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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 Sclerosis34202414823.950 Why?
Frontotemporal Dementia1320242482.780 Why?
RNA-Binding Protein FUS142023772.510 Why?
Pick Disease of the Brain22024421.080 Why?
Nuclear Envelope220181611.060 Why?
Oligonucleotides, Antisense520234620.970 Why?
Motor Neurons1320248710.960 Why?
DNA Repeat Expansion62020740.870 Why?
DNA-Binding Proteins17202496010.850 Why?
Poly A120221800.810 Why?
Active Transport, Cell Nucleus420234310.810 Why?
Frontotemporal Lobar Degeneration320131020.760 Why?
Genes, Regulator120223730.760 Why?
RNA5201927160.720 Why?
Stathmin42024700.680 Why?
RNA Splicing620249020.600 Why?
Frameshifting, Ribosomal12018150.600 Why?
RNA Precursors520231960.580 Why?
Nuclear Pore12018610.570 Why?
Peptide Chain Initiation, Translational120181000.570 Why?
Guanine Nucleotide Exchange Factors320165720.540 Why?
Neostriatum120172310.510 Why?
RNA-Binding Proteins4201918830.500 Why?
RNA Processing, Post-Transcriptional420193920.470 Why?
Induced Pluripotent Stem Cells3202418840.460 Why?
Cerebellar Ataxia420101500.440 Why?
Neurodegenerative Diseases3201810880.410 Why?
RNA, Messenger92024127750.380 Why?
Disease Models, Animal92023183210.360 Why?
Nerve Degeneration520197480.350 Why?
Ubiquinone220101810.340 Why?
Proteins6201659950.340 Why?
Nervous System Diseases2201916570.330 Why?
Spinocerebellar Degenerations32010440.310 Why?
Abnormalities, Multiple3200914240.300 Why?
Dipeptides220223860.300 Why?
Mutation242023302090.290 Why?
Genes, Recessive220086250.290 Why?
Cytoplasm6202314980.280 Why?
Peptides2201743380.280 Why?
Homozygote7201717740.270 Why?
Axons4202316770.260 Why?
Microsatellite Repeats520187840.250 Why?
Autophagy3201913490.250 Why?
Animals3420241688000.240 Why?
TDP-43 Proteinopathies22023400.230 Why?
Polyadenylation220231140.230 Why?
Monosomy12004520.230 Why?
Pedigree11201745350.220 Why?
Gene Expression Regulation62021119060.210 Why?
Chromosome Inversion120041190.210 Why?
Intermediate Filaments120231710.210 Why?
Infertility, Male220213950.210 Why?
Mice202024818390.210 Why?
Chromosomes, Human, Pair 6120043700.210 Why?
Denervation120232650.200 Why?
Trisomy120042600.200 Why?
Chromosomes, Human, Pair 12120044320.200 Why?
Alzheimer Disease1202487240.200 Why?
Chromosomes, Human, Pair 5120033860.200 Why?
Chromosomes, Human, Pair 18120022470.200 Why?
Seminiferous Epithelium1202190.200 Why?
Meiotic Prophase I1202170.190 Why?
Spermatocytes12021400.190 Why?
Nuclear Pore Complex Proteins120231650.190 Why?
Spermatogenesis220212590.190 Why?
Protein Biosynthesis3201820910.190 Why?
Homeostasis5201933380.180 Why?
Antigen-Antibody Complex120225080.180 Why?
Cerebral Cortex1201757580.180 Why?
Mice, Transgenic10202195400.180 Why?
Protein Interaction Domains and Motifs120234470.180 Why?
Nerve Tissue Proteins4201443990.170 Why?
Ataxia320103070.160 Why?
Oligoribonucleotides, Antisense12019140.160 Why?
RNA Transport12019420.160 Why?
Paraneoplastic Syndromes, Nervous System12019240.160 Why?
RNA, Transfer, Met12018140.150 Why?
Cerebellum2201515190.150 Why?
Aging1201787230.150 Why?
Eukaryotic Initiation Factor-4F12018410.140 Why?
Spinocerebellar Ataxias220101080.140 Why?
Humans5720247661170.140 Why?
Fibroblasts5201541620.140 Why?
RNA, Antisense120181350.140 Why?
