Concepts (252)
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.
- Abnormalities, Multiple
- Accidents
- Acetylation
- Actins
- Acyclovir
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Algorithms
- Alleles
- Alternative Splicing
- Amino Acid Substitution
- Amniocentesis
- Anal Canal
- Animals
- Anodontia
- Anophthalmos
- Anus, Imperforate
- Anxiety
- Arginine
- Artificial Intelligence
- Athletes
- Athletic Injuries
- Athletic Performance
- Australia
- Autism Spectrum Disorder
- Base Sequence
- beta Catenin
- Bicycling
- Biomarkers, Tumor
- Brachydactyly
- Brain
- Brain Diseases
- Branchio-Oto-Renal Syndrome
- Carcinoma, Merkel Cell
- Carcinoma, Squamous Cell
- Carrier Proteins
- CDC2 Protein Kinase
- Cell Differentiation
- Cell Line
- Cell Transformation, Viral
- Child
- Child Abuse, Sexual
- Child Behavior Disorders
- Child, Preschool
- Chi-Square Distribution
- Chromatin
- Chromatin Immunoprecipitation
- Chromogranins
- Chromosome Aberrations
- Chromosome Banding
- Chromosome Breakage
- Chromosomes, Human, Pair 12
- Cleft Lip
- Cleft Palate
- Cloaca
- Cognition
- Cohort Studies
- Colon
- Colonic Neoplasms
- Comorbidity
- Comparative Genomic Hybridization
- Congenital Abnormalities
- Congenital Hypothyroidism
- Congenital Microtia
- Craniofacial Abnormalities
- Developmental Disabilities
- Diagnostic Errors
- Disease Susceptibility
- DNA
- DNA Copy Number Variations
- DNA Mutational Analysis
- DNA Probes
- DNA Repair
- DNA Replication
- DNA-Binding Proteins
- Doping in Sports
- Down-Regulation
- Dwarfism
- Dynamins
- Enhancer Elements, Genetic
- Environment
- Epilepsy
- Ergonomics
- Esophagus
- Exome
- Eye Proteins
- Face
- Facial Bones
- Facies
- Failure to Thrive
- Female
- Fibroblasts
- Fingers
- Follow-Up Studies
- Foot Deformities, Congenital
- Fragile X Syndrome
- Gastroschisis
- Gene Expression Profiling
- Gene Ontology
- Genetic Association Studies
- Genetic Counseling
- Genetic Predisposition to Disease
- Genetic Testing
- Genitalia, Male
- Genomics
- Genotype
- Gestational Age
- Glycosylphosphatidylinositols
- GPI-Linked Proteins
- GTP Phosphohydrolases
- GTP-Binding Protein alpha Subunits, Gs
- Haploinsufficiency
- Haplotypes
- Head and Neck Neoplasms
- Health Services Accessibility
- Heart Defects, Congenital
- Hemizygote
- Hernia, Umbilical
- Heterozygote
- High-Throughput Nucleotide Sequencing
- Histones
- Holoprosencephaly
- Homeodomain Proteins
- Homozygote
| - Humans
- Hyperphagia
- Hypospadias
- Hypotrichosis
- Immunohistochemistry
- In Situ Hybridization, Fluorescence
- Incidence
- Incisor
- Induced Pluripotent Stem Cells
- Infant
- Infant, Newborn
- Inheritance Patterns
- Intellectual Disability
- Intelligence
- Intestinal Pseudo-Obstruction
- Kaplan-Meier Estimate
- Kidney
- Laryngeal Neoplasms
- Limb Deformities, Congenital
- Live Birth
- Loss of Function Mutation
- Lymph Node Excision
- Lymphocytes
- Male
- Maternal Age
- Medically Underserved Area
- Melanoma
- Membrane Proteins
- Merkel cell polyomavirus
- Methylation
- Mice
- Microphthalmos
- Microtubule-Associated Proteins
- Middle Aged
- Minor Histocompatibility Antigens
- Mitochondrial Proteins
- Models, Molecular
- Models, Statistical
- Molecular Diagnostic Techniques
- Molecular Sequence Data
- Mouth Abnormalities
- Multivariate Analysis
- Musculoskeletal Abnormalities
- Mutation
- Mutation, Missense
- Neoplasm Metastasis
- Neoplasm Recurrence, Local
- Neoplasm Staging
- Neoplasms
- Nerve Tissue Proteins
- Neural Stem Cells
- Neurodevelopmental Disorders
- Neurons
- Neutrophils
- Obesity
- Oncogenes
- Oxytocin
- Pandemics
- Pedigree
- Penetrance
- Phenotype
- Phosphotransferases (Alcohol Group Acceptor)
- Pneumonia, Viral
- Point Mutation
- Polyhydramnios
- Polyomavirus Infections
- Prader-Willi Syndrome
- Predictive Value of Tests
- Pregnancy
- Pregnancy Complications, Infectious
- Prenatal Diagnosis
- Prevalence
- Prognosis
- Prospective Studies
- Protein Binding
- Protein Domains
- Protein Kinases
- Protein-Arginine N-Methyltransferases
- Pseudohypoparathyroidism
- rab GTP-Binding Proteins
- Registries
- Reproducibility of Results
- Retrospective Studies
- Risk Assessment
- Risk Management
- RNA, Messenger
- RNA-Binding Proteins
- Safety Management
- Schools
- Seizures
- Sentinel Lymph Node Biopsy
- Sequence Deletion
- Sex Factors
- Short Stature Homeobox Protein
- Siblings
- Simplexvirus
- Skin Neoplasms
- Skull
- Soccer
- Software
- Spine
- Sports
- Sports for Persons with Disabilities
- Survival Rate
- Synaptic Vesicles
- Syndrome
- Systems Analysis
- Texas
- Time Factors
- Trachea
- Transcription Factor AP-2
- Transcription, Genetic
- Translocation, Genetic
- Treatment Outcome
- Trinucleotide Repeats
- Trisomy 13 Syndrome
- Tumor Microenvironment
- Ultrasonography
- United States
- Urinary Bladder
- Vidarabine
- Virulence
- Vulnerable Populations
- Wnt Signaling Pathway
- Young Adult
- YY1 Transcription Factor
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Concepts
(252)
Derived automatically from this person's publications.
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Co-Authors
(41)
People in Profiles who have published with this person.
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Similar People
(35)
People who share similar concepts with this person.
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Same Department
People who are also in this person's primary department.
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People whose addresses are nearby this person.
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