Harvard Catalyst Profiles

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Kaitlin Elisabeth Samocha, Ph.D.

Concepts (246)

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Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
Name Number of Publications Most Recent Publication Publications by All Authors Concept Score Why?
Genetic Variation19202465610.820 Why?
Neurobiology120201370.630 Why?
Developmental Disabilities7202415090.630 Why?
Child Development Disorders, Pervasive420146000.570 Why?
Mutation, Missense9202425700.570 Why?
Genes, Essential320201850.440 Why?
Genome, Human7202244210.410 Why?
Autistic Disorder2202012190.400 Why?
Genetic Predisposition to Disease212024178780.400 Why?
High-Throughput Nucleotide Sequencing1202336340.370 Why?
Sensory Gating12010470.360 Why?
5' Untranslated Regions220212530.330 Why?
Quantitative Trait Loci4202421120.320 Why?
Gene Expression Regulation, Developmental1202036080.310 Why?
Databases, Genetic5202017420.290 Why?
Mutation182021300160.290 Why?
Selection, Genetic320228680.280 Why?
Disease320206700.260 Why?
Genetic Diseases, Inborn320236040.260 Why?
Gene Frequency8202036010.250 Why?
DNA Mutational Analysis4202041100.240 Why?
Genetics, Medical220203340.240 Why?
Computational Biology5201635090.230 Why?
Genes, Recessive220246230.230 Why?
Haploinsufficiency320223360.230 Why?
Penetrance420243820.230 Why?
DNA Copy Number Variations4202220200.230 Why?
Phenotype132022165710.230 Why?
Cerebral Cortex1202057760.220 Why?
Genome-Wide Association Study112020126610.220 Why?
Rare Diseases320236220.200 Why?
Genes, X-Linked120211280.180 Why?
Crosses, Genetic320107500.170 Why?
RNA Splice Sites220182100.170 Why?
Sequence Analysis, DNA5201747390.170 Why?
Polymorphism, Single Nucleotide92024159080.170 Why?
Software5201644310.170 Why?
Consanguinity220204560.160 Why?
Proteins3202060300.160 Why?
Sodium, Dietary120224250.160 Why?
Retroelements120191620.150 Why?
Genotype52023129780.150 Why?
Exons4202023810.150 Why?
Molecular Sequence Annotation120205200.150 Why?
Genetics, Population220209350.150 Why?
Reproduction120226450.140 Why?
Choanal Atresia12017410.140 Why?
Genetic Diseases, X-Linked120213860.140 Why?
Multigene Family1202010760.140 Why?
Microphthalmos12017580.140 Why?
Germ-Line Mutation4202018520.140 Why?
RNA Splicing220188980.130 Why?
Genes, Lethal120162230.130 Why?
Heterozygote5202227800.130 Why?
Homozygote2202017760.130 Why?
Nucleotides120184530.130 Why?
Chromosome Mapping3202246110.130 Why?
Genome2201617370.120 Why?
Transcription, Genetic3202075830.120 Why?
Paternal Exposure12015960.120 Why?
Myoclonic Epilepsies, Progressive12014130.120 Why?
Shaw Potassium Channels12014200.120 Why?
Electron Transport120152100.120 Why?
Multifactorial Inheritance3202113800.120 Why?
Prion Diseases120161000.120 Why?
Genetic Association Studies3202327340.120 Why?
Pedigree3201745390.120 Why?
Muscular Dystrophies120173900.120 Why?
Mitochondrial Membranes120151760.120 Why?
Genomics2202358220.120 Why?
Genetic Code120141370.120 Why?
Tourette Syndrome120173950.110 Why?
Nervous System Malformations120152440.110 Why?
Cohort Studies102024414570.110 Why?
Fibronectins120177230.110 Why?
Humans5020247606170.110 Why?
Genes1201718230.110 Why?
Alternative Splicing1201810880.110 Why?
Nose120175210.110 Why?
