Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Lance H Rodan, M.D.

Concepts (403)

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 Syndrome42020562.040 Why?
Muscle Hypotonia420201611.420 Why?
Genetic Variation11202265811.290 Why?
Developmental Disabilities9202115091.260 Why?
Epilepsy11202232900.970 Why?
Arginine320209330.960 Why?
Metabolism, Inborn Errors420212860.850 Why?
Carbohydrate Metabolism, Inborn Errors22020320.790 Why?
F-Box Proteins220202010.760 Why?
Syndactyly12021740.730 Why?
Microcephaly320224250.730 Why?
Transcription Factor 7-Like 2 Protein120211520.730 Why?
Epilepsy, Generalized320191780.720 Why?
Craniofacial Abnormalities220203180.710 Why?
Hemiplegia220181360.700 Why?
Phenotype252022166060.700 Why?
Lymphangiectasis, Intestinal12019100.690 Why?
Nervous System Malformations520222440.680 Why?
Calcium Channels, L-Type120212420.670 Why?
Dicarboxylic Acid Transporters1201840.650 Why?
Cation Transport Proteins220183270.630 Why?
Genetic Predisposition to Disease112022179120.630 Why?
Carbon-Nitrogen Ligases12018270.620 Why?
Metal Metabolism, Inborn Errors12018140.620 Why?
Amino Acid Transport Systems, Acidic12018300.620 Why?
Heterozygote6202428030.610 Why?
Urea Cycle Disorders, Inborn12018320.610 Why?
Hereditary Central Nervous System Demyelinating Diseases12018420.610 Why?
Excitatory Amino Acid Transporter 212019890.610 Why?
Malonates12017430.600 Why?
Maple Syrup Urine Disease12018400.600 Why?
Cerebrovascular Circulation2202027270.590 Why?
Brain Diseases, Metabolic, Inborn12017460.580 Why?
Psychomotor Disorders120181490.580 Why?
Mitochondrial Membrane Transport Proteins120181580.580 Why?
Pedigree13202245890.570 Why?
Anions120171360.570 Why?
Tubulin220206930.560 Why?
Purpura120171170.560 Why?
Antiporters120182780.560 Why?
Lissencephaly12016360.550 Why?
Long QT Syndrome120214670.550 Why?
Dystonic Disorders220183500.540 Why?
Monosaccharide Transport Proteins120184360.530 Why?
Mutation192024300450.510 Why?
Acidosis120172680.490 Why?
Manganese120183950.490 Why?
Parkinsonian Disorders120182840.490 Why?
Autistic Disorder2202112200.480 Why?
Muscle Spasticity320211570.480 Why?
Body Dysmorphic Disorders120182430.480 Why?
Retinal Diseases120207040.470 Why?
Mitochondrial Diseases120183430.470 Why?
Alopecia120184110.460 Why?
Child, Preschool292024422540.450 Why?
Mutation, Missense10202225710.430 Why?
Vision Disorders1202010880.430 Why?
Genetic Association Studies3202127340.430 Why?
Wernicke Encephalopathy12013290.420 Why?
Lymphedema120195250.420 Why?
Spasms, Infantile320222980.420 Why?
Neurotransmitter Agents220246650.420 Why?
Syndrome9202432680.410 Why?
Thiamine Deficiency12013480.410 Why?
Vasospasm, Intracranial120152150.410 Why?
Cerebral Palsy320224740.410 Why?
Ocular Motility Disorders120131440.400 Why?
Brain Ischemia2201830490.390 Why?
Musculoskeletal Abnormalities220221010.390 Why?
Acute Disease3201872380.370 Why?
Muscles1201515760.350 Why?
Eye Movements120135110.350 Why?
Seizures8202429570.350 Why?
Brain Diseases3202215450.350 Why?
Child342024801620.320 Why?
Alleles7202469220.320 Why?
Infant212024362050.310 Why?
Homozygote4202017960.300 Why?
Humans8120247614230.270 Why?
