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Monica Hsiung Wojcik, M.D.
Concepts (297)
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Concepts are derived automatically from a person's publications.
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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.
3' Untranslated Regions
Abnormalities, Multiple
Access to Information
Accidents
Acetyltransferases
Acyl-CoA Oxidase
Adaptor Proteins, Signal Transducing
Adenosine Triphosphatases
Adolescent
Adult
Age of Onset
Aged
Aged, 80 and over
Alleles
Amino Acid Sequence
Amniocentesis
Amyloid
Anemia
Aneuploidy
Angelman Syndrome
Animals
Anodontia
Anorexia Nervosa
Antigens, Surface
Ataxia
Autistic Disorder
Autopsy
Beckwith-Wiedemann Syndrome
Bilirubin
Blood Glucose
Body Height
Body Mass Index
Bone Density
Brain
Brain Diseases
Brain Edema
Canada
Carrier Proteins
Catalytic Domain
Cause of Death
Cell Adhesion
Cell Line
Cell Nucleolus
Cell Nucleus
Cerebellar Ataxia
CHARGE Syndrome
Child
Child, Preschool
Chromatin
Chromosome Aberrations
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 7
Chronic Disease
Chylothorax
Cleft Lip
Cleft Palate
Clubfoot
Cohort Studies
Computational Biology
Congenital Abnormalities
Consensus
Craniofacial Abnormalities
Critical Illness
Cross-Sectional Studies
Cyclin-Dependent Kinase Inhibitor p57
Cytoplasm
Cytoskeletal Proteins
Databases, Genetic
Death, Sudden
Delayed Diagnosis
Delivery of Health Care
Developmental Disabilities
Diabetes Insipidus
Diagnosis, Differential
Diet
DiGeorge Syndrome
Disease Models, Animal
DNA Copy Number Variations
DNA Helicases
DNA Methylation
DNA, Mitochondrial
DNA-Binding Proteins
DNA-Directed RNA Polymerases
Drosophila melanogaster
Drosophila Proteins
Ductus Arteriosus, Patent
Dystonia
Early Diagnosis
Echocardiography
Edema
Elastin
Embryo, Nonmammalian
Epigenesis, Genetic
Epilepsy
Estonia
Exodeoxyribonucleases
Exons
Face
Facies
Family Characteristics
Fatal Outcome
Female
Fetus
Fibroblast Growth Factors
Fibroblasts
Fingers
Finland
Flavoproteins
Focus Groups
Follow-Up Studies
Forecasting
Forkhead Transcription Factors
Gene Deletion
Gene Dosage
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Genes, Dominant
Genetic Association Studies
Genetic Complementation Test
Genetic Diseases, Inborn
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomics
Genotype
Germ-Line Mutation
Glucose Tolerance Test
Glycoproteins
Glycosylation
Growth Disorders
GTPase-Activating Proteins
Haploinsufficiency
Health Personnel
Health Services Accessibility
Health Status Disparities
Healthcare Disparities
Heart Defects, Congenital
Heart Septal Defects, Ventricular
Hematologic Diseases
Hernia, Abdominal
Hernia, Diaphragmatic
Hernia, Ventral
Heterozygote
High-Throughput Nucleotide Sequencing
Hippocampus
Histone Demethylases
Histone-Lysine N-Methyltransferase
Histones
Homozygote
Hospitals
Hospitals, Pediatric
Human Growth Hormone
Humans
Hydrops Fetalis
Hypocalcemia
Hypoxanthine Phosphoribosyltransferase
In Situ Hybridization, Fluorescence
Infant
Infant Mortality
Infant, Low Birth Weight
Infant, Newborn
Infant, Newborn, Diseases
Infant, Premature
Infant, Premature, Diseases
Information Dissemination
Information Storage and Retrieval
Insulin
Insulin Resistance
Intensive Care Units, Neonatal
Intestinal Obstruction
Intracellular Signaling Peptides and Proteins
Introns
Islet Amyloid Polypeptide
Jaundice, Neonatal
Jumonji Domain-Containing Histone Demethylases
Larva
Lesch-Nyhan Syndrome
Lipids
Logistic Models
Loss of Heterozygosity
Magnetic Resonance Imaging
Male
Marfan Syndrome
Methylation
Mice
Middle Aged
Minority Groups
Minority Health
Mitochondria
Mitochondrial Proteins
Mixed Function Oxygenases
Models, Molecular
Multicenter Studies as Topic
Muscle Hypotonia
Mutation
Mutation, Missense
N-Acetylglucosaminyltransferases
Neonatal Screening
Neonatology
Neoplasm Proteins
Neoplasms
Nervous System Diseases
Nervous System Malformations
Neurodegenerative Diseases
Neuropsychological Tests
Noonan Syndrome
Nuclear Proteins
Nuclear Receptor Subfamily 1, Group F, Member 1
Obesity
Olivopontocerebellar Atrophies
Optic Atrophy
Oxidative Phosphorylation
Palliative Care
Patient Discharge
Patient Selection
Pedigree
Peripheral Nervous System Diseases
Phenotype
Phenylketonurias
Phosphoproteins
Phosphoric Monoester Hydrolases
Pierre Robin Syndrome
Point-of-Care Systems
Polyadenylation
Polymerase Chain Reaction
Polymorphism, Genetic
POU Domain Factors
Prader-Willi Syndrome
Predictive Value of Tests
Pregnancy
Prenatal Diagnosis
Prevalence
Prospective Studies
Protein Conformation
Protein Processing, Post-Translational
Protein Subunits
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Pulmonary Emphysema
Purkinje Cells
Quality Improvement
Rare Diseases
Recurrence
Referral and Consultation
Repressor Proteins
Retrospective Studies
Ribonucleoproteins
Risk Assessment
Risk Factors
RNA Splice Sites
RNA Transport
RNA, Messenger
RNA, Small Nuclear
RNA-Binding Proteins
Seizures
Sequence Analysis, DNA
Sequence Homology
Severity of Illness Index
Signal Transduction
Silver-Russell Syndrome
Software
Spasms, Infantile
Spinal Muscular Atrophies of Childhood
Spliceosomes
Stillbirth
Structure-Activity Relationship
Sudden Infant Death
Syndrome
Transcription Factor AP-2
Transcription Factors
Transcription, Genetic
Transcriptional Activation
Turner Syndrome
Ubiquitin-Protein Ligases
Ultrasonography, Prenatal
United States
Vena Cava, Superior
Vestibular Diseases
Vital Statistics
Vomiting
Williams Syndrome
Wolf-Hirschhorn Syndrome
Young Adult
Zebrafish
Zebrafish Proteins
Wojcik's Networks
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Concepts (297)
Derived automatically from this person's publications.
Genetic Testing
Infant Mortality
Intensive Care Units, Neonatal
Genetic Diseases, Inborn
Rare Diseases
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Co-Authors (100)
People in Profiles who have published with this person.
Holm, Ingrid
Rehm, Heidi
Goldstein, Richard
O'Donnell Luria, Anne
Fraiman, Yarden
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_
Similar People (60)
People who share similar concepts with this person.
Green, Robert
Rehm, Heidi
Alkuraya, Fowzan
Chung, Wendy
Inder, Terrie
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_
Same Department
People in same department with this person.
Church, Paige
Cummings, Christy
D'Gama, Alissa
Hay, Susanne
Perrier, Stefanie
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_