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DAVUT PEHLIVAN
Concepts (429)
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Concepts are derived automatically from a person's publications.
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Categories
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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
ADAMTS Proteins
Adaptor Proteins, Signal Transducing
Adaptor Proteins, Vesicular Transport
Adolescent
Adult
Age of Onset
Aged
AlkB Homolog 8, tRNA Methyltransferase
Alleles
Alopecia
Alu Elements
Amines
Amino Acid Sequence
Angelman Syndrome
Animals
Anodontia
Anophthalmos
Anti-Bacterial Agents
Anticoagulants
Antigens, Nuclear
Anti-Inflammatory Agents, Non-Steroidal
Antineoplastic Combined Chemotherapy Protocols
Anxiety
Apoptosis
Apyrase
Armadillo Domain Proteins
Arthrogryposis
ATP-Binding Cassette Transporters
Atrophy
Autistic Disorder
Autoantibodies
Autophagy
Axoneme
Axons
Bardet-Biedl Syndrome
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
Biological Evolution
Biological Variation, Population
Biomarkers, Tumor
Biopsy
Body Patterning
Bone Development
Brain
Brain Diseases
Brain Diseases, Metabolic, Inborn
Brain Edema
Caenorhabditis elegans
Calcium Channels
Calpain
Carcinoma, Squamous Cell
Caregivers
Carrier Proteins
Case-Control Studies
Cataract
Cavernous Sinus Thrombosis
Cell Adhesion Molecules
Cell Cycle Proteins
Cell Differentiation
Cell Line
Cell Movement
Central Nervous System Diseases
Central Nervous System Protozoal Infections
Cerebellar Ataxia
Cerebellar Diseases
Cerebellum
Cerebral Cortex
Cerebral Palsy
Cerebrum
Charcot-Marie-Tooth Disease
Child
Child, Preschool
Chondroitin Sulfate Proteoglycans
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Breakpoints
Chromosome Deletion
Chromosome Duplication
Chromosome Mapping
Chromosome Segregation
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 17
Chromosomes, Human, X
Cilia
Classical Lissencephalies and Subcortical Band Heterotopias
Cleft Palate
Codon, Nonsense
Codon, Terminator
Cohort Studies
Coloboma
Comparative Genomic Hybridization
Congenital Disorders of Glycosylation
Connectin
Consanguinity
Constipation
Contracture
Corneal Opacity
Cranial Sinuses
Craniofacial Abnormalities
CRISPR-Cas Systems
Cross-Sectional Studies
Curcumin
Cytoskeletal Proteins
Databases, Genetic
De Lange Syndrome
DEAD-box RNA Helicases
Deafness
Decompressive Craniectomy
Depression
Developmental Disabilities
Dichlorodiphenyl Dichloroethylene
Disease
Disease Models, Animal
DNA Breaks
DNA Copy Number Variations
DNA Helicases
DNA Mutational Analysis
DNA Repair
DNA Replication
DNA-Binding Proteins
Down-Regulation
Drosophila
Drosophila melanogaster
Drosophila Proteins
Dyneins
Dysarthria
Dystonia
Dystonic Disorders
Eczema
Egypt
Electroencephalography
Electromyography
Encephalitis
Endoplasmic Reticulum Stress
Endoplasmic Reticulum-Associated Degradation
Endoribonucleases
Endothelial Cells
Epilepsy
Epilepsy, Generalized
Esophageal Neoplasms
Exome
Exons
Exonucleases
Extracellular Matrix
Eye Abnormalities
Eye Proteins
Facies
Family
Fatal Outcome
Female
Fibrillar Collagens
Fibroblasts
Fibromatosis, Gingival
Focal Adhesion Protein-Tyrosine Kinases
Follow-Up Studies
Founder Effect
Frameshift Mutation
Gastroesophageal Reflux
Gastrointestinal Diseases
Gastrointestinal Tract
Gastrulation
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Expression Regulation, Neoplastic
Gene Frequency
Gene Order
Gene Rearrangement
Gene Regulatory Networks
Genes, Dominant
Genes, p53
Genes, Recessive
Genes, Tumor Suppressor
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Load
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Gestational Age
Glutamine
Glycogen
Glycosylation
GPI-Linked Proteins
Growth Disorders
GTP Phosphohydrolases
Hamartoma
Head and Neck Neoplasms
Health Status
Hearing Loss, Sensorineural
HEK293 Cells
Hereditary Sensory and Autonomic Neuropathies
Hereditary Sensory and Motor Neuropathy
Heterozygote
High-Throughput Nucleotide Sequencing
Hip Dislocation
Histidine
Histone Deacetylases
Histone-Lysine N-Methyltransferase
Homeodomain Proteins
Homozygote
HSP40 Heat-Shock Proteins
HSP70 Heat-Shock Proteins
Humans
Hydroxymethylglutaryl CoA Reductases
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Hypogonadism
Hypopituitarism
IgA Deficiency
Immunoglobulins
INDEL Mutation
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Infant, Newborn, Diseases
Inflammation
Inheritance Patterns
Intellectual Disability
Intracellular Signaling Peptides and Proteins
Intracranial Hemorrhages
Iran
Kartagener Syndrome
Kidney
Kidney Diseases, Cystic
Klippel-Feil Syndrome
Ligands
Lissencephaly
Loss of Function Mutation
Loss of Heterozygosity
Lysine-tRNA Ligase
Magnetic Resonance Imaging
Male
Mammals
Mediator Complex
MELAS Syndrome
Membrane Proteins
Mendelian Randomization Analysis
Mental Retardation, X-Linked
Metabolome
Methyl-CpG-Binding Protein 2
Mevalonic Acid
Mice
Mice, Inbred C57BL
Mice, Inbred CBA
Mice, Knockout
Mice, Mutant Strains
Microarray Analysis
Microcephaly
Microfilament Proteins
Microphthalmos
Microsatellite Repeats
Microscopy, Fluorescence
Microtubule-Associated Proteins
Microtubules
Middle Aged
Minichromosome Maintenance Proteins
Mitochondrial Diseases
Mitochondrial Myopathies
Mitochondrial Proteins
Models, Genetic
Models, Molecular
Molecular Chaperones
Molecular Diagnostic Techniques
Molecular Sequence Data
Mosaicism
Motor Neurons
Movement Disorders
Multifactorial Inheritance
Muscle Hypotonia
Muscle Proteins
Muscle Spasticity
Muscle, Skeletal
Muscular Diseases
Muscular Dystrophies
Muscular Dystrophies, Limb-Girdle
Muscular Dystrophy, Emery-Dreifuss
Mutation
Mutation, Missense
Myelin P0 Protein
Myelin P2 Protein
Myelin Proteins
Myeloid-Lymphoid Leukemia Protein
Myokymia
Myopathy, Central Core
Myositis
Naegleria fowleri
National Institutes of Health (U.S.)
