Associate Professor Michael Lardelli

• Appointments

  Date	Position	Institution name
  2015 - ongoing	Associate Professor in Genetics	University of Adelaide

• Language Competencies

  Language	Competency
  English	Can read, write, speak, understand spoken and peer review
  Swedish	Can read, write, speak and understand spoken

• Education

  Date	Institution name	Country	Title
  1987 - 1991	Council for National Academic Awards	United Kingdom	Ph.D.
  1981 - 1984	University of Sydney	Australia	B.Sc. (Hons)

• Postgraduate Training

  Date	Title	Institution	Country
  1994 - 1995	ESF Postdoctoral Fellowship	Uppsala University	Sweden
  1991 - 1994	EMBO Long Term Postodoctoral Fellowship	Karolinska Institute	Sweden

• Research Interests

  Animal Developmental Cell Metabolism Cellular Nervous System Central Nervous System Developmental Genetics Genetically Modified Animals Genetics Genomics Medical Genetics Molecular Evolution Neurogenetics Transgenesis

• Journals

  Year	Citation
  2022	Barthelson, K., Newman, M., & Lardelli, M. (2022). Brain transcriptomes of zebrafish and mouse Alzheimer's disease knock-in models imply early disrupted energy metabolism. Disease Models and Mechanisms, 15(1), 1-14. DOI
  2022	Allen, A., Barthelson, K., & Lardelli, M. (2022). pHAPE: a plasmid for production of DNA size marker ladders for gel electrophoresis. DOI
  2021	Jayne, T., Newman, M., Baer, L., & Lardelli, M. (2021). The evolved divergence of γ-secretase-susceptibility of homologous proteins Ngfrb and Nradd in zebrafish. BMC Research Notes, 14(1), 1-5. DOI
  2021	Chin, H. Y., Lardelli, M., Collins-Praino, L., & Barthelson, K. (2021). Differential effects of loss of <i>park7</i> activity on Iron Responsive Element (IRE) gene sets: Implications for the role of iron dyshomeostasis in the pathophysiology of Parkinson’s disease. DOI
  2021	Barthelson, K., Pederson, S. M., Newman, M., Jiang, H., & Lardelli, M. (2021). In-Frame and Frameshift Mutations in Zebrafish Presenilin 2 Affect Different Cellular Functions in Young Adult Brains. Journal of Alzheimer's Disease Reports, 5(1), 395-404. DOI Scopus4 Europe PMC3
  2021	Barthelson, K., Dong, Y., Newman, M., & Lardelli, M. (2021). PRESENILIN 1 mutations causing early-onset familial alzheimer's disease or familial acne inversa differ in their effects on genes facilitating energy metabolism and signal transduction. Journal of Alzheimers Disease, 82(1), 327-347. DOI Scopus2 WoS2 Europe PMC3
  2021	Chin, H. Y., Lardelli, M., Collins-Praino, L., & Barthelson, K. (2021). Loss of park7 activity has differential effects on expression of iron responsive element (IRE) gene sets in the brain transcriptome in a zebrafish model of Parkinson's disease.. Mol Brain, 14(1), 83. DOI Scopus4 WoS4 Europe PMC2
  2021	Barthelson, K., Baer, L., Dong, Y., Hand, M., Pujic, Z., Newman, M., . . . Lardelli, M. (2021). Zebrafish Chromosome 14 Gene Differential Expression in the fmr1hu2787 Model of Fragile X Syndrome. Frontiers in Genetics, 12, 1-11. DOI
  2021	Hin, N., Newman, M., Pederson, S., & Lardelli, M. (2021). Iron responsive element-mediated responses to iron dyshomeostasis in Alzheimer's disease. Journal of Alzheimers Disease, 84(4), 1-34. DOI Scopus2 WoS2 Europe PMC3
  2021	Hin, N., Newman, M., Pederson, S., & Lardelli, M. (2021). Iron Responsive Element (IRE)-mediated responses to iron dyshomeostasis in Alzheimer's disease. Journal of Alzheimer's Disease, 84(4), 1597-1630. DOI
  2021	Barthelson, K., Pederson, S. M., Newman, M., & Lardelli, M. (2021). Brain transcriptome analysis of a protein-truncating mutation in sortilin-related receptor 1 associated with early-onset familial alzheimer's disease indicates early effects on mitochondrial and ribosome function. Journal of Alzheimer's Disease, 79(3), 1105-1119. DOI Scopus4 WoS4 Europe PMC3
