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Barbara R. Pober, M.D.
Concepts (495)
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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
Abortion, Induced
Acetylcysteine
Acidosis
Actins
Adolescent
Adult
Age Factors
Age of Onset
Aged
Aged, 80 and over
Alcohol Drinking
Alleles
alpha-Thalassemia
Amino Acid Sequence
Amino Acid Substitution
Amyloid beta-Peptides
Anemia
Anger
Animals
Anodontia
Anti-Anxiety Agents
Anti-Bacterial Agents
Antifungal Agents
Antigens, Surface
Antihypertensive Agents
Anxiety
Anxiety Disorders
Aorta
Aortic Stenosis, Supravalvular
Aortic Valve Stenosis
Argininosuccinic Acid
Arm
Arnold-Chiari Malformation
Arterial Occlusive Diseases
Autistic Disorder
Autopsy
Bacteria
Base Sequence
Behavior
Binding Sites
Biological Transport, Active
Blood Cell Count
Blood Glucose
Blood Pressure
Blood Pressure Monitoring, Ambulatory
Blood Vessels
Blotting, Northern
Body Composition
Body Constitution
Body Mass Index
Body Weight
Bone and Bones
Bone Density
Brain
Brain Ischemia
Buspirone
Calcium
California
Carboxyhemoglobin
Cardiovascular Abnormalities
Cardiovascular Diseases
Case-Control Studies
Catheterization
Cell Proliferation
Cells, Cultured
Cephalometry
Cerebral Arterial Diseases
Cerebral Palsy
Cerebral Ventricles
Chemokines
Child
Child Behavior Disorders
Child, Preschool
Chromosome Aberrations
Chromosome Banding
Chromosome Deletion
Chromosome Disorders
Chromosome Fragile Sites
Chromosome Fragility
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human, 13-15
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chromosomes, Human, X
Cleft Lip
Cleft Palate
Clone Cells
Coenzyme A Ligases
Cognition
Cognition Disorders
Cohort Studies
Communication
Comorbidity
Computational Biology
Congenital Abnormalities
Consanguinity
Constriction, Pathologic
Conversion Disorder
Copper
CpG Islands
Craniofacial Abnormalities
Culture Techniques
Cytogenetic Analysis
Dandy-Walker Syndrome
Databases, Factual
Databases, Genetic
Deafness
Death, Sudden, Cardiac
Deglutition Disorders
Delayed Diagnosis
Dementia
Demography
Dental Caries
Dental Enamel Hypoplasia
Depressive Disorder, Major
Developmental Disabilities
Diabetes Mellitus
Diabetes Mellitus, Type 2
Diagnosis, Differential
Diagnostic Errors
Diaphragm
Dietary Supplements
Disabled Children
Disease Models, Animal
Diseases in Twins
DNA
DNA Copy Number Variations
DNA Glycosylases
DNA Mutational Analysis
DNA Primers
DNA-(Apurinic or Apyrimidinic Site) Lyase
DNA, Complementary
DNA-Binding Proteins
Down Syndrome
Ductus Arteriosus, Patent
Echocardiography
Elastin
Electric Conductivity
Electrocardiography
Electromyography
Electrophoresis, Gel, Pulsed-Field
Elliptocytosis, Hereditary
Embryo, Mammalian
Emotions
Encephalocele
Ephrin-B1
Epidemiologic Methods
Erythrocyte Indices
Erythrocyte Transfusion
Erythrocytes
Euchromatin
Evaluation Studies as Topic
Exons
Expressed Emotion
Expressed Sequence Tags
Extremities
Exudates and Transudates
Eye Abnormalities
Eye Diseases, Hereditary
Face
Facial Bones
Facial Expression
Failure to Thrive
False Negative Reactions
False Positive Reactions
Family
Family Health
Fatal Outcome
Fathers
Fatty Acids
Fatty Acids, Nonesterified
Female
Fetal Death
Fetal Diseases
Fetal Growth Retardation
Fetus
Fingers
Follicle Stimulating Hormone
Follow-Up Studies
Foot Deformities, Congenital
Forkhead Transcription Factors
Friends
Frizzled Receptors
GATA4 Transcription Factor
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Regulation
Gene Expression Regulation, Developmental
Genes, Dominant
Genes, Overlapping
Genes, Recessive
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Linkage
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genitalia
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genotype
Germ-Line Mutation
Gestational Age
Gonadal Dysgenesis
Growth Disorders
Guidelines as Topic
Hair
Hair Color
Hamartoma Syndrome, Multiple
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Happiness
Head
Health Care Surveys
Health Status Disparities
Health Surveys
Hearing Loss, Sensorineural
Heart Defects, Congenital
Heart Rate
Heart Ventricles
Hedgehog Proteins
Hematologic Diseases
Hemizygote
Hernia, Diaphragmatic
Hernia, Inguinal
Heterozygote
Histocytochemistry
Homeodomain Proteins
Homozygote
Hospitals
Humans
Hydrocephalus
Hypercalcemia
Hypercalciuria
Hypertelorism
Hypertension
Imaging, Three-Dimensional
Immunoenzyme Techniques
In Situ Hybridization
In Situ Hybridization, Fluorescence
Infant
Infant Mortality
Infant, Newborn
Infant, Newborn, Diseases
Infertility
Informed Consent
Insulin
Intelligence
Interferon Regulatory Factors
Interpersonal Relations
Introns
Jamaica
Jaw Relation Record
Karyotyping
Kidney
Kidney Diseases
Kidney Tubules
Kv1.1 Potassium Channel
Lamin Type A
Lamins
Lasers
Lim Kinases
Limb Deformities, Congenital
Linear Models
Lipid Metabolism
Lipid Metabolism, Inborn Errors
Liver
Liver Failure, Acute