Cadherins120179010.100 Why?
Hydrogen Peroxide120157300.100 Why?
Sample Size320208380.100 Why?
Chromosomal Proteins, Non-Histone120177250.100 Why?
Phosphoproteins2201724460.090 Why?
Cell Lineage1202025540.090 Why?
Embryo, Mammalian1201616700.090 Why?
Male2620243603580.090 Why?
CpG Islands2202011920.090 Why?
Genetic Loci2202026240.090 Why?
Species Specificity2201424110.090 Why?
Intracellular Signaling Peptides and Proteins2201728720.080 Why?
Lod Score120106000.080 Why?
Habituation, Psychophysiologic120101470.080 Why?
Chromosomes, Mammalian120101470.080 Why?
Female2620243921480.080 Why?
Testicular Neoplasms120158000.080 Why?
Gene Deletion1201726610.080 Why?
Point Mutation1201415950.080 Why?
Neurogenesis120158620.080 Why?
Models, Genetic5201734310.080 Why?
Molecular Targeted Therapy1202028120.080 Why?
Single-Cell Analysis1202024470.080 Why?
Sequence Homology220201960.080 Why?
Receptors, Cell Surface1201728020.070 Why?
Case-Control Studies42020221480.070 Why?
Mice, Inbred Strains1201017590.070 Why?
Schizophrenia4202069290.070 Why?
Gene Regulatory Networks1201617450.070 Why?
Principal Component Analysis120109430.070 Why?
Chromosomes, Human, X220213210.070 Why?
Child122024800790.060 Why?
Sex Factors12020105480.060 Why?
Sex Characteristics2202126370.060 Why?
Acoustic Stimulation1201012350.060 Why?
Poisson Distribution220205040.060 Why?
Recombination, Genetic1201015190.060 Why?
Synapses1201417550.060 Why?
Congenital Abnormalities220237090.060 Why?
Genetic Markers1201026010.060 Why?
Organ Size1200922520.060 Why?
Prions220161800.050 Why?
Hippocampus1201637610.050 Why?
Ireland120231700.050 Why?
Chromatin1201429550.050 Why?
Acyltransferases120243050.050 Why?
Delivery of Health Care1202053320.050 Why?
Facies120232220.050 Why?
Conserved Sequence2201611620.050 Why?
DNA Replication1200914140.050 Why?
Analysis of Variance1201062240.050 Why?
Reproducibility of Results42020200740.050 Why?
Neurons1202094380.040 Why?
Family Health2201712530.040 Why?
RNA, Messenger32020127580.040 Why?
Heart Defects, Congenital1201546710.040 Why?
Inheritance Patterns120213410.040 Why?
Bone and Bones1200925650.040 Why?
Child Behavior Disorders120238040.040 Why?
Growth Disorders120236340.040 Why?
Gene Dosage1202212170.040 Why?
Automation120205850.040 Why?
Neuregulins12017360.040 Why?
Genetics, Behavioral12017530.040 Why?
Open Reading Frames120208130.030 Why?
1-Alkyl-2-acetylglycerophosphocholine Esterase120171270.030 Why?
Base Sequence22020124210.030 Why?
Reference Standards1202010020.030 Why?
Pakistan120172920.030 Why?
Alleles2201868610.030 Why?
Mental Disorders1201668260.030 Why?
Communication Disorders12016500.030 Why?
Quality-Adjusted Life Years1202217220.030 Why?
Gene Knockdown Techniques1202016080.030 Why?
Apolipoprotein C-III120172100.030 Why?
Postprandial Period120173140.030 Why?
Adult920202209690.030 Why?
Mice52016813680.030 Why?
DNA-Binding Proteins1201295860.030 Why?
Oligonucleotide Array Sequence Analysis1202337770.030 Why?
Biological Specimen Banks120207780.030 Why?
Parents2202035630.030 Why?
Interleukin-8120176960.030 Why?
Animals720171682010.030 Why?
