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William Dobyns
Concepts (1084)
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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.
14-3-3 Proteins
1-Alkyl-2-acetylglycerophosphocholine Esterase
3-Oxo-5-alpha-Steroid 4-Dehydrogenase
46, XX Disorders of Sex Development
Abnormalities, Multiple
Acetazolamide
Acrocallosal Syndrome
Actin-Related Protein 2-3 Complex
Actins
Adaptor Protein Complex sigma Subunits
Adaptor Proteins, Signal Transducing
Adaptor Proteins, Vesicular Transport
Adenosine Triphosphatases
Adenosine Triphosphate
Adolescent
ADP-Ribosylation Factors
Adrenal Gland Diseases
Adrenocorticotropic Hormone
Adrenoleukodystrophy
Adult
Advisory Committees
Age Factors
Age of Onset
Aged
Aged, 80 and over
Agenesis of Corpus Callosum
Aging
Aging, Premature
Aicardi Syndrome
Alanine
Algorithms
Alleles
Alopecia
alpha Catenin
alpha Karyopherins
alpha-Mannosidase
Alternative Splicing
Amino Acid Metabolism, Inborn Errors
Amino Acid Motifs
Amino Acid Sequence
Amino Acid Substitution
Amino Acids
Amniotic Band Syndrome
Amyloid beta-Peptides
Anal Canal
Analysis of Variance
Anemia, Sickle Cell
Aneuploidy
Aneurysm
Animals
Animals, Newborn
Antibodies, Monoclonal
Anticonvulsants
Antigens, Neoplasm
Antiparkinson Agents
Antiphospholipid Syndrome
Antisense Elements (Genetics)
Anus, Imperforate
Aortic Coarctation
Apoptosis
Archaeology
Arginine-tRNA Ligase
Argonaute Proteins
Armadillo Domain Proteins
Arnold-Chiari Malformation
Arthrogryposis
Aspartic Acid
Aspirin
Astrocytes
Ataxia
Ataxia Telangiectasia
Ataxia Telangiectasia Mutated Proteins
Atrophy
Attention Deficit Disorder with Hyperactivity
Auditory Perception
Autism Spectrum Disorder
Autistic Disorder
Autoantibodies
Awards and Prizes
Axon Guidance
Axons
Bacterial Capsules
Bacterial Vaccines
Basal Bodies
Basal Ganglia
Basal Ganglia Diseases
Base Sequence
Basement Membrane
Basilar Artery
beta-Transducin Repeat-Containing Proteins
Biological Evolution
Biological Science Disciplines
Biomarkers
Biopsy
Birth Weight
Bladder Exstrophy
Blastocyst
Blepharophimosis
Blepharoptosis
Blotting, Northern
Blotting, Southern
Blotting, Western
Body Dysmorphic Disorders
Body Mass Index
Body Patterning
Body Size
Bone and Bones
Bone Diseases, Developmental
Brain
Brain Damage, Chronic
Brain Diseases
Brain Mapping
Brain Neoplasms
Brain Stem
Brazil
Bromodeoxyuridine
Bronchi
Butadienes
Cadherins
Calcinosis
Calcium
Calcium Channels
Calcium-Binding Proteins
Calibration
Calreticulin
Capillaries
Carotid Arteries
Carrier Proteins
Case-Control Studies
Caspase 2
Catalytic Domain
Cataract
Catastrophic Illness
Catenins
Cell Adhesion
Cell Adhesion Molecules
Cell Adhesion Molecules, Neuronal
Cell Count
Cell Cycle
Cell Cycle Proteins
Cell Death
Cell Differentiation
Cell Division
Cell Line
Cell Line, Transformed
Cell Line, Tumor
Cell Lineage
Cell Movement
Cell Proliferation
Cell Survival
Cell Transformation, Neoplastic
Cell-Free Nucleic Acids
Cells, Cultured
Central Nervous System
Central Nervous System Cysts
Central Nervous System Neoplasms
Central Nervous System Vascular Malformations
Centromere
Centrosome
Cephalometry
Cerebellar Ataxia
Cerebellar Cortex
Cerebellar Diseases
Cerebellar Vermis
Cerebellum
Cerebral Angiography
Cerebral Cortex
Cerebral Hemorrhage
Cerebral Infarction
Cerebral Small Vessel Diseases
Cerebral Ventricles
Cerebral Ventriculography
Cerebrospinal Fluid Shunts
Cerebrovascular Disorders
Cerebrum
Child
Child Behavior Disorders
Child Development Disorders, Pervasive
