• The University of Western Australia (M409), 35 Stirling Highway,

    6009 Perth

    Australia

  • 506 Citations
  • 13 h-Index
20062020
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Research Output 2006 2019

2019

Analysis of the Epigenome in Multiplex Pre-eclampsia Families Identifies SORD, DGKI, and ICA1 as Novel Candidate Risk Genes

Ariff, A., Melton, P. E., Brennecke, S. P. & Moses, E. K., 19 Mar 2019, In : Frontiers in Genetics. 10, 11 p., 227.

Research output: Contribution to journalArticle

Open Access
1 Citation (Scopus)

Differential SLC6A4 methylation: a predictive epigenetic marker of adiposity from birth to adulthood

EpiGen Consortium, May 2019, In : International Journal of Obesity. 43, 5, p. 974-988 15 p.

Research output: Contribution to journalArticle

Open Access
Adiposity
Epigenomics
Methylation
Parturition
Umbilical Cord

Epigenetic age acceleration in adolescence associates with BMI, inflammation and risk score for middle age cardiovascular disease

Huang, R. C., Lillycrop, K. A., Beilin, L. J., Godfrey, K. M., Anderson, D., Mori, T. A., Rauschert, S., Craig, J. M., Oddy, W. H., Ayonrinde, O. T., Pennell, C. E., Holbrook, J. D. & Melton, P. E., 20 Feb 2019, In : The Journal of clinical endocrinology and metabolism. 104, 7, p. 3012-3024 13 p.

Research output: Contribution to journalArticle

Epigenomics
Cardiovascular Diseases
Inflammation
Adiposity
DNA Methylation

Genetic influence on scar height and pliability after burn injury in individuals of European ancestry: A prospective cohort study

Wallace, H. J., Cadby, G., Melton, P. E., Wood, F. M., Falder, S., Crowe, M. M., Martin, L. J., Marlow, K., Ward, S. V. & Fear, M. W., May 2019, In : Burns. 45, 3, p. 567-578 12 p.

Research output: Contribution to journalArticle

Pliability
Cicatrix
Cohort Studies
Prospective Studies
Wounds and Injuries

Identification of novel sarcoma risk genes using a two-stage genome wide DNA sequencing strategy in cancer cluster families and population case and control cohorts

International Sarcoma Kindred Study, 3 May 2019, In : BMC Medical Genetics. 20, 1, 10 p., 69.

Research output: Contribution to journalArticle

Open Access
Population Control
DNA Sequence Analysis
Sarcoma
Genome
Genes

Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight

Küpers, L. K., Monnereau, C., Sharp, G. C., Yousefi, P., Salas, L. A., Ghantous, A., Page, C. M., Reese, S. E., Wilcox, A. J., Czamara, D., Starling, A. P., Novoloaca, A., Lent, S., Roy, R., Hoyo, C., Breton, C. V., Allard, C., Just, A. C., Bakulski, K. M., Holloway, J. W. & 107 othersEverson, T. M., Xu, C. J., Huang, R. C., van der Plaat, D. A., Wielscher, M., Merid, S. K., Ullemar, V., Rezwan, F. I., Lahti, J., van Dongen, J., Langie, S. A. S., Richardson, T. G., Magnus, M. C., Nohr, E. A., Xu, Z., Duijts, L., Zhao, S., Zhang, W., Plusquin, M., DeMeo, D. L., Solomon, O., Heimovaara, J. H., Jima, D. D., Gao, L., Bustamante, M., Perron, P., Wright, R. O., Hertz-Picciotto, I., Zhang, H., Karagas, M. R., Gehring, U., Marsit, C. J., Beilin, L. J., Vonk, J. M., Jarvelin, M. R., Bergström, A., Örtqvist, A. K., Ewart, S., Villa, P. M., Moore, S. E., Willemsen, G., Standaert, A. R. L., Håberg, S. E., Sørensen, T. I. A., Taylor, J. A., Räikkönen, K., Yang, I. V., Kechris, K., Nawrot, T. S., Silver, M. J., Gong, Y. Y., Richiardi, L., Kogevinas, M., Litonjua, A. A., Eskenazi, B., Huen, K., Mbarek, H., Maguire, R. L., Dwyer, T., Vrijheid, M., Bouchard, L., Baccarelli, A. A., Croen, L. A., Karmaus, W., Anderson, D., de Vries, M., Sebert, S., Kere, J., Karlsson, R., Arshad, S. H., Hämäläinen, E., Routledge, M. N., Boomsma, D. I., Feinberg, A. P., Newschaffer, C. J., Govarts, E., Moisse, M., Fallin, M. D., Melén, E., Prentice, A. M., Kajantie, E., Almqvist, C., Oken, E., Dabelea, D., Boezen, H. M., Melton, P. E., Wright, R. J., Koppelman, G. H., Trevisi, L., Hivert, M. F., Sunyer, J., Munthe-Kaas, M. C., Murphy, S. K., Corpeleijn, E., Wiemels, J., Holland, N., Herceg, Z., Binder, E. B., Davey Smith, G., Jaddoe, V. W. V., Lie, R. T., Nystad, W., London, S. J., Lawlor, D. A., Relton, C. L., Snieder, H. & Felix, J. F., 1 Dec 2019, In : Nature Communications. 10, 1, 1893.

