List of works - Richard Allcock

A haplotype spanning P2X7R, P2X4R and CAMKK2 may mark susceptibility to pulmonary non-tuberculous mycobacterial disease

scientific article published on 23 February 2017

A new species of mesonivirus from the Northern Territory, Australia

scientific article (publication date: 2014)

A promoter polymorphism in the central MHC gene, IKBL, influences the binding of transcription factors USF1 and E47 on disease-associated haplotypes.

scientific article

Alleles of the proximal promoter of BAT1, a putative anti-inflammatory gene adjacent to the TNF cluster, reduce transcription on a disease-associated MHC haplotype

scientific article

Archival Isolates Confirm a Single Topotype of West Nile Virus in Australia

scientific article

Australian bat lyssavirus infection in two horses

scientific article published on 19 August 2014

Characterization and transferability of microsatellites for the Kangaroo Paw, Anigozanthos manglesii (Haemodoraceae).

scientific article

Combined DNA, toxicological and heavy metal analyses provides an auditing toolkit to improve pharmacovigilance of traditional Chinese medicine (TCM)

scientific article

Comparison of faecal microbiota in Blastocystis-positive and Blastocystis-negative irritable bowel syndrome patients.

scientific article published on 31 August 2016

Complete MHC haplotype sequencing for common disease gene mapping

scientific article published on 12 May 2004

Complete coding sequences of three members of the kokobera group of flaviviruses

scientific article published on 18 September 2014

Detection of arboviruses and other micro-organisms in experimentally infected mosquitoes using massively parallel sequencing

scientific article

Detection of variations and identifying genomic breakpoints for large deletions in the LDLR by Ion Torrent semiconductor sequencing

scientific article published on 4 August 2013

Discovery and characterisation of a new insect-specific bunyavirus from Culex mosquitoes captured in northern Australia

scientific article

Erdheim-Chester disease associated with a novel, complex BRAF p.Thr599_Val600delinsArgGlu mutation

scientific article

Genetic Characterization of Archived Bunyaviruses and their Potential for Emergence in Australia

scientific article

Genomic sequence and expression profile of murine Bat1a and Nfkbil1.

scientific article published on August 2006

High-Density SNP genotyping defines 17 distinct haplotypes of the TNF block in the Caucasian population: implications for haplotype tagging

scientific article

Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy

scientific article

Isolation and characterization of 13 microsatellites for the rare endemic shrub Tetratheca erubescens (Elaeocarpaceae).

scientific article published on 09 February 2016

Isolation and characterization of microsatellite primers for the critically endangered shrub Styphelia longissima (Ericaceae).

scientific article

Microbial 16S rRNA Ion Tag and community metagenome sequencing using the Ion Torrent (PGM) Platform

scientific article

Microbial Functional Capacity Is Preserved Within Engineered Soil Formulations Used In Mine Site Restoration

scientific article

Microsatellite markers from the Ion Torrent: a multi-species contrast to 454 shotgun sequencing.

scientific article published on 29 November 2013

Multiple immune factors are involved in controlling acute and chronic chikungunya virus infection

scientific article

Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia.

scientific article published on August 2013

Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy

scientific article published on 06 June 2013

Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita

scientific journal article

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

scientific article

Next generation sequencing of the nidus of early (adenosquamous proliferation rich) radial sclerosing lesions of the breast reveals evidence for a neoplastic precursor lesion

scientific article

Polymorphisms at positions -22 and -348 in the promoter of the BAT1 gene affect transcription and the binding of nuclear factors

scientific article (publication date: May 2004)

Polymorphisms in CAMKK2 may predict sensory neuropathy in African HIV patients

scientific article

Polymorphisms of the CRP gene inhibit inflammatory response and increase susceptibility to depression: the Health in Men Study

scientific article published on 11 May 2009

Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complex.

scientific article published on 2 May 2011

SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathy

scientific article

Scrapheap challenge: a novel bulk-bone metabarcoding method to investigate ancient DNA in faunal assemblages

scientific article (publication date: 28 November 2013)

Susceptibility to non-tuberculous mycobacterial disease is influenced by rs1518111 in IL10.

