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SEEMA LALANI
Concepts (610)
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Concepts are derived automatically from a person's publications.
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Categories
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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.
14-3-3 Proteins
1-Alkyl-2-acetylglycerophosphocholine Esterase
4-Aminobutyrate Transaminase
Abnormalities, Multiple
Aconitate Hydratase
Acrocephalosyndactylia
Actin Cytoskeleton
Actins
Activities of Daily Living
Adaptor Proteins, Signal Transducing
Adenosine Triphosphatases
Adolescent
Adult
Age of Onset
Aged
Aged, 80 and over
Agenesis of Corpus Callosum
Aggrecans
Aging, Premature
Alagille Syndrome
Algorithms
Alleles
alpha7 Nicotinic Acetylcholine Receptor
Alternative Splicing
Alu Elements
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Amino Acyl-tRNA Synthetases
Amish
AMP-Activated Protein Kinases
Anal Canal
Aneuploidy
Animals
Animals, Genetically Modified
Ankyrins
Anthropometry
Anti-Arrhythmia Agents
Antibiotics, Antineoplastic
Antigens, Neoplasm
Anxiety
Aorta
Aortic Coarctation
Arabs
Argonaute Proteins
Arrhythmias, Cardiac
Ataxia
ATPases Associated with Diverse Cellular Activities
Atrial Fibrillation
Atrophy
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Autistic Disorder
Autoimmune Diseases of the Nervous System
Base Composition
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
Bayes Theorem
Biopsy
Blotting, Southern
Body Patterning
Bone Morphogenetic Protein 2
Brachydactyly
Brain
Brain Diseases
Brain Diseases, Metabolic
Branchio-Oto-Renal Syndrome
Caenorhabditis elegans
Caenorhabditis elegans Proteins
Calcineurin
Calcinosis
Calcium Channels
Calcium-Binding Proteins
Cardiac Surgical Procedures
Cardiomyopathies
Cardiomyopathy, Dilated
Cardiovascular Abnormalities
Cardiovascular Diseases
Carotid-Cavernous Sinus Fistula
Carrier Proteins
Case-Control Studies
Cataract
Cause of Death
CDC2 Protein Kinase
Cell Adhesion Molecules
Cell Cycle
Cell Cycle Proteins
Cell Division
Cell Line
Cell Line, Tumor
Cell Nucleolus
Cell Proliferation
Cell Transdifferentiation
Cellular Senescence
Central Nervous System
Cerebellar Ataxia
Cerebellar Vermis
Cerebellum
Cerebral Angiography
Cesarean Section
Charcot-Marie-Tooth Disease
CHARGE Syndrome
Child
Child, Preschool
Choanal Atresia
Cholesterol, HDL
Chondroitin Sulfate Proteoglycans
Chromatin
Chromatin Assembly and Disassembly
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 7
Chromosomes, Human, X
Ciliopathies
Clinical Laboratory Techniques
Cloning, Molecular
Cochlear Implants
Codon, Nonsense
Coenzymes
Cognition
Cognition Disorders
Cohort Studies
Coloboma
Comorbidity
Comparative Genomic Hybridization
Computational Biology
Congenital Abnormalities
Congenital Microtia
Conserved Sequence
Corpus Callosum
COS Cells
Cost-Benefit Analysis
Craniofacial Abnormalities
Craniosynostoses
Creatine Kinase
Cricetinae
Critical Care
Critical Illness
Cytogenetic Analysis
Cytoskeletal Proteins
Databases, Genetic
De Lange Syndrome
DEAD-box RNA Helicases
Deafness
Decision Making
Depression
Developmental Disabilities
Diabetes, Gestational
Diagnosis, Differential
Dichlorodiphenyl Dichloroethylene
Dietary Supplements
DiGeorge Syndrome
Disability Evaluation
Disease
Disease Management
Disease Models, Animal
DNA Copy Number Variations
DNA Damage
DNA Helicases
DNA Methylation
DNA Mutational Analysis
DNA Repair
DNA Replication
DNA, Complementary
DNA, Mitochondrial
DNA-Binding Proteins
Down Syndrome
Drosophila melanogaster
Drug Evaluation, Preclinical
Drug Resistant Epilepsy
Dwarfism
Early Diagnosis
Ectodermal Dysplasia
Electrocardiography
Electron Transport
Electronic Health Records
Embryo, Mammalian
Embryonic Development
Endogenous Retroviruses
Endometriosis
Endoplasmic Reticulum Stress
Energy Metabolism
Epilepsy
Epilepsy, Generalized
Epileptic Syndromes
Esophageal Atresia
Esophagus
Evolution, Molecular
Exome
Exons
Extracorporeal Membrane Oxygenation