Magnetic Resonance Spectroscopy2201537690.270 Why?
Brain112024271070.260 Why?
Male4920243607360.260 Why?
Genes, Recessive220206280.250 Why?
Congenital Abnormalities220227090.250 Why?
Critical Care1201826970.250 Why?
Female4920243925810.250 Why?
Adolescent242024883130.250 Why?
Speech Disorders220181800.240 Why?
Biogenic Amines12024530.230 Why?
Amino Acid Metabolism, Inborn Errors220172830.230 Why?
RNA, Small Nuclear12024750.230 Why?
Drosophila melanogaster3202317120.230 Why?
Pelger-Huet Anomaly1202210.210 Why?
Comparative Genomic Hybridization220204730.200 Why?
Hearing Loss220217830.200 Why?
Phosphatidylinositols120232820.200 Why?
Semaphorins12022960.200 Why?
Hydrocephalus220217640.200 Why?
Facies220212220.190 Why?
DNA-Binding Proteins1201996060.190 Why?
Dwarfism120221380.190 Why?
Thrombolytic Therapy2200920650.190 Why?
Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing)1202180.190 Why?
Dihydroorotase1202180.190 Why?
Aspartate Carbamoyltransferase12021190.190 Why?
Cerebellar Diseases220212200.190 Why?
Myoclonic Epilepsies, Progressive12020130.190 Why?
Cyclin D212021980.190 Why?
Transaldolase12020100.180 Why?
Transketolase1202090.180 Why?
Vacuolar Proton-Translocating ATPases120221950.180 Why?
Ornithine12020790.180 Why?
Cytoplasmic Dyneins12020240.180 Why?
Polydactyly12021560.180 Why?
Uridine120211410.180 Why?
Haploinsufficiency220203370.180 Why?
Genotype42019130090.180 Why?
Uridine Diphosphate Glucose Dehydrogenase1202080.180 Why?
Tumor Suppressor Proteins2202028030.180 Why?
Chromosomes, Human, Pair 21120202280.180 Why?
Procollagen N-Endopeptidase12019190.170 Why?
SKP Cullin F-Box Protein Ligases120201750.170 Why?
Disorders of Sex Development120211290.170 Why?
Jumonji Domain-Containing Histone Demethylases120201710.170 Why?
Spastic Paraplegia, Hereditary120221680.170 Why?
Stroke3201297560.160 Why?
Calcium Channels, R-Type12018150.160 Why?
Malformations of Cortical Development120211760.160 Why?
HEK293 Cells4202242780.160 Why?
Neuroaxonal Dystrophies12018260.160 Why?
Retinitis Pigmentosa120223970.150 Why?
Eye Abnormalities120212420.150 Why?
Folate Receptor 112018400.150 Why?
Exercise1201558840.150 Why?
Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor12017110.150 Why?
Aspartate-Ammonia Ligase12017180.150 Why?
GABA Plasma Membrane Transport Proteins12018300.150 Why?
Acyltransferases120203050.150 Why?
Electroencephalography7202062240.150 Why?
Ceftriaxone120191750.150 Why?
Tetrahydrofolates12018580.150 Why?
Mi-2 Nucleosome Remodeling and Deacetylase Complex120181130.150 Why?
Dyskinesias12018790.150 Why?
Open Reading Frames120218150.150 Why?
Language Disorders120181400.150 Why?
Young Adult122024592070.150 Why?
Pyridoxaminephosphate Oxidase1201780.150 Why?
Nerve Tissue Proteins2202144140.150 Why?
Oxidoreductases120204130.150 Why?
Optic Atrophy12018790.150 Why?
Nucleocytoplasmic Transport Proteins12017730.150 Why?
Stem Cell Niche120213450.140 Why?
Propionic Acidemia1201790.140 Why?
Ubiquitination1202210060.140 Why?
Epilepsies, Myoclonic12018850.140 Why?
Brain Diseases, Metabolic12017440.140 Why?
Muscular Atrophy, Spinal120202580.140 Why?
