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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.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
Name Number of Publications Most Recent Publication Publications by All Authors Concept Score Why?
Genetics, Medical1220243363.860 Why?
Neurofibromatosis 1620235601.410 Why?
Genetic Testing18202435311.270 Why?
Genome, Human15202344170.970 Why?
Neurofibrosarcoma22023260.910 Why?
Neurofibromin 1320201900.900 Why?
Oligonucleotide Array Sequence Analysis11201437750.680 Why?
Chromosome Aberrations11201817640.670 Why?
Genomics14202457940.660 Why?
Policy420235110.600 Why?
Congenital Hypothyroidism12017400.570 Why?
Progeria620161880.550 Why?
Developmental Disabilities8201915040.550 Why?
Facies120172230.540 Why?
Steryl-Sulfatase12016110.540 Why?
Nephrosis12016430.520 Why?
Ichthyosis12016590.510 Why?
Comparative Genomic Hybridization820214730.500 Why?
Congenital Abnormalities320227040.500 Why?
GATA3 Transcription Factor120161520.500 Why?
Incidental Findings420236980.500 Why?
Hypoparathyroidism120161360.470 Why?
Chromosome Disorders320144990.440 Why?
DNA Copy Number Variations6201620130.440 Why?
Pathology, Molecular120163290.420 Why?
Sequence Analysis, DNA7201647130.420 Why?
Hearing Loss, Sensorineural220167810.380 Why?
Chromosome Deletion5202113870.370 Why?
Autistic Disorder6202212160.360 Why?
Genetic Variation9202265510.340 Why?
Genetic Diseases, Inborn220246010.330 Why?
Chromosomes, Human, Pair 15220083620.300 Why?
Health Promotion1201922060.280 Why?
DNA Methylation2202343730.280 Why?
Molecular Diagnostic Techniques220086110.270 Why?
Gene Dosage2200812180.240 Why?
Karyotyping5201811710.240 Why?
Chromosomes, Human, Pair 16320113420.230 Why?
Immunologic Deficiency Syndromes120085570.230 Why?
C-Reactive Protein5200638390.230 Why?
Mosaicism220224660.220 Why?
Mutation82022299320.220 Why?
Penetrance120243880.200 Why?
Atherosclerosis3200735170.200 Why?
Genetic Association Studies5202127170.200 Why?
Practice Guidelines as Topic1201974750.190 Why?
Microarray Analysis520217470.190 Why?
Nerve Sheath Neoplasms120231670.190 Why?
Chromosome Banding220122600.190 Why?
Piperidines3201616500.190 Why?
Base Sequence32023124460.190 Why?
Matrix Attachment Region Binding Proteins12021470.180 Why?
Humans7120247606210.180 Why?
Mutation, Missense4201825660.180 Why?
Chromosomes, Human, Pair 2120213130.170 Why?
Muscular Dystrophy, Duchenne120022680.170 Why?
Language Development Disorders320101920.170 Why?
Genes, Insect120002640.160 Why?
Phenotype132022165460.160 Why?
Child Development Disorders, Pervasive420115990.160 Why?
Photoreceptor Cells, Invertebrate11998390.160 Why?
Edema120027690.160 Why?
Neurofibroma, Plexiform12018660.150 Why?
Pyridines3201628790.150 Why?
Genes, Tumor Suppressor1202210550.150 Why?
Physicians1201645910.150 Why?
Protein Tyrosine Phosphatases120004590.150 Why?
United States102024724610.150 Why?
Chromosomes, Human, Pair 22220093460.150 Why?
Child272021798060.150 Why?
Leg1200210900.150 Why?
Gene Duplication220083130.140 Why?
Body Patterning219986320.140 Why?
Genetic Heterogeneity120207240.140 Why?
Codon120176020.130 Why?
Drosophila2200014920.120 Why?
Uncertainty120207540.120 Why?
Pravastatin120163930.120 Why?
Child, Preschool182021420630.120 Why?
School Health Services120173820.110 Why?
Esophageal Atresia120162170.110 Why?
Bone and Bones3201625600.110 Why?
Quantitative Trait Loci2201421010.110 Why?
Membrane Transport Proteins2200910350.110 Why?
Farnesyltranstransferase12012710.100 Why?
Drosophila Proteins2199816990.100 Why?
Nucleic Acid Hybridization3200813040.100 Why?
Diphosphonates120166380.100 Why?
Proteomics2202038170.090 Why?
Protein Kinases1199816120.090 Why?
Male3420213597440.090 Why?
Loss of Heterozygosity120136590.090 Why?
Genotype92020129600.090 Why?
Galactosemias120111240.090 Why?
Polymorphism, Single Nucleotide72013157890.090 Why?
Imidazoles1201611800.090 Why?
Research Subjects120122490.090 Why?
Disease120156710.090 Why?
Aniridia12009360.080 Why?
Blepharophimosis12008210.080 Why?
Female3320213912700.080 Why?
In Situ Hybridization, Fluorescence2201225060.080 Why?
Chromosome Mapping4202046250.080 Why?
Computational Biology1202035050.070 Why?
