PubRank

Michael R Johnson

Author PubWeight™ 53.57‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 De novo mutations in epileptic encephalopathies. Nature 2013 7.42
2 Faciobrachial dystonic seizures precede Lgi1 antibody limbic encephalitis. Ann Neurol 2011 6.77
3 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Hum Mol Genet 2008 3.93
4 HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans. N Engl J Med 2011 3.93
5 Improved heritability estimation from genome-wide SNPs. Am J Hum Genet 2012 3.48
6 Faciobrachial dystonic seizures: the influence of immunotherapy on seizure control and prevention of cognitive impairment in a broadening phenotype. Brain 2013 3.22
7 Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. Am J Hum Genet 2010 2.61
8 Neural correlates of speech anticipatory anxiety in generalized social phobia. Neuroreport 2004 1.69
9 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. Brain 2010 1.67
10 Heritability of left ventricular mass in a large cohort of twins. J Hypertens 2006 1.65
11 Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study. Lancet Neurol 2006 1.54
12 PTSD symptoms, demographic characteristics, and functional status among veterans treated in VA primary care clinics. J Trauma Stress 2004 1.30
13 A genome-wide association study of neuroticism in a population-based sample. PLoS One 2010 1.09
14 cnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing data. Genome Biol 2012 0.98
15 Intrinsic severity as a determinant of antiepileptic drug refractoriness. Epilepsy Curr 2008 0.98
16 Exon sequencing and high resolution haplotype analysis of ABC transporter genes implicated in drug resistance. Pharmacogenet Genomics 2006 0.97
17 Response to Lee et al.: SNP-based heritability analysis with dense data. Am J Hum Genet 2013 0.97
18 The Social Thoughts and Beliefs Scale: a new inventory for assessing cognitions in social phobia. Psychol Assess 2003 0.96
19 Partial epilepsy with pericentral spikes: a new familial epilepsy syndrome with evidence for linkage to chromosome 4p15. Ann Neurol 2002 0.93
20 Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach. Pharmacogenet Genomics 2007 0.87
21 A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy. Hum Mol Genet 2013 0.87
22 Bayesian survival analysis in genetic association studies. Bioinformatics 2008 0.86
23 Juvenile myoclonic epilepsy and idiopathic photosensitive occipital lobe epilepsy: is there overlap? Brain 2004 0.82
24 Pharmacogenetics in clinical practice: considerations for testing. Expert Rev Mol Diagn 2006 0.80
25 The association between polymorphisms in RLIP76 and drug response in epilepsy. Pharmacogenomics 2007 0.79
26 Increased risk of sudden death among youths and stimulant use: determining alternate potential factors. Am J Psychiatry 2010 0.78
27 Treatment of hamstring strain in a collegiate pole-vaulter integrating dry needling with an eccentric training program: a resident's case report. Int J Sports Phys Ther 2013 0.78
28 Genetics of epilepsy: epilepsy research foundation workshop report. Epileptic Disord 2007 0.77
29 Morel-Lavallée lesion of the lumbar region. J Orthop Sports Phys Ther 2014 0.77
30 Monozygotic twins with LRRK2 mutations: genetically identical but phenotypically discordant. Mov Disord 2012 0.76
31 DIAGNOSTIC IMAGING IN A DIRECT-ACCESS SPORTS PHYSICAL THERAPY CLINIC: A 2-YEAR RETROSPECTIVE PRACTICE ANALYSIS. Int J Sports Phys Ther 2016 0.75
32 Fracture of the capitate. J Orthop Sports Phys Ther 2014 0.75
33 Advances in epilepsy gene discovery and implications for epilepsy diagnosis and treatment. Curr Opin Neurol 2017 0.75
34 Fractures through the base of the second and third metacarpals. J Orthop Sports Phys Ther 2014 0.75
35 Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS). Epilepsy Res 2011 0.75
36 Bayesian variable selection for survival regression in genetics. Genet Epidemiol 2010 0.75