Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Profiles will have a brief outage at 6pm this Friday, 5/30/2025, for system upgrade.

Amy Elizabeth Roberts, M.D.

Concepts (338)

Back to Profile
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 Syndrome2220231223.700 Why?
Heart Defects, Congenital25202446971.280 Why?
Trisomy320172590.940 Why?
Abnormalities, Multiple10202014240.850 Why?
Cardiomyopathy, Dilated520208450.660 Why?
Genetic Testing13202335950.600 Why?
Smith-Lemli-Opitz Syndrome12017460.560 Why?
Chromosomes, Human, Pair 13120171910.550 Why?
DNA Mutational Analysis11202041080.550 Why?
Protein Tyrosine Phosphatase, Non-Receptor Type 111020182250.540 Why?
Executive Function5202413910.530 Why?
Barth Syndrome22014250.510 Why?
SOS1 Protein52013400.490 Why?
Cardiomyopathy, Hypertrophic6202313390.490 Why?
Ectodermal Dysplasia420231060.430 Why?
Growth Charts12012600.390 Why?
LEOPARD Syndrome22023120.380 Why?
Failure to Thrive320231380.360 Why?
Siblings120148280.350 Why?
DiGeorge Syndrome320171870.350 Why?
Intelligence220149230.340 Why?
Facies420232230.310 Why?
Mutation182020301980.300 Why?
Protein Tyrosine Phosphatases420074570.290 Why?
DNA Copy Number Variations5202320450.270 Why?
Genetic Predisposition to Disease82020180710.260 Why?
Induced Pluripotent Stem Cells4201918830.260 Why?
ras Proteins5202210530.240 Why?
Phenotype152020167210.230 Why?
Mutation, Missense5202425890.230 Why?
Genetic Association Studies7201527410.230 Why?
Child342024805640.230 Why?
Memory2201321900.230 Why?
Aortic Stenosis, Supravalvular12024280.220 Why?
Tetralogy of Fallot220216290.220 Why?
Learning1201317550.220 Why?
Chromosomes, Human, Pair 2120043130.210 Why?
Chondroitinsulfatases12023160.210 Why?
Musculoskeletal Abnormalities120241010.210 Why?
Nucleic Acid Hybridization1200413060.210 Why?
Infant172023363860.210 Why?
Germ-Line Mutation3201018840.200 Why?
Child, Preschool202024425000.200 Why?
In Situ Hybridization, Fluorescence3201125050.200 Why?
Costello Syndrome12022190.200 Why?
Acidosis, Lactic120231440.190 Why?
Adolescent282024888350.190 Why?
Williams Syndrome120241960.190 Why?
Chromosome Deletion2201613850.190 Why?
Rare Diseases220246350.180 Why?
Chromosome Aberrations3201417740.180 Why?
Intracellular Signaling Peptides and Proteins6201228800.170 Why?
MAP Kinase Kinase 1220193300.170 Why?
Humans7720247659680.160 Why?
Cardiomyopathies2202320670.160 Why?
Attention Deficit Disorder with Hyperactivity1201437190.160 Why?
MAP Kinase Kinase 212019920.160 Why?
Mitogen-Activated Protein Kinase 712019660.160 Why?
Spasms, Infantile120223020.160 Why?
Muscular Diseases120235500.160 Why?
Cerebrum120201310.150 Why?
Proto-Oncogene Proteins c-raf120192060.150 Why?
Growth Differentiation Factor 11201760.150 Why?
Developmental Disabilities4202415190.150 Why?
Epilepsy2202333200.140 Why?
Heart5202344140.140 Why?
Male4320243636980.140 Why?
Vascular Endothelial Growth Factor Receptor-3120171170.140 Why?
Genes, ras220106580.140 Why?
Chromosomes, Human, Pair 18120172470.140 Why?
Cardiac Myosins120171280.140 Why?
Cataract120238370.140 Why?
Tissue Engineering2201918550.140 Why?
Chromosome Disorders220174980.140 Why?
Proto-Oncogene Proteins B-raf3202220540.130 Why?
Genotype92022130240.130 Why?
Chylothorax12017830.130 Why?
Female4020243961120.130 Why?
Heterozygote2202027940.130 Why?
Myosin Heavy Chains120174020.130 Why?
Son of Sevenless Proteins12015270.130 Why?
