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Siddharth Srivastava, M.D.
Concepts (314)
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Concepts are derived automatically from a person's publications.
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In this concept 'cloud', the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
Abnormalities, Multiple
Aconitate Hydratase
Activities of Daily Living
Acute Disease
Adenosine Triphosphatases
Adolescent
Adult
Age Factors
Age of Onset
Aged
Aged, 80 and over
Alanine-tRNA Ligase
Alleles
Amino Acid Sequence
Ammonia
Amoxapine
Animals
Anisotropy
Anticonvulsants
Anxiety
Ataxia
Atrial Fibrillation
Atrophy
Attention Deficit Disorder with Hyperactivity
Autistic Disorder
Bacterial Translocation
Basal Ganglia
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
beta Catenin
Bifidobacterium
Blepharophimosis
Bone Morphogenetic Protein 4
Brain
Brain-Derived Neurotrophic Factor
California
Carrier Proteins
Case-Control Studies
Cataract
Cell Cycle Proteins
Cell Membrane
Cells, Cultured
Central Nervous System
Cerebellum
Cerebral Palsy
Child
Child Behavior
Child Behavior Disorders
Child Development
Child, Preschool
Chondroitin Sulfate Proteoglycans
Chorea
Chromosomal Proteins, Non-Histone
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Mapping
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 9
Chromosomes, Human, X
Class I Phosphatidylinositol 3-Kinases
Codon, Nonsense
Cognition
Cognition Disorders
Cohort Studies
Communication Disorders
Comorbidity
Comparative Genomic Hybridization
Congenital Hypothyroidism
Consanguinity
Consensus Development Conferences as Topic
Contactins
Corpus Callosum
Craniofacial Abnormalities
Cross-Sectional Studies
Cyclic AMP Response Element-Binding Protein A
Databases, Factual
Databases, Genetic
De Lange Syndrome
Deafness
Death, Sudden, Cardiac
Developmental Disabilities
Diagnosis, Differential
Diagnostic Tests, Routine
Diffusion Tensor Imaging
Disease Management
Disease Models, Animal
Disease Progression
DNA Copy Number Variations
DNA Methylation
DNA Mutational Analysis
DNA-Binding Proteins
Double-Blind Method
Drosophila melanogaster
Drug Discovery
Early Diagnosis
Electrocardiography
Electroencephalography
Electronic Health Records
Endocannabinoids
Endotoxemia
Endotoxins
Epigenesis, Genetic
Epilepsy
Epilepsy, Generalized
Eye Diseases
Face
Facies
Failure to Thrive
Family
Family Health
Female
Forkhead Transcription Factors
Frameshift Mutation
Gene Deletion
Gene Duplication
Gene Expression
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Regulatory Networks
Genetic Association Studies
Genetic Counseling
Genetic Diseases, X-Linked
Genetic Loci
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome-Wide Association Study
Genomics
Genotype
Germ Cells
Germ-Line Mutation
Glutamic Acid
Growth Disorders
GTP-Binding Proteins
Guanine Nucleotide Exchange Factors
Hamartoma Syndrome, Multiple
Haploinsufficiency
Heart Conduction System
Heart Defects, Congenital
Hedgehog Proteins
Hematologic Diseases
Hepatic Encephalopathy
Hereditary Central Nervous System Demyelinating Diseases
Hereditary Sensory and Autonomic Neuropathies
Heterogeneous-Nuclear Ribonucleoproteins
Heterozygote
High-Throughput Nucleotide Sequencing
Histocompatibility Antigens
Histone Acetyltransferases
Histone-Lysine N-Methyltransferase
Histones
History, 19th Century
History, 20th Century
History, 21st Century
Homeodomain Proteins
Humans
Hypertrichosis
Image Processing, Computer-Assisted
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Infant, Newborn, Diseases
Inheritance Patterns
Intelligence
Intelligence Tests
