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NEIL HANCHARD
Concepts (353)
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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.
3' Untranslated Regions
Abnormalities, Multiple
Absorption
Aconitate Hydratase
Actins
Acute Disease
Adaptor Proteins, Signal Transducing
Adolescent
Adult
Africa
Age of Onset
Aging, Premature
Aldosterone
Alleles
Alveolar Epithelial Cells
Amiloride
Amino Acid Metabolism, Inborn Errors
Amino Acid Motifs
Amino Acid Sequence
Amino Acid Substitution
Amino Acids
Anemia, Iron-Deficiency
Anemia, Sickle Cell
Animals
Aortic Coarctation
Arabs
Arginine
Aromatic-L-Amino-Acid Decarboxylases
Arrhythmias, Cardiac
Ascorbic Acid
Autism Spectrum Disorder
Autopsy
Axons
Base Sequence
Benchmarking
beta-Globins
Bias
Bilirubin
Biological Evolution
Biomarkers
Biomedical Research
Birth Rate
Body Patterning
Bone and Bones
Botswana
Brain
Bronchiolitis, Viral
Caenorhabditis elegans
Calcium Channels
Calcium Channels, L-Type
Cameroon
Carbidopa
Carbon
Cardiovascular Diseases
Case-Control Studies
Cell Count
Cell Movement
Cell Proliferation
Cells, Cultured
Cerebral Cortex
Child
Child, Preschool
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Disorders
Chromosome Mapping
Chromosomes, Human
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 8
Citric Acid Cycle
Coat Protein Complex I
Coatomer Protein
Codon
Cohort Studies
Colitis
Collagen Type I
Comparative Genomic Hybridization
Computational Biology
Computer Simulation
CpG Islands
Critical Care
Cross-Sectional Studies
Curriculum
Cysteine
Datasets as Topic
Delayed Diagnosis
Demography
Developmental Disabilities
Diabetes Complications
Diabetes Mellitus
Diaphragmatic Eventration
Disease
Disease Management
Disease Progression
DNA Copy Number Variations
DNA Methylation
DNA Mutational Analysis
DNA Repair
DNA Replication
DNA, Mitochondrial
DNA-Binding Proteins
Dopamine
Dopamine Agonists
Drug Combinations
Edetic Acid
Education
Education, Graduate
Electron Transport
Electron Transport Complex IV
Embryo, Nonmammalian
Embryonic Development
Endemic Diseases
Endoplasmic Reticulum
Endoplasmic Reticulum Stress
England
Epigenomics
Epilepsies, Myoclonic
Epilepsy
Epilepsy, Generalized
Epithelial Sodium Channels
Erythrocytes
Escherichia coli
Exome
Exons
Family
Fatal Outcome
Female
Fetal Diseases
Fetal Hemoglobin
Fibroblasts
Flow Cytometry
Forkhead Transcription Factors
Functional Laterality
Gambia
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Flow
Gene Frequency
Gene Knockdown Techniques
Gene Pool
Genes
Genes, Lethal
Genes, Recessive
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Variation
Genetics, Medical
Genetics, Population
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomics
Genotype
Geography
Germ-Line Mutation
Global Health
Globins
Glucuronosyltransferase
Golgi Apparatus
GTP Phosphohydrolases
Hair
Hair Color
Hair Follicle
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Health
Heart
Heart Defects, Congenital
Heart Ventricles
HEK293 Cells
Hemochromatosis
Hemoglobin, Sickle
Hemolysis
Hepatocyte Nuclear Factor 1-beta
Hernia, Diaphragmatic
Hernias, Diaphragmatic, Congenital
Heterotaxy Syndrome
Heterozygote
High-Throughput Nucleotide Sequencing
Hirschsprung Disease
Histocompatibility Antigens Class II
History, Ancient
HIV Infections
Homeostasis
Homozygote
Human Migration
Humans
Hydrochlorothiazide
Hyperbilirubinemia, Neonatal
Hypertension
Hypertriglyceridemia
Hypokalemia
Hypoplastic Left Heart Syndrome
Immunity
Infant
Infant Care
Infant Nutrition Disorders
Infant, Newborn
Inheritance Patterns
Intellectual Disability
Intensive Care Units, Pediatric
Interleukin-8
International Cooperation
Intracellular Signaling Peptides and Proteins
Introns
Ion Channels
Iron
Isoantibodies
Jamaica
Kwashiorkor
Language
Language Development Disorders
Leigh Disease
Length of Stay
Leukoencephalopathies
Levodopa
Liddle Syndrome
Linkage Disequilibrium
Liver
Lung
Lung Diseases, Interstitial
Magnetic Resonance Imaging
Malaria
Malawi
Male
Malnutrition
MAP Kinase Signaling System
Melanins
Membrane Proteins
Mental Retardation, X-Linked
Metabolic Networks and Pathways
Metabolism
Metabolism, Inborn Errors
Metabolomics
Methyl-CpG-Binding Protein 2
Mice
Micrognathism
Middle Aged
Models, Animal
Models, Molecular
Molecular Sequence Data
Motor Activity
Mouth Mucosa
Multigene Family
Muscle Weakness
Musculoskeletal Abnormalities
Mutation
Mutation, Missense
National Institutes of Health (U.S.)
