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ELIZABETH ROEDER
Concepts (396)
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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
Acidosis, Lactic
Acrocephalosyndactylia
Actins
Adolescent
Adult
Aged
Agenesis of Corpus Callosum
Algorithms
Alleles
alpha-Fetoproteins
Alu Elements
Amino Acid Sequence
Amino Acid Substitution
Amino Acids
Amino Acids, Sulfur
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 and Bones
Bone Diseases, Metabolic
Brain
Brain Neoplasms
Branchio-Oto-Renal Syndrome
Cardiovascular Abnormalities
Carrier Proteins
Cataract
Cataract Extraction
Cell Adhesion Molecules
Cell Cycle Proteins
Cell Movement
Cerebellar Ataxia
Cerebellar Neoplasms
Cerebellum
Cerebral Arteries
Child
Child, Preschool
CHO Cells
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 12
Chromosomes, Human, Pair 13
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 19
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
Corpus Callosum
COS Cells
Cranial Fontanelles
Craniofacial Abnormalities
Craniosynostoses
Cricetinae
CRISPR-Cas Systems
Cyclophosphamide
Cystathionine beta-Synthase
Cystine
Cytoskeleton
Dandy-Walker Syndrome
De Lange Syndrome
Decision Trees
Delivery, Obstetric
Developmental Disabilities
Diagnosis, Differential
Disease Models, Animal
Disorders of Sex Development
DNA
DNA Copy Number Variations
DNA Mutational Analysis
DNA Repair
DNA, Complementary
DNA-Binding Proteins
Down-Regulation
Drosophila
Drosophila Proteins
Drug Resistance
Dysostoses
Dystonic Disorders
Ear, External
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
Fibroblasts
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 Library
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 Testing
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
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Head and Neck Neoplasms
Hearing Disorders
Hearing Loss
Heart Defects, Congenital
Heart Septal Defects, Atrial
HEK293 Cells
Hepatoblastoma
Hepatocyte Nuclear Factor 1-beta
Hernia, Diaphragmatic
Hernia, Hiatal
Hernias, Diaphragmatic, Congenital
Heterozygote
High-Throughput Nucleotide Sequencing
Hirsutism
Histone Acetyltransferases
Histone Deacetylases
Histones
Holoprosencephaly
Homeodomain Proteins
Homocystine
Homocystinuria
Homozygote
Humans
Hybrid Cells
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
Introns
Joint Instability
Karyotyping
Kidney
Kruppel-Like Transcription Factors
Language Development Disorders
Leukocytes, Mononuclear
Leukoencephalopathies
Limb Deformities, Congenital
Lipoprotein(a)
Liver Neoplasms
Lod Score
Long Interspersed Nucleotide Elements
Loss of Function Mutation
Lupus Erythematosus, Systemic
Lymphocytes
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
MAP Kinase Kinase 6
Maternal-Fetal Exchange
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
Micrognathism
Microphthalmos
Microsatellite Repeats
Microtubule-Associated Proteins
Middle Aged
Mitochondria
Models, Genetic
Models, Molecular
Molecular Biology
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
Neoplastic Syndromes, Hereditary
Nephrosis
Nephrotic Syndrome
Neurodegenerative Diseases
Neurodevelopmental Disorders
Nipples
Noonan Syndrome
Nuclear Proteins
Nucleic Acid Hybridization
Nutritional Status
Oligonucleotide Array Sequence Analysis
Osteochondrodysplasias
Otx Transcription Factors
Oxytocin
Pandemics
Paraganglioma
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, Genetic
Polymorphism, Single Nucleotide
Polymorphism, Single-Stranded Conformational
Prader-Willi Syndrome
Pre-Eclampsia
Pregnancy
Pregnancy Complications
Pregnancy Complications, Neoplastic
Pregnancy Outcome
Prenatal Diagnosis
Prevalence
Promoter Regions, Genetic
Prosencephalon
Prostate
Proteasome Endopeptidase Complex
Protein C
Protein Conformation
Protein Isoforms
Protein S
Protein Tyrosine Phosphatases
Prothrombin
Psychomotor Disorders
Pulmonary Alveoli
Pulmonary Veins
Pyridoxine
Radiography
Receptor, Fibroblast Growth Factor, Type 2
Receptors, Odorant
Receptors, Retinoic Acid
Recombination, Genetic
Recurrence
Repetitive Sequences, Nucleic Acid
Repressor Proteins
Reproduction
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 Abnormalities
Skin Neoplasms
Small-Conductance Calcium-Activated Potassium Channels
Smith-Magenis Syndrome
Software
SOX9 Transcription Factor
Spinal Cord Neoplasms
Stroke
Syndrome
Telomere Homeostasis
Teratogens
Tetrasomy
Tomography, X-Ray Computed
TOR Serine-Threonine Kinases
Trans-Activators
Transcription Factors
Transcription, Genetic
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
Zinc Fingers
ROEDER's Networks
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Concepts (396)
Derived automatically from this person's publications.
Neurodevelopmental Disorders
Intellectual Disability
Abnormalities, Multiple
De Lange Syndrome
Phenotype
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Co-Authors (55)
People in Profiles who have published with this person.
CHEUNG, SAU WAI
LUPSKI, JAMES
STANKIEWICZ, PAWEL
LITTLEJOHN, REBECCA
SZAFRANSKI, PRZEMYSLAW
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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.
AKMAN, BENJAMIN
MCLEAN, SCOTT
NUTTER, MORGAN
STUEBBEN, MELISSA
WASKOW, EMILY
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_
Physical Neighbors
People whose addresses are nearby this person.
DONARUMA-KWOH, MARCELLA
DREYER, ZOANN
LITTLEJOHN, REBECCA
MCLEAN, SCOTT
PIERSON, STACY
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