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David Thomas Miller, M.D., Ph.D.

Concepts (315)

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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, Medical1120233373.810 Why?
Neurofibromatosis 1620235621.450 Why?
Genetic Testing17202334391.320 Why?
Genome, Human15202344201.000 Why?
Neurofibrosarcoma22023240.950 Why?
Neurofibromin 1320201960.940 Why?
Oligonucleotide Array Sequence Analysis11201439200.690 Why?
Chromosome Aberrations11201818110.680 Why?
Policy420235040.630 Why?
Genomics13202356920.600 Why?
Congenital Hypothyroidism12017390.590 Why?
Developmental Disabilities8201914520.580 Why?
Progeria620161850.570 Why?
Facies120171970.560 Why?
Steryl-Sulfatase12016110.560 Why?
Nephrosis12016450.540 Why?
Ichthyosis12016600.540 Why?
GATA3 Transcription Factor120161570.520 Why?
Comparative Genomic Hybridization820214960.520 Why?
Incidental Findings420236880.520 Why?
Congenital Abnormalities320227070.520 Why?
Hypoparathyroidism120161200.500 Why?
DNA Copy Number Variations6201619400.470 Why?
Chromosome Disorders320145150.460 Why?
Pathology, Molecular120163250.440 Why?
Sequence Analysis, DNA7201648010.430 Why?
Hearing Loss, Sensorineural220167700.400 Why?
Chromosome Deletion5202114000.390 Why?
Autistic Disorder6202211740.380 Why?
Genetic Variation9202265400.350 Why?
Chromosomes, Human, Pair 15220083740.310 Why?
Genetic Diseases, Inborn120125870.300 Why?
DNA Methylation2202342820.290 Why?
Health Promotion1201921940.290 Why?
Molecular Diagnostic Techniques220086020.280 Why?
Karyotyping5201812430.240 Why?
Gene Dosage2200812510.240 Why?
Immunologic Deficiency Syndromes120085460.240 Why?
Chromosomes, Human, Pair 16320113550.240 Why?
C-Reactive Protein5200637660.240 Why?
Mosaicism220224400.230 Why?
Mutation82022297170.230 Why?
Atherosclerosis3200734280.200 Why?
Practice Guidelines as Topic1201972760.200 Why?
Genetic Association Studies5202126990.200 Why?
Piperidines3201616020.200 Why?
Microarray Analysis520217660.200 Why?
Chromosome Banding220122780.200 Why?
Nerve Sheath Neoplasms120231900.200 Why?
Base Sequence32023127970.190 Why?
Matrix Attachment Region Binding Proteins12021440.190 Why?
Humans7020237420880.190 Why?
Mutation, Missense4201825560.190 Why?
Muscular Dystrophy, Duchenne120022560.180 Why?
Chromosomes, Human, Pair 2120213260.180 Why?
Phenotype132022163310.170 Why?
Language Development Disorders320101960.170 Why?
Genes, Insect120002680.170 Why?
Photoreceptor Cells, Invertebrate11998390.160 Why?
Edema120027900.160 Why?
Child Development Disorders, Pervasive420116150.160 Why?
Pyridines3201628180.160 Why?
Neurofibroma, Plexiform12018690.160 Why?
Physicians1201645540.150 Why?
Child272021774780.150 Why?
Genes, Tumor Suppressor1202210970.150 Why?
Chromosomes, Human, Pair 22220093510.150 Why?
Protein Tyrosine Phosphatases120004730.150 Why?
Leg1200211100.150 Why?
United States92023696930.150 Why?
Body Patterning219986260.150 Why?
Gene Duplication220083300.150 Why?
Genetic Heterogeneity120207320.140 Why?
Codon120176110.140 Why?
Drosophila2200014840.130 Why?
Uncertainty120207250.130 Why?
Child, Preschool182021409550.120 Why?
Pravastatin120163950.120 Why?
School Health Services120173750.120 Why?
Esophageal Atresia120162010.120 Why?
Quantitative Trait Loci2201420150.110 Why?
Bone and Bones3201625750.110 Why?
Membrane Transport Proteins2200910280.110 Why?
Farnesyltranstransferase12012760.110 Why?
Drosophila Proteins2199816990.100 Why?
Proteomics2202036180.100 Why?
Nucleic Acid Hybridization3200813740.100 Why?
Diphosphonates120166250.100 Why?
Male3420213495380.100 Why?
Protein Kinases1199816380.100 Why?
Loss of Heterozygosity120136780.090 Why?
Genotype92020129460.090 Why?
Galactosemias120111250.090 Why?
Polymorphism, Single Nucleotide72013154940.090 Why?
Imidazoles1201612050.090 Why?
Research Subjects120122380.090 Why?
Disease120156810.090 Why?
Aniridia12009360.090 Why?
Female3320213795920.080 Why?
Blepharophimosis12008220.080 Why?
In Situ Hybridization, Fluorescence2201226380.080 Why?
Infant102021350700.080 Why?
Germ-Line Mutation1201617860.080 Why?
