VIICTR Profiles
ORIT
Pediatrics CRA
Home
About
Overview
Sharing Data
ORCID
Help
History (0)
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
CHRISTINE ENG
Concepts (472)
Back to Profile
Concepts are derived automatically from a person's publications.
Cloud
Categories
Timeline
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
Achondroplasia
Acrocephalosyndactylia
Actins
Adaptor Proteins, Signal Transducing
Adaptor Proteins, Vesicular Transport
Adenosine Triphosphatases
Adolescent
Adult
Age of Onset
Aged
Aged, 80 and over
Alleles
alpha-Galactosidase
Alternative Splicing
Alu Elements
Amino Acid Metabolism, Inborn Errors
Amino Acid Motifs
Amino Acid Sequence
Amino Acid Substitution
Amino Acids
Amniocentesis
Amniotic Fluid
Animals
Antigens, Nuclear
Antineoplastic Agents
Arabs
Arrhythmias, Cardiac
Artificial Intelligence
ATPases Associated with Diverse Cellular Activities
ATP-Binding Cassette Transporters
Autism Spectrum Disorder
Autistic Disorder
Autophagy
Autopsy
Awards and Prizes
Axons
Base Sequence
Betacoronavirus
Bile Acids and Salts
Biological Variation, Population
Blotting, Western
Body Height
Body Temperature Regulation
Body Weight
Bone and Bones
Bone Diseases, Developmental
Brain
Brain Diseases
Brain Neoplasms
Brain Waves
Caenorhabditis elegans
Calcineurin
Carcinoma, Renal Cell
Cardiomyopathies
Cardiovascular Diseases
Career Choice
Carrier Proteins
Catalytic Domain
Cell Cycle
Cell Cycle Proteins
Cell Death
Cell Line
Cell Proliferation
Cell Transdifferentiation
Cell-Free Nucleic Acids
Cells, Cultured
Cerebrovascular Disorders
CHARGE Syndrome
Child
Child, Preschool
Choice Behavior
Cholestasis, Intrahepatic
Chorionic Villi Sampling
Chromatin Assembly and Disassembly
Chromosomal Instability
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes, Human
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, X
Chronic Disease
Cloning, Molecular
Codon
Cohort Studies
Collagen Type I
Colorectal Neoplasms
Colorectal Neoplasms, Hereditary Nonpolyposis
Comparative Genomic Hybridization
Computational Biology
Confidentiality
Congenital Abnormalities
Congenital Microtia
Consent Forms
Coronavirus Infections
Coroners and Medical Examiners
Craniofacial Abnormalities
Critical Care
Crystallography, X-Ray
Curriculum
Cysteine
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Cytokine Receptor gp130
Cytokines
Databases, Genetic
De Lange Syndrome
Death, Sudden
Decision Making
Developmental Disabilities
Diagnosis
Diagnosis, Differential
Disclosure
Disease
Disease Management
Disease Models, Animal
Diseases in Twins
DNA
DNA Copy Number Variations
DNA Damage
DNA Helicases
DNA Mismatch Repair
DNA Mutational Analysis
DNA Replication
DNA-Binding Proteins
Double-Blind Method
Down Syndrome
Drosophila
Drosophila melanogaster
Drug Administration Schedule
Drug Resistant Epilepsy
Drug Substitution
Drug Tolerance
Dwarfism
Dynamins
Dystrophin
Electroencephalography
Endocytosis
Endopeptidases
Endoplasmic Reticulum Stress
Endosomes
Enzyme Replacement Therapy
Epilepsy
Ethics, Medical
Everolimus
Exome
Exons
Extracellular Signal-Regulated MAP Kinases
Eye Abnormalities
Fabry Disease
Face
Facies
Failure to Thrive
Family
Family Health
Fathers
Feeding and Eating Disorders
Female
Fetal Diseases
Fetus
Fibroblasts
Follow-Up Studies
Forkhead Transcription Factors
Founder Effect
Fragile X Syndrome
Functional Laterality
Fusion Proteins, bcr-abl
Gastrointestinal Diseases
Gaucher Disease
Geminin
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Frequency
Gene Rearrangement
Genes, Dominant
Genes, Duplicate
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Linkage
Genetic Loci
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetics, Medical
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Genotyping Techniques
Germ Cells
Germ-Line Mutation
Glomerular Filtration Rate
Glucosylceramidase
Glycoproteins
Glycosaminoglycans
Golgi Apparatus
Growth Charts
Growth Disorders
GTP Phosphohydrolases
GTP-Binding Protein alpha Subunits
GTP-Binding Protein alpha Subunits, Gq-G11
GTP-Binding Protein beta Subunits
Hand Deformities, Congenital
Haploinsufficiency
Health Care Costs
Hearing Loss
Heart Defects, Congenital
Heart Diseases
HEK293 Cells
Hemoglobins
Hepatocyte Nuclear Factor 1-beta
Hereditary Central Nervous System Demyelinating Diseases
Heterogeneous-Nuclear Ribonucleoprotein U
Heterotaxy Syndrome
Heterozygote
High-Throughput Nucleotide Sequencing
History, 20th Century
Homologous Recombination
Homozygote
Humans
Hydrops Fetalis
Hypertrophy, Left Ventricular
Iduronate Sulfatase
Immunologic Deficiency Syndromes
Incidence
Incidental Findings
INDEL Mutation
Infant
Infant Care
Infant, Newborn
Informed Consent
Infusions, Intravenous
Inheritance Patterns
Injections, Intravenous
Insurance Coverage
Insurance, Health
Intellectual Disability
Intensive Care Units, Pediatric
Internship and Residency
Interview, Psychological
Intracellular Signaling Peptides and Proteins
Introns
Iris Diseases
Isoenzymes
Job Syndrome
Karyotype
Karyotyping
Kidney
Kidney Diseases
Kidney Failure, Chronic
Kidney Neoplasms
Laboratories
Language Development Disorders
Length of Stay
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Leukoencephalopathies
Limb Deformities, Congenital
Limit of Detection
Liver
Longitudinal Studies
Loss of Function Mutation
Lung Diseases
Lymphangioma, Cystic
Lysosomal Storage Diseases
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Male
MAP Kinase Signaling System
Mass Screening
Mass Spectrometry
Maternal Age
Medical Oncology
Megalencephaly
Membrane Proteins
Metabolomics
Metalloendopeptidases
Methods
Methyl-CpG-Binding Protein 2
Mice
Mice, Knockout
Microarray Analysis
Microcephaly
Microfilament Proteins
Micrognathism
Middle Aged
Minor Histocompatibility Antigens
Mitochondria
Mitochondrial Diseases
Mitochondrial Proteins
Models, Animal
Models, Molecular
Molecular Diagnostic Techniques
Molecular Dynamics Simulation
Molecular Sequence Data
Mosaicism
Mothers
Mucopolysaccharidosis II
Multiprotein Complexes
Munc18 Proteins
Muscle Hypotonia
Muscle Spasticity
Muscle Weakness
Muscles
Muscular Atrophy, Spinal
Muscular Dystrophy, Duchenne
Musculoskeletal Abnormalities
Musculoskeletal System
Mutation
Mutation, Missense
MutL Protein Homolog 1
MutS Homolog 2 Protein
Myelin Sheath
Myoclonic Epilepsies, Progressive
NADPH Oxidases
National Human Genome Research Institute (U.S.)