Child, Preschool
Chi-Square Distribution
CHO Cells
Choline
Chorea
Choristoma
Chromatin
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Fragility
Chromosome Inversion
Chromosome Mapping
Chromosome Segregation
Chromosomes, Artificial, Bacterial
Chromosomes, Human, 16-18
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 21
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 9
Chromosomes, Human, X
Cilia
Ciliopathies
Cisterna Magna
Class I Phosphatidylinositol 3-Kinases
Classical Lissencephalies and Subcortical Band Heterotopias
Cleft Lip
Cleft Palate
Clinical Enzyme Tests
Cloaca
Clonazepam
Cloning, Molecular
Clubfoot
Coatomer Protein
Cobblestone Lissencephaly
Cockayne Syndrome
Codon
Codon, Nonsense
Codon, Terminator
Cognition
Cognition Disorders
Cognitive Dysfunction
Cohort Studies
Collagen Type IV
Coloboma
Combined Modality Therapy
Comparative Genomic Hybridization
Computational Biology
Computer Simulation
Congenital Abnormalities
Congenital Disorders of Glycosylation
Congenital Hypothyroidism
Connective Tissue
Connective Tissue Diseases
Consanguinity
Consensus
Conserved Sequence
Contact Inhibition
Contractile Proteins
Copper
Cornea
Corneal Diseases
Corpus Callosum
COS Cells
Cosmids
Costello Syndrome
CRADD Signaling Adaptor Protein
Cranial Fossa, Posterior
Craniofacial Abnormalities
Craniopharyngioma
Craniosynostoses
Creatine
CREB-Binding Protein
Cricetinae
Cricetulus
Crossing Over, Genetic
Cryptorchidism
Cutis Laxa
Cyclin D2
Cyclin-Dependent Kinase 5
Cyclin-Dependent Kinase Inhibitor p16
Cyclin-Dependent Kinases
Cysteine Endopeptidases
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Cysts
Cytoskeletal Proteins
Dandy-Walker Syndrome
Data Collection
Databases, Factual
Databases, Genetic
DEAD-box RNA Helicases
Decision Making
Deglutition Disorders
Delphi Technique
Demyelinating Diseases
Dendrites
Dendritic Cells
Dentate Gyrus
Dermis
Developmental Disabilities
Diabetes Mellitus, Type 1
Diagnosis, Differential
Diagnostic Errors
Diagnostic Imaging
Diagnostic Tests, Routine
Diazepam
Diencephalon
Diffuse Cerebral Sclerosis of Schilder
Diffusion Tensor Imaging
Digestive System Abnormalities
Dihydrotestosterone
Dimercaprol
Dimerization
Diplopia
Disease
Disease Management
Disease Models, Animal
Disease Progression
Diseases in Twins
Disks Large Homolog 4 Protein
Disorders of Sex Development
DNA
DNA Copy Number Variations
DNA Damage
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA Probes
DNA Repair
DNA Repair Enzymes
DNA, Complementary
DNA-Activated Protein Kinase
DNA-Binding Proteins
Dopamine
Dosage Compensation, Genetic
Drosophila
Drosophila melanogaster
Drosophila Proteins
Drug Resistant Epilepsy
Drug Tolerance
Dwarfism
Dyneins
Dysarthria
Dyskinesias
Dystonia
Dystonic Disorders
Dystroglycans
E1A-Associated p300 Protein
Ear
Echoencephalography
Ectopia Cordis
Edema
Egypt
Ehlers-Danlos Syndrome
Electroencephalography
Electromyography
Electrophoresis, Capillary
Electroporation
Embryo, Mammalian
Embryonic and Fetal Development
Embryonic Stem Cells
Encephalocele
Endoplasmic Reticulum
Endoribonucleases
Endosomal Sorting Complexes Required for Transport
Enhancer of Zeste Homolog 2 Protein
Enzyme Inhibitors
Ependymoglial Cells
Epigenesis, Genetic
Epilepsy
Epistasis, Genetic
Epithelial Cells
Epithelial-Mesenchymal Transition
Erythrocytes
Esophageal Atresia
Esophagus
Evidence-Based Medicine
Evoked Potentials, Visual
Evolution, Molecular
Excitatory Amino Acid Agonists
Exome
Exons
Exonucleases
Exosome Multienzyme Ribonuclease Complex
