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PRZEMYSLAW SZAFRANSKI
Concepts (337)
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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
Acinar Cells
Adaptor Proteins, Signal Transducing
Adolescent
Adult
Aged
Algorithms
Alleles
alpha7 Nicotinic Acetylcholine Receptor
Alternative Splicing
Alu Elements
Amino Acid Sequence
Amino Acid Substitution
Aneuploidy
Angiogenic Proteins
Animals
Animals, Newborn
Antigens, Nuclear
Apoptosis Regulatory Proteins
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Autistic Disorder
Autopsy
Bacterial Proteins
Base Composition
Base Sequence
beta Catenin
Binding Sites
Biopsy
Bone Diseases, Developmental
Bone Diseases, Metabolic
Brain
Bronchopulmonary Dysplasia
Campomelic Dysplasia
Cardiovascular Diseases
Carrier Proteins
Case-Control Studies
Caveolin 3
Cell Adhesion
Cell Adhesion Molecules, Neuronal
Cell Differentiation
Cell Division
Cell Line
Cell Line, Tumor
Cell Movement
Cell Polarity
Cell Proliferation
Cells, Cultured
Chick Embryo
Child
Child, Preschool
Chorionic Villi Sampling
Chromatin
Chromatin Assembly and Disassembly
Chromosome Aberrations
Chromosome Breakage
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 7
Clone Cells
Cloning, Molecular
Codon, Initiator
Codon, Terminator
Cohort Studies
Colitis, Ulcerative
Comparative Genomic Hybridization
Computational Biology
CpG Islands
Craniofacial Abnormalities
Creatine Kinase
CRISPR-Cas Systems
Cyclin E
Cytokine TWEAK
Cytoskeletal Proteins
Databases, Genetic
De Lange Syndrome
Developmental Disabilities
Digestive System Abnormalities
Disease Susceptibility
DNA Copy Number Variations
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA Replication
DNA, Bacterial
DNA, Mitochondrial
DNA-Binding Proteins
DNA-Directed RNA Polymerases
Drosophila
Drosophila melanogaster
Drosophila Proteins
Electron Transport Complex IV
Electrophysiology
Endothelium, Vascular
Enhancer Elements, Genetic
Epilepsy
Epithelial Cells
Estrogen Receptor alpha
Evolution, Molecular
Exons
Eye Abnormalities
Facies
Family
Family Health
Fatal Outcome
Fathers
Female
Fetal Development
Fibroblast Growth Factor 10
Fibroblasts
Forkhead Transcription Factors
Fractures, Bone
Frameshift Mutation
Gametogenesis
GATA3 Transcription Factor
Gene Deletion
Gene Dosage
Gene Duplication
Gene Editing
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Knockdown Techniques
Gene Knockout Techniques
Gene Order
Gene Rearrangement
Genes, Bacterial
Genes, Insect
Genes, Lethal
Genes, Mitochondrial
Genes, Tumor Suppressor
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Structures
Genetic Variation
Genome, Human
Genome, Mitochondrial
Genome-Wide Association Study
Genomic Imprinting
Genomic Instability
Genomics
Genotype
Germ Cells
Germ-Line Mutation
Gestational Age
Glutathione Transferase
Guanine Nucleotide Exchange Factors
Haploinsufficiency
Heart
Hedgehog Proteins
HEK293 Cells
Heterozygote
High-Throughput Nucleotide Sequencing
Hip
Histocytochemistry
Homologous Recombination
Humans
Hydrophobic and Hydrophilic Interactions
Hymenoptera
Hypertension, Pulmonary
Immunohistochemistry
In Situ Hybridization, Fluorescence
INDEL Mutation
Infant
Infant, Newborn
Infant, Newborn, Diseases
Infant, Premature
Inheritance Patterns
Intellectual Disability
Intercellular Junctions
Intestinal Volvulus
Introns
Ischium
Karyotype
Klinefelter Syndrome
Klippel-Trenaunay-Weber Syndrome
Kruppel-Like Transcription Factors
Language Development Disorders
Larva
Long Interspersed Nucleotide Elements
Lower Extremity Deformities, Congenital
Lung
Lung Diseases
Lung Transplantation
Magnetic Resonance Imaging
Male
MAP Kinase Kinase 6
