No photo of Nina Kresoje
  • The University of Western Australia (M504), 35 Stirling Highway,

    6009 Perth


  • 278 Citations
  • 5 h-Index
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Fingerprint Dive into the research topics where Nina Kresoje is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 8 Similar Profiles
Ecology Engineering & Materials Science
macroinvertebrate Earth & Environmental Sciences
Lakes Engineering & Materials Science
Bacteria Engineering & Materials Science
ecology Earth & Environmental Sciences
bacterium Earth & Environmental Sciences
lake Earth & Environmental Sciences
lake ecosystem Earth & Environmental Sciences

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Research Output 2012 2019

  • 278 Citations
  • 5 h-Index
  • 6 Article

Macroinvertebrates and Microbes (Archaea, Bacteria) Offer Complementary Insights into Mine-Pit Lake Ecology

Blanchette, M. L., Allcock, R., Gonzalez, J., Kresoje, N. & Lund, M., 8 Nov 2019, In : Mine Water and the Environment.

Research output: Contribution to journalArticle

Open Access
15 Citations (Scopus)

Detection of Arboviruses and Other Micro-Organisms in Experimentally Infected Mosquitoes Using Massively Parallel Sequencing

Hall-Mendelin, S., Allcock, R., Kresoje, N., Van Den Hurk, A. F. & Warrilow, D., 2013, In : PLoS One. 8, 2, p. 7pp

Research output: Contribution to journalArticle

Open Access
28 Citations (Scopus)

Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia

Gaignard, P., Menezes, M., Schiff, M., Bayot, A., Rak, M., Ogier De Baulny, H., Su, C-H., Gilleron, M., Lombes, A., Abida, H., Tzagoloff, A., Riley, L., Cooper, S. T., Mina, K., Sivadorai, P., Davis, M. R., Allcock, R., Kresoje, N., Laing, N., Thorburn, D. R. & 3 othersSlama, A., Christodoulou, J. & Rustin, P., 2013, In : American Journal of Human Genetics. 93, p. 384-389

Research output: Contribution to journalArticle

Open Access
102 Citations (Scopus)

Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy

Ravenscroft, G., Miyatake, S., Lehtokari, V-L., Todd, E., Vornanen, P., Yau, K., Hayashi, Y. K., Miyake, N., Tsurusaki, Y., Doi, H., Saitsu, H., Osaka, H., Yamashita, S., Ohya, T., Sakamoto, Y., Koshimizu, E., Imamura, S., Yamashita, M., Ogata, K., Shiina, M. & 35 othersBryson-Richardson, R. J., Vaz, R., Ceyhan, O., Brownstein, C. A., Swanson, L. C., Monnot, S., Romero, N. B., Amthor, H., Kresoje, N., Sivadorai, P., Kiraly-Borri, C., Haliloglu, G., Talim, B., Orhan, D., Kale, G., Charles, A., Fabian, V. A., Davis, M. R., Lammens, M., Sewry, C. A., Manzur, A., Muntoni, F., Clarke, N. F., North, K. N., Bertini, E., Nevo, Y., Willichowski, E., Silberg, I. E., Topaloglu, H., Beggs, A. H., Allcock, R., Nishino, I., Wallgren-Pettersson, C., Matsumoto, N. & Laing, N., 2013, In : American Journal of Human Genetics. 93, 1, p. 6-18

Research output: Contribution to journalArticle

Open Access
22 Citations (Scopus)

Whole exome sequencing in foetal akinesia expands the genotype-phenotype spectrum of GBE1 glycogen storage disease mutations

Ravenscroft, G., Thompson, E. M., Todd, E., Yau, K. S., Kresoje, N., Sivadorai, P., Friend, K., Riley, K., Manton, N. D., Blumbergs, P., Fietz, M., Duff, R., Davis, M. R., Allcock, R. & Laing, N., 2013, In : Neuromuscular Disorders. 23, p. 165-169

Research output: Contribution to journalArticle