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Fowzan Sami Alkuraya, M.B.,B.S.
Concepts (1383)
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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.
3' Untranslated Regions
4-1BB Ligand
Abdomen
Abdominal Pain
Abnormalities, Multiple
Abortion, Habitual
Abortion, Induced
Abortion, Spontaneous
Acetylation
Acetylcholinesterase
Acetylcysteine
Acetylesterase
Acetyltransferases
Acidosis, Lactic
Aconitate Hydratase
Acro-Osteolysis
Actins
Acyl Coenzyme A
Acyltransferases
ADAM Proteins
Adaptation, Physiological
Adaptation, Psychological
Adaptor Protein Complex 1
Adaptor Protein Complex alpha Subunits
Adaptor Protein Complex beta Subunits
Adaptor Proteins, Signal Transducing
Adaptor Proteins, Vesicular Transport
Adenine Nucleotide Translocator 1
Adenomatous Polyposis Coli
Adenomatous Polyposis Coli Protein
Adenosine Deaminase
Adenosine Diphosphate
Adenosine Triphosphatases
Adenosine Triphosphate
Adolescent
ADP-Ribosylation Factors
Adrenal Insufficiency
Adrenoleukodystrophy
Adult
Africa
Age of Onset
Aged
Aged, 80 and over
Aging
Aging, Premature
Aicardi Syndrome
Albinism, Oculocutaneous
Alcohol Oxidoreductases
Aldehyde Oxidoreductases
Aldose-Ketose Isomerases
Algorithms
Alleles
Alopecia
alpha-Crystallin B Chain
alpha-Macroglobulins
Alternative Splicing
Amblyopia
Amenorrhea
Amidohydrolases
Amines
Amino Acid Metabolism, Inborn Errors
Amino Acid Motifs
Amino Acid Oxidoreductases
Amino Acid Sequence
Amino Acid Substitution
Amino Acid Transport Systems, Acidic
Amino Acid Transport Systems, Neutral
Anemia
Anemia, Aplastic
Aneurysm
Animals
Animals, Genetically Modified
Animals, Newborn
Anion Transport Proteins
Aniridia
Anophthalmos
Anterior Eye Segment
Anticodon
Antigens, CD
Antigens, Neoplasm
Antihypertensive Agents
Anti-Inflammatory Agents, Non-Steroidal
Antiporters
Anus, Imperforate
Aphakia, Postcataract
Apoptosis Regulatory Proteins
Apraxias
Aqueous Humor
Arabia
Arabs
Arachnodactyly
Armadillo Domain Proteins
Arrhythmias, Cardiac
Arthritis
Arthrogryposis
Artificial Intelligence
Aryl Hydrocarbon Hydroxylases
Aryl Hydrocarbon Receptor Nuclear Translocator
Asia
Aspartate-Ammonia Ligase
Aspartic Acid
Ataxia
ATP-Binding Cassette Transporters
Atrophy
Attitude
Australia
Autoantigens
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Autoimmunity
Autophagy
Autopsy
Axial Length, Eye
Axons
Bardet-Biedl Syndrome
Basal Ganglia Diseases
Base Pairing
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
Beckwith-Wiedemann Syndrome
Behavior, Animal
beta Catenin
beta-Crystallin B Chain
beta-Hexosaminidase alpha Chain
beta-Hexosaminidase beta Chain
Bezoars
Bile Acids and Salts
Binding Sites
Biological Specimen Banks
Biological Transport
Biological Transport, Active
Biometry
Birth Weight
Blepharophimosis
Blepharoptosis
Blepharospasm
Blindness
Blister
Blood Chemical Analysis
Blood Pressure
Blood Proteins
Blood Transfusion
Blotting, Western
B-Lymphocytes
Body Height
Body Patterning
Bone and Bones
Bone Diseases
Bone Diseases, Developmental
Bone Diseases, Metabolic
Bone Marrow
Bone Marrow Cells
Bone Marrow Diseases
Bone Marrow Transplantation
Bone Morphogenetic Protein 2
Bone Morphogenetic Protein 4
Bone Morphogenetic Protein Receptors, Type I
Bone Morphogenetic Proteins
Brain
Brain Diseases
Brain Diseases, Metabolic, Inborn
Brain Ischemia
Brain Stem
Branchial Region
