Harvard Catalyst Profiles

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Amy Elizabeth Roberts, M.D.

Concepts (315)

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Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
Name Number of Publications Most Recent Publication Publications by All Authors Concept Score Why?
Noonan Syndrome2120221333.980 Why?
Heart Defects, Congenital20202342671.110 Why?
Trisomy320172611.080 Why?
Abnormalities, Multiple10202013870.960 Why?
Cardiomyopathy, Dilated520208170.750 Why?
Genetic Testing12202133400.670 Why?
Smith-Lemli-Opitz Syndrome12017230.660 Why?
Chromosomes, Human, Pair 13120172040.630 Why?
Protein Tyrosine Phosphatase, Non-Receptor Type 111020182760.590 Why?
Barth Syndrome22014260.590 Why?
DNA Mutational Analysis11202043120.590 Why?
SOS1 Protein52013470.560 Why?
Growth Charts12012520.460 Why?
Cardiomyopathy, Hypertrophic5202111960.450 Why?
Executive Function3202313210.430 Why?
DiGeorge Syndrome320171830.390 Why?
Siblings120148200.390 Why?
Intelligence220149000.380 Why?
Mutation182020294910.330 Why?
Protein Tyrosine Phosphatases420074930.320 Why?
Induced Pluripotent Stem Cells4201916040.320 Why?
Genetic Predisposition to Disease82020174320.290 Why?
DNA Copy Number Variations4202019020.280 Why?
Phenotype152020164040.270 Why?
Ectodermal Dysplasia320221030.270 Why?
ras Proteins5202211170.270 Why?
Tetralogy of Fallot220215730.270 Why?
Genetic Association Studies7201527210.250 Why?
Memory2201321500.250 Why?
Learning1201316140.250 Why?
Chromosomes, Human, Pair 2120043240.240 Why?
Germ-Line Mutation3201017320.240 Why?
Nucleic Acid Hybridization1200414400.230 Why?
Costello Syndrome12022180.230 Why?
Mutation, Missense4202025110.230 Why?
In Situ Hybridization, Fluorescence3201126610.220 Why?
Child292023743870.220 Why?
Chromosome Deletion2201613780.210 Why?
Infant152022345740.210 Why?
Child, Preschool182020412210.200 Why?
Chromosome Aberrations3201418260.200 Why?
Adolescent252023851390.190 Why?
Intracellular Signaling Peptides and Proteins6201230100.190 Why?
MAP Kinase Kinase 1220193520.190 Why?
Attention Deficit Disorder with Hyperactivity1201436000.180 Why?
LEOPARD Syndrome12018250.180 Why?
Spasms, Infantile120222840.180 Why?
Mitogen-Activated Protein Kinase 712019690.180 Why?
MAP Kinase Kinase 2120191080.180 Why?
Failure to Thrive220221320.180 Why?
Cerebrum120201260.180 Why?
Proto-Oncogene Proteins c-raf120192070.180 Why?
Growth Differentiation Factor 11201750.170 Why?
Cardiac Myosins120171130.160 Why?
Humans6720237172370.160 Why?
Chromosomes, Human, Pair 18120172500.160 Why?
Vascular Endothelial Growth Factor Receptor-3120171260.160 Why?
Chromosome Disorders220174980.160 Why?
Genes, ras220107200.150 Why?
Tissue Engineering2201918550.150 Why?
Chylothorax12017910.150 Why?
Proto-Oncogene Proteins B-raf3202219490.150 Why?
Genotype92022129230.150 Why?
Male4020233513800.150 Why?
Son of Sevenless Proteins12015270.150 Why?
Myosin Heavy Chains120174010.140 Why?
Heterozygote2202027940.140 Why?
Glucose Transporter Type 312015160.140 Why?
Craniofacial Abnormalities220103260.140 Why?
Echocardiography4202050990.140 Why?
Myocytes, Cardiac3201916450.140 Why?
Heart4202243320.140 Why?
Developmental Disabilities3202113780.140 Why?
