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Lance H Rodan, M.D.

Concepts (395)

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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 Syndrome42020502.170 Why?
Muscle Hypotonia420201651.470 Why?
Developmental Disabilities9202114521.340 Why?
Genetic Variation11202265401.330 Why?
Epilepsy11202233011.000 Why?
Arginine320209441.000 Why?
Metabolism, Inborn Errors420212880.890 Why?
Carbohydrate Metabolism, Inborn Errors22020310.830 Why?
F-Box Proteins220201970.790 Why?
Syndactyly12021720.770 Why?
Transcription Factor 7-Like 2 Protein120211540.760 Why?
Epilepsy, Generalized320191740.760 Why?
Microcephaly320224300.760 Why?
Phenotype252022163310.740 Why?
Hemiplegia220181350.740 Why?
Craniofacial Abnormalities220203150.740 Why?
Lymphangiectasis, Intestinal12019100.720 Why?
Nervous System Malformations520222450.720 Why?
Calcium Channels, L-Type120212380.710 Why?
Dicarboxylic Acid Transporters1201850.680 Why?
Genetic Predisposition to Disease112022174000.660 Why?
Cation Transport Proteins220183270.660 Why?
Carbon-Nitrogen Ligases12018280.650 Why?
Excitatory Amino Acid Transporter 212019770.650 Why?
Metal Metabolism, Inborn Errors12018150.650 Why?
Amino Acid Transport Systems, Acidic12018280.650 Why?
Hereditary Central Nervous System Demyelinating Diseases12018390.630 Why?
Urea Cycle Disorders, Inborn12018310.630 Why?
Malonates12017420.630 Why?
Maple Syrup Urine Disease12018390.630 Why?
Cerebrovascular Circulation2202027320.610 Why?
Brain Diseases, Metabolic, Inborn12017440.610 Why?
Mitochondrial Membrane Transport Proteins120181540.610 Why?
Psychomotor Disorders120181520.600 Why?
Heterozygote5202227900.600 Why?
Anions120171330.600 Why?
Pedigree13202246460.590 Why?
Tubulin220206950.580 Why?
Antiporters120182770.580 Why?
Purpura120171220.580 Why?
Lissencephaly12016380.570 Why?
Long QT Syndrome120214530.570 Why?
Dystonic Disorders220183290.570 Why?
Monosaccharide Transport Proteins120184400.550 Why?
Manganese120184080.520 Why?
Acidosis120172720.520 Why?
Parkinsonian Disorders120182720.510 Why?
Autistic Disorder2202111740.510 Why?
Body Dysmorphic Disorders120182290.500 Why?
Muscle Spasticity320211540.500 Why?
Alopecia120183810.500 Why?
Mutation182022297170.490 Why?
Mitochondrial Diseases120183210.490 Why?
Retinal Diseases120206830.490 Why?
Child, Preschool282022409550.470 Why?
Vision Disorders1202010570.450 Why?
Mutation, Missense10202225560.450 Why?
Genetic Association Studies3202126990.450 Why?
Wernicke Encephalopathy12013280.440 Why?
Vasospasm, Intracranial120152060.440 Why?
Thiamine Deficiency12013430.430 Why?
Lymphedema120195280.430 Why?
Spasms, Infantile320223050.430 Why?
Cerebral Palsy320224590.430 Why?
Ocular Motility Disorders120131350.420 Why?
Musculoskeletal Abnormalities22022910.410 Why?
Neurotransmitter Agents120156470.390 Why?
Syndrome8202332480.390 Why?
Brain Ischemia2201832580.390 Why?
Acute Disease3201871410.390 Why?
Eye Movements120135060.360 Why?
Muscles1201516170.360 Why?
Brain Diseases3202215540.360 Why?
Seizures7202128510.340 Why?
Child322022774780.330 Why?
Homozygote4202017770.320 Why?
Alleles6202169310.310 Why?