Spinocerebellar Ataxias120181050.140 Why?
Ataxia220183060.140 Why?
Neurogenesis120238620.140 Why?
Wnt Proteins120217180.140 Why?
Dopamine1202416050.140 Why?
Acid-Base Equilibrium120171810.140 Why?
Gas Chromatography-Mass Spectrometry120173530.130 Why?
Chelating Agents120183870.130 Why?
Language Development Disorders120181930.130 Why?
Recovery of Function1200629770.130 Why?
Nephrosis12016430.130 Why?
Microtubule-Associated Proteins1202110760.130 Why?
Contracture120182350.130 Why?
Carbon Dioxide1202011460.130 Why?
Protein Structure, Secondary1201912290.130 Why?
Myokymia12015110.130 Why?
Hyperkinesis12016890.130 Why?
Chromosome Deletion1202013870.130 Why?
Kv1.1 Potassium Channel12015300.130 Why?
Carnitine120172520.130 Why?
Ergometry12015170.130 Why?
Histones2202325800.130 Why?
Medulloblastoma120216780.130 Why?
Chorea12016790.130 Why?
Heart Defects, Congenital1201246960.130 Why?
Chromosomal Proteins, Non-Histone120207270.130 Why?
beta Catenin1202010400.120 Why?
Cataplexy12015610.120 Why?
Infant, Newborn52021262120.120 Why?
PTEN Phosphohydrolase1202011150.120 Why?
Carrier Proteins2201949360.120 Why?
Molecular Diagnostic Techniques120196110.120 Why?
Quadriplegia120162260.120 Why?
Phosphocreatine120152610.120 Why?
In Situ Hybridization, Fluorescence1202025100.120 Why?
Serine120188300.120 Why?
Movement Disorders120184590.110 Why?
Diarrhea1202113180.110 Why?
Amino Acid Sequence32021134490.110 Why?
Cell Adhesion Molecules1202016000.110 Why?
Limbic Encephalitis12013360.110 Why?
Hypoxia-Ischemia, Brain120173520.110 Why?
Vigabatrin12013880.110 Why?
Magnetic Resonance Imaging102020364230.110 Why?
DNA Helicases120188510.110 Why?
Glycoproteins1202122080.110 Why?
Disease Management3201825070.100 Why?
Glutamate Decarboxylase120132390.100 Why?
Visual Cortex1202011070.100 Why?
Foot Deformities12012350.100 Why?
Administration, Oral1202040160.100 Why?
Down Syndrome120209010.100 Why?
Chromosome Mapping1202046380.100 Why?
Genome, Human2202244250.100 Why?
Gastroschisis12013990.100 Why?
DNA Copy Number Variations1202120200.100 Why?
Mitochondrial Proteins120179760.100 Why?
Emergency Medicine2201811970.100 Why?
Metabolic Diseases120186810.100 Why?
Pupil120121460.100 Why?
Toes120122090.090 Why?
Paresis120121760.090 Why?
Leukocytosis120122510.090 Why?
Chick Embryo220239820.090 Why?
Drosophila3202314950.090 Why?
Glasgow Coma Scale120125800.090 Why?
Rest120159190.090 Why?
Monitoring, Physiologic1201817800.090 Why?
Amino Acids1201617180.090 Why?
Fatty Acids1201718080.080 Why?
Gene Expression Regulation32022119020.080 Why?
Oxygen1202042280.080 Why?
Intracranial Thrombosis120091080.080 Why?
Animals1220231684410.080 Why?
Adult1420212211480.070 Why?
Anticonvulsants2201819060.070 Why?
Deep Brain Stimulation120168320.070 Why?
Corpus Callosum120127510.070 Why?
Case-Control Studies22015221680.070 Why?
Pilot Projects1202086330.070 Why?
DNA, Mitochondrial120128650.070 Why?
Psychotic Disorders1202232230.070 Why?
Atrophy2202216330.070 Why?
Diffusion Magnetic Resonance Imaging1201827900.070 Why?