Nuclear Matrix-Associated Proteins12015460.140 Why?
Female3720233779090.130 Why?
Fatal Outcome2201718920.130 Why?
MAP Kinase Signaling System3201415870.130 Why?
Muscle Proteins1202012350.130 Why?
Nervous System Malformations120152250.130 Why?
Syndrome5202232010.120 Why?
Ductus Arteriosus, Patent120152100.120 Why?
Facies320221930.120 Why?
Aortic Coarctation120152660.120 Why?
Therapies, Investigational120141110.120 Why?
Protein Interaction Domains and Motifs120155120.120 Why?
Fetal Distress12012460.110 Why?
Protein Kinases1202016840.110 Why?
Nuchal Translucency Measurement12012540.110 Why?
Infant, Newborn52020247420.110 Why?
Hand Deformities, Congenital120121470.110 Why?
Angiography1201716690.110 Why?
Heart Ventricles3201538370.100 Why?
Tachycardia, Ventricular1201912170.100 Why?
Mitochondrial Diseases120143150.100 Why?
Cell Culture Techniques1201817220.100 Why?
Heart Transplantation2202030830.100 Why?
Receptors, G-Protein-Coupled1201712070.100 Why?
Fontan Procedure120157410.090 Why?
Prognosis42021292260.090 Why?
Aniridia12009280.090 Why?
Arrhythmias, Cardiac1201921400.090 Why?
Neurogenesis120158330.090 Why?
Gene Regulatory Networks1201817300.090 Why?
Chromosomes, Human, Pair 15220203740.090 Why?
Autistic Disorder1201710720.090 Why?
RNA-Binding Proteins2201519230.090 Why?
Young Adult92021562470.090 Why?
Cardiomyopathies1202018310.090 Why?
Branchio-Oto-Renal Syndrome12008250.090 Why?
High-Throughput Nucleotide Sequencing3201736980.090 Why?
Disease Management3201425370.090 Why?
Microarray Analysis120117810.080 Why?
Transcription Factor AP-212008820.080 Why?
Cognition Disorders2201539900.080 Why?
Epilepsy1202229400.080 Why?
Cohort Studies62022398870.080 Why?
Neck120127100.080 Why?
Karyotyping2201112720.080 Why?
Heart Valve Diseases1201510570.080 Why?
Quantitative Trait Loci1201419790.080 Why?
Severe Combined Immunodeficiency120092340.080 Why?
Leukemia, Myelomonocytic, Chronic12007920.070 Why?
Infant, Premature, Diseases120127000.070 Why?
Environment1201211010.070 Why?
Activin Receptors, Type I120061450.070 Why?
Hypoplastic Left Heart Syndrome120115350.070 Why?
Cardiovascular System120127700.070 Why?
Prenatal Diagnosis1201211720.070 Why?
Cardiovascular Diseases32019143810.070 Why?
Genetic Variation2201966640.070 Why?
Nuclear Proteins2201259880.070 Why?
Receptors, Transforming Growth Factor beta120063170.070 Why?
Risk Factors42022708640.070 Why?
Adult1520212124510.070 Why?
Aortic Valve1201518350.070 Why?
Cardiomegaly120086500.070 Why?
Translocation, Genetic2201514260.070 Why?
Retinaldehyde12003270.060 Why?
Models, Molecular3201555420.060 Why?
Retrospective Studies52020726140.060 Why?
Neuropsychological Tests4202169290.060 Why?
Attention1201424140.060 Why?
Predictive Value of Tests12020152710.060 Why?
Models, Biological2201498920.060 Why?
Reproducibility of Results22020195380.060 Why?
Brain42021252810.060 Why?
Rod Opsins120031180.060 Why?
Sequence Deletion1200815510.060 Why?
Rhodopsin120032090.060 Why?
Chromatin3202327410.060 Why?
Dark Adaptation120032310.060 Why?
Histones1201325880.060 Why?
Spasm120221070.060 Why?
