Andreas Brunklaus
Andreas Brunklaus
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Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome
A Brunklaus, R Ellis, E Reavey, GH Forbes, SM Zuberi
Brain 135 (8), 2329-2336, 2012
Genotype–phenotype associations in SCN1A-related epilepsies
SM Zuberi, A Brunklaus, R Birch, E Reavey, J Duncan, GH Forbes
Neurology 76 (7), 594-600, 2011
Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort
JD Symonds, SM Zuberi, K Stewart, A McLellan, M O ‘Regan, S MacLeod, ...
Brain 142 (8), 2303-2318, 2019
Evidence for oxidative stress in the frontal cortex in patients with recurrent depressive disorder—a postmortem study
TM Michel, S Frangou, D Thiemeyer, S Camara, J Jecel, K Nara, ...
Psychiatry research 151 (1-2), 145-150, 2007
Dravet syndrome—from epileptic encephalopathy to channelopathy
A Brunklaus, SM Zuberi
Epilepsia 55 (7), 979-984, 2014
Dravet syndrome and its mimics: Beyond SCN1A
D Steel, JD Symonds, SM Zuberi, A Brunklaus
Epilepsia 58 (11), 1807-1816, 2017
Outcome and prognostic features in opsoclonus-myoclonus syndrome from infancy to adult life
A Brunklaus, K Pohl, SM Zuberi, C de Sousa
Pediatrics 128 (2), e388-e394, 2011
Comorbidities and predictors of health‐related quality of life in Dravet syndrome
A Brunklaus, L Dorris, SM Zuberi
Epilepsia 52 (8), 1476-1482, 2011
The genetic landscape of epilepsy of infancy with migrating focal seizures
R Burgess, S Wang, A McTague, KE Boysen, X Yang, Q Zeng, KA Myers, ...
Annals of neurology 86 (6), 821-831, 2019
Genotype phenotype associations across the voltage-gated sodium channel family
A Brunklaus, R Ellis, E Reavey, C Semsarian, SM Zuberi
Journal of medical genetics 51 (10), 650-658, 2014
Investigating neuroblastoma in childhood opsoclonus-myoclonus syndrome
A Brunklaus, K Pohl, SM Zuberi, C de Sousa
Archives of disease in childhood 97 (5), 461-463, 2012
The clinical utility of an SCN1A genetic diagnosis in infantile‐onset epilepsy
A Brunklaus, L Dorris, R Ellis, E Reavey, E Lee, G Forbes, R Appleton, ...
Developmental Medicine & Child Neurology 55 (2), 154-161, 2013
Predicting functional effects of missense variants in voltage-gated sodium and calcium channels
HO Heyne, D Baez-Nieto, S Iqbal, DS Palmer, A Brunklaus, P May, ...
Science translational medicine 12 (556), eaay6848, 2020
Phenotypic spectrum and genetics of SCN2A‐related disorders, treatment options, and outcomes in epilepsy and beyond
M Wolff, A Brunklaus, SM Zuberi
Epilepsia 60, S59-S67, 2019
Biological concepts in human sodium channel epilepsies and their relevance in clinical practice
A Brunklaus, J Du, F Steckler, II Ghanty, KM Johannesen, CD Fenger, ...
Epilepsia 61 (3), 387-399, 2020
A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants
JA López-Rivera, E Pérez-Palma, J Symonds, AS Lindy, DA McKnight, ...
Brain 143 (4), 1099-1105, 2020
Anakinra usage in febrile infection related epilepsy syndrome: an international cohort
YC Lai, E Muscal, E Wells, N Shukla, K Eschbach, K Hyeong Lee, ...
Annals of clinical and translational neurology 7 (12), 2467-2474, 2020
The humanistic and economic burden of Dravet syndrome on caregivers and families: implications for future research
MP Jensen, A Brunklaus, L Dorris, SM Zuberi, KG Knupp, BS Galer, ...
Epilepsy & Behavior 70, 104-109, 2017
The value of cardiac MRI versus echocardiography in the pre-operative assessment of patients with Duchenne muscular dystrophy
A Brunklaus, E Parish, F Muntoni, S Scuplak, SK Tucker, M Fenton, ...
european journal of paediatric neurology 19 (4), 395-401, 2015
Health-related quality-of-life and behavioural outcome in survivors of childhood meningitis
R Sumpter, A Brunklaus, R McWilliam, L Dorris
Brain injury 25 (13-14), 1288-1295, 2011
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