Research output: Contribution to journalArticle

Open Access
methylation
DNA Methylation
Meta-Analysis
Methylation
deoxyribonucleic acid

Statins do not directly inhibit the activity of major epigenetic modifying enzymes

Bridgeman, S., Northrop, W., Ellison, G., Sabapathy, T., Melton, P. E., Newsholme, P. & Mamotte, C. D. S., 10 Apr 2019, In : Cancers. 11, 4, 516.

Research output: Contribution to journalArticle

Open Access
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Epigenomics
Enzymes
Histones
Acetylation

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
2018
1 Citation (Scopus)
36 Downloads (Pure)
Open Access
File
Personality Assessment
Endophenotypes
Cognition
Schizophrenia
Personality
1 Citation (Scopus)

Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults

for the BIOS Consortium & for the GLOBAL Meth QTL Consortium, Dec 2018, In : EBioMedicine. 38, p. 206-216

Research output: Contribution to journalArticle

Open Access
DNA Methylation
Smoking
Mothers
Phenotype
Waist Circumference

Bile Acids, Hepatic Steatosis and Gut Microbiome in Patients Undergoing Dietary Intervention for Non-Alcoholic Fatty Liver Disease

Wang, Z., Properzi, C., Liddle, C., Melton, P., Ariff, A., O'Sullivan, T., Sherriff, J., Coulter, S., Christophersen, C., Morrison, M., Jeffrey, G. P. & Adams, L. A., Oct 2018, In : Hepatology. 68, p. 972A-972A 1 p., 1706.