Extracellular Matrix
Extracellular Matrix Proteins
Extremities
Eye
Eye Abnormalities
Eye Diseases
Eye Diseases, Hereditary
Eye Movements
Eye Neoplasms
Eye Proteins
Face
Facial Asymmetry
Facial Bones
Facial Expression
Facial Neoplasms
Facial Nerve
Facial Paralysis
Facies
Family
Family Health
Fatal Outcome
Female
Fetal Death
Fetal Diseases
Fetal Growth Retardation
Fetus
Fibroblast Growth Factor 8
Fibroblasts
Fibroma
Fibrous Dysplasia, Polyostotic
Filamins
Fingers
Finland
Fluorescence
Fluorescent Antibody Technique, Indirect
Focal Dermal Hypoplasia
Follow-Up Studies
Forkhead Transcription Factors
Fossils
Founder Effect
Fragile X Syndrome
Frameshift Mutation
Frontal Bone
Frontal Lobe
Functional Laterality
Gain of Function Mutation
Gastroesophageal Reflux
Gene Amplification
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Gene Knockdown Techniques
Gene Knockout Techniques
Gene Ontology
Gene Order
Gene Regulatory Networks
Genes
Genes, Dominant
Genes, Lethal
Genes, Overlapping
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Carrier Screening
Genetic Complementation Test
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Linkage
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetic Vectors
Genetics
Genitalia
Genitalia, Female
Genitalia, Male
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Genotyping Techniques
Germ-Line Mutation
Gestational Age
Glaucoma
Glucuronosyltransferase
Glutamate Decarboxylase
Glutamic Acid
Glutamine
Glutathione Reductase
Glutathione Transferase
Glycine
Glycosylation
Gonadal Dysgenesis, 46,XY
Gray Matter
Green Fluorescent Proteins
Growth Disorders
GTPase-Activating Proteins
GTP-Binding Proteins
Guanylate Kinases
Guidelines as Topic
Gyrus Cinguli
Haemophilus Infections
Haemophilus influenzae
Haemophilus Vaccines
Hair
Hair Follicle
Hamartoma
Hand Deformities, Congenital
Haploidy
Haploinsufficiency
Haplotypes
Head Movements
Headache
Hearing Loss
Hearing Loss, Sensorineural
Heart
Heart Defects, Congenital
Hedgehog Proteins
HEK293 Cells
HeLa Cells
Hemangioma
Hemangioma, Cavernous
Hematopoietic Stem Cell Transplantation
Hemimegalencephaly
Hemiterpenes
Hepatolenticular Degeneration
Hernia, Umbilical
Heterozygote
High-Throughput Nucleotide Sequencing
Hippocampus
Hirschsprung Disease
Histone Deacetylases
Histone-Lysine N-Methyltransferase
History, 20th Century
History, 21st Century
History, Ancient
Holoprosencephaly
Homeodomain Proteins
Hominidae
Homovanillic Acid
Homozygote
Humans
Hybrid Cells
Hydrocephalus
Hydrolases
Hydrops Fetalis
Hydroxyindoleacetic Acid
Hyperkinesis
Hypertension, Portal
Hypertrophy
Hypesthesia
Hypogonadism
Hypothalamic Diseases
Hypothalamus
Image Processing, Computer-Assisted
Imaging, Three-Dimensional
Imatinib Mesylate
Immune Evasion
Immunoenzyme Techniques
Immunoglobulin G
Immunohistochemistry
Immunoprecipitation
In Situ Hybridization
In Situ Hybridization, Fluorescence
Incidence
Indonesia
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Infant, Premature
Inheritance Patterns
Inositol
Intellectual Disability
Intelligence
Intercellular Signaling Peptides and Proteins
Interferon-Induced Helicase, IFIH1
Internationality
Internet
Interneurons
Intestinal Atresia
Intestines
Intracellular Signaling Peptides and Proteins
Intracranial Aneurysm
Intracranial Arterial Diseases
Introns
Isoelectric Focusing
Isotretinoin
Italy
Jejunum
Jews
Karyotyping
Katanin
KCNQ Potassium Channels
Kidney
Kidney Diseases
Kidney Diseases, Cystic
Kinetochores
Klippel-Trenaunay-Weber Syndrome
Knowledge Bases
