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PENGFEI LIU
Concepts (334)
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Concepts are derived automatically from a person's publications.
Cloud
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.
Abnormalities, Multiple
Acromegaly
Adaptor Proteins, Signal Transducing
Adenoma
Adenosine Triphosphatases
Adenosine Triphosphate
Adolescent
Adult
Age Factors
Age of Onset
Alleles
Alu Elements
Alzheimer Disease
Amino Acid Sequence
Amino Acids
Aneuploidy
Animals
Animals, Genetically Modified
Antigens, Nuclear
Arabs
Arrhythmias, Cardiac
Arthralgia
ATPases Associated with Diverse Cellular Activities
ATP-Binding Cassette Transporters
Attention Deficit Disorder with Hyperactivity
Autistic Disorder
Autoantigens
Bardet-Biedl Syndrome
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
Bile Acids and Salts
Biological Variation, Population
Biomarkers, Tumor
Biopsy
Bone and Bones
Bone Marrow
Bone Morphogenetic Proteins
Brain
Brain Diseases
CA3 Region, Hippocampal
Carboxypeptidases
Cardiovascular Abnormalities
Carrier Proteins
Cation Transport Proteins
CDC2 Protein Kinase
Cell Cycle
Cell Cycle Proteins
Cell Line
Cell Nucleus
Cell Proliferation
Cells, Cultured
Cerebellum
Charcot-Marie-Tooth Disease
Chick Embryo
Child
Child Behavior Disorders
Child, Preschool
China
Cholestasis, Intrahepatic
Chromatin Assembly and Disassembly
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Breakage
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Mapping
Chromosome Pairing
Chromosomes, Human
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, X
Cleft Lip
Cleft Palate
Clone Cells
Cohort Studies
Collagen Type III
Comparative Genomic Hybridization
Computational Biology
Congenital Abnormalities
Craniofacial Abnormalities
Critical Care
Crossing Over, Genetic
Cytoskeletal Proteins
Databases, Factual
Databases, Genetic
De Lange Syndrome
Developmental Disabilities
Disease Management
Disease Models, Animal
DNA
DNA Breaks
DNA Copy Number Variations
DNA End-Joining Repair
DNA Helicases
DNA Repair
DNA Replication
DNA-Binding Proteins
Dura Mater
Dwarfism
Dynamins
Embryonic Development
Endocytosis
Endoplasmic Reticulum Stress
Endosomes
Enhancer Elements, Genetic
Epilepsy
Evolution, Molecular
Excitatory Postsynaptic Potentials
Exome
Exons
Extremities
Face
Facies
Failure to Thrive
Family
Fanconi Anemia
Female
Fetus
Fibrillin-1
Fibroblasts
Follow-Up Studies
GABAergic Neurons
Gametogenesis
Gastrulation
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Frequency
Gene Order
Gene Rearrangement
Genes, Recessive
Genes, Reporter
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Loci
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome, Human
Genome-Wide Association Study
Genomic Instability
Genomic Structural Variation
Genomics
Genotype
Genotyping Techniques
Gigantism
Golgi Apparatus
Growth Disorders
GTP Phosphohydrolases
GTP-Binding Protein beta Subunits
GTP-Binding Proteins
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Hearing Loss
Heart Defects, Congenital
Hematologic Neoplasms
Hereditary Sensory and Motor Neuropathy
Heterozygote
High-Throughput Nucleotide Sequencing
Histone Deacetylase 1
Histone-Lysine N-Methyltransferase
Holoprosencephaly
Homeodomain Proteins
Homologous Recombination
Homozygote
Human Growth Hormone
Humans
Hypothalamus
In Situ Hybridization, Fluorescence
Incidental Findings
INDEL Mutation
Induced Pluripotent Stem Cells
Infant
Infant Care
Infant, Newborn
Inheritance Patterns
Intellectual Disability
Intensive Care Units, Pediatric
Intracellular Signaling Peptides and Proteins
Intracranial Aneurysm
Intracranial Arteriovenous Malformations
Introns
Inverted Repeat Sequences
Kidney
Kidney Diseases, Cystic
Language Development Disorders
Length of Stay
Limit of Detection
Loss of Function Mutation
Loss of Heterozygosity
Lumbar Vertebrae
Magnetic Resonance Imaging
Male
MAP Kinase Signaling System
Megakaryocyte Progenitor Cells
Megalencephaly
Membrane Proteins
Memory
Memory Disorders
Meningioma
Metalloendopeptidases
Methyl-CpG-Binding Protein 2
Mi-2 Nucleosome Remodeling and Deacetylase Complex
Mice
Mice, Transgenic
Microarray Analysis
Microcephaly
Micrognathism
Microsatellite Repeats
Middle Aged
Minor Histocompatibility Antigens
Mitochondria
Mitochondrial Proteins
Models, Genetic
Models, Molecular
Molecular Diagnostic Techniques
Molecular Motor Proteins
Molecular Sequence Data
Mosaicism
Motor Neurons
Muscle Hypotonia
Muscle Weakness
Muscles
Muscular Atrophy
Muscular Atrophy, Spinal
Musculoskeletal Abnormalities
Mutation
Mutation, Missense
Myelin Proteins
Myelin Sheath
Myeloid-Lymphoid Leukemia Protein
Myosin Heavy Chains
National Institutes of Health (U.S.)
