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Maureen Bocian
Concepts (238)
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Concepts are derived automatically from a person's publications.
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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.
Abdominal Muscles
Abnormalities, Multiple
Abortion, Spontaneous
Achondroplasia
Acidosis, Lactic
Acyl-CoA Dehydrogenase
Adolescent
Adult
Algorithms
Alleles
alpha-Fetoproteins
Amino Acid Sequence
Amniocentesis
Aneuploidy
Animals
Anterior Horn Cells
Arthrogryposis
Autistic Disorder
Autoradiography
Azure Stains
Base Sequence
Behavior
Bicarbonates
Blotting, Southern
B-Lymphocytes
Body Height
Bone and Bones
Bone Diseases
Brain
British Columbia
Carnitine
Case-Control Studies
Cell Line
Cells, Cultured
Cephalometry
Child
Child, Preschool
Chromosome Aberrations
Chromosome Banding
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes, Artificial, Bacterial
Chromosomes, Artificial, Yeast
Chromosomes, Human, 16-18
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 13
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Cloning, Molecular
Congenital Abnormalities
Contig Mapping
Contracture
Cooperative Behavior
Cosmids
Craniofacial Abnormalities
Craniofacial Dysostosis
Cri-du-Chat Syndrome
Crossing Over, Genetic
Cytogenetic Analysis
Cytoskeletal Proteins
Developmental Disabilities
Diaphragm
Diseases in Twins
DNA
DNA Mutational Analysis
DNA Probes
DNA, Complementary
DNA-Binding Proteins
Dwarfism
Ear
Edema
Exome
Exons
Extremities
Eye Abnormalities
Face
Fatal Outcome
Fathers
Fatty Acids
Female
Fetal Diseases
Fetal Growth Retardation
Fetus
Fibroblasts
Fibula
Fingers
Follow-Up Studies
Foot Deformities, Congenital
Frameshift Mutation
Functional Laterality
Gene Amplification
Gene Deletion
Gene Duplication
Gene Expression
Gene Frequency
Gene Library
Genes, Recessive
Genetic Carrier Screening
Genetic Counseling
Genetic Linkage
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genomic Library
Genotype
Gestational Age
Growth
Growth Disorders
Head
Hearing Disorders
Heart Septal Defects, Ventricular
Hedgehog Proteins
Heterozygote
High-Throughput Nucleotide Sequencing
Holoprosencephaly
Homozygote
Humans
Hydrops Fetalis
Image Processing, Computer-Assisted
In Situ Hybridization, Fluorescence
In Vitro Techniques
Infant
Infant, Newborn
Intellectual Disability
Intelligence
Intestinal Atresia
Intestines
Ion Channels
Joint Diseases
Karyotyping
Kruppel-Like Transcription Factors
Lactic Acid
Language Disorders
Limb Deformities, Congenital
Lip
Magnetic Resonance Imaging
Male
Mandible
Maxillofacial Abnormalities
Membrane Proteins
Microcephaly
Microsatellite Repeats
Microscopy, Fluorescence
Middle Aged
Mitochondria, Muscle
Mitochondrial Diseases
Molecular Sequence Data
Mosaicism
Mouth Abnormalities
Muscle Hypotonia
Muscle, Skeletal
Mutagenesis, Insertional
Mutation
Mutation, Missense
NADH Dehydrogenase
Nasopharyngeal Neoplasms
National Institutes of Health (U.S.)
Neoplasms
Nerve Tissue Proteins
Nervous System Neoplasms
Neural Tube Defects
Neurofibromatosis 1
Nuclear Proteins
Oxidation-Reduction
Oxidative Phosphorylation
Pallister-Hall Syndrome
Parents
Pediatrics
Pedigree
Phenotype
Point Mutation
Polydactyly
Polyhydramnios
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Polymorphism, Single-Stranded Conformational
Preconception Care
Pregnancy
Pregnancy Trimester, Second
Prenatal Diagnosis
Protein Subunits
Proteins
Protein-Tyrosine Kinases
Psychometrics
Quinacrine
Radiography
Receptor, Fibroblast Growth Factor, Type 3
Receptors, AMPA
Receptors, Fibroblast Growth Factor
Receptors, Glycine
Receptors, Neuropeptide Y
Receptors, Neurotransmitter
Recombination, Genetic
Reference Values
Repetitive Sequences, Nucleic Acid
Rhabdomyosarcoma, Embryonal
Risk Factors
Sequence Alignment
Sequence Tagged Sites
Siblings
Skin
Skin Abnormalities
Skin Diseases, Vascular
Skin Neoplasms
Socioeconomic Factors
Sodium Channels
Somatotypes
Speech Perception
Spinal Cord
Stomach
Syndactyly
Syndrome
Telangiectasis
Terminology as Topic
Thoracic Vertebrae
Tomography, X-Ray Computed
Trans-Activators
Translocation, Genetic
Trisomy
Tritium
Twins, Monozygotic
Ultrasonography
Ultrasonography, Prenatal
United States
Urogenital Abnormalities
Uterine Diseases
Vertebrates
X Chromosome
Y Chromosome
Zinc Finger Protein Gli3
Maureen's Networks
Concepts (238)
Derived automatically from this person's publications.
Abnormalities, Multiple
Chromosome Deletion
Prenatal Diagnosis
Autistic Disorder
Chromosome Aberrations
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Co-Authors (9)
People in Profiles who have published with this person.
Spence, M
UCI
Gargus, John
UCI
Flodman, Pamela
UCI
Osann, Kathryn
UCI
Curry, Cynthia
UCSF
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_
Similar People (60)
People who share similar concepts with this person.
Norton, Mary
UCSF
Gleeson, Joseph
UCSD
Kimonis, Virginia
UCI
Rauen, Katherine
UC Davis
Sparks, Teresa
UCSF
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_
Same Department
Baram, Tallie Z
Batra, Anjan
Gray, Wendy
Haier, Richard
Rasmussen, Jerod
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