Proteins2201860320.060 Why?
Zebrafish3202330070.060 Why?
Neuropsychological Tests1201870450.060 Why?
Attention Deficit Disorder with Hyperactivity1202137040.060 Why?
Antibodies1201324210.060 Why?
Siblings220218250.060 Why?
Referral and Consultation1201836000.060 Why?
Brain Mapping1202066260.060 Why?
Fatigue1201215510.060 Why?
Temporal Lobe1201216950.060 Why?
Genomics1202058200.060 Why?
Cell Nucleus2202329080.060 Why?
Membrane Proteins2202278560.060 Why?
Clinical Protocols1200914400.060 Why?
Spliceosomes120241300.060 Why?
RNA Splice Sites120242110.050 Why?
Dose-Response Relationship, Drug12015107660.050 Why?
Anemia1201215080.050 Why?
Phosphatidylinositol Phosphates120232010.050 Why?
Extracellular Matrix2202017250.050 Why?
Protein-Arginine N-Methyltransferases120221290.050 Why?
Calpain120221450.050 Why?
Phosphoric Monoester Hydrolases120234120.050 Why?
Autoimmune Diseases1201322480.050 Why?
rhoB GTP-Binding Protein12020170.050 Why?
Chromatin2202329600.050 Why?
Diagnosis, Differential22016129700.050 Why?
Ubiquitin-Protein Ligases2202218930.050 Why?
Lower Extremity Deformities, Congenital12020120.050 Why?
Tissue Plasminogen Activator1200611640.050 Why?
Practice Guidelines as Topic1201873890.050 Why?
Dendritic Spines120222430.050 Why?
Cyclin D12020720.050 Why?
DNA Mutational Analysis2202041100.040 Why?
Genitalia120211130.040 Why?
Methyltransferases120233770.040 Why?
Focal Adhesions120201150.040 Why?
Casein Kinase II120201220.040 Why?
Loss of Heterozygosity120226620.040 Why?
Physicians1201845910.040 Why?
Pentose Phosphate Pathway120201260.040 Why?
Histone Demethylases120223200.040 Why?
Recurrence1201284690.040 Why?
Lupus Erythematosus, Systemic1201221630.040 Why?
Sequence Analysis, DNA2202147410.040 Why?
Codon, Nonsense120202850.040 Why?
Polymorphism, Single Nucleotide12018159410.040 Why?
DNA, Complementary1202219920.040 Why?
Rare Diseases120246210.040 Why?
Frameshift Mutation120203920.040 Why?
Neurites120203910.040 Why?
Class I Phosphatidylinositol 3-Kinases120228980.040 Why?
Germ Cells120226340.040 Why?
Models, Molecular2201854390.040 Why?
Emergency Medical Services1200919230.040 Why?
Genes, Dominant120208630.040 Why?
Methylation1202010830.040 Why?
Gastric Mucosa120216040.040 Why?
Asparagine120171190.040 Why?
Treatment Outcome32020646510.040 Why?
Pyridoxal Phosphate120171250.040 Why?
Algorithms12018140260.040 Why?
Microfilament Proteins1202211340.040 Why?
Leigh Disease12018890.040 Why?
Severity of Illness Index12015158380.030 Why?
Lysosomes120229230.030 Why?
Sequence Alignment1202121790.030 Why?
Face1202210260.030 Why?
Chromatography, Liquid120209830.030 Why?
RNA Splicing120219180.030 Why?
Adenosine Triphosphate1202219890.030 Why?
Registries1201282230.030 Why?
DEAD-box RNA Helicases120193840.030 Why?
Longitudinal Studies12012145990.030 Why?
Prospective Studies12020544150.030 Why?
Actins1202320500.030 Why?
Consanguinity120174560.030 Why?
Proteasome Endopeptidase Complex1202213200.030 Why?
Cytoskeleton1202011700.030 Why?
Basal Ganglia120185540.030 Why?
Valproic Acid120184430.030 Why?
