Harvard Catalyst Profiles
Contact, publication, and social network information about Harvard faculty and fellows.
Home
About
Overview
Open Source Software
Help
History (0)
Find People
Find Everything
Login
to
edit your profile
(add a photo, education, awards, etc.), search
student opportunities
, and
create reports
.
Edit My Profile
My Person List (
0
)
Opportunity Search
Return to Top
Anne O'Donnell Luria, M.D., Ph.D.
Concepts (358)
Back to Profile
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.
1-Alkyl-2-acetylglycerophosphocholine Esterase
5' Untranslated Regions
Abnormalities, Multiple
Abortion, Spontaneous
Access to Information
Actinin
Adaptor Proteins, Signal Transducing
Adenosine Deaminase
Adolescent
Adult
Age Factors
Aged
Aged, 80 and over
Aging
Algorithms
Alleles
alpha-Glucosidases
Alternative Splicing
Amino Acid Sequence
Amino Acid Substitution
Anemia, Diamond-Blackfan
Anemia, Megaloblastic
Aneuploidy
Animals
Apolipoprotein C-III
Arginine
Arthrogryposis
Australia
Autistic Disorder
Autopsy
Base Sequence
Bayes Theorem
Binding Sites
Blepharophimosis
Blood Chemical Analysis
Blood Transfusion
Body Patterning
Bone Morphogenetic Proteins
Brain
BRCA1 Protein
Breast
Breast Neoplasms
Buffers
Calibration
Cardiomyopathies
Cardiovascular Diseases
Carrier Proteins
Case-Control Studies
Cell Cycle Proteins
Cell Line
Cell Line, Tumor
Cerebral Palsy
Child
Child, Preschool
Chloride Channels
Chondroitin Sulfate Proteoglycans
Chromatin
Chromosomal Proteins, Non-Histone
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes, Human, Pair 9
Codon, Nonsense
Cognition
Cohort Studies
Collagen Type VI
Coma
Computational Biology
Congenital Hypothyroidism
Connexins
Consanguinity
Consensus
Conserved Sequence
Coronary Disease
CpG Islands
Craniofacial Abnormalities
Craniosynostoses
Cytosine
Databases, Genetic
Databases, Nucleic Acid
De Lange Syndrome
Delivery of Health Care
Deuterium Oxide
Developmental Disabilities
Diabetes Mellitus, Type 2
Dietary Fats
Disease
Disease Models, Animal
Disease Progression
DNA
DNA Copy Number Variations
DNA Damage
DNA Methylation
DNA Mutational Analysis
DNA-Binding Proteins
Drosophila melanogaster
Drosophila Proteins
Drug Prescriptions
Dyslipidemias
Dystroglycans
Dystrophin
Dystrophin-Associated Proteins
Early Diagnosis
Eczema
Educational Status
Embryo, Nonmammalian
Embryonic Stem Cells
Enzyme Inhibitors
Enzyme Stability
Epigenesis, Genetic
Epigenomics
Epilepsy
Evolution, Molecular
Exons
Face
Facies
Failure to Thrive
Fasting
Fatal Outcome
Fathers
Female
Fertility
Fibrosis
Filipin
G2 Phase
Gastric Bypass
Gene Deletion
Gene Dosage
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Gene Knockout Techniques
Genes
Genes, BRCA1
Genes, Essential
Genes, Lethal
Genes, Recessive
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Loci
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetics, Medical
Genetics, Population
Genome
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomics
Genotype
Germ Cells
Germ-Line Mutation
Glomerulosclerosis, Focal Segmental
Glucose
Glucosyltransferases
Glutamates
Glutamine
Glycine
Growth Disorders
Haploinsufficiency
Haplotypes
Health
Heart Defects, Congenital
HEK293 Cells
HeLa Cells
Hematologic Diseases
Hematologic Tests
Hematopoiesis
Heterozygote
High-Throughput Nucleotide Sequencing
Histone Acetyltransferases
Histone Deacetylases
Histone-Lysine N-Methyltransferase
Histones
Homozygote
Humans
Hydrogen-Ion Concentration
Hydrolysis
Hydrops Fetalis
Hydroxocobalamin
Hyperammonemia
Hypertrichosis
Immune System Diseases
Infant
Infant, Newborn
Infertility, Female
Informatics
Information Dissemination
Information Storage and Retrieval
Inheritance Patterns
Injections, Intramuscular
Intercellular Signaling Peptides and Proteins
Interleukin-8
Internet
Intracellular Signaling Peptides and Proteins
Intranuclear Space
Ion Channels
Isotopes
Joint Instability
Karyotyping
Kidney
Kinetics
Liver
Liver Failure, Acute
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Male
Malformations of Cortical Development
Mammals
Marfan Syndrome
Membrane Glycoproteins
Membrane Proteins
Mental Disorders
Mental Health
Methylglucosides
Methyltransferases
Mice
Mice, 129 Strain
Mice, Knockout
Microcephaly
Middle Aged
Models, Genetic
Models, Molecular
Molecular Sequence Annotation
Mood Disorders
Mothers
Motor Activity
Movement Disorders
Multifactorial Inheritance
Multigene Family
Muscle, Skeletal
Muscles
Muscular Diseases
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Mutation
Mutation, Missense
Myoblasts
Myocardial Infarction
Nanopores
National Human Genome Research Institute (U.S.)