Chromosomes, Human, Pair 9120045450.060 Why?
Cardiac Surgical Procedures1201734690.060 Why?
Diagnosis, Differential32014132740.060 Why?
Mitogen-Activated Protein Kinases2202213200.050 Why?
Language1201012600.050 Why?
Genome-Wide Association Study22017119510.050 Why?
Comparative Genomic Hybridization220145140.050 Why?
Aortic Aneurysm120066680.050 Why?
Aneuploidy120044800.050 Why?
Cross-Sectional Studies32023234090.050 Why?
Heart Diseases1201327620.050 Why?
Comorbidity12014104510.050 Why?
Time Factors22020410950.050 Why?
Chromosomes, Human, Pair 3120203220.050 Why?
Massachusetts1201287490.050 Why?
Growth Disorders120046480.050 Why?
Homeodomain Proteins1200924590.050 Why?
Desmoplakins12019660.050 Why?
KCNQ1 Potassium Channel12019990.040 Why?
Telomere120048290.040 Why?
Face120049840.040 Why?
Age of Onset2202033330.040 Why?
Light1200314440.040 Why?
Practice Guidelines as Topic1201474860.040 Why?
Cells, Cultured32019200950.040 Why?
Longitudinal Studies12012136120.040 Why?
Registries1201280950.040 Why?
Chromosomes, Human, Pair 5120174120.040 Why?
Mitochondria1200936410.040 Why?
Electrocardiography2202064090.040 Why?
DNA-Binding Proteins2201598040.040 Why?
Signal Transduction32022239960.040 Why?
Prevalence12012148960.040 Why?
Pedigree2201747230.030 Why?
Case-Control Studies32021218050.030 Why?
Follow-Up Studies12017393020.030 Why?
Ethics, Medical120008000.030 Why?
Chromosomes, Human, Pair 22120163480.030 Why?
Proteins1201061660.030 Why?
Leukemia, Myelomonocytic, Juvenile12014240.030 Why?
Oncogene Protein v-akt120141410.030 Why?
Reactive Oxygen Species2201421470.030 Why?
Odds Ratio2202099740.030 Why?
Transcription Factors12014120730.030 Why?
Genes, Developmental12013380.030 Why?
Alleles2201571010.030 Why?
Base Sequence22018133170.030 Why?
Neurofibromin 1120142040.030 Why?
Homozygote1201718450.030 Why?
MAP Kinase Kinase Kinases120142720.030 Why?
Linkage Disequilibrium1201720650.030 Why?
Acyltransferases120143060.030 Why?
Mutagenesis, Insertional120156640.030 Why?
Educational Status2201023400.030 Why?
Action Potentials1201917910.030 Why?
Smith-Magenis Syndrome12011190.030 Why?
Extracellular Signal-Regulated MAP Kinases120146490.030 Why?
Chromosome Duplication12011630.030 Why?
Polymorphism, Single Nucleotide32017156000.030 Why?
RNA Splicing120158830.030 Why?
Dyslexia, Acquired12010160.030 Why?
Articulation Disorders12010110.030 Why?
Magnetics120146470.030 Why?
DNA1200571660.030 Why?
Promoter Regions, Genetic2201360510.030 Why?
Congenital Abnormalities120156980.020 Why?
Genetic Diseases, Inborn120155960.020 Why?
Amino Acid Substitution1201518360.020 Why?
Heart Failure12014101850.020 Why?
Genetic Markers1201726920.020 Why?
Methylation1201311230.020 Why?
Pregnancy32022273060.020 Why?
Seizures1202225920.020 Why?
Language Disorders120101300.020 Why?
HEK293 Cells1201943290.020 Why?
Molecular Sequence Annotation120125500.020 Why?
Sarcomeres120123530.020 Why?
Electron Transport Complex IV120092060.020 Why?
Chromosomes, Human120114780.020 Why?
Cytochromes c120091860.020 Why?
Kaplan-Meier Estimate1202067780.020 Why?
