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STEPHANIE SHERMAN
Concepts (245)
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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.
5' Untranslated Regions
Abnormalities, Multiple
Adolescent
Adult
Affect
Age of Onset
Aged
Aged, 80 and over
Algorithms
Alleles
Amniotic Fluid
Analysis of Variance
Animals
Antigens, Neoplasm
Anxiety
Ataxia
Atrial Pressure
Attention
Attention Deficit Disorder with Hyperactivity
Attitude
Autism Spectrum Disorder
Autistic Disorder
Base Sequence
Body Mass Index
Brain
Case-Control Studies
Causality
Cell Cycle Proteins
Cells, Cultured
Child
Child Rearing
Child, Preschool
Chromosome Mapping
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 21
Chronic Disease
Clinical Competence
Clinical Trials as Topic
Cluster Analysis
Cognition
Cohort Studies
Comorbidity
Confidence Intervals
Cotinine
Cross-Sectional Studies
Curriculum
Cytoskeletal Proteins
Decision Making
Delayed Diagnosis
Delivery of Health Care
Demography
Dental Care
Depression
Dietary Supplements
Disabled Persons
Disease Models, Animal
Dizziness
DNA
DNA Copy Number Variations
DNA Methylation
DNA Mutational Analysis
DNA Primers
Documentation
Down Syndrome
Drosophila melanogaster
Dyspnea
Echocardiography
Education
Education, Medical, Undergraduate
Educational Measurement
Educational Status
Embryonic Development
Executive Function
Exercise
Family
Fathers
Female
Fertility
Fetal Development
Fever
Fibroblasts
Focus Groups
Folic Acid
Follicular Phase
Fragile X Mental Retardation Protein
Fragile X Syndrome
Gene Expression Regulation
Gene Frequency
Gene Silencing
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Heterogeneity
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Ghana
Haplotypes
Headache
Health Behavior
Health Education
Health Status
Heart Defects, Congenital
Heart Failure
Heart Septal Defects
Heterozygote
Homozygote
Hormone Replacement Therapy
Humans
Hypersensitivity
Immunization
Incidence
Infant
Infant, Newborn
Infertility, Female
Influenza, Human
Information Systems
Intellectual Disability
Intelligence
Intelligence Tests
Internship and Residency
Interspersed Repetitive Sequences
Interviews as Topic
Klinefelter Syndrome
Language
Linear Models
Linkage Disequilibrium
Logistic Models
Magnetic Resonance Imaging
Male
Maternal Age
Maternal Exposure
Mathematical Computing
Meiosis
Memory
Menarche
Menopause
Menopause, Premature
Menstruation
Mental Processes
Metabolomics
Microarray Analysis
Microsatellite Repeats
Middle Aged
Mitral Valve Prolapse
Models, Genetic
Models, Statistical
Molecular Sequence Data
Mothers
Motivation
Multivariate Analysis
Muscle Proteins
Mutagenesis
Mutation
Neonatal Screening
Nerve Tissue Proteins
Neurologic Examination
Neuropsychological Tests
Nicotine
Nondisjunction, Genetic
Occupational Exposure
Occupations
Olfaction Disorders
Oocytes
Oogenesis
Parents
Paternal Age
Patient Education as Topic
Patient Positioning
Peer Group
Personality Inventory
Phenotype
Pneumonia
Point Mutation
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Preconception Care
Predictive Value of Tests
Pregnancy
Pregnancy Outcome
Pregnancy Trimester, Second
Premenopause
Prenatal Diagnosis
Prevalence
Preventive Health Services
Primary Ovarian Insufficiency
Principal Component Analysis
Program Development
Promoter Regions, Genetic
Proportional Hazards Models
Proteasome Endopeptidase Complex
Protein Biosynthesis
Qualitative Research
Quality Improvement
Quality of Life
Quantitative Trait, Heritable
Radiography
Radiography, Thoracic
Receptor, Notch4
Receptors, Corticotropin-Releasing Hormone
Recombination, Genetic
Regression Analysis
Reproduction
Research Subjects
Reverse Transcriptase Polymerase Chain Reaction
Risk
Risk Assessment
Risk Factors
RNA, Messenger
RNA-Binding Proteins
Seizures
Sensitivity and Specificity
Sequence Analysis, DNA
Sequence Homology, Nucleic Acid
Severity of Illness Index
Sex Ratio
Sister Chromatid Exchange
Smoking
Social Class
Socioeconomic Factors
Spermatogenesis
Steroid 17-alpha-Hydroxylase
Students, Medical
Surveys and Questionnaires
Syndrome
Teaching
Telomere
Telomere Homeostasis
Thinking
Transcription, Genetic
Tremor
Trinucleotide Repeat Expansion
Trinucleotide Repeats
Trisomy
Trisomy 18 Syndrome
United States
Vaccination
Whole Genome Sequencing
Young Adult
SHERMAN's Networks
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Concepts (245)
Derived automatically from this person's publications.
Fragile X Syndrome
Fragile X Mental Retardation Protein
Down Syndrome
Chromosomes, Human, Pair 21
Nondisjunction, Genetic
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Co-Authors (17)
People in Profiles who have published with this person.
SARGSYAN, ZAVEN
TURNER, TERI
LIM, JONATHAN
MISRA, ARUNIMA
REZIGH, ALEC
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Similar People (60)
People who share similar concepts with this person.
NELSON, DAVID
BOERWINKLE, ERIC
JANKOVIC, JOSEPH
LUPSKI, JAMES
AMOS, CHRIS
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Same Department
People who are also in this person's primary department.
GAY, LINDSEY
ISMAIL, NADIA
KHAWAJA, LUBNA
LESCINSKAS, ERICA
RUEDA, JAIME
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