Harvard Catalyst Profiles

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Amy Elizabeth Roberts, M.D.

Concepts (338)

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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 Syndrome2220231203.810 Why?
Heart Defects, Congenital25202446731.310 Why?
Trisomy320172600.970 Why?
Abnormalities, Multiple10202014150.870 Why?
Cardiomyopathy, Dilated520208190.680 Why?
Genetic Testing13202335310.620 Why?
Smith-Lemli-Opitz Syndrome12017460.580 Why?
Chromosomes, Human, Pair 13120171940.570 Why?
DNA Mutational Analysis11202041080.560 Why?
Protein Tyrosine Phosphatase, Non-Receptor Type 111020182240.560 Why?
Executive Function5202413740.550 Why?
Barth Syndrome22014250.530 Why?
SOS1 Protein52013400.500 Why?
Cardiomyopathy, Hypertrophic6202313110.500 Why?
Ectodermal Dysplasia420231060.450 Why?
Growth Charts12012600.400 Why?
LEOPARD Syndrome22023120.390 Why?
Failure to Thrive320231400.370 Why?
Siblings120148240.360 Why?
DiGeorge Syndrome320171850.350 Why?
Intelligence220149190.350 Why?
Facies420232230.320 Why?
Mutation182020299570.310 Why?
Protein Tyrosine Phosphatases420074580.300 Why?
DNA Copy Number Variations5202320130.280 Why?
Genetic Predisposition to Disease82020177900.270 Why?
Induced Pluripotent Stem Cells4201918460.270 Why?
ras Proteins5202210510.250 Why?
Phenotype152020165480.240 Why?
Mutation, Missense5202425670.240 Why?
Genetic Association Studies7201527160.230 Why?
Child342024797990.230 Why?
Memory2201321790.230 Why?
Aortic Stenosis, Supravalvular12024280.230 Why?
Tetralogy of Fallot220216310.230 Why?
Learning1201317390.230 Why?
Chromosomes, Human, Pair 2120043130.220 Why?
Chondroitinsulfatases12023160.220 Why?
Musculoskeletal Abnormalities120241000.210 Why?
Germ-Line Mutation3201018420.210 Why?
Nucleic Acid Hybridization1200413040.210 Why?
Infant172023360530.210 Why?
Child, Preschool202024420560.210 Why?
In Situ Hybridization, Fluorescence3201125050.210 Why?
Costello Syndrome12022190.200 Why?
Adolescent282024878090.200 Why?
Acidosis, Lactic120231450.200 Why?
Williams Syndrome120241930.190 Why?
Chromosome Deletion2201613870.190 Why?
Rare Diseases220246190.190 Why?
Chromosome Aberrations3201417670.180 Why?
Intracellular Signaling Peptides and Proteins6201228730.180 Why?
MAP Kinase Kinase 1220193320.170 Why?
Cardiomyopathies2202319510.170 Why?
Humans7720247606130.170 Why?
MAP Kinase Kinase 212019920.160 Why?
Attention Deficit Disorder with Hyperactivity1201437010.160 Why?
Mitogen-Activated Protein Kinase 712019660.160 Why?
Spasms, Infantile120222960.160 Why?
Muscular Diseases120235510.160 Why?
Cerebrum120201320.160 Why?
Proto-Oncogene Proteins c-raf120192030.160 Why?
Growth Differentiation Factor 11201760.150 Why?
Developmental Disabilities4202415040.150 Why?
Epilepsy2202332670.150 Why?
Heart5202343930.150 Why?
Male4320243597180.140 Why?
Vascular Endothelial Growth Factor Receptor-3120171190.140 Why?
Chromosomes, Human, Pair 18120172460.140 Why?
Cardiac Myosins120171270.140 Why?
Genes, ras220106540.140 Why?
Cataract120238270.140 Why?
Chromosome Disorders220174990.140 Why?
Tissue Engineering2201918700.140 Why?
Proto-Oncogene Proteins B-raf3202220530.140 Why?
Genotype92022129570.140 Why?
Chylothorax12017830.130 Why?
Female4020243912460.130 Why?
Heterozygote2202027980.130 Why?
Myosin Heavy Chains120174020.130 Why?
