Concepts (126)
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
- Achondroplasia
- Adaptor Proteins, Signal Transducing
- Adolescent
- Adult
- Alcohol Drinking
- Alternative Splicing
- Amino Acid Sequence
- Animals
- Atrophy
- Autistic Disorder
- Base Sequence
- Brain
- Brain Diseases
- Cadherins
- Cell Adhesion Molecules, Neuronal
- Central Nervous System Diseases
- Cerebellar Ataxia
- Cerebellum
- Cerebral Cortex
- Cerebral Ventricles
- Cerebral Ventriculography
- Child
- Child, Preschool
- Choristoma
- Chromosome Deletion
- Chromosome Disorders
- Chromosome Inversion
- Chromosome Mapping
- Chromosomes, Human, Pair 1
- Chromosomes, Human, Pair 7
- Cognition Disorders
- Colorectal Neoplasms
- Consanguinity
- Contractile Proteins
- Cytogenetics
- Disease Progression
- DNA Mutational Analysis
- DNA Primers
- Elastin
- Epilepsy
- Exons
- Extracellular Matrix Proteins
- Family
- Family Health
- Fatal Outcome
- Female
- Gene Deletion
- Gene Dosage
- Gene Expression Profiling
- Gene Expression Regulation
- Genes, Dominant
- Genes, Recessive
- Genes, X-Linked
- Genetic Diseases, X-Linked
- Genetic Linkage
- Genetic Markers
- Genetic Predisposition to Disease
- Genetic Privacy
- Genetic Techniques
- Genetic Testing
- Genome, Human
- Genotype
| - Haplotypes
- Health Policy
- Health Surveys
- Heterozygote
- Homeodomain Proteins
- Homozygote
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Infant, Newborn
- Karyotyping
- Lod Score
- Logistic Models
- Loss of Heterozygosity
- Lung Diseases
- Magnetic Resonance Imaging
- Male
- Malformations of Cortical Development
- Maternal Age
- Mental Disorders
- Mice
- Microfilament Proteins
- Microsatellite Repeats
- Middle Aged
- Models, Genetic
- Molecular Sequence Data
- Movement Disorders
- Mutation
- Nerve Tissue Proteins
- Nervous System Malformations
- Neurons
- Oligonucleotide Array Sequence Analysis
- Patients
- Pedigree
- Phenotype
- Physical Chromosome Mapping
- Point Mutation
- Polymorphism, Genetic
- Polymorphism, Single Nucleotide
- Prejudice
- Prenatal Care
- Prenatal Diagnosis
- Public Health
- Radiography
- Rats
- Recovery of Function
- Remission, Spontaneous
- Retrospective Studies
- Risk Factors
- RNA Splice Sites
- RNA, Messenger
- Sequence Analysis, DNA
- Sequence Homology, Amino Acid
- Serine Endopeptidases
- Syndrome
- Transcription Factors
- Trinucleotide Repeat Expansion
- Turkey
- Twins, Dizygotic
- United States
- Vesicular Transport Proteins
- Williams Syndrome
- Young Adult
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Concepts
(126)
Derived automatically from this person's publications.
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Co-Authors
(8)
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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