National Institutes of Health (U.S.)
Neoplasms
Neoplastic Syndromes, Hereditary
Nephrons
Nerve Tissue Proteins
Nervous System Diseases
Neuralgia
Neurocutaneous Syndromes
Neurodevelopmental Disorders
Neurons
NF-kappa B
Noonan Syndrome
Nuchal Translucency Measurement
Nuclear Proteins
Nucleic Acid Amplification Techniques
Nucleic Acid Hybridization
Oligonucleotide Array Sequence Analysis
Optic Atrophy
Organ Size
Organ Specificity
Oryzias
Osteochondrodysplasias
Osteogenesis Imperfecta
Otorhinolaryngologic Diseases
Outpatients
p21-Activated Kinases
Pandemics
Parents
Patella
Pathology, Molecular
Patient Preference
Patient Satisfaction
Patients
PAX2 Transcription Factor
Pedigree
Peroxisomes
Phenotype
Philadelphia Chromosome
Phosphoprotein Phosphatases
Phosphorylation
Physical and Rehabilitation Medicine
Physical Examination
Physicians
Pilot Projects
Platelet Count
Pneumonia, Viral
Point Mutation
Polyhydramnios
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Potassium Channels
Practice Guidelines as Topic
Predictive Value of Tests
Pregnancy
Prenatal Diagnosis
Problem Behavior
Proline-Rich Protein Domains
Prospective Studies
Proteasome Endopeptidase Complex
Protein Binding
Protein Conformation
Protein Stability
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Protein Tyrosine Phosphatases
Protein-Tyrosine Kinases
Proteolysis
Proto-Oncogene Proteins
Psychomotor Disorders
Pyrroline Carboxylate Reductases
Quality of Life
Rare Diseases
ras GTPase-Activating Proteins
Receptors, Cytoplasmic and Nuclear
Recombinant Proteins
Recombination, Genetic
Referral and Consultation
Registries
Renal Dialysis
Repressor Proteins
Reproducibility of Results
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
Rhabdomyolysis
RNA Splice Sites
RNA Splicing
Safety
Segmental Duplications, Genomic
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology, Amino Acid
Sex Characteristics
Signal Transduction
Sirolimus
Situs Inversus
Skin
Sleep Apnea Syndromes
Smith-Magenis Syndrome
Software
Spectrin
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Spinocerebellar Ataxias
Spleen
Students, Medical
Sudden Infant Death
Surveys and Questionnaires
Survival of Motor Neuron 1 Protein
Survival of Motor Neuron 2 Protein
Sweating
Syndrome
Telemedicine
Texas
Thanatophoric Dysplasia
TOR Serine-Threonine Kinases
Transcription Factors
Transcriptome
Transfection
Transferrin
Translocation, Genetic
Transposases
Treatment Outcome
Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
Tumor Protein p73
Tumor Suppressor Proteins
Twins, Monozygotic
Ubiquitin-Protein Ligases
Ultrasonography
Ultrasonography, Prenatal
Uniparental Disomy
United States
Urinary Tract
Urogenital Abnormalities
Vesico-Ureteral Reflux
Vesicular Transport Proteins
Vital Capacity
Xenopus laevis
Young Adult
Zebrafish
ENG's Networks
Click the
Explore
buttons for more information and interactive visualizations!
Concepts (472)
Derived automatically from this person's publications.
Genetic Diseases, Inborn
Exome
Sequence Analysis, DNA
Genetic Testing
Prenatal Diagnosis
Explore
_
Co-Authors (141)
People in Profiles who have published with this person.
GIBBS, RICHARD
LUPSKI, JAMES
XIA, FAN
PLON, SHARON
MUZNY, DONNA
Explore
_
Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
GIBBS, RICHARD
BOERWINKLE, ERIC
MUZNY, DONNA
STANKIEWICZ, PAWEL
Explore
_
Same Department
People who are also in this person's primary department.
BONNEN, PENELOPE
GIJAVANEKAR, CHARUL
JEONG, MIRA
LORENZO, ISABEL
SZAFRANSKI, PRZEMYSLAW
Explore
_