Research output: Contribution to journalAbstract/Meeting Abstract

10 Citations (Scopus)

Cohort profile: Pregnancy and childhood epigenetics (PACE) consortium

Felix, J. F., Joubert, B. R., Baccarelli, A. A., Sharp, G. C., Almqvist, C., Annesi-Maesano, I., Arshad, H., Baiz, N., Bakermans-Kranenburg, M. J., Bakulski, K. M., Binder, E. B., Bouchard, L., Breton, C. V., Brunekreef, B., Brunst, K. J., Burchard, E. G., Bustamante, M., Chatzi, L., Munthe-Kaas, M. C., Corpeleijn, E. & 104 othersCzamara, D., Dabelea, D., Smith, G. D., De Boever, P., Duijts, L., Dwyer, T., Eng, C., Eskenazi, B., Everson, T. M., Falahi, F., Fallin, M. D., Farchi, S., Fernandez, M. F., Gao, L., Gaunt, T. R., Ghantous, A., Gillman, M. W., Gonseth, S., Grote, V., Gruzieva, O., Håberg, S. E., Herceg, Z., Hivert, M. F., Holland, N., Holloway, J. W., Hoyo, C., Hu, D., Huang, R. C., Huen, K., Järvelin, M. R., Jima, D. D., Just, A. C., Karagas, M. R., Karlsson, R., Karmaus, W., Kechris, K. J., Kere, J., Kogevinas, M., Koletzko, B., Koppelman, G. H., Kupers, L. K., Ladd-Acosta, C., Lahti, J., Lambrechts, N., Langie, S. A. S., Lie, R. T., Liu, A. H., Magnus, M. C., Magnus, P., Maguire, R. L., Marsit, C. J., McArdle, W., Melen, E., Melton, P., Murphy, S. K., Nawrot, T. S., Nisticò, L., Nohr, E. A., Nordlund, B., Nystad, W., Oh, S. S., Oken, E., Page, C. M., Perron, P., Pershagen, G., Pizzi, C., Plusquin, M., Raikkonen, K., Reese, S. E., Reischl, E., Richiardi, L., Ring, S., Roy, R. P., Rzehak, P., Schoeters, G., Schwartz, D. A., Sebert, S., Snieder, H., Sørensen, T. I. A., Starling, A. P., Sunyer, J., Taylor, J. A., Tiemeier, H., Ullemar, V., Vafeiadi, M., Van Ijzendoorn, M. H., Vonk, J. M., Vriens, A., Vrijheid, M., Wang, P., Wiemels, J. L., Wilcox, A. J., Wright, R. J., Xu, C. J., Xu, Z., Yang, I. V., Yousefi, P., Zhang, H., Zhang, W., Zhao, S., Agha, G., Relton, C. L., Jaddoe, V. W. V. & London, S. J., 1 Feb 2018, In : International Journal of Epidemiology. 47, 1, p. 22-23u dyx218.

Research output: Contribution to journalArticle

Open Access
19 Citations (Scopus)

Epigenetic effects of metformin: From molecular mechanisms to clinical implications

Bridgeman, S. C., Ellison, G. C., Melton, P. E., Newsholme, P. & Mamotte, C. D. S., 22 Mar 2018, In : Diabetes, Obesity and Metabolism.

Research output: Contribution to journalReview article

Metformin
Epigenomics
Hypoglycemic Agents
Gene Expression
AMP-Activated Protein Kinases

Epigenetics, heritability and longitudinal analysis

Nustad, H. E., Almeida, M., Canty, A. J., LeBlanc, M., Page, C. M. & Melton, P. E., 17 Sep 2018, In : BMC Genetics. 19, Suppl 1, p. 77

Research output: Contribution to journalArticle

Open Access
DNA Methylation
Epigenomics
Quality Control
Cytosine
Guanine
7 Citations (Scopus)

Epigenome-wide Meta-analysis of DNA Methylation and Childhood Asthma

BIOS consortium, 20 Dec 2018, In : The Journal of Allergy and Clinical Immunology.

Research output: Contribution to journalArticle

Open Access
DNA Methylation
Meta-Analysis
Asthma
Methylation
Newborn Infant
1 Citation (Scopus)

GAW20: Methods and strategies for the new frontiers of epigenetics and pharmacogenomics

Tintle, N. L., Fardo, D. W., De Andrade, M., Aslibekyan, S., Bailey, J. N., Bermejo, J. L., Cantor, R. M., Ghosh, S., Melton, P., Wang, X., MacCluer, J. W. & Almasy, L., 17 Sep 2018, In : BMC Proceedings. 12, 26.

Research output: Contribution to journalArticle

Open Access
Pharmacogenetics
DNA Methylation
Epigenomics
Nucleotides
Fenofibrate
1 Citation (Scopus)

Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study

Cadby, G., Melton, P. E., McCarthy, N. S., Almeida, M., Williams-Blangero, S., Curran, J. E., VandeBerg, J. L., Hui, J., Beilby, J., Musk, A. W., James, A. L., Hung, J., Blangero, J. & Moses, E. K., 2018, In : Human Genetics. 137, 1, p. 45–53 9 p.

Research output: Contribution to journalArticle

Obesity
Health
Single Nucleotide Polymorphism
Triglycerides
Body Mass Index
1 Citation (Scopus)

Retinal genes are differentially expressed in areas of primary versus secondary degeneration following partial optic nerve injury

Chiha, W., LeVaillant, C. J., Bartlett, C. A., Hewitt, A. W., Melton, P. E., Fitzgerald, M. & Harvey, A. R., 1 Feb 2018, In : PLoS One. 13, 2, e0192348.

