Bree Hodgson
Bree Hodgson
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GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies
LM Dibbens, HJ Feng, MC Richards, LA Harkin, BL Hodgson, D Scott, ...
Human molecular genetics 13 (13), 1315-1319, 2004
Benign familial neonatal‐infantile seizures: characterization of a new sodium channelopathy
SF Berkovic, SE Heron, L Giordano, C Marini, R Guerrini, RE Kaplan, ...
Annals of neurology 55 (4), 550-557, 2004
Surgical wound infection as a performance indicator: agreement of common definitions of wound infection in 4773 patients
APR Wilson, C Gibbons, BC Reeves, B Hodgson, M Liu, D Plummer, ...
Bmj 329 (7468), 720, 2004
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
LM Dibbens, B De Vries, S Donatello, SE Heron, BL Hodgson, ...
Nature genetics 45 (5), 546, 2013
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis
SF Berkovic, LM Dibbens, A Oshlack, JD Silver, M Katerelos, DF Vears, ...
The American Journal of Human Genetics 82 (3), 673-684, 2008
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
SE Heron, BE Grinton, S Kivity, Z Afawi, SM Zuberi, JN Hughes, ...
The American Journal of Human Genetics 90 (1), 152-160, 2012
Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms
RH Wallace, BL Hodgson, BE Grinton, RM Gardiner, R Robinson, ...
Neurology 61 (6), 765-769, 2003
GABRA1 and STXBP1: novel genetic causes of Dravet syndrome
GL Carvill, S Weckhuysen, JM McMahon, C Hartmann, RS Møller, ...
Neurology 82 (14), 1245-1253, 2014
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations
IE Scheffer, SE Heron, BM Regan, S Mandelstam, DE Crompton, ...
Annals of neurology 75 (5), 782-787, 2014
Epilepsy and mental retardation limited to females: an under-recognized disorder
IE Scheffer, SJ Turner, LM Dibbens, MA Bayly, K Friend, B Hodgson, ...
Brain 131 (4), 918-927, 2008
Augmented currents of an HCN2 variant in patients with febrile seizure syndromes
LM Dibbens, CA Reid, B Hodgson, EA Thomas, AM Phillips, E Gazina, ...
Annals of neurology 67 (4), 542-546, 2010
Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy
MG Ricos, BL Hodgson, T Pippucci, A Saidin, YS Ong, SE Heron, ...
Annals of neurology 79 (1), 120-131, 2016
Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome
JC Mulley, B Hodgson, JM McMahon, X Iona, S Bellows, SA Mullen, ...
Epilepsia 54 (9), e122-e126, 2013
NEDD4‐2 as a potential candidate susceptibility gene for epileptic photosensitivity
LM Dibbens, J Ekberg, I Taylor, BL Hodgson, SJ Conroy, IL Lensink, ...
Genes, Brain and Behavior 6 (8), 750-755, 2007
The role of neuronal GABAA receptor subunit mutations in idiopathic generalized epilepsies
LM Dibbens, LA Harkin, M Richards, BL Hodgson, AL Clarke, S Petrou, ...
Neuroscience letters 453 (3), 162-165, 2009
Screening and cell‐based assessment of mutations in the Aristaless‐related homeobox (ARX) gene
T Fullston, M Finnis, A Hackett, B Hodgson, L Brueton, G Baynam, ...
Clinical genetics 80 (6), 510-522, 2011
Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26
KM Klein, CJ Bromhead, KR Smith, CJ O’Callaghan, SJ Corcoran, ...
Neurology 80 (16), 1485-1493, 2013
The role of seizure-related SEZ6 as a susceptibility gene in febrile seizures
JC Mulley, X Iona, B Hodgson, SE Heron, SF Berkovic, IE Scheffer, ...
Neurology research international 2011, 2011
Ability to detect aneuploidy from cell free DNA collected from media is dependent on the stage of development of the embryo
M Lane, DL Zander-Fox, H Hamilton, MJ Jasper, BL Hodgson, M Fraser, ...
Fertility and Sterility 108 (3), e61, 2017
Rare protein sequence variation in SV2A gene does not affect response to levetiracetam
LM Dibbens, BL Hodgson, KL Helbig, KL Oliver, JC Mulley, SF Berkovic, ...
Epilepsy research 101 (3), 277-279, 2012
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