Concepts (214)
Concepts are derived automatically from a person's publications.
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.
- Absorptiometry, Photon
- Adolescent
- Adult
- Age Factors
- Age of Onset
- Aged
- Aged, 80 and over
- Albuminuria
- Alleles
- Amino Acid Metabolism, Inborn Errors
- Animals
- Animals, Genetically Modified
- Aorta
- Aortic Aneurysm, Thoracic
- Arginine-tRNA Ligase
- Atrial Natriuretic Factor
- Autistic Disorder
- Autoantigens
- beta Catenin
- beta-Thalassemia
- Biopsy
- Blood Pressure
- Blood Transfusion
- Body Mass Index
- Bone Density
- Bone Diseases, Metabolic
- Brain
- Brain Diseases, Metabolic, Inborn
- Calcium
- Cardiac Output, Low
- Cardiovascular Diseases
- Caribbean Region
- Carrier Proteins
- Case-Control Studies
- Cataract
- Cell Cycle
- Cell Cycle Proteins
- Centrioles
- Child
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 15
- Chromosomes, Human, Pair 2
- Cohort Studies
- Collagen Type III
- Collagen Type IV
- Collagen Type V
- Creatinine
- Cross Infection
- Databases, Genetic
- DEAD-box RNA Helicases
- Denys-Drash Syndrome
- Developmental Disabilities
- Diabetes Mellitus, Type 2
- Diabetic Angiopathies
- Diagnosis, Differential
- Disease Management
- Disease Models, Animal
- Disease Progression
- Disease Transmission, Infectious
- DNA
- DNA Copy Number Variations
- DNA Mutational Analysis
- DNA Polymerase gamma
- DNA-Directed DNA Polymerase
- Dogs
- Drosophila
- Drosophila Proteins
- Dwarfism
- Edema
- Electroencephalography
- Enoyl-CoA Hydratase
- Epilepsy
- Exome
- Exons
- Eye Diseases, Hereditary
- Face
- Female
- Fetus
- Fibrillin-1
- Fibrillins
- Follow-Up Studies
- Forkhead Transcription Factors
- Fractures, Bone
- Frameshift Mutation
- Genes, Dominant
- Genes, Recessive
- Genes, X-Linked
- Genetic Association Studies
- Genetic Diseases, Inborn
- Genetic Loci
- Genetic Predisposition to Disease
- Genetic Testing
- Genome-Wide Association Study
- Genomic Instability
- Genomics
- Genotype
- Genotyping Techniques
- Gestational Age
- Glutarates
- Glycine
- Haploinsufficiency
- Hearing Loss
- Heart Ventricles
- Hematuria
- Hemolytic-Uremic Syndrome
- Hepatitis C
| - Hepatocyte Nuclear Factor 1-beta
- Heterozygote
- Homozygote
- Humans
- Hypertension
- Hypertension, Pulmonary
- Hypertension, Renal
- Incidental Findings
- Infant
- Infant, Newborn
- Integrins
- Intellectual Disability
- Intestinal Polyposis
- Intracellular Signaling Peptides and Proteins
- Iran
- Kidney
- Kidney Diseases
- Kidney Diseases, Cystic
- Kidney Failure, Chronic
- Leigh Disease
- Linkage Disequilibrium
- Longitudinal Studies
- Loss of Function Mutation
- Magnetic Resonance Imaging
- Male
- Marfan Syndrome
- Mass Screening
- Matrix Attachment Region Binding Proteins
- Mice
- Microcephaly
- Microfilament Proteins
- Microtubule-Associated Proteins
- Middle Aged
- Mitochondrial Diseases
- Mitral Valve
- Models, Molecular
- Molecular Diagnostic Techniques
- Multivariate Analysis
- Muscle Hypotonia
- Muscle Weakness
- Muscular Atrophy
- Mutant Proteins
- Mutation
- Mutation, Missense
- Myocardial Infarction
- Neoplasm Proteins
- Neoplastic Syndromes, Hereditary
- Nephrectomy
- Nephritis, Hereditary
- Nephrons
- Neurodevelopmental Disorders
- Nuclear Proteins
- Obesity
- Osteoporosis
- Ovarian Diseases
- Ovary
- PAX2 Transcription Factor
- Pedigree
- Phenotype
- Pleckstrin Homology Domains
- Polycystic Kidney, Autosomal Dominant
- Polymorphism, Single Nucleotide
- Potassium Channels, Tandem Pore Domain
- Pregnancy
- Prevalence
- Problem Behavior
- Proportional Hazards Models
- Prospective Studies
- Protein Tyrosine Phosphatases
- Proteins
- Protein-Tyrosine Kinases
- Proteinuria
- Purpura
- Referral and Consultation
- Renal Dialysis
- Repressor Proteins
- Retina
- Retrospective Studies
- Rho Guanine Nucleotide Exchange Factors
- Risk Factors
- RNA Helicases
- RNA Splice Sites
- Seizures
- Sequence Analysis, DNA
- Sex Factors
- Smad4 Protein
- Sodium
- Spectrin
- Stroke
- Surveys and Questionnaires
- Survival Analysis
- Survivors
- Thinness
- Time
- Transcription Factors
- Trinucleotide Repeats
- Ultrasonography
- United States
- Universal Precautions
- Urinary Tract
- Urine
- Urogenital Abnormalities
- Vesico-Ureteral Reflux
- WT1 Proteins
- Xenopus laevis
- Young Adult
- Zinc
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Concepts
(214)
Derived automatically from this person's publications.
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(54)
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(60)
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