Neck
Neoplasm Grading
Neoplasm Proteins
Neoplasm Recurrence, Local
Neoplasms
Netherlands
Neural Pathways
Neural Stem Cells
Neurodevelopmental Disorders
Neuronal Plasticity
Neurosurgical Procedures
Nuclear Proteins
Nuclear Receptor Co-Repressor 1
Nuclear Receptor Co-Repressor 2
Nucleic Acid Hybridization
Oligonucleotide Array Sequence Analysis
Oligonucleotides
Osteochondrodysplasias
Paralysis
Pedigree
Peptides
Peripheral Nerves
Peroxisomes
Phenotype
Phosphoprotein Phosphatases
Pilot Projects
Pituitary Neoplasms
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Polyneuropathies
Primates
Prognosis
Protein Conformation
Protein Processing, Post-Translational
Proto-Oncogene Proteins
Purkinje Cells
Radiography
Receptors, Cytoplasmic and Nuclear
Receptors, GABA-A
Receptors, G-Protein-Coupled
Receptors, Vascular Endothelial Growth Factor
Recombination, Genetic
Referral and Consultation
Repetitive Sequences, Nucleic Acid
Repressor Proteins
Reproducibility of Results
Retrospective Studies
Rhabdomyolysis
Scoliosis
Segmental Duplications, Genomic
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Serine-Type D-Ala-D-Ala Carboxypeptidase
Sex Chromosomes
Short Stature Homeobox Protein
Signal Transduction
Smith-Magenis Syndrome
Spastic Paraplegia, Hereditary
Spastin
Spheroids, Cellular
Spinal Cord Compression
Spinal Cord Neoplasms
Spine
Spinocerebellar Degenerations
Structure-Activity Relationship
Subarachnoid Space
Survival of Motor Neuron 1 Protein
Survival of Motor Neuron 2 Protein
Syndrome
T-Box Domain Proteins
Templates, Genetic
Texas
Trans-Activators
Transcription Factors
Transcription, Genetic
Transferrin
Transforming Growth Factor beta
Translocation, Genetic
Treatment Outcome
Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
Twins, Monozygotic
Ultrasonography, Prenatal
Uniparental Disomy
United States
Vascular Endothelial Growth Factor A
Whole Genome Sequencing
Young Adult
Zebrafish
Zebrafish Proteins
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Concepts (334)
Derived automatically from this person's publications.
DNA Copy Number Variations
Genetic Diseases, Inborn
Gene Rearrangement
Gene Duplication
DNA Replication
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Co-Authors (86)
People in Profiles who have published with this person.
LUPSKI, JAMES
YUAN, BO
POSEY, JENNIFER
LALANI, SEEMA
ENG, CHRISTINE
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
STANKIEWICZ, PAWEL
GIBBS, RICHARD
CHEUNG, SAU WAI
BOERWINKLE, ERIC
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Same Department
People who are also in this person's primary department.
ATKINSON, ELIZABETH
MURALI, CHAYA
NAGAMANI, SANDESH
PANDEY, ASHUTOSH
POTOCKI, LORRAINE
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Physical Neighbors
People whose addresses are nearby this person.
BAJIC, ALEKSANDAR
LEE, KWANGHYUK
SMITH, JANICE
YAMAMOTO, SHINYA
ZONG, CHENGHANG
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