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Lance H Rodan, M.D.

Concepts (410)

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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?
MELAS Syndrome42020542.000 Why?
Muscle Hypotonia420201671.380 Why?
Developmental Disabilities10202415191.360 Why?
Genetic Variation11202266101.270 Why?
Epilepsy11202233200.950 Why?
Arginine320209330.930 Why?
Metabolism, Inborn Errors420212910.830 Why?
Carbohydrate Metabolism, Inborn Errors22020320.770 Why?
F-Box Proteins220201990.740 Why?
Microcephaly320224260.720 Why?
Syndactyly12021740.720 Why?
Transcription Factor 7-Like 2 Protein120211520.710 Why?
Phenotype272024167210.710 Why?
Epilepsy, Generalized320191830.700 Why?
Craniofacial Abnormalities220203110.700 Why?
Hemiplegia220181360.690 Why?
Lymphangiectasis, Intestinal12019100.670 Why?
Nervous System Malformations520222430.670 Why?
Calcium Channels, L-Type120212420.660 Why?
Dicarboxylic Acid Transporters1201840.640 Why?
Cation Transport Proteins220183250.620 Why?
Genetic Predisposition to Disease112022180710.610 Why?
Carbon-Nitrogen Ligases12018270.610 Why?
Metal Metabolism, Inborn Errors12018140.610 Why?
Amino Acid Transport Systems, Acidic12018300.600 Why?
Heterozygote6202427940.600 Why?
Urea Cycle Disorders, Inborn12018310.600 Why?
Excitatory Amino Acid Transporter 212019890.590 Why?
Hereditary Central Nervous System Demyelinating Diseases12018430.590 Why?
Malonates12017430.590 Why?
Maple Syrup Urine Disease12018410.580 Why?
Cerebrovascular Circulation2202026730.580 Why?
Brain Diseases, Metabolic, Inborn12017460.570 Why?
Psychomotor Disorders120181490.570 Why?
Pedigree13202245260.560 Why?
Mitochondrial Membrane Transport Proteins120181690.560 Why?
Anions120171360.550 Why?
Tubulin220206920.550 Why?
Purpura120171150.550 Why?
Antiporters120182750.550 Why?
Lissencephaly12016360.540 Why?
Long QT Syndrome120214740.530 Why?
Dystonic Disorders220183530.530 Why?
Mutation212024301960.520 Why?
Monosaccharide Transport Proteins120184370.520 Why?
Acidosis120172710.480 Why?
Manganese120183950.480 Why?
Parkinsonian Disorders120182860.480 Why?
Autistic Disorder2202112390.470 Why?
Body Dysmorphic Disorders120182420.470 Why?
Muscle Spasticity320211600.470 Why?
Retinal Diseases120207090.460 Why?
Mitochondrial Diseases120183450.460 Why?
Child, Preschool302024425000.450 Why?
Alopecia120184140.450 Why?
Mutation, Missense10202225890.420 Why?
Genetic Association Studies3202127410.420 Why?
Vision Disorders1202010870.420 Why?
Wernicke Encephalopathy12013290.410 Why?
Lymphedema120195250.410 Why?
Spasms, Infantile320223020.410 Why?
Neurotransmitter Agents220246630.410 Why?
Syndrome9202432710.400 Why?
Vasospasm, Intracranial120152060.400 Why?
Thiamine Deficiency12013480.400 Why?
Cerebral Palsy320224810.400 Why?
Ocular Motility Disorders120131440.390 Why?
Brain Ischemia2201830000.390 Why?
Musculoskeletal Abnormalities220221010.380 Why?
Acute Disease3201872320.360 Why?
Muscles1201515780.340 Why?
Alleles8202468970.340 Why?
Eye Movements120135100.340 Why?
Brain Diseases3202215460.340 Why?
Seizures8202430000.340 Why?
Child352024805630.330 Why?
Infant222024363850.310 Why?
Homozygote4202017750.300 Why?
Humans8320247659560.270 Why?
Magnetic Resonance Spectroscopy2201536720.270 Why?