Son of Sevenless Proteins12015270.130 Why?
Craniofacial Abnormalities220103150.130 Why?
Echocardiography4202049810.130 Why?
Glucose Transporter Type 312015160.130 Why?
Myocytes, Cardiac3201916570.130 Why?
MAP Kinase Signaling System3201414830.120 Why?
Nuclear Matrix-Associated Proteins12015380.120 Why?
Fatal Outcome2201718320.120 Why?
Muscle Proteins1202011520.120 Why?
Nervous System Malformations120152440.110 Why?
Infant, Newborn62023261790.110 Why?
Syndrome5202232800.110 Why?
Protein Interaction Domains and Motifs120154530.110 Why?
Ductus Arteriosus, Patent120152180.110 Why?
Protein Kinases1202016120.110 Why?
Therapies, Investigational120141120.110 Why?
Aortic Coarctation120152820.100 Why?
Fetal Distress12012390.100 Why?
Nuchal Translucency Measurement12012590.100 Why?
Angiography1201716050.100 Why?
Heart Ventricles3201538120.100 Why?
Young Adult112024587480.100 Why?
Hand Deformities, Congenital120121740.090 Why?
Cell Culture Techniques1201816640.090 Why?
Brain52024269510.090 Why?
Tachycardia, Ventricular1201913030.090 Why?
Mitochondrial Diseases120143400.090 Why?
Receptors, G-Protein-Coupled1201712450.090 Why?
Prognosis42021296610.090 Why?
Heart Transplantation2202032240.080 Why?
Fontan Procedure120157910.080 Why?
Arrhythmias, Cardiac1201922550.080 Why?
Aniridia12009360.080 Why?
RNA-Binding Proteins2201518940.080 Why?
Neurogenesis120158550.080 Why?
Gene Regulatory Networks1201817410.080 Why?
Disease Management3201425140.080 Why?
High-Throughput Nucleotide Sequencing3201736170.080 Why?
Adult1920242200070.080 Why?
Chromosomes, Human, Pair 15220203630.080 Why?
Microarray Analysis120117470.080 Why?
Cognition Disorders2201539760.080 Why?
Branchio-Oto-Renal Syndrome12008250.080 Why?
Transcription Factor AP-212008790.080 Why?
Autistic Disorder1201712140.070 Why?
Cohort Studies62022413370.070 Why?
Karyotyping2201111720.070 Why?
Neck120127310.070 Why?
Heart Valve Diseases1201510470.070 Why?
Severe Combined Immunodeficiency120092260.070 Why?
Quantitative Trait Loci1201421010.070 Why?
Environment1201211180.070 Why?
Infant, Premature, Diseases120127080.070 Why?
Leukemia, Myelomonocytic, Chronic12007930.070 Why?
Activin Receptors, Type I120061360.070 Why?
Nuclear Proteins2201257950.060 Why?
Genetic Variation2201965520.060 Why?
Hypoplastic Left Heart Syndrome120115940.060 Why?
Retrospective Studies62023803450.060 Why?
Genome-Wide Association Study32024126280.060 Why?
Cardiomegaly120085930.060 Why?
Magnetic Resonance Imaging52024362860.060 Why?
Receptors, Transforming Growth Factor beta120063010.060 Why?
Prenatal Diagnosis1201212640.060 Why?
Risk Factors42022743330.060 Why?
Translocation, Genetic2201513880.060 Why?
Models, Molecular3201554340.060 Why?
Aortic Valve1201519960.060 Why?
Cardiovascular Diseases32019157600.060 Why?
Cardiovascular System120128500.060 Why?
Models, Biological2201494680.060 Why?
Retinaldehyde12003240.060 Why?
Neuropsychological Tests4202170220.060 Why?
Attention1201423870.060 Why?
Predictive Value of Tests12020152860.060 Why?
Amino Acid Transport System y+L12023170.060 Why?
Sequence Deletion1200814930.060 Why?
Reproducibility of Results22020200800.060 Why?
Rod Opsins120031080.050 Why?
Rhodopsin120032030.050 Why?
Dark Adaptation120032210.050 Why?
Histones1201325820.050 Why?
Chromosomes, Human, Pair 9120045340.050 Why?
Diagnosis, Differential32014129680.050 Why?