Kruppel-Like Transcription Factors
Laminin
Language
Language Development Disorders
Language Tests
Laser Capture Microdissection
Lateral Ventricles
Leukoencephalopathies
Ligands
Limb Deformities, Congenital
Linkage Disequilibrium
Lipomatosis
Lissencephaly
Liver
Liver Cirrhosis
Liver Diseases
Liver Failure, Acute
Lod Score
Longevity
Longitudinal Studies
Loose Anagen Hair Syndrome
Loss of Function Mutation
Lumbosacral Region
Luminescent Proteins
Lupus Coagulation Inhibitor
Lupus Erythematosus, Systemic
Lymphatic Abnormalities
Lymphatic Vessels
Lymphedema
Lymphocytes
Macaca nemestrina
Macrophages
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Male
Malformations of Cortical Development
Malformations of Cortical Development, Group II
Mandibulofacial Dysostosis
Mannose
Mannosyltransferases
Matched-Pair Analysis
Mechanistic Target of Rapamycin Complex 1
Mediator Complex
Medulla Oblongata
MEF2 Transcription Factors
Megalencephaly
Memantine
Membrane Glycoproteins
Membrane Potentials
Membrane Proteins
Membrane Transport Proteins
Mental Disorders
Mental Retardation, X-Linked
Mesencephalon
Methoxyhydroxyphenylglycol
Methyl-CpG-Binding Protein 2
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Mutant Strains
Mice, Neurologic Mutants
Microbodies
Microcephaly
Microfilament Proteins
Microphthalmos
Microsatellite Repeats
Microscopy, Fluorescence
Microtubule-Associated Proteins
Microtubules
Middle Aged
Middle East
Migraine with Aura
Mitogen-Activated Protein Kinase 7
Mitosis
Models, Anatomic
Models, Genetic
Models, Molecular
Molecular Biology
Molecular Conformation
Molecular Diagnostic Techniques
Molecular Sequence Data
Molecular Targeted Therapy
Molecular Typing
Monosaccharide Transport Proteins
Morphogenesis
Mosaicism
Motor Activity
Mouse Embryonic Stem Cells
Movement Disorders
Mullerian Ducts
Multiplex Polymerase Chain Reaction
Multiprotein Complexes
Multivariate Analysis
Muscle Hypotonia
Muscle Spasticity
Muscle, Skeletal
Muscles
Muscular Diseases
Muscular Dystrophies
Musculoskeletal Abnormalities
Mutagenesis
Mutagenesis, Site-Directed
Mutant Proteins
Mutation
Mutation, Missense
Myoclonus
Myofibromatosis
Myosin Heavy Chains
N-Acetylgalactosaminyltransferases
N-Acetylglucosaminyltransferases
Naphthyridines
Necrosis
Neocortex
Neoplasm Metastasis
Neoplasm Proteins
Neoplasms
Nerve Degeneration
Nerve Net
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Neural Cell Adhesion Molecules
Neural Conduction
Neural Pathways
Neural Stem Cells
Neural Tube
Neurobiology
Neurocutaneous Syndromes
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neurogenesis
Neuroglia
Neuroimaging
Neurologic Examination
Neurology
Neurons
Neuropeptides
Neuropsychological Tests
Nevus
Nevus, Pigmented
NFI Transcription Factors
NIH 3T3 Cells
N-Methylaspartate
Nonmuscle Myosin Type IIB
Nonsense Mediated mRNA Decay
Noonan Syndrome
Norepinephrine
Nose
Nuclear Family
Nuclear Proteins
Nuclear Respiratory Factor 1
Nucleic Acid Hybridization
Nucleotidyltransferases
Nystagmus, Pathologic
Occipital Bone
Occludin
Ocular Motility Disorders
Oligonucleotide Array Sequence Analysis
Oligonucleotide Probes
Olivopontocerebellar Atrophies
Oman
Oncogene Proteins, Fusion
Open Reading Frames
Optic Atrophy
Optic Disk
Optic Lobe, Nonmammalian
Optic Nerve
Orbit
Organ Size
Organogenesis
Orofaciodigital Syndromes
Orphan Nuclear Receptors
Osteochondrodysplasias
Osteogenesis Imperfecta
Ouabain
Pakistan
Paleopathology
Paraparesis, Spastic
Parents
Paresis
Parietal Lobe
Parkinson Disease
Parkinson Disease, Secondary