scientific article published on 4 February 2017

The human TREM gene cluster at 6p21.1 encodes both activating and inhibitory single IgV domain receptors and includes NKp44

scientific article

The major histocompatibility complex: a paradigm for studies of the human genome

scientific article published on January 2012

Towards a universal molecular microbiological test

scientific article

Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project

scientific article

Whole exome sequencing in foetal akinesia expands the genotype-phenotype spectrum of GBE1 glycogen storage disease mutations

scientific article

Whole exome sequencing of an asbestos-induced wild-type murine model of malignant mesothelioma

scientific article

List of works by Richard Allcock

A haplotype spanning P2X7R, P2X4R and CAMKK2 may mark susceptibility to pulmonary non-tuberculous mycobacterial disease

A new species of mesonivirus from the Northern Territory, Australia

A promoter polymorphism in the central MHC gene, IKBL, influences the binding of transcription factors USF1 and E47 on disease-associated haplotypes.

Alleles of the proximal promoter of BAT1, a putative anti-inflammatory gene adjacent to the TNF cluster, reduce transcription on a disease-associated MHC haplotype

Archival Isolates Confirm a Single Topotype of West Nile Virus in Australia

Australian bat lyssavirus infection in two horses

Characterization and transferability of microsatellites for the Kangaroo Paw, Anigozanthos manglesii (Haemodoraceae).

Combined DNA, toxicological and heavy metal analyses provides an auditing toolkit to improve pharmacovigilance of traditional Chinese medicine (TCM)

Comparison of faecal microbiota in Blastocystis-positive and Blastocystis-negative irritable bowel syndrome patients.

Complete MHC haplotype sequencing for common disease gene mapping

Complete coding sequences of three members of the kokobera group of flaviviruses

Detection of arboviruses and other micro-organisms in experimentally infected mosquitoes using massively parallel sequencing

Detection of variations and identifying genomic breakpoints for large deletions in the LDLR by Ion Torrent semiconductor sequencing

Discovery and characterisation of a new insect-specific bunyavirus from Culex mosquitoes captured in northern Australia

Erdheim-Chester disease associated with a novel, complex BRAF p.Thr599_Val600delinsArgGlu mutation

Genetic Characterization of Archived Bunyaviruses and their Potential for Emergence in Australia

Genomic sequence and expression profile of murine Bat1a and Nfkbil1.

High-Density SNP genotyping defines 17 distinct haplotypes of the TNF block in the Caucasian population: implications for haplotype tagging

Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy

Isolation and characterization of 13 microsatellites for the rare endemic shrub Tetratheca erubescens (Elaeocarpaceae).

Isolation and characterization of microsatellite primers for the critically endangered shrub Styphelia longissima (Ericaceae).

Microbial 16S rRNA Ion Tag and community metagenome sequencing using the Ion Torrent (PGM) Platform

Microbial Functional Capacity Is Preserved Within Engineered Soil Formulations Used In Mine Site Restoration

Microsatellite markers from the Ion Torrent: a multi-species contrast to 454 shotgun sequencing.

Multiple immune factors are involved in controlling acute and chronic chikungunya virus infection

Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia.

Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy

Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

Next generation sequencing of the nidus of early (adenosquamous proliferation rich) radial sclerosing lesions of the breast reveals evidence for a neoplastic precursor lesion

Polymorphisms at positions -22 and -348 in the promoter of the BAT1 gene affect transcription and the binding of nuclear factors

Polymorphisms in CAMKK2 may predict sensory neuropathy in African HIV patients

Polymorphisms of the CRP gene inhibit inflammatory response and increase susceptibility to depression: the Health in Men Study

Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complex.

SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathy

Scrapheap challenge: a novel bulk-bone metabarcoding method to investigate ancient DNA in faunal assemblages

Susceptibility to non-tuberculous mycobacterial disease is influenced by rs1518111 in IL10.

The human TREM gene cluster at 6p21.1 encodes both activating and inhibitory single IgV domain receptors and includes NKp44

The major histocompatibility complex: a paradigm for studies of the human genome

Towards a universal molecular microbiological test

Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project

Whole exome sequencing in foetal akinesia expands the genotype-phenotype spectrum of GBE1 glycogen storage disease mutations

Whole exome sequencing of an asbestos-induced wild-type murine model of malignant mesothelioma