Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Kira Apse, M.Sc.

Concepts (126)

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?
Malformations of Cortical Development220121740.240 Why?
Prejudice120045670.170 Why?
Maternal Age120128040.170 Why?
Patients120049080.150 Why?
Genetic Testing3200635940.120 Why?
Contractile Proteins220062400.120 Why?
Prenatal Care1201211580.120 Why?
Cerebral Ventricles220065500.110 Why?
Family1200432080.110 Why?
Homeodomain Proteins3201224300.090 Why?
Microfilament Proteins2200611300.090 Why?
Alcohol Drinking1201240410.080 Why?
Genes, Dominant320068550.080 Why?
Nervous System Malformations220062430.070 Why?
Vesicular Transport Proteins120093760.060 Why?
Cell Adhesion Molecules, Neuronal120072620.060 Why?
Pedigree6200945350.060 Why?
Colorectal Neoplasms1200469580.060 Why?
Cerebellar Ataxia120061500.060 Why?
Choristoma120062050.060 Why?
Genetic Privacy12004590.060 Why?
Abnormalities, Multiple2200914240.060 Why?
Chromosomes, Human, Pair 1120066400.060 Why?
Williams Syndrome120061950.060 Why?
Microsatellite Repeats420067840.050 Why?
Chromosome Disorders120064980.050 Why?
Chromosome Mapping2200846170.050 Why?
Extracellular Matrix Proteins120078330.050 Why?
Cerebellum2200715190.050 Why?
Chromosome Deletion1200613840.050 Why?
Serine Endopeptidases1200710240.050 Why?
Point Mutation1200615900.040 Why?
Transcription Factors42012121290.040 Why?
Movement Disorders120124600.040 Why?
Autistic Disorder1200812380.040 Why?
DNA Mutational Analysis4200941110.040 Why?
Brain Diseases1200615520.030 Why?
Syndrome3200932710.030 Why?
Lod Score220085990.030 Why?
In Situ Hybridization, Fluorescence3200725100.030 Why?
Mutation52012301920.030 Why?
Chromosomes, Human, Pair 7220073100.030 Why?
Nerve Tissue Proteins1200743940.030 Why?
Gene Expression Profiling1200995250.030 Why?
Homozygote2200817740.030 Why?
Health Surveys1201240580.030 Why?
Health Policy1200526990.020 Why?
Public Health1200526800.020 Why?
Brain32008271790.020 Why?
Family Health2200612530.020 Why?
Genetic Predisposition to Disease32008180740.020 Why?
Gene Deletion2200826670.020 Why?
Cognition Disorders1201239650.020 Why?
Logistic Models12012132730.020 Why?
RNA Splice Sites120092120.020 Why?
Epilepsy1201233170.020 Why?
Magnetic Resonance Imaging52012365470.020 Why?
Cerebral Ventriculography12006440.020 Why?
Cytogenetics120071970.020 Why?
Consanguinity120084600.020 Why?
Chromosome Inversion120071190.020 Why?
Female1020123961410.020 Why?
Physical Chromosome Mapping120061830.020 Why?
Genes, X-Linked120061290.020 Why?
Genes, Recessive120086250.020 Why?
Twins, Dizygotic120062360.020 Why?
Remission, Spontaneous120063840.020 Why?
Sequence Analysis, DNA2200647800.020 Why?
Male820123638150.010 Why?
Achondroplasia12005280.010 Why?
Molecular Sequence Data22009175960.010 Why?
Elastin120062980.010 Why?
Turkey120052810.010 Why?
Trinucleotide Repeat Expansion120062530.010 Why?
Karyotyping1200611750.010 Why?
Loss of Heterozygosity120066630.010 Why?
Gene Dosage1200812130.010 Why?
Alternative Splicing1200911030.010 Why?
Cadherins120088990.010 Why?
Polymorphism, Single Nucleotide32008160390.010 Why?
Genetic Techniques120064290.010 Why?
Adult420122230880.010 Why?
Exons1200923930.010 Why?
DNA Primers1200728240.010 Why?
Humans1220127659260.010 Why?
Haplotypes1200927260.010 Why?
Central Nervous System Diseases120075190.010 Why?
Genetic Diseases, X-Linked120063860.010 Why?
Sequence Homology, Amino Acid1200627430.010 Why?
Middle Aged320122230160.010 Why?
Fatal Outcome1200618350.010 Why?
Atrophy1200616290.010 Why?
Cerebral Cortex2200757650.010 Why?
Gene Expression Regulation22009118950.010 Why?
Child, Preschool32009425100.010 Why?
Heterozygote1200727960.010 Why?
Genetic Markers1200626030.010 Why?
Oligonucleotide Array Sequence Analysis1200837960.010 Why?
Genetic Linkage1200523420.010 Why?
United States22005729090.010 Why?
Adolescent22012888110.010 Why?
Child42009805680.010 Why?
Polymorphism, Genetic1200942490.010 Why?
Base Sequence12009124050.010 Why?
Adaptor Proteins, Signal Transducing1200828970.010 Why?
Prenatal Diagnosis1200512710.010 Why?
Models, Genetic1200634470.010 Why?
Young Adult12012598570.010 Why?
Lung Diseases1200619390.010 Why?
Recovery of Function1200629630.010 Why?
Risk Factors12012748500.010 Why?
Infant22009364260.010 Why?
Amino Acid Sequence12006133980.010 Why?
Radiography1200569410.010 Why?
RNA, Messenger12009127680.010 Why?
Retrospective Studies12012815370.010 Why?
Genotype12007130260.010 Why?
Genome, Human1200544430.010 Why?
Rats12008237080.010 Why?
Neurons1200895270.000 Why?
Disease Progression12006136140.000 Why?
Phenotype12007167140.000 Why?
Infant, Newborn12007263800.000 Why?
Mental Disorders1200768700.000 Why?
Animals220091687350.000 Why?
Mice12009817820.000 Why?
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Concepts (126)
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.