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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, Medical1220243343.800 Why?
Neurofibromatosis 1620235611.380 Why?
Genetic Testing18202435911.240 Why?
Genome, Human15202344430.960 Why?
Neurofibrosarcoma22023280.890 Why?
Neurofibromin 1320201900.890 Why?
Oligonucleotide Array Sequence Analysis11201437960.670 Why?
Chromosome Aberrations11201817760.650 Why?
Genomics14202459220.640 Why?
Policy420235120.590 Why?
Congenital Hypothyroidism12017400.560 Why?
Progeria620161820.550 Why?
Developmental Disabilities8201915190.540 Why?
Facies120172240.530 Why?
Steryl-Sulfatase12016110.530 Why?
Nephrosis12016430.510 Why?
Ichthyosis12016590.500 Why?
Comparative Genomic Hybridization820214740.490 Why?
Congenital Abnormalities320227030.490 Why?
Incidental Findings420236980.490 Why?
GATA3 Transcription Factor120161630.480 Why?
Hypoparathyroidism120161360.460 Why?
Chromosome Disorders320144980.440 Why?
DNA Copy Number Variations6201620450.430 Why?
Pathology, Molecular120163290.420 Why?
Sequence Analysis, DNA7201647800.420 Why?
Hearing Loss, Sensorineural220167830.380 Why?
Chromosome Deletion5202113840.370 Why?
Autistic Disorder6202212380.350 Why?
Genetic Variation9202266130.340 Why?
Genetic Diseases, Inborn220246060.330 Why?
Chromosomes, Human, Pair 15220083610.300 Why?
Health Promotion1201922090.280 Why?
DNA Methylation2202344270.270 Why?
Molecular Diagnostic Techniques220086140.260 Why?
Gene Dosage2200812110.230 Why?
Karyotyping5201811760.230 Why?
Immunologic Deficiency Syndromes120085490.230 Why?
Chromosomes, Human, Pair 16320113410.230 Why?
C-Reactive Protein5200638530.230 Why?
Mosaicism220224800.210 Why?
Mutation82022302140.210 Why?
Penetrance120243880.200 Why?
Atherosclerosis3200734210.200 Why?
Genetic Association Studies5202127440.190 Why?
Practice Guidelines as Topic1201974300.190 Why?
Microarray Analysis520217510.190 Why?
Nerve Sheath Neoplasms120231690.190 Why?
Chromosome Banding220122610.190 Why?
Base Sequence32023124150.190 Why?
Piperidines3201616630.190 Why?
Humans7120247668120.180 Why?
Mutation, Missense4201825910.180 Why?
Matrix Attachment Region Binding Proteins12021480.180 Why?
Chromosomes, Human, Pair 2120213130.170 Why?
Muscular Dystrophy, Duchenne120022710.170 Why?
Language Development Disorders320101940.160 Why?
Genes, Insect120002650.160 Why?
Child Development Disorders, Pervasive420115970.160 Why?
Phenotype132022167220.160 Why?
Edema120027640.150 Why?
Photoreceptor Cells, Invertebrate11998390.150 Why?
Neurofibroma, Plexiform12018660.150 Why?
Pyridines3201628880.150 Why?
Physicians1201645910.150 Why?
Genes, Tumor Suppressor1202210570.150 Why?
Protein Tyrosine Phosphatases120004570.150 Why?
United States102024729450.140 Why?
Leg1200210870.140 Why?
Chromosomes, Human, Pair 22220093480.140 Why?
Child272021806700.140 Why?
Body Patterning219986340.140 Why?
Gene Duplication220083150.140 Why?
Genetic Heterogeneity120207350.130 Why?
Codon120175990.130 Why?
Drosophila2200015090.120 Why?
Uncertainty120207650.120 Why?
Pravastatin120163910.110 Why?
Child, Preschool182021425770.110 Why?
School Health Services120173880.110 Why?
Esophageal Atresia120162260.110 Why?
Bone and Bones3201625590.110 Why?
Quantitative Trait Loci2201421330.110 Why?
Membrane Transport Proteins2200910290.110 Why?
Farnesyltranstransferase12012700.100 Why?
Drosophila Proteins2199817050.100 Why?
Nucleic Acid Hybridization3200813050.100 Why?
Diphosphonates120166250.090 Why?
Protein Kinases1199816100.090 Why?
Proteomics2202039150.090 Why?
Loss of Heterozygosity120136630.090 Why?
Male3420213641540.090 Why?
Genotype92020130360.090 Why?
Galactosemias120111240.090 Why?
Imidazoles1201611680.090 Why?
Polymorphism, Single Nucleotide72013160440.090 Why?
Disease120156750.080 Why?
Research Subjects120122480.080 Why?
Aniridia12009360.080 Why?
Blepharophimosis12008210.080 Why?
Female3320213965320.080 Why?
In Situ Hybridization, Fluorescence2201225100.080 Why?
Chromosome Mapping4202046180.070 Why?
Computational Biology1202035640.070 Why?
Truth Disclosure120124330.070 Why?
