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MICHAEL WANGLER
Concepts (360)
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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.
Abdominal Neoplasms
Abnormalities, Multiple
Actins
Acyl-CoA Oxidase
Adenocarcinoma, Mucinous
Adenosine Triphosphatases
Adolescent
Adrenoleukodystrophy
Adult
Age of Onset
Aged
Aged, 80 and over
Algorithms
Alleles
alpha-Fetoproteins
Amino Acid Sequence
Amino Acid Substitution
Animals
Animals, Genetically Modified
Aortic Aneurysm
Arginine
Ataxia
Ataxia Telangiectasia
Ataxia Telangiectasia Mutated Proteins
ATPases Associated with Diverse Cellular Activities
ATP-Binding Cassette Transporters
Autism Spectrum Disorder
Autistic Disorder
Autophagy
Axons
Base Sequence
Beckwith-Wiedemann Syndrome
Behavior, Animal
beta Catenin
beta Karyopherins
Bias
Biomarkers
Blastomeres
Body Dysmorphic Disorders
Bone Morphogenetic Proteins
Brain
Brain Diseases
Caenorhabditis elegans
Calcium Channels
Calcium Channels, N-Type
Carbohydrate Metabolism
Carcinoma, Hepatocellular
Cardiovascular Abnormalities
Cardiovascular System
Carrier Proteins
Cartilage
Cataract
Cell Nucleus
Cell Polarity
Central Nervous System
Cerebellar Ataxia
Cerebellum
Channelopathies
Child
Child, Preschool
Chromatography, Liquid
Chromosomal Proteins, Non-Histone
Cluster Analysis
Cognition
Cohort Studies
Collagen Type XI
Coloboma
Colon
Combined Modality Therapy
Computational Biology
Congenital Abnormalities
Corpus Callosum
Craniofacial Abnormalities
Critical Care
Cross-Sectional Studies
Cyclin-Dependent Kinase 8
Cyclin-Dependent Kinases
Cytoskeletal Proteins
Cytoskeleton
Databases, Factual
Databases, Genetic
Developmental Disabilities
Diagnosis, Computer-Assisted
Diagnosis, Differential
DiGeorge Syndrome
Disease
Disease Management
Disease Models, Animal
DNA (Cytosine-5-)-Methyltransferases
DNA Copy Number Variations
DNA Helicases
DNA Mutational Analysis
DNA, Complementary
DNA, Mitochondrial
DNA-Binding Proteins
Drosophila
Drosophila melanogaster
Drosophila Proteins
Dynamins
Dystonia
Electron Transport Chain Complex Proteins
Embryo Transfer
Endoplasmic Reticulum
Enhancer of Zeste Homolog 2 Protein
Epilepsy
Epilepsy, Generalized
Escherichia coli
Exome
Eye Diseases, Hereditary
Eye Movements
Eye Proteins
Face
Family Health
Fatty Acids
Female
Fertilization in Vitro
Fibroblasts
Gain of Function Mutation
Gene Dosage
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Expression Regulation, Enzymologic
Gene Knockdown Techniques
Genes
Genes, Dominant
Genes, Homeobox
Genes, Insect
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Predisposition to Disease
Genetic Research
Genetic Testing
Genetic Variation
Genitalia
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Gestational Age
Glucose
Growth Differentiation Factors
GTP Phosphohydrolases
GTP-Binding Protein beta Subunits
GTP-Binding Proteins
Hand Deformities, Congenital
Haploinsufficiency
Health Care Costs
Health Services Accessibility
Hearing Loss
Hearing Loss, Sensorineural
Heart Defects, Congenital
Hemiplegia
Hernias, Diaphragmatic, Congenital
Heterozygote
Histone-Lysine N-Methyltransferase
Histones
Homozygote
Humans
Hypertension
Hypoglycemia
Infant
Infant Care
Infant, Newborn
Inheritance Patterns
Intellectual Disability
Intensive Care Units, Pediatric
Intestinal Neoplasms
Intestinal Pseudo-Obstruction
Intestine, Small
Intussusception
Karyopherins
Ketoglutarate Dehydrogenase Complex
Ketoglutaric Acids
Language Development Disorders
Leigh Disease
Length of Stay
Leukoencephalopathies
Lipid Droplets
Lipid Metabolism
Liver Diseases
Liver Neoplasms
Liver Transplantation
Logistic Models
Loss of Function Mutation
Lysine
Lysosomal Storage Diseases
Lysosomes
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Male
Mammals
Mechanistic Target of Rapamycin Complex 1
Mediator Complex
Medically Underserved Area
Membrane Proteins
Mental Disorders
Metabolic Diseases
Metabolomics
Metalloendopeptidases
Methylation
Methyltransferases
Mice
Microcephaly
Microfilament Proteins
Micrognathism
MicroRNAs
Microscopy, Confocal
Microscopy, Electron, Transmission
Microtubule-Associated Proteins
Middle Aged
Missouri
Mitochondria
Mitochondrial Dynamics
Mitochondrial Membrane Transport Proteins
Mitochondrial Proteins
Mitochondrial Proton-Translocating ATPases
Models, Animal
Models, Genetic
Molecular Chaperones
Molecular Diagnostic Techniques
Molecular Sequence Annotation
Molecular Sequence Data
Mouth Mucosa
Multiprotein Complexes
Multivariate Analysis
Muscle Hypotonia
Muscle Proteins
Muscle, Skeletal
Muscle, Smooth
Muscles
Musculoskeletal Abnormalities
Mutation
Mutation, Missense
Myocytes, Smooth Muscle
Myosin-Light-Chain Kinase
National Institutes of Health (U.S.)
