Harvard Catalyst Profiles

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Amy Elizabeth Roberts, M.D.

Concepts (337)

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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 Syndrome2220231223.960 Why?
Heart Defects, Congenital23202345841.210 Why?
Trisomy320172661.000 Why?
Abnormalities, Multiple10202014160.900 Why?
Cardiomyopathy, Dilated520208510.690 Why?
Genetic Testing13202334440.650 Why?
Smith-Lemli-Opitz Syndrome12017460.600 Why?
Chromosomes, Human, Pair 13120171970.590 Why?
Protein Tyrosine Phosphatase, Non-Receptor Type 111020182340.580 Why?
DNA Mutational Analysis11202041860.570 Why?
Barth Syndrome22014250.550 Why?
Cardiomyopathy, Hypertrophic6202312650.530 Why?
Executive Function4202313640.530 Why?
SOS1 Protein52013410.520 Why?
Ectodermal Dysplasia420231060.470 Why?
Growth Charts12012610.420 Why?
LEOPARD Syndrome22023140.400 Why?
Failure to Thrive320231360.390 Why?
DiGeorge Syndrome320171770.370 Why?
Siblings120148540.360 Why?
Intelligence220149200.360 Why?
Facies420231970.330 Why?
Mutation182020297860.320 Why?
Protein Tyrosine Phosphatases420074730.310 Why?
DNA Copy Number Variations5202319410.290 Why?
Induced Pluripotent Stem Cells4201917360.280 Why?
Genetic Predisposition to Disease82020174460.280 Why?
ras Proteins5202210600.260 Why?
Phenotype152020163650.260 Why?
Mutation, Missense5202425640.250 Why?
Genetic Association Studies7201527030.240 Why?
Tetralogy of Fallot220216230.240 Why?
Aortic Stenosis, Supravalvular12024300.240 Why?
Memory2201321740.240 Why?
Learning1201317130.230 Why?
Chondroitinsulfatases12023160.230 Why?
Chromosomes, Human, Pair 2120043260.230 Why?
Child322024777090.230 Why?
Germ-Line Mutation3201017880.230 Why?
Musculoskeletal Abnormalities12024950.220 Why?
Infant172023351360.220 Why?
Nucleic Acid Hybridization1200413750.220 Why?
In Situ Hybridization, Fluorescence3201126490.210 Why?
Costello Syndrome12022190.210 Why?
Child, Preschool192023410060.210 Why?
Williams Syndrome120241870.200 Why?
Acidosis, Lactic120231420.200 Why?
Rare Diseases220245530.200 Why?
Chromosome Deletion2201614010.200 Why?
Adolescent262023857810.190 Why?
Chromosome Aberrations3201418130.190 Why?
Intracellular Signaling Peptides and Proteins6201229150.180 Why?
MAP Kinase Kinase 1220193370.180 Why?
Cardiomyopathies2202319120.180 Why?
MAP Kinase Kinase 212019960.170 Why?
Mitogen-Activated Protein Kinase 712019660.170 Why?
Attention Deficit Disorder with Hyperactivity1201436580.170 Why?
Humans7520247443430.170 Why?
Spasms, Infantile120223050.170 Why?
Muscular Diseases120235560.160 Why?
Cerebrum120201370.160 Why?
Proto-Oncogene Proteins c-raf120192030.160 Why?
Developmental Disabilities4202414560.160 Why?
Growth Differentiation Factor 11201760.160 Why?
Epilepsy2202333100.150 Why?
Heart5202344670.150 Why?
Cardiac Myosins120171170.150 Why?
Vascular Endothelial Growth Factor Receptor-3120171180.150 Why?
Chromosomes, Human, Pair 18120172450.150 Why?
Cataract120238340.150 Why?
Genes, ras220106900.150 Why?
Male4120233501180.140 Why?
Chromosome Disorders220175140.140 Why?
Tissue Engineering2201918800.140 Why?
Genotype92022129510.140 Why?
Proto-Oncogene Proteins B-raf3202220430.140 Why?
Chylothorax12017840.140 Why?
Heterozygote2202028040.140 Why?
Son of Sevenless Proteins12015270.140 Why?
Myosin Heavy Chains120174140.130 Why?