Chromatin3202329380.050 Why?
Spasm120221310.050 Why?
Cardiac Surgical Procedures1201736200.050 Why?
Mitogen-Activated Protein Kinases2202212460.050 Why?
Antiporters120232780.050 Why?
Comparative Genomic Hybridization220144730.050 Why?
Aortic Aneurysm120066460.050 Why?
Monosaccharide Transport Proteins120234400.050 Why?
Phosphotransferases (Alcohol Group Acceptor)120234360.050 Why?
Aneuploidy120045510.050 Why?
Language1201015330.050 Why?
Transcription Factors22024121020.040 Why?
Time Factors22020401390.040 Why?
Cross-Sectional Studies32023259410.040 Why?
Heart Diseases1201328090.040 Why?
Seizures2202329170.040 Why?
Comorbidity12014105530.040 Why?
Massachusetts1201288030.040 Why?
Homeodomain Proteins1200924140.040 Why?
Growth Disorders120046530.040 Why?
Chromosomes, Human, Pair 3120203150.040 Why?
Desmoplakins12019620.040 Why?
KCNQ1 Potassium Channel120191030.040 Why?
Neonatal Screening120235950.040 Why?
Face1200410170.040 Why?
Mammals1202411310.040 Why?
Age of Onset2202033020.040 Why?
Telomere120049340.040 Why?
Light1200313440.040 Why?
Cells, Cultured32019189550.040 Why?
Practice Guidelines as Topic1201474750.040 Why?
Cerebral Cortex2202457610.030 Why?
Drosophila1202414920.030 Why?
Mitochondria1200936010.030 Why?
Registries1201284580.030 Why?
DNA-Binding Proteins2201595910.030 Why?
Signal Transduction32022233740.030 Why?
Longitudinal Studies12012144940.030 Why?
Chromosomes, Human, Pair 5120173850.030 Why?
Electrocardiography2202064150.030 Why?
Pedigree2201745780.030 Why?
Case-Control Studies32021220520.030 Why?
Follow-Up Studies12017392620.030 Why?
Prevalence12012156860.030 Why?
Ventricular Remodeling1202312610.030 Why?
Ethics, Medical120007830.030 Why?
Proteins1201060290.030 Why?
Chromosomes, Human, Pair 22120163460.030 Why?
Odds Ratio2202097160.030 Why?
Leukemia, Myelomonocytic, Juvenile12014250.030 Why?
Oncogene Protein v-akt120141290.030 Why?
Reactive Oxygen Species2201421380.030 Why?
Base Sequence22018124440.030 Why?
Anticonvulsants1202318790.030 Why?
Alleles2201569000.030 Why?
Genes, Developmental12013380.030 Why?
Neurofibromin 1120141900.030 Why?
Homozygote1201717880.030 Why?
MAP Kinase Kinase Kinases120142560.030 Why?
Diffusion Magnetic Resonance Imaging1202427820.030 Why?
Linkage Disequilibrium1201719960.030 Why?
Acyltransferases120143050.030 Why?
Mutagenesis, Insertional120156520.020 Why?
Action Potentials1201918160.020 Why?
Educational Status2201025140.020 Why?
Extracellular Signal-Regulated MAP Kinases120146160.020 Why?
Polymorphism, Single Nucleotide32017157900.020 Why?
Smith-Magenis Syndrome12011190.020 Why?
Promoter Regions, Genetic2201357820.020 Why?
Magnetics120146000.020 Why?
DNA1200572330.020 Why?
Genetic Diseases, Inborn120156010.020 Why?
RNA Splicing120159150.020 Why?
Chromosome Duplication12011750.020 Why?
Dyslexia, Acquired12010140.020 Why?
Amino Acid Substitution1201517370.020 Why?
Articulation Disorders12010110.020 Why?
Congenital Abnormalities120157040.020 Why?
Genetic Markers1201726090.020 Why?
Methylation1201310810.020 Why?
Proteomics1202438170.020 Why?
HEK293 Cells1201942630.020 Why?
Animals720241679600.020 Why?
Molecular Sequence Annotation120125240.020 Why?
Kaplan-Meier Estimate1202065440.020 Why?
Chromosomes, Human120114420.020 Why?