Truth Disclosure120124320.070 Why?
Infant102021360600.070 Why?
Diagnosis, Differential22019129650.070 Why?
Germ-Line Mutation1201618410.070 Why?
Pain1200250660.070 Why?
Chromosomes, Human, Pair 8120094520.070 Why?
Coronary Artery Disease1200766590.070 Why?
Information Dissemination1201511310.070 Why?
Pulmonary Surfactant-Associated Protein B12006420.070 Why?
Frameshift Mutation120083880.070 Why?
Severe Combined Immunodeficiency120092260.070 Why?
Human Genome Project120071990.070 Why?
Chromosomes, Human, Pair 7120073100.070 Why?
Abnormalities, Multiple2201114150.070 Why?
Genetic Predisposition to Disease62024177900.070 Why?
Inheritance Patterns120083400.060 Why?
Gene Frequency4201636150.060 Why?
Carotid Artery Diseases120118830.060 Why?
Williams Syndrome120071930.060 Why?
Adolescent152018878100.060 Why?
Carotid Arteries320169510.060 Why?
Social Behavior2201011310.060 Why?
Genes1200818450.060 Why?
Cardiotonic Agents120075460.060 Why?
High-Throughput Nucleotide Sequencing1201636160.050 Why?
Nervous System Diseases1201316470.050 Why?
Aging2201186510.050 Why?
Myotonic Dystrophy12002780.050 Why?
Apoptosis1199895010.050 Why?
Transcription Factors22021121030.050 Why?
Hearing Loss120097800.050 Why?
Enzyme Inhibitors1201237260.050 Why?
Neoplasms22021220720.050 Why?
Heart Defects, Congenital2201646730.050 Why?
Child Behavior120078470.050 Why?
Collagen Type V12021160.050 Why?
Heterozygote2201827980.050 Why?
Forkhead Transcription Factors1200816120.050 Why?
Sequence Alignment2200821760.050 Why?
Sex Characteristics1201126290.050 Why?
Collagen Type III12021910.050 Why?
Sequence Deletion2201814930.040 Why?
Amino Acid Sequence32017134510.040 Why?
Dwarfism120211370.040 Why?
Databases, Factual1201580350.040 Why?
Homeodomain Proteins1200924140.040 Why?
Embryo, Nonmammalian220009000.040 Why?
Neuregulins11998360.040 Why?
Receptors, Invertebrate Peptide11998120.040 Why?
Pupa11998420.040 Why?
Genetic Counseling120026240.040 Why?
Epilepsy1201432670.040 Why?
Macular Degeneration1200610020.040 Why?
Pigment Epithelium of Eye119982090.040 Why?
Blotting, Northern1200015430.040 Why?
Class I Phosphatidylinositol 3-Kinases120228950.040 Why?
Gene Expression Regulation, Developmental2200036040.040 Why?
Young Adult72018587410.040 Why?
Molecular Weight1200021860.040 Why?
Retina2199826350.040 Why?
Thinness120214910.040 Why?
Microcephaly120214250.030 Why?
Protein Prenylation12016700.030 Why?
Cohort Studies42020413350.030 Why?
Germ Cells120206350.030 Why?
Gene Expression Profiling2201494110.030 Why?
Women's Health1200520560.030 Why?
In Situ Hybridization1200019000.030 Why?
DNA Mutational Analysis3200941070.030 Why?
Tissue Distribution1200022620.030 Why?
Myocardial Ischemia1200621640.030 Why?
Limb Deformities, Congenital120161360.030 Why?
Sequence Homology, Amino Acid1200027530.030 Why?
Brain12022269510.030 Why?
Isoenzymes1200016900.030 Why?
Chromosomes120185750.030 Why?
Gene Expression Regulation, Enzymologic1200011730.030 Why?
Tracheoesophageal Fistula120161310.030 Why?
Sensitivity and Specificity22007146600.030 Why?
Models, Educational120173730.030 Why?
Face1202110170.030 Why?
Immunity, Innate1200630470.030 Why?
Nuclear Proteins1200957910.030 Why?
Anal Canal120163720.030 Why?
Crohn Disease1200622750.030 Why?
Proto-Oncogene Proteins c-akt1202224480.030 Why?
Diagnostic Tests, Routine120197860.030 Why?
Receptors, Notch119987430.030 Why?
DNA-Binding Proteins2200995850.030 Why?
TOR Serine-Threonine Kinases1202220580.030 Why?
Uniparental Disomy12013450.030 Why?
Phosphatidylinositol 3-Kinases1202228640.030 Why?
ras Proteins1199810520.030 Why?
Demography1201716500.030 Why?
China2200923390.030 Why?
Molecular Sequence Data22008176240.030 Why?
Histones1202325830.030 Why?
Prospective Studies42016543030.030 Why?
Patients120189060.030 Why?
DNA Probes120135510.020 Why?
Gestational Age1202135650.020 Why?
Cardiac Surgical Procedures1200736200.020 Why?
Growth and Development12011470.020 Why?
Pulmonary Disease, Chronic Obstructive1200632240.020 Why?
