Harvard Catalyst Profiles

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Bernard S Chang, M.D.

Concepts (300)

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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?
Periventricular Nodular Heterotopia102016532.710 Why?
Epilepsy15202032691.470 Why?
Malformations of Cortical Development920151761.310 Why?
Cerebral Cortex16201557591.120 Why?
Transcranial Magnetic Stimulation6202014691.050 Why?
Electroencephalography17201661870.990 Why?
Seizures12202029190.940 Why?
Nerve Net5201522630.880 Why?
Brain212018269470.760 Why?
Brain Mapping7201665700.750 Why?
Scalp220133890.660 Why?
Nervous System Malformations620112440.640 Why?
Brain Waves220134010.610 Why?
Dyslexia320122080.570 Why?
Neurology220147780.520 Why?
Neuroanatomy12015700.490 Why?
Models, Neurological3201217570.480 Why?
Information Theory12013490.430 Why?
Epilepsies, Partial320124300.400 Why?
Career Choice220147520.370 Why?
Leukoencephalopathies120132490.360 Why?
Biological Clocks120123160.340 Why?
Cognition Disorders5201539750.330 Why?
Arthrogryposis12009680.320 Why?
Neurogenesis120148550.290 Why?
Child Behavior Disorders120118050.270 Why?
Receptors, G-Protein-Coupled5201512450.270 Why?
Magnetic Resonance Imaging252016362840.260 Why?
Diagnosis, Computer-Assisted120117060.260 Why?
Frontal Lobe4201414190.250 Why?
Cell Adhesion Molecules, Neuronal120072630.250 Why?
Students, Medical2201919270.250 Why?
Chromosomes, Human, Pair 16220043420.240 Why?
Rest120109140.240 Why?
Parietal Lobe320118490.220 Why?
Signal Processing, Computer-Assisted4201314890.220 Why?
Reading320135290.220 Why?
Education, Medical1201517250.220 Why?
Curriculum3202237170.210 Why?
Epilepsy, Post-Traumatic12003400.210 Why?
Anticonvulsants3202018810.210 Why?
Pedigree11201445780.210 Why?
Extracellular Matrix Proteins120078290.210 Why?
Entropy220132100.200 Why?
Functional Laterality2200622530.190 Why?
Societies, Medical1201438910.190 Why?
Serine Endopeptidases1200710200.190 Why?
Neuropsychological Tests6201370210.190 Why?
Syndrome6200932620.190 Why?
Education, Medical, Undergraduate2202010660.180 Why?
Developmental Disabilities3201015040.170 Why?
Epilepsy, Temporal Lobe220053880.160 Why?
Microcephaly320104250.160 Why?
Monitoring, Ambulatory120023520.160 Why?
Humans5920227584060.160 Why?
Thinking120203190.140 Why?
Electrocardiography1201163630.140 Why?
Mutation112015299150.140 Why?
Problem-Based Learning120203520.140 Why?
DNA Mutational Analysis7201441060.140 Why?
Adult2420182199350.140 Why?
Young Adult122018588080.140 Why?
Neural Pathways1200730390.140 Why?
Sleep2201347440.140 Why?
Algorithms32013139610.130 Why?
Male3420183587470.130 Why?
Homeodomain Proteins4201224130.130 Why?
Clinical Clerkship120225630.130 Why?
Mind-Body Relations, Metaphysical12015360.130 Why?
Image Processing, Computer-Assisted4201389450.120 Why?
Abnormalities, Multiple3200814140.120 Why?
Faculty, Medical2202011920.120 Why?
Female3220183903230.110 Why?
Outpatients1200215910.110 Why?
Nerve Tissue Proteins1200744060.110 Why?
Immunoglobulin Variable Region119944190.110 Why?
Preoperative Care1200222490.110 Why?
Cerebral Ventricles320045420.110 Why?
Choristoma220052070.100 Why?
Phonetics120131980.100 Why?
Cognition1200969530.100 Why?
Child132018798180.100 Why?
Contractile Proteins120122400.090 Why?
Aortic Aneurysm, Thoracic120186950.090 Why?
Oxygen2201341910.090 Why?
Body Patterning220146320.090 Why?
Genetic Predisposition to Disease32018177680.090 Why?
Child, Preschool92018420620.090 Why?
Stochastic Processes120123540.090 Why?
Adolescent122018878920.090 Why?
Brain Injuries1200320440.090 Why?
Computer Simulation3202062010.090 Why?
Oligodendroglia120155360.090 Why?
Genetic Association Studies2201827170.090 Why?
Congresses as Topic120157990.090 Why?
DNA Repair-Deficiency Disorders12010360.090 Why?
Internationality1201510000.080 Why?
Maternal Age120128070.080 Why?
Infant82018360550.080 Why?