  2021	Barthelson, K., Newman, M., Nowell, C. J., & Lardelli, M. (2021). No observed effect on brain vasculature of Alzheimer's disease-related mutations in the zebrafish presenilin 1 gene. Molecular Brain, 14(1), 22-1-22-4. DOI
  2021	Barthelson, K., Dong, Y., Newman, M., & Lardelli, M. (2021). <i>PRESENILIN 1</i>mutations causing early-onset familial Alzheimer’s disease or familial acne inversa differ in their effects on genes facilitating energy metabolism and signal transduction. DOI
  2021	Barthelson, K., Newman, M., & Lardelli, M. (2021). Comparative analysis of Alzheimer’s disease knock-in model brain transcriptomes implies changes to energy metabolism as a causative pathogenic stress. DOI
  2021	Dong, Y., Newman, M., Pederson, S. M., Barthelson, K., Hin, N., & Lardelli, M. (2021). Transcriptome analyses of 7-day-old zebrafish larvae possessing a familial Alzheimer’s disease-like mutation in psen1 indicate effects on oxidative phosphorylation, ECM and MCM functions, and iron homeostasis. BMC Genomics, 22(1), 211-1-211-16. DOI Scopus4 WoS4 Europe PMC3
  2021	Moussavi Nik, S. H., Porter, T., Newman, M., Bartlett, B., Khan, I., Sabale, M., . . . Verdile, G. (2021). Relevance of a truncated PRESENILIN 2 transcript to Alzheimer's disease and neurodegeneration.. Journal of Alzheimer's Disease, 80(4), 1-11. DOI WoS1
  2020	Barthelson, K., Pederson, S. M., Newman, M., & Lardelli, M. (2020). Brain transcriptome analysis reveals subtle effects on mitochondrial function and iron homeostasis of mutations in the SORL1 gene implicated in early onset familial Alzheimer’s disease. biorxiv. DOI
  2020	Jiang, H., Pederson, S. M., Newman, M., Dong, Y., & Lardelli, M. (2020). Transcriptome analysis indicates dominant effects on ribosome and mitochondrial function of a premature termination codon mutation in the zebrafish gene<i>psen2</i>. DOI
  2020	Newman, M., Moussavi Nik, S. H., Sutherland, G. T., Hin, N., Kim, W. S., Halliday, G. M., . . . Lardelli, M. (2020). Accelerated loss of hypoxia response in zebrafish with familial Alzheimer's disease-like mutation of Presenilin 1. Human Molecular Genetics, 29(14), 2379-2394. DOI Scopus7 WoS6 Europe PMC4
  2020	Barthelson, K., Newman, M., & Lardelli, M. (2020). Sorting Out the Role of the Sortilin-Related Receptor 1 in Alzheimer's Disease.. J Alzheimers Dis Rep, 4(1), 123-140. DOI Europe PMC10
  2020	Jiang, H., Pederson, S. M., Newman, M., Dong, Y., Barthelson, K., & Lardelli, M. (2020). Transcriptome analysis indicates dominant effects on ribosome and mitochondrial function of a premature termination codon mutation in the zebrafish gene psen2. PLoS One, 15(7), e0232559-1-e0232559-25. DOI Scopus3 WoS3 Europe PMC2
  2020	Barthelson, K., Pederson, S. M., Newman, M., & Lardelli, M. (2020). Brain transcriptome analysis reveals subtle effects on mitochondrial function and iron homeostasis of mutations in the SORL1 gene implicated in early onset familial Alzheimer's disease.. Molecular brain, 13(1), 142. DOI Scopus12 WoS12 Europe PMC8
  2020	Barthelson, K., Pederson, S., Newman, M., & Lardelli, M. (2020). Transcriptome analysis of a protein-truncating mutation in sortilin-related receptor 1 associated with early-onset familial Alzheimer’s disease indicates effects on mitochondrial and ribosome function in young-adult zebrafish brains. biorxiv. DOI
  2020	Barthelson, K., Pederson, S. M., Newman, M., Jiang, H., & Lardelli, M. (2020). Frameshift and frame-preserving mutations in zebrafish presenilin 2 affect different cellular functions in young adult brains. DOI
  2020	Hin, N., Newman, M., Kaslin, J., Douek, A. M., Lumsden, A., Moussavi Nik, S. H., . . . Lardelli, M. (2020). Accelerated brain aging towards transcriptional inversion in a zebrafish model of the K115fs mutation of human PSEN2. PloS one, 15(1), e0227258. DOI Scopus14 WoS14 Europe PMC10
