Harvard Catalyst Profiles

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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 Development220121760.240 Why?
Prejudice120045710.180 Why?
Maternal Age120128090.170 Why?
Patients120049060.150 Why?
Genetic Testing3200635330.130 Why?
Contractile Proteins220062400.120 Why?
Prenatal Care1201211400.120 Why?
Cerebral Ventricles220065420.110 Why?
Family1200431930.110 Why?
Homeodomain Proteins3201224130.100 Why?
Microfilament Proteins2200611300.090 Why?
Alcohol Drinking1201240280.080 Why?
Genes, Dominant320068510.080 Why?
Nervous System Malformations220062440.070 Why?
Vesicular Transport Proteins120093760.070 Why?
Cell Adhesion Molecules, Neuronal120072630.060 Why?
Pedigree6200945390.060 Why?
Colorectal Neoplasms1200469270.060 Why?
Cerebellar Ataxia120061500.060 Why?
Choristoma120062050.060 Why?
Genetic Privacy12004590.060 Why?
Abnormalities, Multiple2200914220.060 Why?
Chromosomes, Human, Pair 1120066380.060 Why?
Williams Syndrome120061940.060 Why?
Microsatellite Repeats420067830.060 Why?
Chromosome Disorders120064970.050 Why?
Chromosome Mapping2200846110.050 Why?
Extracellular Matrix Proteins120078290.050 Why?
Cerebellum2200715010.050 Why?
Chromosome Deletion1200613860.050 Why?
Serine Endopeptidases1200710220.050 Why?
Point Mutation1200615950.050 Why?
Transcription Factors42012121160.040 Why?
Movement Disorders120124590.040 Why?
Autistic Disorder1200812190.040 Why?
DNA Mutational Analysis4200941100.040 Why?
Brain Diseases1200615460.030 Why?
Syndrome3200932680.030 Why?
Lod Score220086000.030 Why?
In Situ Hybridization, Fluorescence3200725090.030 Why?
Mutation52012300150.030 Why?
Chromosomes, Human, Pair 7220073100.030 Why?
Nerve Tissue Proteins1200744080.030 Why?
Gene Expression Profiling1200994170.030 Why?
Health Surveys1201240360.030 Why?
Homozygote2200817760.030 Why?
Health Policy1200526820.030 Why?
Public Health1200526710.020 Why?
Brain32008271000.020 Why?
Family Health2200612530.020 Why?
Genetic Predisposition to Disease32008178780.020 Why?
Gene Deletion2200826590.020 Why?
Cognition Disorders1201239790.020 Why?
Logistic Models12012132480.020 Why?
RNA Splice Sites120092100.020 Why?
Epilepsy1201233030.020 Why?
Magnetic Resonance Imaging52012364010.020 Why?
Cerebral Ventriculography12006440.020 Why?
Cytogenetics120071980.020 Why?
Consanguinity120084560.020 Why?
Chromosome Inversion120071200.020 Why?
Female1020123922030.020 Why?
Physical Chromosome Mapping120061830.020 Why?
Genes, X-Linked120061280.020 Why?
Genes, Recessive120086230.020 Why?
Twins, Dizygotic120062360.020 Why?
Remission, Spontaneous120063840.020 Why?
Sequence Analysis, DNA2200647390.020 Why?
Male820123604020.020 Why?
Achondroplasia12005280.020 Why?
Molecular Sequence Data22009176300.010 Why?
Elastin120062980.010 Why?
Turkey120052530.010 Why?
Trinucleotide Repeat Expansion120062470.010 Why?
Karyotyping1200611710.010 Why?
Loss of Heterozygosity120066620.010 Why?
Gene Dosage1200812170.010 Why?
Alternative Splicing1200910880.010 Why?
Cadherins120089010.010 Why?
Polymorphism, Single Nucleotide32008159080.010 Why?
Genetic Techniques120064280.010 Why?
Adult420122209950.010 Why?
Exons1200923810.010 Why?
DNA Primers1200728170.010 Why?
Haplotypes1200927130.010 Why?
Humans1220127607400.010 Why?
Central Nervous System Diseases120075210.010 Why?
Genetic Diseases, X-Linked120063860.010 Why?
Sequence Homology, Amino Acid1200627470.010 Why?
Middle Aged320122206030.010 Why?
Fatal Outcome1200618350.010 Why?
Atrophy1200616320.010 Why?
Cerebral Cortex2200757760.010 Why?
Gene Expression Regulation22009118740.010 Why?
Child, Preschool32009421930.010 Why?
Heterozygote1200727800.010 Why?
Genetic Markers1200626010.010 Why?
Oligonucleotide Array Sequence Analysis1200837760.010 Why?
Genetic Linkage1200523400.010 Why?
United States22005722920.010 Why?
Adolescent22012882470.010 Why?
Child42009800890.010 Why?
Polymorphism, Genetic1200942420.010 Why?
Adaptor Proteins, Signal Transducing1200828960.010 Why?
Base Sequence12009124200.010 Why?
Prenatal Diagnosis1200512650.010 Why?
Models, Genetic1200634310.010 Why?
Young Adult12012591910.010 Why?
Lung Diseases1200619090.010 Why?
Recovery of Function1200629770.010 Why?
Risk Factors12012741280.010 Why?
Infant22009361570.010 Why?
Amino Acid Sequence12006134420.010 Why?
Radiography1200569610.010 Why?
Retrospective Studies12012805830.010 Why?
RNA, Messenger12009127590.010 Why?
Genotype12007129770.010 Why?
Genome, Human1200544210.010 Why?
Rats12008237160.010 Why?
Disease Progression12006134950.000 Why?
Neurons1200894360.000 Why?
Phenotype12007165720.000 Why?
Infant, Newborn12007261830.000 Why?
Mental Disorders1200768260.000 Why?
Animals220091682020.000 Why?
Mice12009813680.000 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.