Craniofacial Abnormalities220103110.130 Why?
Echocardiography4202050450.120 Why?
Myocytes, Cardiac3201916680.120 Why?
Glucose Transporter Type 312015170.120 Why?
MAP Kinase Signaling System3201414900.120 Why?
Fatal Outcome2201718310.120 Why?
Nuclear Matrix-Associated Proteins12015390.120 Why?
Muscle Proteins1202011580.120 Why?
Nervous System Malformations120152430.110 Why?
Infant, Newborn62023263460.110 Why?
Syndrome5202232710.110 Why?
Protein Interaction Domains and Motifs120154460.100 Why?
Ductus Arteriosus, Patent120152140.100 Why?
Protein Kinases1202016110.100 Why?
Therapies, Investigational120141100.100 Why?
Aortic Coarctation120152770.100 Why?
Fetal Distress12012390.100 Why?
Angiography1201715810.100 Why?
Nuchal Translucency Measurement12012590.100 Why?
Heart Ventricles3201538320.090 Why?
Young Adult112024598890.090 Why?
Cell Culture Techniques1201816520.090 Why?
Hand Deformities, Congenital120121750.090 Why?
Brain52024271710.090 Why?
Tachycardia, Ventricular1201913100.090 Why?
Mitochondrial Diseases120143450.090 Why?
Receptors, G-Protein-Coupled1201712420.080 Why?
Prognosis42021299220.080 Why?
Heart Transplantation2202033100.080 Why?
Arrhythmias, Cardiac1201922470.080 Why?
RNA-Binding Proteins2201518740.080 Why?
Fontan Procedure120158050.080 Why?
Neurogenesis120158660.080 Why?
Aniridia12009360.080 Why?
Gene Regulatory Networks1201817480.080 Why?
Disease Management3201425350.080 Why?
High-Throughput Nucleotide Sequencing3201736550.080 Why?
Chromosomes, Human, Pair 15220203600.080 Why?
Adult1920242230440.080 Why?
Cognition Disorders2201539670.080 Why?
Microarray Analysis120117520.080 Why?
Branchio-Oto-Renal Syndrome12008250.070 Why?
Transcription Factor AP-212008780.070 Why?
Autistic Disorder1201712390.070 Why?
Cohort Studies62022416490.070 Why?
Neck120127330.070 Why?
Karyotyping2201111780.070 Why?
Heart Valve Diseases1201510300.070 Why?
Severe Combined Immunodeficiency120092350.070 Why?
Quantitative Trait Loci1201421400.070 Why?
Environment1201211140.070 Why?
Infant, Premature, Diseases120127130.060 Why?
Leukemia, Myelomonocytic, Chronic12007930.060 Why?
Nuclear Proteins2201257830.060 Why?
Activin Receptors, Type I120061330.060 Why?
Genetic Variation2201966100.060 Why?
Hypoplastic Left Heart Syndrome120115950.060 Why?
Retrospective Studies62023815140.060 Why?
Cardiomegaly120085890.060 Why?
Genome-Wide Association Study32024128070.060 Why?
Magnetic Resonance Imaging52024365320.060 Why?
Receptors, Transforming Growth Factor beta120063060.060 Why?
Prenatal Diagnosis1201212680.060 Why?
Models, Molecular3201553790.060 Why?
Risk Factors42022748400.060 Why?
Aortic Valve1201519680.060 Why?
Cardiovascular Diseases32019156520.060 Why?
Translocation, Genetic2201513940.060 Why?
Cardiovascular System120128410.060 Why?
Models, Biological2201494430.060 Why?
Retinaldehyde12003230.060 Why?
Neuropsychological Tests4202171230.060 Why?
Attention1201424190.060 Why?
Reproducibility of Results22020201240.050 Why?
Sequence Deletion1200814950.050 Why?
Predictive Value of Tests12020153980.050 Why?
Amino Acid Transport System y+L12023170.050 Why?
Rod Opsins120031080.050 Why?
Rhodopsin120032020.050 Why?
Diagnosis, Differential32014129760.050 Why?
Dark Adaptation120032240.050 Why?
Histones1201325840.050 Why?
Chromosomes, Human, Pair 9120045330.050 Why?
Spasm120221310.050 Why?
Chromatin3202329800.050 Why?
