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ZEYNEP COBAN-AKDEMIR
Concepts (451)
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Concepts are derived automatically from a person's publications.
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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.
46, XX Disorders of Sex Development
Abnormalities, Multiple
ABO Blood-Group System
Actins
Adaptor Proteins, Signal Transducing
Adaptor Proteins, Vesicular Transport
Adenosine Triphosphatases
Adolescent
ADP-Ribosylation Factor 1
Adult
Agammaglobulinemia
Age of Onset
Aged
Algorithms
AlkB Homolog 8, tRNA Methyltransferase
Alleles
Alternative Splicing
Alu Elements
Amino Acid Sequence
Amino Acid Substitution
Amino Acids
AMP-Activated Protein Kinases
Angelman Syndrome
Animals
Animals, Genetically Modified
Ankyrins
Anodontia
Antigens, Neoplasm
Apoptosis Regulatory Proteins
Apyrase
Arabs
Arginine
Arteries
Arthrogryposis
Ataxia
ATPases Associated with Diverse Cellular Activities
Atrial Fibrillation
Atrioventricular Block
Atrophy
Autistic Disorder
Autoantibodies
Autoimmunity
Autophagy
Autopsy
Axons
Base Sequence
Behavior
beta Catenin
Binding Sites
Biological Variation, Population
B-Lymphocytes
Body Patterning
Bone and Bones
Bone Morphogenetic Protein 4
Bone Morphogenetic Protein 7
Brain
Calcium Channels
Calpain
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Carrier Proteins
Case-Control Studies
Cation Transport Proteins
CD4-Positive T-Lymphocytes
CD56 Antigen
CDC2 Protein Kinase
cdc42 GTP-Binding Protein
Cell Adhesion Molecules
Cell Cycle
Cell Cycle Proteins
Cell Differentiation
Cell Line
Cell Line, Tumor
Cell Movement
Cell Proliferation
Cells, Cultured
Cellular Reprogramming
Central Nervous System
Cerebellar Ataxia
Cerebellum
Cerebral Cortex
Cerebral Palsy
Charcot-Marie-Tooth Disease
Child
Child, Preschool
Chile
Chloride Channels
Choline
Chromosome Aberrations
Chromosome Breakpoints
Chromosome Disorders
Chromosome Duplication
Chromosome Inversion
Chromosome Segregation
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 5
Class I Phosphatidylinositol 3-Kinases
Cleft Lip
Cleft Palate
Codon, Nonsense
Codon, Terminator
Cohort Studies
Colon
Common Variable Immunodeficiency
Comparative Genomic Hybridization
Computational Biology
Congenital Abnormalities
Congenital Disorders of Glycosylation
Connectin
Consanguinity
Craniofacial Abnormalities
Crohn Disease
Cytidine Deaminase
Cytokines
Cytomegalovirus
Cytomegalovirus Infections
Cytoplasm
Cytoskeletal Proteins
Cytotoxicity, Immunologic
Data Mining
Databases, Genetic
DEAD-box RNA Helicases
Deafness
Death, Sudden, Cardiac
Democratic Republic of the Congo
Demyelinating Diseases
Developmental Disabilities
Diagnosis, Differential
Dichlorodiphenyl Dichloroethylene
Disease Management
Disease Models, Animal
Disease Susceptibility
DNA
DNA Copy Number Variations
DNA Helicases
DNA Methylation
DNA Mutational Analysis
DNA Replication
DNA-Binding Proteins
Drosophila melanogaster
Dwarfism
Dysarthria
Echocardiography
Egypt
Electrocardiography
Embryo, Mammalian
Embryonic Development
Embryonic Stem Cells
Endoplasmic Reticulum Stress
Endoplasmic Reticulum-Associated Degradation
Epigenomics
Epilepsy
Epstein-Barr Virus Infections
Essential Hypertension
Ethanolamine
Exome
Exons
Exosome Multienzyme Ribonuclease Complex
Eye Abnormalities
Eye Proteins
Face
Facies
Family
Fatal Outcome
F-Box Proteins
Female
Fibrillin-1
Fibroblast Growth Factor 10
Fibroblasts
Fibromatosis, Gingival
Forkhead Transcription Factors
Frameshift Mutation
Gain of Function Mutation
Gametogenesis
Gene Deletion
Gene Duplication
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Gene Regulatory Networks
Genes, Dominant
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Linkage
Genetic Markers
Genetic Pleiotropy
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetics, Medical
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomic Instability
Genomics
Genotype
Genotyping Techniques
Gestational Age
Glycosylation
GPI-Linked Proteins
GTP Phosphohydrolases
GTP-Binding Protein beta Subunits
Hearing Loss, Sensorineural
Heart Atria
Heart Defects, Congenital
Hedgehog Proteins
HEK293 Cells
Hemorrhage
Hepatocyte Nuclear Factor 1-beta
Hereditary Sensory and Autonomic Neuropathies
Hernia, Diaphragmatic
Hernias, Diaphragmatic, Congenital
Herpesvirus 4, Human
Heterotaxy Syndrome
Heterozygote
High-Throughput Nucleotide Sequencing
Histone Acetyltransferases
Homeodomain Proteins
Homozygote
Humans
Hyaluronoglucosaminidase
Hypertension, Pulmonary
Hypogonadism
Immunity
Immunoglobulins
Immunohistochemistry
Immunologic Deficiency Syndromes
Immunologic Memory
Immunological Synapses
Immunophenotyping
Infant
Infant, Newborn
Infant, Newborn, Diseases
Inflammation
Information Dissemination
Intellectual Disability
Intercellular Signaling Peptides and Proteins
Interferon Regulatory Factors
Interferon Type I
