Concepts (153)
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.
- Adolescent
- Adrenal Insufficiency
- Adult
- Age of Onset
- Aged
- Aged, 80 and over
- Alleles
- Amino Acid Sequence
- Amino Acid Transport System y+L
- Amino Acid Transport Systems, Basic
- Animals
- Antiporters
- Arachnodactyly
- Basal Cell Nevus Syndrome
- Bayes Theorem
- Biological Specimen Banks
- Carcinoma, Basal Cell
- Cardiovascular Diseases
- Case-Control Studies
- Casein Kinase II
- Cell Differentiation
- Cell Proliferation
- Child
- Child, Preschool
- Chondroitinsulfatases
- Cohort Studies
- Comparative Genomic Hybridization
- Computational Biology
- Confusion
- Connective Tissue
- Connective Tissue Diseases
- Constipation
- Contraception
- Contraceptive Agents
- Contracture
- Critical Illness
- Delayed Diagnosis
- Developmental Disabilities
- Diabetes Mellitus
- Disclosure
- Disease
- Disease Management
- DNA
- DNA, Mitochondrial
- Duty to Recontact
- Emergency Service, Hospital
- Endocrine System Diseases
- Epilepsy
- Executive Function
- Fabry Disease
- Failure to Thrive
- Female
- Fetus
- Follow-Up Studies
- Gene Targeting
- Genes, Dominant
- Genetic Association Studies
- Genetic Counseling
- Genetic Diseases, Inborn
- Genetic Predisposition to Disease
- Genetic Research
- Genetic Testing
- Genetic Variation
- Genetics, Medical
- Genome, Human
- Genomics
- Genotype
- Growth Disorders
- Health Services Accessibility
- Health Status Disparities
- Heterozygote
- Histone-Lysine N-Methyltransferase
- Hospitals
- Humans
- Hyperparathyroidism
- Hyperthyroidism
- Hypertrichosis
| - Infant
- Infant, Newborn
- Informed Consent
- Jamaica
- Kidney
- Kidney Diseases, Cystic
- Laboratories
- Limb Deformities, Congenital
- Loeys-Dietz Syndrome
- Longevity
- Longitudinal Studies
- Male
- Maple Syrup Urine Disease
- Massachusetts
- Medical History Taking
- Medicine
- Mental Retardation, X-Linked
- Metabolic Diseases
- Metabolism, Inborn Errors
- Mice
- Microarray Analysis
- Middle Aged
- Minority Groups
- Minority Health
- Mitochondrial Diseases
- Molecular Sequence Data
- Monosaccharide Transport Proteins
- Multicenter Studies as Topic
- Mutation
- Mutation, Missense
- Myeloid-Lymphoid Leukemia Protein
- Neonatal Screening
- Nerve Tissue Proteins
- Neural Stem Cells
- Neurogenesis
- Neuropsychological Tests
- Odds Ratio
- Pancreatitis
- Parents
- Patient Education as Topic
- Pedigree
- Penetrance
- Phenotype
- Physicians
- Physician's Role
- Physicians, Primary Care
- Point Mutation
- Practice Guidelines as Topic
- Pregnancy
- Prenatal Diagnosis
- Prevalence
- Primary Health Care
- Prospective Studies
- Puberty, Precocious
- Pyruvate Dehydrogenase Complex Deficiency Disease
- Randomized Controlled Trials as Topic
- Rare Diseases
- Referral and Consultation
- Reproducibility of Results
- Retinitis Pigmentosa
- Retrospective Studies
- Risk Factors
- RNA-Binding Proteins
- Seizures
- Sensitivity and Specificity
- Sequence Analysis, DNA
- Skin Abnormalities
- Smad2 Protein
- Syndrome
- Transcription Factors
- Ultrasonography, Prenatal
- United States
- Urea Cycle Disorders, Inborn
- Williams Syndrome
- Young Adult
- Zebrafish
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Concepts
(153)
Derived automatically from this person's publications.
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Co-Authors
(77)
People in Profiles who have published with this person.
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Similar People
(60)
People who share similar concepts with this person.
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Same Department
People in same department with this person.
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