| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Cerebral white matter lesions, vascular risk factors, and cognitive function in a population-based study: the Rotterdam Study.
|
Neurology
|
1994
|
3.75
|
|
2
|
Intracerebral hematomas during anticoagulant treatment.
|
Stroke
|
1990
|
2.97
|
|
3
|
Distinct genetic forms of frontotemporal dementia.
|
Neurology
|
2008
|
2.15
|
|
4
|
Cognitive correlates of ventricular enlargement and cerebral white matter lesions on magnetic resonance imaging. The Rotterdam Study.
|
Stroke
|
1994
|
2.14
|
|
5
|
[Familial forms of fronto-temporal dementia].
|
Ned Tijdschr Geneeskd
|
1995
|
2.04
|
|
6
|
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism.
|
Neurol Sci
|
2003
|
1.90
|
|
7
|
Octapeptide repeat insertions in the prion protein gene and early onset dementia.
|
J Neurol Neurosurg Psychiatry
|
2004
|
1.87
|
|
8
|
Incidence of dementia: does gender make a difference?
|
Neurobiol Aging
|
2001
|
1.81
|
|
9
|
Familial aggregation in frontotemporal dementia.
|
Neurology
|
1998
|
1.76
|
|
10
|
Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options.
|
Eur J Neurol
|
2009
|
1.76
|
|
11
|
Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.
|
Am J Hum Genet
|
2001
|
1.71
|
|
12
|
Familial aggregation of parkinsonism in progressive supranuclear palsy.
|
Neurology
|
2009
|
1.68
|
|
13
|
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.
|
Brain
|
2001
|
1.59
|
|
14
|
Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau.
|
Am J Pathol
|
1998
|
1.50
|
|
15
|
Cerebral white matter lesions and atherosclerosis in the Rotterdam Study.
|
Lancet
|
1993
|
1.49
|
|
16
|
Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology.
|
J Neurol Neurosurg Psychiatry
|
2009
|
1.43
|
|
17
|
[Clinical thinking and decision making in practice. A student with sudden headache].
|
Ned Tijdschr Geneeskd
|
2000
|
1.39
|
|
18
|
Prognostic factors in patients with intracerebral haematoma.
|
J Neurol Neurosurg Psychiatry
|
1992
|
1.38
|
|
19
|
Diagnosis and management of early- and late-onset cerebellar ataxia.
|
Clin Genet
|
2007
|
1.22
|
|
20
|
Frontal presentation in progressive supranuclear palsy.
|
Neurology
|
2007
|
1.12
|
|
21
|
Medical and environmental risk factors for sporadic frontotemporal dementia: a retrospective case-control study.
|
J Neurol Neurosurg Psychiatry
|
2003
|
1.09
|
|
22
|
Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families.
|
Ann Neurol
|
1997
|
1.09
|
|
23
|
Molecular analysis of mutant and wild-type tau deposited in the brain affected by the FTDP-17 R406W mutation.
|
Am J Pathol
|
2001
|
1.02
|
|
24
|
Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathology.
|
Brain
|
2005
|
1.01
|
|
25
|
Familial clustering and genetic risk for dementia in a genetically isolated Dutch population.
|
Brain
|
2004
|
1.00
|
|
26
|
Familial aggregation, the PDE4D gene, and ischemic stroke in a genetically isolated population.
|
Neurology
|
2005
|
0.99
|
|
27
|
Insulin-resistance and metabolic syndrome are related to executive function in women in a large family-based study.
|
Eur J Epidemiol
|
2010
|
0.99
|
|
28
|
Complex compulsive behaviour in the temporal variant of frontotemporal dementia.
|
J Neurol
|
2001
|
0.98
|
|
29
|
Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohort.
|
J Neurol
|
2014
|
0.98
|
|
30
|
Vascular risk factors, atherosclerosis, cerebral white matter lesions and cerebral perfusion in a population-based study.
|
Eur J Nucl Med
|
1996
|
0.96
|
|
31
|
Cerebrovascular risk factors do not contribute to genetic variance of cognitive function: the ERF study.
|
Neurobiol Aging
|
2006
|
0.96
|
|
32
|
Apolipoprotein E gene and sporadic frontal lobe dementia.
|
Neurology
|
1997
|
0.93
|
|
33
|
Reproductive period and risk of dementia in postmenopausal women.
|
JAMA
|
2001
|
0.92
|
|
34
|
Loss of frontal fMRI activation in early frontotemporal dementia compared to early AD.
|
Neurology
|
2003
|
0.91
|
|
35
|
Recurrent stroke after transient ischaemic attack or minor ischaemic stroke: does the distinction between small and large vessel disease remain true to type? Dutch TIA Trial Study Group.
|
J Neurol Neurosurg Psychiatry
|
1995
|
0.90
|
|
36
|
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7.
|
Neurol Sci
|
2002
|
0.89
|
|
37
|
The apolipoprotein E epsilon 4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations.
|
Ann Neurol
|
1994
|
0.89
|
|
38
|
Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patients.
|
Hum Mol Genet
|
2000
|
0.88
|
|
39
|
Preparing for presymptomatic DNA testing for early onset Alzheimer's disease/cerebral haemorrhage and hereditary Pick disease.
|
J Med Genet
|
1997
|
0.88
|
|
40
|
Cathepsin D gene and the risk of Alzheimer's disease: a population-based study and meta-analysis.
|
Neurobiol Aging
|
2009
|
0.87
|
|
41
|
Coexistent tau and amyloid pathology in hereditary frontotemporal dementia with tau mutations.
|
Ann N Y Acad Sci
|
2000
|
0.87
|
|
42
|
Genetic risk factors for cerebral small-vessel disease in hypertensive patients from a genetically isolated population.
|
J Neurol Neurosurg Psychiatry
|
2010
|
0.86
|
|
43
|
Choroid plexus papilloma in the posterior fossa.
|
Surg Neurol
|
1987
|
0.86
|
|
44
|
Residual lesions on computed tomography after intracerebral hemorrhage.
|
Stroke
|
1991
|
0.84
|
|
45
|
Brain perfusion patterns in familial frontotemporal lobar degeneration.
|
Neurology
|
2011
|
0.83
|
|
46
|
Apolipoprotein E4 in the temporal variant of frontotemporal dementia.
|
J Neurol Neurosurg Psychiatry
|
2002
|
0.81
|
|
47
|
A new locus for a childhood onset, slowly progressive autosomal recessive spinocerebellar ataxia maps to chromosome 11p15.
|
J Med Genet
|
2004
|
0.80
|
|
48
|
Meningitis, cranial nerve palsies and bilateral cerebral infarcts : a neurological variant of Lemierre's syndrome.
|
J Neurol
|
2008
|
0.80
|
|
49
|
A clinical-genetic study of Parkinson's disease in a genetically isolated community.
|
J Neurol
|
2003
|
0.79
|
|
50
|
Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations.
|
Neurosci Lett
|
1999
|
0.78
|
|
51
|
Does cerebral infarction after a previous warning occur in the same vascular territory?
|
Stroke
|
1993
|
0.78
|
|
52
|
Recent advances in progressive supranuclear palsy: a review.
|
Curr Alzheimer Res
|
2011
|
0.76
|
|
53
|
The Dutch Vascular Factors in Dementia Study: rationale and design.
|
J Neurol
|
1998
|
0.75
|
|
54
|
[Progressive supranuclear palsy; an unusual form of parkinsonism].
|
Ned Tijdschr Geneeskd
|
2004
|
0.75
|
|
55
|
[New insights in frontotemporal dementia].
|
Ned Tijdschr Geneeskd
|
2000
|
0.75
|