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Maya Chopra, M.B.,B.S.

Concepts (144)

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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?
Craniofacial Abnormalities320213201.080 Why?
Cerebral Palsy320244800.860 Why?
DNA Polymerase III12022520.790 Why?
Iron-Sulfur Proteins12022850.780 Why?
Lipodystrophy120221450.730 Why?
Language Development Disorders120211930.660 Why?
Databases, Genetic1202317580.540 Why?
Dwarfism120161370.500 Why?
Limb Deformities, Congenital120161360.500 Why?
Heterozygote1202127980.460 Why?
Urogenital Abnormalities120162550.440 Why?
RNA-Binding Proteins1202118910.400 Why?
Phenotype122024167310.400 Why?
Syndrome6202232740.350 Why?
Genetic Variation1202366110.300 Why?
Tuberous Sclerosis2201410420.270 Why?
Child, Preschool152024426830.220 Why?
5' Untranslated Regions120242550.210 Why?
Genetic Predisposition to Disease22022180680.210 Why?
Developmental Disabilities4202115200.210 Why?
Genetic Testing3202435910.200 Why?
Facies320212240.190 Why?
Pedigree5202445450.190 Why?
Spastic Paraplegia, Hereditary120241710.190 Why?
Practice Guidelines as Topic2202474600.180 Why?
Spasms, Infantile120243010.180 Why?
Population Surveillance1201125970.180 Why?
Chromosome Disorders120234990.180 Why?
Pathology, Molecular120223290.170 Why?
Mutation52024302660.160 Why?
Histone-Lysine N-Methyltransferase120247010.160 Why?
Haploinsufficiency120213340.160 Why?
Ephrin-B112017240.150 Why?
Child142024809600.140 Why?
Mediator Complex120171060.140 Why?
Cognition Disorders1201139850.140 Why?
Mutation, Missense2202225920.130 Why?
Persistent Fetal Circulation Syndrome12016800.130 Why?
Pierre Robin Syndrome120171180.130 Why?
Alleles4202469010.120 Why?
Genomic Imprinting120163260.110 Why?
Infant82024365560.110 Why?
Point Mutation1201915960.110 Why?
Craniosynostoses120174160.110 Why?
Pulmonary Alveoli120166650.110 Why?
Orofaciodigital Syndromes12012210.100 Why?
GTPase-Activating Proteins120164690.100 Why?
Australia2201712650.100 Why?
Nerve Tissue Proteins2202344130.100 Why?
Basic Helix-Loop-Helix Transcription Factors1201711430.090 Why?
Adolescent92024892440.090 Why?
Histones1202226030.090 Why?
Caregivers1202423080.090 Why?
China1201623950.090 Why?
Zebrafish1202230370.090 Why?
Ehlers-Danlos Syndrome12011940.090 Why?
Pulmonary Veins120167580.090 Why?
Humans2620247689700.090 Why?
Astrocytoma120147810.080 Why?
Male1720243652030.080 Why?
Kyphosis120112530.080 Why?
Genotype32024130480.080 Why?
Attention Deficit Disorder with Hyperactivity1202437300.080 Why?
Female1820243975150.080 Why?
Brain Diseases1201615580.070 Why?
Sirolimus1201415400.070 Why?
Sequence Deletion2202414980.070 Why?
Cohort Studies32022418080.070 Why?
Transcription Factors32024121740.060 Why?
Gene Deletion1201226740.060 Why?
Membrane Proteins1202178850.060 Why?
Scoliosis120117930.060 Why?
Genetic Association Studies3202127480.060 Why?
Abnormalities, Multiple1201114230.060 Why?
Anticonvulsants1201419240.060 Why?
Exons2202423950.060 Why?
Genome, Human1201644560.050 Why?
Molecular Sequence Data22016176290.050 Why?
Chromosomes, Human, Pair 22120233480.050 Why?
DNA Mutational Analysis3201741240.050 Why?
Tumor Suppressor Proteins1201128120.050 Why?
DEAD-box RNA Helicases120243850.040 Why?
Polymorphism, Genetic1201142510.040 Why?
Brain32023274530.040 Why?
Signal Transduction22021236530.040 Why?
Young Adult22021601310.040 Why?
Codon, Nonsense120212870.040 Why?
Microarray Analysis120227550.040 Why?
Frameshift Mutation120213930.040 Why?
Chromosome Deletion1202313900.040 Why?
Epilepsy1201433260.040 Why?
Fibroblast Growth Factor 1012017310.040 Why?
Proteins1201260110.040 Why?
Cranial Sutures12017990.040 Why?
Age of Onset1202433460.030 Why?
New Zealand120173600.030 Why?
Receptor, Fibroblast Growth Factor, Type 1120172600.030 Why?
Adult520212238510.030 Why?
TOR Serine-Threonine Kinases2201620630.030 Why?
Genes, Lethal120162240.030 Why?
Comparative Genomic Hybridization120164740.030 Why?
Chromosomes, Human, Pair 16120163440.030 Why?
High-Throughput Nucleotide Sequencing2201736710.030 Why?
DNA-Binding Proteins2202496180.030 Why?
DNA Copy Number Variations1202220550.030 Why?
Societies, Medical1202439680.020 Why?
Self Report1202437730.020 Why?
Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase1201170.020 Why?
Foot Deformities, Congenital12011590.020 Why?
Corpus Callosum120167530.020 Why?
Antineoplastic Agents12014136980.020 Why?
X Chromosome Inactivation120122290.020 Why?
Hand Deformities, Congenital120111750.020 Why?
Chromatin1202229810.020 Why?
Muscle Hypotonia120111660.020 Why?
Introns120129690.020 Why?
Forkhead Transcription Factors1201616250.020 Why?
Protein Conformation1201639560.020 Why?
DNA1202272140.020 Why?
Family Health1201212550.020 Why?
Alternative Splicing1201211050.020 Why?
Repressor Proteins1201729860.020 Why?
Sequence Analysis, DNA1201747850.020 Why?
Cognition1202470810.020 Why?
Retrospective Studies32024819030.020 Why?
Face1201110310.020 Why?
Amino Acids1201117160.020 Why?
Amino Acid Sequence12016134270.010 Why?
Magnetic Resonance Imaging32017368540.010 Why?
Risk Factors12011749760.010 Why?
Nuclear Proteins1201758040.010 Why?
Base Sequence12012124300.010 Why?
Prospective Studies22017549620.010 Why?
Fibroblasts1201141790.010 Why?
Middle Aged220112237370.010 Why?
Biopsy1201168050.010 Why?
Animals220221693350.010 Why?
Skin1201145060.010 Why?
United States12024731860.010 Why?
Infant, Newborn12016264280.010 Why?
Cells, Cultured12011190230.010 Why?
Mice12019820720.010 Why?
Aged120211717860.000 Why?
Treatment Outcome12014654800.000 Why?
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Concepts (144)
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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.