Mitogen-Activated Protein Kinases2202212400.050 Why?
Cardiac Surgical Procedures1201736750.050 Why?
Antiporters120232750.050 Why?
Aortic Aneurysm120066230.050 Why?
Comparative Genomic Hybridization220144760.050 Why?
Monosaccharide Transport Proteins120234370.050 Why?
Phosphotransferases (Alcohol Group Acceptor)120234340.040 Why?
Language1201015500.040 Why?
Aneuploidy120045780.040 Why?
Transcription Factors22024121310.040 Why?
Time Factors22020400650.040 Why?
Heart Diseases1201328210.040 Why?
Cross-Sectional Studies32023263180.040 Why?
Comorbidity12014105630.040 Why?
Seizures2202330000.040 Why?
Growth Disorders120046330.040 Why?
Massachusetts1201288750.040 Why?
Homeodomain Proteins1200924280.040 Why?
Chromosomes, Human, Pair 3120203230.040 Why?
Desmoplakins12019650.040 Why?
KCNQ1 Potassium Channel120191030.040 Why?
Mammals1202411250.040 Why?
Face1200410280.040 Why?
Neonatal Screening120236270.040 Why?
Age of Onset2202033440.040 Why?
Telomere120049430.040 Why?
Light1200313650.040 Why?
Cells, Cultured32019189730.040 Why?
Practice Guidelines as Topic1201474250.030 Why?
Cerebral Cortex2202457670.030 Why?
Drosophila1202415010.030 Why?
DNA-Binding Proteins2201596010.030 Why?
Registries1201282970.030 Why?
Signal Transduction32022236010.030 Why?
Electrocardiography2202064040.030 Why?
Mitochondria1200936730.030 Why?
Chromosomes, Human, Pair 5120173860.030 Why?
Longitudinal Studies12012147510.030 Why?
Pedigree2201745260.030 Why?
Case-Control Studies32021222230.030 Why?
Follow-Up Studies12017391930.030 Why?
Ventricular Remodeling1202312720.030 Why?
Prevalence12012158420.030 Why?
Proteins1201059950.030 Why?
Ethics, Medical120007830.030 Why?
Odds Ratio2202096490.030 Why?
Chromosomes, Human, Pair 22120163480.030 Why?
Leukemia, Myelomonocytic, Juvenile12014240.030 Why?
Oncogene Protein v-akt120141300.030 Why?
Reactive Oxygen Species2201421400.030 Why?
Base Sequence22018124030.030 Why?
Alleles2201568970.030 Why?
Anticonvulsants1202319210.030 Why?
Genes, Developmental12013380.030 Why?
Neurofibromin 1120141900.030 Why?
Homozygote1201717750.030 Why?
MAP Kinase Kinase Kinases120142520.030 Why?
Linkage Disequilibrium1201719970.030 Why?
Diffusion Magnetic Resonance Imaging1202427980.020 Why?
Acyltransferases120143050.020 Why?
Mutagenesis, Insertional120156610.020 Why?
Educational Status2201025130.020 Why?
Action Potentials1201918380.020 Why?
Extracellular Signal-Regulated MAP Kinases120146120.020 Why?
Polymorphism, Single Nucleotide32017160470.020 Why?
Promoter Regions, Genetic2201357860.020 Why?
Magnetics120145850.020 Why?
Smith-Magenis Syndrome12011190.020 Why?
DNA1200572020.020 Why?
RNA Splicing120159030.020 Why?
Genetic Diseases, Inborn120156050.020 Why?
Amino Acid Substitution1201517400.020 Why?
Chromosome Duplication12011790.020 Why?
Dyslexia, Acquired12010140.020 Why?
Congenital Abnormalities120157040.020 Why?
Articulation Disorders12010130.020 Why?
Genetic Markers1201726010.020 Why?
Methylation1201310730.020 Why?
Proteomics1202439100.020 Why?
HEK293 Cells1201942600.020 Why?
Animals720241687640.020 Why?
Kaplan-Meier Estimate1202064990.020 Why?
Molecular Sequence Annotation120125230.020 Why?
Chromosomes, Human120114370.020 Why?
Heart Failure12014118400.020 Why?
Language Disorders120101400.020 Why?
Amino Acid Sequence22012134000.020 Why?
