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B. Grinton · SciRah

Researcher profile · Semantic Scholar

B. Grinton

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B. Grinton — researcher profile on SciRah

h-index: 21
Works: 40
Citations: 2,721

Most-cited papers

Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations.
I. Scheffer, L. Harkin, B. Grinton, L. Dibbens +12 more
2006Brain : a journal of neurology278 citations Open access
Semantic Scholar
Benign familial neonatal‐infantile seizures: Characterization of a new sodium channelopathy
S. Berkovic, S. Heron, L. Giordano, C. Marini +12 more
2004Annals of Neurology268 citations
Semantic Scholar
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.
S. Heron, B. Grinton, S. Kivity, Z. Afawi +20 more
2012American Journal of Human Genetics256 citations Open access
Semantic Scholar
Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms
R. Wallace, B. Hodgson, B. Grinton, R. Gardiner +11 more
2003Neurology202 citations
Semantic Scholar
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study.
G. Cavalleri, M. Weale, K. Shianna, Rinki Singh +37 more
2007Lancet Neurology193 citations Open access
Semantic Scholar
A variant of KCC2 from patients with febrile seizures impairs neuronal Cl− extrusion and dendritic spine formation
Martin Puskarjov, Patricia Seja, S. Heron, Tristiana C. Williams +11 more
2014EMBO Reports189 citations Open access
Semantic Scholar
Genes4Epilepsy: An epilepsy gene resource
Karen L. Oliver, I. Scheffer, M. Bennett, B. Grinton +2 more
2023Epilepsia152 citations Open access
Semantic Scholar
Genetic Architecture of Idiopathic Generalized Epilepsy: Clinical Genetic Analysis of 55 Multiplex Families
C. Marini, I. Scheffer, K. Crossland, B. Grinton +13 more
2004Epilepsia148 citations Open access
Semantic Scholar
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome
B. Grinton, S. Heron, James T. Pelekanos, S. Zuberi +19 more
2015Epilepsia111 citations
Semantic Scholar
SCN2A Mutations and Benign Familial Neonatal‐Infantile Seizures: The Phenotypic Spectrum
E. Herlenius, S. Heron, B. Grinton, Deborah Keay +3 more
2007Epilepsia111 citations Open access
Semantic Scholar
Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance.
Douglas E. Crompton, I. Scheffer, I. Taylor, M. Cook +7 more
2010Brain : a journal of neurology86 citations Open access
Semantic Scholar
Genetic epilepsy with febrile seizures plus
Yuehua Zhang, R. Burgess, Jodie P. Malone, Georgie C. Glubb +17 more
2017Neurology81 citations
Semantic Scholar
PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures
I. Scheffer, B. Grinton, S. Heron, S. Kivity +10 more
2012Neurology81 citations Open access
Semantic Scholar
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures
S. Heron, K. Cox, B. Grinton, S. Zuberi +6 more
2007Journal of Medical Genetics77 citations Open access
Semantic Scholar
Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction
M. Richards, S. Heron, H. E. Spendlove, I. Scheffer +4 more
2004Journal of Medical Genetics72 citations Open access
Semantic Scholar
The health‐related quality of life of childhood epilepsy syndromes
M. Sabaz, D. Cairns, A. Bleasel, J. A. Lawson +3 more
2003Journal of Paediatrics and Child Health65 citations
Semantic Scholar
Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes
D. Vears, Meng-Han Tsai, L. Sadleir, B. Grinton +5 more
2012Epilepsia58 citations Open access
Semantic Scholar
Familial clustering of seizure types within the idiopathic generalized epilepsies
M. Winawer, C. Marini, B. Grinton, Daniel Rabinowitz +3 more
2005Neurology58 citations Open access
Semantic Scholar
Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3
S. Heron, I. Scheffer, B. Grinton, H. Eyre +4 more
2010Epilepsia37 citations Open access
Semantic Scholar
Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families
Karen L. Oliver, I. Scheffer, Colin A. Ellis, B. Grinton +44 more
2024EBioMedicine35 citations Open access
Semantic Scholar
Randomized Controlled Trial of Melatonin for Sleep Disturbance in Dravet Syndrome: The DREAMS Study
K. Myers, M. Davey, Michael S. Ching, Colin A. Ellis +4 more
2018Journal of Clinical Sleep Medicine (JCSM)25 citations Open access
Semantic Scholar
Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic Architecture
