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Pediatrics CRA
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FAN XIA
Concepts (300)
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Concepts are derived automatically from a person's publications.
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Categories
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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.
Abnormalities, Multiple
Achondroplasia
Acrocephalosyndactylia
Actins
Adaptor Proteins, Signal Transducing
Adenosine Triphosphatases
Adipose Tissue, White
Adolescent
Adult
Alleles
Amino Acid Sequence
Amino Acid Substitution
Animals
Animals, Genetically Modified
Antibodies
Antigens, Neoplasm
Arabs
Arrhythmias, Cardiac
Arthralgia
Artificial Intelligence
Ataxia
ATPases Associated with Diverse Cellular Activities
Autism Spectrum Disorder
Autistic Disorder
Axons
Bacillus megaterium
Base Sequence
beta Catenin
Biomarkers
Bone and Bones
Bone Diseases, Developmental
Brain
Caenorhabditis elegans
Calcineurin
Calcium Channels
Cardiomyopathies
Carrier Proteins
CDC2 Protein Kinase
Cell Cycle
Cell Cycle Proteins
Cell Line
Cell Line, Tumor
Cell Proliferation
Cell-Free Nucleic Acids
Central Nervous System
Cerebellar Ataxia
Child
Child, Preschool
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Mapping
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 8
Chromosomes, Human, X
Circadian Rhythm
Codon
Cognition
Cohort Studies
Collagen Type I
Colon
Comamonas
Comparative Genomic Hybridization
Computational Biology
Congenital Microtia
Consanguinity
Corpus Callosum
Craniofacial Abnormalities
Critical Care
Cyclic AMP
Cyclic AMP-Dependent Protein Kinases
CYS2-HIS2 Zinc Fingers
Cytoskeletal Proteins
Data Mining
Databases, Genetic
De Lange Syndrome
Developmental Disabilities
Diet
Disease Management
DNA
DNA Copy Number Variations
DNA Mutational Analysis
DNA-Binding Proteins
Drosophila melanogaster
Drug Resistant Epilepsy
Dwarfism
Electroencephalography
Endocytosis
Endoplasmic Reticulum Stress
Endosomes
Enzyme Activation
Enzyme Stability
Epilepsy
Escherichia coli
Exome
Exons
Face
Facies
Family
Fasting
Feeding and Eating Disorders
Female
Fetal Growth Retardation
Fetal Hemoglobin
Fetus
Fibrillin-1
Fibroblasts
Fluorescent Dyes
Fluorometry
Food Chain
Fusion Proteins, bcr-abl
gamma-Globins
Geminin
Gene Deletion
Gene Dosage
Gene Expression
Genes, Dominant
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Loci
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genitalia
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomics
Genotype
Genotyping Techniques
Germ Cells
Germ-Line Mutation
Glucose
Glutathione
Golgi Apparatus
Growth Charts
Growth Disorders
GTP-Binding Protein beta Subunits
Hand Deformities, Congenital
Haploinsufficiency
Heart Defects, Congenital
Heart Ventricles
HEK293 Cells
HeLa Cells
Hemoglobinopathies
Hereditary Central Nervous System Demyelinating Diseases
Heterozygote
High-Throughput Nucleotide Sequencing
Homozygote
Humans
Hydrops Fetalis
In Situ Hybridization, Fluorescence
Incidental Findings
INDEL Mutation
Infant
Infant Care
Infant, Newborn
Inflammation
Inheritance Patterns
Insulin
Intellectual Disability
Intensive Care Units, Pediatric
Intestinal Pseudo-Obstruction
Karyotyping
Kidney Diseases
Kinetics
Laboratories
Language Development Disorders
Length of Stay
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Limb Deformities, Congenital
Liver
Loss of Function Mutation
Lymphangioma, Cystic
Male
Membrane Proteins
Metabolomics
Metal Metabolism, Inborn Errors
Metalloendopeptidases
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Obese
Microcephaly
Microfilament Proteins
Micrognathism
MicroRNAs
Microscopy, Electron, Transmission
Mitochondria
Mitochondrial Diseases
Mitochondrial Proteins
Models, Molecular
Molecular Diagnostic Techniques
Molecular Sequence Data
Mosaicism
Muscle Hypotonia
Muscle Weakness
Muscle, Smooth
Muscles
Muscular Atrophy, Spinal
Mutation
Mutation, Missense
Myelin Sheath
Neoplasm Proteins
Nervous System Diseases
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neuroimaging
Neurons
Neurosecretory Systems
Neutropenia
N-Terminal Acetyltransferase A
N-Terminal Acetyltransferase E
Nuchal Translucency Measurement
Nuclear Matrix-Associated Proteins
Nuclear Proteins
Octamer Transcription Factors
Olfactory Perception
Optic Atrophy
Osteogenesis Imperfecta
Patella
Pathology, Molecular
Pedigree
Peptide Fragments
Peptide Hormones
Peptide Termination Factors
Phenotype
Philadelphia Chromosome
Phosphoprotein Phosphatases
Phosphorylation
Pilot Projects
Point Mutation
Polymorphism, Single Nucleotide
Prader-Willi Syndrome
Predictive Value of Tests
Pregnancy
Prenatal Diagnosis
Problem Behavior
Progeria
Prognosis
Prospective Studies
Protein Conformation
Protein Stability
Proteins
Proteolysis
Pyrroline Carboxylate Reductases
Rare Diseases
Recombinant Proteins
Referral and Consultation
Registries
Repressor Proteins
Reproducibility of Results
Reproduction
Retrospective Studies
Rhabdomyolysis
Ring Chromosomes
RNA Splice Sites
RNA Splicing
RNA-Binding Proteins
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology, Amino Acid
Signal Transduction
Single-Cell Analysis
Sleep Apnea Syndromes
Species Specificity
Spectrin
Speech Disorders
Structure-Activity Relationship
Sudden Infant Death
Survival of Motor Neuron 1 Protein
Survival of Motor Neuron 2 Protein
Syndrome
Texas
Thanatophoric Dysplasia
Thyroid Neoplasms
Transcription Factors
Transferrin
Translocation, Genetic
Transposases
Tumor Cells, Cultured
Ubiquitin-Protein Ligases
Ultrasonography, Prenatal
Urinary Bladder
Wnt Signaling Pathway
X Chromosome Inactivation
Young Adult
Zinc Fingers
XIA's Networks
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Concepts (300)
Derived automatically from this person's publications.
Muscle Hypotonia
Genetic Diseases, Inborn
Intellectual Disability
Exome
Language Development Disorders
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Co-Authors (95)
People in Profiles who have published with this person.
ENG, CHRISTINE
LUPSKI, JAMES
LALANI, SEEMA
GIBBS, RICHARD
BI, WEIMIN
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
GIBBS, RICHARD
BOERWINKLE, ERIC
STANKIEWICZ, PAWEL
LALANI, SEEMA
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_
Same Department
People who are also in this person's primary department.
HONKOMP, JESSICA
KETKAR, SHAMIKA
LUPSKI, JAMES
SONG, I-WEN
WORLEY, KIM
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Physical Neighbors
People whose addresses are nearby this person.
DANG, WEIWEI
LANZA, DENISE
QIN, XIANG
SMITH, JANICE
SZAFRANSKI, PRZEMYSLAW
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