Myopathies, Nemaline12017730.140 Why?
Huntington Disease2201411470.140 Why?
Neuromuscular Junction120193990.140 Why?
RNA Stability120193190.140 Why?
Nucleocytoplasmic Transport Proteins12017720.140 Why?
Cell Death2201416760.130 Why?
Spinal Cord5201918110.130 Why?
Prions120181770.130 Why?
Cell Nucleus2201728640.130 Why?
Neural Stem Cells220138970.130 Why?
Family Health4200612530.130 Why?
SMN Complex Proteins12015410.120 Why?
RNA, Small Interfering3201434240.120 Why?
Ribonucleoprotein, U1 Small Nuclear12015360.120 Why?
Ribosomes120184950.120 Why?
Open Reading Frames120188200.120 Why?
GTPase-Activating Proteins120174650.110 Why?
Genetic Linkage3200423420.110 Why?
Receptors, Cytoplasmic and Nuclear120188530.110 Why?
Lysosomes120199320.110 Why?
Chromosome Mapping6201046170.100 Why?
Blotting, Southern120137720.100 Why?
Superoxide Dismutase120155930.100 Why?
Cell Dedifferentiation120131250.100 Why?
Shal Potassium Channels12012200.100 Why?
Gene Knock-In Techniques320214190.100 Why?
Kv Channel-Interacting Proteins12012390.100 Why?
Genotype62013130280.100 Why?
DNA Primers2201328240.100 Why?
Oligonucleotide Array Sequence Analysis2201237960.100 Why?
Troponin T120177850.100 Why?
Neural Cell Adhesion Molecules120121220.100 Why?
Frontal Lobe2201514080.100 Why?
Mice, Inbred C57BL82021223410.100 Why?
Protein Binding5202193010.100 Why?
Membrane Glycoproteins1202336920.100 Why?
HEK293 Cells2201842630.100 Why?
Excitatory Amino Acid Transporter 212012880.090 Why?
Synapses1202117590.090 Why?
Adaptor Proteins, Signal Transducing3201528980.090 Why?
Protein Structure, Tertiary3201537510.090 Why?
Carrier Proteins2201649100.090 Why?
Cell Line, Transformed120128580.090 Why?
Syndrome4200932700.090 Why?
Neurons3201695210.090 Why?
Gene Expression Profiling3201995270.090 Why?
Neurofilament Proteins120123350.090 Why?
Immunoprecipitation120128740.090 Why?
Alternative Splicing2201511030.080 Why?
Neuroglia120159630.080 Why?
Alleles3202168920.080 Why?
Mice, Knockout42023144560.080 Why?
Astrocytes2201513530.080 Why?
Genetic Vectors1201934000.080 Why?
Myotonic Dystrophy12010780.080 Why?
Subcellular Fractions120105280.080 Why?
Membrane Proteins2201978500.080 Why?
Trinucleotide Repeats120102570.080 Why?
Muscular Dystrophies, Limb-Girdle12009620.080 Why?
Frameshift Mutation120103920.080 Why?
Female2920213962330.080 Why?
Trinucleotide Repeat Expansion120102530.080 Why?
Paraplegia120091590.070 Why?
Histone-Lysine N-Methyltransferase120126980.070 Why?
Amino Acid Sequence52017134000.070 Why?
Coenzymes120081010.070 Why?
Brain82016271770.070 Why?
Molecular Chaperones220187600.070 Why?
Molecular Targeted Therapy1201928240.070 Why?
Sequence Analysis, DNA4201747800.070 Why?
In Situ Hybridization, Fluorescence1201325100.070 Why?
Epilepsy, Tonic-Clonic12007540.070 Why?
Male2520213639350.070 Why?
Face2200410290.070 Why?
Phosphotransferases120083020.070 Why?
Yeasts120082780.070 Why?
Cell Cycle Proteins3201534360.070 Why?
Cataract220038370.070 Why?
HeLa Cells4201830730.070 Why?
DNA Mutational Analysis6201041120.070 Why?
Cell Line22018155460.070 Why?
Central Nervous System1201313430.070 Why?
Developmental Disabilities2200615190.060 Why?
Introns220219650.060 Why?
Heat-Shock Proteins220107900.060 Why?
Parkinsonian Disorders120092850.060 Why?
