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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.
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Timeline
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In this concept 'cloud', the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
3' Untranslated Regions
Abnormalities, Multiple
Active Transport, Cell Nucleus
Adaptor Proteins, Signal Transducing
Adaptor Proteins, Vesicular Transport
Adolescent
Adult
Age of Onset
Aged
Aged, 80 and over
Aging
Alleles
Alternative Splicing
Alzheimer Disease
Amino Acid Motifs
Amino Acid Sequence
Amino Acids
Amyotrophic Lateral Sclerosis
Analysis of Variance
Animals
Antigen-Antibody Complex
Antigens, Neoplasm
Arabs
Astrocytes
Ataxia
Ataxia Telangiectasia
Atrophy
Autophagy
Axons
Base Sequence
Behavior, Animal
beta Karyopherins
Binding Sites
Biological Transport
Biopsy
Blotting, Northern
Blotting, Southern
Brain
Brain Diseases
Brain Stem
Calcium Chloride
Carrier Proteins
Case-Control Studies
Cataract
Cell Communication
Cell Culture Techniques
Cell Cycle Proteins
Cell Death
Cell Dedifferentiation
Cell Differentiation
Cell Line
Cell Line, Transformed
Cell Line, Tumor
Cell Nucleus
Cells, Cultured
Central Nervous System
Cerebellar Ataxia
Cerebellum
Cerebral Cortex
Child
Child, Preschool
Chromatography, Affinity
Chromosome Banding
Chromosome Disorders
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, X
Cilia
Cloning, Molecular
Coenzymes
Cognition Disorders
Cohort Studies
Consanguinity
Cytoplasm
Cytoskeletal Proteins
Denervation
Deoxyuridine
Developmental Disabilities
Diagnosis, Differential
Dipeptides
Diphosphates
Disease Models, Animal
Disease Progression
DNA
DNA Mutational Analysis
DNA Primers
DNA Repeat Expansion
DNA, Complementary
DNA, Mitochondrial
DNA-Binding Proteins
Drosophila melanogaster
Electroencephalography
Energy Metabolism
Epilepsy, Tonic-Clonic
Eukaryotic Initiation Factor-4F
Excitatory Amino Acid Transporter 2
Exons
Face
Family
Family Health
Female
Fetus
Fibroblasts
Finland
Fluorescent Antibody Technique
Frameshift Mutation
Frameshifting, Ribosomal
France
Frontal Lobe
Frontotemporal Dementia
Frontotemporal Lobar Degeneration
Gene Deletion
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Enzymologic
Gene Frequency
Gene Knock-In Techniques
Genes
Genes, Lethal
Genes, Recessive
Genes, Regulator
Genetic Association Studies
Genetic Complementation Test
Genetic Linkage
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetic Vectors
Genome-Wide Association Study
Genotype
Green Fluorescent Proteins
Growth Disorders
GTPase-Activating Proteins
Guanine Nucleotide Exchange Factors
Haplotypes
Heat-Shock Proteins
HEK293 Cells
HeLa Cells
Heterozygote
High-Throughput Nucleotide Sequencing
Hippocampus
Histone-Lysine N-Methyltransferase
Homeodomain Proteins
Homeostasis
Homozygote
Humans
Huntington Disease
Hydrolysis
Immunoblotting
Immunoprecipitation
In Situ Hybridization, Fluorescence
Inclusion Bodies
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Infertility, Male
Inflammation
Injections, Intraventricular
Inorganic Pyrophosphatase
Intermediate Filaments
Intracellular Signaling Peptides and Proteins
Introns
Isoenzymes
Isotope Labeling
Karyopherins
Karyotyping
Kidney
Kv Channel-Interacting Proteins
Lipids
Lod Score
Lysosomes
Magnetic Resonance Imaging
Male
Meiotic Prophase I
Membrane Glycoproteins
Membrane Proteins
Membrane Transport Proteins
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Transgenic
Microglia
Microsatellite Repeats
Microscopy, Electron
Microscopy, Fluorescence
Middle Aged
Mitochondrial Encephalomyopathies
Mitochondrial Myopathies
Mitochondrial Proteins
Models, Biological
Models, Genetic
Models, Molecular
Molecular Chaperones
Molecular Sequence Data
Molecular Targeted Therapy
