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A Singleton
Author PubWeight™ 63.99
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
alpha-Synuclein locus triplication causes Parkinson's disease.
Science
2003
20.20
2
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
N Engl J Med
2009
7.53
3
Lewy bodies and parkinsonism in families with parkin mutations.
Ann Neurol
2001
2.50
4
D2 dopamine receptor gene (DRD2) Taq1 A polymorphism: reduced dopamine D2 receptor binding in the human striatum associated with the A1 allele.
Pharmacogenetics
1997
2.28
5
General practitioners' continuing education: a review of policies, strategies and effectiveness, and their implications for the future.
Br J Gen Pract
1998
2.20
6
alpha-Synuclein gene haplotypes are associated with Parkinson's disease.
Hum Mol Genet
2001
2.07
7
SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia.
Neurology
2008
1.79
8
Genome-wide association study of obsessive-compulsive disorder.
Mol Psychiatry
2012
1.57
9
LRRK2 gene in Parkinson disease: mutation analysis and case control association study.
Neurology
2005
1.56
10
Genome-wide association study of Tourette's syndrome.
Mol Psychiatry
2012
1.42
11
Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.
Neurology
2000
1.31
12
Prophylactic immunization against experimental leishmaniasis. V. Mechanism of the anti-protective blocking effect induced by subcutaneous immunization against Leishmania major infection.
J Immunol
1985
1.29
13
Genomic biomarkers and cellular pathways of ischemic stroke by RNA gene expression profiling.
Neurology
2010
1.23
14
Neurocirculatory and nigrostriatal abnormalities in Parkinson disease from LRRK2 mutation.
Neurology
2007
1.16
15
Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family.
Arch Neurol
2001
1.01
16
The genetics of ischaemic stroke.
J Intern Med
2010
1.01
17
Lack of association with TorsinA haplotype in German patients with sporadic dystonia.
Neurology
2006
1.01
18
Clinical features of patients with blepharospasm: a report of 240 patients.
Eur J Neurol
2011
0.99
19
Whole genome analysis in a consanguineous family with early onset Alzheimer's disease.
Neurobiol Aging
2008
0.95
20
The future of genetic analysis of neurological disorders.
Neurobiol Dis
2000
0.93
21
Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes.
Eur J Hum Genet
2001
0.93
22
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion.
Hum Mol Genet
1999
0.90
23
Clinical heterogeneity and genotype-phenotype correlations in hereditary spastic paraplegia because of Spatacsin mutations (SPG11).
Eur J Neurol
2008
0.90
24
Lack of aggregation of ischemic stroke subtypes within affected sibling pairs.
Neurology
2007
0.90
25
Lymphopain, a cytotoxic T and natural killer cell-associated cysteine proteinase.
Leukemia
1998
0.82
26
Genetic analysis of synphilin-1 in familial Parkinson's disease.
Neurobiol Dis
2001
0.81
27
Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19.
Neurogenetics
2009
0.81
28
A variant in the HS1-BP3 gene is associated with familial essential tremor.
Neurology
2005
0.80
29
Autoradiographic localization of atrial natriuretic peptide receptor subtypes in rat kidney.
Am J Physiol
1990
0.78
30
Heterogeneous binding sites for alpha-atrial natriuretic peptide in human umbilical cord and placenta.
Am J Physiol
1991
0.76
31
Small de novo duplication in the repeat region of the TATA-box-binding protein gene manifest with a phenotype similar to variant Creutzfeldt-Jakob disease.
Clin Genet
2004
0.76
32
Low prevalence of PANK2 mutations in Brazilian patients with early onset generalised dystonia and basal ganglia abnormalities on MRI.
J Neurol Neurosurg Psychiatry
2010
0.75
33
Community care and general practice. Multidisciplinary, proactive care is needed.
BMJ
1996
0.75
34
Peptide inhibitors of C3 breakdown.
Clin Exp Immunol
1990
0.75
35
Adolescent fertility management: the Sierra Leone experience.
J Famil Health Train
1982
0.75
36
LRRK2 mutations in a clinic-based cohort of Parkinson's disease.
Eur J Neurol
2006
0.75
37
Patient classification systems.
J N Y State Nurses Assoc
1980
0.75
38
[Increment in height of the upper segment and bi-iliac diameter after menarche in young girls. Longitudinal study of 40 adolescents].
Arch Fr Pediatr
1975
0.75
39
The 'anatomy' of infection.
Aust Nurses J
1983
0.75
40
Referrals and relationships: in-practice referrals meetings in a general practice.
Fam Pract
2001
0.75