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Amanda Krause
Concepts (266)
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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.
5' Untranslated Regions
Abetalipoproteinemia
Abnormalities, Multiple
Abortion, Spontaneous
Acanthocytes
Acrocephalosyndactylia
Adolescent
Adult
Africa
Africa South of the Sahara
Age of Onset
Aged
Aged, 80 and over
Aggression
Albinism, Oculocutaneous
Alleles
alpha-Thalassemia
Anal Canal
Anemia, Sickle Cell
Anticoagulants
Apathy
Aryl Hydrocarbon Hydroxylases
Ataxin-1
Ataxin-2
Ataxin-7
Ataxins
Autoantibodies
Base Sequence
beta-Thalassemia
Biomarkers
Blepharophimosis
Blood Cell Count
Blood Coagulation Factor Inhibitors
Blood Glucose
Brain
Brain Stem
BRCA2 Protein
C9orf72 Protein
Cardiomyopathy, Dilated
Case-Control Studies
Cauda Equina
Cell Cycle Proteins
Cerebellar Diseases
Child
Child, Preschool
Chorea
Chromatography, Thin Layer
Chromosome Aberrations
Chromosome Disorders
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human, Pair 5
Cognition Disorders
Cohort Studies
Contrast Media
Copper Sulfate
Costs and Cost Analysis
Cross-Sectional Studies
Cyclic AMP Response Element-Binding Protein
Cytochrome P-450 CYP2C9
De Lange Syndrome
Deafness
Dementia
Depression
Developing Countries
Disease Progression
DNA
DNA Mutational Analysis
DNA-Binding Proteins
Dose-Response Relationship, Drug
Ear
Early Diagnosis
Early Medical Intervention
Echocardiography
Ectromelia
Electrocardiography
Embryo Implantation
Esophagus
Europe
Exons
Eye Abnormalities
Facies
Factor VIII
False Negative Reactions
False Positive Reactions
Family
Family Health
Family Leave
Fanconi Anemia
Fanconi Anemia Complementation Group G Protein
Fanconi Anemia Complementation Group Proteins
Fatal Outcome
Female
Fertilization in Vitro
Filamins
Flow Cytometry
Forkhead Box Protein L2
Forkhead Transcription Factors
Founder Effect
Fragile X Mental Retardation Protein
Fragile X Syndrome
Frameshift Mutation
Gadolinium
Galactosemias
Gastrointestinal Tract
Gene Conversion
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Frequency
Gene Rearrangement
Gene Silencing
Genes, BRCA2
Genes, Dominant
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Linkage
Genetic Loci
Genetic Predisposition to Disease
Genetic Privacy
Genetic Testing
Genetic Variation
Genetics, Medical
Genome-Wide Association Study
Genomics
Genotype
Germ-Line Mutation
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Heart Defects, Congenital
Heart Failure
Hematopoietic Stem Cell Transplantation
Hemoglobinopathies
Hemophilia A
Heredodegenerative Disorders, Nervous System
Heterozygote
History, 20th Century
HIV
HIV Infections
Homozygote
Humans
Huntingtin Protein
Huntington Disease
In Situ Hybridization, Fluorescence
Incidence
Indicators and Reagents
Infant
Infant, Newborn
Insulin
Insulin-Like Growth Factor Binding Protein 3
Insulin-Like Growth Factor I
Intellectual Disability
Introns
Irritable Mood
Japan
Kaplan-Meier Estimate
Kidney
Kruppel-Like Transcription Factors
Li-Fraumeni Syndrome
Limb Deformities, Congenital
Linkage Disequilibrium
Lower Extremity Deformities, Congenital
Magnetic Resonance Imaging
Magnetic Resonance Imaging, Cine
Male
Mali
Mass Screening
Maternal Age
Membrane Proteins
Microphthalmia-Associated Transcription Factor
Microsatellite Repeats
Middle Aged
Mixed Function Oxygenases
Molecular Epidemiology
Multiplex Polymerase Chain Reaction
Muscular Atrophy, Spinal
Muscular Dystrophy, Duchenne
Mutation
Mutation Rate
Mutation, Missense
Neoplasms
Nerve Tissue Proteins
Neural Tube Defects
Neurodegenerative Diseases
Neurofilament Proteins
Neuromuscular Diseases
Neuronal Apoptosis-Inhibitory Protein
Neuropsychological Tests
North America
Nuclear Proteins
Nucleic Acid Conformation
Oligonucleotides, Antisense
Open Reading Frames
Osteochondrodysplasias
Parity
Patient Acceptance of Health Care
Pedigree
Phenotype
Polycystic Kidney, Autosomal Recessive
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Population Surveillance
Predictive Value of Tests
Pregnancy
Pregnancy Outcome
Pregnancy Rate
Preimplantation Diagnosis
Prenatal Diagnosis
Prevalence
Primary Ovarian Insufficiency
Professional Role
Prognosis
Promoter Regions, Genetic
Prospective Studies
Protein Biosynthesis
Psychomotor Performance
Puberty
Quality of Life
Radiography
Rare Diseases
Receptors, Cell Surface
Recurrence
Repetitive Sequences, Nucleic Acid
Reproducibility of Results
Research Design
Retrospective Studies
Risk Assessment
Risk Factors
RNA-Binding Proteins
Sequence Analysis, DNA
Sequence Deletion
Skin Pigmentation
Sleep Wake Disorders
SMN Complex Proteins
Societies, Medical
South Africa
Spine
Spinocerebellar Ataxias
Stillbirth
Stroke Volume
Surveys and Questionnaires
Survival of Motor Neuron 1 Protein
Syndrome
TATA-Box Binding Protein
Thyroid Hormones
Trachea
Transcription Factors
Trinucleotide Repeat Expansion
Trinucleotide Repeats
Tumor Suppressor Protein p53
Universities
Upper Extremity Deformities, Congenital
UTP-Hexose-1-Phosphate Uridylyltransferase
Ventricular Function, Left
Vitamin K Epoxide Reductases
Waardenburg Syndrome
Warfarin
Young Adult
Zinc Finger Protein Gli3
Krause's Networks
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Concepts (266)
Derived automatically from this person's publications.
Huntington Disease
Chorea
Dementia
Heredodegenerative Disorders, Nervous System
Cognition Disorders
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Co-Authors (14)
People in Profiles who have published with this person.
Tsabedze, Nqoba
Poole, Janet
Mpangase, Phelelani
Manga, Pravin
Ramsay, Michele
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Similar People (60)
People who share similar concepts with this person.
Norris, Shane
Madhi, Shabir
Cohen, Cheryl
Kahn, Kathleen
Raal, Frederick
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