Neoplasm Metastasis
Neoplasm Proteins
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Netrins
Neural Conduction
Neurodevelopmental Disorders
Neuromuscular Diseases
Neurons
Nitrogen
Nuclear Proteins
Nucleic Acid Amplification Techniques
Optic Atrophies, Hereditary
Orofaciodigital Syndromes
Osteogenesis Imperfecta
Osteomyelitis
Oxidoreductases
Paraplegia
Parents
Pathology, Molecular
Pedigree
Penetrance
Peripheral Nervous System Diseases
Peru
Phenotype
Phosphotransferases
Pituitary Gland
Polymorphism, Single Nucleotide
Polyneuropathies
Prevalence
Primary Ovarian Insufficiency
Prognosis
Protein Conformation
Protein Folding
Protein Isoforms
Protein Structure, Tertiary
Proteins
Proteolysis
Proteome
Proto-Oncogene Proteins
Psychometrics
Quadriplegia
Quality of Life
Quantitative Trait, Heritable
Radiography
Rare Diseases
Rats
Receptor, EphA2
Receptors, Cell Surface
Receptors, G-Protein-Coupled
Receptors, Immunologic
Receptors, Metabotropic Glutamate
Receptors, Notch
Recombination, Genetic
Refsum Disease
Renal Insufficiency
Repetitive Sequences, Nucleic Acid
Repressor Proteins
Reproducibility of Results
Respiratory System
Retina
Retrospective Studies
Rett Syndrome
Reverse Genetics
Ribosomes
RNA Interference
RNA Splice Sites
RNA Splicing
RNA, Messenger
RNA, Transfer
RNA-Binding Proteins
Ryanodine Receptor Calcium Release Channel
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Sciatic Nerve
Scoliosis
Seizures
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Serine C-Palmitoyltransferase
Sex Factors
Siblings
Signal Transduction
Sinus Thrombosis, Intracranial
Sodium-Calcium Exchanger
Software
Spasms, Infantile
Spastic Paraplegia, Hereditary
Spinal Muscular Atrophies of Childhood
Spine
Spinocerebellar Ataxias
Stroke
Suppression, Genetic
Surveys and Questionnaires
Survival Analysis
Survival Rate
Symporters
Syndrome
T-Box Domain Proteins
Tight Junctions
TOR Serine-Threonine Kinases
Trans-Activators
Transcription Factors
Transcriptome
Translocation, Genetic
Tremor
Trichothiodystrophy Syndromes
Tubulin
Tumor Suppressor Proteins
Turkey
Ubiquitin
Ubiquitin-Protein Ligases
Unfolded Protein Response
United States
Urinary Tract
Urogenital Abnormalities
Vesico-Ureteral Reflux
Vesicular Monoamine Transport Proteins
Vesicular Transport Proteins
Vocal Cord Paralysis
White Matter
X Chromosome
X Chromosome Inactivation
Xeroderma Pigmentosum Group D Protein
Young Adult
Zebrafish
Zebrafish Proteins
PEHLIVAN's Networks
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Concepts (429)
Derived automatically from this person's publications.
Mental Retardation, X-Linked
Neurodevelopmental Disorders
Sinus Thrombosis, Intracranial
Charcot-Marie-Tooth Disease
Microcephaly
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Co-Authors (86)
People in Profiles who have published with this person.
LUPSKI, JAMES
GIBBS, RICHARD
POSEY, JENNIFER
CALAME, DANIEL
MUZNY, DONNA
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_
Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
GIBBS, RICHARD
ZOGHBI, HUDA
BOERWINKLE, ERIC
STANKIEWICZ, PAWEL
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Same Department
People who are also in this person's primary department.
EL-HALLAL, MARIA
EMRICK, LISA
GLAZE, DANIEL
LYONS-WARREN, ARIEL
QUACH, MICHAEL
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