Richard Allcock

Associate Professor, BSc PhD W.Aust.

  • The University of Western Australia (M504), 35 Stirling Highway, Room G3, M Block, QEII Medical Centre, Nedlands

    6009 Perth

    Australia

  • 1943 Citations
  • 24 h-Index
19952020
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Personal profile

Biography

Following my PhD, I undertook postdoctoral studies with John Trowsdale in Cambridge. I also spent time at the Cambridge Institute for Medical Research and the Wellcome Trust Sanger Institute. I returned to Perth in 2003 as a UWA postdoctoral Fellow and subsequently took up a Lectureship within the School of Surgery and Pathology. I have focussed on undergradaute teaching and curriculum devlopment in the BSc Patholgoy major. In 2009 I was promoted to Associate Professor within the new School of Pathology and Laboratory Medicine and moved to take over running of the LotteryWest State Biomedical Facility Genomics based at Royal Perth Hospital.

Keywords

  • Next-generation sequencing
  • Genomics
  • Bioinformatics
  • Immunogenetics
  • Exome sequencing
  • Whole-genome sequencing

Fingerprint Fingerprint is based on mining the text of the person's scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 19 Similar Profiles
Haplotypes Medicine & Life Sciences
Genes Medicine & Life Sciences
Major Histocompatibility Complex Medicine & Life Sciences
Exome Medicine & Life Sciences
Alleles Medicine & Life Sciences
Mutation Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences
Inclusion Body Myositis Medicine & Life Sciences

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Research Output 1995 2019

Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes

Melton, P. E., Johnson, M. P., Gokhale-Agashe, D., Rea, A. J., Ariff, A., Cadby, G., Peralta, J. M., Mcnab, T. J., Allcock, R. J., Abraham, L. J., Blangero, J., Brennecke, S. P. & Moses, E. K., 9 Jan 2019, In : Journal of Hypertension. 15 p.

Research output: Contribution to journalArticle

Exome
Pre-Eclampsia
Genes
Chromosomes, Human, Pair 1
Open Reading Frames
2 Citations (Scopus)

An examination of multiple classes of rare variants in extended families with bipolar disorder

Toma, C., Shaw, A. D., Allcock, R. J. N., Heath, A., Pierce, K. D., Mitchell, P. B., Schofield, P. R. & Fullerton, J. M., 1 Dec 2018, In : Translational Psychiatry. 8, 1, 65.

Research output: Contribution to journalArticle

Open Access
Bipolar Disorder
Exome
Penetrance
Genetic Association Studies
Genes

A Pilot Study to Non-Invasively Track PIK3CA Mutation in Head and Neck Cancer

Schmidt, H., Kulasinghe, A., Allcock, R. J. N., Tan, L. Y., Mokany, E., Kenny, L. & Punyadeera, C., Dec 2018, In : Diagnostics. 8, 4, 9 p., 79.

Research output: Contribution to journalArticle

1 Citation (Scopus)
Open Access
Molecular Biology
Genes
Carcinoma
Tumors
Mutation
3 Citations (Scopus)

Malignant cells from pleural fluids in malignant mesothelioma patients reveal novel mutations

Sneddon, S. A., Dick, I. M., Lee, Y. C., Musk, A. W., Allcock, R. J., Waddell, N., Patch, A-M., Pearson, J. V., Holt, R. A., Robinson, B. W. & Creaney, J., May 2018, In : Lung Cancer. 119, p. 64-70

Research output: Contribution to journalArticle

Open Access
Mesothelioma
Mutation
Pleural Effusion
Neoplasms
Malignant Mesothelioma

Projects 2000 2020