Research output: Contribution to journalArticle

Open Access
Optic Nerve Injuries
optics
retina
Retina
Optics
1 Citation (Scopus)
Genetic Heterogeneity
Schizophrenia
Genome
Psychotic Disorders
Base Pairing
2017
13 Citations (Scopus)

ANRIL Promoter DNA Methylation: A Perinatal Marker for Later Adiposity

Lillycrop, K., Murray, R., Cheong, C., Teh, A. L., Clarke-Harris, R., Barton, S., Costello, P., Garratt, E., Cook, E., Titcombe, P., Shunmuganathan, B., Liew, S. J., Chua, Y-C., Lin, X., Wu, Y., Burdge, G. C., Cooper, C., Inskip, H. M., Karnani, N., Hopkins, J. C. & 14 othersChilds, C. E., Chavez, C. P., Calder, P. C., Yap, F., Lee, Y. S., Chong, Y. S., Melton, P., Beilin, L., Huang, R-C., Gluckman, P. D., Harvey, N., Hanson, M. A., Holbrook, J. D. & Godfrey, K. M., Mar 2017, In : EBioMedicine. 19, p. 60–72

Research output: Contribution to journalArticle

Open Access
Methylation
Adiposity
DNA Methylation
Genetic Epigenesis
Parturition
6 Citations (Scopus)
Exome
Schizophrenia
Genetic Association Studies
Gene Frequency
Population
21 Citations (Scopus)

Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: findings from the pregnancy and childhood epigenetics (PACE) consortium

Sharp, G. C., Salas, L. A., Monnereau, C., Allard, C., Yousefi, P., Everson, T. M., Bohlin, J., Xu, Z., Huang, R-C., Reese, S. E., Xu, C-J., Baiz, N., Hoyo, C., Agha, G., Roy, R., Holloway, J. W., Ghantous, A., Merid, S. K., Bakulski, K. M., Kupers, L. K. & 65 othersZhang, H., Richmond, R. C., Page, C. M., Duijts, L., Lie, R. T., Melton, P. E., Vonk, J. M., Nohr, E. A., Williams-DeVane, C., Huen, K., Rifas-Shiman, S. L., Ruiz-Arenas, C., Gonseth, S., Rezwan, F. I., Herceg, Z., Ekstrom, S., Croen, L., Falahi, F., Perron, P., Karagas, M. R., Quraishi, B. M., Suderman, M., Magnus, M. C., Jaddoe, V. W. V., Taylor, J. A., Anderson, D., Zhao, S., Smit, H. A., Josey, M. J., Bradman, A., Baccarelli, A. A., Bustamante, M., Haberg, S. E., Pershagen, G., Hertz-Picciotto, I., Newschaffer, C., Corpeleijn, E., Bouchard, L., Lawlor, D. A., Maguire, R. L., Barcellos, L. F., Smith, G. D., Eskenazi, B., Karmaus, W., Marsit, C. J., Hivert, M-F., Snieder, H., Fallin, M. D., Melen, E., Munthe-Kaas, M. C., Arshad, H., Wiemels, J. L., Annesi-Maesano, I., Vrijheid, M., Oken, E., Holland, N., Murphy, S. K., Sorensen, T. I. A., Koppelman, G. H., Newnham, J. P., Wilcox, A. J., Nystad, W., London, S. J., Felix, J. F. & Relton, C. L., 15 Oct 2017, In : Human Molecular Genetics. 26, 20, p. 4067-4085 19 p.

Research output: Contribution to journalArticle

Open Access
3 Citations (Scopus)

The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia

Thomsen, L. C. V., McCarthy, N. S., Melton, P. E., Cadby, G., Austgulen, R., Nygård, O. K., Johnson, M. P., Brennecke, S., Moses, E. K., Bjørge, L. & Iversen, A-C., Jan 2017, In : Journal of Hypertension. 35, 1, p. 132-139 8 p.