Infant192022350700.300 Why?
Humans7920237420880.280 Why?
Magnetic Resonance Spectroscopy2201537600.280 Why?
Male4820223495380.270 Why?
Genes, Recessive220206420.260 Why?
Brain102022263430.260 Why?
Female4820223795920.260 Why?
Critical Care1201826400.260 Why?
Congenital Abnormalities220227070.260 Why?
Adolescent232022856490.250 Why?
Amino Acid Metabolism, Inborn Errors220172550.250 Why?
Speech Disorders220181890.250 Why?
Drosophila melanogaster3202317040.240 Why?
Pelger-Huet Anomaly1202210.220 Why?
Hearing Loss220217650.210 Why?
Comparative Genomic Hybridization220204960.210 Why?
Phosphatidylinositols120232910.210 Why?
Hydrocephalus220217460.210 Why?
Semaphorins120221010.210 Why?
Facies220211970.210 Why?
DNA-Binding Proteins1201996390.200 Why?
Dwarfism120221450.200 Why?
Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing)12021110.200 Why?
Dihydroorotase12021110.200 Why?
Aspartate Carbamoyltransferase12021220.200 Why?
Cerebellar Diseases220212220.200 Why?
Myoclonic Epilepsies, Progressive12020110.200 Why?
Thrombolytic Therapy2200921610.190 Why?
Cyclin D2120211010.190 Why?
Transaldolase1202090.190 Why?
Transketolase1202090.190 Why?
Vacuolar Proton-Translocating ATPases120221950.190 Why?
Haploinsufficiency220203290.190 Why?
Ornithine12020780.190 Why?
Cytoplasmic Dyneins12020250.190 Why?
Polydactyly12021570.190 Why?
Genotype42019129460.190 Why?
Uridine120211460.190 Why?
Uridine Diphosphate Glucose Dehydrogenase1202090.190 Why?
Chromosomes, Human, Pair 21120202300.180 Why?
Procollagen N-Endopeptidase12019190.180 Why?
Tumor Suppressor Proteins2202028420.180 Why?
Disorders of Sex Development120211220.180 Why?
SKP Cullin F-Box Protein Ligases120201770.180 Why?
Spastic Paraplegia, Hereditary120221570.170 Why?
Jumonji Domain-Containing Histone Demethylases120201820.170 Why?
Calcium Channels, R-Type12018140.170 Why?
Stroke3201299630.160 Why?
Neuroaxonal Dystrophies12018220.160 Why?
Exercise1201556110.160 Why?
Retinitis Pigmentosa120223860.160 Why?
HEK293 Cells4202242000.160 Why?
Folate Receptor 112018360.160 Why?
Malformations of Cortical Development120212000.160 Why?
Electroencephalography7202061420.160 Why?
Eye Abnormalities120212460.160 Why?
Ceftriaxone120191680.160 Why?
Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor12017100.160 Why?
Aspartate-Ammonia Ligase12017160.160 Why?
GABA Plasma Membrane Transport Proteins12018300.160 Why?
Acyltransferases120202940.160 Why?
Dyskinesias12018780.160 Why?
Mi-2 Nucleosome Remodeling and Deacetylase Complex120181130.160 Why?
Tetrahydrofolates12018610.160 Why?
Open Reading Frames120218100.150 Why?
Pyridoxaminephosphate Oxidase1201780.150 Why?
Language Disorders120181400.150 Why?
Optic Atrophy12018790.150 Why?
Oxidoreductases120204240.150 Why?
Nucleocytoplasmic Transport Proteins12017760.150 Why?
Stem Cell Niche120213420.150 Why?
Nerve Tissue Proteins2202144650.150 Why?
Propionic Acidemia1201790.150 Why?
Ubiquitination1202210110.150 Why?
Epilepsies, Myoclonic12018800.150 Why?
Spinocerebellar Ataxias12018880.150 Why?