Craniofacial Abnormalities220103150.130 Why?
Echocardiography4202051020.130 Why?
Glucose Transporter Type 312015160.130 Why?
Myocytes, Cardiac3201916370.130 Why?
Female3820233801940.130 Why?
Nuclear Matrix-Associated Proteins12015450.130 Why?
MAP Kinase Signaling System3201415260.130 Why?
Fatal Outcome2201718500.120 Why?
Muscle Proteins1202011590.120 Why?
Nervous System Malformations120152470.120 Why?
Infant, Newborn62023256250.120 Why?
Syndrome5202232510.110 Why?
Ductus Arteriosus, Patent120152090.110 Why?
Protein Interaction Domains and Motifs120154740.110 Why?
Protein Kinases1202016400.110 Why?
Therapies, Investigational120141120.110 Why?
Aortic Coarctation120152810.110 Why?
Fetal Distress12012400.110 Why?
Nuchal Translucency Measurement12012560.100 Why?
Angiography1201716390.100 Why?
Heart Ventricles3201538210.100 Why?
Hand Deformities, Congenital120121460.100 Why?
Cell Culture Techniques1201816780.100 Why?
Tachycardia, Ventricular1201912730.090 Why?
Mitochondrial Diseases120143200.090 Why?
Heart Transplantation2202031100.090 Why?
Receptors, G-Protein-Coupled1201712220.090 Why?
Prognosis42021290630.090 Why?
Fontan Procedure120157780.090 Why?
Arrhythmias, Cardiac1201922680.090 Why?
Aniridia12009370.090 Why?
Gene Regulatory Networks1201817080.080 Why?
Neurogenesis120158380.080 Why?
RNA-Binding Proteins2201519030.080 Why?
Chromosomes, Human, Pair 15220203730.080 Why?
Disease Management3201424590.080 Why?
High-Throughput Nucleotide Sequencing3201735970.080 Why?
Young Adult92021564300.080 Why?
Microarray Analysis120117670.080 Why?
Branchio-Oto-Renal Syndrome12008240.080 Why?
Cognition Disorders2201540430.080 Why?
Adult1820232140550.080 Why?
Transcription Factor AP-212008820.080 Why?
Autistic Disorder1201711850.080 Why?
Neck120126970.080 Why?
Cohort Studies62022405610.080 Why?
Karyotyping2201112430.070 Why?
Heart Valve Diseases1201510730.070 Why?
Quantitative Trait Loci1201420190.070 Why?
Severe Combined Immunodeficiency120092230.070 Why?
Environment1201211240.070 Why?
Infant, Premature, Diseases120127060.070 Why?
Activin Receptors, Type I120061420.070 Why?
Leukemia, Myelomonocytic, Chronic12007970.070 Why?
Nuclear Proteins2201258530.070 Why?
Retrospective Studies62023774490.070 Why?
Genetic Variation2201965440.070 Why?
Genome-Wide Association Study32024122610.070 Why?
Hypoplastic Left Heart Syndrome120115740.070 Why?
Cardiomegaly120086200.060 Why?
Receptors, Transforming Growth Factor beta120063140.060 Why?
Prenatal Diagnosis1201212360.060 Why?
Risk Factors42022722900.060 Why?
Cardiovascular Diseases32019151650.060 Why?
Aortic Valve1201519220.060 Why?
Translocation, Genetic2201514200.060 Why?
Models, Molecular3201554560.060 Why?
Cardiovascular System120128320.060 Why?
Models, Biological2201495830.060 Why?
Retinaldehyde12003250.060 Why?
Neuropsychological Tests4202169930.060 Why?
Predictive Value of Tests12020150760.060 Why?
Attention1201424000.060 Why?
Amino Acid Transport System y+L12023170.060 Why?
Reproducibility of Results22020199050.060 Why?
Sequence Deletion1200815260.060 Why?
Brain42021263850.060 Why?
Rod Opsins120031110.060 Why?
Rhodopsin120032030.060 Why?
Dark Adaptation120032190.050 Why?
Histones1201325990.050 Why?
Diagnosis, Differential32014129590.050 Why?
Chromosomes, Human, Pair 9120045350.050 Why?
