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David Thomas Miller, M.D., Ph.D.
Concepts (316)
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Concepts are derived automatically from a person's publications.
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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.
Abnormalities, Multiple
Absorptiometry, Photon
Acute Disease
Acute-Phase Reaction
Adaptation, Psychological
Adolescent
Adult
Age Determination by Skeleton
Aged
Aging
Alleles
Amino Acid Sequence
Anal Canal
Animals
Aniridia
Ankle Brachial Index
Anthropometry
Apoptosis
Atherosclerosis
Autistic Disorder
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
Blepharophimosis
Blood Flow Velocity
Blood Pressure
Blotting, Northern
Body Height
Body Patterning
Bone and Bones
Bone Density
Bone Remodeling
Boston
Brain
Cardiac Surgical Procedures
Cardiotonic Agents
Carotid Arteries
Carotid Artery Diseases
Case-Control Studies
Child
Child Behavior
Child Development Disorders, Pervasive
Child, Preschool
China
Chlorides
Chromatography, High Pressure Liquid
Chromosome Aberrations
Chromosome Banding
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes
Chromosomes, Human
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chronic Disease
Class I Phosphatidylinositol 3-Kinases
Codon
Codon, Nonsense
Cohort Studies
Collagen Type III
Collagen Type V
Comparative Genomic Hybridization
Complement Factor H
Computational Biology
Computer Simulation
Congenital Abnormalities
Congenital Hypothyroidism
Connexins
Consanguinity
Coronary Artery Disease
C-Reactive Protein
Crohn Disease
Cytogenetic Analysis
Data Mining
Databases, Factual
Databases, Genetic
Demography
Developmental Disabilities
Diagnosis, Differential
Diagnostic Tests, Routine
Diarrhea
Diphosphonates
Disease
Disease Management
Disease Progression
DNA Copy Number Variations
DNA Methylation
DNA Mutational Analysis
DNA Probes
DNA-Binding Proteins
Dose-Response Relationship, Drug
Double-Blind Method
Down Syndrome
Drosophila
Drosophila melanogaster
Drosophila Proteins
Drug Administration Schedule
Drug Therapy, Combination
Dwarfism
Edema
Electroencephalography
Embryo, Nonmammalian
Enzyme Inhibitors
Epilepsy
Esophageal Atresia
Esophagus
Eyelids
Face
Facies
Farnesyltranstransferase
Fatigue
Female
Femoral Artery
Fertilization in Vitro
Forced Expiratory Volume
Forkhead Transcription Factors
Frameshift Mutation
Galactosemias
Gamma Rays
GATA3 Transcription Factor
Gene Dosage
Gene Duplication
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Expression Regulation, Enzymologic
Gene Frequency
Genes
Genes, Insect
Genes, ras
Genes, Tumor Suppressor
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Linkage
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetics, Medical
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Geography
Germ Cells
Germ-Line Mutation
Gestational Age
Growth and Development
Growth Plate
Haplotypes
Health Promotion
Hearing Loss
Hearing Loss, Sensorineural
Heart Defects, Congenital
Helix-Loop-Helix Motifs
Heterozygote
High-Throughput Nucleotide Sequencing
Histones
Homeodomain Proteins
Homozygote
Human Genome Project
Humans
Hypertension, Pulmonary
Hypoparathyroidism
Ichthyosis
Imidazoles
Immunity, Innate
Immunologic Deficiency Syndromes
In Situ Hybridization
In Situ Hybridization, Fluorescence
Incidental Findings
Infant
Infant, Newborn
Information Dissemination
Inheritance Patterns
Insect Proteins
International Classification of Diseases
Ion Transport
Isoenzymes
Karyotyping
Kidney
Language Development Disorders
Leg
Limb Deformities, Congenital
Loss of Heterozygosity
Macular Degeneration
Male
Matrix Attachment Region Binding Proteins
Medical Informatics
Medical Records
Membrane Proteins
Membrane Transport Proteins
Microarray Analysis
Microcephaly
Microscopy, Confocal
Middle Aged
Mitosis
Models, Educational
Molecular Diagnostic Techniques
Molecular Epidemiology
Molecular Sequence Data
Molecular Weight
Mosaicism
Muscular Dystrophy, Duchenne
Mutagenesis
Mutation
Mutation, Missense
Myocardial Ischemia
Myotonic Dystrophy
Neonatal Screening
Neoplasms
Nephrosis
Nerve Sheath Neoplasms
Nervous System Diseases
Neuregulins
Neurodegenerative Diseases
Neurofibroma, Plexiform
Neurofibromatosis 1
Neurofibromin 1
Neurofibrosarcoma
Nuclear Proteins
Nucleic Acid Hybridization
Nutritional Physiological Phenomena
Obesity
Oligonucleotide Array Sequence Analysis
Oocytes
Pain
Pathology, Molecular
Patient Participation
Patients
Pedigree
Penetrance
Phenotype
Phosphatidylinositol 3-Kinases
Phosphorylation
Photoreceptor Cells
Photoreceptor Cells, Invertebrate
Physicians
Pigment Epithelium of Eye
Piperidines
Policy
Polymorphism, Single Nucleotide
Practice Guidelines as Topic
Pravastatin
Pregnancy
Prevalence
Primary Ovarian Insufficiency
Progeria
Prognosis
Prospective Studies
Protein Kinases
Protein Prenylation
Protein Tyrosine Phosphatases
Proteomics
Proto-Oncogene Proteins c-akt
Pulmonary Disease, Chronic Obstructive
Pulmonary Surfactant-Associated Protein B
Pulsatile Flow
Pupa
Pyridines
Quality of Life
Quantitative Trait Loci
Radiography
Randomized Controlled Trials as Topic
ras Proteins
Receptors, Invertebrate Peptide
Receptors, Notch
Recombination, Genetic
Reproducibility of Results
Research Subjects
Retina
Retrospective Studies
Risk Factors
RNA, Messenger
Schizophrenia
School Health Services
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Severe Combined Immunodeficiency
Severity of Illness Index
Sex Characteristics
Signal Transduction
Social Behavior
Spine
Steryl-Sulfatase
Syndrome
Thinness
Tissue Distribution
Tomography, X-Ray Computed
TOR Serine-Threonine Kinases
Trachea
Tracheoesophageal Fistula
Transcription Factors
Treatment Outcome
Trisomy
Truth Disclosure
Uncertainty
Uniparental Disomy
United States
User-Computer Interface
UTP-Hexose-1-Phosphate Uridylyltransferase
Vestibular Aqueduct
Vomiting
Weight Gain
Williams Syndrome
Women's Health
Xenopus laevis
Young Adult
Miller's Networks
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Concepts (316)
Derived automatically from this person's publications.
Neurofibrosarcoma
Genetics, Medical
Neurofibromatosis 1
Genome, Human
Genetic Testing
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Co-Authors (97)
People in Profiles who have published with this person.
Kwiatkowski, David
Ullrich, Nicole
Wu, Bai-Lin
Kalia, Sarah
Chung, Wendy
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_
Similar People (60)
People who share similar concepts with this person.
Green, Robert
Rehm, Heidi
Alkuraya, Fowzan
Daly, Mark
Chung, Wendy
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_
Same Department
People in same department with this person.
Abu-El-Haija, Aya
Exposito-Alonso, David
Holm, Ingrid
Kriz, Andrea
Sacharow, Stephanie
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Physical Neighbors
People whose addresses are nearby this person.
Cox, Gerald
Beggs, Alan
Irons, Mira
Tan, Wen-Hann
Neilan, Edward
_