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History (18)
Clonorchis sinensis
Casualties abroad and at home.
N-Methylaspartate
Myosarcoma
Coronavirus OC43, Human
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Kevin Strauss
Concepts (545)
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Concepts are derived automatically from a person's publications.
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Categories
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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.
3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
Abnormalities, Multiple
Abortion, Spontaneous
Acids
Active Transport, Cell Nucleus
Acute Disease
Acyltransferases
Adaptor Proteins, Vesicular Transport
Adenine Nucleotide Translocator 1
Adolescent
Adrenal Hyperplasia, Congenital
Adult
Affect
Age of Onset
Aged
Aged, 80 and over
Agenesis of Corpus Callosum
Alanine
Albumins
Algorithms
Alleles
Alu Elements
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Amino Acids
Amino Acids, Branched-Chain
Amino Acyl-tRNA Synthetases
Amish
AMP-Activated Protein Kinases
Amyloid beta-Peptides
Anemia, Hemolytic
Animals
Antibody Specificity
Antigens, CD
Anxiety
Apc7 Subunit, Anaphase-Promoting Complex-Cyclosome
Apgar Score
Apolipoproteins B
Apoptosis
Arginine
Arkansas
Arterioles
Aspartic Acid
Atherosclerosis
ATP-Dependent Proteases
Attention
Autism Spectrum Disorder
Autoantibodies
Autoantigens
Autoimmune Diseases
Autopsy
Axons
Azo Compounds
Basal Ganglia Diseases
Base Sequence
Behavior, Animal
Betaine
Bile Acids and Salts
Bilirubin
Biological Products
Biomarkers
Bipolar Disorder
Blood Volume
Blood-Brain Barrier
Blotting, Western
Body Composition
Body Weights and Measures
Bone and Bones
Bone Diseases
Bone Marrow Transplantation
Bone Morphogenetic Protein 2
Brain
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Brazil
Cadherins
Carbon-Carbon Ligases
Cardiac Surgical Procedures
Cardiomyopathies
Carnitine
Carotid Intima-Media Thickness
Case-Control Studies
Caspase 2
Catalytic Domain
Catheterization
Catheters
Cattle
Cell Cycle
Cell Differentiation
Cell Line
Cell Line, Tumor
Cell Movement
Cell Nucleus
Cell Proliferation
Cell Separation
Cell Survival
Cells, Cultured
Central Nervous System Diseases
Cerebrovascular Circulation
Charcot-Marie-Tooth Disease
Chemical and Drug Induced Liver Injury
Child
Child Development Disorders, Pervasive
Child, Preschool
Cholagogues and Choleretics
Cholestasis, Intrahepatic
Cholesterol, LDL
Chromatography, Liquid
Chromosome Mapping
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 7
Chronic Disease
Cleft Palate
Clinical Protocols
Clinical Trials as Topic
Cloning, Molecular
Codon, Nonsense
Cognition
Cognitive Dysfunction
Cohort Studies
Combined Modality Therapy
Comorbidity
Computational Biology
Consanguinity
Conserved Sequence
COP-Coated Vesicles
Corpus Callosum
Corpus Striatum
Cost of Illness
CRADD Signaling Adaptor Protein
Craniofacial Abnormalities
Creatine
Crigler-Najjar Syndrome
Cross-Cultural Comparison
Cross-Sectional Studies
Cystathionine beta-Synthase
Cysteine Endopeptidases
Cytarabine
DEAD-box RNA Helicases
Deafness
Dendritic Cells
Dependovirus
Depression
Depressive Disorder, Major
Developmental Disabilities
Diet
Diet Therapy
Diet, Protein-Restricted
Dietary Proteins
Diffusion Magnetic Resonance Imaging
Diffusion Tensor Imaging
Disease Management
Disease Models, Animal
Disease Progression
DNA
DNA Copy Number Variations
DNA Methylation
DNA Mutational Analysis
DNA, Mitochondrial
DNA-Binding Proteins
Dopamine Plasma Membrane Transport Proteins
Dose-Response Relationship, Drug
Dwarfism
Dyskeratosis Congenita
Dystonia
Echocardiography
Electroencephalography
Ellis-Van Creveld Syndrome
Embryo, Nonmammalian
Encephalitis
End Stage Liver Disease
Endocrine System Diseases
Endoribonucleases
Epilepsies, Partial
Epilepsy