Rebekah V. Harris, Karen L. Oliver, P. Perucca, P. Striano +17 more
2023Annals of Neurology21 citations Open access
Semantic Scholar
Epidemiology and etiology of infantile developmental and epileptic encephalopathies in Tasmania
Tyson L. Ware, Shannon R. Huskins, B. Grinton, Yu-Chi Liu +17 more
2019Epilepsia Open21 citations Open access
Semantic Scholar
In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remission.
S. Tomlinson, H. Bostock, B. Grinton, M. Hanna +5 more
2012Brain : a journal of neurology21 citations Open access
Semantic Scholar
Novel Missense CACNA1G Mutations Associated with Infantile-Onset Developmental and Epileptic Encephalopathy
G. Berecki, K. Helbig, Tyson L. Ware, B. Grinton +4 more
2020International Journal of Molecular Sciences17 citations Open access
Semantic Scholar
Association of SLC32A1 Missense Variants With Genetic Epilepsy With Febrile Seizures Plus
S. Heron, Brigid M. Regan, Rebekah V. Harris, A. Gardner +17 more
2021Neurology15 citations Open access
Semantic Scholar
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes
J. Mulley, I. Scheffer, Tarishi Desai, M. Bayly +4 more
2011Epilepsia12 citations Open access
Semantic Scholar
Contribution of rare genetic variants to drug response in absence epilepsy.
K. Myers, M. Bennett, B. Grinton, G. Dabscheck +11 more
2021Epilepsy Research10 citations
Semantic Scholar
A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressure.
B. Grinton, E. Robertson, L. Fearnley, I. Scheffer +10 more
2022American Journal of Human Genetics8 citations Open access
Semantic Scholar
Splice variant in ARX leading to loss of C‐terminal region in a boy with intellectual disability and infantile onset developmental and epileptic encephalopathy
C. Shoubridge, Matilda R. Jackson, B. Grinton, S. Berkovic +4 more
2019American Journal of Medical Genetics. Part A8 citations Open access
Semantic Scholar
Novel mutations in the KCNQ 2 gene link epilepsy to a dysfunction of the KCNQ 2-calmodulin interaction
M. Richards, S. Heron, H. E. Spendlove, I. Scheffer +4 more
20043 citations
Semantic Scholar
Recognition and epileptology of protracted CLN3 disease
J. Cameron, J. Damiano, B. Grinton, P. Carney +7 more
2023Epilepsia2 citations Open access
Semantic Scholar
Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array data
E. Robertson, B. Grinton, Karen L. Oliver, L. Fearnley +6 more
2023medRxiv1 citations Open access
Semantic Scholar
Invited comments on the shostak and ottman review. Commentary and Authors' reply
V. Andersen, P. Benson, A. Kleinman, Thomas D. Bird +15 more
20061 citations
Semantic Scholar
The non-neurologists' view on epilepsy syndromes classification.
D. Vears, B. Grinton
2006Epileptic disorders1 citations
Semantic Scholar
SLC7A6OS Founder Mutation: A Rare Cause of Progressive Myoclonus Epilepsy Dated to 1100 Years Ago.
B. Grinton, Colin A. Ellis, M. Parnes, L. Stripe +14 more
2026Movement Disorders0 citations Open access
Semantic Scholar
35. Peripheral nerve excitability testing shows distinctive ion channel dysfunction in patients with KCNQ2 mutations and epilepsy
S. Tomlinson, B. Grinton, H. Bostock, M. Hanna +4 more
20100 citations
Semantic Scholar
FAMILIAL TEMPORAL LOBE EPILEPSY: A BENIGN EPILEPSY SYNDROME WITHOUT HIPPOCAMPAL SCLEROSIS, SHOWING COMPLEX INHERITANCE
Douglas E. Crompton, I. Scheffer, A. McIntosh, M. Cook +7 more
20090 citations
Semantic Scholar
Benign familial neonatal-infantile seizures: The mutational and phenotypic spectrum
S. Heron, B. Grinton, E. Herlenius, Deborah Keay +4 more
20070 citations
Semantic Scholar
ELO01 Phenotypic characterisation of a large family with benign familial neonatal seizures associated with an exon duplication of the KCNQ2 gene
R. Lunan, S. Heron, K. Cox, B. Grinton +4 more
20070 citations
Semantic Scholar

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I. Scheffer×36
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S. Berkovic×33
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J. Mulley×15
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S. Heron×13
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Karen L. Oliver

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L. Sadleir — researcher profile on SciRah

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