Diagnosis, Differential22019129850.070 Why?
Infant102021364590.070 Why?
Pain1200250980.070 Why?
Germ-Line Mutation1201618860.070 Why?
Chromosomes, Human, Pair 8120094510.070 Why?
Coronary Artery Disease1200765750.070 Why?
Information Dissemination1201511420.070 Why?
Pulmonary Surfactant-Associated Protein B12006440.070 Why?
Frameshift Mutation120083920.070 Why?
Abnormalities, Multiple2201114240.070 Why?
Chromosomes, Human, Pair 7120073100.070 Why?
Human Genome Project120072020.070 Why?
Severe Combined Immunodeficiency120092350.070 Why?
Genetic Predisposition to Disease62024180760.060 Why?
Inheritance Patterns120083450.060 Why?
Gene Frequency4201636240.060 Why?
Carotid Artery Diseases120118720.060 Why?
Williams Syndrome120071950.060 Why?
Carotid Arteries320169320.060 Why?
Adolescent152018889020.060 Why?
Social Behavior2201011470.060 Why?
Genes1200818240.060 Why?
Cardiotonic Agents120075410.060 Why?
High-Throughput Nucleotide Sequencing1201636670.050 Why?
Nervous System Diseases1201316590.050 Why?
Aging2201187280.050 Why?
Myotonic Dystrophy12002770.050 Why?
Apoptosis1199895140.050 Why?
Enzyme Inhibitors1201237230.050 Why?
Transcription Factors22021121590.050 Why?
Hearing Loss120097850.050 Why?
Neoplasms22021223500.050 Why?
Heart Defects, Congenital2201647120.050 Why?
Child Behavior120078640.050 Why?
Collagen Type V12021160.050 Why?
Heterozygote2201827950.050 Why?
Forkhead Transcription Factors1200816270.050 Why?
Sequence Alignment2200821770.050 Why?
Sex Characteristics1201126450.050 Why?
Collagen Type III12021920.040 Why?
Sequence Deletion2201814940.040 Why?
Amino Acid Sequence32017134110.040 Why?
Dwarfism120211370.040 Why?
Databases, Factual1201580650.040 Why?
Homeodomain Proteins1200924290.040 Why?
Embryo, Nonmammalian220009100.040 Why?
Neuregulins11998360.040 Why?
Receptors, Invertebrate Peptide11998130.040 Why?
Pupa11998420.040 Why?
Genetic Counseling120026340.040 Why?
Epilepsy1201433170.040 Why?
Macular Degeneration1200610150.040 Why?
Pigment Epithelium of Eye119982090.040 Why?
Blotting, Northern1200015500.040 Why?
Gene Expression Regulation, Developmental2200036100.040 Why?
Class I Phosphatidylinositol 3-Kinases120229040.040 Why?
Young Adult72018599390.040 Why?
Molecular Weight1200021680.040 Why?
Retina2199826600.040 Why?
Thinness120214820.040 Why?
Microcephaly120214270.030 Why?
Protein Prenylation12016690.030 Why?
Cohort Studies42020417060.030 Why?
Germ Cells120206440.030 Why?
Myocardial Ischemia1200621310.030 Why?
In Situ Hybridization1200018920.030 Why?
Gene Expression Profiling2201495280.030 Why?
Women's Health1200520810.030 Why?
DNA Mutational Analysis3200941140.030 Why?
Tissue Distribution1200022750.030 Why?
Limb Deformities, Congenital120161360.030 Why?
Sequence Homology, Amino Acid1200027460.030 Why?
Brain12022271580.030 Why?
Gene Expression Regulation, Enzymologic1200011680.030 Why?
Isoenzymes1200016880.030 Why?
Chromosomes120185780.030 Why?
Tracheoesophageal Fistula120161310.030 Why?
Sensitivity and Specificity22007146530.030 Why?
Models, Educational120173750.030 Why?
Face1202110290.030 Why?
Nuclear Proteins1200957950.030 Why?
Immunity, Innate1200630790.030 Why?
Anal Canal120163750.030 Why?
Crohn Disease1200622860.030 Why?
Proto-Oncogene Proteins c-akt1202224560.030 Why?
Diagnostic Tests, Routine120197880.030 Why?
Receptors, Notch119987510.030 Why?
DNA-Binding Proteins2200996130.030 Why?
TOR Serine-Threonine Kinases1202220600.030 Why?
Uniparental Disomy12013460.030 Why?
Phosphatidylinositol 3-Kinases1202228820.030 Why?
Demography1201716410.030 Why?
ras Proteins1199810550.030 Why?
Molecular Sequence Data22008176090.030 Why?
China2200923860.030 Why?
Histones1202325950.030 Why?
Patients120189080.020 Why?
DNA Probes120135410.020 Why?
Prospective Studies42016548720.020 Why?
Gestational Age1202136170.020 Why?
Cardiac Surgical Procedures1200736830.020 Why?
Growth and Development12011460.020 Why?
Pulmonary Disease, Chronic Obstructive1200632460.020 Why?
