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Christelle Moufawad El Achkar, M.D.

Concepts (119)

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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?
Epilepsy10202333101.020 Why?
Calcium Channels, R-Type12018140.670 Why?
Dyskinesias12018780.630 Why?
Developmental Disabilities4202114560.600 Why?
Contracture120182240.550 Why?
Cation Transport Proteins120183270.540 Why?
Genetic Variation5202065420.500 Why?
Spasms, Infantile120183050.500 Why?
Epilepsy, Generalized420201740.470 Why?
Ataxia220203040.460 Why?
Ocular Motility Disorders120141350.450 Why?
Genetic Diseases, X-Linked120143720.370 Why?
Microcephaly120144320.360 Why?
Receptors, GABA-A320226270.330 Why?
Lissencephaly12016380.290 Why?
Seizures4202328590.250 Why?
PTEN Phosphohydrolase1202011420.250 Why?
Cadherins120189070.220 Why?
Nerve Tissue Proteins2202144630.220 Why?
Tubulin120166950.220 Why?
Intranuclear Space12021150.200 Why?
Child, Preschool132021410050.190 Why?
Excitatory Amino Acid Transporter 212019770.160 Why?
Mutation62022297860.160 Why?
Neuronal Ceroid-Lipofuscinoses120191420.160 Why?
Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor12017100.160 Why?
Aspartate-Ammonia Ligase12017160.160 Why?
Facies120181970.150 Why?
Glomerulosclerosis, Focal Segmental120213570.150 Why?
Oligonucleotides, Antisense120194330.150 Why?
Movement Disorders120204460.150 Why?
Nephrotic Syndrome120213890.140 Why?
Mutagenesis, Insertional120196550.140 Why?
Infant82020351340.130 Why?
Cerebellar Diseases120182260.130 Why?
Amino Acid Metabolism, Inborn Errors120172550.130 Why?
Vesicular Transport Proteins120183770.130 Why?
Phenotype72022163670.120 Why?
Rare Diseases120195530.120 Why?
Receptors, N-Methyl-D-Aspartate120198960.120 Why?
Membrane Transport Proteins1201910310.120 Why?
Child112021777090.110 Why?
Mutation, Missense2202025660.110 Why?
Quinidine12020570.090 Why?
Electroencephalography3202061510.090 Why?
Adolescent62020857790.080 Why?
Male1520233501150.080 Why?
Carrier Proteins1202150230.070 Why?
Syndrome2202232520.070 Why?
Channelopathies12015320.070 Why?
Autistic Disorder1201411850.060 Why?
Female1420233801930.060 Why?
Regression Analysis1201464590.060 Why?
Genotype22020129520.060 Why?
Humans2020237443660.060 Why?
Young Adult52020564290.060 Why?
Databases, Genetic1202017830.060 Why?
Age of Onset2202032700.050 Why?
Genetic Counseling120156000.050 Why?
Athetosis12020160.050 Why?
Neuropsychological Tests2201969940.050 Why?
Chorea12020740.050 Why?
Cohort Studies42023405590.050 Why?
Pedigree1201846420.040 Why?
HEK293 Cells2201942080.040 Why?
Anticonvulsants1202019160.040 Why?
Brain32020263880.040 Why?
Genetic Testing2202034440.040 Why?
Codon, Nonsense120212810.040 Why?
Ceftriaxone120191680.040 Why?
Patch-Clamp Techniques120209640.040 Why?
Adult620212140520.040 Why?
Asparagine120171220.040 Why?
Disease Progression12014132860.040 Why?
Chromosomes, Human120204570.040 Why?
Massachusetts1202086620.040 Why?
Drugs, Investigational120192140.040 Why?
Dystonia120203630.040 Why?
Amino Acid Sequence22019138140.040 Why?
Podocytes120213960.040 Why?
Xenopus laevis120209570.040 Why?
Microarray Analysis120207670.040 Why?
Animals620221687680.030 Why?
Polymorphism, Single Nucleotide22020155200.030 Why?
Comorbidity12020103880.030 Why?
Consanguinity120174540.030 Why?
Protein Structure, Secondary1201912470.030 Why?
gamma-Aminobutyric Acid1202211210.030 Why?
Oocytes1202011880.030 Why?
Magnetic Resonance Imaging22020354250.030 Why?
Glutamine120175790.030 Why?
Arginine120179440.030 Why?
Glutamic Acid1201911690.030 Why?
Siblings120178540.030 Why?
Synaptic Transmission1201911780.030 Why?
Homozygote1201717870.030 Why?
Registries1201880910.030 Why?
Drug Discovery1201910580.020 Why?
Heterozygote1201828040.020 Why?
Brain Diseases1202015630.020 Why?
DNA Mutational Analysis1201741850.020 Why?
Binding Sites1201761110.020 Why?
Infant, Newborn22019256280.020 Why?
Rats, Sprague-Dawley1201983000.020 Why?
Child Development1201922230.020 Why?
Biopsy1201967550.020 Why?
Models, Molecular1201754510.020 Why?
Fibroblasts1201741620.020 Why?
Cell Line12021160000.020 Why?
Skin1201943720.020 Why?
Kidney1202171840.020 Why?
Genetic Predisposition to Disease12016174460.020 Why?
Mice22022812010.020 Why?
RNA, Messenger12019130350.020 Why?
Rats12019242520.010 Why?
Gene Expression Regulation12019120730.010 Why?
Neurons1201993400.010 Why?
Retrospective Studies12018774600.010 Why?
Middle Aged120202133900.000 Why?
Moufawad El Achkar's Networks
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Concepts (119)
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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.