Michael R Johnson
Michael R Johnson
Verified email at imperial.ac.uk - Homepage
Title
Cited by
Cited by
Year
HLA-A* 3101 and carbamazepine-induced hypersensitivity reactions in Europeans
M McCormack, A Alfirevic, S Bourgeois, JJ Farrell, D Kasperavičiūtė, ...
New England Journal of Medicine 364 (12), 1134-1143, 2011
9082011
De novo mutations in epileptic encephalopathies
AS Allen, SF Berkovic, P Cossette, N Delanty, D Dlugos, EE Eichler, ...
Nature 501 (7466), 217, 2013
8422013
Faciobrachial dystonic seizures precede Lgi1 antibody limbic encephalitis
SR Irani, AW Michell, B Lang, P Pettingill, P Waters, MR Johnson, ...
Annals of neurology 69 (5), 892-900, 2011
7282011
Improved heritability estimation from genome-wide SNPs
D Speed, G Hemani, MR Johnson, DJ Balding
The American Journal of Human Genetics 91 (6), 1011-1021, 2012
5312012
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
SE Baranzini, J Wang, RA Gibson, N Galwey, Y Naegelin, F Barkhof, ...
Human molecular genetics 18 (4), 767-778, 2009
5132009
De novo mutations in epileptic encephalopathies
KC Epi, PE Phenome, AS Allen, SF Berkovic, P Cossette, N Delanty, ...
Nature 501 (7466), 217-221, 2013
4742013
Faciobrachial dystonic seizures: the influence of immunotherapy on seizure control and prevention of cognitive impairment in a broadening phenotype
SR Irani, CJ Stagg, JM Schott, CR Rosenthal, SA Schneider, P Pettingill, ...
Brain 136 (10), 3151-3162, 2013
3492013
ABCB1 genotype and PGP expression, function and therapeutic drug response: a critical review and recommendations for future research
GD Leschziner, T Andrew, M Pirmohamed, MR Johnson
The pharmacogenomics journal 7 (3), 154-179, 2007
3172007
Reevaluation of SNP heritability in complex human traits
D Speed, N Cai, MR Johnson, S Nejentsev, DJ Balding
Nature genetics 49 (7), 986-992, 2017
2942017
Rare deletions at 16p13. 11 predispose to a diverse spectrum of sporadic epilepsy syndromes
EL Heinzen, RA Radtke, TJ Urban, GL Cavalleri, C Depondt, AC Need, ...
The American Journal of Human Genetics 86 (5), 707-718, 2010
2562010
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ...
The American Journal of Human Genetics 95 (4), 360-370, 2014
2112014
The role of [18F]fluoro-2-deoxyglucose-PET scanning in the diagnosis of paraneoplastic neurological disorders
JH Rees, SF Hain, MR Johnson, RAC Hughes, DC Costa, PJ Ell, G Keir, ...
Brain 124 (11), 2223-2231, 2001
1692001
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
D Kasperavičiūtė, CB Catarino, EL Heinzen, C Depondt, GL Cavalleri, ...
Brain 133 (7), 2136-2147, 2010
1622010
De novo mutations in SLC1A2 and CACNA1A are important causes of epileptic encephalopathies
CT Myers, JM McMahon, AL Schneider, S Petrovski, AS Allen, GL Carvill, ...
The American Journal of Human Genetics 99 (2), 287-298, 2016
1572016
Immunotherapy-responsive seizure-like episodes with potassium channel antibodies
SR Irani, C Buckley, A Vincent, OC Cockerell, P Rudge, MR Johnson, ...
Neurology 71 (20), 1647-1648, 2008
1342008
Intrinsic severity as a determinant of antiepileptic drug refractoriness
MA Rogawski, MR Johnson
Epilepsy currents 8 (5), 127-130, 2008
1272008
Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus
MR Johnson, J Behmoaras, L Bottolo, ML Krishnan, K Pernhorst, ...
Nature communications 6 (1), 1-11, 2015
1152015
Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease
MR Johnson, K Shkura, SR Langley, A Delahaye-Duriez, P Srivastava, ...
Nature neuroscience 19 (2), 223-232, 2016
1022016
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study
AS Allen, ST Bellows, SF Berkovic, J Bridgers, R Burgess, G Cavalleri, ...
The Lancet Neurology 16 (2), 135-143, 2017
1012017
Neurofibromatous neuropathy in neurofibromatosis 1 (NF1)
RE Ferner, RAC Hughes, SM Hall, M Upadhyaya, MR Johnson
Journal of medical genetics 41 (11), 837-841, 2004
1002004
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Articles 1–20