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Stephanie Sacharow, M.D.
Concepts (186)
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Concepts are derived automatically from a person's publications.
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Categories
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Details
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
Acidosis, Lactic
Adenosine Triphosphate
Adolescent
Adult
Alleles
Amidohydrolases
Amino Acid Metabolism, Inborn Errors
Animals
Arginine
Arthrogryposis
Asparagine
Aspartate-Ammonia Ligase
Asperger Syndrome
Atrophy
Attitude to Health
Autistic Disorder
Autoantigens
Bacteria
Binding Sites
Biological Therapy
Bone Diseases, Developmental
Brain Diseases
Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor
Cardiomyopathies
Carrier Proteins
Cataract
Child
Child Development Disorders, Pervasive
Child, Preschool
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes, Artificial, Bacterial
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Clinical Trials as Topic
Cognition
Cohort Studies
Comorbidity
Comparative Genomic Hybridization
Consanguinity
Consensus
Cosmetics
Cross-Sectional Studies
DEAD-box RNA Helicases
Developmental Disabilities
Diagnosis, Differential
Diet
Dietary Proteins
Disease Models, Animal
DNA Copy Number Variations
DNA Mutational Analysis
DNA, Mitochondrial
Dose-Response Relationship, Drug
Down-Regulation
Drug Packaging
Drug Stability
Endopeptidases
Epilepsy
Escherichia coli
Executive Function
Facies
Family
Fatty Acids, Essential
Female
Fibroblasts
Fungi
GATA4 Transcription Factor
Gene Deletion
Gene Duplication
Gene Frequency
Genetic Association Studies
Genetic Engineering
Genetic Linkage
Genetic Predisposition to Disease
Genome-Wide Association Study
Genotype
Germ-Line Mutation
Glutamine
Glycoproteins
GTP-Binding Protein beta Subunits
Guanosine Triphosphate
Haploinsufficiency
Health Education
Health Personnel
Heart Defects, Congenital
HEK293 Cells
Heredodegenerative Disorders, Nervous System
Herpes Simplex
Heterozygote
Homeostasis
Homozygote
Humans
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Jaundice
Lethargy
Lipid Metabolism, Inborn Errors
Liver
Liver Diseases
Liver Failure, Acute
Longitudinal Studies
Lysosomes
Male
Mass Screening
Membrane Proteins
Metals
Methylenetetrahydrofolate Dehydrogenase (NADP)
Mice
Microarray Analysis
Microcephaly
Micronutrients
Microsatellite Repeats
Middle Aged
Minor Histocompatibility Antigens
Mitochondria
Mitochondrial Diseases
Mitochondrial Proteins
Models, Molecular
Monomeric GTP-Binding Proteins
Muscular Diseases
Mutation
Mutation, Missense
Needs Assessment
Neonatal Screening
Neoplastic Syndromes, Hereditary
Nerve Tissue Proteins
Nervous System
Neuropeptides
Neuropsychological Tests
Noonan Syndrome
Nucleic Acid Hybridization
Nutritional Status
Oligonucleotide Array Sequence Analysis
Oligonucleotide Probes
Oxidoreductases Acting on CH-CH Group Donors
Pedigree
Peripheral Nervous System Diseases
Phenotype
Phenylalanine
Phenylalanine Ammonia-Lyase
Phenylalanine Hydroxylase
Phenylketonurias
Phosphotransferases (Alcohol Group Acceptor)
Plastics
Polymorphism, Single Nucleotide
Pregnancy
Prognosis
Program Development
Proteasome Endopeptidase Complex
Protein Conformation
Protein Structure, Tertiary
Puerto Rico
Recombinant Proteins
Repressor Proteins
Retinitis Pigmentosa
Retrospective Studies
Ribonuclease III
Risk Factors
RNA-Binding Proteins
Rodentia
Seizures
Sequence Deletion
Siblings
Spasms, Infantile
Spherocytosis, Hereditary
Syndrome
Tooth Abnormalities
Transcription Factors
Treatment Outcome
Tubulin
Ubiquitin Thiolesterase
Ubiquitins
User-Computer Interface
Vacuolar Proton-Translocating ATPases
Vomiting
Young Adult
Zebrafish
Sacharow's Networks
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Concepts (186)
Derived automatically from this person's publications.
Phenylketonurias
Neonatal Screening
Abnormalities, Multiple
Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor
Phenylalanine Ammonia-Lyase
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_
Co-Authors (18)
People in Profiles who have published with this person.
O'Connell, Amy
Waisbren, Susan
Rodan, Lance
Bodamer, Olaf
Goodlett, Benjamin
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_
Similar People (60)
People who share similar concepts with this person.
Levy, Harvey
Alkuraya, Fowzan
Waisbren, Susan
Chung, Wendy
Pearl, Phillip
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_
Same Department
People in same department with this person.
Brownstein, Catherine
Cox, Gerald
Kim, Sonia
O'Donnell Luria, Anne
Zhou, Zinan
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_