• The University of Western Australia (M560), 35 Stirling Highway,

    6009 Perth

    Australia

  • 2219 Citations
  • 11 h-Index
20142019
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Fingerprint Dive into the research topics where Denise Anderson is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 1 Similar Profiles
Genome-Wide Association Study Medicine & Life Sciences
Precursor Cell Lymphoblastic Leukemia-Lymphoma Medicine & Life Sciences
Vitamin D Medicine & Life Sciences
Epigenomics Medicine & Life Sciences
DNA Methylation Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma Medicine & Life Sciences
Type 2 Diabetes Mellitus Medicine & Life Sciences

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Research Output 2014 2019

  • 2219 Citations
  • 11 h-Index
  • 27 Article
  • 1 Letter
1 Citation (Scopus)

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., Jul 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

Innate immune activation occurs in acute food protein–induced enterocolitis syndrome reactions

Mehr, S., Lee, E., Hsu, P., Anderson, D., de Jong, E., Bosco, A. & Campbell, D. E., 4 May 2019, In : Journal of Allergy and Clinical Immunology. 5 p.

Research output: Contribution to journalLetter

1 Citation (Scopus)

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
2 Citations (Scopus)

Personalized Transcriptomics Reveals Heterogeneous Immunophenotypes in Children with Viral Bronchiolitis

Jones, A. C., Anderson, D., Galbraith, S., Fantino, E., Cardenas, D. G., Read, J. F., Serralha, M., Holt, B. J., Strickland, D. H., Sly, P. D., Bosco, A. & Holt, P. G., 15 Jun 2019, In : American Journal of Respiratory and Critical Care Medicine. 199, 12, p. 1537-1549 13 p.

Research output: Contribution to journalArticle

Open Access
2 Citations (Scopus)

A phenotype centric benchmark of variant prioritisation tools

Anderson, D. & Lassmann, T., 1 Dec 2018, In : npj Genomic Medicine. 3, 1, 5.

Research output: Contribution to journalArticle

Open Access
Benchmarking
Phenotype
Inborn Genetic Diseases
Rare Diseases