Long QT Syndrome
Lung
Luteinizing Hormone
Lyases
Lymphedema
Lymphocytes
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Male
Malocclusion
Mandibulofacial Dysostosis
Maternal Exposure
Maternal Nutritional Physiological Phenomena
Maternal-Fetal Exchange
Medical Records
Membrane Proteins
Memory
Meningomyelocele
Mental Disorders
Mental Recall
Mesoderm
Meta-Analysis as Topic
Mice
Mice, Inbred C57BL
Mice, Knockout
Microsatellite Repeats
Middle Aged
Models, Anatomic
Models, Biological
Models, Genetic
Molecular Sequence Data
Mosaicism
Multigene Family
Multiple Endocrine Neoplasia
Muscle Proteins
Muscle Tonus
Muscle, Smooth, Vascular
Muscular Atrophy, Spinal
Muscular Dystrophies
Muscular Dystrophy, Emery-Dreifuss
Musculoskeletal Abnormalities
Musculoskeletal Diseases
Mutation
Mutation, Missense
Myocytes, Smooth Muscle
Myokymia
Myopia
Nails, Malformed
Necrosis
Neoplasms
Nephritis, Hereditary
Nephrocalcinosis
Nephrolithiasis
Nerve Tissue Proteins
Neural Crest
Neural Tube Defects
Neurofibrillary Tangles
Neurologic Examination
Nicotine
Nonprescription Drugs
Noonan Syndrome
Nuclear Proteins
Nucleic Acid Hybridization
Nutritional Physiological Phenomena
Obsessive Behavior
Obsessive-Compulsive Disorder
Organ Size
Orofaciodigital Syndromes
Osteoblasts
Osteogenesis
Osteoporosis
Oxidation-Reduction
Oxidative Stress
Parenteral Nutrition
Parenteral Nutrition, Total
Parents
Patient Care Team
Patient Education as Topic
Patient Preference
Pattern Recognition, Automated
Pedigree
Peer Group
Penetrance
Perception
Persistent Fetal Circulation Syndrome
Phenotype
Phosphoric Monoester Hydrolases
Phylogeny
Physical Chromosome Mapping
Physical Examination
Physical Therapy Modalities
Placenta
Point Mutation
Polymerase Chain Reaction
Polymorphism, Genetic
Potassium Channels
Potassium Channels, Voltage-Gated
Prediabetic State
Pregnancy
Pregnancy Complications
Pregnancy Trimester, Second
Pregnancy Trimester, Third
Prenatal Diagnosis
Prevalence
Primary Ovarian Insufficiency
Professional-Patient Relations
Prognosis
Prospective Studies
Protein Kinases
Proteins
Proteinuria
Proteomics
Pseudogenes
Psychiatric Status Rating Scales
Psychopharmacology
Psychotic Disorders
Psychotropic Drugs
PTEN Phosphohydrolase
Puberty, Precocious
Pulmonary Circulation
Pulmonary Disease, Chronic Obstructive
Pulmonary Emphysema
Pulmonary Valve
Quality of Life
Rare Diseases
Receptors, G-Protein-Coupled
Receptors, Neurotransmitter
Renal Tubular Transport, Inborn Errors
Repressor Proteins
Reproduction
Research Design
Respiration, Artificial
Respiratory Function Tests
Respiratory System Abnormalities
Retinal Diseases
Retroelements
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
Review Literature as Topic
Ring Chromosomes
Risk
Risk Factors
RNA
Saccharomyces cerevisiae Proteins
Sensitivity and Specificity
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Severity of Illness Index
Sex Characteristics
Sex Factors
Siblings
Signal Transduction
Sirolimus
Skin
Skin Abnormalities
Skull
Smoking
SOXF Transcription Factors
Spasms, Infantile
Spinal Cord
Stroke
Structure-Activity Relationship
Sulfur
Survival Rate
Syndrome
Syntaxin 1
Tetralogy of Fallot
Thiocyanates
Tics
Time Factors
Tissue Distribution
Toes
Tomography, X-Ray Computed
Tongue Habits
Tooth Abnormalities
Tooth Diseases
TOR Serine-Threonine Kinases
Trachea
Trans-Activators
Transcription Factor AP-2
Transcription Factors
Transcription, Genetic
Translocation, Genetic
Treatment Outcome
Trisomy
Truth Disclosure
Tumor Suppressor Proteins
Twins, Monozygotic
Ultrasonography
Ultrasonography, Doppler, Transcranial
Ultrasonography, Prenatal
Uniparental Disomy
United States
Urinary Tract Infections
Vascular Diseases
Vascular Resistance
Vasoconstriction
Vertical Dimension
Vitreous Body
Williams Syndrome
Wnt Proteins
X Chromosome
X Chromosome Inactivation
Y Chromosome
Young Adult
Zinc Fingers
Pober's Networks
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Concepts (495)
Derived automatically from this person's publications.
Chromosome Deletion
Diaphragm
Abnormalities, Multiple
Hernia, Diaphragmatic
Williams Syndrome
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Co-Authors (51)
People in Profiles who have published with this person.
Stanley, Takara
Donahoe, Patricia
Lin, Angela
McDougle, Christopher
Thom, Robyn
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Similar People (60)
People who share similar concepts with this person.
Galaburda, Al
Alkuraya, Fowzan
McDougle, Christopher
Chung, Wendy
Thom, Robyn
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_
Same Department
People in same department with this person.
Black, Peter
Kleinman, Paul
Neutra, Marian
Taylor, George
Treves, Ted
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_
Physical Neighbors
People whose addresses are nearby this person.
Wilhelm, Sabine
Fischer, Sylvia
Wang, Betty
Wittner, Ben
Flannick, Jason
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