PubRank

Jim Stankovich

Author PubWeight™ 47.91‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature 2011 13.23
2 Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. Ann Neurol 2011 3.52
3 Common variants at 12q14 and 12q24 are associated with hippocampal volume. Nat Genet 2012 1.79
4 The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis. Hum Mol Genet 2010 1.73
5 Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis. Am J Hum Genet 2008 1.69
6 A clinical screening tool identifies autoimmune diabetes in adults. Diabetes Care 2006 1.59
7 Human leukocyte antigen-DR15, low infant sibling exposure and multiple sclerosis: gene-environment interaction. Ann Neurol 2010 1.55
8 A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis. PLoS One 2010 1.38
9 Vitamin D status: multifactorial contribution of environment, genes and other factors in healthy Australian adults across a latitude gradient. J Steroid Biochem Mol Biol 2013 1.33
10 Saliva-derived DNA performs well in large-scale, high-density single-nucleotide polymorphism microarray studies. Cancer Epidemiol Biomarkers Prev 2010 1.27
11 The apolipoprotein epsilon4 gene is associated with elevated risk of normal tension glaucoma. Mol Vis 2002 1.19
12 Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand. Hum Genet 2010 0.97
13 Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study. Hum Genet 2007 0.95
14 A genome-wide association study in progressive multiple sclerosis. Mult Scler 2012 0.93
15 Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis. Hum Genet 2004 0.89
16 Tonography demonstrates reduced facility of outflow of aqueous humor in myocilin mutation carriers. J Glaucoma 2003 0.88
17 Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus. J Neuroimmunol 2009 0.87
18 Investigating a cluster of vulvar cancer in young women: a cross-sectional study of genital human papillomavirus prevalence. BMC Infect Dis 2012 0.87
19 Linkage replication of the MYP12 locus in common myopia. Invest Ophthalmol Vis Sci 2007 0.86
20 Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data. Hum Genet 2005 0.86
21 Polymorphisms in the receptor tyrosine kinase MERTK gene are associated with multiple sclerosis susceptibility. PLoS One 2011 0.86
22 Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients. PLoS One 2010 0.85
23 Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes. Hum Mol Genet 2013 0.85
24 Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis. PLoS One 2013 0.85
25 Multipoint approximations of identity-by-descent probabilities for accurate linkage analysis of distantly related individuals. Am J Hum Genet 2008 0.84
26 The advantages of dense marker sets for linkage analysis with very large families. Hum Genet 2007 0.80
27 An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3. Arthritis Res Ther 2014 0.79
28 CTLA-4 and multiple sclerosis: the A49G single nucleotide polymorphism shows no association with multiple sclerosis in a Southern Australian population. J Neuroimmunol 2008 0.79
29 Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patients. Immunogenetics 2007 0.78
30 Association of ACE gene polymorphism with genetic susceptibility to systemic lupus erythematosus in a Chinese population: a family-based association study. J Rheumatol 2007 0.78
31 Common variation in the MOG gene influences transcript splicing in humans. J Neuroimmunol 2010 0.77
32 Misclassification due to body hair and seasonal variation on melanin density estimates for skin type using spectrophotometry. J Photochem Photobiol B 2002 0.77
33 Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypes. Br J Haematol 2010 0.76
34 The use of computer-assisted-telephone-interviewing to diagnose seizures, epilepsy and idiopathic generalized epilepsy. Epilepsy Res 2010 0.75
35 Multiple sclerosis: a haplotype association study. Novartis Found Symp 2005 0.75