Consanguinity320104560.080 Why?
Genetic Diseases, X-Linked120133780.080 Why?
SOXB1 Transcription Factors120102860.080 Why?
Middle Aged1320182195680.080 Why?
Wechsler Scales120092570.080 Why?
Cerebellum3200714970.080 Why?
Alternative Splicing1201410900.080 Why?
Phenotype62018165340.080 Why?
Reproducibility of Results32013200550.080 Why?
DNA Repair Enzymes120103440.080 Why?
Microsatellite Repeats320057850.080 Why?
Phosphotransferases (Alcohol Group Acceptor)120104350.070 Why?
Microfilament Proteins1201211330.070 Why?
Eye Abnormalities220082410.070 Why?
Muscular Dystrophies220083890.070 Why?
Family Health3200612570.070 Why?
Neural Stem Cells120148820.070 Why?
Cytogenetics120071980.070 Why?
Chromosome Inversion120071200.070 Why?
Chromosomes, Human, Pair 7120073100.070 Why?
Statistics, Nonparametric1201128500.060 Why?
Organ Size1201022520.060 Why?
Brain Diseases2200515410.060 Why?
In Situ Hybridization, Fluorescence2201325040.060 Why?
Mannosyltransferases12005230.060 Why?
Anterior Temporal Lobectomy12005460.060 Why?
Information Storage and Retrieval120118210.060 Why?
Prenatal Care1201211290.060 Why?
Chromosomes, Human, Pair 1120076350.060 Why?
Adaptation, Physiological1201212950.060 Why?
Analysis of Variance1201362340.060 Why?
Clinical Competence1202047750.060 Why?
Heterozygote2201327970.060 Why?
Paresis120061760.060 Why?
Quality Improvement1201938060.060 Why?
Schools, Medical220228770.060 Why?
Hemianopsia120051210.060 Why?
Point Mutation2201315930.060 Why?
Inheritance Patterns120063400.060 Why?
Radiation Dosage1201219560.060 Why?
Sequence Analysis, DNA2201347110.050 Why?
Time Factors32013398720.050 Why?
Sclerosis120032100.050 Why?
Randomized Controlled Trials as Topic12020101460.050 Why?
Executive Function1201113740.050 Why?
Models, Statistical2202050700.050 Why?
Transcription Factors42012120940.050 Why?
Chromosome Deletion1200713870.050 Why?
Predictive Value of Tests22012152250.050 Why?
Quadriplegia120042260.050 Why?
Aged, 80 and over32013586830.050 Why?
Central Nervous System Diseases120075200.050 Why?
Phenytoin120031880.050 Why?
Controlled Clinical Trials as Topic120031860.050 Why?
Carbamazepine120032240.050 Why?
Homozygote1200717880.050 Why?
Nerve Fibers, Myelinated120079520.050 Why?
Terminology as Topic1200915330.050 Why?
Ocular Motility Disorders120031440.050 Why?
Genes, Recessive120046260.050 Why?
Neuromuscular Diseases120042550.050 Why?
Psychiatric Status Rating Scales1201160130.050 Why?
Visual Pathways120055340.050 Why?
Models, Theoretical1201335610.050 Why?
Neurofibromatosis 1120065600.050 Why?
Tomography, Emission-Computed1200311210.050 Why?
Genetic Heterogeneity120047230.050 Why?
Aged520181682180.040 Why?
Base Sequence42014124360.040 Why?
Intelligence120059210.040 Why?
Alcohol Drinking1201240180.040 Why?
Fatal Outcome1200418290.040 Why?
Severity of Illness Index22010157850.040 Why?
Tomography, Emission-Computed, Single-Photon1200310660.040 Why?
Software1201344150.040 Why?
Ion Channels1200310430.040 Why?
Brain Stem120038570.040 Why?
Neuroglia120039440.040 Why?
Parents1201135480.040 Why?
Epilepsies, Myoclonic11998850.040 Why?
Olivary Nucleus119981280.040 Why?
Thalamus1200310400.040 Why?
Gene Expression Regulation12015118920.030 Why?
Models, Animal1200321120.030 Why?
Genotype42018129450.030 Why?
Myoclonic Epilepsy, Juvenile12015130.030 Why?
Diagnostic Errors1200312630.030 Why?
Czech Republic12015730.030 Why?
Organizational Culture120195060.030 Why?
Sequence Deletion2201414920.030 Why?
Classical Lissencephalies and Subcortical Band Heterotopias12014130.030 Why?
Compulsive Behavior120151170.030 Why?
Lissencephaly12014360.030 Why?
Lod Score220056020.030 Why?
Needs Assessment1202011410.030 Why?
Longitudinal Studies12010144900.030 Why?
Biological Evolution2201410740.030 Why?
rhoA GTP-Binding Protein120152340.030 Why?