Spasm120221210.050 Why?
Chromatin3202329340.050 Why?
Cardiac Surgical Procedures1201735370.050 Why?
Mitogen-Activated Protein Kinases2202212850.050 Why?
Antiporters120232770.050 Why?
Aortic Aneurysm120066430.050 Why?
Comparative Genomic Hybridization220144960.050 Why?
Monosaccharide Transport Proteins120234400.050 Why?
Aneuploidy120045300.050 Why?
Phosphotransferases (Alcohol Group Acceptor)120234370.050 Why?
Language1201014710.050 Why?
Cross-Sectional Studies32023250430.050 Why?
Seizures2202328590.050 Why?
Comorbidity12014103880.050 Why?
Transcription Factors22024122080.040 Why?
Time Factors22020400750.040 Why?
Heart Diseases1201327880.040 Why?
Massachusetts1201286630.040 Why?
Homeodomain Proteins1200924210.040 Why?
Growth Disorders120046450.040 Why?
Chromosomes, Human, Pair 3120203230.040 Why?
Desmoplakins12019620.040 Why?
KCNQ1 Potassium Channel120191040.040 Why?
Neonatal Screening120235910.040 Why?
Age of Onset2202032710.040 Why?
Face120049940.040 Why?
Mammals1202411430.040 Why?
Telomere120049100.040 Why?
Light1200313740.040 Why?
Cells, Cultured32019192290.040 Why?
Practice Guidelines as Topic1201472790.040 Why?
Registries1201280890.040 Why?
Mitochondria1200935200.030 Why?
Longitudinal Studies12012139890.030 Why?
Drosophila1202414910.030 Why?
Signal Transduction32022234030.030 Why?
DNA-Binding Proteins2201596480.030 Why?
Chromosomes, Human, Pair 5120174030.030 Why?
Electrocardiography2202064420.030 Why?
Case-Control Studies32021217460.030 Why?
Prevalence12012152260.030 Why?
Pedigree2201746440.030 Why?
Follow-Up Studies12017390500.030 Why?
Ventricular Remodeling1202312240.030 Why?
Ethics, Medical120007920.030 Why?
Proteins1201061030.030 Why?
Chromosomes, Human, Pair 22120163510.030 Why?
Odds Ratio2202098490.030 Why?
Reactive Oxygen Species2201420770.030 Why?
Leukemia, Myelomonocytic, Juvenile12014200.030 Why?
Oncogene Protein v-akt120141350.030 Why?
Anticonvulsants1202319160.030 Why?
Alleles2201569330.030 Why?
Base Sequence22018127970.030 Why?
Genes, Developmental12013400.030 Why?
Neurofibromin 1120141960.030 Why?
Homozygote1201717850.030 Why?
MAP Kinase Kinase Kinases120142610.030 Why?
Linkage Disequilibrium1201719970.030 Why?
Acyltransferases120142940.030 Why?
Mutagenesis, Insertional120156550.030 Why?
Action Potentials1201918060.030 Why?
Educational Status2201025400.020 Why?
Polymorphism, Single Nucleotide32017155190.020 Why?
Smith-Magenis Syndrome12011190.020 Why?
Extracellular Signal-Regulated MAP Kinases120146250.020 Why?
Promoter Regions, Genetic2201358670.020 Why?
Magnetics120146060.020 Why?
RNA Splicing120159070.020 Why?
Chromosome Duplication12011740.020 Why?
Dyslexia, Acquired12010140.020 Why?
Genetic Diseases, Inborn120155870.020 Why?
Articulation Disorders12010140.020 Why?
DNA1200573010.020 Why?
Congenital Abnormalities120157070.020 Why?
Proteomics1202436380.020 Why?
Amino Acid Substitution1201517910.020 Why?
Genetic Markers1201726340.020 Why?
Methylation1201311060.020 Why?
HEK293 Cells1201942040.020 Why?
Heart Failure12014109000.020 Why?
Animals720241687570.020 Why?
Molecular Sequence Annotation120125280.020 Why?
Kaplan-Meier Estimate1202065380.020 Why?
Electron Transport Complex IV120091890.020 Why?
Chromosomes, Human120114570.020 Why?
Parents1202334070.020 Why?
