Research output per year
Research output per year
Personal profile
Roles and responsibilities
Head, Statistical Genetics
Funding overview
Ada Bartholomew Medical Trust
National Health & Medical Research Council
National Institute of Health
Royal Perth Hospital Medical Research Found.
Texas Biomedical Research Institute
National Health & Medical Research Council
National Institute of Health
Royal Perth Hospital Medical Research Found.
Texas Biomedical Research Institute
Previous positions
Postdoctoral Scientist, Department of Genetics, Texas Biomedical Research Institute, San Antonio, Texas, USA
Teaching overview
Fundamentals of Genetic Epidemiology
Research
Genetic epidemiology of complex disease in families.
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
Research expertise keywords
- Statistical genetics
- Bioinformatics
- Genetic epidemiology
- Population genetics
- Computational Biology
- Transcriptomics
- Cardiovascular disease, genetics of
- Complex disease, genetics of
- Family-based genetic studies
- Phylogeography
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Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Author Correction: Topical application of an irreversible small molecule inhibitor of lysyl oxidases ameliorates skin scarring and fibrosis
Chaudhari, N., Findlay, A. D., Stevenson, A. W., Clemons, T. D., Yao, Y., Joshi, A., Sayyar, S., Wallace, G., Rea, S., Toshniwal, P., Deng, Z., Melton, P. E., Hortin, N., Iyer, K. S., Jarolimek, W., Wood, F. M. & Fear, M. W., Dec 2023, In: Nature Communications. 14, 1, p. 135 135.Research output: Contribution to journal › Article
Open Access -
Adiposity associated DNA methylation signatures in adolescents are related to leptin and perinatal factors
Huang, R. C., Melton, P. E., Burton, M. A., Beilin, L. J., Clarke-Harris, R., Cook, E., Godfrey, K. M., Burdge, G. C., Mori, T. A., Anderson, D., Rauschert, S., Craig, J. M., Kobor, M. S., MacIsaac, J. L., Morin, A. M., Oddy, W. H., Pennell, C. E., Holbrook, J. D. & Lillycrop, K. A., 2022, In: Epigenetics. 17, 8, p. 819-836 18 p.Research output: Contribution to journal › Article › peer-review
Open Access3 Citations (Web of Science) -
A methylome and transcriptome analysis of normal human scar cells reveals a role for FOXF2 in scar maintenance
Stevenson, A. W., Melton, P. E., Moses, E. K., Wallace, H. J., Wood, F. M., Rea, S., Danielsen, P. L., Alghamdi, M., Hortin, N., Borowczyk, J., Deng, Z., Manzur, M. & Fear, M. W., May 2022, In: The Journal of Investigative Dermatology. 142, 5, p. 1489-1498.e12Research output: Contribution to journal › Article › peer-review
2 Citations (Scopus) -
Association of protein function-altering variants with cardiometabolic traits: the strong heart study
Shan, Y., Cole, S. A., Haack, K., Melton, P. E., Best, L. G., Bizon, C., Kobes, S., Köroğlu, Ç., Baier, L. J., Hanson, R. L., Sanna, S., Li, Y. & Franceschini, N., Dec 2022, In: Scientific Reports. 12, 1, p. 9317 9317.Research output: Contribution to journal › Article › peer-review
Open Access -
Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease
Cadby, G., Giles, C., Melton, P. E., Huynh, K., Mellett, N. A., Duong, T., Nguyen, A., Cinel, M., Smith, A., Olshansky, G., Wang, T., Brozynska, M., Inouye, M., McCarthy, N. S., Ariff, A., Hung, J., Hui, J., Beilby, J., Dubé, M-P., Watts, G. F., & 24 others, Dec 2022, In: Nature Communications. 13, 1, 3124.Research output: Contribution to journal › Article › peer-review
Open Access3 Citations (Web of Science)
Datasets
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Supplemental Data: Heritability of 596 lipid species and genetic correlation with cardiovascular traits in the Busselton Family Heart Study
Cadby, G. (Creator), Melton, P. (Creator), McCarthy, N. (Creator), Giles, C. (Creator), Mellett, N. A. (Creator), Huynh, K. (Creator), Hung, J. (Creator), Beilby, J. (Creator), Dube, M. (Creator), Watts, G. (Creator), Blangero, J. (Creator), Meikle, P. J. (Creator) & Moses, E. (Creator), American Society for Biochemistry and Molecular Biology, 14 Feb 2020
DOI: 10.1194/jlr.RA119000594, https://www.jlr.org/content/early/2020/02/14/jlr.RA119000594/suppl/DC1
Dataset
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Using whole genome sequencing to identify pathogenic cop number variants in children with congenital heart defects
Zhang, B., Pachter, N. & Melton, P.
1/01/17 → 31/12/17
Project: Research
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Microbiome and Liver Injury in Nonalcoholic Fatty Liver Disease
Adams, L., Morrison, M. & Melton, P.
1/01/16 → 31/12/16
Project: Research
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NIRIS 2016 - Philip Melton
Department of Health (Western Australia)
1/01/16 → 31/12/16
Project: Research
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N/3 Pedigree Based Whole Genome Sequencing of Affective & Psychotic Disorders
Jablensky, A., McCarthy, N., Melton, P. & Moses, E.
1/03/15 → 28/02/19
Project: Research
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Prevalence, phenotype and genotype of common sleep disorders
Eastwood, P., Hillman, D., Moses, E., McArdle, N. & Melton, P.
National Health & Medical Research Council NHMRC
1/01/15 → 31/12/17
Project: Research