Branchio-Oto-Renal Syndrome
BRCA1 Protein
BRCA2 Protein
Breast Diseases
CADASIL
Cadherins
Caenorhabditis elegans
Caenorhabditis elegans Proteins
Cafe-au-Lait Spots
Calcinosis
Calcium
Calcium Channels
Calcium-Binding Proteins
Calpain
Capillaries
Carbohydrate Metabolism, Inborn Errors
Carboxylic Ester Hydrolases
Carboxypeptidases
Carcinoma, Papillary
Cardiomyopathies
Cardiomyopathy, Dilated
Cardiomyopathy, Hypertrophic
Carrier Proteins
Carrier State
Case-Control Studies
Casein Kinase I
Caspase 7
Cataplexy
Cataract
Cataract Extraction
Cathepsin H
Cation Transport Proteins
Causality
Cause of Death
CD8-Positive T-Lymphocytes
CDC2 Protein Kinase
cdc42 GTP-Binding Protein
Cell Adhesion
Cell Adhesion Molecules
Cell Cycle
Cell Cycle Proteins
Cell Differentiation
Cell Division
Cell Line
Cell Line, Tumor
Cell Lineage
Cell Movement
Cell Nucleus
Cell Polarity
Cell Proliferation
Cell Separation
Cells, Cultured
Central Nervous System
Central Nervous System Diseases
Central Nervous System Vascular Malformations
Centrioles
Centrosome
Cerebellar Diseases
Cerebellum
Cerebral Cortex
Charcot-Marie-Tooth Disease
CHARGE Syndrome
Cheilitis
Chick Embryo
Child
Child Development Disorders, Pervasive
Child, Preschool
Chloride Channels
Chloride-Bicarbonate Antiporters
Choanal Atresia
Cholangitis
Cholestasis
Cholestasis, Intrahepatic
Chondrocytes
Chondroitin Sulfate Proteoglycans
Chromatin
Chromatin Assembly and Disassembly
Chromatography, High Pressure Liquid
Chromogranins
Chromosomal Position Effects
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Breakage
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 13
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Chromosomes, Human, X
Chromosomes, Human, Y
Chronic Disease
Cilia
Ciliary Motility Disorders
Claudins
Cleft Lip
Cleft Palate
Clubfoot
Cockayne Syndrome
Codon
Codon, Nonsense
Cogan Syndrome
Cognition
Cognition Disorders
Cohort Studies
Collagen
Collagen Diseases
Collagen Type I
Collagen Type II
Collagen Type IV
Collagen Type IX
Collagen Type V
Collagen Type VI
Collagen Type VIII
Collagen Type XI
Collagen Type XVIII
Collectins
Coloboma
Colorectal Neoplasms
Colorectal Neoplasms, Hereditary Nonpolyposis
Comet Assay
Comorbidity
Comparative Genomic Hybridization
Complement Pathway, Mannose-Binding Lectin
Computational Biology
Computer Simulation
Congenital Abnormalities
Congenital Disorders of Glycosylation
Congenital Hypothyroidism
Connective Tissue
Connective Tissue Diseases
Connexin 43
Connexins
Consanguinity
Consensus Sequence
Conserved Sequence
Constipation
Contracture
Cor Triatriatum
Co-Repressor Proteins
Cornea
Corneal Diseases
Corneal Dystrophies, Hereditary
Corneal Opacity
Corneal Topography
Coronary Artery Disease
Corpus Callosum
Cost of Illness
COUP Transcription Factor I
Cranial Nerves
Craniofacial Abnormalities
Craniofacial Dysostosis
Craniosynostoses
Crossing Over, Genetic
Cross-Sectional Studies
Crystallins
Cutis Laxa
Cyprus
Cystadenocarcinoma, Serous
Cysteine Endopeptidases
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Cystinosis
Cysts
Cytogenetic Analysis
Cytokine Receptor gp130
Cytokines
Cytokinesis
Cytoplasm
Cytoplasmic Granules
Cytosine
Cytoskeletal Proteins
Cytoskeleton
Cytosol
Dandy-Walker Syndrome
Databases, Factual
Databases, Genetic
De Lange Syndrome
DEAD-box RNA Helicases
Deaf-Blind Disorders
Deafness
Death, Sudden
Delivery of Health Care
