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Amy Elizabeth Roberts, M.D.
Concepts (338)
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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
Acidosis, Lactic
Action Potentials
Activin Receptors, Type I
Acyltransferases
Adaptation, Psychological
Adolescent
Adult
Age Factors
Age of Onset
Aged
Aged, 80 and over
Alleles
Amino Acid Sequence
Amino Acid Substitution
Amino Acid Transport System y+L
Aneuploidy
Angiography
Animals
Aniridia
Anticonvulsants
Antiporters
Aorta, Thoracic
Aortic Aneurysm
Aortic Coarctation
Aortic Stenosis, Supravalvular
Aortic Valve
Arrhythmias, Cardiac
Arteries
Articulation Disorders
Attention
Attention Deficit Disorder with Hyperactivity
Autistic Disorder
Barth Syndrome
Base Sequence
B-Lymphocytes
Brain
Branchio-Oto-Renal Syndrome
Caenorhabditis elegans
Cardiac Myosins
Cardiac Surgical Procedures
Cardiomegaly
Cardiomyopathies
Cardiomyopathy, Dilated
Cardiomyopathy, Hypertrophic
Cardiovascular Diseases
Cardiovascular System
Carrier Proteins
Case-Control Studies
Cataract
Cell Culture Techniques
Cell Line
Cell Separation
Cells, Cultured
Cerebral Cortex
Cerebrum
Child
Child Development Disorders, Pervasive
Child, Preschool
Chondroitinsulfatases
Chromatin
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Mapping
Chromosomes, Human
Chromosomes, Human, Pair 13
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 9
Chylothorax
Cognition
Cognition Disorders
Cohort Studies
Collagen Type III
Comorbidity
Comparative Genomic Hybridization
Congenital Abnormalities
COS Cells
Costello Syndrome
Craniofacial Abnormalities
Cross-Sectional Studies
Cytochromes c
Dark Adaptation
Databases, Genetic
Desmoplakins
Developmental Disabilities
Diagnosis, Differential
Diffusion Magnetic Resonance Imaging
DiGeorge Syndrome
Disease Management
Disease Progression
DNA
DNA Copy Number Variations
DNA Mutational Analysis
DNA-Binding Proteins
Dose-Response Relationship, Radiation
Drosophila
Ductus Arteriosus, Patent
Dyslexia, Acquired
Dyspnea
Echocardiography
Echocardiography, Transesophageal
Ectodermal Dysplasia
Educational Status
Ehlers-Danlos Syndrome
Electrocardiography
Electron Transport Complex IV
Enhancer Elements, Genetic
Environment
Epigenomics
Epilepsy
Ethics, Medical
Executive Function
Extracellular Signal-Regulated MAP Kinases
Face
Facies
Failure to Thrive
Fatal Outcome
Female
Fetal Distress
Fibroblasts
Follow-Up Studies
Fontan Procedure
Gene Expression
Gene Expression Profiling
Gene Frequency
Gene Regulatory Networks
Gene Silencing
Genes, Developmental
Genes, ras
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Linkage
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome-Wide Association Study
Genomics
Genotype
Germ-Line Mutation
Glucose Transporter Type 3
Growth Charts
Growth Differentiation Factor 1
Growth Disorders
GTPase-Activating Proteins
Hand Deformities, Congenital
Health Knowledge, Attitudes, Practice
Hearing
Hearing Loss
Heart
Heart Defects, Congenital
Heart Diseases
Heart Failure
Heart Transplantation
Heart Valve Diseases
Heart Ventricles
HEK293 Cells
Hemodynamics
Heterozygote
High-Throughput Nucleotide Sequencing
Histones
Homeodomain Proteins
Homozygote
Humans
Hypoplastic Left Heart Syndrome
In Situ Hybridization, Fluorescence
Incidence
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Infant, Premature
Infant, Premature, Diseases
Intelligence
Internship and Residency
Intracellular Signaling Peptides and Proteins
Kaplan-Meier Estimate
Karyotyping
KCNQ1 Potassium Channel
Kinetics
Language
Language Disorders
Learning
LEOPARD Syndrome
Leukemia, Myeloid, Acute
Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Juvenile
Light
Linkage Disequilibrium
Longitudinal Studies
Lysine
Magnetic Resonance Imaging
Magnetics
Male
Mammals
