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Pediatrics CRA
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LISA EMRICK
Concepts (333)
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Concepts are derived automatically from a person's publications.
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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.
14-3-3 Proteins
1-Alkyl-2-acetylglycerophosphocholine Esterase
Abnormalities, Multiple
Acidosis, Lactic
Adolescent
Adult
Age of Onset
AIDS-Related Opportunistic Infections
Alleles
Alternative Splicing
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Amitriptyline
Amniotic Fluid
Animals
Animals, Genetically Modified
Aniridia
Apyrase
Arabs
Arginine
Arginine-tRNA Ligase
Argininosuccinate Lyase
Argininosuccinate Synthase
Aromatic-L-Amino-Acid Decarboxylases
Arrhythmias, Cardiac
Ascorbic Acid
Ataxia
Autism Spectrum Disorder
Autistic Disorder
Autoimmune Diseases of the Nervous System
Base Sequence
Behavior, Animal
Bicarbonates
Biomedical Research
Bone and Bones
Brain
Brain Diseases
Caenorhabditis elegans
Caenorhabditis elegans Proteins
Calcineurin
Calcium Channels
Calcium Channels, L-Type
Calcium Channels, R-Type
Case-Control Studies
Cation Transport Proteins
CDC2 Protein Kinase
Cell Line
Cell Transdifferentiation
Cells, Cultured
Cerebellar Ataxia
Cerebellum
Cerebral Palsy
Cerebroside-Sulfatase
Child
Child, Preschool
Chloride-Bicarbonate Antiporters
Chromosomal Instability
Chromosome Deletion
Chromosomes, Human, Pair 17
Chronic Disease
Citrulline
Class I Phosphatidylinositol 3-Kinases
Clinical Trials as Topic
Coat Protein Complex I
Coatomer Protein
Codon, Nonsense
Cohort Studies
Collagen Type I
Common Data Elements
Congenital Abnormalities
Consensus
Craniofacial Abnormalities
Craniosynostoses
Cross-Over Studies
Cross-Sectional Studies
Cytomegalovirus Retinitis
Data Collection
Developmental Disabilities
Diabetes Mellitus
Diagnosis, Differential
Dietary Supplements
Dihydroxyphenylalanine
Disease Management
Disease Progression
DNA Copy Number Variations
DNA Damage
DNA Mutational Analysis
DNA-Binding Proteins
Dopa Decarboxylase
Drosophila melanogaster
Drosophila Proteins
Drug Administration Schedule
Drug Resistant Epilepsy
Drug Therapy, Combination
Dwarfism
Dysarthria
Dystonic Disorders
Early Diagnosis
Ectodermal Dysplasia
eIF-2 Kinase
Electroencephalography
Electron Transport
Electron Transport Complex IV
Embryo, Nonmammalian
Endoplasmic Reticulum
Endoplasmic Reticulum Stress
Epilepsy
Esophageal Motility Disorders
Exodeoxyribonucleases
Exome
Exons
Face
Facies
Family
F-Box Proteins
Female
Fetal Development
Fetus
Fibroblasts
Foscarnet
Frameshift Mutation
Fucosyltransferases
Gain of Function Mutation
Gait
Ganciclovir
Gene Deletion
Gene Expression
Gene Expression Regulation, Developmental
Genes, Mitochondrial
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Linkage
Genetic Predisposition to Disease
Genetic Testing
Genetic Therapy
Genetic Variation
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Gestational Age
Gluconeogenesis
Glucose
Glutathione
Glycosylation
Golgi Apparatus
Guanosine Diphosphate Fucose
Guanosine Diphosphate Mannose
Haploinsufficiency
Hearing Loss, Sensorineural
Heart Defects, Congenital
HeLa Cells
Hematopoietic Stem Cell Transplantation
Hemiplegia
Hereditary Central Nervous System Demyelinating Diseases
Hernias, Diaphragmatic, Congenital
Heterozygote
Homeodomain Proteins
Homozygote
Hospice and Palliative Care Nursing
Humans
Hydrocephalus
Immunologic Deficiency Syndromes
Immunophenotyping
Infant
Infant, Newborn
Infant, Newborn, Diseases
Inflammation
Inositol 1,4,5-Trisphosphate Receptors
Insulin
Insulin Resistance
Intellectual Disability
Interferon Type I
Interferon-Induced Helicase, IFIH1
Intracellular Signaling Peptides and Proteins
Introns
Iron
Isotope Labeling
Karyotyping
KCNQ2 Potassium Channel
Language Development Disorders
Leukodystrophy, Metachromatic
Leukoencephalopathies
Levodopa
Limb Deformities, Congenital
Lipoma
Liver Transplantation
Long QT Syndrome
Longitudinal Studies
Loss of Function Mutation
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Mandibulofacial Dysostosis
MAP Kinase Kinase Kinases
Matrix Attachment Region Binding Proteins
Megalencephaly
MELAS Syndrome
Membrane Proteins
Membrane Transport Proteins
Mental Disorders
Metabolomics
Mice
Mice, Knockout
Microcephaly
Microscopy, Electron, Transmission
Microtubule-Associated Proteins
Middle Aged
Migraine with Aura
Mitochondria
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Molecular Chaperones
Molecular Sequence Data
Mosaicism
Movement Disorders
Muscle Hypotonia
Muscle Proteins
Muscle Weakness
Musculoskeletal Abnormalities
Mutant Proteins
Mutation
Mutation, Missense
National Institute of Neurological Disorders and Stroke (U.S.)