Demyelinating Diseases
Deoxyribonucleases, Type II Site-Specific
Dependovirus
Dermatitis, Exfoliative
Developmental Disabilities
Diabetes Complications
Diabetes Mellitus
Diabetes Mellitus, Type 2
Diabetic Retinopathy
Diagnosis
Diagnosis, Differential
Diagnostic Imaging
Diagnostic Techniques and Procedures
Diffuse Cerebral Sclerosis of Schilder
Disease
Disease Management
Disease Models, Animal
Disease Progression
Disease Susceptibility
Disorders of Sex Development
DNA
DNA Adducts
DNA Copy Number Variations
DNA Damage
DNA Glycosylases
DNA Helicases
DNA Methylation
DNA Modification Methylases
DNA Mutational Analysis
DNA Repair
DNA Replication
DNA Transposable Elements
DNA, Complementary
DNA, Mitochondrial
DNA-Binding Proteins
Down-Regulation
Drosophila
Drosophila melanogaster
Drosophila Proteins
Drug Evaluation, Preclinical
Drug Therapy, Combination
Duane Retraction Syndrome
Dwarfism
Dysphonia
Dyspnea
Dystonia
Ear
Ear Diseases
Ear, External
Ear, Inner
Echocardiography
Ectodermal Dysplasia
Ectopia Lentis
Ectromelia
Ectropion
Egypt
Ehlers-Danlos Syndrome
Electroencephalography
Electromyography
Electrophoresis, Agar Gel
Electroretinography
Ellis-Van Creveld Syndrome
Embryo Transfer
Embryo, Mammalian
Embryonic Development
Emulsions
Encephalitis
Encephalocele
Endodeoxyribonucleases
Endonucleases
Endopeptidases
Endoplasmic Reticulum
Endothelin-1
Endothelin-3
Endothelium, Corneal
Endpoint Determination
Enhancer Elements, Genetic
Enkephalins
Enoyl-CoA Hydratase
Enzyme Activation
Enzyme Stability
Epidermal Growth Factor
Epidermis
Epigenesis, Genetic
Epilepsies, Myoclonic
Epilepsy
Epilepsy, Generalized
Epistasis, Genetic
Epithelial Cells
Epstein-Barr Virus Infections
Esophagus
Esotropia
Eukaryotic Initiation Factor-2B
Europe
Evolution, Molecular
Exocrine Pancreatic Insufficiency
Exons
Exonucleases
Exophthalmos
Exoribonucleases
Exosomes
Exostoses, Multiple Hereditary
Exotropia
Extracellular Matrix
Extracellular Matrix Proteins
Extracellular Signal-Regulated MAP Kinases
Eye
Eye Abnormalities
Eye Diseases, Hereditary
Eye Proteins
Eyeglasses
Eyelid Diseases
Face
Facies
Failure to Thrive
Family
Family Health
Fanconi Anemia
Fatal Outcome
Fatty Acids
F-Box Proteins
Female
Ferrets
Fertilization in Vitro
Fetal Death
Fetal Development
Fetal Diseases
Fetal Growth Retardation
Fetal Proteins
Fetus
Fibroblast Growth Factor 3
Fibroblasts
Fibrosis
Fingers
Flow Cytometry
Fluorescein Angiography
Fluorescent Antibody Technique
Follow-Up Studies
Foot
Foot Deformities, Congenital
Forkhead Transcription Factors
Founder Effect
Fragile X Mental Retardation Protein
Frameshift Mutation
Fundus Oculi
GA-Binding Protein Transcription Factor
gamma-Aminobutyric Acid
gamma-Crystallins
gamma-Glutamyltransferase
Gangliosidoses, GM2
Gastrointestinal Diseases
Gene Components
Gene Conversion
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Expression Regulation, Enzymologic
Gene Frequency
Gene Knockdown Techniques
Gene Knockout Techniques
Gene Order
Gene Rearrangement
Gene Regulatory Networks
Gene Silencing
General Practice
Genes
Genes, Dominant
Genes, Lethal
Genes, p53
Genes, Recessive
Genes, Reporter
Genes, Tumor Suppressor
Genes, X-Linked
Genetic Association Studies
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, Medical
Genetics, Population
Genitalia
Genitalia, Male
Genome
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomic Instability