Erlotinib Hydrochloride
Erythrocytes
Ether-A-Go-Go Potassium Channels
Evoked Potentials, Auditory, Brain Stem
Exome
Exons
Eye Abnormalities
Family Health
Fatal Outcome
Female
Fibrinogen
Fibroblasts
Flow Cytometry
Follow-Up Studies
Food, Formulated
Forkhead Transcription Factors
Frameshift Mutation
Furosemide
G(M3) Ganglioside
Gait Disorders, Neurologic
Gangliosides
Gene Deletion
Gene Dosage
Gene Expression
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Genes
Genes, RAG-1
Genes, Recessive
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Predisposition to Disease
Genetic Testing
Genetic Therapy
Genetic Variation
Genetic Vectors
Genetics, Medical
Genetics, Population
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomics
Genotype
Glomerulosclerosis, Focal Segmental
Glucose
Glucuronosyltransferase
Glutamic Acid
Glutarates
Glutaryl-CoA Dehydrogenase
Glycine N-Methyltransferase
Glycosphingolipids
Golgi Apparatus
Gonadal Dysgenesis
Graft Rejection
Graft Survival
Gray Matter
Growth and Development
Growth Disorders
Guanine Nucleotide Exchange Factors
Gyrus Cinguli
Hair
Hair Cells, Auditory
Haploinsufficiency
Haplotypes
Head
Health Care Costs
Health Services Accessibility
Healthcare Disparities
Hearing
Hearing Loss, Central
Hearing Loss, Sensorineural
Heart
Heart Defects, Congenital
HEK293 Cells
HeLa Cells
Hereditary Sensory and Autonomic Neuropathies
Hernia, Hiatal
Heterochromatin
Heterozygote
High-Throughput Nucleotide Sequencing
Hip Dislocation, Congenital
Hirschsprung Disease
Histidine
Histocompatibility Testing
HLA Antigens
Homeostasis
Homocysteine
Homocystinuria
Homozygote
Hospitalization
Humans
Hydrazines
Hyperbilirubinemia
Hyperhomocysteinemia
Hyperlipoproteinemia Type II
Image Processing, Computer-Assisted
Imidazoles
Immunization
Immunoblotting
Immunohistochemistry
Immunologic Deficiency Syndromes
Immunoprecipitation
Impulsive Behavior
Incidental Findings
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Infusions, Intravenous
Injections, Spinal
Intellectual Disability
Intelligence
Intracellular Signaling Peptides and Proteins
Isaacs Syndrome
Isoleucine
Kaplan-Meier Estimate
Kartagener Syndrome
Kernicterus
Ketoglutaric Acids
Ketone Oxidoreductases
Ki-67 Antigen
Kidney
Kruppel-Like Transcription Factors
Laminin
Leucine
Linkage Disequilibrium
Lissencephaly
Liver
Liver Cirrhosis
Liver Function Tests
Liver Transplantation
Living Donors
Long Interspersed Nucleotide Elements
Longitudinal Studies
Loss of Function Mutation
Lymphocyte Activation
Lymphocytes
Lysine
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Malabsorption Syndromes
Male
Malformations of Cortical Development
Mannitol
Maple Syrup Urine Disease
Maryland
Mechanistic Target of Rapamycin Complex 1
Megalencephaly
Membrane Microdomains
Membrane Proteins
Membrane Transport Proteins
Mental Disorders
Metabolic Diseases
Methionine
Methylenetetrahydrofolate Reductase (NADPH2)
Methyltransferases
Mice
Mice, Inbred C57BL
Mice, Knockout
Microcephaly
Microscopy, Electron, Transmission
Microtubule-Associated Proteins
Middle Aged
Mitochondria
Mitochondrial Proteins
Mitosis
Models, Biological
Models, Neurological
Molecular Diagnostic Techniques
Molecular Sequence Data
Motor Neurons
Motor Skills Disorders
Movement Disorders
Multienzyme Complexes
Multiprotein Complexes
Muscle Weakness
Muscle, Skeletal
Muscular Atrophy, Spinal
Muscular Diseases
Musculoskeletal Abnormalities
Mutagenesis, Insertional
Mutation
Mutation, Missense
Myasthenic Syndromes, Congenital
Myocardium
Myopathies, Nemaline
N-Acetylgalactosaminyltransferases
Necrosis
Neonatal Screening
Nephrosis
Nephrotic Syndrome
Nerve Tissue Proteins
Neural Stem Cells
Neurodevelopmental Disorders
Neurogenesis
Neurons
Neurotoxins
Nitro Compounds
Nuclear Proteins
Nucleosomes
Nutritional Physiological Phenomena
Nutritional Requirements
Octamer Transcription Factor-3