Research output: Contribution to journalArticle

Open Access
Methylenetetrahydrofolate Reductase (NADPH2)
Pre-Eclampsia
Antihypertensive Agents
Genes
Single Nucleotide Polymorphism
2016
66 Downloads (Pure)

Constrained multivariate association with longitudinal phenotypes

Melton, P. E., Peralta, J. M. & Almasy, L., 2016, BMC Proceedings. Greenwood, C. M. T., MacCluer, J. W. & Almasy, L. (eds.). 7 ed. New York: Springer Nature, Vol. 10. p. 329-332 4 p.

Research output: Chapter in Book/Conference paperConference paper

Open Access
File
Blood Pressure
Phenotype
Genes
Education
Pedigree
1 Citation (Scopus)
81 Downloads (Pure)

Genetic Analysis Workshop 19: Methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals

Engelman, C. D., Greenwood, C. M. T., Bailey, J. N., Cantor, R. M., Kent, J. W., König, I. R., Bermejo, J. L., Melton, P. E., Santorico, S. A., Schillert, A., Wijsman, E. M., MacCluer, J. W. & Almasy, L., 2016, BMC Proceedings: Proceedings of Genetic Analysis Workshop 19 . Greenwood, C. M. T., MacCluer, J. W. & Almasy, L. (eds.). New York: Springer Nature, Vol. 10. p. 67-70 4 p.

Research output: Chapter in Book/Conference paperConference paper

Open Access
File
Exome
Pedigree
Genome
Gene Expression
Education
8 Citations (Scopus)

Longitudinal analytical approaches to genetic data

Chiu, Y. F., Justice, A. E. & Melton, P. E., 2016, BMC Genetics. Greenwood, C. M. T., MacCluer, J. W. & Almasy, L. (eds.). Supp. 2 ed. United Kingdom: BioMed Central, Vol. 17. 4

Research output: Chapter in Book/Conference paperConference paper

Open Access
Genome
Blood Pressure
Phenotype
Education
Growth

Paternal genetic structure in contemporary mennonite communities from the American midwest

Beaty, K. G., Mosher, M. J., Crawford, M. H. & Melton, P., 2016, In : Human Biology. 88, 2, p. 95-108

Research output: Contribution to journalArticle

Genetic Structures
Y Chromosome
Y chromosome
genetic structure
chromosome
4 Citations (Scopus)

Patterns of DNA methylation across the leptin core promoter in four diverse Asian and north American populations

Mosher, M. J., Melton, P., Stapleton, P., Schanfield, M. S. & Crawford, M. H., 2016, In : Human Biology. 88, 2, p. 121-135

Research output: Contribution to journalArticle

Asian Americans
methylation
DNA methylation
DNA Methylation
Leptin
11 Citations (Scopus)

Transcriptome analysis of human ageing in male skin shows mid-life period of variability and central role of NF-κB

Haustead, D. J., Stevenson, A., Saxena, V., Marriage, F., Firth, M., Silla, R., Martin, L., Adcroft, K. F., Rea, S., Day, P. J., Melton, P., Wood, F. M. & Fear, M. W., 31 May 2016, In : Scientific Reports. 6, 26846.

Research output: Contribution to journalArticle

Open Access
Gene Expression Profiling
Transcriptome
Skin
NF-kappa B
Meta-Analysis
2015
16 Citations (Scopus)

Absence of germline mutations in BAP1 in sporadic cases of malignant mesothelioma

Sneddon, S., Leon, J., Dick, I., Cadby, G., Olsen, N., Brims, F., Allcock, R., Moses, E., Melton, P., De Klerk, N., Musk, A., Robinson, B. & Creaney, J., 25 May 2015, In : Gene. 563, 1, p. 103-105

Research output: Contribution to journalArticle

Open Access
Germ-Line Mutation
Mesothelioma
Exome
High-Throughput Nucleotide Sequencing
Neoplasms

A genetic connection between preeclampsia and chronic hypertension in Norwegian families.