Truth Disclosure120124350.080 Why?
Chromosome Mapping4202047420.080 Why?
Diagnosis, Differential22019129580.080 Why?
Computational Biology1202035180.080 Why?
Pain1200249610.080 Why?
Chromosomes, Human, Pair 8120094620.070 Why?
Coronary Artery Disease1200764540.070 Why?
Information Dissemination1201511000.070 Why?
Pulmonary Surfactant-Associated Protein B12006420.070 Why?
Severe Combined Immunodeficiency120092210.070 Why?
Frameshift Mutation120083990.070 Why?
Human Genome Project120071920.070 Why?
Chromosomes, Human, Pair 7120073210.070 Why?
Abnormalities, Multiple2201114160.070 Why?
Inheritance Patterns120083400.070 Why?
Gene Frequency4201635870.070 Why?
Adolescent152018856490.060 Why?
Williams Syndrome120071870.060 Why?
Carotid Artery Diseases120118820.060 Why?
Carotid Arteries320169520.060 Why?
Social Behavior2201011280.060 Why?
Genes1200818920.060 Why?
Cardiotonic Agents120075350.060 Why?
High-Throughput Nucleotide Sequencing1201635850.060 Why?
Genetic Predisposition to Disease52018174000.060 Why?
Nervous System Diseases1201316170.050 Why?
Aging2201186260.050 Why?
Myotonic Dystrophy12002780.050 Why?
Apoptosis1199897150.050 Why?
Hearing Loss120097650.050 Why?
Transcription Factors22021121640.050 Why?
Heart Defects, Congenital2201645660.050 Why?
Neoplasms22021215960.050 Why?
Enzyme Inhibitors1201238000.050 Why?
Heterozygote2201827900.050 Why?
Collagen Type V12021160.050 Why?
Child Behavior120078380.050 Why?
Forkhead Transcription Factors1200816130.050 Why?
Sex Characteristics1201125850.050 Why?
Collagen Type III12021900.050 Why?
Sequence Alignment2200822570.050 Why?
Sequence Deletion2201815260.050 Why?
Databases, Factual1201577160.050 Why?
Amino Acid Sequence32017138140.040 Why?
Dwarfism120211450.040 Why?
Homeodomain Proteins1200924170.040 Why?
Embryo, Nonmammalian220008940.040 Why?
Neuregulins11998350.040 Why?
Genetic Counseling120026000.040 Why?
Receptors, Invertebrate Peptide11998110.040 Why?
Pupa11998370.040 Why?
Macular Degeneration120069800.040 Why?
Epilepsy1201433010.040 Why?
Pigment Epithelium of Eye119982200.040 Why?
Class I Phosphatidylinositol 3-Kinases120228900.040 Why?
Young Adult72018563500.040 Why?
Blotting, Northern1200015810.040 Why?
Gene Expression Regulation, Developmental2200036170.040 Why?
Molecular Weight1200022550.040 Why?
Retina2199826110.040 Why?
Thinness120214790.040 Why?
Cohort Studies42020404500.040 Why?
Microcephaly120214300.040 Why?
Protein Prenylation12016730.040 Why?
Germ Cells120206280.030 Why?
Women's Health1200520340.030 Why?
Myocardial Ischemia1200621450.030 Why?
Gene Expression Profiling2201494100.030 Why?
In Situ Hybridization1200019500.030 Why?
Limb Deformities, Congenital120161360.030 Why?
Tissue Distribution1200023350.030 Why?
DNA Mutational Analysis3200941870.030 Why?
Brain12022263430.030 Why?
Sequence Homology, Amino Acid1200028370.030 Why?
Chromosomes120185950.030 Why?
Isoenzymes1200017250.030 Why?
Tracheoesophageal Fistula120161290.030 Why?
Sensitivity and Specificity22007147200.030 Why?
Gene Expression Regulation, Enzymologic1200012130.030 Why?
Models, Educational120173770.030 Why?
Face120219930.030 Why?
Immunity, Innate1200629560.030 Why?
Nuclear Proteins1200958510.030 Why?
Anal Canal120163760.030 Why?
Proto-Oncogene Proteins c-akt1202225020.030 Why?
Crohn Disease1200623010.030 Why?
Receptors, Notch119987390.030 Why?
Diagnostic Tests, Routine120197830.030 Why?
Uniparental Disomy12013430.030 Why?
DNA-Binding Proteins2200996390.030 Why?
TOR Serine-Threonine Kinases1202221070.030 Why?
China2200922460.030 Why?
Demography1201716500.030 Why?
ras Proteins1199810600.030 Why?
Phosphatidylinositol 3-Kinases1202229380.030 Why?
Histones1202325970.030 Why?
Prospective Studies42016531870.030 Why?
Molecular Sequence Data22008181120.030 Why?
Gestational Age1202134900.030 Why?
Patients120188920.030 Why?
DNA Probes120135600.030 Why?
Cardiac Surgical Procedures1200735260.030 Why?
Pulmonary Disease, Chronic Obstructive1200630380.030 Why?
Growth and Development12011510.020 Why?