Oligonucleotide Array Sequence Analysis
Oligonucleotides
Open Reading Frames
Organic Anion Transporters
Organic Chemicals
Organogenesis
Organoids
Osmolar Concentration
Osteochondrodysplasias
Otoacoustic Emissions, Spontaneous
Outpatients
Oxidation-Reduction
Oxidoreductases Acting on CH-CH Group Donors
Pain Management
Parents
Parkinsonian Disorders
Pathology, Molecular
Patient-Centered Care
PC12 Cells
Pediatrics
Pedigree
Pennsylvania
Peripheral Nerves
Phenotype
Phototherapy
Pilot Projects
Piperazines
Polyhydramnios
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Population Surveillance
Positron-Emission Tomography
Postmortem Changes
Postoperative Complications
Prednisolone
Pregnancy
Prevalence
Primary Cell Culture
Progesterone Reductase
Prognosis
Propionates
Propionic Acidemia
Prosencephalon
Prospective Studies
Protein Isoforms
Protein Structure, Tertiary
Protein Transport
Proteins
Proteolysis
Protestantism
Proto-Oncogene Proteins c-myc
Psychiatric Status Rating Scales
Psychomotor Agitation
Psychomotor Disorders
Pulse Wave Analysis
Pupil Disorders
Putamen
Pyrimidines
Pyruvate Kinase
Quality of Life
Quantitative Trait, Heritable
Radiography
Rare Diseases
Rats
Receptors, LDL
Receptors, Virus
Recombinant Proteins
Reflex, Stretch
Registries
Repressor Proteins
Reproducibility of Results
Respiration, Artificial
Respiratory Rate
Retrospective Studies
Ribonucleoproteins
Risk
Risk Assessment
Risk Factors
RNA, Long Noncoding
RNA, Untranslated
RNA-Binding Proteins
S-Adenosylhomocysteine
S-Adenosylmethionine
Saline Solution, Hypertonic
Secondary Prevention
Seizures
Sensitivity and Specificity
Sequence Analysis, DNA
Sequence Analysis, RNA
Serine Proteases
Serum Albumin
Severe Combined Immunodeficiency
Severity of Illness Index
Sex Characteristics
Sex-Determining Region Y Protein
Sialic Acid Storage Disease
Sialyltransferases
Siblings
Signal Transduction
Sirolimus
Sodium
SOX Transcription Factors
Spastic Paraplegia, Hereditary
Species Specificity
Spinal Cord
Spinal Fusion
Spinal Muscular Atrophies of Childhood
Stem Cells
Stereocilia
Stillbirth
Sudden Infant Death
Survival of Motor Neuron 1 Protein
Survival of Motor Neuron 2 Protein
Survival Rate
Survivors
Sweetening Agents
Symporters
Syndrome
Tandem Mass Spectrometry
Telomere
Telomere Homeostasis
Temporal Lobe
Thoracotomy
Thymus Gland
Tight Junctions
Time Factors
Tissue and Organ Procurement
Tissue Donors
T-Lymphocytes
Tomography, X-Ray Computed
Tooth Abnormalities
TOR Serine-Threonine Kinases
Transcription Factors
Transforming Growth Factor beta
Transplant Recipients
Treatment Outcome
Troponin T
Tryptophan
Tubulin
Tumor Suppressor Proteins
Tyrosine-tRNA Ligase
Ubiquitination
Ubiquitin-Protein Ligases
United States
Ursodeoxycholic Acid
Usher Syndromes
Valine
Vasoconstriction
Vitamin B 12 Deficiency
Vulnerable Populations
Water-Electrolyte Imbalance
Weight Gain
White Matter
Wisconsin
Wnt Signaling Pathway
Workflow
Yeasts
Young Adult
Zebrafish
Zonula Occludens-2 Protein
Strauss's Networks
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Concepts (545)
Derived automatically from this person's publications.
Muscular Atrophy, Spinal
Maple Syrup Urine Disease
Liver Transplantation
Child, Preschool
Infant
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Co-Authors (6)
People in Profiles who have published with this person.
Wang, Dan
Gao, Guangping
Brown, Robert
Gruntman, Alisha
Gray-Edwards, Heather
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Similar People (60)
People who share similar concepts with this person.
Maron, Barry
Flotte, Terence
Krings, Timo
Tucker, Katherine
Seddon, Johanna
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Same Department
People who are also in this person's primary department.
Ezzio, Catherine
Garg, Arvin
Gauguet, Stefanie
Greenstein, Emily
Horgan, Megan
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