Genomics
Genotype
Germ Cells
Germ-Line Mutation
Glaucoma
Glaucoma, Open-Angle
Globus Pallidus
Glucose-6-Phosphatase
Glucosyltransferases
Glutamate Decarboxylase
Glutamine
Glutarates
Glutathione
Glutathione Synthase
Glycine
Glycine Plasma Membrane Transport Proteins
Glycogen Debranching Enzyme System
Glycogen Storage Disease Type III
Glycoproteins
Glycosylation
Glycosylphosphatidylinositols
Golgi Apparatus
Gonads
Gonioscopy
gp100 Melanoma Antigen
GPI-Linked Proteins
Granulomatous Disease, Chronic
Growth Disorders
Growth Hormone
GTP Phosphohydrolases
GTPase-Activating Proteins
GTP-Binding Protein alpha Subunits, Gi-Go
GTP-Binding Protein alpha Subunits, Gs
GTP-Binding Proteins
Guanine Nucleotide Exchange Factors
Hand
Hand Deformities, Congenital
Haploidy
Haploinsufficiency
Haplotypes
Head Movements
Health Policy
Hearing Disorders
Hearing Loss
Hearing Loss, Bilateral
Hearing Loss, Sensorineural
Heart Defects, Congenital
Heart Diseases
Heart Failure
Heart Septal Defects, Atrial
Heat-Shock Proteins
Hedgehog Proteins
HEK293 Cells
HeLa Cells
Helicobacter Infections
Helicobacter pylori
Hematologic Diseases
Hematopoietic Stem Cell Transplantation
Hemizygote
Hemoglobinopathies
Hemoglobinuria, Paroxysmal
Hep G2 Cells
Hepatitis B, Chronic
Hepatolenticular Degeneration
Hereditary Central Nervous System Demyelinating Diseases
Hereditary Sensory and Autonomic Neuropathies
Hereditary Sensory and Motor Neuropathy
Heredity
Heredodegenerative Disorders, Nervous System
Hernia, Diaphragmatic
Herpesvirus 4, Human
Heterogeneous-Nuclear Ribonucleoprotein K
Heterozygote
Hidradenitis Suppurativa
High-Throughput Nucleotide Sequencing
Hirschsprung Disease
Histidine
Histone Deacetylases
Histone-Lysine N-Methyltransferase
Histones
History, Ancient
Hoarseness
Holoprosencephaly
Homeodomain Proteins
Homeostasis
Homozygote
Horses
HSP40 Heat-Shock Proteins
Human Development
Human Genome Project
Humans
Hyaluronoglucosaminidase
Hydranencephaly
Hydrocephalus
Hydro-Lyases
Hydrophthalmos
Hydrops Fetalis
Hyperglycinemia, Nonketotic
Hyperhidrosis
Hyperopia
Hypertelorism
Hypertrichosis
Hypoglycemia
Hypogonadism
Hypohidrosis
Hypopigmentation
Hypopituitarism
Hypospadias
Hypothalamus
Hypothyroidism
Hypoventilation
Hypoxia-Ischemia, Brain
Ichthyosis
I-kappa B Kinase
Immune System Diseases
Immunoglobulins
Immunohistochemistry
Immunologic Deficiency Syndromes
Immunophenotyping
Immunoprecipitation
In Situ Hybridization
In Situ Hybridization, Fluorescence
Inbreeding
INDEL Mutation
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Infant, Newborn, Diseases
Infertility
Infertility, Female
Infertility, Male
Inflammatory Bowel Diseases
Information Dissemination
Infusions, Intravenous
Inheritance Patterns
Injections
Inosine
Inosine Triphosphate
Insulin Resistance
Insulin-Like Growth Factor Binding Proteins
Intercellular Signaling Peptides and Proteins
Interleukin-11
Interleukin-6
Intermediate Filament Proteins
International Cooperation
Internationality
Interviews as Topic
Intestinal Mucosa
Intracellular Signaling Peptides and Proteins
Intraocular Pressure
Introns
Ion Channels
Iris
Islam
Israel
Italy
Jaundice, Obstructive
Joint Diseases
Joint Instability
Kaplan-Meier Estimate
Kartagener Syndrome
Karyotyping
Keratinocytes
Keratoconus
Keratosis
Kidney
Kidney Diseases
Kidney Diseases, Cystic
Killer Cells, Natural
Kinetics
