PubRank

Marsel Mesulam

Author PubWeight™ 62.38‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet 2011 10.07
2 Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 2011 9.90
3 Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nat Genet 2010 5.52
4 Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum Mol Genet 2006 4.80
5 Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. Lancet Neurol 2007 2.72
6 The arcuate fasciculus and the disconnection theme in language and aphasia: history and current state. Cortex 2008 2.45
7 Diagnostic criteria for the behavioral variant of frontotemporal dementia (bvFTD): current limitations and future directions. Alzheimer Dis Assoc Disord 2007 2.43
8 Novel late-onset Alzheimer disease loci variants associate with brain gene expression. Neurology 2012 2.08
9 TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia. Acta Neuropathol 2014 1.90
10 C9ORF72 repeat expansions in cases with previously identified pathogenic mutations. Neurology 2013 1.70
11 An ALS-associated mutation affecting TDP-43 enhances protein aggregation, fibril formation and neurotoxicity. Nat Struct Mol Biol 2011 1.58
12 TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy. Acta Neuropathol 2009 1.56
13 Increased frequency of learning disability in patients with primary progressive aphasia and their first-degree relatives. Arch Neurol 2008 1.34
14 What is a disconnection syndrome? Cortex 2008 1.24
15 TDP-43 pathology in primary progressive aphasia and frontotemporal dementia with pathologic Alzheimer disease. Acta Neuropathol 2010 1.19
16 With or without FUS, it is the anatomy that dictates the dementia phenotype. Brain 2009 1.12
17 Imaging connectivity in the human cerebral cortex: the next frontier? Ann Neurol 2005 1.12
18 Left hemicranial hypoplasia in 2 patients with primary progressive aphasia. Arch Neurol 2004 1.08
19 Expression of human FUS protein in Drosophila leads to progressive neurodegeneration. Protein Cell 2011 1.06
20 Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration. Arch Neurol 2011 1.01
21 Association of GSK3B with Alzheimer disease and frontotemporal dementia. Arch Neurol 2008 0.98
22 Covert processing of words and pictures in nonsemantic variants of primary progressive aphasia. Alzheimer Dis Assoc Disord 2008 0.97
23 Primary progressive aphasia pathology. Ann Neurol 2008 0.94
24 Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid. Acta Neuropathol 2013 0.91
25 An update on primary progressive aphasia. Curr Neurol Neurosci Rep 2007 0.90
26 Pilot trial of memantine in primary progressive aphasia. Alzheimer Dis Assoc Disord 2010 0.88
27 Anatomical physiology of spatial extinction. Cereb Cortex 2007 0.86
28 Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene. Mol Neurodegener 2014 0.84
29 A novel GRN mutation (GRN c.708+6_+9delTGAG) in frontotemporal lobar degeneration with TDP-43-positive inclusions: clinicopathologic report of 6 cases. J Neuropathol Exp Neurol 2014 0.77
30 Adult polyglucosan body disease with GBE1 haploinsufficiency and concomitant frontotemporal lobar degeneration. Neuropathol Appl Neurobiol 2014 0.77