Rhys H Thomas
Rhys H Thomas
Intermediate Clinical Lecturer / Honorary Consultant in Epilepsy
Verified email at - Homepage
Cited by
Cited by
Neurological and neuropsychiatric complications of COVID-19 in 153 patients: a UK-wide surveillance study
A Varatharaj, N Thomas, M Ellul, NWS Davies, T Pollak, M Sultan, ...
Lancet Psychiatry, 2020
Pathophysiological mechanisms of dominant and recessive GLRA1 mutations in hyperekplexia
SK Chung, JF Vanbellinghen, JGL Mullins, A Robinson, J Hantke, ...
Journal of Neuroscience 30 (28), 9612-9620, 2010
High rate of recurrent de novo mutations in developmental and epileptic encephalopathies
FF Hamdan, C Myers, P Cossette, P Lemay, D Spiegelman, ...
AJHG 101 (5), 664-685, 2017
The hidden genetics of epilepsy - a clinically important new paradigm
RH Thomas, SF Berkovic
Nature Reviews Neurology 10 (5), 283-292, 2014
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study
CD Whelan, S Adams, S Alhusaini, N Bargalló, E Bartolini, A Bernasconi, ...
Brain 141 (2), 391-408, 2018
Hyperekplexia: stiffness, startle and syncope
RH Thomas, JBP Stephenson, RJ Harvey, MI Rees
Journal of Pediatric Neurology; JPN 8 (1), 11, 2010
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study
EPGP Epi4K consortium
Lancet Neurology 16 (2), 135-143, 2017
Cognitive performance among carriers of pathogenic copy number variants: Analysis of 152,000 UK Biobank subjects
KG Kendall KM, Rees E, Escott-Price V, Mark Eynon, Thomas RH, Hewitt J, O ...
Biological Psychiatry, 2016
Twenty-Nine Cases of Enterovirus-D68 Associated Acute Flaccid Myelitis in Europe 2016; A Case Series and Epidemiologic Overview.
M Knoester, J Helfferich, R Poelman, C Van Leer-Buter, O Brouwer, ...
Pediatr Infect Dis Journal 38 (1), 16-21, 2018
Cerebral venous thrombosis after vaccination against COVID-19 in the UK: a multicentre cohort study
RJ Perry, A Tamborska, B Singh, B Craven, R Marigold, P Arthur-Farraj, ...
Lancet, 2021
Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease
E Carta, SK Chung, VM James, A Robinson, JL Gill, N Remy, ...
Journal of Biological Chemistry 287 (34), 28975-28985, 2012
CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures
RH Thomas, LM Zhang, GL Carvill, JS Archer, SB Heavin, ...
Neurology 84 (9), 951-958, 2015
Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay
RH Thomas, SK Chung, SE Wood, TD Cushion, CJG Drew, CL Hammond, ...
Brain 136 (10), 3085-3095, 2013
Neurological phenotypes associated with COL4A1/2 mutations: expanding the spectrum of disease
S Zagaglia, C Selch, JR Nisevic, D Mei, Z Michalak, ...
Neurology 91 (22), e2078-e2088, 2018
The glycinergic system in human startle disease: a genetic screening approach
JS Davies, SK Chung, RH Thomas, A Robinson, CL Hammond, ...
Frontiers in molecular neuroscience 3, 2010
Weight change associated with antiepileptic drugs
WO Pickrell, AS Lacey, RH Thomas, PEM Smith, MI Rees
Journal of Neurology, Neurosurgery & Psychiatry 84 (7), 796-799, 2013
Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle disease
VM James, A Bode, SK Chung, JL Gill, M Nielsen, FM Cowan, M Vujic, ...
Neurobiology of disease 52, 137-149, 2013
COVID-19 and psychosis risk: real or delusional concern?
CJ Watson, RH Thomas, T Solomon, BD Michael, TR Nicholson, ...
Neuroscience letters 741, 135491, 2021
Cluster Of Atypical Adult Guillain-Barré Syndrome Temporally Associated With Neurological Illness Due To Ev-D68 In Children, South Wales, United Kingdom, October 2015 To …
BWM CJ Williams, RH Thomas, TP Pickersgill, M Lyons, G Lowe, RE Stiff, C ...
EuroSurveillance 21 (4), 2016
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA Epilepsy study
SN Hatton, KH Huynh, L Bonilha, E Abela, S Alhusaini, AN Altmann, ...
Brain, 2020
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