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ELIZABETH ROEDER
Concepts (328)
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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.
Abnormalities, Multiple
Acidosis, Lactic
Acrocephalosyndactylia
Actins
Adolescent
Adult
Aged
Agenesis of Corpus Callosum
Alleles
alpha-Fetoproteins
Alu Elements
Amino Acid Sequence
Amino Acid Substitution
Amino Acyl-tRNA Synthetases
Amniocentesis
Anemia, Diamond-Blackfan
Animals
Antibodies, Antiphospholipid
Antithrombin III
Anxiety
Apoptosis
Arginine
Arrhythmias, Cardiac
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Autistic Disorder
Autopsy
Base Sequence
Beckwith-Wiedemann Syndrome
Blepharophimosis
Bone Diseases, Metabolic
Carrier Proteins
Cataract
Cataract Extraction
Cell Adhesion Molecules
Cell Cycle Proteins
Cell Movement
Cerebellar Ataxia
Cerebellar Neoplasms
Cerebral Arteries
Child
Child, Preschool
Chondroitin Sulfate Proteoglycans
Chromatin Assembly and Disassembly
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Mapping
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chromosomes, Human, X
Cleavage And Polyadenylation Specificity Factor
Cleft Palate
Cockayne Syndrome
Codon, Terminator
Cognition Disorders
Cohort Studies
Colon
Comparative Genomic Hybridization
Congenital Hypothyroidism
Cornea
COS Cells
Cranial Fontanelles
Craniofacial Abnormalities
Craniosynostoses
CRISPR-Cas Systems
Cystine
Cytoskeleton
De Lange Syndrome
Developmental Disabilities
Diagnosis, Differential
Disease Models, Animal
Disorders of Sex Development
DNA Copy Number Variations
DNA Mutational Analysis
DNA Repair
DNA, Complementary
DNA-Binding Proteins
Down-Regulation
Dysostoses
Dystonic Disorders
Electrophysiological Phenomena
Endopeptidases
Endoplasmic Reticulum Stress
Epilepsy
Evolution, Molecular
Exome
Exons
Extracellular Matrix Proteins
Eye Abnormalities
Face
Facies
Factor V
Family
Family Health
Fatal Outcome
Female
Follow-Up Studies
Forkhead Transcription Factors
Fractures, Bone
Fragile X Mental Retardation Protein
Frameshift Mutation
Gain of Function Mutation
Gene Deletion
Gene Dosage
Gene Duplication
Gene Knockout Techniques
Gene Order
Gene Rearrangement
Genes, Dominant
Genes, Lethal
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Linkage
Genetic Loci
Genetic Predisposition to Disease
Genetic Variation
Genitalia
Genitalia, Female
Genitalia, Male
Genome, Human
Genomic Imprinting
Genomic Instability
Genomics
Genotype
Germ Cells
Gigantism
Glaucoma
Glutamate-tRNA Ligase
Glycoproteins
Glypicans
Growth Disorders
Haploinsufficiency
Hearing Loss
Heart Defects, Congenital
HEK293 Cells
Hepatocyte Nuclear Factor 1-beta
Hernia, Diaphragmatic
Hernia, Hiatal
Hernias, Diaphragmatic, Congenital
Heterozygote
High-Throughput Nucleotide Sequencing
Histone Acetyltransferases
Histone Deacetylases
Holoprosencephaly
Homeodomain Proteins
Homozygote
Humans
Hyperphagia
Hypertelorism
Image Processing, Computer-Assisted
In Situ Hybridization, Fluorescence
INDEL Mutation
Infant
Infant, Newborn
Inheritance Patterns
Intellectual Disability
Intestinal Pseudo-Obstruction
Intracellular Signaling Peptides and Proteins
Intracranial Thrombosis
Joint Instability
Karyotyping
Kidney
Kruppel-Like Transcription Factors
Language Development Disorders
Leukocytes, Mononuclear
Leukoencephalopathies
Lipoprotein(a)
Long Interspersed Nucleotide Elements
Loss of Function Mutation
Lymphocytes
Magnetic Resonance Imaging
Male
MAP Kinase Kinase 6
Matrix Attachment Region Binding Proteins
Medulloblastoma
Megalencephaly
Membrane Proteins
Mental Disorders