Language Disorders120101390.020 Why?
Electron Transport Complex IV120091900.020 Why?
Heart Failure12014118480.020 Why?
Pregnancy32022297460.020 Why?
Sarcomeres120123670.020 Why?
Amino Acid Sequence22012134510.020 Why?
Parents1202335490.020 Why?
Cytochromes c120091730.020 Why?
Oligonucleotide Array Sequence Analysis1201737740.020 Why?
GTPase-Activating Proteins120124750.020 Why?
Myocardial Contraction1201415160.020 Why?
Aorta, Thoracic1201510950.020 Why?
Lysine1201310010.020 Why?
Age Factors22019184130.020 Why?
Cell Separation1201417200.020 Why?
Mitochondrial Membranes120091720.020 Why?
Motor Skills Disorders12008890.020 Why?
Gene Silencing1201515120.020 Why?
Molecular Sequence Data22012176240.020 Why?
Medical History Taking120127730.020 Why?
Genetic Loci1201726180.020 Why?
Epigenomics120149360.020 Why?
COS Cells1200911290.020 Why?
Gene Frequency1201436130.020 Why?
Protein Conformation1201539700.020 Why?
Oxidative Phosphorylation120094950.020 Why?
Motor Skills120105200.020 Why?
Genomics1202357950.020 Why?
Chromosomes, Human, Pair 6120083750.020 Why?
Statistics, Nonparametric1201228520.020 Why?
Child Development Disorders, Pervasive120115990.020 Why?
Reading120105300.020 Why?
Sequence Analysis, DNA1201747160.020 Why?
Enhancer Elements, Genetic1201313560.020 Why?
Collagen Type III12006910.020 Why?
Chromosome Mapping1201446260.020 Why?
Mice, Mutant Strains1200917540.020 Why?
Membrane Potentials1200910950.020 Why?
Hearing120105010.020 Why?
Health Knowledge, Attitudes, Practice1200039850.020 Why?
Proportional Hazards Models12020125310.020 Why?
Mice, Knockout22012143740.020 Why?
Databases, Genetic1201217380.020 Why?
Ehlers-Danlos Syndrome12006920.020 Why?
Sequence Homology, Amino Acid1200927530.020 Why?
Risk1201796320.020 Why?
Caenorhabditis elegans1201414440.020 Why?
Gene Expression1201775870.010 Why?
Repressor Proteins1201529820.010 Why?
Cell Line12018156200.010 Why?
Ventricular Outflow Obstruction120062650.010 Why?
Mice42015812090.010 Why?
Hemodynamics1201441730.010 Why?
Protein Structure, Tertiary1200938000.010 Why?
Genetic Linkage1200823810.010 Why?
Infant, Premature1201220920.010 Why?
Reference Values1200949250.010 Why?
Dose-Response Relationship, Radiation120038810.010 Why?
Kinetics1200963770.010 Why?
Transcription, Genetic1201575930.010 Why?
Transfection1200957810.010 Why?
Arteries1200611260.010 Why?
Hearing Loss120087800.010 Why?
RNA, Messenger12015127620.010 Why?
Echocardiography, Transesophageal1200611080.010 Why?
Middle Aged420232203590.010 Why?
Myocardium1201247000.010 Why?
Fibroblasts1200940890.010 Why?
Adaptation, Psychological1201026280.010 Why?
Prospective Studies12023543060.010 Why?
Carrier Proteins1201249380.010 Why?
Phosphorylation1200983110.010 Why?
Dyspnea1200613530.010 Why?
Leukemia, Myeloid, Acute1201436100.010 Why?
Aged, 80 and over12023589800.010 Why?
Photic Stimulation1200319670.010 Why?
Disease Progression12014135050.010 Why?
B-Lymphocytes1200947420.010 Why?
Gene Expression Profiling1201294060.010 Why?
Survival Analysis12006101850.010 Why?
Cognition1201069640.010 Why?
Pregnancy Complications1200629420.010 Why?
Incidence12010213910.010 Why?
United States22014724480.010 Why?
Aged120231691430.010 Why?
Students, Medical1200019270.000 Why?
Physicians1200045910.000 Why?
Internship and Residency1200058700.000 Why?
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.