  2019	Newman, M., Hin, N., Pederson, S., & Lardelli, M. (2019). A familial Alzheimer's disease-like mutation in the zebrafish presenilin 1 gene affects brain energy production. DOI
  2019	Newman, M., Nik, H. M., Sutherland, G., Hin, N., Kim, W., Halliday, G., . . . Lardelli, M. (2019). Accelerated loss of hypoxia response in zebrafish with familial Alzheimer’s disease-like mutation of Presenilin 1. DOI
  2019	Newman, M., Hin, N., Pederson, S., & Lardelli, M. (2019). Brain transcriptome analysis of a familial Alzheimer's disease-like mutation in the zebrafish presenilin 1 gene implies effects on energy production. Molecular Brain, 12(1), 1-5. DOI Scopus17 WoS16 Europe PMC12
  2019	Braggin, J. E., Bucks, S. A., Course, M. M., Smith, C. L., Sopher, B., Osnis, L., . . . Jayadev, S. (2019). Alternative splicing in a presenilin 2 variant associated with Alzheimer disease. Annals of Clinical and Translational Neurology, 6(4), 762-777. DOI Scopus18 WoS19 Europe PMC14
  2018	Lumsden, A., Rogers, J., Majd, S., Newman, M., Sutherland, G., Verdile, G., & Lardelli, M. (2018). Dysregulation of neuronal iron homeostasis as an alternative unifying effect of mutations causing familial Alzheimer's disease. Frontiers in Neuroscience, 12(AUG), 533-1-533-21. DOI Scopus28 WoS26 Europe PMC18
  2018	Nik, S. H. M., Newman, M., Lumsden, A., Jayne, T., & Lardelli, M. (2018). HMGA1 zebrafish co-orthologue hmga1b can modulate p53-dependent cellular responses but is unable to control the alternative splicing of psen1. DOI
  2018	Jiang, H., Newman, M., & Lardelli, M. (2018). The zebrafish orthologue of familial Alzheimer's disease gene PRESENILIN 2 is required for normal adult melanotic skin pigmentation. PLoS ONE, 13(10), e0206155-1-e0206155-20. DOI Scopus12 WoS13 Europe PMC6
  2018	Jiang, H., Jayadev, S., Lardelli, M., & Newman, M. (2018). A Review of the Familial Alzheimer's Disease Locus PRESENILIN 2 and Its Relationship to PRESENILIN 1. Journal of Alzheimer's Disease, 66(4), 1323-1339. DOI Scopus8 WoS8 Europe PMC6
  2018	Ratnayake, D., Newman, M., & Lardelli, M. (2018). Degenerate codon mixing for PCR-based manipulation of highly repetitive sequences. BMC Research Notes, 11(1), 202-1-202-7. DOI Scopus1 Europe PMC1
  2018	Hin, N., Newman, M., Kaslin, J., Douek, A. M., Lumsden, A., Zhou, X., . . . Lardelli, M. (2018). Accelerated brain aging towards transcriptional inversion in a zebrafish model of familial Alzheimer's disease. BioRxiv, OnlinePubl. DOI
  2017	Newman, M., Halter, L., Lim, A., & Lardelli, M. (2017). Mitochondrion to endoplasmic reticulum apposition length in zebrafish embryo spinal progenitors is unchanged in response to perturbations associated with Alzheimer’s disease. PLoS ONE, 12(6), e0179859-1-e0179859-17. DOI Scopus2 WoS2 Europe PMC1
  2016	Ebrahimie, E., Moussavi Nik, S., Newman, M., Van Der Hoek, M., & Lardelli, M. (2016). The Zebrafish equivalent of Alzheimer's disease-associated PRESENILIN Isoform PS2V regulates inflammatory and other responses to hypoxic stress. Journal of Alzheimer's Disease, 52(2), 581-608. DOI Scopus14 WoS12 Europe PMC12
  2016	Jayne, T., Newman, M., Verdile, G., Sutherland, G., Münch, G., Musgrave, I., . . . Lardelli, M. (2016). Evidence for and against a pathogenic role of reduced γ-secretase activity in familial Alzheimer's disease. Journal of Alzheimer's Disease, 52(3), 781-799. DOI Scopus27 WoS27 Europe PMC21
  2016	Richards, R., Robertson, S., O'Keefe, L., Fornarino, D., Scott, A., Lardelli, M., & Baune, B. (2016). The enemy within: innate surveillance-mediated cell death, the common mechanism of neurodegenerative disease. Frontiers in Neuroscience, 10(MAY), 193-1-193-20. DOI Scopus27 WoS27 Europe PMC18