Brain Diseases, Metabolic12017420.150 Why?
Young Adult112021563500.150 Why?
Ataxia220183040.150 Why?
Muscular Atrophy, Spinal120202580.150 Why?
Wnt Proteins120217210.140 Why?
Neurogenesis120238290.140 Why?
Acid-Base Equilibrium120171850.140 Why?
Chelating Agents120183800.140 Why?
Gas Chromatography-Mass Spectrometry120173610.140 Why?
Recovery of Function1200629240.140 Why?
Contracture120182230.140 Why?
Carbon Dioxide1202011410.140 Why?
Nephrosis12016450.140 Why?
Language Development Disorders120181960.140 Why?
Hyperkinesis12016890.140 Why?
Myokymia12015110.140 Why?
Carnitine120172390.140 Why?
Microtubule-Associated Proteins1202110860.140 Why?
Chromosome Deletion1202014000.130 Why?
Chorea12016740.130 Why?
Protein Structure, Secondary1201912450.130 Why?
Kv1.1 Potassium Channel12015290.130 Why?
Ergometry12015170.130 Why?
Histones2202325970.130 Why?
Heart Defects, Congenital1201245660.130 Why?
Chromosomal Proteins, Non-Histone120207300.130 Why?
Medulloblastoma120216810.130 Why?
beta Catenin1202010580.130 Why?
Cataplexy12015600.130 Why?
Infant, Newborn52021255750.130 Why?
Molecular Diagnostic Techniques120196020.120 Why?
PTEN Phosphohydrolase1202011440.120 Why?
Quadriplegia120162250.120 Why?
Phosphocreatine120152690.120 Why?
Movement Disorders120184440.120 Why?
Carrier Proteins2201950190.120 Why?
In Situ Hybridization, Fluorescence1202026380.120 Why?
Serine120188280.120 Why?
Hypoxia-Ischemia, Brain120173260.120 Why?
Diarrhea1202113430.120 Why?
Cell Adhesion Molecules1202015990.120 Why?
Limbic Encephalitis12013340.120 Why?
Amino Acid Sequence32021138140.110 Why?
Magnetic Resonance Imaging102020353420.110 Why?
Vigabatrin12013920.110 Why?
DNA Helicases120188610.110 Why?
Glycoproteins1202122600.110 Why?
Disease Management3201824500.110 Why?
Glutamate Decarboxylase120132460.110 Why?
Administration, Oral1202039130.110 Why?
Foot Deformities12012360.110 Why?
Down Syndrome120208800.110 Why?
DNA Copy Number Variations1202119400.110 Why?
Visual Cortex1202011490.110 Why?
Gastroschisis12013970.100 Why?
Chromosome Mapping1202047420.100 Why?
Genome, Human2202244200.100 Why?
Pupil120121490.100 Why?
Metabolic Diseases120186570.100 Why?
Emergency Medicine2201812050.100 Why?
Mitochondrial Proteins120179950.100 Why?
Toes120122070.100 Why?
Paresis120121790.100 Why?
Leukocytosis120122470.100 Why?
Chick Embryo220239810.100 Why?
Drosophila3202314840.090 Why?
Glasgow Coma Scale120125700.090 Why?
Rest120159000.090 Why?
Monitoring, Physiologic1201817370.090 Why?
Amino Acids1201617270.090 Why?
Fatty Acids1201718060.080 Why?
Oxygen1202041690.080 Why?
Intracranial Thrombosis120091130.080 Why?
Gene Expression Regulation32022120710.080 Why?
Adult1420212137120.080 Why?
Animals1220231685610.080 Why?
Deep Brain Stimulation120167460.080 Why?
Anticonvulsants2201819140.080 Why?
Corpus Callosum120127370.080 Why?
Pilot Projects1202082970.070 Why?
Case-Control Studies22015217190.070 Why?
DNA, Mitochondrial120128140.070 Why?
Psychotic Disorders1202230400.070 Why?
