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?
Epilepsy10202333260.980 Why?
Calcium Channels, R-Type12018130.640 Why?
Dyskinesias12018790.590 Why?
Developmental Disabilities4202115210.560 Why?
Contracture120182360.520 Why?
Cation Transport Proteins120183260.520 Why?
Genetic Variation5202066100.480 Why?
Spasms, Infantile120183010.480 Why?
Epilepsy, Generalized420201810.440 Why?
Ataxia220203070.440 Why?
Ocular Motility Disorders120141440.420 Why?
Genetic Diseases, X-Linked120143910.350 Why?
Microcephaly120144260.350 Why?
Receptors, GABA-A320226250.310 Why?
Lissencephaly12016360.270 Why?
PTEN Phosphohydrolase1202011200.240 Why?
Seizures4202330000.230 Why?
Nerve Tissue Proteins2202144150.210 Why?
Cadherins120189060.210 Why?
Tubulin120166950.210 Why?
Intranuclear Space12021150.190 Why?
Child, Preschool132021426840.170 Why?
Neuronal Ceroid-Lipofuscinoses120191340.150 Why?
Mutation62022302660.150 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 Segmental120213360.140 Why?
Facies120182240.140 Why?
Nephrotic Syndrome120213810.140 Why?
Mutagenesis, Insertional120196620.140 Why?
Oligonucleotides, Antisense120194610.140 Why?
Movement Disorders120204640.140 Why?
Cerebellar Diseases120182280.130 Why?
Infant82020365410.130 Why?
Vesicular Transport Proteins120183770.120 Why?
Amino Acid Metabolism, Inborn Errors120172840.120 Why?
Phenotype72022167350.110 Why?
Receptors, N-Methyl-D-Aspartate120199050.110 Why?
Rare Diseases120196300.110 Why?
Membrane Transport Proteins1201910390.110 Why?
Child112021809690.100 Why?
Mutation, Missense2202025920.100 Why?
Quinidine12020520.090 Why?
Electroencephalography3202063180.080 Why?
Carrier Proteins1202149400.070 Why?
Adolescent62020892470.070 Why?
Male1520233652490.070 Why?
Syndrome2202232740.060 Why?
Channelopathies12015320.060 Why?
Regression Analysis1201463460.060 Why?
Autistic Disorder1201412400.060 Why?
Female1420233974640.060 Why?
Genotype22020130480.060 Why?
Humans2020237688870.060 Why?
Databases, Genetic1202017580.050 Why?
Young Adult52020601100.050 Why?
Age of Onset2202033460.050 Why?
Athetosis12020150.050 Why?
Genetic Counseling120156340.050 Why?
Neuropsychological Tests2201971480.050 Why?
Cohort Studies42023418000.040 Why?
Chorea12020800.040 Why?
Pedigree1201845450.040 Why?
HEK293 Cells2201942910.040 Why?
Anticonvulsants1202019240.040 Why?
Brain32020274760.040 Why?
Genetic Testing2202035900.040 Why?
Codon, Nonsense120212870.040 Why?
Patch-Clamp Techniques120209270.040 Why?
Ceftriaxone120191750.040 Why?
Chromosomes, Human120204380.040 Why?
Asparagine120171200.040 Why?
Adult620212238180.040 Why?
Amino Acid Sequence22019134270.040 Why?
Drugs, Investigational120192130.040 Why?
Massachusetts1202088880.040 Why?
Disease Progression12014136770.040 Why?
Dystonia120203780.040 Why?
Microarray Analysis120207550.030 Why?
Xenopus laevis120209660.030 Why?
Podocytes120214030.030 Why?
Animals620221694080.030 Why?
Protein Structure, Secondary1201912160.030 Why?
Polymorphism, Single Nucleotide22020160510.030 Why?
Oocytes1202011720.030 Why?
Consanguinity120174600.030 Why?
Comorbidity12020105910.030 Why?
gamma-Aminobutyric Acid1202211430.030 Why?
Magnetic Resonance Imaging22020368610.030 Why?
Glutamine120175780.030 Why?
Arginine120179320.030 Why?
Glutamic Acid1201911930.030 Why?
Siblings120178290.030 Why?
Synaptic Transmission1201911770.030 Why?
Homozygote1201717790.030 Why?
Drug Discovery1201910680.020 Why?
Registries1201883840.020 Why?
Heterozygote1201827980.020 Why?
Brain Diseases1202015580.020 Why?
DNA Mutational Analysis1201741230.020 Why?
Binding Sites1201760230.020 Why?
Rats, Sprague-Dawley1201982000.020 Why?
Infant, Newborn22019263940.020 Why?
Child Development1201923370.020 Why?
Models, Molecular1201754040.020 Why?
Biopsy1201968050.020 Why?
Fibroblasts1201741780.020 Why?
Cell Line12021156030.020 Why?
Skin1201945070.020 Why?
Kidney1202170570.020 Why?
Genetic Predisposition to Disease12016180650.010 Why?
RNA, Messenger12019128090.010 Why?
Mice22022820740.010 Why?
Rats12019238470.010 Why?
Gene Expression Regulation12019119340.010 Why?
Neurons1201995240.010 Why?
Retrospective Studies12018818920.010 Why?
Middle Aged120202237400.000 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.