PubRank

A Singleton

Author PubWeight™ 63.99‹?›

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