Klippel-Feil Syndrome
Kruppel-Like Transcription Factors
Kuwait
Lamin Type A
Langer-Giedion Syndrome
Large-Conductance Calcium-Activated Potassium Channel alpha Subunits
Latent TGF-beta Binding Proteins
LDL-Receptor Related Protein-Associated Protein
LDL-Receptor Related Proteins
Leber Congenital Amaurosis
Leigh Disease
Lens Subluxation
Lens, Crystalline
Leukemia Inhibitory Factor
Leukemia, Myeloid, Acute
Leukemia, Myelomonocytic, Juvenile
Leukoencephalopathies
Leukopenia
Leviviridae
Libya
Ligase Chain Reaction
Ligases
Limb Deformities, Congenital
Linkage Disequilibrium
Lipid Metabolism
Lipoid Proteinosis of Urbach and Wiethe
Lipopolysaccharides
Lipoproteins
Lissencephaly
Livedo Reticularis
Liver
Liver Cirrhosis
Liver Diseases
Liver Failure
Liver Failure, Acute
Lod Score
Loss of Heterozygosity
Luciferases
Lung
Lupus Erythematosus, Systemic
Lymph Nodes
Lymphocyte Count
Lymphohistiocytosis, Hemophagocytic
Lymphoma
Lymphoma, B-Cell
Lymphoproliferative Disorders
Lysine-tRNA Ligase
Lysosomes
Macaca
Macula Lutea
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Malabsorption Syndromes
Malate Dehydrogenase
Malates
Malaysia
Male
Malformations of Cortical Development
Malignant Hyperthermia
Mammals
Mannose-Binding Protein-Associated Serine Proteases
Mannosidases
Mannosyltransferases
MAP Kinase Signaling System
Marfan Syndrome
Matrix Attachment Region Binding Proteins
Maxillofacial Abnormalities
Mediator Complex
Megacolon
Meiosis
Melanosomes
Membrane Glycoproteins
Membrane Potential, Mitochondrial
Membrane Proteins
Membrane Transport Proteins
Mendelian Randomization Analysis
Meningocele
Mental Disorders
Mental Retardation, X-Linked
Meta-Analysis as Topic
Metabolic Diseases
Metabolism, Inborn Errors
Metabolome
Metalloendopeptidases
Metalloproteases
Methanol
Methylation
Methyltransferases
Mice
Mice, Inbred C3H
Mice, Inbred C57BL
Mice, Knockout
Mice, Transgenic
Microcephaly
Microfilament Proteins
Micrognathism
Microphthalmos
Microsatellite Repeats
Microscopy, Electron, Transmission
Microscopy, Phase-Contrast
Microscopy, Video
Microtubule Proteins
Microtubule-Associated Proteins
Microtubules
Microvilli
Middle Aged
Middle East
Milk
Minor Histocompatibility Antigens
Mitochondria
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Membrane Transport Proteins
Mitochondrial Myopathies
Mitochondrial Proteins
Mitochondrial Proton-Translocating ATPases
Mitogen-Activated Protein Kinase Kinases
Mitosis
Mixed Function Oxygenases
Models, Animal
Models, Biological
Models, Genetic
Models, Molecular
Molecular Chaperones
Molecular Conformation
Molecular Diagnostic Techniques
Molecular Probe Techniques
Molecular Sequence Annotation
Molecular Sequence Data
Monoamine Oxidase
Monomeric GTP-Binding Proteins
Monosaccharide Transport Proteins
Monosomy
Morbidity
Morphogenesis
Mosaicism
Motor Neurons
Mouth
Movement Disorders
Mucociliary Clearance
Mucolipidoses
Mucopolysaccharidosis IV
Multienzyme Complexes
Multivariate Analysis
Muscle Cramp
Muscle Hypotonia
Muscle Proteins
Muscle Spasticity
Muscle, Skeletal
Muscular Atrophy
Muscular Diseases
Muscular Dystrophies
Musculoskeletal Abnormalities
Musculoskeletal System
Mutant Proteins
Mutation
Mutation, Missense
Mydriasis
Myelin Sheath
Myeloid-Lymphoid Leukemia Protein
Myofibrils
Myopathies, Nemaline
Myopia
Myopia, Degenerative
Myosins
N-Acetylglucosaminyltransferases
NADP
Nail Diseases