Eye Abnormalities
Eye Diseases, Hereditary
Face
Facial Asymmetry
Facial Paralysis
Facies
Failure to Thrive
Family
Family Health
F-Box Proteins
Female
Fibroblasts
Fibrosis
Filamins
Fingers
Flicker Fusion
Folic Acid
Foot Deformities, Congenital
Forkhead Transcription Factors
Frameshift Mutation
Gametogenesis
gamma-Aminobutyric Acid
Geminin
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Regulation, Developmental
Gene Frequency
Gene Knockdown Techniques
Gene Order
Gene Rearrangement
Genes, Dominant
Genes, Duplicate
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Services
Genetic Testing
Genetic Variation
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomic Instability
Genomics
Genotype
Genotyping Techniques
Germ Cells
Germ-Line Mutation
Glaucoma
Glaucoma, Open-Angle
Golgi Apparatus
Growth
Growth Disorders
Growth Hormone
GTP Phosphohydrolases
GTP-Binding Protein beta Subunits
Guanine Nucleotide Exchange Factors
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Hartnup Disease
Health Services Accessibility
Health Services Misuse
Health Status
Healthcare Disparities
Hearing Loss
Hearing Loss, Sensorineural
Heart
Heart Arrest
Heart Atria
Heart Defects, Congenital
Heart Ventricles
Hepatocyte Nuclear Factor 1-beta
Hernias, Diaphragmatic, Congenital
Heterotaxy Syndrome
Heterozygote
High-Throughput Nucleotide Sequencing
Hirsutism
Histidine
Histone Acetyltransferases
Histone Chaperones
Histone Deacetylases
Histones
Homeodomain Proteins
Homologous Recombination
Homozygote
Hospital Mortality
Hospitals, Pediatric
Humans
Hybrid Cells
Hydroxyurea
Hypertension, Pulmonary
Hypoplastic Left Heart Syndrome
Hypoxia-Ischemia, Brain
Ikaros Transcription Factor
Imaging, Three-Dimensional
In Situ Hybridization, Fluorescence
INDEL Mutation
Induced Pluripotent Stem Cells
Infant
Infant Care
Infant, Newborn
Inheritance Patterns
Intellectual Disability
Intensive Care Units, Pediatric
Intercellular Signaling Peptides and Proteins
Intervertebral Disc Degeneration
Intervertebral Disc Displacement
Intracellular Signaling Peptides and Proteins
Intraocular Pressure
Isoproterenol
Jagged-1 Protein
Kaplan-Meier Estimate
Karyotyping
Kidney
Lactic Acid
Language Development Disorders
Leg
Length of Stay
Leukoencephalopathies
Ligases
Light
LIM Domain Proteins
Limb Deformities, Congenital
Limit of Detection
Locomotion
Loss of Function Mutation
Loss of Heterozygosity
Lung Diseases
Lung Diseases, Obstructive
Lung Transplantation
Magnesium
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Mammals
Mandibulofacial Dysostosis
MAP Kinase Kinase Kinases
Mediator Complex
Medically Underserved Area
Membrane Glycoproteins
Membrane Proteins
Membrane Transport Proteins
Mental Disorders
Metalloendopeptidases
Mice
Mice, Knockout
Mice, Transgenic
Microarray Analysis
Microcephaly
Micrognathism
Microsatellite Repeats
Microscopy, Electron, Transmission
Microtubule-Associated Proteins
Middle Aged
Minor Histocompatibility Antigens
Mitochondria
Mitochondria, Muscle
Mitochondrial Diseases
Mitochondrial Myopathies
Mitochondrial Proteins
Mobius Syndrome
Models, Animal
Models, Genetic
Models, Theoretical
Molecular Probe Techniques
Molecular Sequence Data
Mosaicism
Movement Disorders
Moyamoya Disease
Multicenter Studies as Topic
Muscle Hypotonia
Muscle Proteins
Muscle Weakness
Muscle, Skeletal
Muscular Atrophy, Spinal
Muscular Diseases
Mutation
Mutation, Missense
Myocytes, Cardiac
Myopathies, Nemaline
Myopia
Neonatal Screening
Neonatology
Neoplasm Proteins
Neoplasms
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Neural Crest
Neurocognitive Disorders
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neurogenesis
Neuroimaging
Neuronal Plasticity
Neurons
Neurotransmitter Agents
NF-kappa B
Niacin
Nondisjunction, Genetic
Nuclear Matrix-Associated Proteins
Nuclear Proteins
Nucleic Acid Hybridization
Nucleosides
Nucleosome Assembly Protein 1
Nucleotide Motifs
Obesity
Octamer Transcription Factors
Ocular Motility Disorders
Olfaction Disorders
Olfactory Mucosa
Oligonucleotide Array Sequence Analysis