Neuroglia120209550.030 Why?
Receptors, GABA-A120196230.030 Why?
Glutamine120175770.030 Why?
Microscopy, Confocal1202019700.030 Why?
Adenosine Triphosphatases120188340.030 Why?
Zebrafish Proteins1202010140.030 Why?
Chromatin Assembly and Disassembly120186330.030 Why?
Epilepsies, Partial120184310.030 Why?
Incidence12012213410.030 Why?
Germ-Line Mutation1202218580.030 Why?
Proto-Oncogene Proteins c-akt1202224550.030 Why?
Organoids120207400.030 Why?
Databases, Genetic1202017420.030 Why?
Cohort Studies32022414460.030 Why?
TOR Serine-Threonine Kinases1202220570.030 Why?
RNA-Binding Proteins1202218970.030 Why?
Mass Spectrometry1202021920.030 Why?
Gene Expression Regulation, Developmental1202436120.030 Why?
Phosphatidylinositol 3-Kinases1202228630.030 Why?
Protein Processing, Post-Translational1202019740.030 Why?
Central Nervous System1202013370.030 Why?
Abnormalities, Multiple1202014240.030 Why?
Chromatography, High Pressure Liquid1201615400.030 Why?
Lower Extremity1202012010.030 Why?
Kinetics1202063740.020 Why?
Early Diagnosis1201711860.020 Why?
Genetic Heterogeneity120157320.020 Why?
Health Services Accessibility1200954410.020 Why?
Drosophila Proteins1202016990.020 Why?
Homeostasis1202233210.020 Why?
Metabolomics1202016570.020 Why?
Oxidation-Reduction1201722300.020 Why?
Risk Factors22020741670.020 Why?
Cytoskeletal Proteins1201613420.020 Why?
Intestinal Mucosa1202130300.020 Why?
Hotlines12009550.020 Why?
Genetic Testing1202235380.020 Why?
Ambulances12009910.020 Why?
Binding Sites1201760550.020 Why?
Tomography, X-Ray Computed12012205560.020 Why?
Emergency Medical Technicians120091190.020 Why?
Ontario120093980.020 Why?
Transportation of Patients120091740.020 Why?
Interinstitutional Relations120092360.020 Why?
Protein Binding1202093520.020 Why?
Nuclear Proteins1202257940.020 Why?
Hippocampus1202037630.020 Why?
Massachusetts1202088320.020 Why?
Cell Cycle Proteins1201934470.020 Why?
Signal Transduction22020234410.020 Why?
Fibroblasts1201741400.020 Why?
High-Throughput Nucleotide Sequencing1201936390.020 Why?
Epigenesis, Genetic1202037980.020 Why?
Hospitals, Community120093650.020 Why?
Cell Line12021156050.020 Why?
Retina1201726580.020 Why?
RNA, Messenger12021127960.020 Why?
Comorbidity12020104980.020 Why?
Gene Expression1201875840.020 Why?
Intracellular Signaling Peptides and Proteins1201628710.020 Why?
Cell Differentiation12023115260.020 Why?
Adaptor Proteins, Signal Transducing1201628980.020 Why?
Rats12021237420.020 Why?
Mice22021815090.010 Why?
Disease Progression12021135020.010 Why?
Retrospective Studies12012805820.010 Why?
Mice, Inbred C57BL12021221630.010 Why?
Cross-Sectional Studies12024261120.010 Why?
Triage120099850.010 Why?
Patient Transfer120097940.010 Why?
Aged, 80 and over12006589560.010 Why?
Neurons1202094620.010 Why?
Transcription Factors12021121250.010 Why?
Obesity12022129380.010 Why?
Follow-Up Studies12021391170.010 Why?
Patient Care Team1200925230.010 Why?
Middle Aged220152208260.010 Why?
Patient Selection1200942440.010 Why?
Hospitals1200938820.010 Why?
Emergency Service, Hospital1200978740.010 Why?
Time Factors12009399750.000 Why?
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Concepts (403)
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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.