Nails, Malformed
Nanopores
Narcolepsy
Nasal Mucosa
Neoplasm Metastasis
Neoplasm Proteins
Neoplasm Recurrence, Local
Neoplasm Staging
Neoplasms
Nephritis, Hereditary
Nephrotic Syndrome
Nerve Fibers, Myelinated
Nerve Growth Factors
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Netherlands
Neural Crest
Neural Stem Cells
Neural Tube Defects
Neuroaxonal Dystrophies
Neurodegenerative Diseases
Neurofibromin 1
Neurogenesis
Neuroglia
Neuromuscular Junction
Neuronal Ceroid-Lipofuscinoses
Neurons
Neuropilin-1
Neurotransmitter Agents
Neutropenia
NFI Transcription Factors
NF-kappa B
Niacin
Night Blindness
Nitrogen
NM23 Nucleoside Diphosphate Kinases
Nodal Protein
Nose
Nose Diseases
Nuclear Family
Nuclear Pore Complex Proteins
Nuclear Proteins
Nucleic Acid Amplification Techniques
Nucleic Acid Conformation
Nucleic Acid Synthesis Inhibitors
Nucleocytoplasmic Transport Proteins
Nucleotidases
Nucleotide Transport Proteins
Nucleotidyltransferases
Nystagmus, Pathologic
Obesity
Ocular Motility Disorders
Oligonucleotide Array Sequence Analysis
Oligospermia
Oncogene Proteins
Oncostatin M
Oocyte Retrieval
Oocytes
Open Reading Frames
Ophthalmoscopy
Optic Atrophy
Optic Atrophy, Hereditary, Leber
Optic Disk
Optic Nerve Diseases
Organogenesis
Organoids
Orofaciodigital Syndromes
Orphan Nuclear Receptors
Ossification, Heterotopic
Osteoblasts
Osteochondrodysplasias
Osteogenesis
Osteogenesis Imperfecta
Osteosclerosis
Ovarian Neoplasms
Oxidation-Reduction
Oxidative Phosphorylation
Oxidative Stress
Oxidoreductases
Oxidoreductases Acting on CH-CH Group Donors
Oxidoreductases Acting on CH-NH Group Donors
Oxygen
Oxygenases
Paired Box Transcription Factors
Pakistan
Palate
Pancreas
Pancreatic Diseases
Parkinson Disease, Secondary
Patella
Pathology, Molecular
Patient Education as Topic
Pedigree
Pelizaeus-Merzbacher Disease
Pellagra
Pelvic Bones
Penetrance
Pentosyltransferases
Peptic Ulcer
Peptic Ulcer Hemorrhage
Peptides
Peptidylprolyl Isomerase
Periosteum
Peripheral Nerves
Peripheral Nervous System Diseases
Periventricular Nodular Heterotopia
Peroxisomal Disorders
Peroxisomes
Phagocytes
Pharmacogenetics
Phenotype
Phenylalanine-tRNA Ligase
Phosphate Transport Proteins
Phosphates
Phosphoglycerate Dehydrogenase
Phospholipase C beta
Phospholipids
Phosphoprotein Phosphatases
Phosphoproteins
Phosphoric Monoester Hydrolases
Phosphorylation
Phosphotransferases (Alcohol Group Acceptor)
Photoreceptor Cells
Phylogeny
Physical Chromosome Mapping
Physical Examination
Pituitary Gland
Pituitary Hormones
Plasma Membrane Neurotransmitter Transport Proteins
Plasmids
Pneumonia
Point Mutation
Poisoning
Pol1 Transcription Initiation Complex Proteins
Policy Making
Polycystic Kidney Diseases
Polydactyly
Polyhydramnios
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Polymorphism, Single Nucleotide
Polysaccharides
Population Groups
Population Surveillance
Positron-Emission Tomography
Posterior Eye Segment
Postoperative Complications
Potassium Channels
Potassium Channels, Inwardly Rectifying
Potassium Channels, Voltage-Gated
Practice Guidelines as Topic
Prader-Willi Syndrome
Preconception Care
Predictive Value of Tests
Pregnancy
Pregnancy Proteins
Preimplantation Diagnosis
Prenatal Diagnosis
Prevalence
Primates
Principal Component Analysis
Procollagen
Procollagen-Proline Dioxygenase
Prognosis
Program Development
Program Evaluation
Proline