Monosomy
Motor Activity
Motor Cortex
Motor Neuron Disease
Motor Neurons
Muscle Fibers, Skeletal
Muscle Hypotonia
Muscle, Skeletal
Muscular Dystrophies, Limb-Girdle
Mutant Proteins
Mutation
Mutation, Missense
Myeloid Cells
Myopathies, Nemaline
Myopathies, Structural, Congenital
Myotonic Dystrophy
Neoplasm Proteins
Neostriatum
Nerve Degeneration
Nerve Tissue Proteins
Nervous System Diseases
Neural Cell Adhesion Molecules
Neural Stem Cells
Neurodegenerative Diseases
Neurofilament Proteins
Neuroglia
Neuromuscular Junction
Neurons
Nuclear Envelope
Nuclear Pore
Nuclear Pore Complex Proteins
Nuclear Proteins
Nucleocytoplasmic Transport Proteins
Oculomotor Nerve Diseases
Oligodendroglia
Oligonucleotide Array Sequence Analysis
Oligonucleotides, Antisense
Oligoribonucleotides, Antisense
Open Reading Frames
Oxidative Stress
Paraneoplastic Syndromes, Nervous System
Paraplegia
Parkinsonian Disorders
Pedigree
Peptide Chain Initiation, Translational
Peptides
Phenotype
Phosphotransferases
Pick Disease of the Brain
Point Mutation
Poly A
Polyadenylation
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Polymorphism, Single-Stranded Conformational
Pregnancy
Prions
Promoter Regions, Genetic
Protein Binding
Protein Biosynthesis
Protein Folding
Protein Interaction Domains and Motifs
Protein Sorting Signals
Protein Stability
Protein Structure, Tertiary
Protein Tyrosine Phosphatases
Protein Tyrosine Phosphatases, Non-Receptor
Proteins
Proteomics
Psychomotor Disorders
Pyrophosphatases
Quadriceps Muscle
Reactive Oxygen Species
Receptors, Cholinergic
Receptors, Cytoplasmic and Nuclear
Recombinant Fusion Proteins
Recombinant Proteins
Reverse Transcriptase Polymerase Chain Reaction
Ribonucleoprotein, U1 Small Nuclear
Ribosomes
Risk
Risk Factors
RNA
RNA Interference
RNA Precursors
RNA Processing, Post-Transcriptional
RNA Splice Sites
RNA Splicing
RNA Stability
RNA Transport
RNA, Antisense
RNA, Messenger
RNA, Small Interfering
RNA, Transfer, Met
RNA-Binding Protein EWS
RNA-Binding Protein FUS
RNA-Binding Proteins
Saudi Arabia
Seminiferous Epithelium
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology, Amino Acid
Shal Potassium Channels
SMN Complex Proteins
Spermatocytes
Spermatogenesis
Spermatozoa
Spinal Cord
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Stathmin
Structure-Activity Relationship
Subcellular Fractions
Superoxide Dismutase
Survival Analysis
Synapses
Synaptic Transmission
Syndrome
TATA-Binding Protein Associated Factors
tau Proteins
TDP-43 Proteinopathies
Thymidine
Thymidine Phosphorylase
Tissue Banks
Transcription Factor TFIIIA
Transcription Factors
Transfection
Transgenes
Trinucleotide Repeat Expansion
Trinucleotide Repeats
Trisomy
Troponin T
Ubiquinone
Ubiquitinated Proteins
Ubiquitination
Ubiquitin-Protein Ligases
Vacuoles
Vesicular Transport Proteins
Yeasts
Young Adult
Lagier-Tourenne's Networks
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Concepts (346)
Derived automatically from this person's publications.
Nuclear Envelope
Frontotemporal Dementia
Pick Disease of the Brain
RNA-Binding Protein FUS
Amyotrophic Lateral Sclerosis
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_
Co-Authors (26)
People in Profiles who have published with this person.
Marques, Christine
Held, Aaron
Wainger, Brian
Hyman, Bradley
Oakley, Derek
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_
Similar People (60)
People who share similar concepts with this person.
Cudkowicz, Merit
Rutkove, Seward
Berry, James
Paganoni, Sabrina
Weisskopf, Marc
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_
Same Department
People in same department with this person.
Geffrey, Alexandra
Kwak, Sang
Tan, Yong Qiang Benjamin
Waite, Shelley
Yadav, Rachita
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_