Male5120243636910.260 Why?
Adolescent262024888320.260 Why?
Brain112024271780.250 Why?
Female5020243961010.250 Why?
Genes, Recessive220206240.250 Why?
Congenital Abnormalities220227040.250 Why?
Critical Care1201827120.250 Why?
Speech Disorders220181780.230 Why?
Biogenic Amines12024530.230 Why?
Amino Acid Metabolism, Inborn Errors220172840.230 Why?
Iron-Binding Proteins12024830.230 Why?
RNA, Small Nuclear12024700.230 Why?
Drosophila melanogaster3202317210.220 Why?
Friedreich Ataxia12024820.220 Why?
Spastic Paraplegia, Hereditary220241720.210 Why?
Pelger-Huet Anomaly1202210.210 Why?
Hearing Loss220217840.200 Why?
Comparative Genomic Hybridization220204760.200 Why?
Phosphatidylinositols120232760.200 Why?
Semaphorins12022960.200 Why?
Hydrocephalus220217620.190 Why?
DNA-Binding Proteins1201996010.190 Why?
Facies220212230.190 Why?
Dwarfism120221370.190 Why?
Thrombolytic Therapy2200920590.190 Why?
Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing)1202180.180 Why?
Dihydroorotase1202180.180 Why?
Aspartate Carbamoyltransferase12021180.180 Why?
Cerebellar Diseases220212260.180 Why?
Myoclonic Epilepsies, Progressive12020130.180 Why?
Cyclin D212021970.180 Why?
Vacuolar Proton-Translocating ATPases120221960.180 Why?
Transaldolase12020100.180 Why?
Transketolase1202090.180 Why?
Ornithine12020800.180 Why?
Uridine120211350.180 Why?
Haploinsufficiency220203340.180 Why?
Genotype42019130240.180 Why?
Cytoplasmic Dyneins12020240.180 Why?
Polydactyly12021570.180 Why?
Tumor Suppressor Proteins2202027960.170 Why?
Uridine Diphosphate Glucose Dehydrogenase1202080.170 Why?
Chromosomes, Human, Pair 21120202280.170 Why?
Procollagen N-Endopeptidase12019190.170 Why?
SKP Cullin F-Box Protein Ligases120201730.170 Why?
Disorders of Sex Development120211290.170 Why?
Jumonji Domain-Containing Histone Demethylases120201690.170 Why?
Stroke3201297470.160 Why?
Calcium Channels, R-Type12018130.160 Why?
Malformations of Cortical Development120211740.160 Why?
Membrane Transport Proteins1202410280.150 Why?
HEK293 Cells4202242580.150 Why?
Retinitis Pigmentosa120223940.150 Why?
Eye Abnormalities120212430.150 Why?
Neuroaxonal Dystrophies12018260.150 Why?
Exercise1201559370.150 Why?
Folate Receptor 112018410.150 Why?
Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor12017110.150 Why?
Acyltransferases120203050.150 Why?
Aspartate-Ammonia Ligase12017180.150 Why?
GABA Plasma Membrane Transport Proteins12018300.150 Why?
Ceftriaxone120191760.150 Why?
Electroencephalography7202062730.150 Why?
Tetrahydrofolates12018580.150 Why?
Mi-2 Nucleosome Remodeling and Deacetylase Complex120181160.150 Why?
Dyskinesias12018790.150 Why?
Open Reading Frames120218200.140 Why?
Nerve Tissue Proteins2202143920.140 Why?
Language Disorders120181400.140 Why?
Young Adult122024598860.140 Why?
Pyridoxaminephosphate Oxidase1201780.140 Why?
Oxidoreductases120204090.140 Why?
Optic Atrophy12018780.140 Why?
Stem Cell Niche120213460.140 Why?
Nucleocytoplasmic Transport Proteins12017730.140 Why?
Ubiquitination120229960.140 Why?
Propionic Acidemia1201790.140 Why?
Epilepsies, Myoclonic12018830.140 Why?
Brain Diseases, Metabolic12017440.140 Why?