Thymidine Phosphorylase12005160.060 Why?
Sequence Analysis, RNA1201320390.060 Why?
Chromosomes, Human, Pair 16120073400.060 Why?
Ubiquitin-Protein Ligases2201218970.060 Why?
Biological Transport1201020800.060 Why?
Cilia120094980.060 Why?
Pyrophosphatases120051430.060 Why?
Mutant Proteins220194870.060 Why?
Motor Neuron Disease22015980.060 Why?
Microglia1201413710.060 Why?
Molecular Sequence Data42014175970.060 Why?
Base Sequence52017124050.060 Why?
DNA, Mitochondrial220108700.060 Why?
Chromosome Banding120042610.060 Why?
Gene Expression3202375820.050 Why?
Spermatozoa120076270.050 Why?
Lod Score120036000.050 Why?
Muscle Hypotonia120041660.050 Why?
Green Fluorescent Proteins3201820620.050 Why?
Reactive Oxygen Species1201021440.050 Why?
Karyotyping1200411750.050 Why?
tau Proteins1201221100.050 Why?
RNA Splice Sites120232120.050 Why?
Psychomotor Disorders120021490.050 Why?
Myopathies, Structural, Congenital120021040.050 Why?
Genetic Markers2200926030.050 Why?
Antigens, Neoplasm1200919960.050 Why?
Genes, Lethal120212240.050 Why?
Polymorphism, Single Nucleotide52017160400.050 Why?
Genetic Complementation Test120215560.040 Why?
Chromosomes, Human, X120023190.040 Why?
Protein Tyrosine Phosphatases120024570.040 Why?
Genetic Predisposition to Disease22015180760.040 Why?
Intracellular Signaling Peptides and Proteins1201028790.040 Why?
Mitochondrial Proteins120059750.040 Why?
Cells, Cultured42019189670.040 Why?
Motor Cortex2201910040.040 Why?
Muscle, Skeletal5201749590.040 Why?
Nuclear Proteins1201457910.040 Why?
Case-Control Studies12017222280.040 Why?
Aged, 80 and over42017595150.040 Why?
Young Adult52019598680.040 Why?
Oxidative Stress1201031400.040 Why?
Adolescent102017888190.040 Why?
Heterozygote2201527960.040 Why?
Receptors, Cholinergic120192430.040 Why?
Adult1020192231390.040 Why?
Consanguinity220104600.040 Why?
Sequence Alignment2201721740.040 Why?
beta Karyopherins12018460.040 Why?
Homeodomain Proteins1200724300.040 Why?
Transgenes1202110140.040 Why?
Growth Disorders120026330.040 Why?
Karyopherins120181330.040 Why?
TATA-Binding Protein Associated Factors120181030.040 Why?
Neoplasm Proteins1200935940.040 Why?
Reverse Transcriptase Polymerase Chain Reaction2201745650.030 Why?
Brain Diseases1200615520.030 Why?
RNA-Binding Protein EWS120182110.030 Why?
Ubiquitinated Proteins12016320.030 Why?
Cell Differentiation12013116420.030 Why?
Muscle Fibers, Skeletal120195520.030 Why?
Genetic Association Studies2201527440.030 Why?
Child, Preschool52007425110.030 Why?
Transcription Factor TFIIIA12015250.030 Why?
Synaptic Transmission1202111750.030 Why?
Tissue Banks120151830.030 Why?
Inclusion Bodies120162770.030 Why?
Mutation, Missense2201725900.030 Why?
Hippocampus2201837730.030 Why?
Injections, Intraventricular120142270.030 Why?
Chromatography, Affinity120155210.030 Why?
Models, Genetic1200334480.030 Why?
Isotope Labeling120153900.030 Why?
Middle Aged620182230830.030 Why?
Oligodendroglia120175430.030 Why?
Sequence Deletion2201014940.030 Why?
Amino Acid Motifs120159240.020 Why?
Recombinant Proteins1202164930.020 Why?
Models, Biological3201594450.020 Why?
Infant42010364270.020 Why?
Genes1201518240.020 Why?
Atrophy1201616290.020 Why?
Gene Frequency2200936230.020 Why?
Transfection2201057390.020 Why?
Gene Deletion2200926670.020 Why?
Oculomotor Nerve Diseases12010530.020 Why?
