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.
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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Research output
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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., 8 Feb 2021, (E-pub ahead of print) In: Epigenetics.Research output: Contribution to journal › Article › peer-review
Open Access -
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., 21 Oct 2021, (E-pub ahead of print) In: The Journal of Investigative Dermatology.Research output: Contribution to journal › Article › peer-review
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DNA methylation patterns within whole blood of adolescents born from assisted reproductive technology are not different from adolescents born from natural conception
Penova-Veselinovic, B., Melton, P. E., Huang, R. C., Yovich, J. L., Burton, P., Wijs, L. A. & Hart, R. J., 18 Jun 2021, In: Human Reproduction. 36, 7, p. 2035 - 2049Research output: Contribution to journal › Article › peer-review
2 Citations (Scopus) -
Epigenome-Wide Association Study of Thyroid Function Traits Identifies Novel Associations of fT3 With KLF9 and DOT1L
Lafontaine, N., Campbell, P. J., Castillo-Fernandez, J. E., Mullin, S., Lim, E. M., Kendrew, P., Lewer, M., Brown, S. J., Huang, R-C., Melton, P. E., Mori, T. A., Beilin, L. J., Dudbridge, F., Spector, T. D., Wright, M. J., Martin, N. G., McRae, A. F., Panicker, V., Zhu, G., Walsh, J. P. & 2 others, , May 2021, In: The Journal of clinical endocrinology and metabolism. 106, 5, p. e2191–e2202Research output: Contribution to journal › Article › peer-review
2 Citations (Scopus) -
Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3
Nolan, J., Campbell, P. J., Brown, S. J., Zhu, G., Gordon, S., Lim, E. M., Joseph, J., Cross, S., Panicker, V., Medland, S. E., Melton, P., Beilin, L. J., Mori, T. A., Mullin, B., Pennell, C., Wang, C., Dudbridge, F., Walsh, J. P., Martin, N. G. & Wilson, S. G., Nov 2021, In: European Journal of Endocrinology. 185, 5, p. 743-753Research output: Contribution to journal › Article › peer-review
Open AccessFile13 Downloads (Pure)
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.
Royal Perth Hospital Medical Research Foundation
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.
The University of Western Australia
1/01/16 → 31/12/16
Project: Research
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NIRIS 2016 - Philip Melton
Government of Western Australia, Department of Health
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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Microbiome Diversity, Nutritional Status and Gut Dysbiosis in Amerindians
Melton, P., Baldi, N. & Rea, A.
Royal Perth Hospital Medical Research Foundation
1/01/15 → 31/12/15
Project: Research