Intestines
Intracellular Signaling Peptides and Proteins
Joint Instability
Kidney
Lactobacillus
Language
Language Development
Language Development Disorders
Language Disorders
Lethargy
Leukoencephalopathies
Linear Models
Lipomatosis
Liver Cirrhosis
Longitudinal Studies
Magnetic Resonance Imaging
Male
Mammals
Massachusetts
Mediator Complex
Membrane Proteins
Meningeal Neoplasms
Meningioma
Mental Disorders
Mental Retardation, X-Linked
Methyl-CpG-Binding Protein 2
Methyltransferases
Mice
Microarray Analysis
Microcephaly
Microphthalmos
Middle Aged
Migraine with Aura
Mitochondria
Models, Molecular
Molecular Diagnostic Techniques
Molecular Sequence Data
Movement Disorders
Moyamoya Disease
Muscle Hypotonia
Muscle Spasticity
Mutant Proteins
Mutation
Mutation, Missense
Myostatin
Neonatal Screening
Neoplasm Proteins
Nerve Tissue Proteins
Nervous System Diseases
Neurocutaneous Syndromes
Neurodegenerative Diseases
Neurologic Examination
Neuroprotective Agents
Neuropsychological Tests
Nuclear Proteins
Obsessive-Compulsive Disorder
Organ Size
Pancreatitis
Parents
Patella
Pathology, Molecular
Pediatrics
Pedigree
Permeability
Phenotype
Port-Wine Stain
POU Domain Factors
Practice Guidelines as Topic
Predictive Value of Tests
Pregnancy
Prenatal Diagnosis
Prevalence
Probiotics
Prognosis
Prospective Studies
Protein Conformation
Protein Phosphatase 2
Psychometrics
Psychomotor Agitation
Psychomotor Disorders
PTEN Phosphohydrolase
PubMed
Quadriplegia
Quality of Life
Quantitative Trait, Heritable
rab GTP-Binding Proteins
Receptors, GABA-A
Receptors, Granulocyte-Macrophage Colony-Stimulating Factor
Receptors, Retinoic Acid
Registries
Repetitive Sequences, Nucleic Acid
Repressor Proteins
Retina
Retinitis Pigmentosa
Retinoids
Retrospective Studies
Rett Syndrome
Risk Factors
RNA Polymerase III
RNA Processing, Post-Transcriptional
Scrotum
Seizures
Self-Injurious Behavior
Sequence Alignment
Sequence Analysis, DNA
Serine C-Palmitoyltransferase
Severity of Illness Index
Sex Factors
Shab Potassium Channels
Sialyltransferases
Siblings
Signal Transduction
Single-Cell Analysis
Social Behavior
Socialization
Societies, Medical
Sodium Channel Blockers
Sodium-Potassium-Exchanging ATPase
Spastic Paraplegia, Hereditary
Speech
Speech Disorders
Speech-Language Pathology
Sphingolipids
Standard of Care
Stereotyped Behavior
Sturge-Weber Syndrome
Syndrome
Tachycardia
Thyroid Diseases
TOR Serine-Threonine Kinases
Transcription Factors
Treatment Outcome
TRPM Cation Channels
Tryptophan-tRNA Ligase
Tuberous Sclerosis
Ubiquitin-Protein Ligases
Ultrasonography
United States
Urogenital Abnormalities
Vascular Malformations
Vesicular Transport Proteins
Vestibular Diseases
Vomiting
X Chromosome Inactivation
Young Adult
Zebrafish
Srivastava's Networks
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Concepts (314)
Derived automatically from this person's publications.
De Lange Syndrome
Genetic Association Studies
Cerebral Palsy
Phenotype
Chromosome Disorders
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Co-Authors (86)
People in Profiles who have published with this person.
Santana Almansa, Alexandra
Sahin, Mustafa
Chopra, Maya
Ebrahimi-Fakhari, Darius
Mo, Alisa
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_
Similar People (60)
People who share similar concepts with this person.
Kohane, Zak
Walsh, Christopher
Alkuraya, Fowzan
Sahin, Mustafa
Chung, Wendy
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_
Same Department
People in same department with this person.
Bellinger, David
Fagiolini, Michela
Glass, Madison
Lee, Henry
Patel, Archana
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_