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Clotilde Delphine Lagier-Tourenne, M.D., Ph.D.

Concepts (346)

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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?
Amyotrophic Lateral Sclerosis34202414813.970 Why?
Frontotemporal Dementia1320242492.800 Why?
RNA-Binding Protein FUS142023772.530 Why?
Pick Disease of the Brain22024421.090 Why?
Nuclear Envelope220181631.060 Why?
Oligonucleotides, Antisense520234620.970 Why?
Motor Neurons1320248700.970 Why?
DNA Repeat Expansion62020740.880 Why?
DNA-Binding Proteins17202496150.850 Why?
Poly A120221800.820 Why?
Active Transport, Cell Nucleus420234320.820 Why?
Frontotemporal Lobar Degeneration320131020.770 Why?
Genes, Regulator120223730.770 Why?
RNA5201927200.730 Why?
Stathmin42024700.690 Why?
RNA Splicing620249050.600 Why?
Frameshifting, Ribosomal12018150.600 Why?
RNA Precursors520231960.580 Why?
Nuclear Pore12018620.580 Why?
Peptide Chain Initiation, Translational120181000.570 Why?
Guanine Nucleotide Exchange Factors320165720.550 Why?
Neostriatum120172360.510 Why?
RNA-Binding Proteins4201918900.500 Why?
RNA Processing, Post-Transcriptional420193930.470 Why?
Induced Pluripotent Stem Cells3202418870.460 Why?
Cerebellar Ataxia420101510.450 Why?
Neurodegenerative Diseases3201810950.410 Why?
RNA, Messenger92024128000.380 Why?
Disease Models, Animal92023183490.360 Why?
Nerve Degeneration520197490.350 Why?
Ubiquinone220101810.350 Why?
Proteins6201660090.340 Why?
Nervous System Diseases2201916620.330 Why?
Spinocerebellar Degenerations32010440.310 Why?
Dipeptides220223860.310 Why?
Abnormalities, Multiple3200914240.310 Why?
Mutation242023302380.290 Why?
Genes, Recessive220086250.290 Why?
Cytoplasm6202315050.280 Why?
Peptides2201743540.280 Why?
Homozygote7201717790.280 Why?
Axons4202316770.260 Why?
Microsatellite Repeats520187850.250 Why?
Autophagy3201913490.250 Why?
Animals3420241692460.240 Why?
TDP-43 Proteinopathies22023400.230 Why?
Polyadenylation220231140.230 Why?
Monosomy12004520.230 Why?
Pedigree11201745390.220 Why?
Chromosome Inversion120041190.220 Why?
Gene Expression Regulation62021119280.220 Why?
Intermediate Filaments120231710.210 Why?
Infertility, Male220213970.210 Why?
Mice202024820290.210 Why?
Chromosomes, Human, Pair 6120043700.210 Why?
Denervation120232650.210 Why?
Trisomy120042600.200 Why?
Chromosomes, Human, Pair 12120044320.200 Why?
Alzheimer Disease1202487590.200 Why?
Chromosomes, Human, Pair 5120033870.200 Why?
Chromosomes, Human, Pair 18120022470.200 Why?
Seminiferous Epithelium1202190.200 Why?
Meiotic Prophase I1202170.200 Why?
Spermatocytes12021400.190 Why?
Nuclear Pore Complex Proteins120231650.190 Why?
Spermatogenesis220212600.190 Why?
Protein Biosynthesis3201820940.190 Why?
Homeostasis5201933480.180 Why?
Antigen-Antibody Complex120225130.180 Why?
Mice, Transgenic10202195610.180 Why?
Cerebral Cortex1201758120.180 Why?
Protein Interaction Domains and Motifs120234510.180 Why?
Nerve Tissue Proteins4201444130.170 Why?
Ataxia320103070.170 Why?
Oligoribonucleotides, Antisense12019140.170 Why?
RNA Transport12019420.160 Why?
Paraneoplastic Syndromes, Nervous System12019240.160 Why?
RNA, Transfer, Met12018140.150 Why?
Cerebellum2201515220.150 Why?
Aging1201787440.150 Why?
Eukaryotic Initiation Factor-4F12018410.150 Why?
Spinocerebellar Ataxias220101080.150 Why?
Humans5720247681660.140 Why?
