Publications

Publications 2013

Journal articles

  • Berndt, S. I., S. Gustafsson, R. Magi, …, G. Cadby, …, K. E. North, R. J. Loos and E. Ingelsson (2013). “Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.” Nat Genet 45(5): 501-512. [pubmed]
  • Cadby, G., S. Mukherjee, A. W. Musk, A. Reid, M. Garlepp, I. Dick, C. Robinson, J. Hui, G. Fiorito, S. Guarrera, J. Beilby, P. E. Melton, E. K. Moses, D. Ugolini, D. Mirabelli, S. Bonassi, C. Magnani, I. Dianzani, G. Matullo, B. Robinson, J. Creaney and L. J. Palmer (2013). “A genome-wide association study for malignant mesothelioma risk.” Lung Cancer 82(1): 1-8. [pubmed]
  • Chittoor, G., V. S. Farook, S. Puppala, S. P. Fowler, J. Schneider, T. D. Dyer, S. A. Cole, J. L. Lynch, J. E. Curran, L. Almasy, J. W. Maccluer, A. G. Comuzzie, D. E. Hale, R. S. Ramamurthy, D. J. Dudley, E. K. Moses, R. Arya, D. M. Lehman, C. P. Jenkinson, B. S. Bradshaw, R. A. Defronzo, J. Blangero and R. Duggirala (2013). “Localization of a major susceptibility locus influencing preterm birth.” Mol Hum Reprod 19(10): 687-96. [pubmed]
  • Johnson, M. P., S. P. Brennecke, C. E. East, T. D. Dyer, L. T. Roten, J. M. Proffitt, P. E. Melton, M. H. Fenstad, T. Aalto-Viljakainen, K. Makikallio, S. Heinonen, E. Kajantie, J. Kere, H. Laivuori, R. Austgulen, J. Blangero and E. K. Moses (2013). “Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease.” Mol Hum Reprod 19(7): 423-437. [pubmed]
  • Jones, R. M., G. Cadby, P. E. Melton, L. J. Abraham, A. J. Whitehouse and E. K. Moses (2013). “Genome-wide association study of autistic-like traits in a general population study of young adults.” Front Hum Neurosci 7: 658. [pubmed]
  • Jones, R. M., Wood, D. (2013). “Sarcoma genomics.” Bone and Joint360 2(6): 2-8. [link]
  • Kochunov, P., J. Charlesworth, A. Winkler, L. E. Hong, T. E. Nichols, J. E. Curran, E. Sprooten, N. Jahanshad, P. M. Thompson, M. P. Johnson, J. W. Kent, Jr., B. A. Landman, B. Mitchell, S. A. Cole, T. D. Dyer, E. K. Moses, H. H. Goring, L. Almasy, R. Duggirala, R. L. Olvera, D. C. Glahn and J. Blangero (2013). “Transcriptomics of cortical gray matter thickness decline during normal aging.” Neuroimage 82C: 273-283. [pubmed]
  • Lian, I. A., M. Langaas, E. Moses and A. Johansson (2013). “Differential gene expression at the maternal-fetal interface in preeclampsia is influenced by gestational age.” PLoS One 8(7): e69848. [pubmed]
  • Matullo, G., S. Guarrera, M. Betti, G. Fiorito, D. Ferrante, F. Voglino, G. Cadby, C. Di Gaetano, F. Rosa, A. Russo, A. Hirvonen, E. Casalone, S. Tunesi, M. Padoan, M. Giordano, A. Aspesi, C. Casadio, F. Ardissone, E. Ruffini, P. G. Betta, R. Libener, R. Guaschino, E. Piccolini, M. Neri, A. W. Musk, N. H. de Klerk, J. Hui, J. Beilby, A. L. James, J. Creaney, B. W. Robinson, S. Mukherjee, L. J. Palmer, D. Mirabelli, D. Ugolini, S. Bonassi, C. Magnani and I. Dianzani (2013). “Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study.” PLoS One 8(4): e61253. [pubmed]
  • Melton, P. E., N. F. Baldi, R. Barrantes and M. H. Crawford (2013). “Microevolution, migration, and the population structure of five Amerindian populations from Nicaragua and Costa Rica.” Am J Hum Biol 25(4): 480-490. [link]
  • Melton, P. E., M. A. Carless, J. E. Curran, T. D. Dyer, H. H. Goring, J. W. Kent, Jr., E. Drigalenko, M. P. Johnson, J. W. Maccluer, E. K. Moses, A. G. Comuzzie, M. C. Mahaney, D. H. O’Leary, J. Blangero and L. Almasy (2013). “Genetic architecture of carotid artery intima-media thickness in Mexican Americans.” Circ Cardiovasc Genet 6(2): 211-221. [pubmed]
  • Pandey, G. S., C. Yanover, L. M. Miller-Jenkins, S. Garfield, S. A. Cole, J. E. Curran, E. K. Moses, N. Rydz, V. Simhadri, C. Kimchi-Sarfaty, D. Lillicrap, K. R. Viel, T. M. Przytycka, G. F. Pierce, T. E. Howard, Z. E. Sauna, J. Lusher, M. Chitlur, A. Ameri, K. Natarajan, R. V. Iyer, A. A. Thompson, R. G. Watts, C. L. Kempton, C. Kessler, J. C. Barrett, E. J. Martin, N. Key, R. Kruse-Jarres, C. Lessinger, K. P. Pratt, N. Josephson, K. McRedmond, J. Withycombe, C. Walsh, D. Matthews, J. Mahlangu, A. Krause, R. Schwyzer, R. Thejpal, N. Rapiti, Y. Goga, M. Coetzee, D. Stones, K. Mann, S. Butenas, L. Almasy, J. Blangero, M. Carless, R. Raja and E. Reed (2013). “Endogenous factor VIII synthesis from the intron 22-inverted F8 locus may modulate the immunogenicity of replacement therapy for hemophilia A.” Nat Med 19(10): 1318-1324. [pubmed]
  • Peters, K. E., J. Beilby, G. Cadby, N. M. Warrington, D. G. Bruce, W. A. Davis, T. M. Davis, S. Wiltshire, M. Knuiman, B. M. McQuillan, L. J. Palmer, P. L. Thompson and J. Hung (2013). “A comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/R2), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndrome.” BMC Med Genet 14: 15. [pubmed]
  • Rubicz, R., R. Yolken, E. Drigalenko, M. A. Carless, T. D. Dyer, L. Bauman, P. E. Melton, J. W. Kent, Jr., J. B. Harley, J. E. Curran, M. P. Johnson, S. A. Cole, L. Almasy, E. K. Moses, N. V. Dhurandhar, E. Kraig, J. Blangero, C. T. Leach and H. H. Goring (2013). “A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).” PLoS Genet 9(1): e1003147. [pubmed]
  • Voruganti, V. S., J. W. Kent, Jr., S. Debnath, S. A. Cole, K. Haack, H. H. Goring, M. A. Carless, J. E. Curran, M. P. Johnson, L. Almasy, T. D. Dyer, J. W. Maccluer, E. K. Moses, H. E. Abboud, M. C. Mahaney, J. Blangero and A. G. Comuzzie (2013). “Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans.” Front Genet 4: 279. [pubmed]
  • Yadav, S., I. Cotlarciuc, P. B. Munroe, M. S. Khan, M. A. Nalls, S. Bevan, Y. C. Cheng, W. M. Chen, R. Malik, N. S. McCarthy, E. G. Holliday, D. Speed, N. Hasan, M. Pucek, P. E. Rinne, P. Sever, A. Stanton, D. C. Shields, J. M. Maguire, M. McEvoy, R. J. Scott, L. Ferrucci, M. J. Macleod, J. Attia, H. S. Markus, M. M. Sale, B. B. Worrall, B. D. Mitchell, M. Dichgans, C. Sudlow, J. F. Meschia, P. M. Rothwell, M. Caulfield and P. Sharma (2013). “Genome-Wide Analysis of Blood Pressure Variability and Ischemic Stroke.” Stroke 44(10): 2703-2709. [pubmed]

