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Alissa Maria D'Gama, M.D., Ph.D.
Concepts (112)
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Concepts are derived automatically from a person's publications.
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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.
Abnormalities, Multiple
Adolescent
Adult
Amino Acid Metabolism, Inborn Errors
Animals
Autistic Disorder
Biopsy
Brain
Cation Transport Proteins
Cell Division
Cell Lineage
Cells, Cultured
Central Nervous System
Cerebral Cortex
Chelating Agents
Child
Child, Preschool
Chromatin
Chromosome Aberrations
Chromosomes, Human
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Class I Phosphatidylinositol 3-Kinases
Classical Lissencephalies and Subcortical Band Heterotopias
Cohort Studies
Colorectal Neoplasms
Congenital Hypothyroidism
Consanguinity
Databases, Genetic
Diabetes Insipidus
DNA Mutational Analysis
DNA Replication
DNA-Binding Proteins
Ductus Arteriosus, Patent
Dystonic Disorders
Embryonic Development
Epigenesis, Genetic
Exons
Face
Female
Fingers
Gene Expression Regulation, Developmental
Gene Regulatory Networks
Genetic Association Studies
Genetic Loci
Genetic Predisposition to Disease
Genetic Variation
Genome, Human
Genome-Wide Association Study
Genotype
Germ-Line Mutation
Growth Substances
Hand
High-Throughput Nucleotide Sequencing
Histone-Lysine N-Methyltransferase
Homeodomain Proteins
Humans
Hypoventilation
Infant
Infant, Newborn
Insulin-Like Growth Factor I
Lissencephaly
Loss of Heterozygosity
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Manganese
Metal Metabolism, Inborn Errors
Mice
Middle Aged
Mitosis
Mosaicism
Muscle Proteins
Muscle Weakness
Muscle, Skeletal
Mutation
Mutation, Missense
Myopathies, Structural, Congenital
Neurons
Oligonucleotide Array Sequence Analysis
Parkinsonian Disorders
Pedigree
Periventricular Nodular Heterotopia
Phenotype
Phosphatidylinositol 3-Kinases
Polymorphism, Single Nucleotide
Prefrontal Cortex
Pregnancy
Prognosis
Protein-Serine-Threonine Kinases
Proto-Oncogene Proteins c-akt
Rats
Receptors, Cell Surface
Recombinant Proteins
Repressor Proteins
Rett Syndrome
Sequence Analysis
Sequence Analysis, DNA
Signal Transduction
Single-Cell Analysis
Sleep Apnea, Central
Stem Cells
Stereotypic Movement Disorder
Telencephalon
Thiolester Hydrolases
TOR Serine-Threonine Kinases
Transcription Factor AP-2
Transcription Factors
Transcription, Genetic
Video Recording
Young Adult
Zygote
D'Gama's Networks
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Concepts (112)
Derived automatically from this person's publications.
Malformations of Cortical Development
Amino Acid Metabolism, Inborn Errors
Telencephalon
Mutation
Thiolester Hydrolases
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Co-Authors (59)
People in Profiles who have published with this person.
Poduri, Annapurna
Yu, Tim
Walsh, Christopher
Agrawal, Pankaj
Jamuar, Saumya
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_
Similar People (60)
People who share similar concepts with this person.
Poduri, Annapurna
Kwiatkowski, David
Walsh, Christopher
Alkuraya, Fowzan
Hildebrandt, Friedhelm
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_
Same Department
People in same department with this person.
Amirault, Janine
Dodderer, Joshua
Marrinan, Jaclyn
Nunneley, Chloe
Szuch, Eliza
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