National Institutes of Health (U.S.)
Neoplasm Proteins
Nephrotic Syndrome
Nerve Tissue Proteins
Neuregulins
Neuromuscular Diseases
Neuropeptides
Niemann-Pick Disease, Type C
Nucleosomes
Open Reading Frames
Ophthalmoplegia
Pakistan
Pan troglodytes
Patella
Pathology, Molecular
Patient Selection
Pedigree
Penetrance
Phenotype
Phenylacetates
Phosphoproteins
Phosphorylation
Physicians
Podocytes
Poisson Distribution
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Postprandial Period
Pregnancy
Pregnancy Trimester, First
Prenatal Diagnosis
Prevalence
Primates
Prion Diseases
Prions
Prognosis
Protein Biosynthesis
Protein Structure, Tertiary
Proteins
Proteome
Protons
Psychiatry
Psychomotor Disorders
Psychopathology
Radiation Tolerance
Rare Diseases
Receptors, Notch
Recombinant Proteins
Reference Standards
Regulatory Sequences, Nucleic Acid
Repressor Proteins
Reproducibility of Results
Reproductive Techniques, Assisted
Retrospective Studies
Ribosomal Proteins
Ribosomes
Risk Assessment
Risk Factors
RNA Splice Sites
RNA, Messenger
RNA, Small Nuclear
S Phase
Saccharomyces cerevisiae
Sample Size
Scrotum
Seizures
Selection, Genetic
Sequence Analysis, DNA
Sequence Analysis, RNA
Serine
Severity of Illness Index
Siblings
Signal Transduction
Sodium Benzoate
Software
Solvents
Spasms, Infantile
Species Specificity
Spermatozoa
Spliceosomes
Substrate Specificity
Suicide
Syndrome
Temperature
Thrombocytopenia
Thrombotic Microangiopathies
TOR Serine-Threonine Kinases
Transcription Factors
Transcription, Genetic
Transfection
Treatment Outcome
Triglycerides
Tubulin
Tumor Cells, Cultured
Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
Tumor Suppressor Proteins
Turner Syndrome
Ultrasonography, Prenatal
Uncertainty
Uniparental Disomy
United States
Urogenital Abnormalities
User-Computer Interface
Validation Studies as Topic
Vestibular Diseases
Virulence
Vitamin B 12 Deficiency
Xenopus laevis
Xenopus Proteins
Young Adult
Zebrafish
O'Donnell Luria's Networks
Click the
Explore
buttons for more information and interactive visualizations!
Concepts (358)
Derived automatically from this person's publications.
Genome, Human
Genomics
Inheritance Patterns
Genetic Variation
Rare Diseases
Explore
_
Co-Authors (160)
People in Profiles who have published with this person.
Wojcik, Monica
Rehm, Heidi
Talkowski, Michael
Stenton, Sarah
Karczewski, Konrad
Explore
_
Similar People (60)
People who share similar concepts with this person.
Kohane, Zak
Rehm, Heidi
Alkuraya, Fowzan
Daly, Mark
Chung, Wendy
Explore
_
Same Department
People in same department with this person.
Boone, Philip
Power, Kaiden
Rockowitz, Shira
Vilanova-Velez, Luis
Voshall, Adam
Explore
_