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Christopher Balak
Concepts (115)
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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.
Adolescent
Adult
Aicardi Syndrome
Algorithms
Alleles
Amino Acid Sequence
Animals
Arthrogryposis
Athletes
Autism Spectrum Disorder
Binding Sites
Body Dysmorphic Disorders
Brain
Brain Diseases
Cataract
Cell Adhesion
Cell-Free Nucleic Acids
Cells, Cultured
Central Nervous System
Cerebellum
Child
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 1
Codon, Nonsense
Cohort Studies
Contracture
Craniofacial Abnormalities
DEAD-box RNA Helicases
Developmental Disabilities
Diagnosis, Differential
Diagnostic Errors
Disease Models, Animal
DNA
DNA Copy Number Variations
DNA Methylation
Drug Resistant Epilepsy
Dysarthria
Electroencephalography
Epigenesis, Genetic
Epilepsy
Epileptic Syndromes
Exome
Female
Fibroblast Growth Factors
Frameshift Mutation
Gait Ataxia
Gene Expression
Gene Expression Regulation
Gene Regulatory Networks
Genetic Diseases, X-Linked
GTP-Binding Protein alpha Subunits, Gi-Go
Healthy Volunteers
HEK293 Cells
Hereditary Central Nervous System Demyelinating Diseases
Heterogeneous-Nuclear Ribonucleoprotein Group F-H
Heterozygote
Humans
Infant
Infant, Newborn
Intellectual Disability
Intracellular Signaling Peptides and Proteins
Lysosomal-Associated Membrane Protein 1
Lysosomes
Magnetic Resonance Imaging
Male
Metabolic Networks and Pathways
Methyl-CpG-Binding Protein 2
Mice
Mice, Knockout
Microglia
Models, Molecular
Molecular Diagnostic Techniques
Muscle Hypotonia
Muscular Atrophy, Spinal
Muscular Diseases
Mutation
Mutation, Missense
Myoclonic Epilepsies, Progressive
Nerve Tissue Proteins
Neural Tube Defects
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neurons
Nuclear Proteins
Olivopontocerebellar Atrophies
Pedigree
Phenotype
Pol1 Transcription Initiation Complex Proteins
Prevalence
Prognosis
Promoter Regions, Genetic
Protein Conformation
Proto-Oncogene Proteins
Qb-SNARE Proteins
Qc-SNARE Proteins
Rats
Rett Syndrome
RNA
RNA, Ribosomal, 18S
Saliva
SKP Cullin F-Box Protein Ligases
Spasms, Infantile
Spinal Muscular Atrophies of Childhood
Synapses
Syndrome
TATA-Binding Protein Associated Factors
Transcription Factors
Transforming Growth Factor beta
Vacuolar Proton-Translocating ATPases
Vesicular Transport Proteins
Whole Genome Sequencing
Young Adult
Zebrafish
Zinc Fingers
Christopher's Networks
Concepts (115)
Derived automatically from this person's publications.
SKP Cullin F-Box Protein Ligases
Frameshift Mutation
Body Dysmorphic Disorders
Intellectual Disability
Chromosomes, Human, Pair 1
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Co-Authors (20)
People in Profiles who have published with this person.
Glass, Christopher
UCSD
Pasillas, Martina
UCSD
Gordts, Philip
UCSD
Schlachetzki, Johannes
UCSD
Moskowitz, Abby
UCSD
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_
Similar People (60)
People who share similar concepts with this person.
Gleeson, Joseph
UCSD
Nagata, Jason
UCSF
Brown, Hilary
USC
Sherr, Elliott
UCSF
Martinez, Julian
UCLA
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Same Department
Blue, Steven
Concepcion, Dorothy
Fu, Xiang-dong
Ren, Bing
Willert, Karl
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