Harvard Catalyst Profiles

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Christelle Moufawad El Achkar, M.D.

Concepts (119)

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?
Epilepsy10202332900.990 Why?
Calcium Channels, R-Type12018150.640 Why?
Dyskinesias12018790.600 Why?
Developmental Disabilities4202115090.570 Why?
Contracture120182350.520 Why?
Cation Transport Proteins120183270.520 Why?
Genetic Variation5202065670.480 Why?
Spasms, Infantile120182980.480 Why?
Epilepsy, Generalized420201780.440 Why?
Ataxia220203060.440 Why?
Ocular Motility Disorders120141440.420 Why?
Genetic Diseases, X-Linked120143860.360 Why?
Microcephaly120144250.350 Why?
Receptors, GABA-A320226230.320 Why?
Lissencephaly12016360.270 Why?
PTEN Phosphohydrolase1202011150.240 Why?
Seizures4202329570.240 Why?
Nerve Tissue Proteins2202144140.210 Why?
Cadherins120189030.210 Why?
Tubulin120166930.210 Why?
Intranuclear Space12021150.190 Why?
Child, Preschool132021422300.180 Why?
Neuronal Ceroid-Lipofuscinoses120191340.160 Why?
Mutation62022300520.160 Why?
Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor12017110.150 Why?
Aspartate-Ammonia Ligase12017180.150 Why?
Excitatory Amino Acid Transporter 212019890.150 Why?
Glomerulosclerosis, Focal Segmental120213350.140 Why?
Facies120182220.140 Why?
Movement Disorders120204590.140 Why?
Mutagenesis, Insertional120196560.140 Why?
Nephrotic Syndrome120213900.140 Why?
Oligonucleotides, Antisense120194610.140 Why?
Cerebellar Diseases120182200.130 Why?
Infant82020361920.130 Why?
Vesicular Transport Proteins120183760.120 Why?
Amino Acid Metabolism, Inborn Errors120172830.120 Why?
Phenotype72022165910.120 Why?
Receptors, N-Methyl-D-Aspartate120198940.120 Why?
Rare Diseases120196220.110 Why?
Membrane Transport Proteins1201910350.110 Why?
Child112021801530.110 Why?
Mutation, Missense2202025710.100 Why?
Quinidine12020520.090 Why?
Electroencephalography3202062250.080 Why?
Adolescent62020883190.070 Why?
Carrier Proteins1202149360.070 Why?
Male1520233608040.070 Why?
Syndrome2202232670.060 Why?
Channelopathies12015300.060 Why?
Autistic Disorder1201412200.060 Why?
Regression Analysis1201463430.060 Why?
Female1420233926440.060 Why?
Genotype22020129900.060 Why?
Humans2020237615040.060 Why?
Databases, Genetic1202017420.060 Why?
Young Adult52020592430.050 Why?
Age of Onset2202033050.050 Why?
Athetosis12020150.050 Why?
Genetic Counseling120156270.050 Why?
Neuropsychological Tests2201970450.050 Why?
Cohort Studies42023414870.040 Why?
Chorea12020790.040 Why?
Pedigree1201845420.040 Why?
HEK293 Cells2201942780.040 Why?
Anticonvulsants1202019060.040 Why?
Brain32020271120.040 Why?
Genetic Testing2202035370.040 Why?
Codon, Nonsense120212850.040 Why?
Patch-Clamp Techniques120209270.040 Why?
Ceftriaxone120191750.040 Why?
Chromosomes, Human120204410.040 Why?
Asparagine120171190.040 Why?
Adult620212211770.040 Why?
Amino Acid Sequence22019134460.040 Why?
Drugs, Investigational120192120.040 Why?
Massachusetts1202088300.040 Why?
Disease Progression12014135060.040 Why?
Dystonia120203700.040 Why?
Microarray Analysis120207490.030 Why?
Xenopus laevis120209630.030 Why?
Podocytes120214050.030 Why?
Animals620221684590.030 Why?
Protein Structure, Secondary1201912290.030 Why?
Polymorphism, Single Nucleotide22020159360.030 Why?
Comorbidity12020105080.030 Why?
Consanguinity120174560.030 Why?
Oocytes1202011660.030 Why?
gamma-Aminobutyric Acid1202211410.030 Why?
Magnetic Resonance Imaging22020364260.030 Why?
Glutamine120175770.030 Why?
Arginine120179340.030 Why?
Glutamic Acid1201911760.030 Why?
Siblings120178250.030 Why?
Synaptic Transmission1201911730.030 Why?
Homozygote1201717760.030 Why?
Registries1201882240.020 Why?
Drug Discovery1201910510.020 Why?
Heterozygote1201827870.020 Why?
Brain Diseases1202015450.020 Why?
DNA Mutational Analysis1201741110.020 Why?
Binding Sites1201760550.020 Why?
Rats, Sprague-Dawley1201981810.020 Why?
Infant, Newborn22019261980.020 Why?
Child Development1201923060.020 Why?
Biopsy1201967660.020 Why?
Models, Molecular1201754390.020 Why?
Fibroblasts1201741410.020 Why?
Cell Line12021156010.020 Why?
Skin1201944840.020 Why?
Kidney1202170480.020 Why?
Genetic Predisposition to Disease12016179040.010 Why?
RNA, Messenger12019127950.010 Why?
Mice22022815250.010 Why?
Rats12019237420.010 Why?
Gene Expression Regulation12019119030.010 Why?
Neurons1201994630.010 Why?
Retrospective Studies12018806360.010 Why?
Middle Aged120202208950.000 Why?
Moufawad El Achkar's Networks
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Concepts (119)
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Co-Authors (51)
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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.