Muscular Atrophy, Spinal120202600.140 Why?
Ataxia220183070.140 Why?
Spinocerebellar Ataxias120181090.140 Why?
Dopamine1202415820.140 Why?
Neurogenesis120238650.140 Why?
Wnt Proteins120217220.130 Why?
Acid-Base Equilibrium120171800.130 Why?
Chelating Agents120183800.130 Why?
Gas Chromatography-Mass Spectrometry120173550.130 Why?
Recovery of Function1200629660.130 Why?
Language Development Disorders120181940.130 Why?
Microtubule-Associated Proteins1202110660.130 Why?
Carbon Dioxide1202011370.130 Why?
Protein Structure, Secondary1201912100.130 Why?
Nephrosis12016430.130 Why?
Contracture120182340.130 Why?
Myokymia12015110.130 Why?
Hyperkinesis12016880.130 Why?
Chromosome Deletion1202013850.130 Why?
Medulloblastoma120216580.130 Why?
Kv1.1 Potassium Channel12015290.130 Why?
Carnitine120172530.130 Why?
Ergometry12015170.120 Why?
Histones2202325840.120 Why?
Chorea12016800.120 Why?
Heart Defects, Congenital1201246980.120 Why?
Chromosomal Proteins, Non-Histone120207220.120 Why?
beta Catenin1202010430.120 Why?
Cataplexy12015610.120 Why?
Carrier Proteins2201949130.120 Why?
Infant, Newborn52021263490.120 Why?
PTEN Phosphohydrolase1202011190.120 Why?
Molecular Diagnostic Techniques120196180.120 Why?
Quadriplegia120162270.120 Why?
Phosphocreatine120152580.120 Why?
In Situ Hybridization, Fluorescence1202025050.120 Why?
Serine120188240.110 Why?
Movement Disorders120184610.110 Why?
Diarrhea1202113160.110 Why?
Amino Acid Sequence32021134000.110 Why?
Cell Adhesion Molecules1202016120.110 Why?
Limbic Encephalitis12013360.110 Why?
Hypoxia-Ischemia, Brain120173610.110 Why?
DNA Helicases120188520.110 Why?
Magnetic Resonance Imaging102020365320.110 Why?
Vigabatrin12013880.110 Why?
Glycoproteins1202121950.110 Why?
Disease Management3201825350.100 Why?
Visual Cortex1202010840.100 Why?
Glutamate Decarboxylase120132400.100 Why?
Administration, Oral1202040150.100 Why?
Foot Deformities12012350.100 Why?
Chromosome Mapping1202046180.100 Why?
Down Syndrome120209150.100 Why?
Genome, Human2202244480.100 Why?
DNA Copy Number Variations1202120450.100 Why?
Gastroschisis12013990.100 Why?
Mitochondrial Proteins120179750.090 Why?
Metabolic Diseases120186870.090 Why?
Emergency Medicine2201812210.090 Why?
Pupil120121470.090 Why?
Toes120122090.090 Why?
Paresis120121760.090 Why?
Leukocytosis120122480.090 Why?
Chick Embryo220239640.090 Why?
Drosophila3202315010.090 Why?
Glasgow Coma Scale120125750.090 Why?
Rest120159410.080 Why?
Monitoring, Physiologic1201817920.080 Why?
Amino Acids1201617090.080 Why?
Animals1320241687590.080 Why?
Fatty Acids1201718060.080 Why?
Gene Expression Regulation32022118880.080 Why?
Adult1520242230380.080 Why?
Oxygen1202042410.080 Why?
Intracranial Thrombosis120091090.080 Why?
Anticonvulsants2201819210.070 Why?
Corpus Callosum120127510.070 Why?
Deep Brain Stimulation120168500.070 Why?
Case-Control Studies22015222220.070 Why?
Pilot Projects1202087330.070 Why?
DNA, Mitochondrial120128690.070 Why?
Psychotic Disorders1202232680.070 Why?
Atrophy2202216350.070 Why?
Diffusion Magnetic Resonance Imaging1201828030.060 Why?
