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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 Development220121740.240 Why?
Prejudice120045690.170 Why?
Maternal Age120128040.170 Why?
Patients120049080.150 Why?
Genetic Testing3200635910.120 Why?
Contractile Proteins220062400.120 Why?
Prenatal Care1201211580.120 Why?
Cerebral Ventricles220065500.110 Why?
Family1200432100.110 Why?
Homeodomain Proteins3201224290.090 Why?
Microfilament Proteins2200611300.090 Why?
Alcohol Drinking1201240450.080 Why?
Genes, Dominant320068550.080 Why?
Nervous System Malformations220062430.070 Why?
Vesicular Transport Proteins120093770.060 Why?
Cell Adhesion Molecules, Neuronal120072620.060 Why?
Pedigree6200945390.060 Why?
Colorectal Neoplasms1200469660.060 Why?
Cerebellar Ataxia120061510.060 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 Mapping2200846160.050 Why?
Extracellular Matrix Proteins120078320.050 Why?
Cerebellum2200715210.050 Why?
Chromosome Deletion1200613840.050 Why?
Serine Endopeptidases1200710270.050 Why?
Point Mutation1200615910.050 Why?
Transcription Factors42012121580.040 Why?
Movement Disorders120124620.040 Why?
Autistic Disorder1200812390.040 Why?
DNA Mutational Analysis4200941140.040 Why?
Brain Diseases1200615510.030 Why?
Syndrome3200932710.030 Why?
Lod Score220086000.030 Why?
In Situ Hybridization, Fluorescence3200725090.030 Why?
Mutation52012302110.030 Why?
Chromosomes, Human, Pair 7220073100.030 Why?
Nerve Tissue Proteins1200744010.030 Why?
Gene Expression Profiling1200995320.030 Why?
Homozygote2200817740.030 Why?
Health Surveys1201240560.030 Why?
Health Policy1200526980.020 Why?
Public Health1200526810.020 Why?
Brain32008271630.020 Why?
Family Health2200612540.020 Why?
Genetic Predisposition to Disease32008180630.020 Why?
Gene Deletion2200826680.020 Why?
Cognition Disorders1201239680.020 Why?
Logistic Models12012132840.020 Why?
RNA Splice Sites120092120.020 Why?
Epilepsy1201233170.020 Why?
Magnetic Resonance Imaging52012365820.020 Why?
Cerebral Ventriculography12006440.020 Why?
Cytogenetics120071980.020 Why?
Consanguinity120084600.020 Why?
Chromosome Inversion120071190.020 Why?
Female1020123966600.020 Why?
Physical Chromosome Mapping120061830.020 Why?
Genes, X-Linked120061290.020 Why?
Genes, Recessive120086240.020 Why?
Twins, Dizygotic120062360.020 Why?
Remission, Spontaneous120063840.020 Why?
Sequence Analysis, DNA2200647800.020 Why?
Male820123642030.020 Why?
Achondroplasia12005280.010 Why?
Molecular Sequence Data22009176080.010 Why?
Elastin120062990.010 Why?
Turkey120052560.010 Why?
Trinucleotide Repeat Expansion120062530.010 Why?
Karyotyping1200611760.010 Why?
Loss of Heterozygosity120066630.010 Why?
Gene Dosage1200812110.010 Why?
Alternative Splicing1200911030.010 Why?
Genetic Techniques120064270.010 Why?
Cadherins120089030.010 Why?
Polymorphism, Single Nucleotide32008160360.010 Why?
Adult420122233170.010 Why?
Exons1200923910.010 Why?
DNA Primers1200728270.010 Why?
Haplotypes1200927220.010 Why?
Humans1220127670400.010 Why?
Central Nervous System Diseases120075180.010 Why?
Genetic Diseases, X-Linked120063860.010 Why?
Sequence Homology, Amino Acid1200627450.010 Why?
Middle Aged320122232330.010 Why?
Fatal Outcome1200618360.010 Why?
Atrophy1200616310.010 Why?
Cerebral Cortex2200757540.010 Why?
Gene Expression Regulation22009119230.010 Why?
Child, Preschool32009426060.010 Why?
Genetic Markers1200626020.010 Why?
Heterozygote1200727940.010 Why?
Oligonucleotide Array Sequence Analysis1200837970.010 Why?
Genetic Linkage1200523420.010 Why?
United States22005729710.010 Why?
Adolescent22012890460.010 Why?
Child42009807710.010 Why?
Polymorphism, Genetic1200942470.010 Why?
Base Sequence12009124140.010 Why?
Adaptor Proteins, Signal Transducing1200829020.010 Why?
Prenatal Diagnosis1200512710.010 Why?
Models, Genetic1200634450.010 Why?
Young Adult12012599800.010 Why?
Lung Diseases1200619420.010 Why?
Recovery of Function1200629780.010 Why?
Risk Factors12012748860.010 Why?
Infant22009364850.010 Why?
Amino Acid Sequence12006134110.010 Why?
Radiography1200569750.010 Why?
RNA, Messenger12009127930.010 Why?
Retrospective Studies12012816590.010 Why?
Genotype12007130350.010 Why?
Genome, Human1200544410.010 Why?
Rats12008237130.010 Why?
Neurons1200895170.000 Why?
Disease Progression12006136460.000 Why?
Phenotype12007167180.000 Why?
Infant, Newborn12007263960.000 Why?
Mental Disorders1200768730.000 Why?
Animals220091689650.000 Why?
Mice12009819120.000 Why?
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Concepts (126)
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Co-Authors (8)
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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.