UTP-Hexose-1-Phosphate Uridylyltransferase12011680.020 Why?
Cytogenetic Analysis120122950.020 Why?
Ankle Brachial Index120111540.020 Why?
Consanguinity120134560.020 Why?
Age Determination by Skeleton120111290.020 Why?
Boston2201693050.020 Why?
Trachea1201610750.020 Why?
Esophagus1201610170.020 Why?
Pulsatile Flow120113320.020 Why?
Prevalence22022151940.020 Why?
Hypertension, Pulmonary1202115270.020 Why?
Haplotypes2200627810.020 Why?
Pedigree2200846460.020 Why?
Growth Plate120112740.020 Why?
Drosophila melanogaster1199817040.020 Why?
Nutritional Physiological Phenomena120113700.020 Why?
Vomiting120126320.020 Why?
Chromosomes, Human120114570.020 Why?
Spine1201611430.020 Why?
Obesity12011127050.020 Why?
International Classification of Diseases120148650.020 Why?
Gene Expression Regulation12007120710.020 Why?
Vestibular Aqueduct12009660.020 Why?
User-Computer Interface1201514260.020 Why?
Treatment Outcome32013629660.020 Why?
Homozygote1201317770.020 Why?
Down Syndrome120168800.020 Why?
Infant, Newborn32016255750.020 Why?
Ion Transport120093200.020 Why?
Primary Ovarian Insufficiency120081150.020 Why?
Case-Control Studies12005217190.020 Why?
Blood Flow Velocity1201114230.020 Why?
Bone Remodeling120115750.020 Why?
Codon, Nonsense120082810.020 Why?
Femoral Artery120118430.020 Why?
Risk Factors42006721450.020 Why?
Data Mining120125370.020 Why?
Neonatal Screening120115910.020 Why?
Acute-Phase Reaction12006910.020 Why?
Alleles2200969310.020 Why?
Connexins120083590.020 Why?
Chlorides120096670.020 Why?
Eyelids120082630.020 Why?
Anthropometry1201113500.020 Why?
Prognosis12007290100.020 Why?
Trisomy120072660.020 Why?
Patient Participation1201514450.020 Why?
Geography120086690.020 Why?
Complement Factor H120061100.020 Why?
Drug Therapy, Combination1201664830.020 Why?
Adult620212137120.020 Why?
Diarrhea1201213430.020 Why?
Chromatography, High Pressure Liquid1200915740.020 Why?
Retrospective Studies42016770980.020 Why?
Xenopus laevis120099560.020 Why?
Fatigue1201215260.020 Why?
Absorptiometry, Photon1201117260.020 Why?
Medical Records1201014130.020 Why?
Databases, Genetic1201217800.020 Why?
Medical Informatics120127420.020 Why?
Body Height1201115740.020 Why?
Middle Aged620112131270.020 Why?
RNA, Messenger12000130290.020 Why?
Membrane Proteins2199878730.020 Why?
Drug Administration Schedule1201249290.020 Why?
Computer Simulation1201761910.010 Why?
Syndrome1201032480.010 Why?
Oocytes1200911860.010 Why?
Molecular Epidemiology120064680.010 Why?
Microscopy, Confocal1200919690.010 Why?
Chronic Disease1201791440.010 Why?
Weight Gain1201222820.010 Why?
Neurodegenerative Diseases1201110600.010 Why?
Reproducibility of Results12020198620.010 Why?
Forced Expiratory Volume1200617410.010 Why?
Animals420091685610.010 Why?
Radiography1201270100.010 Why?
Genetic Linkage1200624220.010 Why?
Kidney1201671670.010 Why?
Disease Management1201124500.010 Why?
Dose-Response Relationship, Drug12012109430.010 Why?
Adaptation, Psychological1201025750.010 Why?
Fertilization in Vitro1200712840.010 Why?
Helix-Loop-Helix Motifs11998960.010 Why?
Electroencephalography1201461420.010 Why?
Quality of Life12020127300.010 Why?
Signal Transduction21998233870.010 Why?
Bone Density1201134690.010 Why?
Photoreceptor Cells119982440.010 Why?
Gamma Rays119983200.010 Why?
Insect Proteins119982580.010 Why?
Acute Disease1200671410.010 Why?
Blood Pressure1201185410.010 Why?
Genes, ras119986910.010 Why?
Disease Progression12011132560.010 Why?
Mutagenesis1199812630.010 Why?
Recombination, Genetic1199815860.010 Why?
Mitosis1199812080.010 Why?
Genome-Wide Association Study12012122200.010 Why?
Basic Helix-Loop-Helix Transcription Factors1199811140.010 Why?
Severity of Illness Index12010155300.010 Why?
Double-Blind Method12006120170.010 Why?
Schizophrenia1201068740.010 Why?
Pregnancy12011290870.010 Why?
Randomized Controlled Trials as Topic1200699410.010 Why?
Tomography, X-Ray Computed12011200860.000 Why?
Phosphorylation1199884360.000 Why?
Aged220061629440.000 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.