Fibroblasts5201541760.140 Why?
RNA, Antisense120181360.140 Why?
Myopathies, Nemaline12017730.140 Why?
Huntington Disease2201411470.140 Why?
RNA Stability120193190.140 Why?
Neuromuscular Junction120194070.140 Why?
Nucleocytoplasmic Transport Proteins12017730.140 Why?
Cell Death2201416790.140 Why?
Spinal Cord5201918110.130 Why?
Prions120181770.130 Why?
Cell Nucleus2201728850.130 Why?
Neural Stem Cells220138950.130 Why?
Family Health4200612550.130 Why?
SMN Complex Proteins12015410.120 Why?
Ribonucleoprotein, U1 Small Nuclear12015360.120 Why?
RNA, Small Interfering3201434280.120 Why?
Ribosomes120184970.120 Why?
Open Reading Frames120188180.120 Why?
GTPase-Activating Proteins120174670.110 Why?
Genetic Linkage3200423420.110 Why?
Receptors, Cytoplasmic and Nuclear120188590.110 Why?
Lysosomes120199380.110 Why?
Blotting, Southern120137750.110 Why?
Chromosome Mapping6201046200.110 Why?
Cell Dedifferentiation120131250.110 Why?
Superoxide Dismutase120155960.110 Why?
Shal Potassium Channels12012200.100 Why?
Gene Knock-In Techniques320214220.100 Why?
Kv Channel-Interacting Proteins12012390.100 Why?
Genotype62013130450.100 Why?
DNA Primers2201328280.100 Why?
Oligonucleotide Array Sequence Analysis2201238000.100 Why?
Troponin T120177870.100 Why?
Neural Cell Adhesion Molecules120121220.100 Why?
Frontal Lobe2201514260.100 Why?
Mice, Inbred C57BL82021223790.100 Why?
Protein Binding5202193430.100 Why?
Membrane Glycoproteins1202337110.100 Why?
HEK293 Cells2201842830.100 Why?
Excitatory Amino Acid Transporter 212012890.100 Why?
Synapses1202117650.090 Why?
Adaptor Proteins, Signal Transducing3201529090.090 Why?
Protein Structure, Tertiary3201537720.090 Why?
Cell Line, Transformed120128660.090 Why?
Carrier Proteins2201649370.090 Why?
Syndrome4200932720.090 Why?
Neurons3201695140.090 Why?
Gene Expression Profiling3201995380.090 Why?
Neurofilament Proteins120123360.090 Why?
Immunoprecipitation120128740.090 Why?
Alternative Splicing2201511050.080 Why?
Neuroglia120159600.080 Why?
Alleles3202168940.080 Why?
Mice, Knockout42023144880.080 Why?
Astrocytes2201513500.080 Why?
Myotonic Dystrophy12010800.080 Why?
Genetic Vectors1201934020.080 Why?
Subcellular Fractions120105250.080 Why?
Membrane Proteins2201978760.080 Why?
Trinucleotide Repeats120102570.080 Why?
Muscular Dystrophies, Limb-Girdle12009620.080 Why?
Frameshift Mutation120103920.080 Why?
Female2920213971920.080 Why?
Trinucleotide Repeat Expansion120102540.080 Why?
Paraplegia120091610.080 Why?
Histone-Lysine N-Methyltransferase120127010.070 Why?
Amino Acid Sequence52017134210.070 Why?
Coenzymes120081010.070 Why?
Molecular Chaperones220187620.070 Why?
Brain82016273600.070 Why?
Molecular Targeted Therapy1201928300.070 Why?
Sequence Analysis, DNA4201747860.070 Why?
In Situ Hybridization, Fluorescence1201325210.070 Why?
Epilepsy, Tonic-Clonic12007540.070 Why?
Face2200410290.070 Why?
Male2520213647190.070 Why?
Phosphotransferases120083020.070 Why?
Yeasts120082790.070 Why?
Cataract220038370.070 Why?
Cell Cycle Proteins3201534450.070 Why?
HeLa Cells4201830740.070 Why?
DNA Mutational Analysis6201041200.070 Why?
Cell Line22018155970.070 Why?
Central Nervous System1201313460.070 Why?
Developmental Disabilities2200615180.070 Why?
Introns220219660.060 Why?
Heat-Shock Proteins220107970.060 Why?
