Caitlin A Bennett
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Explore the profile of Caitlin A Bennett including associated specialties, affiliations and a list of published articles.
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5
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37
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Recent Articles
1.
Chen S, Abou-Khalil B, Afawi Z, Ali Q, Amadori E, Anderson A, et al.
medRxiv
. 2023 Mar;
PMID: 36865150
Identifying genetic risk factors for highly heterogeneous disorders like epilepsy remains challenging. Here, we present the largest whole-exome sequencing study of epilepsy to date, with >54,000 human exomes, comprising 20,979...
2.
Gozzelino L, Kochlamazashvili G, Baldassari S, Mackintosh A, Licchetta L, Iovino E, et al.
Brain
. 2022 Jul;
145(7):2313-2331.
PMID: 35786744
Epilepsy is one of the most frequent neurological diseases, with focal epilepsy accounting for the largest number of cases. The genetic alterations involved in focal epilepsy are far from being...
3.
Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice
Scheffer I, Bennett C, Gill D, de Silva M, Boggs K, Marum J, et al.
Dev Med Child Neurol
. 2022 Jun;
65(1):50-57.
PMID: 35701389
Aim: To assess the clinical utility of exome sequencing for patients with developmental and epileptic encephalopathies (DEEs). Method: Over 2 years, patients with DEEs were recruited for singleton exome sequencing....
4.
Green T, Motelow J, Bennett M, Ye Z, Bennett C, Griffin N, et al.
Hum Mol Genet
. 2022 Feb;
31(14):2307-2316.
PMID: 35137044
Hypothalamic hamartoma with gelastic seizures is a well-established cause of drug-resistant epilepsy in early life. The development of novel surgical techniques has permitted the genomic interrogation of hypothalamic hamartoma tissue....
5.
Bennett C, Petrovski S, Oliver K, Berkovic S
Neurol Genet
. 2017 Jul;
3(4):e163.
PMID: 28717674
Objective: To assist the interpretation of genomic data for common epilepsies, we asked whether variants implicated in mild epilepsies in autosomal dominant families are present in the general population. Methods:...