List of works - Justin P Rubio

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

scientific article

A YAC contig map of Plasmodium falciparum chromosome 4: characterization of a DNA amplification between two recently separated isolates

scientific article published on 01 March 1995

A conserved sorting-associated protein is mutant in chorea-acanthocytosis

scientific article published in June 2001

A genome-wide association study in progressive multiple sclerosis

scientific journal article

A genomewide association study of smoking relapse in four European population-based samples

scientific article published on 01 August 2013

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

scientific article (publication date: 26 October 2010)

An 18-kDa translocator protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28

scientific article

CD127 immunophenotyping suggests altered CD4+ T cell regulation in primary progressive multiple sclerosis

scientific article published on 11 April 2008

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

scientific article published on 30 August 2010

Current status of the Plasmodium falciparum genome project.

scientific article published on July 1996

Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe.

scientific article published on 4 April 2012

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

scientific article

Effects of enzyme inducers efavirenz and tipranavir/ritonavir on the pharmacokinetics of the HIV integrase inhibitor dolutegravir

scientific article

Estimation of the Antirelapse Efficacy of Tafenoquine, Using Plasmodium vivax Genotyping.

scientific article published on 23 October 2015

Evaluation of the effect of UGT1A1 polymorphisms on dolutegravir pharmacokinetics

scientific article published on January 2014

Exome array analysis suggests an increased variant burden in families with schizophrenia.

scientific article

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

scientific article

Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosis

article

Genetic deficiency of plasma lipoprotein-associated phospholipase A2 (PLA2G7 V297F null mutation) and risk of Alzheimer's disease in Japan

scientific article published on 01 January 2010

Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis

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

Haplotypes of the interleukin 7 receptor alpha gene are correlated with altered expression in whole blood cells in multiple sclerosis.

scientific article published on 11 October 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

Interleukin-2 receptor-α proximal promoter hypomethylation is associated with multiple sclerosis

scientific article

Leptin's metabolic and immune functions can be uncoupled at the ligand/receptor interaction level

scientific article

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

scientific article

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

scientific article

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease

scientific article published in May 2007

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

scientific article published on 03 March 2010

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

scientific article

Tafenoquine treatment of Plasmodium vivax malaria: suggestive evidence that CYP2D6 reduced metabolism is not associated with relapse in the Phase 2b DETECTIVE trial.

scientific article published on 18 February 2016

The ATP-binding cassette (ABC) gene family of Plasmodium falciparum.

scientific article published on April 1996

The chorea of McLeod syndrome

scientific article published on 01 September 2001

The chromosomal organization of the Plasmodium falciparum var gene family is conserved

scientific article published on 01 July 1997

Validation of linear cerebral atrophy markers in multiple sclerosis

scientific article published on 01 February 2008

Variants of ST8SIA1 are associated with risk of developing multiple sclerosis

scientific article

List of works by Justin P Rubio

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

A YAC contig map of Plasmodium falciparum chromosome 4: characterization of a DNA amplification between two recently separated isolates

A conserved sorting-associated protein is mutant in chorea-acanthocytosis

A genome-wide association study in progressive multiple sclerosis

A genomewide association study of smoking relapse in four European population-based samples

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

An 18-kDa translocator protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28

CD127 immunophenotyping suggests altered CD4+ T cell regulation in primary progressive multiple sclerosis

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

Current status of the Plasmodium falciparum genome project.

Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe.

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

Effects of enzyme inducers efavirenz and tipranavir/ritonavir on the pharmacokinetics of the HIV integrase inhibitor dolutegravir

Estimation of the Antirelapse Efficacy of Tafenoquine, Using Plasmodium vivax Genotyping.

Evaluation of the effect of UGT1A1 polymorphisms on dolutegravir pharmacokinetics

Exome array analysis suggests an increased variant burden in families with schizophrenia.

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

Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosis

Genetic deficiency of plasma lipoprotein-associated phospholipase A2 (PLA2G7 V297F null mutation) and risk of Alzheimer's disease in Japan

Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis

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

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

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

Haplotypes of the interleukin 7 receptor alpha gene are correlated with altered expression in whole blood cells in multiple sclerosis.

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

Interleukin-2 receptor-α proximal promoter hypomethylation is associated with multiple sclerosis

Leptin's metabolic and immune functions can be uncoupled at the ligand/receptor interaction level

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

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

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease

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

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

Tafenoquine treatment of Plasmodium vivax malaria: suggestive evidence that CYP2D6 reduced metabolism is not associated with relapse in the Phase 2b DETECTIVE trial.

The ATP-binding cassette (ABC) gene family of Plasmodium falciparum.

The chorea of McLeod syndrome

The chromosomal organization of the Plasmodium falciparum var gene family is conserved

Validation of linear cerebral atrophy markers in multiple sclerosis

Variants of ST8SIA1 are associated with risk of developing multiple sclerosis