UTP-Hexose-1-Phosphate Uridylyltransferase12011670.020 Why?
Cytogenetic Analysis120122700.020 Why?
Consanguinity120134600.020 Why?
Ankle Brachial Index120111630.020 Why?
Age Determination by Skeleton120111240.020 Why?
Boston2201693460.020 Why?
Pulsatile Flow120113180.020 Why?
Esophagus1201610400.020 Why?
Trachea1201610940.020 Why?
Haplotypes2200627260.020 Why?
Prevalence22022158350.020 Why?
Hypertension, Pulmonary1202116040.020 Why?
Pedigree2200845390.020 Why?
Growth Plate120112750.020 Why?
Spine1201611340.020 Why?
Drosophila melanogaster1199817250.020 Why?
Nutritional Physiological Phenomena120113570.020 Why?
Chromosomes, Human120114370.020 Why?
Vomiting120126520.020 Why?
Gene Expression Regulation12007119240.020 Why?
Obesity12011130900.020 Why?
User-Computer Interface1201514090.020 Why?
Vestibular Aqueduct12009730.020 Why?
International Classification of Diseases120149350.020 Why?
Treatment Outcome32013652860.020 Why?
Primary Ovarian Insufficiency120081040.020 Why?
Homozygote1201317750.020 Why?
Ion Transport120093220.020 Why?
Down Syndrome120169160.020 Why?
Infant, Newborn32016263870.020 Why?
Blood Flow Velocity1201113740.020 Why?
Case-Control Studies12005222480.020 Why?
Bone Remodeling120115770.020 Why?
Femoral Artery120118270.020 Why?
Codon, Nonsense120082870.020 Why?
Data Mining120125600.020 Why?
Risk Factors42006748890.020 Why?
Alleles2200968960.020 Why?
Acute-Phase Reaction12006910.020 Why?
Anthropometry1201113360.020 Why?
Connexins120083550.020 Why?
Neonatal Screening120116190.020 Why?
Chlorides120096660.020 Why?
Eyelids120082780.020 Why?
Prognosis12007299590.020 Why?
Drug Therapy, Combination1201663060.020 Why?
Patient Participation1201514450.020 Why?
Geography120086510.020 Why?
Trisomy120072600.020 Why?
Complement Factor H120061100.020 Why?
Diarrhea1201213170.020 Why?
Chromatography, High Pressure Liquid1200915290.020 Why?
Fatigue1201215550.020 Why?
Absorptiometry, Photon1201117070.020 Why?
Adult620212233050.020 Why?
Xenopus laevis120099660.020 Why?
Retrospective Studies42016816570.010 Why?
Medical Records1201014080.010 Why?
Databases, Genetic1201217560.010 Why?
Body Height1201115620.010 Why?
RNA, Messenger12000127950.010 Why?
Medical Informatics120127440.010 Why?
Membrane Proteins2199878690.010 Why?
Drug Administration Schedule1201248530.010 Why?
Oocytes1200911680.010 Why?
Middle Aged620112232670.010 Why?
Syndrome1201032710.010 Why?
Computer Simulation1201762580.010 Why?
Molecular Epidemiology120064730.010 Why?
Microscopy, Confocal1200919690.010 Why?
Chronic Disease1201793580.010 Why?
Weight Gain1201223560.010 Why?
Neurodegenerative Diseases1201110890.010 Why?
Reproducibility of Results12020201460.010 Why?
Animals420091689390.010 Why?
Forced Expiratory Volume1200618280.010 Why?
Radiography1201269680.010 Why?
Kidney1201670730.010 Why?
Genetic Linkage1200623420.010 Why?
Disease Management1201125330.010 Why?
Dose-Response Relationship, Drug12012107450.010 Why?
Adaptation, Psychological1201026620.010 Why?
Fertilization in Vitro1200713010.010 Why?
Helix-Loop-Helix Motifs11998970.010 Why?
Electroencephalography1201462820.010 Why?
Bone Density1201134910.010 Why?
Quality of Life12020134760.010 Why?
Signal Transduction21998236180.010 Why?
Photoreceptor Cells119982340.010 Why?
Insect Proteins119982530.010 Why?
Gamma Rays119983240.010 Why?
Genes, ras119986560.010 Why?
Acute Disease1200672400.010 Why?
Blood Pressure1201185330.010 Why?
Mutagenesis1199812280.010 Why?
Disease Progression12011136420.010 Why?
Recombination, Genetic1199815240.010 Why?
Mitosis1199811760.010 Why?
Basic Helix-Loop-Helix Transcription Factors1199811440.010 Why?
Severity of Illness Index12010159120.010 Why?
Genome-Wide Association Study12012128080.010 Why?
Double-Blind Method12006124300.010 Why?
Schizophrenia1201069760.010 Why?
Pregnancy12011302360.010 Why?
Randomized Controlled Trials as Topic12006103840.000 Why?
Tomography, X-Ray Computed12011207100.000 Why?
Phosphorylation1199883100.000 Why?
Aged220061713440.000 Why?
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.