Thomsen, L. C., Mccarthy, N., Melton, P., Tollaksen, K., Lyslo, I., Solberg, P., Roten, L. T., Nygard, O. K., Cadby, G., Austgulen, R., Moses, E., Iversen, A. C. & Bjorge, L., 2015, Abstracts of the XIXth World Congress for the Study of Hypertension in Pregnancy Preeclampsia/Hypertension - Future Risks and Novel Therapies. Netherlands: Elsevier, Vol. 5. p. 1

Research output: Chapter in Book/Conference paperConference paper

Genome-wide transcriptome directed pathway analysis of maternal preeclampsia susceptibility genes

Yong, H. E. J., Melton, P., Johnson, M. P., Freed, K. A., Kalionis, B., Murthi, P., Brennecke, S. P., Keogh, R. J. & Moses, E., 2015, XIXth World Congress for the Study of Hypertension in Pregnancy — Preeclampsia/Hypertension - Future Risks and Novel Therapies. Netherlands: Elsevier, Vol. 5. p. 1

Research output: Chapter in Book/Conference paperConference paper

19 Citations (Scopus)

Genome-wide transcriptome directed pathway analysis of maternal pre-eclampsia susceptibility genes

Yong, H. E. J., Melton, P., Johnson, M. P., Freed, K. A., Kalionis, B., Murthi, P., Brennecke, S. P., Keogh, R. J. & Moses, E., 26 May 2015, In : PLoS One. 10, 5, p. 1-15

Research output: Contribution to journalArticle

Open Access
pre-eclampsia
Pre-Eclampsia
Transcriptome
transcriptome
Genes
6 Citations (Scopus)

Refined phenotyping identifies links between preeclampsia and related diseases in a Norwegian preeclampsia family cohort

Thomsen, L. C. V., Melton, P., Tollaksen, K., Lyslo, I., Roten, L. T., Odland, M. L., Strand, K. M., Nygard, O., Sun, C., Iversen, A. C., Austgulen, R., Moses, E. & Bjørge, L., 2015, In : Journal of Hypertension. 33, 11, p. 2294-2302

Research output: Contribution to journalArticle

Open Access
Pre-Eclampsia
Gestational Age
Phenotype
Cardiovascular Diseases
Lung Diseases
2014
3 Citations (Scopus)

Bivariate association analysis of longitudinal phenotypes in families

Melton, P. & Almasy, L. A., 2014, In : BMC Proceedings. 8, p. S90

Research output: Contribution to journalArticle

Open Access
2 Citations (Scopus)

Effect of recent historical events on migration and isonymic stratification among the Rama Amerindians from Nicaragua

Baldi, N. F., Melton, P. & Crawford, M. H., 2014, In : Human Biology. 86, 1, p. 37-50

Research output: Contribution to journalArticle

8 Citations (Scopus)

Evidence of heterogeneity by race/ethnicity in genetic determinants of QT interval

Seyerle, A. A., Young, A. M., Jeff, J. M., Melton, P., Jorgensen, N. W., Lin, Y., Carty, C. L., Deelman, E., Heckbert, S. R., Hindorff, L. A., Jackson, R. D., Martin, L. W., Okin, P. M., Perez, M. V., Psaty, B. M., Soliman, E. Z., Whitsel, E. A., North, K. E., Laston, S., Kooperberg, C. & 1 othersAvery, C. L., Nov 2014, In : Epidemiology. 25, 6, p. 790-798 9 p.

Research output: Contribution to journalArticle

11 Citations (Scopus)

Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees

Bickeboller, H., Bailey, J. N., Beyene, J., Cantor, R. M., Cordell, H. J., Culverhouse, R. C., Engelman, C. D., Fardo, D. W., Ghosh, S., Konig, I. R., Bermejo, J. L., Melton, P., Santorico, S. A., Satten, G. A., Sun, L., Tintle, N. L., Ziegler, A., Maccluer, J. W. & Almasy, L., 2014, Genetic Analysis Workshop 18. United Kingdom: BioMed Central, p. 1-4

Research output: Chapter in Book/Conference paperOther chapter contribution

Open Access
9 Citations (Scopus)

Longitudinal data analysis for genetic studies in the whole-genome sequencing era

Wu, Z., Hu, Y. & Melton, P., 2014, In : Genetic Epidemiology. 38, SUPPL.1, p. S74-S80

Research output: Contribution to journalArticle

Genome
Phenotype
Genome-Wide Association Study
Linear Models
Blood Pressure
29 Citations (Scopus)

Meta-analysis of human methylation data for evidence of sex-specific autosomal patterns

Mccarthy, N., Melton, P., Cadby, G., Yazar, S., Franchina, M., Moses, E., Mackey, D. & Hewitt, A., 18 Nov 2014, In : BMC Genomics. 15, p. 1-11 12 p., 981.

