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Deb Pal
Professor
Professor of Epilepsy
,
Basic and Clinical Neuroscience
https://orcid.org/0000-0003-2655-0564
Phone
85762
6375
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Research output
(131)
Projects
(52)
Similar Profiles
(6)
Supervised Work
(4)
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Dive into the research topics where Deb Pal is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Medicine and Dentistry
Anticonvulsant
15%
Benign Childhood Epilepsy
42%
Benign Epilepsy
9%
Brain Disease
18%
Case-Control Study
7%
Clinical Trial
12%
Clinician
12%
Cohort Effect
7%
Counseling
8%
Developmental Verbal Dyspraxia
7%
Disease
7%
Dyslexia
13%
Endophenotype
6%
Epilepsy Syndromes
16%
Epileptic Seizure
55%
Febrile Seizure
9%
Generalised Epilepsy
9%
Genetic Evaluation
12%
Genetic Heterogeneity
10%
Genetic Risk Factor
7%
Genetic Screening
9%
GRIN2A
29%
Health Care Cost
11%
Health Outcomes
12%
Landau-Kleffner Syndrome
8%
Language Disorder
9%
Magnetic Resonance Imaging
7%
Magnetic Resonance Imaging
7%
Mass Screening
9%
Mental Health
26%
Migraine
7%
Narcolepsy
12%
Neonates
8%
Observational Study
6%
Outpatient
7%
Partial Seizure
19%
Patient with Epilepsy
8%
Patient-Reported Outcome
22%
Pediatric Epilepsy
22%
Pediatrics
8%
Quality of Life
11%
Randomized Controlled Trial
16%
Rating Scale
8%
Rolandic Epilepsy
100%
SCN8A
14%
Specific Language Impairment
11%
Speech and Language
7%
Speech Disorder
9%
Speech Sound Disorder
15%
Systematic Review
44%
Neuroscience
Adverse Effect
6%
Anticonvulsant
17%
Antiseizure Medication
7%
Apraxia
10%
Attention Deficit Hyperactivity Disorder
10%
Autism
16%
Brain Disease
12%
Brain Network
10%
Channelopathy
12%
Childhood Absence Epilepsy
11%
CHRNA4
9%
Cognitive Disorders
9%
Comorbidity
8%
Copy Number Variation
19%
Electroencephalogram
11%
Epileptic Absence
21%
Epileptic Seizure
9%
Febrile Seizure
9%
Focal Epilepsy
9%
Generalised Epilepsy
22%
Genetic Generalized Epilepsy
12%
GRIN2A
21%
Impulsivity
16%
Intractable Epilepsy
15%
Juvenile Myoclonic Epilepsy
47%
Language Disorder
8%
Language Disorders
15%
Lennox-Gastaut Syndrome
9%
Magnetic Resonance Imaging
21%
Mammalian Target of Rapamycin
7%
Meta-Analysis
13%
Migraine
7%
Myoclonic Epilepsy
11%
Myoclonic Seizure
12%
Nerve Cell Differentiation
8%
Neurodevelopmental Disorder
9%
Night Sleep
9%
Pediatric Epilepsy
22%
Pervasive Developmental Disorder
9%
Positive Allosteric Modulator
8%
Primary Generalized Epilepsy
16%
Randomized Controlled Trial
9%
Rolandic Epilepsy
74%
SCN8A
19%
Seizure Types
12%
Single-Nucleotide Polymorphism
11%
Speech Disorder
6%
Stereotypic Movement Disorder
7%
Synapse
7%
Tonic-Clonic Seizure
8%
Biochemistry, Genetics and Molecular Biology
ABCC6
6%
Agonist
6%
Array Comparative Genomic Hybridization
11%
Autosomal Dominant Inheritance
14%
BRD2
6%
Copy-Number Variation
15%
Cytochrome C Oxidase
6%
DNM1
6%
Electroencephalogram
7%
Enzyme
6%
Exome Sequencing
10%
Factor Analysis
6%
Family Size
6%
GABRB2
6%
Gene Frequency
9%
Gene Linkage
26%
Gene Locus
6%
Genetic Disorder
7%
Genetic Heterogeneity
12%
Genetic Screening
12%
Genetics
52%
Genomics
8%
GRIN2A
24%
Juvenile Myoclonic Epilepsy
12%
Linkage Analysis
10%
Maternal Inheritance
6%
Medical Genetics
9%
Missense
14%
Missense Mutation
7%
Mosaicism
7%
Nav1.1
6%
Nerve Cell Differentiation
6%
NMDA Receptor
7%
Offspring
7%
PAX6
15%
Pedigree
9%
Penetrance
10%
Phenocopy
6%
Prevalence
12%
Proband
17%
Rare Variant
15%
Rolandic Epilepsy
60%
SCN8A
10%
Sex Difference
8%
Single-Nucleotide Polymorphism
10%
SMARCA2
6%
SNAP25
6%
Spike
13%
Synaptic Transmission
7%
Transmission Disequilibrium Test
6%
