Concepts (152)
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
- Adult
- Algorithms
- Alleles
- Alternative Splicing
- Amino Acid Sequence
- Anaphase
- Aneuploidy
- Animals
- Animals, Genetically Modified
- Autistic Disorder
- Base Sequence
- Bayes Theorem
- Body Patterning
- Breast Neoplasms
- Cadherins
- Calcium-Binding Proteins
- Cardiovascular Diseases
- Case-Control Studies
- Cell Adhesion Molecules, Neuronal
- Cell Movement
- Child
- Child Development Disorders, Pervasive
- Child, Preschool
- Choanal Atresia
- Cholesterol
- Cholesterol, HDL
- Chromosomal Instability
- Chromosomal Proteins, Non-Histone
- Chromosome Aberrations
- Chromosome Breakage
- Chromosome Breakpoints
- Chromosome Deletion
- Chromosome Inversion
- Chromosome Mapping
- Chromosome Painting
- Chromosomes, Human
- Chromosomes, Human, Pair 11
- Chromosomes, Human, Pair 2
- Cluster Analysis
- Cohort Studies
- Computational Biology
- Congenital Abnormalities
- CpG Islands
- Cytoskeletal Proteins
- Developmental Disabilities
- Disease Models, Animal
- DNA Barcoding, Taxonomic
- DNA Breaks
- DNA Copy Number Variations
- DNA Mutational Analysis
- DNA Replication
- DNA, Single-Stranded
- DNA-Binding Proteins
- Embryo, Nonmammalian
- Endpoint Determination
- Epigenesis, Genetic
- Epilepsy
- Evolution, Molecular
- Exons
- Facies
- Female
- Finland
- Gene Deletion
- Gene Dosage
- Gene Expression Profiling
- Gene Expression Regulation
- Gene Frequency
- Gene Library
- Gene Order
- Gene Rearrangement
- Genetic Association Studies
- Genetic Markers
- Genetic Predisposition to Disease
- Genetic Variation
- Genetics, Population
| - Genome
- Genome, Human
- Genome-Wide Association Study
- Genomic Instability
- Genomic Structural Variation
- Genomics
- Genotype
- Germ-Line Mutation
- High-Throughput Nucleotide Sequencing
- Homozygote
- Humans
- Huntington Disease
- INDEL Mutation
- Infant
- Interspersed Repetitive Sequences
- Inverted Repeat Sequences
- Karyotyping
- Linear Models
- Lymphocytes
- Major Histocompatibility Complex
- Male
- Mental Disorders
- Mice
- Mice, Transgenic
- Microphthalmos
- Mitochondrial Proteins
- Mitosis
- Mitral Valve
- Mitral Valve Prolapse
- Models, Genetic
- Models, Statistical
- Molecular Sequence Annotation
- Molecular Sequence Data
- Multifactorial Inheritance
- Muscular Dystrophies
- Mutation
- Neoplasms
- Nerve Tissue Proteins
- Nervous System
- Neural Cell Adhesion Molecules
- Neural Stem Cells
- Nose
- Oligonucleotide Array Sequence Analysis
- Organ Specificity
- Pedigree
- Phenotype
- Phylogeny
- Phylogeography
- Polymorphism, Single Nucleotide
- Promoter Regions, Genetic
- Protein Isoforms
- Protein Stability
- Proteins
- Pyruvate Dehydrogenase (Lipoamide)-Phosphatase
- Pyruvic Acid
- Quantitative Trait Loci
- Reproducibility of Results
- RNA, Messenger
- ROC Curve
- Schizophrenia
- Sequence Analysis, DNA
- Sequence Analysis, RNA
- Sequence Deletion
- Signal Transduction
- Software
- Suppression, Genetic
- Syndrome
- Terminal Repeat Sequences
- Transcription Factors
- Transcription, Genetic
- Translocation, Genetic
- Workflow
- Xenopus
- Young Adult
- Zebrafish
- Zebrafish Proteins
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Concepts
(152)
Derived automatically from this person's publications.
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Co-Authors
(32)
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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