Proteins2201859950.060 Why?
Attention Deficit Disorder with Hyperactivity1202137180.060 Why?
Zebrafish3202330350.060 Why?
Neuropsychological Tests1201871220.060 Why?
Antibodies1201324170.060 Why?
Siblings220218280.060 Why?
Brain Mapping1202065980.060 Why?
Referral and Consultation1201836150.060 Why?
Fatigue1201215490.060 Why?
Ethanolamine1202490.060 Why?
Temporal Lobe1201217140.060 Why?
Genomics1202059290.060 Why?
Cell Nucleus2202328670.060 Why?
Spliceosomes120241160.060 Why?
Membrane Proteins2202278510.060 Why?
Clinical Protocols1200914410.050 Why?
RNA Splice Sites120242120.050 Why?
Dose-Response Relationship, Drug12015107290.050 Why?
Trinucleotide Repeat Expansion120242540.050 Why?
Anemia1201215110.050 Why?
Phosphatidylinositol Phosphates120232010.050 Why?
Choline120245100.050 Why?
Extracellular Matrix2202017270.050 Why?
Protein-Arginine N-Methyltransferases120221270.050 Why?
Autoimmune Diseases1201322260.050 Why?
Calpain120221450.050 Why?
Phosphoric Monoester Hydrolases120234160.050 Why?
Diagnosis, Differential22016129760.050 Why?
Ubiquitin-Protein Ligases2202218920.050 Why?
rhoB GTP-Binding Protein12020160.050 Why?
Chromatin2202329800.050 Why?
Receptors, Virus120246510.040 Why?
Tissue Plasminogen Activator1200611670.040 Why?
Lower Extremity Deformities, Congenital12020120.040 Why?
Practice Guidelines as Topic1201874250.040 Why?
Dendritic Spines120222450.040 Why?
Cyclin D12020700.040 Why?
DNA Mutational Analysis2202041080.040 Why?
Methyltransferases120233710.040 Why?
Genitalia120211140.040 Why?
Focal Adhesions120201130.040 Why?
Casein Kinase II120201200.040 Why?
Physicians1201845880.040 Why?
Loss of Heterozygosity120226630.040 Why?
Pentose Phosphate Pathway120201250.040 Why?
Histone Demethylases120223280.040 Why?
Lupus Erythematosus, Systemic1201221590.040 Why?
Sequence Analysis, DNA2202147720.040 Why?
Recurrence1201285010.040 Why?
Codon, Nonsense120202880.040 Why?
Polymorphism, Single Nucleotide12018160470.040 Why?
DNA, Complementary1202219840.040 Why?
Frameshift Mutation120203930.040 Why?
Rare Diseases120246350.040 Why?
Neurites120203890.040 Why?
Models, Molecular2201853790.040 Why?
Germ Cells120226470.040 Why?
Class I Phosphatidylinositol 3-Kinases120229040.040 Why?
Emergency Medical Services1200919380.040 Why?
Genes, Dominant120208560.040 Why?
Methylation1202010730.040 Why?
Gastric Mucosa120216020.040 Why?
Treatment Outcome32020651890.040 Why?
Asparagine120171200.040 Why?
Pyridoxal Phosphate120171230.030 Why?
Microfilament Proteins1202211300.030 Why?
Algorithms12018140710.030 Why?
Leigh Disease12018880.030 Why?
Severity of Illness Index12015158800.030 Why?
Lysosomes120229320.030 Why?
Sequence Alignment1202121710.030 Why?
Face1202210280.030 Why?
Chromatography, Liquid120209900.030 Why?
RNA Splicing120219030.030 Why?
Adenosine Triphosphate1202219990.030 Why?
Registries1201282970.030 Why?
DEAD-box RNA Helicases120193840.030 Why?
Actins1202320560.030 Why?
Prospective Studies12020548060.030 Why?
Longitudinal Studies12012147490.030 Why?
Consanguinity120174600.030 Why?
Proteasome Endopeptidase Complex1202213140.030 Why?
Cytoskeleton1202011780.030 Why?