Parkinsonian Disorders
Patch-Clamp Techniques
PAX2 Transcription Factor
PAX6 Transcription Factor
PAX9 Transcription Factor
PC12 Cells
Pediatric Obesity
Pedigree
Penetrance
Penicillamine
Pentanes
Pentosyltransferases
Peptide Elongation Factors
Peptides
Periaqueductal Gray
Peripheral Nerves
Peripheral Nervous System Diseases
Periventricular Nodular Heterotopia
Phenotype
Phosphatidylinositol 3-Kinases
Phosphatidylinositols
Phospholipases A
Phosphoprotein Phosphatases
Phosphoproteins
Phosphoric Diester Hydrolases
Phosphorylation
Phylogeny
Physical Chromosome Mapping
Physostigmine
Pierre Robin Syndrome
Pigmentation
Pilot Projects
Pituitary Gland
Pituitary Neoplasms
Placenta
Plasmapheresis
Platelet-Derived Growth Factor
Point Mutation
Poliovirus Vaccine, Oral
Polycomb Repressive Complex 2
Polydactyly
Polymerase Chain Reaction
Polymicrogyria
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Polymorphism, Single Nucleotide
Polymorphism, Single-Stranded Conformational
Polyradiculoneuropathy
Polysaccharides
Polysaccharides, Bacterial
Pons
Postmortem Changes
Practice Guidelines as Topic
Precision Medicine
Predictive Value of Tests
Pregnancy
Pregnancy Complications, Infectious
Pregnancy Outcome
Prenatal Diagnosis
Prevalence
Primary Myelofibrosis
Primates
Probability
Prognosis
Promoter Regions, Genetic
Prosencephalon
Prospective Studies
Prosthesis Failure
Protein Aggregation, Pathological
Protein Binding
Protein Conformation
Protein Domains
Protein Isoforms
Protein Kinase C
Protein Kinase C-epsilon
Protein Kinase Inhibitors
Protein Multimerization
Protein Phosphatase 1
Protein Phosphatase 2
Protein Structure, Secondary
Protein Structure, Tertiary
Protein Subunits
Proteins
Proteomics
Proto-Oncogene Proteins c-akt
Proto-Oncogene Proteins c-sis
Proto-Oncogene Proteins p21(ras)
Pseudopseudohypoparathyroidism
Pseudotumor Cerebri
Psychomotor Disorders
Psychotic Disorders
PTEN Phosphohydrolase
Purkinje Cells
Pyramidal Tracts
Pyrophosphatases
Quadriplegia
Quantitative Trait Loci
rab GTP-Binding Proteins
rab3 GTP-Binding Proteins
Rabbits
Radiography
Radioimmunoassay
Radionuclide Imaging
ras Proteins
Rats
Rats, Wistar
Real-Time Polymerase Chain Reaction
Receptor Protein-Tyrosine Kinases
Receptor, Fibroblast Growth Factor, Type 1
Receptor, Metabotropic Glutamate 5
Receptor, Platelet-Derived Growth Factor beta
Receptors, Androgen
Receptors, Cytoplasmic and Nuclear
Receptors, Glycine
Receptors, G-Protein-Coupled
Receptors, Metabotropic Glutamate
Receptors, N-Methyl-D-Aspartate
Receptors, Retinoic Acid
Receptors, Virus
Recombinant Proteins
Recombination, Genetic
Recovery of Function
Rectum
Recurrence
Reference Values
Regulatory Elements, Transcriptional
Regulatory Factor X Transcription Factors
Remission, Spontaneous
Repetitive Sequences, Amino Acid
Repetitive Sequences, Nucleic Acid
Replication Protein A
Replication Protein C
Repressor Proteins
Reproducibility of Results
Reproduction
Research
Respiratory Rate
Restriction Mapping
Retina
Retinal Degeneration
Retinal Diseases
Retinal Dysplasia
Retinitis Pigmentosa
Retinoids
Retrospective Studies
Rett Syndrome
Review Literature as Topic
Reye Syndrome
Rhabdoid Tumor
rhoA GTP-Binding Protein
Rhombencephalon
Ribonucleoprotein, U5 Small Nuclear
Ribonucleoproteins, Small Nuclear
Ribosomal Protein S6 Kinases
Ring Chromosomes
Risk
Risk Assessment
Risk Factors
RNA
RNA Interference
RNA Polymerase II
RNA Splice Sites
RNA Splicing
RNA, Messenger
RNA, Small Interfering
RNA, Small Nuclear
RNA, Viral
RNA-Binding Proteins
