UCLA.edu
Profiles
Home
About
Help/FAQs
History (0)
Search Options
UC Davis
UCI
UCLA
UCSD
UCSF
All UC Health
USC
All
Everything
Research
Concepts
Awards
People
UC Health People
UC Davis People
UCI People
UCLA People
UCSD People
UCSF People
USC People
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Naghmeh Dorrani
Concepts (198)
Back to Profile
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.
Abnormalities, Multiple
Acetylation
Active Transport, Cell Nucleus
Acyl Coenzyme A
Acyl-CoA Dehydrogenase
Adaptation, Psychological
Adolescent
Adult
Age of Onset
Alleles
Amino Acid Sequence
Ammonia
Angelman Syndrome
Animals
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Base Sequence
Biomarkers, Pharmacological
Biopsy
Blotting, Southern
Brain
Brain Diseases
CADASIL
California
Carnitine
Carrier Proteins
Case-Control Studies
Cataract
Cell Line
Cells, Cultured
Cerebellar Neoplasms
Child
Child Development Disorders, Pervasive
Child, Preschool
CHO Cells
Chromogranins
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders
Chromosome Inversion
Chromosomes, Artificial, Bacterial
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 18
Chromosomes, Human, X
Chromothripsis
Clinical Laboratory Services
Codon, Nonsense
Cohort Studies
Computational Biology
Computer Simulation
Congenital Disorders of Glycosylation
Constipation
CpG Islands
Craniosynostoses
Cricetulus
Cross-Over Studies
Decision Making
Developmental Disabilities
Diabetes Mellitus
Diagnosis
Disease Management
DNA Methylation
DNA Mutational Analysis
DNA-Binding Proteins
Down Syndrome
Drug Administration Schedule
Electroencephalography
Electromyography
Electronic Health Records
Epilepsy
Exome
Facies
Failure to Thrive
Female
Flow Cytometry
Follow-Up Studies
Foot Deformities, Congenital
Forkhead Transcription Factors
Fragile X Syndrome
Frameshift Mutation
Furin
GATA6 Transcription Factor
Gene Duplication
Gene Expression Profiling
Gene Order
Gene Rearrangement
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Linkage
Genetic Predisposition to Disease
Genetic Privacy
Genetic Testing
Genetic Variation
Genome, Human
Genome-Wide Association Study
Genomic Structural Variation
Genomics
Genotype
Germ-Line Mutation
Glutamine
Glycerol
Growth Disorders
GTP-Binding Protein alpha Subunits, Gs
Haploinsufficiency
Heart Defects, Congenital
Hedgehog Proteins
Heterozygote
High-Throughput Nucleotide Sequencing
Histone Acetyltransferases
Histone-Lysine N-Methyltransferase
Histones
Humans
Huntington Disease
Hyperammonemia
Hypertrichosis
Hypotrichosis
Immunoglobulin J Recombination Signal Sequence-Binding Protein
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Intellectual Disability
Isochromosomes
Karyotyping
Kidney
Ligands
Lipid Metabolism, Inborn Errors
Liver Transplantation
Loss of Function Mutation
Magnetic Resonance Imaging
Male
Malonates
Medulloblastoma
Methyl-CpG-Binding Protein 2
Microcephaly
Molecular Diagnostic Techniques
Monosaccharide Transport Proteins
Multicenter Studies as Topic
Mutation
Mutation, Missense
MutL Proteins
Myeloid-Lymphoid Leukemia Protein
Neonatal Screening
Neoplasm Proteins
Nerve Tissue Proteins
Neurodevelopmental Disorders
Nuclear Proteins
Osteochondroma
Parents
Pathology, Molecular
Patient Reported Outcome Measures
Pedigree
Phenotype
Phenylacetates
Phenylbutyrates
Phenylketonurias
Phosphoric Monoester Hydrolases
Pilot Projects
Polymorphism, Single Nucleotide
Polyneuropathies
Prader-Willi Syndrome
Pregnancy
Prognosis
Protein-Tyrosine Kinases
Proto-Oncogene Proteins
Quality of Life
Rare Diseases
Receptor, Notch3
Receptors, Cell Surface
Receptors, Notch
Repressor Proteins
Reproducibility of Results
Retrospective Studies
Rett Syndrome
Sequence Analysis, DNA
Sequence Deletion
Severity of Illness Index
Sex Chromosome Aberrations
SOXD Transcription Factors
Spasms, Infantile
Spinal Neoplasms
Succinates
Surveys and Questionnaires
Syndrome
Transcription Factors
Transcription, Genetic
Transcriptome
Translocation, Genetic
Trisomy
Uncertainty
United States
Urea Cycle Disorders, Inborn
Uridine Diphosphate Galactose
Whole Genome Sequencing
X Chromosome
Young Adult
Naghmeh's Networks
Concepts (198)
Derived automatically from this person's publications.
Intellectual Disability
Urea Cycle Disorders, Inborn
Developmental Disabilities
Myeloid-Lymphoid Leukemia Protein
Microcephaly
Explore
_
Co-Authors (50)
People in Profiles who have published with this person.
Nelson, Stanley
UCLA
Martinez, Julian
UCLA
Quintero-Rivera, Fabiola
UCI
Grody, Wayne
UCLA
Palmer, Christina
UCLA
Explore
_
Similar People (60)
People who share similar concepts with this person.
Gleeson, Joseph
UCSD
Martinez, Julian
UCLA
Anderson, Peter
UCI
Longo, Nicola
UCLA
Hagerman, Randi
UC Davis
Explore
_
Same Department
Combs, Monica
Kohn, Donald
Leifheit, Kathryn
Srivastava, Neeraj
Wong, Derek
Search Department
_