Ophthalmoplegia
Optic Atrophy
Optic Disk
Optic Nerve
Orbital Diseases
Osteochondritis Dissecans
Osteogenesis
Outpatients
Palliative Care
Parents
Patella
PAX5 Transcription Factor
Pediatrics
Pedigree
Peptide Elongation Factors
Peptide Termination Factors
Perinatal Death
Peripheral Nervous System
Peripheral Nervous System Diseases
Peroxidases
Phenotype
Philippines
Phosphofructokinase-1
Phosphoprotein Phosphatases
Phosphoric Monoester Hydrolases
Phosphorylation
Physical Chromosome Mapping
Pilot Projects
Placenta Previa
Point Mutation
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Postpartum Hemorrhage
Precision Medicine
Pre-Eclampsia
Pregnancy
Premature Birth
Prenatal Care
Prenatal Diagnosis
Primary Health Care
Prognosis
Prospective Studies
Protein Interaction Maps
Protein Phosphatase 1
Protein Stability
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Protein Tyrosine Phosphatases
Proteins
Proteolysis
Quality of Life
Rabbits
Radiography
Rare Diseases
Rats
Receptor, IGF Type 1
Receptors, Cell Surface
Receptors, Nicotinic
Receptors, Transforming Growth Factor beta
Recurrence
Repressor Proteins
Reproducibility of Results
Respiratory Insufficiency
Retina
Retinal Degeneration
Retrospective Studies
Rett Syndrome
Rhabdomyolysis
rho-Associated Kinases
Ribonucleoprotein, U5 Small Nuclear
Ribonucleoproteins
Risk
Risk Assessment
RNA Polymerase II
RNA Processing, Post-Transcriptional
RNA Recognition Motif Proteins
RNA Splice Sites
RNA Splicing
RNA, Messenger
RNA, Small Nuclear
RNA-Binding Proteins
Rothmund-Thomson Syndrome
Sarcomeres
Schizophrenia
Scimitar Syndrome
Scleroderma, Systemic
Segmental Duplications, Genomic
Seizures
Self Report
Self-Examination
Semaphorins
Sensitivity and Specificity
Sensory Receptor Cells
Sensory Thresholds
Separase
Sequence Alignment
Sequence Analysis
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Serine-Arginine Splicing Factors
Serrate-Jagged Proteins
Severity of Illness Index
Sex Characteristics
Siblings
Sick Role
Sickness Impact Profile
Signal Processing, Computer-Assisted
Sirolimus
Sister Chromatid Exchange
Skull
Smell
Smith-Magenis Syndrome
Spasms, Infantile
Spine
Spliceosomes
Staining and Labeling
Stem Cells
Stillbirth
Stroke
Sudden Infant Death
Surveys and Questionnaires
Survival Analysis
Survival of Motor Neuron 1 Protein
Synapses
Synaptic Transmission
Syndactyly
Syndrome
Tachycardia, Supraventricular
Tachycardia, Ventricular
Telemedicine
Telomere
Testis
Tetraspanins
Texas
Thumb
Tomography, X-Ray Computed
Trachea
Tracheoesophageal Fistula
Transcription Factor AP-1
Transcription Factors
Transcription Factors, General
Transcriptome
Translocation, Genetic
Treatment Outcome
Trisomy
Troponin T
Tubulin
Tumor Suppressor Protein p53
Twist-Related Protein 1
Ubiquinone
Ubiquitin-Protein Ligases
Ubiquitins
Ultrasonography
Ultrasonography, Prenatal
Verapamil
Vesicular Transport Proteins
Veterans
Virulence
Visual Acuity
Visual Field Tests
Visual Fields
Vitamin A
Vitamin B Complex
Vitamin K
Vitamins
Vulnerable Populations
WD40 Repeats
Whole Genome Sequencing
Wolff-Parkinson-White Syndrome
X Chromosome Inactivation
Xenopus laevis
Young Adult
Zebrafish
Zebrafish Proteins
Zinc Fingers
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Concepts (610)
Derived automatically from this person's publications.
Abnormalities, Multiple
Heart Defects, Congenital
Sequence Deletion
Chromosome Deletion
Intellectual Disability
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Co-Authors (165)
People in Profiles who have published with this person.
BELMONT, JOHN
MIYAKE, CHRISTINA
LUPSKI, JAMES
SCOTT, DARYL
CHEUNG, SAU WAI
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
STANKIEWICZ, PAWEL
GIBBS, RICHARD
BOERWINKLE, ERIC
CHEUNG, SAU WAI
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Same Department
People who are also in this person's primary department.
ARENKIEL, BENJAMIN
BONNEN, PENELOPE
ERWIN, GRAHAM
MILOSAVLJEVIC, ALEKSANDAR
SCHULZE, KATHARINA
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