Language Disorders120101410.020 Why?
Pregnancy32022291440.020 Why?
Sarcomeres120123740.020 Why?
Cytochromes c120091800.020 Why?
Amino Acid Sequence22012138150.020 Why?
Aorta, Thoracic1201510820.020 Why?
GTPase-Activating Proteins120124980.020 Why?
Oligonucleotide Array Sequence Analysis1201739200.020 Why?
Myocardial Contraction1201415850.020 Why?
Motor Skills Disorders12008900.020 Why?
Mitochondrial Membranes120091750.020 Why?
Lysine1201310070.020 Why?
Age Factors22019183700.020 Why?
Epigenomics120149030.020 Why?
Cell Separation1201417510.020 Why?
Gene Silencing1201515380.020 Why?
Medical History Taking120127830.020 Why?
Genetic Loci1201725750.020 Why?
Magnetic Resonance Imaging32021354210.020 Why?
Molecular Sequence Data22012181110.020 Why?
Gene Frequency1201435880.020 Why?
COS Cells1200911610.020 Why?
Oxidative Phosphorylation120094810.020 Why?
Protein Conformation1201540110.020 Why?
Motor Skills120105220.020 Why?
Chromosomes, Human, Pair 6120083800.020 Why?
Genomics1202357200.020 Why?
Statistics, Nonparametric1201228860.020 Why?
Enhancer Elements, Genetic1201313410.020 Why?
Collagen Type III12006900.020 Why?
Hearing120104820.020 Why?
Child Development Disorders, Pervasive120116150.020 Why?
Chromosome Mapping1201447400.020 Why?
Reading120105580.020 Why?
Membrane Potentials1200911370.020 Why?
Mice, Mutant Strains1200918660.020 Why?
Sequence Analysis, DNA1201748030.020 Why?
Health Knowledge, Attitudes, Practice1200039230.020 Why?
Mice, Knockout22012145570.020 Why?
Proportional Hazards Models12020123540.020 Why?
Ehlers-Danlos Syndrome12006890.020 Why?
Databases, Genetic1201217830.020 Why?
Sequence Homology, Amino Acid1200928390.020 Why?
Risk1201796870.020 Why?
Cerebral Cortex1202157080.020 Why?
Caenorhabditis elegans1201414190.020 Why?
Repressor Proteins1201530230.020 Why?
Gene Expression1201777990.020 Why?
Cell Line12018159970.020 Why?
Ventricular Outflow Obstruction120062720.010 Why?
Mice42015811830.010 Why?
Hemodynamics1201441990.010 Why?
Infant, Premature1201220440.010 Why?
Genetic Linkage1200824210.010 Why?
Protein Structure, Tertiary1200938460.010 Why?
Reference Values1200949820.010 Why?
Dose-Response Relationship, Radiation120038760.010 Why?
Kinetics1200964730.010 Why?
Transcription, Genetic1201577220.010 Why?
Transfection1200958920.010 Why?
Arteries1200611190.010 Why?
Hearing Loss120087650.010 Why?
RNA, Messenger12015130330.010 Why?
Middle Aged420232133830.010 Why?
Echocardiography, Transesophageal1200611330.010 Why?
Adaptation, Psychological1201025760.010 Why?
Prospective Studies12023532880.010 Why?
Myocardium1201247760.010 Why?
Fibroblasts1200941610.010 Why?
Dyspnea1200613030.010 Why?
Carrier Proteins1201250210.010 Why?
Phosphorylation1200984360.010 Why?
Leukemia, Myeloid, Acute1201435230.010 Why?
Aged, 80 and over12023577760.010 Why?
Photic Stimulation1200320250.010 Why?
Disease Progression12014132840.010 Why?
B-Lymphocytes1200946650.010 Why?
Gene Expression Profiling1201294380.010 Why?
Survival Analysis12006102520.010 Why?
Cognition1201067700.010 Why?
Pregnancy Complications1200628610.010 Why?
Incidence12010209470.010 Why?
United States22014698720.010 Why?
Aged120231632800.010 Why?
Students, Medical1200018620.000 Why?
Physicians1200045670.000 Why?
Internship and Residency1200057880.000 Why?
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© 2024 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.