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Sacrum
Scalp
Schizophrenia
Sebaceous Glands
Segmental Duplications, Genomic
Seizures
Septo-Optic Dysplasia
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology
Sequence Homology, Amino Acid
Serine Endopeptidases
Serotonin
Severe Combined Immunodeficiency
Severity of Illness Index
Sex Characteristics
Sex Chromosome Aberrations
Sex Chromosome Disorders
Sex Distribution
Sex Factors
Signal Transduction
Single-Cell Analysis
Skin
Skin Abnormalities
Skin Diseases
Skin Diseases, Vascular
Skin Neoplasms
Skin Pigmentation
Skull
SMARCB1 Protein
Smoothened Receptor
Sodium-Phosphate Cotransporter Proteins, Type III
Sodium-Potassium-Exchanging ATPase
Software
Sotos Syndrome
Spasms, Infantile
Spatio-Temporal Analysis
Species Specificity
Sphingomyelin Phosphodiesterase
Spinal Cord
Spinal Puncture
Spindle Apparatus
Spine
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Spliceosomes
src Homology Domains
Statistics, Nonparametric
Stem Cells
Stereotypic Movement Disorder
Steroids
Stiff-Person Syndrome
Stroke
Structure-Activity Relationship
Survival Rate
Synaptic Transmission
Syndactyly
Syndrome
T-Box Domain Proteins
Telangiectasis
Telomere
Teratoma
Terminology as Topic
Testis
Testosterone
Tight Junctions
Time Factors
Tissue Distribution
Toes
Tomography, X-Ray Computed
TOR Serine-Threonine Kinases
Touch
Trachea
Tracheoesophageal Fistula
Trans-Activators
Transcription Factor TFIID
Transcription Factors
Transcription, Genetic
Transcriptional Activation
Transcriptome
Transfection
Translocation, Genetic
Treatment Outcome
Tremor
Tretinoin
Trinucleotide Repeat Expansion
Trinucleotide Repeats
Trisomy
Tuberous Sclerosis
Tubulin
Tumor Suppressor Proteins
Turkey
Twin Studies as Topic
Twins, Dizygotic
Twins, Monozygotic
Two-Hybrid System Techniques
Tyrosine 3-Monooxygenase
Ubiquitin Thiolesterase
Ubiquitin-Protein Ligases
Ultrasonography
Ultrasonography, Prenatal
Ultraviolet Rays
Unfolded Protein Response
United States
Up-Regulation
Uridine Diphosphate Galactose
Urogenital Abnormalities
Vacuolar Proton-Translocating ATPases
Valproic Acid
Vascular Diseases
Vascular Malformations
Velopharyngeal Insufficiency
Vesico-Ureteral Reflux
Vesicular Transport Proteins
Vestibular Diseases
Vestibular Function Tests
Virus Internalization
Virus Replication
Visual Fields
Visual Perception
Walker-Warburg Syndrome
WD40 Repeats
Weight Gain
White Matter
Whole Genome Sequencing
Williams Syndrome
Wnt1 Protein
Wolff-Parkinson-White Syndrome
X Chromosome
X Chromosome Inactivation
Young Adult
Zebrafish
Zebrafish Proteins
Zika Virus
Zika Virus Infection
Zinc
Zinc Finger E-box Binding Homeobox 2
Zinc Finger Protein Gli3
Zinc Fingers
Zygote
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Concepts (1084)
Derived automatically from this person's publications.
Abnormalities, Multiple
Brain
Cerebellum
Nervous System Malformations
Mutation
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Co-Authors (12)
People in Profiles who have published with this person.
Das, Soma
Gershon, Elliot
Keedy, Sarah
Haverfield, Eden
Tao, James
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People who share similar concepts with this person.
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People who are also in this person's primary department.
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Physical Neighbors
People whose addresses are nearby this person.
Caliskan, Minal
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