NAV1.4 Voltage-Gated Sodium Channel
Nerve Net
Neurodevelopmental Disorders
Neurofibromatosis 1
Neurofibromin 1
Neuromuscular Diseases
Neurons
Nigeria
Nuclear Family
Nuclear Proteins
Organ Size
Organogenesis
Oryzias
Osteoporosis
PAX2 Transcription Factor
Pedigree
Peroxidases
Pharmacogenetics
Phenotype
Phosphotransferases (Alcohol Group Acceptor)
Phylogeny
Polymorphism, Restriction Fragment Length
Polymorphism, Single Nucleotide
Pregnancy
Principal Component Analysis
Prospective Studies
Protein Precursors
Protein Tyrosine Phosphatases
Protein-Energy Malnutrition
Pulmonary Surfactant-Associated Protein C
Pulmonary Surfactant-Associated Proteins
Pulmonary Surfactants
Quantitative Trait Loci
rab GTP-Binding Proteins
rab5 GTP-Binding Proteins
Radiography
Receptors, Adrenergic, alpha-1
Receptors, Lipoprotein
Renin
Repressor Proteins
Research Personnel
Respiratory Syncytial Virus Infections
Retrospective Studies
Rhabdomyolysis
Risk Factors
RNA Splicing
RNA, Long Noncoding
RNA, Messenger
RNA, Small Interfering
Scalp
Seizures
Selection, Genetic
Sequence Analysis, DNA
Sequence Deletion
Severe Acute Malnutrition
Severity of Illness Index
Sickle Cell Trait
Situs Inversus
Skin
Spastic Paraplegia, Hereditary
Statistics, Nonparametric
Status Epilepticus
Students
Survivors
Syndrome
Tetraspanins
Texas
Thinness
Transcription Factors
Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
Tumor Necrosis Factor-alpha
Uganda
Uniparental Disomy
United Kingdom
United States
Universities
Urogenital Abnormalities
Vanilmandelic Acid
Vesico-Ureteral Reflux
Waardenburg Syndrome
Whole Genome Sequencing
Xenopus laevis
Young Adult
Zebrafish
Zebrafish Proteins
HANCHARD's Networks
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Concepts (353)
Derived automatically from this person's publications.
Anemia, Sickle Cell
Exome
Genomics
Genetic Variation
Chromosomes, Human, Pair 20
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Co-Authors (100)
People in Profiles who have published with this person.
SCHULZE, KATHARINA
BELMONT, JOHN
LUPSKI, JAMES
LALANI, SEEMA
MARDON, GRAEME
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
BOERWINKLE, ERIC
AMOS, CHRIS
GIBBS, RICHARD
STANKIEWICZ, PAWEL
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_
Same Department
People who are also in this person's primary department.
BEKHEIRNIA, MIR REZA
MACHOL, KEREN
ROBAK, LAURIE
ROSENBERG, SUSAN
YAMAMOTO, SHINYA
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Physical Neighbors
People whose addresses are nearby this person.
BEKHEIRNIA, MIR REZA
CRAIGEN, WILLIAM
DHAR, SHWETA
EBLE, TANYA
SCAGLIA, FERNANDO
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