UTP-Hexose-1-Phosphate Uridylyltransferase12011680.020 Why?
Cytogenetic Analysis120122710.020 Why?
Consanguinity120134560.020 Why?
Ankle Brachial Index120111630.020 Why?
Boston2201692800.020 Why?
Age Determination by Skeleton120111260.020 Why?
Trachea1201610820.020 Why?
Pulsatile Flow120113210.020 Why?
Esophagus1201610230.020 Why?
Haplotypes2200627640.020 Why?
Prevalence22022156870.020 Why?
Hypertension, Pulmonary1202115700.020 Why?
Pedigree2200845780.020 Why?
Spine1201611110.020 Why?
Growth Plate120112740.020 Why?
Drosophila melanogaster1199817100.020 Why?
Nutritional Physiological Phenomena120113630.020 Why?
Chromosomes, Human120114420.020 Why?
Vomiting120126500.020 Why?
Obesity12011129220.020 Why?
Gene Expression Regulation12007119030.020 Why?
User-Computer Interface1201514030.020 Why?
International Classification of Diseases120148940.020 Why?
Vestibular Aqueduct12009730.020 Why?
Down Syndrome120168920.020 Why?
Treatment Outcome32013650170.020 Why?
Homozygote1201317880.020 Why?
Primary Ovarian Insufficiency120081050.020 Why?
Ion Transport120093180.020 Why?
Infant, Newborn32016261810.020 Why?
Blood Flow Velocity1201113770.020 Why?
Case-Control Studies12005220530.020 Why?
Bone Remodeling120115800.020 Why?
Femoral Artery120118350.020 Why?
Codon, Nonsense120082810.020 Why?
Data Mining120125530.020 Why?
Neonatal Screening120115950.020 Why?
Risk Factors42006743590.020 Why?
Alleles2200968980.020 Why?
Acute-Phase Reaction12006910.020 Why?
Connexins120083510.020 Why?
Chlorides120096630.020 Why?
Anthropometry1201113480.020 Why?
Eyelids120082770.020 Why?
Prognosis12007296580.020 Why?
Patient Participation1201514390.020 Why?
Geography120086610.020 Why?
Trisomy120072600.020 Why?
Drug Therapy, Combination1201664980.020 Why?
Complement Factor H120061090.020 Why?
Diarrhea1201213190.020 Why?
Chromatography, High Pressure Liquid1200915440.020 Why?
Fatigue1201215440.020 Why?
Adult620212199940.020 Why?
Absorptiometry, Photon1201117360.020 Why?
Xenopus laevis120099650.020 Why?
Retrospective Studies42016803720.020 Why?
Databases, Genetic1201217380.020 Why?
Medical Records1201014070.020 Why?
Medical Informatics120127320.020 Why?
Body Height1201115700.020 Why?
RNA, Messenger12000127660.020 Why?
Membrane Proteins2199878500.010 Why?
Drug Administration Schedule1201248990.010 Why?
Oocytes1200911650.010 Why?
Middle Aged620112203520.010 Why?
Computer Simulation1201762180.010 Why?
Syndrome1201032800.010 Why?
Molecular Epidemiology120064690.010 Why?
Microscopy, Confocal1200919720.010 Why?
Chronic Disease1201792870.010 Why?
Weight Gain1201223470.010 Why?
Neurodegenerative Diseases1201110840.010 Why?
Reproducibility of Results12020200800.010 Why?
Animals420091679630.010 Why?
Forced Expiratory Volume1200618090.010 Why?
Radiography1201269650.010 Why?
Kidney1201670640.010 Why?
Genetic Linkage1200623810.010 Why?
Disease Management1201125140.010 Why?
Dose-Response Relationship, Drug12012108270.010 Why?
Adaptation, Psychological1201026280.010 Why?
Fertilization in Vitro1200712920.010 Why?
Helix-Loop-Helix Motifs11998960.010 Why?
Electroencephalography1201461890.010 Why?
Quality of Life12020133080.010 Why?
Signal Transduction21998233760.010 Why?
Bone Density1201135340.010 Why?
Photoreceptor Cells119982360.010 Why?
Gamma Rays119983170.010 Why?
Insect Proteins119982540.010 Why?
Genes, ras119986550.010 Why?
Blood Pressure1201185250.010 Why?
Acute Disease1200672690.010 Why?
Mutagenesis1199812340.010 Why?
Disease Progression12011135020.010 Why?
Recombination, Genetic1199815260.010 Why?
Mitosis1199811910.010 Why?
Genome-Wide Association Study12012126260.010 Why?
Basic Helix-Loop-Helix Transcription Factors1199811390.010 Why?
Severity of Illness Index12010158400.010 Why?
Double-Blind Method12006124270.010 Why?
Schizophrenia1201069150.010 Why?
Pregnancy12011297490.010 Why?
Randomized Controlled Trials as Topic12006103440.010 Why?
Tomography, X-Ray Computed12011205090.000 Why?
Phosphorylation1199883130.000 Why?
Aged220061691520.000 Why?
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© 2024 President and Fellows of Harvard College
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.