MAP Kinase Kinase 1
MAP Kinase Kinase 2
MAP Kinase Kinase Kinases
MAP Kinase Signaling System
Massachusetts
Medical History Taking
Membrane Potentials
Memory
Methylation
Mice
Mice, Knockout
Mice, Mutant Strains
Microarray Analysis
Middle Aged
Mitochondria
Mitochondrial Diseases
Mitochondrial Membranes
Mitogen-Activated Protein Kinase 7
Mitogen-Activated Protein Kinases
Models, Biological
Models, Molecular
Molecular Sequence Annotation
Molecular Sequence Data
Monosaccharide Transport Proteins
Motor Skills
Motor Skills Disorders
Muscle Proteins
Muscular Diseases
Musculoskeletal Abnormalities
Mutagenesis, Insertional
Mutation
Mutation, Missense
Myocardial Contraction
Myocardium
Myocytes, Cardiac
Myosin Heavy Chains
Neck
Neonatal Screening
Nervous System Malformations
Neurofibromin 1
Neurogenesis
Neuropsychological Tests
Noonan Syndrome
Nuchal Translucency Measurement
Nuclear Matrix-Associated Proteins
Nuclear Proteins
Nucleic Acid Hybridization
Odds Ratio
Oligonucleotide Array Sequence Analysis
Oncogene Protein v-akt
Oxidative Phosphorylation
Parents
Pedigree
Phenotype
Phosphorylation
Phosphotransferases (Alcohol Group Acceptor)
Photic Stimulation
Physicians
Polymorphism, Single Nucleotide
Practice Guidelines as Topic
Predictive Value of Tests
Pregnancy
Pregnancy Complications
Prenatal Diagnosis
Prevalence
Prognosis
Promoter Regions, Genetic
Proportional Hazards Models
Prospective Studies
Protein Conformation
Protein Interaction Domains and Motifs
Protein Kinases
Protein Structure, Tertiary
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Protein Tyrosine Phosphatases
Proteins
Proteomics
Proto-Oncogene Proteins B-raf
Proto-Oncogene Proteins c-raf
Quantitative Trait Loci
Rare Diseases
ras Proteins
Reactive Oxygen Species
Reading
Receptors, G-Protein-Coupled
Receptors, Transforming Growth Factor beta
Reference Values
Registries
Repressor Proteins
Reproducibility of Results
Retinaldehyde
Retrospective Studies
Rhodopsin
Risk
Risk Factors
RNA Splicing
RNA, Messenger
RNA-Binding Proteins
Rod Opsins
Sarcomeres
Seizures
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Severe Combined Immunodeficiency
Siblings
Signal Transduction
Smith-Lemli-Opitz Syndrome
Smith-Magenis Syndrome
Son of Sevenless Proteins
SOS1 Protein
Spasm
Spasms, Infantile
Statistics, Nonparametric
Students, Medical
Survival Analysis
Syndrome
Tachycardia, Ventricular
Telomere
Tetralogy of Fallot
Therapies, Investigational
Time Factors
Tissue Engineering
Transcription Factor AP-2
Transcription Factors
Transcription, Genetic
Transfection
Translocation, Genetic
Trisomy
United States
Vascular Endothelial Growth Factor Receptor-3
Ventricular Outflow Obstruction
Ventricular Remodeling
Williams Syndrome
Young Adult
Roberts's Networks
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Concepts (338)
Derived automatically from this person's publications.
Heart Defects, Congenital
Noonan Syndrome
Cardiomyopathy, Dilated
Abnormalities, Multiple
Trisomy
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_
Co-Authors (110)
People in Profiles who have published with this person.
Newburger, Jane
Morton, Sarah
Kucherlapati, Raju
Jenkins, Kathy
Chung, Wendy
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_
Similar People (60)
People who share similar concepts with this person.
Newburger, Jane
Faraone, Stephen
Alkuraya, Fowzan
Seidman, Christine
Chung, Wendy
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_
Same Department
People in same department with this person.
Farias, Michael
Gupta, Krishan
Lyon, Shannon
Newburger, Jane
Wypij, David
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_
Physical Neighbors
People whose addresses are nearby this person.
Church, George
Horwitz, Bruce
Kucherlapati, Raju
Mochida, Ganeshwaran
Seidman, Jonathan