)
Derived automatically from this person's publications.
Lissencephaly
Atrophy
Mitochondrial Diseases
Cytochrome Reductases
Plasma Membrane Neurotransmitter Transport Proteins
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_
Co-Authors (63)
People in Profiles who have published with this person.
Yang, Edward
Berry, Gerard
Darras, Basil
Prabhu, Sanjay
Rodan, Lance
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_
Similar People (60)
People who share similar concepts with this person.
Mootha, Vamsi
Walsh, Christopher
Faraone, Stephen
Alkuraya, Fowzan
Chung, Wendy
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_
Same Department
People in same department with this person.
Afshar Saber, Wardiya
Jayakar, Selwyn
Klein, Jessica
Rostamian, Sahar
Seiglie, Mariel
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_
Physical Neighbors
People whose addresses are nearby this person.
Maski, Kiran
Mazumdar, Maitreyi
LaRovere, Kerri
Takeoka, Masanori
Levin, April
_