Promoter Regions, Genetic
Prospective Studies
Proteasome Endopeptidase Complex
Protein Binding
Protein Biosynthesis
Protein Conformation
Protein Folding
Protein Interaction Domains and Motifs
Protein Interaction Mapping
Protein Isoforms
Protein Kinase C
Protein Precursors
Protein Processing, Post-Translational
Protein Sorting Signals
Protein Stability
Protein Structure, Tertiary
Protein Subunits
Protein Transport
Protein Tyrosine Phosphatases
Protein Tyrosine Phosphatases, Non-Receptor
Protein-Arginine N-Methyltransferases
Proteins
Proteinuria
Proteoglycans
Proteome
Proteomics
Proto-Oncogene Proteins
Proto-Oncogene Proteins B-raf
Proto-Oncogene Proteins c-abl
Pruritus
Pseudohypoparathyroidism
Pseudouridine
Psychomotor Disorders
Public Health
Pulmonary Valve Stenosis
Purine-Nucleoside Phosphorylase
Purine-Pyrimidine Metabolism, Inborn Errors
Purkinje Cells
Pyroglutamate Hydrolase
Pyrophosphatases
Pyrrolidonecarboxylic Acid
Qa-SNARE Proteins
Qatar
Quadriplegia
Quantitative Trait Loci
rab GTP-Binding Proteins
Rabbits
rac1 GTP-Binding Protein
Radiography
Ranvier's Nodes
Rare Diseases
ras GTPase-Activating Proteins
ras Proteins
Rats
Rats, Mutant Strains
Rats, Sprague-Dawley
Reactive Oxygen Species
Receptor Protein-Tyrosine Kinases
Receptor, EphA2
Receptor, TIE-2
Receptors, AMPA
Receptors, Antigen, T-Cell, alpha-beta
Receptors, Cell Surface
Receptors, Cytokine
Receptors, Cytoplasmic and Nuclear
Receptors, Glycine
Receptors, Interleukin
Receptors, Lipoprotein
Receptors, Nicotinic
Recombinant Proteins
Recurrence
Reflex, Abnormal
Refraction, Ocular
Refractive Errors
Remission Induction
Renal Insufficiency
Repetitive Sequences, Nucleic Acid
Repressor Proteins
Reproducibility of Results
Research
Respiratory Burst
Respiratory Distress Syndrome, Newborn
Respiratory Mucosa
Respiratory System
Respiratory System Abnormalities
Retina
Retinal Artery
Retinal Cone Photoreceptor Cells
Retinal Degeneration
Retinal Detachment
Retinal Diseases
Retinal Dystrophies
Retinal Perforations
Retinal Pigment Epithelium
Retinal Rod Photoreceptor Cells
Retinitis Pigmentosa
Retinoschisis
Retinoscopy
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
RGS Proteins
Rhabdomyolysis
rho GTP-Binding Proteins
Ribonucleases
Ribonucleoproteins
Ribonucleoproteins, Small Nuclear
Rifampin
Ring Chromosomes
Risk Factors
RNA
RNA Helicases
RNA Interference
RNA Processing, Post-Transcriptional
RNA Splice Sites
RNA Splicing
RNA Stability
RNA, Messenger
RNA, Small Interfering
RNA, Transfer
RNA, Transfer, Amino Acid-Specific
RNA, Transfer, Arg
RNA, Untranslated
RNA-Binding Proteins
Ryanodine Receptor Calcium Release Channel
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Sacrum
Sarcomeres
Saudi Arabia
Scalp Dermatoses
Scavenger Receptors, Class F
Sclera
Scleral Buckling
Scleral Diseases
Scoliosis
Scotoma
Secretory Pathway
Seizures
Seminiferous Tubules
Sensitivity and Specificity
Sensory Rhodopsins
Septo-Optic Dysplasia
Sequence Alignment
Sequence Analysis
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology
Sequence Homology, Amino Acid
Serine
Serine Endopeptidases
Serine Proteases
Severe Combined Immunodeficiency
Severity of Illness Index
Sex Chromosome Aberrations
Siblings
Signal Transduction
Sinusitis
Skin
Skin Abnormalities
Skin Diseases
Skin Diseases, Genetic
Skin Diseases, Vascular
SKP Cullin F-Box Protein Ligases
Sleep