Neck
Neoplasm Proteins
Neoplasms
Neoplasms, Adipose Tissue
Nerve Degeneration
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Neurobiology
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neurofibroma, Plexiform
Neurofibromatosis 1
Neurofibromin 1
Neuroglia
Neuroimaging
Neuromuscular Junction
Neurons
Nuclear Proteins
Optic Atrophy, Autosomal Dominant
Optic Atrophy, Hereditary, Leber
Organ Specificity
Osteochondrodysplasias
Ovulation Induction
Paraganglioma
Pedigree
Peroxiredoxins
Peroxisomal Biogenesis Factor 2
Peroxisomal Disorders
Peroxisomes
Peutz-Jeghers Syndrome
Phenotype
PHEX Phosphate Regulating Neutral Endopeptidase
Phosphatidylinositols
Pilot Projects
Point Mutation
Polycomb Repressive Complex 1
Polycomb Repressive Complex 2
Polycomb-Group Proteins
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Practice Guidelines as Topic
Precision Medicine
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
Pregnancy
Pregnancy Complications
Premature Birth
Presenilins
Prognosis
Proprotein Convertases
Protein Binding
Protein Domains
Protein Subunits
Proteins
Proteinuria
PTEN Phosphohydrolase
Pupa
Quantitative Trait, Heritable
ran GTP-Binding Protein
Rare Diseases
Rats
Receptors, Glycine
Receptors, Notch
Recurrence
Reflex, Abnormal
Registries
Repressor Proteins
Research Personnel
Retina
Retinal Dystrophies
Retinitis Pigmentosa
Retrospective Studies
Ribonuclease III
Risk Factors
RNA Interference
RNA, Messenger
RNA, Small Interfering
Seizures
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Serine Endopeptidases
Signal Transduction
Sleep Apnea Syndromes
Sodium-Potassium-Exchanging ATPase
Software
Spasms, Infantile
Speech Disorders
Sperm Injections, Intracytoplasmic
Sphingomyelins
Spine
Sterol Regulatory Element Binding Protein 2
Syndrome
Tandem Mass Spectrometry
T-Box Domain Proteins
Texas
TOR Serine-Threonine Kinases
Transcription Factors
Transcription Initiation, Genetic
Transcriptome
Tumor Suppressor Proteins
Ubiquitination
Ubiquitin-Protein Ligases
Ultrasonography, Prenatal
United Kingdom
United States
Urinary Bladder
Vesicular Transport Proteins
Vulnerable Populations
WD40 Repeats
Whole Genome Sequencing
X Chromosome
Young Adult
Zebrafish
Zebrafish Proteins
Zellweger Syndrome
Zinc Fingers
WANGLER's Networks
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Concepts (360)
Derived automatically from this person's publications.
Peroxisomal Disorders
Drosophila melanogaster
Peroxisomes
Intellectual Disability
Mutation, Missense
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Co-Authors (123)
People in Profiles who have published with this person.
BELLEN, HUGO
YAMAMOTO, SHINYA
BACINO, CARLOS
KANCA, OGUZ
Andrews, Jonathan
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Similar People (60)
People who share similar concepts with this person.
BELLEN, HUGO
LUPSKI, JAMES
GIBBS, RICHARD
BOERWINKLE, ERIC
YAMAMOTO, SHINYA
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_
Same Department
People who are also in this person's primary department.
DILEEP, VISHNU
LADHA, FARAH
LI, HONGJIE
MATHUR, VEENA
MEHTA, HEER
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