Europe1202034130.030 Why?
Odds Ratio2201796430.030 Why?
Population Control12013220.030 Why?
Risk Factors52022741150.030 Why?
Chickens120158580.030 Why?
Intelligence Tests120145030.030 Why?
Amino Acid Sequence22014134410.030 Why?
Embryonic Stem Cells1202012620.030 Why?
Sequence Deletion1201714900.030 Why?
Longevity1202010640.030 Why?
Signal Transduction12015234160.030 Why?
Phylogeny1202028060.030 Why?
Transcription Factors12012121160.030 Why?
Testis120157920.030 Why?
Lymphocytes1202026040.030 Why?
Intelligence120179230.020 Why?
Genes, Dominant120148510.020 Why?
Molecular Sequence Data22014176290.020 Why?
Behavior120145400.020 Why?
GTPase-Activating Proteins120144710.020 Why?
Spermatozoa120156290.020 Why?
Artifacts1202019100.020 Why?
Mice, Knockout22017143890.020 Why?
Myocytes, Cardiac1202016670.020 Why?
Tyrosine1201514400.020 Why?
Neurodegenerative Diseases1202010850.020 Why?
Fasting1201716030.020 Why?
Heat-Shock Proteins120147950.020 Why?
High-Throughput Screening Assays120169330.020 Why?
Health Status Indicators120169690.020 Why?
Sequence Homology, Amino Acid1201427470.020 Why?
Sequence Alignment1201421780.020 Why?
User-Computer Interface1201613970.020 Why?
Amino Acid Substitution1201417390.020 Why?
Chromatin Assembly and Disassembly120146340.020 Why?
Enzyme Activation1201535910.020 Why?
tau Proteins1202020940.020 Why?
Educational Status1201725090.020 Why?
Health Status1202240750.020 Why?
Triglycerides1201724590.020 Why?
Hybridization, Genetic120091020.020 Why?
Dietary Fats1201719950.020 Why?
Bayes Theorem1201723260.020 Why?
Family1202031930.020 Why?
Reactive Oxygen Species1201521370.020 Why?
Genetic Testing1202035330.020 Why?
Protein Conformation1201439650.020 Why?
RNA-Binding Proteins1201518900.020 Why?
Linear Models1201658660.020 Why?
Proteome1201618570.020 Why?
Protein-Tyrosine Kinases1201524250.020 Why?
Algorithms22017140180.020 Why?
Cell Line12020155760.020 Why?
Parkinson Disease1202028780.020 Why?
Cell Cycle Proteins1201734470.020 Why?
Regression Analysis1201463380.020 Why?
Genetic Linkage1201023400.010 Why?
Repressor Proteins1201529850.010 Why?
Phosphorylation1201583110.010 Why?
Infant22017361520.010 Why?
Child, Preschool22017421880.010 Why?
Imaging, Three-Dimensional1201640580.010 Why?
Internet1201530900.010 Why?
Coronary Disease1201759120.010 Why?
Nerve Net1201422900.010 Why?
Behavior, Animal1201018720.010 Why?
Nerve Tissue Proteins1201444080.010 Why?
Seizures1201429540.010 Why?
Carrier Proteins1201449350.010 Why?
Brain22020271010.010 Why?
Models, Statistical1201550730.010 Why?
Middle Aged320202205840.010 Why?
Cognition Disorders1201439790.010 Why?
Cells, Cultured12015189370.010 Why?
Mice, Inbred C57BL12016221150.010 Why?
Membrane Proteins1201478470.010 Why?
Bipolar Disorder1201450910.010 Why?
Myocardial Infarction12017114590.010 Why?
Prognosis12015296000.010 Why?
Aged, 80 and over12020588940.010 Why?
Cardiovascular Diseases12020154980.010 Why?
Adolescent12017882340.000 Why?
Aged120201690420.000 Why?
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Concepts (246)
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© 2025 President and Fellows of Harvard College
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.