Basal Ganglia120185490.030 Why?
Valproic Acid120184450.030 Why?
Neuroglia120209640.030 Why?
Receptors, GABA-A120196240.030 Why?
Glutamine120175760.030 Why?
Microscopy, Confocal1202019650.030 Why?
Adenosine Triphosphatases120188370.030 Why?
Zebrafish Proteins1202010170.030 Why?
Chromatin Assembly and Disassembly120186320.030 Why?
Epilepsies, Partial120184310.030 Why?
Incidence12012214800.030 Why?
Proto-Oncogene Proteins c-akt1202224530.030 Why?
Organoids120207390.030 Why?
Databases, Genetic1202017510.030 Why?
Germ-Line Mutation1202218840.030 Why?
Cohort Studies32022416470.030 Why?
TOR Serine-Threonine Kinases1202220560.030 Why?
RNA-Binding Proteins1202218740.030 Why?
Mass Spectrometry1202021940.030 Why?
Gene Expression Regulation, Developmental1202436060.030 Why?
Phosphatidylinositol 3-Kinases1202228780.030 Why?
Protein Processing, Post-Translational1202019570.030 Why?
Abnormalities, Multiple1202014240.030 Why?
Central Nervous System1202013410.030 Why?
Chromatography, High Pressure Liquid1201615260.020 Why?
Lower Extremity1202012260.020 Why?
Kinetics1202062740.020 Why?
Early Diagnosis1201711870.020 Why?
Genetic Heterogeneity120157350.020 Why?
Health Services Accessibility1200955060.020 Why?
Drosophila Proteins1202016970.020 Why?
Homeostasis1202233360.020 Why?
Mice32024818180.020 Why?
Metabolomics1202016680.020 Why?
Oxidation-Reduction1201722180.020 Why?
Cytoskeletal Proteins1201613250.020 Why?
Risk Factors22020748360.020 Why?
Intestinal Mucosa1202130460.020 Why?
Hotlines12009550.020 Why?
Genetic Testing1202235950.020 Why?
Ambulances12009940.020 Why?
Binding Sites1201760010.020 Why?
Tomography, X-Ray Computed12012206600.020 Why?
Emergency Medical Technicians120091190.020 Why?
Ontario120094020.020 Why?
Transportation of Patients120091780.020 Why?
Interinstitutional Relations120092340.020 Why?
Protein Binding1202092960.020 Why?
Nuclear Proteins1202257830.020 Why?
Hippocampus1202037750.020 Why?
Massachusetts1202088710.020 Why?
Cell Cycle Proteins1201934300.020 Why?
Signal Transduction22020236000.020 Why?
High-Throughput Nucleotide Sequencing1201936550.020 Why?
Fibroblasts1201741590.020 Why?
Epigenesis, Genetic1202038190.020 Why?
Hospitals, Community120093630.020 Why?
Cell Line12021155430.020 Why?
Retina1201726570.020 Why?
RNA, Messenger12021127690.020 Why?
Gene Expression1201875840.020 Why?
Comorbidity12020105630.020 Why?
Intracellular Signaling Peptides and Proteins1201628800.020 Why?
Cell Differentiation12023116400.020 Why?
Adaptor Proteins, Signal Transducing1201628990.020 Why?
Rats12021237070.020 Why?
Disease Progression12021136310.010 Why?
Retrospective Studies12012815150.010 Why?
Cross-Sectional Studies12024263130.010 Why?
Mice, Inbred C57BL12021223310.010 Why?
Triage120099960.010 Why?
Patient Transfer120097900.010 Why?
Aged, 80 and over12006594880.010 Why?
Transcription Factors12021121310.010 Why?
Neurons1202095240.010 Why?
Obesity12022130750.010 Why?
Follow-Up Studies12021391940.010 Why?
Patient Care Team1200925170.010 Why?
Middle Aged220152230040.010 Why?
Patient Selection1200942550.010 Why?
Hospitals1200938880.010 Why?
Emergency Service, Hospital1200978750.010 Why?
Time Factors12009400650.000 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.