Metabolism, Inborn Errors
Metalloendopeptidases
Methyl-CpG-Binding Protein 2
Methylenetetrahydrofolate Reductase (NADPH2)
Mi-2 Nucleosome Remodeling and Deacetylase Complex
Mice
Mice, Inbred C3H
Mice, Inbred C57BL
Microcephaly
Microphthalmos
Microsatellite Repeats
Microtubule-Associated Proteins
Middle Aged
Mitochondria
Models, Genetic
Models, Molecular
Molecular Diagnostic Techniques
Molecular Sequence Data
Mosaicism
Movement Disorders
Multigene Family
Multiprotein Complexes
Muscle Hypotonia
Musculoskeletal Abnormalities
Mutagenesis, Site-Directed
Mutation
Mutation, Missense
Myotonic Dystrophy
Myotonin-Protein Kinase
Nephrosis
Nephrotic Syndrome
Neurodevelopmental Disorders
Noonan Syndrome
Nuclear Proteins
Nucleic Acid Hybridization
Oligonucleotide Array Sequence Analysis
Otx Transcription Factors
Oxytocin
Pandemics
Patch-Clamp Techniques
Patella
Pathology, Molecular
Pedigree
Pelvis
Penis
Persistent Fetal Circulation Syndrome
Phenotype
Phylogeny
Pierre Robin Syndrome
Pituitary Gland
Placenta
Podocytes
Point Mutation
Polyadenylation
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Prader-Willi Syndrome
Pre-Eclampsia
Pregnancy
Pregnancy Outcome
Prevalence
Promoter Regions, Genetic
Prosencephalon
Prostate
Proteasome Endopeptidase Complex
Protein C
Protein Conformation
Protein Isoforms
Protein S
Prothrombin
Psychomotor Disorders
Pulmonary Alveoli
Pulmonary Veins
Radiography
Receptor, Fibroblast Growth Factor, Type 2
Receptors, Odorant
Receptors, Retinoic Acid
Recombination, Genetic
Recurrence
Repressor Proteins
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
Ring Chromosomes
Risk Factors
RNA Processing, Post-Transcriptional
RNA Splicing
RNA, Messenger
RNA, Transfer
Saccule and Utricle
Scapula
Schizophrenia
Scrotum
Segmental Duplications, Genomic
Seizures
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Serine
Sex Distribution
Shoulder
Siblings
Skin Neoplasms
Small-Conductance Calcium-Activated Potassium Channels
Smith-Magenis Syndrome
SOX9 Transcription Factor
Spinal Cord Neoplasms
Stroke
Syndrome
Telomere Homeostasis
Tetrasomy
Tomography, X-Ray Computed
TOR Serine-Threonine Kinases
Trans-Activators
Transcription Factors
Transcriptional Activation
Transcriptional Elongation Factors
Transfection
Translocation, Genetic
Trisomy
Ubiquitin-Protein Ligases
Ultraviolet Rays
Urethral Diseases
Urinary Bladder
Urogenital Abnormalities
White Matter
Whole Genome Sequencing
X Chromosome Inactivation
Xenopus
Young Adult
Zebrafish
Zebrafish Proteins
Zinc Finger Protein Gli2
ROEDER's Networks
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Concepts (328)
Derived automatically from this person's publications.
Neurodevelopmental Disorders
Intellectual Disability
De Lange Syndrome
Abnormalities, Multiple
Chromosomes, Human, X
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Co-Authors (54)
People in Profiles who have published with this person.
CHEUNG, SAU WAI
LUPSKI, JAMES
STANKIEWICZ, PAWEL
SZAFRANSKI, PRZEMYSLAW
BI, WEIMIN
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
STANKIEWICZ, PAWEL
GIBBS, RICHARD
CHEUNG, SAU WAI
ELSEA, SARAH
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_
Same Department
People who are also in this person's primary department.
JUAREZ, OLIVIA
LITTLEJOHN, REBECCA
NUTTER, MORGAN
ODOM, JOHN
SCHMID, CARRIE
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Physical Neighbors
People whose addresses are nearby this person.
CHACKO, SHEEBU
GREEN, CAROL
LITTLEJOHN, REBECCA
MCLEAN, SCOTT
RUSSELL, HEIDI
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