Maternal Inheritance
Megalencephaly
Membrane Proteins
Membrane Transport Proteins
Mental Disorders
Mesoderm
Metabolic Networks and Pathways
Mice
Mice, Inbred CBA
Mice, Knockout
Microcephaly
Microchip Analytical Procedures
Middle Aged
Minisatellite Repeats
Mitochondrial Dynamics
Models, Animal
Models, Biological
Models, Genetic
Molecular Sequence Data
Morphogenesis
Mosaicism
Mouth Mucosa
Multigene Family
Muscle Hypotonia
Muscle Proteins
Muscle Spasticity
Muscle, Skeletal
Muscular Diseases
Mutagenesis
Mutagenesis, Insertional
Mutation
Mutation, Missense
Myalgia
NAV1.5 Voltage-Gated Sodium Channel
Neoplasm Invasiveness
Neoplasms
Neovascularization, Pathologic
Nerve Tissue Proteins
Neurons
Nuclear Proteins
Nucleotide Motifs
Nucleotides
Oligonucleotide Array Sequence Analysis
Oogenesis
Open Reading Frames
Operon
Organ Specificity
Organogenesis
Ovarian Follicle
Ovarian Neoplasms
Ovary
Patella
Paternal Inheritance
Pedigree
Persistent Fetal Circulation Syndrome
Phenotype
Phylogeny
Pierre Robin Syndrome
Point Mutation
Polyadenylation
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Pregnancy
Prognosis
Promoter Regions, Genetic
Prospective Studies
Protein Binding
Protein Interaction Domains and Motifs
Protein Interaction Maps
Protein Kinases
Pseudomonas putida
Pulmonary Alveoli
Pulmonary Veins
Radiography
Radiography, Thoracic
ran GTP-Binding Protein
Real-Time Polymerase Chain Reaction
Receptor, Fibroblast Growth Factor, Type 2
Receptor, IGF Type 1
Receptors, Cell Surface
Receptors, G-Protein-Coupled
Receptors, Nicotinic
Receptors, Odorant
Recombination, Genetic
Recurrence
Regulatory Sequences, Nucleic Acid
Respiratory Insufficiency
Respiratory System Abnormalities
Rho Guanine Nucleotide Exchange Factors
Risk
RNA Interference
RNA, Long Noncoding
RNA, Messenger
RNA, Transfer
Segmental Duplications, Genomic
Semaphorins
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Sertoli Cells
Sex Characteristics
Sigma Factor
Signal Transduction
Sjogren's Syndrome
Skin
Smith-Magenis Syndrome
Sodium Channels
SOX9 Transcription Factor
Survival Rate
Tandem Repeat Sequences
T-Box Domain Proteins
Thigh
Transcription Factors
Transcription, Genetic
Transcriptome
Translocation, Genetic
Tumor Necrosis Factors
Tumor Suppressor Proteins
Two-Hybrid System Techniques
Ubiquitin-Protein Ligases
Umbilical Veins
Uniparental Disomy
Vascular Endothelial Growth Factor A
Wasps
Williams Syndrome
X Chromosome Inactivation
Young Adult
YY1 Transcription Factor
Zebrafish
Zinc Finger Protein Gli2
SZAFRANSKI's Networks
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Concepts (337)
Derived automatically from this person's publications.
Persistent Fetal Circulation Syndrome
Forkhead Transcription Factors
Enhancer Elements, Genetic
RNA, Long Noncoding
T-Box Domain Proteins
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Co-Authors (41)
People in Profiles who have published with this person.
STANKIEWICZ, PAWEL
LALANI, SEEMA
LUPSKI, JAMES
CHEUNG, SAU WAI
BACINO, CARLOS
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Similar People (60)
People who share similar concepts with this person.
STANKIEWICZ, PAWEL
LUPSKI, JAMES
BOERWINKLE, ERIC
AMOS, CHRIS
GIBBS, RICHARD
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_
Same Department
People who are also in this person's primary department.
AL-RAMAHI, ISMAEL
HARRIS, RONALD
JEONG, MIRA
LIU, NING
VENNER, ERIC
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Physical Neighbors
People whose addresses are nearby this person.
DARILEK, SANDRA
DODDAPANENI, HARSHAVARDHAN
JEONG, MIRA
POTOCKI, LORRAINE
WANG, MENG
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