Thymidine Phosphorylase12005160.060 Why?
Parkinsonian Disorders120092850.060 Why?
Sequence Analysis, RNA1201320400.060 Why?
Chromosomes, Human, Pair 16120073410.060 Why?
Biological Transport1201020850.060 Why?
Ubiquitin-Protein Ligases2201219010.060 Why?
Cilia120094980.060 Why?
Pyrophosphatases120051420.060 Why?
Mutant Proteins220194880.060 Why?
Motor Neuron Disease22015980.060 Why?
Microglia1201413760.060 Why?
Molecular Sequence Data42014176220.060 Why?
Base Sequence52017124210.060 Why?
DNA, Mitochondrial220108720.060 Why?
Chromosome Banding120042610.060 Why?
Gene Expression3202375980.050 Why?
Spermatozoa120076320.050 Why?
Lod Score120036000.050 Why?
Muscle Hypotonia120041660.050 Why?
Green Fluorescent Proteins3201820650.050 Why?
Reactive Oxygen Species1201021490.050 Why?
Karyotyping1200411770.050 Why?
Psychomotor Disorders120021490.050 Why?
Myopathies, Structural, Congenital120021040.050 Why?
RNA Splice Sites120232130.050 Why?
tau Proteins1201221440.050 Why?
Genetic Markers2200926030.050 Why?
Antigens, Neoplasm1200919970.050 Why?
Genes, Lethal120212240.050 Why?
Polymorphism, Single Nucleotide52017160450.050 Why?
Genetic Complementation Test120215570.040 Why?
Chromosomes, Human, X120023200.040 Why?
Protein Tyrosine Phosphatases120024580.040 Why?
Genetic Predisposition to Disease22015180650.040 Why?
Intracellular Signaling Peptides and Proteins1201028920.040 Why?
Mitochondrial Proteins120059790.040 Why?
Cells, Cultured42019190150.040 Why?
Muscle, Skeletal5201749780.040 Why?
Motor Cortex2201910130.040 Why?
Nuclear Proteins1201458040.040 Why?
Case-Control Studies12017222910.040 Why?
Aged, 80 and over42017596290.040 Why?
Young Adult52019600660.040 Why?
Oxidative Stress1201031390.040 Why?
Adolescent102017891690.040 Why?
Heterozygote2201527980.040 Why?
Receptors, Cholinergic120192440.040 Why?
Adult1020192236460.040 Why?
Consanguinity220104600.040 Why?
Sequence Alignment2201721790.040 Why?
beta Karyopherins12018460.040 Why?
Homeodomain Proteins1200724290.040 Why?
Transgenes1202110160.040 Why?
Growth Disorders120026350.040 Why?
Karyopherins120181340.040 Why?
TATA-Binding Protein Associated Factors120181030.040 Why?
Neoplasm Proteins1200936030.040 Why?
Reverse Transcriptase Polymerase Chain Reaction2201745800.030 Why?
Brain Diseases1200615540.030 Why?
RNA-Binding Protein EWS120182110.030 Why?
Ubiquitinated Proteins12016320.030 Why?
Muscle Fibers, Skeletal120195530.030 Why?
Cell Differentiation12013116690.030 Why?
Genetic Association Studies2201527440.030 Why?
Child, Preschool52007426690.030 Why?
Transcription Factor TFIIIA12015240.030 Why?
Synaptic Transmission1202111770.030 Why?
Tissue Banks120151830.030 Why?
Inclusion Bodies120162780.030 Why?
Mutation, Missense2201725920.030 Why?
Hippocampus2201837850.030 Why?
Injections, Intraventricular120142270.030 Why?
Chromatography, Affinity120155250.030 Why?
Models, Genetic1200334470.030 Why?
Isotope Labeling120153940.030 Why?
Middle Aged620182234920.030 Why?
Oligodendroglia120175400.030 Why?
Sequence Deletion2201014970.030 Why?
Amino Acid Motifs120159300.030 Why?
Recombinant Proteins1202165140.020 Why?
Models, Biological3201594950.020 Why?
Genes1201518240.020 Why?
Infant42010365350.020 Why?
Atrophy1201616460.020 Why?
Gene Frequency2200936230.020 Why?
Transfection2201057550.020 Why?
Gene Deletion2200926750.020 Why?