Electron Transport Complex IV120091880.020 Why?
Pregnancy32022302600.020 Why?
Parents1202335920.020 Why?
Oligonucleotide Array Sequence Analysis1201737970.020 Why?
Sarcomeres120123790.020 Why?
GTPase-Activating Proteins120124650.020 Why?
Cytochromes c120091730.020 Why?
Myocardial Contraction1201415150.020 Why?
Cell Separation1201417180.020 Why?
Aorta, Thoracic1201511030.020 Why?
Age Factors22019183800.020 Why?
Lysine120139910.020 Why?
Gene Silencing1201515050.020 Why?
Motor Skills Disorders12008890.020 Why?
Mitochondrial Membranes120091840.020 Why?
Molecular Sequence Data22012175940.020 Why?
Genetic Loci1201726310.020 Why?
Medical History Taking120127770.020 Why?
Epigenomics120149590.020 Why?
COS Cells1200911360.020 Why?
Gene Frequency1201436240.020 Why?
Protein Conformation1201539460.020 Why?
Oxidative Phosphorylation120095020.020 Why?
Motor Skills120105160.020 Why?
Chromosomes, Human, Pair 6120083710.020 Why?
Genomics1202359290.020 Why?
Statistics, Nonparametric1201228440.020 Why?
Child Development Disorders, Pervasive120115970.020 Why?
Sequence Analysis, DNA1201747720.020 Why?
Reading120105390.020 Why?
Chromosome Mapping1201446180.020 Why?
Enhancer Elements, Genetic1201313650.020 Why?
Mice, Mutant Strains1200917450.020 Why?
Membrane Potentials1200910830.020 Why?
Collagen Type III12006920.020 Why?
Hearing120105050.020 Why?
Health Knowledge, Attitudes, Practice1200040580.020 Why?
Proportional Hazards Models12020125090.020 Why?
Risk1201795910.020 Why?
Mice, Knockout22012144480.020 Why?
Databases, Genetic1201217510.020 Why?
Sequence Homology, Amino Acid1200927450.020 Why?
Ehlers-Danlos Syndrome12006940.020 Why?
Gene Expression1201775840.010 Why?
Repressor Proteins1201529680.010 Why?
Cell Line12018155430.010 Why?
Caenorhabditis elegans1201414770.010 Why?
Ventricular Outflow Obstruction120062620.010 Why?
Mice42015818190.010 Why?
Hemodynamics1201441840.010 Why?
Protein Structure, Tertiary1200937500.010 Why?
Genetic Linkage1200823410.010 Why?
Infant, Premature1201221220.010 Why?
Reference Values1200949080.010 Why?
Kinetics1200962740.010 Why?
Dose-Response Relationship, Radiation120038690.010 Why?
Transfection1200957430.010 Why?
Transcription, Genetic1201575990.010 Why?
Arteries1200611180.010 Why?
Hearing Loss120087840.010 Why?
RNA, Messenger12015127680.010 Why?
Echocardiography, Transesophageal1200610930.010 Why?
Middle Aged420232230090.010 Why?
Myocardium1201247600.010 Why?
Adaptation, Psychological1201026600.010 Why?
Fibroblasts1200941590.010 Why?
Prospective Studies12023548020.010 Why?
Carrier Proteins1201249130.010 Why?
Phosphorylation1200982780.010 Why?
Dyspnea1200613520.010 Why?
Leukemia, Myeloid, Acute1201436460.010 Why?
Aged, 80 and over12023594890.010 Why?
Photic Stimulation1200319930.010 Why?
Disease Progression12014136320.010 Why?
B-Lymphocytes1200947780.010 Why?
Gene Expression Profiling1201295250.010 Why?
Survival Analysis12006100700.010 Why?
Cognition1201070490.010 Why?
Pregnancy Complications1200629750.010 Why?
Incidence12010214800.010 Why?
United States22014729030.010 Why?
Aged120231711170.010 Why?
Students, Medical1200019590.000 Why?
Physicians1200045880.000 Why?
Internship and Residency1200059460.000 Why?
Roberts's Networks
Click the
Explore
buttons for more information and interactive visualizations!
Concepts (338)
Explore
_
Co-Authors (110)
Explore
_
Similar People (60)
Explore
_
Same Department 
Explore
_
Physical Neighbors
_
© 2025 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.