Small Ubiquitin-Related Modifier Proteins
Smith-Lemli-Opitz Syndrome
Sodium Channels
Sodium-Bicarbonate Symporters
Sodium-Calcium Exchanger
Sodium-Phosphate Cotransporter Proteins, Type III
Software
Sotos Syndrome
Soybean Oil
Spasms, Infantile
Spastic Paraplegia, Hereditary
Speech Disorders
Sperm Injections, Intracytoplasmic
Sperm Motility
Spermatids
Spermatogenesis
Sphingomyelin Phosphodiesterase
Spinal Cord
Spine
Spinocerebellar Ataxias
Statistics, Nonparametric
Stem Cells
Sterol 14-Demethylase
Stiff-Person Syndrome
Stillbirth
Stomach
Strabismus
Stroke
Structure-Activity Relationship
Subcellular Fractions
Subretinal Fluid
Sulfonamides
SUMO-1 Protein
Suppressor Factors, Immunologic
Symporters
Synaptic Transmission
Synaptic Vesicles
Syndactyly
Syndrome
Syntaxin 16
Tacrolimus Binding Proteins
Tandem Mass Spectrometry
Tay-Sachs Disease
T-Box Domain Proteins
Telangiectasis
Telomere
Thalassemia
Thiophenes
Threonine
Thrombocytopenia
Thrombopoietin
Thrombosis
Thyroglobulin
Thyroid Neoplasms
Tibia
Time Factors
Timolol
Tissue Distribution
Tissue Plasminogen Activator
T-Lymphocytes
T-Lymphocytes, Helper-Inducer
Tolloid-Like Metalloproteinases
Tomography, Optical Coherence
Tomography, X-Ray Computed
Tonometry, Ocular
Tooth Abnormalities
Trans-Activators
Transaldolase
Transaminases
Transcription Factor AP-2
Transcription Factor Pit-1
Transcription Factors
Transfection
Transferases
Transforming Growth Factor beta
Transgenes
Translocation, Genetic
Treatment Outcome
Trichothiodystrophy Syndromes
Trismus
Trisomy
tRNA Methyltransferases
TRPM Cation Channels
Truncus Arteriosus, Persistent
Tubulin
Tumor Suppressor Proteins
Tunisia
Turkey
Twins, Monozygotic
Two-Hybrid System Techniques
Type C Phospholipases
Tyrosine
Tyrosine-tRNA Ligase
Ubiquitin
Ubiquitin-Activating Enzymes
Ubiquitination
Ubiquitin-Conjugating Enzymes
Ubiquitin-Protein Ligase Complexes
Ubiquitin-Protein Ligases
Ubiquitins
Ulna
Ultrasonography
Ultrasonography, Prenatal
Umbilicus
United Arab Emirates
United States
Up-Regulation
Ureter
Urethral Obstruction
Uridine
Uridine Diphosphate Glucose Dehydrogenase
Urinalysis
Urinary Bladder
Urogenital Abnormalities
Urticaria
Uterus
Vascular Malformations
Vasculitis
Vesico-Ureteral Reflux
Vesicular Monoamine Transport Proteins
Vesicular Transport Proteins
Vestibular Diseases
Viscera
Visual Acuity
Visual Fields
Visual Perception
Vitamin D
Vitamin D Deficiency
Vitamin D-Binding Protein
Vitiligo
Vitrectomy
Voice Disorders
Vomiting
Walker-Warburg Syndrome
Weill-Marchesani Syndrome
Wnt Proteins
Wnt1 Protein
Wolf-Hirschhorn Syndrome
Workflow
X Chromosome Inactivation
Xanthomatosis, Cerebrotendinous
Xenopus laevis
Xenopus Proteins
Xeroderma Pigmentosum
X-Ray Microtomography
Young Adult
Zebrafish
Zebrafish Proteins
Zellweger Syndrome
Zona Pellucida
Zygote
Alkuraya's Networks
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Concepts (1383)
Derived automatically from this person's publications.
Genes, Recessive
Abnormalities, Multiple
Pedigree
Mutation
Consanguinity
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Co-Authors (112)
People in Profiles who have published with this person.
Walsh, Christopher
Lin, Angela
Aldeeri, Abdulrahman
Faquih, Tariq
Altuame, Fadie
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People whose addresses are nearby this person.
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