PubRank

Janice Holton

Author PubWeight™ 30.06‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease. Brain 2009 4.01
2 SNCA variants are associated with increased risk for multiple system atrophy. Ann Neurol 2009 3.55
3 A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. Brain 2008 2.13
4 Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress. J Neurochem 2006 1.91
5 The midbrain to pons ratio: a simple and specific MRI sign of progressive supranuclear palsy. Neurology 2013 1.74
6 Gene expression in Huntington's disease skeletal muscle: a potential biomarker. Hum Mol Genet 2005 1.51
7 Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11. Nat Genet 2007 1.38
8 Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions. Neurosci Lett 2003 1.27
9 An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies. Acta Neuropathol 2006 1.24
10 Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene. Arch Neurol 2008 1.20
11 Familial Danish dementia: co-existence of Danish and Alzheimer amyloid subunits (ADan AND A{beta}) in the absence of compact plaques. J Biol Chem 2005 1.18
12 Down-regulation of the dopamine receptor D2 in mice lacking ataxin 1. Hum Mol Genet 2007 1.12
13 Complement activation in chromosome 13 dementias. Similarities with Alzheimer's disease. J Biol Chem 2002 1.04
14 The clinical and neuroanatomical phenotype of FUS associated frontotemporal lobar degeneration. J Neurol Neurosurg Psychiatry 2010 0.91
15 Hyposmia in progressive supranuclear palsy. Mov Disord 2010 0.88
16 Sporadic inclusion body myositis: an unsolved mystery. Acta Reumatol Port 2009 0.86
17 TDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT. Neurobiol Aging 2013 0.81
18 Preferential association of serum amyloid P component with fibrillar deposits in familial British and Danish dementias: similarities with Alzheimer's disease. J Neurol Sci 2007 0.81
19 Diagnostic implications of histological analysis of neurosurgical aspirate in addition to routine resections. Neuropathology 2011 0.80
20 Sporadic and familial dementia with ubiquitin-positive tau-negative inclusions: clinical features of one histopathological abnormality underlying frontotemporal lobar degeneration. Arch Neurol 2005 0.80
21 Abundant pyroglutamate-modified ABri and ADan peptides in extracellular and vascular amyloid deposits in familial British and Danish dementias. Neurobiol Aging 2012 0.78
22 Parkinson's disease with Onuf's nucleus involvement mimicking multiple system atrophy. BMJ Case Rep 2009 0.75
23 DYT6 Dystonia: A Neuropathological Study. Neurodegener Dis 2015 0.75
24 Progressive parkinsonism, oculomotor abnormalities and autonomic dysfunction: clinicopathological case. Mov Disord 2011 0.75