Atrophy2202215760.070 Why?
Diffusion Magnetic Resonance Imaging1201827360.070 Why?
Zebrafish3202329900.070 Why?
Neuropsychological Tests1201869740.070 Why?
Proteins2201860960.070 Why?
Attention Deficit Disorder with Hyperactivity1202136490.070 Why?
Antibodies1201324590.060 Why?
Referral and Consultation1201835270.060 Why?
Fatigue1201215260.060 Why?
Siblings220218540.060 Why?
Brain Mapping1202066690.060 Why?
Temporal Lobe1201216690.060 Why?
Genomics1202056920.060 Why?
Cell Nucleus2202329680.060 Why?
Membrane Proteins2202278730.060 Why?
Clinical Protocols1200914590.060 Why?
Anemia1201214990.050 Why?
Dose-Response Relationship, Drug12015109430.050 Why?
Phosphatidylinositol Phosphates120232090.050 Why?
Extracellular Matrix2202017400.050 Why?
Protein-Arginine N-Methyltransferases120221310.050 Why?
Autoimmune Diseases1201321300.050 Why?
Calpain120221500.050 Why?
Phosphoric Monoester Hydrolases120234300.050 Why?
Chromatin2202329170.050 Why?
rhoB GTP-Binding Protein12020160.050 Why?
Ubiquitin-Protein Ligases2202218600.050 Why?
Diagnosis, Differential22016129580.050 Why?
Lower Extremity Deformities, Congenital12020120.050 Why?
Dendritic Spines120222330.050 Why?
Practice Guidelines as Topic1201872760.050 Why?
Cyclin D12020710.050 Why?
Methyltransferases120233670.050 Why?
Genitalia120211110.050 Why?
Recurrence1201283330.050 Why?
DNA Mutational Analysis2202041870.050 Why?
Pentose Phosphate Pathway120201240.050 Why?
Casein Kinase II120201280.050 Why?
Tissue Plasminogen Activator1200612620.050 Why?
Histone Demethylases120223200.050 Why?
Loss of Heterozygosity120226780.050 Why?
Focal Adhesions120201210.050 Why?
Physicians1201845540.040 Why?
Lupus Erythematosus, Systemic1201220990.040 Why?
Codon, Nonsense120202810.040 Why?
Sequence Analysis, DNA2202148010.040 Why?
Polymorphism, Single Nucleotide12018154940.040 Why?
DNA, Complementary1202220490.040 Why?
Frameshift Mutation120203990.040 Why?
Neurites120203800.040 Why?
Class I Phosphatidylinositol 3-Kinases120228900.040 Why?
Germ Cells120226280.040 Why?
Treatment Outcome32020629660.040 Why?
Models, Molecular2201854540.040 Why?
Asparagine120171220.040 Why?
Emergency Medical Services1200919140.040 Why?
Genes, Dominant120208800.040 Why?
Methylation1202011070.040 Why?
Gastric Mucosa120215980.040 Why?
Leigh Disease12018750.040 Why?
Pyridoxal Phosphate120171270.040 Why?
Lysosomes120228930.040 Why?
Algorithms12018138530.040 Why?
Severity of Illness Index12015155300.040 Why?
Microfilament Proteins1202211520.040 Why?
Face120229930.040 Why?
Registries1201280770.040 Why?
Chromatography, Liquid120209770.040 Why?
Sequence Alignment1202122570.040 Why?
RNA Splicing120219070.030 Why?
Longitudinal Studies12012139210.030 Why?
DEAD-box RNA Helicases120193750.030 Why?
Adenosine Triphosphate1202220240.030 Why?
Prospective Studies12020531870.030 Why?
Consanguinity120174560.030 Why?
Proteasome Endopeptidase Complex1202213330.030 Why?
Actins1202321200.030 Why?
Cytoskeleton1202011850.030 Why?
Neuroglia120209250.030 Why?