  2015	Moussavi Nik, S., Newman, M., Wilson, L., Ebrahimie, E., Wells, S., Musgrave, I., . . . Lardelli, M. (2015). Alzheimer's disease-related peptide PS2V plays ancient, conserved roles in suppression of the unfolded protein response under hypoxia and stimulation of γ-secretase activity. Human Molecular Genetics, 24(13), 3662-3678. DOI Scopus22 WoS21 Europe PMC13
  2015	Lim, A., Moussavi Nik, S., Ebrahimie, E., & Lardelli, M. (2015). Analysis of nicastrin gene phylogeny and expression in zebrafish. Development Genes and Evolution, 225(3), 171-178. DOI Scopus4 WoS4 Europe PMC3
  2014	Newman, M., Ebrahimie, E., & Lardelli, M. (2014). Using the zebrafish model for Alzheimer's disease research. Frontiers in Genetics, 5(JUN), 189-1-189-10. DOI Scopus88 WoS82 Europe PMC43
  2014	Ganesan, S., Moussavi Nik, S., Newman, M., & Lardelli, M. (2014). Identification and expression analysis of the zebrafish orthologues of the mammalian MAP1LC3 gene family. Experimental Cell Research, 328(1), 228-237. DOI Scopus10 WoS11 Europe PMC5
  2014	Nik, S., Croft, K., Mori, T., & Lardelli, M. (2014). The comparison of methods for measuring oxidative stress in zebrafish brains. Zebrafish, 11(3), 248-254. DOI Scopus10 WoS9 Europe PMC7
  2014	Newman, M., Wilson, L., Verdile, G., Lim, A., Khan, I., Nik, S., . . . Lardelli, M. (2014). Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease. Human Molecular Genetics, 23(3), 602-617. DOI Scopus40 WoS37 Europe PMC25
  2014	Moussavi Nik, S. H., Newman, M., Ganesan, S., Chen, M., Martins, R., Verdile, G., & Lardelli, M. (2014). Hypoxia alters expression of Zebrafish Microtubule-associated protein Tau (mapta, maptb) gene transcripts. BMC Research Notes, 7(1), 767-1-767-9. DOI Scopus16 Europe PMC5
  2014	Klarić, T., Lardelli, M., Key, B., Koblar, S., & Lewis, M. (2014). Activity-dependent expression of neuronal PAS domain-containing protein 4 (npas4a) in the developing zebrafish brain. Frontiers in Neuroanatomy, 8(DEC), 148-1-148-13. DOI Scopus15 WoS15 Europe PMC10
  2013	Wilson, L., & Lardelli, M. (2013). The development of an in vivo γ-secretase assay using zebrafish embryos. Journal of Alzheimer's Disease, 36(3), 521-534. DOI Scopus8 WoS8 Europe PMC4
  2013	Sharman, M., Moussavi Nik, S., Chen, M., Ong, D., Wijaya, L., Laws, S., . . . Verdile, G. (2013). The Guinea Pig as a model for sporadic Alzheimer's Disease (AD): the impact of cholesterol intake on expression of AD-related genes. PLoS One, 8(6), 1-12. DOI Scopus28 WoS28 Europe PMC22
  2012	Avdesh, A., Chen, M., Martin-Iverson, M., Mondal, A., Ong, D., Rainey-Smith, S., . . . Martins, R. (2012). Regular care and maintenance of a Zebrafish (Danio rerio) laboratory: an introduction. Journal of Visualized Experiments, (69), 1-8. DOI Scopus218 WoS197 Europe PMC91
  2012	Newman, M., Nornes, S., Martins, R., & Lardelli, M. (2012). Robust homeostasis of Presenilin1 protein levels by transcript regulation. Neuroscience Letters, 519(1), 14-19. DOI Scopus4 WoS5 Europe PMC2
  2012	Moussavi Nik, S., Wilson, L., Newman, M., Croft, K., Mori, T., Musgrave, I., & Lardelli, M. (2012). The BACE1-PSEN-AβPP regulatory axis has an ancient role in response to low oxygen/oxidative stress. Journal of Alzheimer's Disease, 28(3), 515-530. DOI Scopus36 WoS21 Europe PMC24
  2012	Avdesh, A., Martin-Iverson, M., Mondal, A., Chen, M., Askraba, S., Newman, M., . . . Martins, R. (2012). Evaluation of color preference in zebrafish for learning and memory. Journal of Alzheimer's Disease, 28(2), 459-469. DOI Scopus88 WoS83 Europe PMC36
  2012	Chen, M., Tegg, M., Avdesh, A., Mondal, A., Lardelli, M., Verdile, G., & Martins, R. (2012). P4‐121: Analysis of insulin‐degrading enzyme (IDE) expression and function in zebrafish embryos. Alzheimer's &amp; Dementia, 8(4S_Part_18). DOI
  2011	Sugano, Y., & