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

Concepts (142)

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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 Abnormalities320213151.100 Why?
Cerebral Palsy320244720.880 Why?
DNA Polymerase III12022510.800 Why?
Iron-Sulfur Proteins12022830.790 Why?
Lipodystrophy120221480.740 Why?
Language Development Disorders120211920.670 Why?
Databases, Genetic1202317370.550 Why?
Dwarfism120161370.510 Why?
Limb Deformities, Congenital120161360.510 Why?
Heterozygote1202127970.460 Why?
Urogenital Abnormalities120162560.440 Why?
RNA-Binding Proteins1202118940.400 Why?
Phenotype112024165340.390 Why?
Syndrome6202232620.350 Why?
Genetic Variation1202365480.310 Why?
Tuberous Sclerosis2201410300.280 Why?
Genetic Predisposition to Disease22022177680.210 Why?
Developmental Disabilities4202115040.210 Why?
Child, Preschool142024420620.210 Why?
Genetic Testing3202435300.200 Why?
Facies320212220.200 Why?
Pedigree5202445780.200 Why?
Spastic Paraplegia, Hereditary120241680.200 Why?
Practice Guidelines as Topic2202473780.180 Why?
Population Surveillance1201126060.180 Why?
Chromosome Disorders120234990.180 Why?
Histone-Lysine N-Methyltransferase120246770.170 Why?
Pathology, Molecular120223280.170 Why?
Mutation52024299150.170 Why?
Haploinsufficiency120213270.160 Why?
Ephrin-B112017240.150 Why?
Mediator Complex120171060.140 Why?
Child132024798180.140 Why?
Cognition Disorders1201139750.140 Why?
Mutation, Missense2202225640.130 Why?
Persistent Fetal Circulation Syndrome12016800.130 Why?
Pierre Robin Syndrome120171170.130 Why?
Alleles4202468950.120 Why?
Genomic Imprinting120163300.120 Why?
Point Mutation1201915930.110 Why?
Craniosynostoses120174120.110 Why?
Pulmonary Alveoli120166510.110 Why?
Orofaciodigital Syndromes12012210.110 Why?
GTPase-Activating Proteins120164740.110 Why?
Nerve Tissue Proteins2202344060.100 Why?
Australia2201712760.100 Why?
Infant72024360550.100 Why?
Adolescent92024878920.100 Why?
Basic Helix-Loop-Helix Transcription Factors1201711360.100 Why?
Caregivers1202422250.100 Why?
Histones1202225770.100 Why?
Zebrafish1202229930.090 Why?
China1201623330.090 Why?
Ehlers-Danlos Syndrome12011920.090 Why?
Pulmonary Veins120167450.090 Why?
Humans2520247584060.080 Why?
Astrocytoma120147750.080 Why?
Kyphosis120112370.080 Why?
Male1620243587470.080 Why?
Genotype32024129450.080 Why?
Attention Deficit Disorder with Hyperactivity1202437010.080 Why?
Female1720243903230.070 Why?
Brain Diseases1201615410.070 Why?
Sirolimus1201415330.070 Why?
Cohort Studies32022412560.070 Why?
Transcription Factors32024120940.060 Why?
Gene Deletion1201226660.060 Why?
Scoliosis120117340.060 Why?
Membrane Proteins1202178430.060 Why?
Anticonvulsants1201418810.060 Why?
Genetic Association Studies3202127170.060 Why?
Abnormalities, Multiple1201114140.060 Why?
Genome, Human1201644160.050 Why?
Molecular Sequence Data22016176170.050 Why?
Chromosomes, Human, Pair 22120233460.050 Why?
DNA Mutational Analysis3201741060.050 Why?
DEAD-box RNA Helicases120243830.050 Why?
Tumor Suppressor Proteins1201128000.050 Why?
Polymorphism, Genetic1201142840.040 Why?
Brain32023269470.040 Why?
Signal Transduction22021233420.040 Why?
Young Adult22021588080.040 Why?
Codon, Nonsense120212810.040 Why?
Microarray Analysis120227460.040 Why?
Frameshift Mutation120213880.040 Why?
Chromosome Deletion1202313870.040 Why?
Epilepsy1201432690.040 Why?
Fibroblast Growth Factor 1012017310.040 Why?
Proteins1201260260.040 Why?
Cranial Sutures12017920.040 Why?
Age of Onset1202432980.040 Why?
New Zealand120173520.040 Why?
Adult520212199350.030 Why?
Receptor, Fibroblast Growth Factor, Type 1120172560.030 Why?
TOR Serine-Threonine Kinases2201620570.030 Why?
Genes, Lethal120162250.030 Why?
Comparative Genomic Hybridization120164730.030 Why?
Chromosomes, Human, Pair 16120163420.030 Why?
High-Throughput Nucleotide Sequencing2201736150.030 Why?
DNA Copy Number Variations1202220120.030 Why?
DNA-Binding Proteins2202495740.030 Why?
Societies, Medical1202438910.030 Why?
Self Report1202437140.030 Why?
Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase1201170.020 Why?
Sequence Deletion1201614920.020 Why?
Foot Deformities, Congenital12011590.020 Why?
Corpus Callosum120167490.020 Why?
Antineoplastic Agents12014135910.020 Why?
X Chromosome Inactivation120122260.020 Why?
Hand Deformities, Congenital120111740.020 Why?
Chromatin1202229380.020 Why?
Muscle Hypotonia120111600.020 Why?
Introns120129780.020 Why?
Forkhead Transcription Factors1201616110.020 Why?
Protein Conformation1201639660.020 Why?
DNA1202271990.020 Why?
Family Health1201212570.020 Why?
Alternative Splicing1201210900.020 Why?
Repressor Proteins1201729800.020 Why?
Sequence Analysis, DNA1201747110.020 Why?
Exons1201223870.020 Why?
Cognition1202469530.020 Why?
Retrospective Studies32024801680.020 Why?
Face1201110170.020 Why?
Amino Acids1201117130.020 Why?
Amino Acid Sequence12016134470.010 Why?
Magnetic Resonance Imaging32017362840.010 Why?
Risk Factors12011738090.010 Why?
Nuclear Proteins1201757860.010 Why?
Base Sequence12012124360.010 Why?
Prospective Studies22017541370.010 Why?
Fibroblasts1201140870.010 Why?
Middle Aged220112195680.010 Why?
Biopsy1201167680.010 Why?
Animals220221677680.010 Why?
Skin1201144640.010 Why?
United States12024721360.010 Why?
Infant, Newborn12016261830.010 Why?
Cells, Cultured12011189400.010 Why?
Mice12019811010.010 Why?
Aged120211682180.000 Why?
Treatment Outcome12014643780.000 Why?
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Concepts (142)
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Co-Authors (39)
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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.