Basal Ganglia120185450.030 Why?
Valproic Acid120184460.030 Why?
Glutamine120175740.030 Why?
Microscopy, Confocal1202019690.030 Why?
Receptors, GABA-A120196270.030 Why?
Adenosine Triphosphatases120188360.030 Why?
Zebrafish Proteins1202010040.030 Why?
Chromatin Assembly and Disassembly120186280.030 Why?
Germ-Line Mutation1202217860.030 Why?
Organoids120206920.030 Why?
Incidence12012209280.030 Why?
Epilepsies, Partial120184360.030 Why?
Proto-Oncogene Proteins c-akt1202225020.030 Why?
Cohort Studies32022404500.030 Why?
Databases, Genetic1202017800.030 Why?
TOR Serine-Threonine Kinases1202221070.030 Why?
Mass Spectrometry1202022030.030 Why?
RNA-Binding Proteins1202218990.030 Why?
Phosphatidylinositol 3-Kinases1202229380.030 Why?
Protein Processing, Post-Translational1202019890.030 Why?
Abnormalities, Multiple1202014160.030 Why?
Central Nervous System1202013540.030 Why?
Lower Extremity1202011510.030 Why?
Health Services Accessibility1200951330.030 Why?
Chromatography, High Pressure Liquid1201615740.030 Why?
Kinetics1202064740.030 Why?
Early Diagnosis1201711840.030 Why?
Genetic Heterogeneity120157320.030 Why?
Metabolomics1202014670.030 Why?
Oxidation-Reduction1201721870.020 Why?
Drosophila Proteins1202016990.020 Why?
Homeostasis1202233350.020 Why?
Risk Factors22020721450.020 Why?
Cytoskeletal Proteins1201613630.020 Why?
Hotlines12009550.020 Why?
Intestinal Mucosa1202130380.020 Why?
Genetic Testing1202234390.020 Why?
Ambulances12009950.020 Why?
Tomography, X-Ray Computed12012200860.020 Why?
Emergency Medical Technicians120091160.020 Why?
Binding Sites1201761150.020 Why?
Ontario120093810.020 Why?
Transportation of Patients120091850.020 Why?
Interinstitutional Relations120092400.020 Why?
Protein Binding1202093870.020 Why?
Hippocampus1202036610.020 Why?
Nuclear Proteins1202258510.020 Why?
Massachusetts1202086620.020 Why?
Epigenesis, Genetic1202036390.020 Why?
Cell Cycle Proteins1201934440.020 Why?
Signal Transduction22020233870.020 Why?
Hospitals, Community120093480.020 Why?
High-Throughput Nucleotide Sequencing1201935850.020 Why?
Fibroblasts1201741430.020 Why?
Cell Line12021159940.020 Why?
Retina1201726110.020 Why?
Comorbidity12020103720.020 Why?
Cell Differentiation12023114700.020 Why?
RNA, Messenger12021130290.020 Why?
Intracellular Signaling Peptides and Proteins1201629060.020 Why?
Gene Expression1201877900.020 Why?
Adaptor Proteins, Signal Transducing1201629150.020 Why?
Rats12021242650.020 Why?
Disease Progression12021132560.010 Why?
Mice22021810450.010 Why?
Retrospective Studies12012770980.010 Why?
Mice, Inbred C57BL12021218210.010 Why?
Triage120099770.010 Why?
Patient Transfer120097600.010 Why?
Aged, 80 and over12006576830.010 Why?
Neurons1202093250.010 Why?
Transcription Factors12021121640.010 Why?
Obesity12022127050.010 Why?
Follow-Up Studies12021390040.010 Why?
Patient Care Team1200925270.010 Why?
Middle Aged220152131270.010 Why?
Patient Selection1200942140.010 Why?
Hospitals1200939370.010 Why?
Emergency Service, Hospital1200976450.010 Why?
Time Factors12009400540.000 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.