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List of works by Jim Stankovich

2-D and 3-D Interactions in Random Sequential Adsorption of Charged Particles

scientific article published in October 1997

A DNA resequencing array for genes involved in Parkinson's disease.

scientific article

A clinical screening tool identifies autoimmune diabetes in adults

scientific article published on 01 May 2006

A genome-wide association study in progressive multiple sclerosis

scientific journal article

A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis

scientific article (publication date: 26 October 2010)

A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis.

scientific article published on 17 July 2015

An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3

scientific article

Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patients

scientific article published on 26 January 2007

Anticipation in familial hematologic malignancies

article

Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy

scientific article published in September 2009

Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis

scientific article

Association of ACE gene polymorphism with genetic susceptibility to systemic lupus erythematosus in a Chinese population: a family-based association study

scientific article published on 15 October 2007

CTLA-4 and multiple sclerosis: the A49G single nucleotide polymorphism shows no association with multiple sclerosis in a Southern Australian population

article

Combined approach for finding susceptibility genes in DISH/chondrocalcinosis families: whole-genome-wide linkage and IBS/IBD studies

scientific article published on 2 November 2017

Common variants at 12q14 and 12q24 are associated with hippocampal volume

scientific article

Common variation in the MOG gene influences transcript splicing in humans.

scientific article published on 30 August 2010

Confirmation of the Adult-Onset Primary Open Angle Glaucoma Locus GLC1B at 2cen-q13 in an Australian Family

article

Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data.

scientific article

Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations

scientific article published on 8 June 2017

Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus.

scientific article

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

scientific article

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

scientific article

HLA-DRB1 associations with disease susceptibility and clinical course in Australians with multiple sclerosis.

scientific article published on 21 April 2009

Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study

scientific article published on 5 January 2007

Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition

scientific article published on 13 December 2010

Human leukocyte antigen-DR15, low infant sibling exposure and multiple sclerosis: Gene-environment interaction

article

Identifying nineteenth century genealogical links from genotypes

scientific article published on 10 May 2005

Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis

scientific article

Individual and joint action of environmental factors and risk of MS.

scientific article published on May 2011

Interactions between Two Spherical Particles with Nonuniform Surface Potentials: The Linearized Poisson-Boltzmann Theory

scientific article published in August 1999

Investigating a cluster of vulvar cancer in young women: a cross-sectional study of genital human papillomavirus prevalence

scientific article

Investigation of chromosome 2q in osteoarthritis of the hand: no significant linkage in a Tasmanian population

scientific article published on December 2002

Linkage Replication of theMYP12Locus in Common Myopia

scientific article published in October 2007

Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree

scientific article published on October 2005

Measuring environmental factors can enhance the search for disease causing genes?

scientific article

Melanocortin 1 receptor genotype, past environmental sun exposure, and risk of multiple sclerosis.

scientific article published on August 2008

Misclassification due to body hair and seasonal variation on melanin density estimates for skin type using spectrophotometry

scientific article published on August 2002

Modelling genetic susceptibility to multiple sclerosis with family data.

scientific article

Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients

scientific article

Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

scientific article

On the utility of data from the International HapMap Project for Australian association studies.

scientific article

Past environmental sun exposure and risk of multiple sclerosis: a role for the Cdx-2 Vitamin D receptor variant in this interaction.

scientific article published on 21 April 2009

Planning for the future: Emergency department presentation patterns in Tasmania, Australia

scientific article published on 22 September 2017

Polymorphisms in the receptor tyrosine kinase MERTK gene are associated with multiple sclerosis susceptibility

scientific article (publication date: 8 February 2011)

Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes

scientific article published on 12 February 2013

Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies

scientific article published on 03 March 2010

Sequence variants of alpha-methylacyl-CoA racemase are associated with prostate cancer risk: a replication study in an ethnically homogeneous population

scientific article published on 01 September 2008

Syndrome X in 8-y-old Australian children: stronger associations with current body fatness than with infant size or growth

scientific article published on 01 October 2002

The advantages of dense marker sets for linkage analysis with very large families.

scientific article published on 25 January 2007

The association between hormonal and reproductive factors and hand osteoarthritis.

scientific article

The genetic contribution and relevance of knee cartilage defects: case-control and sib-pair studies

scientific article published on 01 October 2005

The genetic contribution to longitudinal changes in knee structure and muscle strength: a sibpair study

scientific article published on 01 September 2005

The use of computer-assisted-telephone-interviewing to diagnose seizures, epilepsy and idiopathic generalized epilepsy

scientific article

Tonography Demonstrates Reduced Facility of Outflow of Aqueous Humor in Myocilin Mutation Carriers

scientific article published on 01 June 2003

Trends in diabetes management practices of patients from an Australian insulin-treated diabetes register.

scientific article published on February 2004

Using genetic advances to investigate diabetes in Tasmania

scientific article published on 01 January 2001

Vitamin D status: multifactorial contribution of environment, genes and other factors in healthy Australian adults across a latitude gradient

scientific article published on 08 February 2013

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