Oculomotor Nerve Diseases12010530.020 Why?
Saudi Arabia120102120.020 Why?
Ataxia Telangiectasia120101070.020 Why?
Fluorescent Antibody Technique1201324740.020 Why?
Transcription Factors12009121680.020 Why?
DNA3201072140.020 Why?
Membrane Transport Proteins1201510370.020 Why?
Myeloid Cells120148390.020 Why?
Drosophila melanogaster1201817260.020 Why?
3' Untranslated Regions120115150.020 Why?
Amino Acids1201517160.020 Why?
Structure-Activity Relationship1201430550.020 Why?
Protein Stability120105800.020 Why?
Magnetic Resonance Imaging42009367430.020 Why?
Ubiquitination1201310090.020 Why?
Behavior, Animal1201618620.020 Why?
France120094970.020 Why?
Diagnosis, Differential12002130140.020 Why?
Immunoblotting1201016470.020 Why?
Motor Activity1201727110.020 Why?
Arabs120091900.020 Why?
Polymerase Chain Reaction2200960820.020 Why?
Phenotype22021167260.020 Why?
Cell Communication1201316600.020 Why?
Vacuoles120072240.020 Why?
Child52010809170.020 Why?
Inorganic Pyrophosphatase1200530.020 Why?
Aged520181715040.020 Why?
Cell Culture Techniques1201316670.020 Why?
Genetic Testing2200935910.020 Why?
Calcium Chloride12005790.020 Why?
Deoxyuridine12005340.020 Why?
Quadriceps Muscle120071570.020 Why?
Diphosphates12005890.020 Why?
Mitochondrial Myopathies12005500.020 Why?
Mitochondrial Encephalomyopathies12005400.020 Why?
RNA Interference1201428320.020 Why?
Thymidine120052970.020 Why?
Genetic Variation2201566110.020 Why?
Analysis of Variance1201362290.020 Why?
Point Mutation1201015960.020 Why?
Protein Sorting Signals120052740.020 Why?
Vesicular Transport Proteins120073770.010 Why?
Chromosomes, Human, Pair 4120053780.010 Why?
Hydrolysis120056460.010 Why?
Adaptor Proteins, Vesicular Transport120063010.010 Why?
Finland120056090.010 Why?
Promoter Regions, Genetic1201557970.010 Why?
Blotting, Northern1200515500.010 Why?
Cytoskeletal Proteins1200913270.010 Why?
Microscopy, Electron1200725600.010 Why?
Age of Onset1201033470.010 Why?
Risk Factors12010749440.010 Why?
Microscopy, Fluorescence1201026330.010 Why?
Chromosome Disorders120064980.010 Why?
Lipids1201433430.010 Why?
Risk1201596130.010 Why?
Survival Analysis12015101010.010 Why?
Polymorphism, Single-Stranded Conformational120023250.010 Why?
Protein Tyrosine Phosphatases, Non-Receptor12002690.010 Why?
High-Throughput Nucleotide Sequencing1201536710.010 Why?
Disease Progression12019136710.010 Why?
DNA, Complementary1200519890.010 Why?
Fetus1200918830.010 Why?
Protein Folding120058710.010 Why?
Binding Sites1201060200.010 Why?
Sequence Homology, Amino Acid1200527480.010 Why?
Cognition Disorders1201539800.010 Why?
Haplotypes1200727220.010 Why?
Proteomics1201539120.010 Why?
Gene Expression Regulation, Enzymologic1200511690.010 Why?
Isoenzymes1200516880.010 Why?
Brain Stem120068590.010 Why?
Cloning, Molecular1200541680.010 Why?
Family1201032090.010 Why?
Energy Metabolism1201029070.010 Why?
Recombinant Fusion Proteins1200537400.010 Why?
Exons1200223940.010 Why?
Pregnancy12018302560.010 Why?
Models, Molecular1200654030.010 Why?
Polymorphism, Genetic1200642490.010 Why?
Biopsy1200767930.010 Why?
Genome-Wide Association Study12014127950.010 Why?
Inflammation12014108730.010 Why?
Cohort Studies12015417540.010 Why?
Electroencephalography1200763140.010 Why?
Kidney1200570640.010 Why?
Cell Line, Tumor12005171400.000 Why?
Infant, Newborn12002264220.000 Why?
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© 2025 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.