Saudi Arabia120102110.020 Why?
Ataxia Telangiectasia120101070.020 Why?
Fluorescent Antibody Technique1201324690.020 Why?
Transcription Factors12009121300.020 Why?
DNA3201071930.020 Why?
Membrane Transport Proteins1201510290.020 Why?
Myeloid Cells120148390.020 Why?
Drosophila melanogaster1201817250.020 Why?
3' Untranslated Regions120115140.020 Why?
Amino Acids1201517100.020 Why?
Structure-Activity Relationship1201430510.020 Why?
Protein Stability120105760.020 Why?
Magnetic Resonance Imaging42009365480.020 Why?
Ubiquitination1201310000.020 Why?
Behavior, Animal1201618670.020 Why?
France120094950.020 Why?
Diagnosis, Differential12002129760.020 Why?
Immunoblotting1201016440.020 Why?
Motor Activity1201727110.020 Why?
Polymerase Chain Reaction2200960590.020 Why?
Arabs120091900.020 Why?
Phenotype22021167160.020 Why?
Child52010805730.020 Why?
Cell Communication1201316600.020 Why?
Vacuoles120072240.020 Why?
Cell Culture Techniques1201316510.020 Why?
Aged520181712190.020 Why?
Inorganic Pyrophosphatase1200530.020 Why?
Genetic Testing2200935940.020 Why?
Calcium Chloride12005780.020 Why?
Deoxyuridine12005340.020 Why?
Quadriceps Muscle120071560.020 Why?
Diphosphates12005910.020 Why?
Mitochondrial Myopathies12005490.020 Why?
Mitochondrial Encephalomyopathies12005400.020 Why?
RNA Interference1201428280.020 Why?
Thymidine120052940.020 Why?
Genetic Variation2201566120.020 Why?
Analysis of Variance1201362080.020 Why?
Point Mutation1201015910.020 Why?
Protein Sorting Signals120052730.010 Why?
Vesicular Transport Proteins120073760.010 Why?
Chromosomes, Human, Pair 4120053780.010 Why?
Hydrolysis120056430.010 Why?
Adaptor Proteins, Vesicular Transport120062990.010 Why?
Finland120056080.010 Why?
Promoter Regions, Genetic1201557840.010 Why?
Blotting, Northern1200515460.010 Why?
Cytoskeletal Proteins1200913220.010 Why?
Microscopy, Electron1200725430.010 Why?
Age of Onset1201033440.010 Why?
Risk Factors12010748570.010 Why?
Microscopy, Fluorescence1201026270.010 Why?
Chromosome Disorders120064980.010 Why?
Lipids1201433160.010 Why?
Risk1201595990.010 Why?
Survival Analysis12015100870.010 Why?
Polymorphism, Single-Stranded Conformational120023250.010 Why?
Protein Tyrosine Phosphatases, Non-Receptor12002690.010 Why?
High-Throughput Nucleotide Sequencing1201536650.010 Why?
Disease Progression12019136160.010 Why?
DNA, Complementary1200519840.010 Why?
Fetus1200918780.010 Why?
Protein Folding120058680.010 Why?
Binding Sites1201060010.010 Why?
Sequence Homology, Amino Acid1200527430.010 Why?
Cognition Disorders1201539660.010 Why?
Haplotypes1200727260.010 Why?
Proteomics1201539070.010 Why?
Gene Expression Regulation, Enzymologic1200511670.010 Why?
Isoenzymes1200516880.010 Why?
Brain Stem120068520.010 Why?
Cloning, Molecular1200541630.010 Why?
Family1201032080.010 Why?
Energy Metabolism1201028940.010 Why?
Recombinant Fusion Proteins1200537330.010 Why?
Exons1200223930.010 Why?
Pregnancy12018302330.010 Why?
Models, Molecular1200653820.010 Why?
Polymorphism, Genetic1200642490.010 Why?
Biopsy1200767680.010 Why?
Genome-Wide Association Study12014128030.010 Why?
Inflammation12014108600.010 Why?
Cohort Studies12015416840.010 Why?
Electroencephalography1200762790.010 Why?
Kidney1200570720.010 Why?
Cell Line, Tumor12005170710.000 Why?
Infant, Newborn12002263810.000 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.