Aorta, Thoracic1201510390.020 Why?
Mitochondrial Membranes120091670.020 Why?
GTPase-Activating Proteins120124960.020 Why?
Motor Skills Disorders12008880.020 Why?
Lysine1201310420.020 Why?
Oligonucleotide Array Sequence Analysis1201739930.020 Why?
Amino Acid Sequence22012142430.020 Why?
Myocardial Contraction1201416490.020 Why?
Epigenomics120148130.020 Why?
Cell Separation1201418290.020 Why?
Age Factors22019187980.020 Why?
Gene Silencing1201516160.020 Why?
Magnetic Resonance Imaging32021345020.020 Why?
Medical History Taking120128010.020 Why?
Genetic Loci1201726140.020 Why?
COS Cells1200912110.020 Why?
Gene Frequency1201437140.020 Why?
Oxidative Phosphorylation120094880.020 Why?
Molecular Sequence Data22012187380.020 Why?
Protein Conformation1201540720.020 Why?
Motor Skills120105250.020 Why?
Chromosomes, Human, Pair 6120083910.020 Why?
Hearing120104310.020 Why?
Collagen Type III12006910.020 Why?
Enhancer Elements, Genetic1201313770.020 Why?
Child Development Disorders, Pervasive120116010.020 Why?
Statistics, Nonparametric1201229350.020 Why?
Reading120105490.020 Why?
Membrane Potentials1200911840.020 Why?
Chromosome Mapping1201448250.020 Why?
Mice, Mutant Strains1200919520.020 Why?
Sequence Analysis, DNA1201749160.020 Why?
Ehlers-Danlos Syndrome12006850.020 Why?
Health Knowledge, Attitudes, Practice1200039560.020 Why?
Proportional Hazards Models12020124170.020 Why?
Mice, Knockout22012152580.020 Why?
Databases, Genetic1201218000.020 Why?
Caenorhabditis elegans1201414230.020 Why?
Sequence Homology, Amino Acid1200929310.020 Why?
Risk1201797730.020 Why?
Cerebral Cortex1202157280.020 Why?
Animals620151708900.020 Why?
Repressor Proteins1201530890.020 Why?
Ventricular Outflow Obstruction120062720.020 Why?
Gene Expression1201780130.020 Why?
Cell Line12018166930.020 Why?
Mice42015811260.020 Why?
Hemodynamics1201442310.010 Why?
Infant, Premature1201220150.010 Why?
Genetic Linkage1200825160.010 Why?
Protein Structure, Tertiary1200939910.010 Why?
Reference Values1200950580.010 Why?
Dose-Response Relationship, Radiation120039210.010 Why?
Hearing Loss120087140.010 Why?
Arteries1200611080.010 Why?
Kinetics1200968050.010 Why?
Transcription, Genetic1201579520.010 Why?
Transfection1200961420.010 Why?
Aneurysm, Dissecting120066440.010 Why?
RNA, Messenger12015133010.010 Why?
Echocardiography, Transesophageal1200611110.010 Why?
Adaptation, Psychological1201025450.010 Why?
Dyspnea1200612560.010 Why?
Leukemia, Myeloid, Acute1201433330.010 Why?
Fibroblasts1200942860.010 Why?
Myocardium1201249430.010 Why?
Carrier Proteins1201251350.010 Why?
Phosphorylation1200987430.010 Why?
Photic Stimulation1200320230.010 Why?
Disease Progression12014133070.010 Why?
B-Lymphocytes1200949260.010 Why?
Gene Expression Profiling1201295320.010 Why?
Cognition1201061090.010 Why?
Survival Analysis12006105420.010 Why?
Pregnancy Complications1200628300.010 Why?
Incidence12010206530.010 Why?
Middle Aged320122150410.010 Why?
United States22014677980.010 Why?
Students, Medical1200017730.010 Why?
Physicians1200043540.000 Why?
Internship and Residency1200056340.000 Why?
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© 2023 President and Fellows of Harvard College
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.