Harvard Catalyst Profiles
Contact, publication, and social network information about Harvard faculty and fellows.
Home
About
Overview
Open Source Software
Help
History (0)
Find People
Find Everything
Login
to
edit your profile
(add a photo, education, awards, etc.), search
student opportunities
, and
create reports
.
Edit My Profile
My Person List (
0
)
Opportunity Search
Return to Top
Kaitlin Elisabeth Samocha, Ph.D.
Concepts (246)
Back to Profile
Concepts are derived automatically from a person's publications.
Cloud
Categories
Timeline
Details
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.
1-Alkyl-2-acetylglycerophosphocholine Esterase
5' Untranslated Regions
Acoustic Stimulation
Acyltransferases
Adolescent
Adult
Aged
Aged, 80 and over
Algorithms
Alleles
Alternative Splicing
Amino Acid Sequence
Amino Acid Substitution
Analysis of Variance
Animals
Apolipoprotein C-III
Artifacts
Autistic Disorder
Automation
Base Sequence
Bayes Theorem
Behavior
Behavior, Animal
Biological Specimen Banks
Bipolar Disorder
Bone and Bones
Brain
Cadherins
Cardiovascular Diseases
Carrier Proteins
Case-Control Studies
Cell Cycle Proteins
Cell Line
Cell Lineage
Cells, Cultured
Cerebral Cortex
Chickens
Child
Child Behavior Disorders
Child Development Disorders, Pervasive
Child, Preschool
Choanal Atresia
Chromatin
Chromatin Assembly and Disassembly
Chromosomal Proteins, Non-Histone
Chromosome Mapping
Chromosomes, Human, X
Chromosomes, Mammalian
Cognition Disorders
Cohort Studies
Communication Disorders
Computational Biology
Congenital Abnormalities
Consanguinity
Conserved Sequence
Coronary Disease
CpG Islands
Crosses, Genetic
Databases, Genetic
Delivery of Health Care
Developmental Disabilities
Dietary Fats
Disease
DNA Copy Number Variations
DNA Mutational Analysis
DNA Replication
DNA-Binding Proteins
Educational Status
Electron Transport
Embryo, Mammalian
Embryonic Stem Cells
Enzyme Activation
Europe
Exons
Facies
Family
Family Health
Fasting
Female
Fibronectins
Gene Deletion
Gene Dosage
Gene Expression Regulation, Developmental
Gene Frequency
Gene Knockdown Techniques
Gene Regulatory Networks
Genes
Genes, Dominant
Genes, Essential
Genes, Lethal
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Code
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Linkage
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetics, Behavioral
Genetics, Medical
Genetics, Population
Genome
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Germ-Line Mutation
Growth Disorders
GTPase-Activating Proteins
Habituation, Psychophysiologic
Haploinsufficiency
Health Status
Health Status Indicators
Heart Defects, Congenital
Heat-Shock Proteins
Heterozygote
High-Throughput Nucleotide Sequencing
High-Throughput Screening Assays
Hippocampus
Homozygote
Humans
Hybridization, Genetic
Hydrogen Peroxide
Imaging, Three-Dimensional
Infant
Inheritance Patterns
Intelligence
Intelligence Tests
Interleukin-8
Internet
Intracellular Signaling Peptides and Proteins
Ireland
Linear Models
Lod Score
Longevity
Lymphocytes
Male
Membrane Proteins
Mental Disorders
Mice
Mice, Inbred C57BL
Mice, Inbred Strains
Mice, Knockout
Microphthalmos
Middle Aged
Mitochondrial Membranes
Models, Genetic
Models, Statistical
Molecular Sequence Annotation
Molecular Sequence Data
Molecular Targeted Therapy
Multifactorial Inheritance
Multigene Family
Muscular Dystrophies
Mutation
Mutation, Missense
Myocardial Infarction
Myoclonic Epilepsies, Progressive
Myocytes, Cardiac
Nerve Net
Nerve Tissue Proteins
Nervous System Malformations
Neuregulins
Neurobiology
Neurodegenerative Diseases
Neurogenesis
Neurons
Nose
Nucleotides
Odds Ratio
Oligonucleotide Array Sequence Analysis
Open Reading Frames
Organ Size
Pakistan
Parents
Parkinson Disease
Paternal Exposure
Pedigree
Penetrance
Phenotype
Phosphoproteins
Phosphorylation
Phylogeny
Point Mutation
Poisson Distribution
Polymorphism, Single Nucleotide
Population Control
Postprandial Period
Principal Component Analysis
Prion Diseases
Prions
Prognosis
Protein Conformation
Proteins
Protein-Tyrosine Kinases
Proteome
Quality-Adjusted Life Years
Quantitative Trait Loci
Rare Diseases
Reactive Oxygen Species
Receptors, Cell Surface
Recombination, Genetic
Reference Standards
Regression Analysis
Repressor Proteins
Reproducibility of Results
Reproduction
Retroelements
Risk Factors
RNA Splice Sites
RNA Splicing
RNA, Messenger
RNA-Binding Proteins
Sample Size
Schizophrenia
Seizures
Selection, Genetic
Sensory Gating
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology
Sequence Homology, Amino Acid
Sex Characteristics
Sex Factors
Shaw Potassium Channels
Signal Transduction
Single-Cell Analysis
Sodium, Dietary
Software
Species Specificity
Spermatozoa
Synapses
tau Proteins
Testicular Neoplasms
Testis
Tourette Syndrome
Transcription Factors
Transcription, Genetic
Triglycerides
Tyrosine
User-Computer Interface
Samocha's Networks
Click the
Explore
buttons for more information and interactive visualizations!
Concepts (246)
Derived automatically from this person's publications.
Developmental Disabilities
Mutation, Missense
Child Development Disorders, Pervasive
Genetic Variation
Neurobiology
Explore
_
Co-Authors (66)
People in Profiles who have published with this person.
Neale, Benjamin
Talkowski, Michael
Daly, Mark
O'Donnell Luria, Anne
Karczewski, Konrad
Explore
_
Similar People (60)
People who share similar concepts with this person.
Neale, Benjamin
Rehm, Heidi
Alkuraya, Fowzan
Daly, Mark
Chung, Wendy
Explore
_
Same Department
People in same department with this person.
Dron, Jacqueline
Shim, Injeong
Stuhr, Nicole
Szczerbinski, Lukasz
Torabi Dashti, Hesamaddin
Explore
_