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Rebecca Mardach
Concepts (124)
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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.
Actins
Adolescent
Adult
Aged
Amidohydrolases
Amino Acid Metabolism, Inborn Errors
Amino Acid Substitution
Amino Acid Transport Systems, Basic
Amniotic Fluid
Asperger Syndrome
Autism Spectrum Disorder
Base Sequence
Biological Transport
Biotin
Biotinidase
Carbon-Carbon Ligases
Carboxy-Lyases
Cardiomyopathies
Carnitine
Carrier Proteins
Cell Line, Transformed
Cells, Cultured
Child
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 10
Citrullinemia
Comparative Genomic Hybridization
Constipation
Critical Illness
Developmental Disabilities
DNA Copy Number Variations
DNA Mutational Analysis
DNA, Mitochondrial
Drug Administration Schedule
Drug Substitution
Electrocardiography
Enzyme Replacement Therapy
Failure to Thrive
Family Health
Fatal Outcome
Female
Fibroblasts
Fragile X Syndrome
Gaucher Disease
Genetic Association Studies
Genetic Carrier Screening
Genetic Predisposition to Disease
Genetic Testing
Genotype
Glucosylceramidase
Growth Disorders
Haplotypes
Hemoglobins
Histone-Lysine N-Methyltransferase
Homocystine
Homocystinuria
Homozygote
Humans
Hyperammonemia
Hypertrichosis
Ileus
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Injections, Intravenous
Intellectual Disability
Intestinal Pseudo-Obstruction
Lactic Acid
Leukocytes, Mononuclear
Loss of Function Mutation
Male
Marfan Syndrome
Membrane Glycoproteins
Metabolic Diseases
Metabolism, Inborn Errors
Methionine
Methylmalonic Acid
Methylmalonyl-CoA Decarboxylase
Middle Aged
Mitochondrial Membrane Transport Proteins
Mitochondrial Myopathies
Muscle, Skeletal
Mutation
Myeloid-Lymphoid Leukemia Protein
Myocardium
Neonatal Screening
Nucleic Acid Conformation
Nucleic Acid Hybridization
Ornithine
Oxidoreductases
Oxidoreductases Acting on CH-CH Group Donors
Palmitic Acids
Pedigree
Phenotype
Platelet Count
Pneumothorax
Point Mutation
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Precision Medicine
Pregnancy
Prenatal Diagnosis
Propionates
Proteins
Pyridoxine
Pyruvate Carboxylase
Recombinant Proteins
Retrospective Studies
RNA, Messenger
RNA, Transfer, Arg
Sequence Deletion
Sexual Maturation
Substance Withdrawal Syndrome
Substrate Specificity
Symporters
Syndrome
Thymidine Kinase
Treatment Outcome
Valerates
Valine
Vitamin B 12
Vitamin B 12 Deficiency
Whole Genome Sequencing
Rebecca's Networks
Concepts (124)
Derived automatically from this person's publications.
Amino Acid Metabolism, Inborn Errors
Carnitine
Glucosylceramidase
Propionates
Gaucher Disease
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Co-Authors (23)
People in Profiles who have published with this person.
Besterman, Aaron
UCSD
James, Kiely
UCSD
Quintero-Rivera, Fabiola
UCI
Feigenbaum, Annette
UCSD
Perry, James
UCSD
Explore
_
Similar People (60)
People who share similar concepts with this person.
Said, Hamid
UCI
Hagerman, Randi
UC Davis
Harmatz, Paul
UCSF
Nyhan, William
UCSD
Gleeson, Joseph
UCSD
Explore
_
Same Department
Barbera, Nicole
Demeterco-berggren, Carla
Gomez-arostegui, Juliana
Mills, Tatyana
Shapiro, Warren
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