Research output: Contribution to journalArticle

Open Access
7 Citations (Scopus)

Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22

Løset, M., Johnson, M. P., Melton, P., Ang, W., Huang, R-C., Mori, T., Beilin, L., Pennell, C., Roten, L. T., Iversen, A. C., Austgulen, R., East, C. E., Blangero, J. C., Brennecke, S. P. & Moses, E., 2014, In : Pregnancy Hypertension. 4, 2, p. 178-185

Research output: Contribution to journalArticle

Pre-Eclampsia
Single Nucleotide Polymorphism
Cardiovascular Diseases
Chromosomes
Mothers
2013
19 Citations (Scopus)

A genome-wide association study for malignant mesothelioma risk

Cadby, G., Mukherjee, S., Musk, A., Reid, A., Garlepp, M., Dick, I., Robinson, C., Hui, J., Fiorito, G., Guarrera, S., Beilby, J., Melton, P., Moses, E., Ugolini, D., Mirabelli, D., Bonassi, S., Magnani, C., Dianzani, I., Matullo, G., Robinson, B. & 2 othersCreaney, J. & Palmer, L. J., Oct 2013, In : Lung Cancer. 82, 1, p. 1-8

Research output: Contribution to journalArticle

Genome-Wide Association Study
Asbestos
Single Nucleotide Polymorphism
Western Australia
Malignant Mesothelioma
51 Citations (Scopus)

A Genome-Wide Integrative Genomic Study Localizes Genetic Factors Influencing Antibodies against Epstein-Barr Virus Nuclear Antigen 1 (EBNA-1)

Rubicz, R., Yolken, R., Drigalenko, E., Carless, M. A., Dyer, T. D., Bauman, L., Melton, P., Kent Jr, J. W., Harley, J. B., Curran, J. E., Johnson, M. P., Cole, S. A., Almasy, L., Moses, E., Dhurandhar, N. V., Kraig, E., Blangero, J., Leach, C. T. & Goring, H. H. H., 2013, In : PLoS Genetics. 9, 1, p. 17pp

Research output: Contribution to journalArticle

Open Access
18 Citations (Scopus)

Genetic architecture of carotid artery intima-media thickness in Mexican Americans

Melton, P., Carless, M. A., Curran, J. E., Dyer, T. D., Göring, H. H. H., Kent Jr., J. W., Drigalenko, E., Johnson, M. P., Maccluer, J. W., Moses, E., Comuzzie, A. G., Mahaney, M. C., O'Leary, D. H., Blangero, J. & Almasy, L., 2013, In : Circulation: Cardiovascular Genetics. 6, 2, p. 211-221

Research output: Contribution to journalArticle

Open Access
19 Citations (Scopus)

Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease

Johnson, M. P., Brennecke, S. P., East, C. E., Dyer, T. D., Roten, L. T., Proffitt, J. M., Melton, P., Fenstad, M. H., Aalto-Viljakainen, T., Makikallio, K., Heinonen, S., Kajantie, E., Kere, J., Laivuori, H., Pouta, A., Kivinen, K., Ekholm, E., Hietala, R., Sainio, S., Saisto, T. & 7 othersUotila, J., Klemetti, M., Inkeri Lokki, A., Georgiadis, L., Austgulen, R., Blangero, J. & Moses, E., 2013, In : Molecular Human Reproduction. 19, 7, p. 423-437

Research output: Contribution to journalArticle

12 Citations (Scopus)
Open Access
10 Citations (Scopus)

Microevolution, migration, and the population structure of five amerindian populations from nicaragua and costa rica

Melton, P., Baldi, N. F., Barrantes, R. & Crawford, M. H., 2013, In : American Journal of Human Biology. 25, 4, p. 480-490

Research output: Contribution to journalArticle