Neonatal Screening
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Neural Cell Adhesion Molecule L1
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neuroglia
Neuroimaging
Neurologists
Neurology
Neurons
Nevus
NF-kappa B
Nitric Oxide
Nitric Oxide Donors
Nitric Oxide Synthase Type III
Nonsense Mediated mRNA Decay
Noonan Syndrome
Nuclear Proteins
Osteochondrodysplasias
Osteoporosis
Paraparesis, Spastic
Paraplegia
Pediatric Nursing
Pedigree
Peptide Elongation Factors
Peripheral Nervous System Diseases
Phenotype
Phosphatidylinositol 3-Kinases
Phosphoprotein Phosphatases
Phosphoproteins
Phosphotransferases (Alcohol Group Acceptor)
Physical Examination
Pigmentation Disorders
Pilot Projects
Point Mutation
Polymorphism, Single Nucleotide
Practice Guidelines as Topic
Pregnancy
Prenatal Diagnosis
Prognosis
Prospective Studies
Proteasome Endopeptidase Complex
Protein Isoforms
Protein Structure, Secondary
Proteins
Proteomics
rab GTP-Binding Proteins
Radiography
Rare Diseases
Reactive Nitrogen Species
Receptors, AMPA
Reproducibility of Results
Research Design
Retrospective Studies
Rhabdomyolysis
Ribonuclease H
Ribonucleoprotein, U5 Small Nuclear
RNA Splicing
RNA, Long Noncoding
RNA, Messenger
RNA, Small Interfering
RNA, Small Nuclear
RNA, Transfer, Leu
SAM Domain and HD Domain-Containing Protein 1
Scoliosis
Seizures
Separase
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Severity of Illness Index
Siblings
Signal Transduction
Skin
Sleep Stages
Sleep Wake Disorders
Sodium
Sodium Bicarbonate
Sodium-Bicarbonate Symporters
Sodium-Potassium-Exchanging ATPase
Spastic Paraplegia, Hereditary
Stroke
Symptom Assessment
Syndactyly
Syndrome
Thymidine
Thymidine Phosphorylase
TOR Serine-Threonine Kinases
Transcription Factors
Transcriptome
Transposases
Treatment Outcome
Tremor
Tyrosine
Ubiquitin
Ultrasonography, Prenatal
Unfolded Protein Response
United States
Vascular Malformations
Weight Gain
White Matter
Whole Genome Sequencing
Young Adult
Zebrafish
EMRICK's Networks
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Concepts (333)
Derived automatically from this person's publications.
Neurodevelopmental Disorders
Mitochondrial Diseases
Intellectual Disability
Leukoencephalopathies
Developmental Disabilities
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Co-Authors (107)
People in Profiles who have published with this person.
CALAME, DANIEL
BURRAGE, LINDSAY
SCAGLIA, FERNANDO
LALANI, SEEMA
ELSEA, SARAH
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
SCAGLIA, FERNANDO
GIBBS, RICHARD
BELLEN, HUGO
ELSEA, SARAH
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Same Department
People who are also in this person's primary department.
CHAO, HSIAO-TUAN
DUDLEY-HARRELL, HOLLY
DUGGAN, DEANNA
HULL, MARIAM
LAZAR, STEVEN
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Physical Neighbors
People whose addresses are nearby this person.
ABID, FARIDA
CASTRO-REYES, WILFRED
DIAZ-MEDINA, GLORIA
QUACH, MICHAEL
SETO, ELAINE
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