Genes, Immunoglobulin119942850.030 Why?
Educational Measurement1202012480.030 Why?
Death, Sudden120153020.030 Why?
rho GTP-Binding Proteins120152770.030 Why?
Age Factors12010183580.030 Why?
Serotonin1199810400.030 Why?
Microscopy, Electron, Transmission120156950.030 Why?
Positron-Emission Tomography1200964570.030 Why?
Teaching1202011680.030 Why?
Cell Movement1200552010.030 Why?
Codon, Nonsense120142810.030 Why?
Cats120149760.030 Why?
Animals620151677680.030 Why?
Learning1202217390.030 Why?
Acute Disease1200372250.020 Why?
RNA Splice Sites120132110.020 Why?
Case-Control Studies12010220290.020 Why?
Interpersonal Relations1201914330.020 Why?
Membrane Proteins1200878430.020 Why?
Molecular Sequence Data22014176170.020 Why?
Optic Nerve120155670.020 Why?
Septo-Optic Dysplasia1201080.020 Why?
Myelin Sheath120156520.020 Why?
Hippocampus1200337360.020 Why?
Program Evaluation1201924920.020 Why?
Risk1200395990.020 Why?
Dose-Response Relationship, Drug12003107480.020 Why?
Aggression120157450.020 Why?
Genes, Dominant120138620.020 Why?
Tamoxifen120159630.020 Why?
Fathers120133770.020 Why?
Corpus Callosum120157490.020 Why?
Mosaicism120134650.020 Why?
Genetic Linkage2200523810.020 Why?
Cobblestone Lissencephaly1200820.020 Why?
Movement Disorders120124590.020 Why?
Chromosomes, Human, Pair 19120103470.020 Why?
Neurons2200594160.020 Why?
Radiography2201369540.020 Why?
Cell Proliferation22015104160.020 Why?
Amino Acids1199417130.020 Why?
Infant, Newborn32018261830.020 Why?
Middle East120082300.020 Why?
Polymorphism, Single Nucleotide42010157730.020 Why?
Central Nervous System1201513330.020 Why?
Haplotypes1201427640.020 Why?
Mental Disorders1200768030.020 Why?
Axons1201516730.020 Why?
Psychomotor Disorders120071490.020 Why?
Alleles1201868950.020 Why?
History, 19th Century120097200.020 Why?
Mice, Inbred BALB C1201562090.020 Why?
Cell Lineage1201525330.020 Why?
Treatment Outcome22003643780.020 Why?
United States12014721360.020 Why?
Karyotyping1200711710.020 Why?
Echocardiography1201849620.020 Why?
Cell Survival1201557810.020 Why?
Turkey120052490.010 Why?
Antisense Elements (Genetics)12004370.010 Why?
Embryo, Mammalian1201016740.010 Why?
Gene Order120041690.010 Why?
Genome, Human2200844160.010 Why?
Chromosomes, Human, Pair 9120055340.010 Why?
DNA Primers1200728160.010 Why?
Visual Field Tests120054110.010 Why?
Health Surveys1201240640.010 Why?
Amino Acid Sequence11994134470.010 Why?
Promoter Regions, Genetic1201457790.010 Why?
DNA2200771990.010 Why?
Brain Neoplasms1200389810.010 Why?
Frameshift Mutation120043880.010 Why?
Risk Assessment12003238840.010 Why?
History, 20th Century1200927720.010 Why?
DNA Repair1201020380.010 Why?
Mice32015811010.010 Why?
Pain1201550650.010 Why?
Artifacts1200918970.010 Why?
Sequence Homology, Amino Acid1200427530.010 Why?
Mice, Knockout12015143540.010 Why?
Amino Acid Substitution1200417340.010 Why?
Chromosome Mapping1200746240.010 Why?
Family1201031880.010 Why?
Genetic Variation1201465480.010 Why?
Harmaline1199840.010 Why?
Visual Fields1200510540.010 Why?
Prospective Studies12003541370.010 Why?
Logistic Models12012132760.010 Why?
Signal Transduction22015233420.010 Why?
Ligands1200432580.010 Why?
Mice, Inbred C57BL12015220030.010 Why?
Disease Models, Animal12015181190.010 Why?
Mutation, Missense1200425640.010 Why?
Acoustic Stimulation1199812320.010 Why?
Stem Cells1200435210.010 Why?
Genome-Wide Association Study12010126040.010 Why?
Cohort Studies12010412560.000 Why?
Rats, Sprague-Dawley1199881430.000 Why?
Pyridines1199828590.000 Why?
Risk Factors12012738090.000 Why?
Immunohistochemistry11998110700.000 Why?
Retrospective Studies12012801680.000 Why?
Rats11998236790.000 Why?
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Concepts (300)
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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.