Published abstracts

  • Løset, M., M. P. Johnson, P. E. Melton, W. Ang, J. Marsh, R.-C. Huang, T. Mori, L. Beilin, C. Pennell, L. T. Roten, A.-C. Iversen, R. Austgulen, C. E. East, J. Blangero, S. P. Brennecke and E. K. Moses (2013). OP004. A SNP associated with susceptibility to preeclampsia near the inhibin, beta B gene, is also associated with cardiovascular disease risk traits. Pregnancy Hypertens. 3: 63.
  • Roten, L. T., M. P. Johnson, L. C. Thompsen, A. S. Gundersen, P. Solberg, K. Tollaksen, I. Lyslo, C. Tappert, M. L. Odland, K. M. Strand, M. H. Fenstad, F. Drablos, F. Skorpen, E. K. Moses, R. Austgulen and L. Bjorge (2013). OP006. A preeclampsia genome-wide linkage scan in norwegian families. Pregnancy Hypertens. 3: 64.
  • Ward, S., L. Palmer, J. Cole, F. Wood and J. Heyworth (2013). Validation of self-reported melanoma diagnosis history. Pigment Cell and Melanoma Research. 26: 1013.
  • Ward, S., L. Palmer, J. M. Cole, F. Wood and J. Heyworth (2013). Validation of self-reported melanoma diagnosis history. Society for Melanoma Research 2013 Congress, Wiley-Blackwell. 26: 932-1019.

Theses

  • Simpson, L. (2013). Investigating the contribution of genes, fat distribution, and physical inactibity in obstructive sleep apnoea. Doctor of Philosophy, The University of Western Australia. [link]
  • Ward, S. (2013). The genetic epidemiology of melanoma in Western Australia: the Western Australian melanoma health study, familial aggregation of melanoma and scar outcome post-melanoma excision. Doctor of Philosophy, The University of Western Australia. [link]