Intestinal Pseudo-Obstruction
Intracellular Signaling Peptides and Proteins
Iran
Karyotype
Kidney Diseases, Cystic
Killer Cells, Natural
Laminin
LIM Domain Proteins
Limb Deformities, Congenital
Lipodystrophy
Lissencephaly
Loss of Function Mutation
Low Density Lipoprotein Receptor-Related Protein-6
Lung
Lung Diseases
Lymphocyte Activation
Lymphohistiocytosis, Hemophagocytic
Lymphopenia
Lymphoproliferative Disorders
Magnetic Resonance Imaging
Male
Mammals
Marfan Syndrome
Maternal Inheritance
Mechanistic Target of Rapamycin Complex 2
Mediator Complex
Megalencephaly
Membrane Proteins
Membrane Transport Proteins
Mendelian Randomization Analysis
Metalloendopeptidases
Mice
Mice, Inbred C57BL
Mice, Knockout
Microcephaly
Micrognathism
Microsatellite Repeats
Microscopy, Confocal
Microscopy, Electron, Transmission
Microscopy, Fluorescence
Microtubule-Associated Proteins
Microtubules
Middle Aged
Minichromosome Maintenance Proteins
Mitochondria
Mitochondrial Proteins
Models, Molecular
Molecular Chaperones
Molecular Conformation
Molecular Diagnostic Techniques
Molecular Sequence Data
Mosaicism
Mullerian Ducts
Multifactorial Inheritance
Muscle Hypotonia
Muscle Proteins
Muscle Spasticity
Muscle, Skeletal
Muscles
Muscular Dystrophies, Limb-Girdle
Muscular Dystrophy, Emery-Dreifuss
Musculoskeletal Abnormalities
Mutant Proteins
Mutation
Mutation, Missense
Myelin P2 Protein
Myokymia
National Institutes of Health (U.S.)
Neoplasm Proteins
Neoplasms
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Netrins
Neural Conduction
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neuroimaging
Neurons
Neutropenia
Nonsense Mediated mRNA Decay
Nuclear Proteins
Nucleotides
Oncogene Proteins
Optic Atrophy
Organogenesis
Osteomyelitis
Osteoporosis
Pakistan
Paraplegia
Parkinsonian Disorders
Paternal Inheritance
Pathology, Molecular
PAX2 Transcription Factor
PAX8 Transcription Factor
Pedigree
Penetrance
Peptide Chain Termination, Translational
Peptides
Peripheral Nervous System Diseases
Peroxidases
Phenotype
Phosphatidylinositol 3-Kinases
Phosphorylation
Pilot Projects
Pluripotent Stem Cells
Point Mutation
Polydactyly
Polymorphism, Single Nucleotide
Primary Ovarian Insufficiency
Progeria
Prognosis
Proteasome Endopeptidase Complex
Protein Binding
Protein Domains
Protein Folding
Protein Tyrosine Phosphatases
Protein-Arginine N-Methyltransferases
Proteins
Protein-Tyrosine Kinases
Proteomics
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-myc
Quadriplegia
Radiography, Thoracic
Rare Diseases
Real-Time Polymerase Chain Reaction
Receptor Tyrosine Kinase-like Orphan Receptors
Receptor, Fibroblast Growth Factor, Type 2
Receptor, Platelet-Derived Growth Factor beta
Receptors, Virus
Reference Values
Renal Insufficiency
Repressor Proteins
Retina
Retinal Cone Photoreceptor Cells
Retinal Rod Photoreceptor Cells
Retinitis Pigmentosa
Retrospective Studies
Reverse Genetics
Reverse Transcriptase Polymerase Chain Reaction
rhoA GTP-Binding Protein
Risk Assessment
Risk Factors
RNA
RNA Helicases
RNA Interference
RNA Processing, Post-Transcriptional
RNA Splice Sites
RNA Splicing
RNA, Messenger
RNA-Binding Proteins
Ryanodine Receptor Calcium Release Channel
Scoliosis
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology
Severity of Illness Index
Siblings
Signal Transduction
Sirolimus
Smad2 Protein
Smith-Magenis Syndrome
Software
Somatic Hypermutation, Immunoglobulin
Spastic Paraplegia, Hereditary
Stem Cell Transplantation
Syndrome
T-Box Domain Proteins
Tenascin
Tomography, X-Ray Computed
Trans-Activators
Transcription Factors
Transcriptome
Transposition of Great Vessels
Trinucleotide Repeat Expansion
Trinucleotide Repeats
Tubulin
Turkey
Ubiquitin
Ubiquitin-Protein Ligases
Unfolded Protein Response
Uniparental Disomy
United States
Urinary Bladder
Urogenital Abnormalities
Uterus
Vagina
Vesico-Ureteral Reflux
Vesicular Transport Proteins
Viremia
Virus Diseases
Vocal Cord Paralysis
von Willebrand Diseases
von Willebrand Factor
White Matter
Whole Genome Sequencing
Wiskott-Aldrich Syndrome Protein Family
Wnt Proteins
Wnt Signaling Pathway
Wolffian Ducts
Wolff-Parkinson-White Syndrome
Workflow
X Chromosome Inactivation
Young Adult
Zebrafish
Zebrafish Proteins
Zinc
COBAN-AKDEMIR's Networks
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Concepts (451)
Derived automatically from this person's publications.
Phenotype
Exome
Pedigree
Genetic Variation
Neurodevelopmental Disorders
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Co-Authors (108)
People in Profiles who have published with this person.
LUPSKI, JAMES
GIBBS, RICHARD
POSEY, JENNIFER
PEHLIVAN, DAVUT
MUZNY, DONNA
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Same Department
People who are also in this person's primary department.
EBLE, TANYA
KETKAR, SHAMIKA
LICHTARGE, OLIVIER
MUZNY, DONNA
PARVANDEH, SAEID
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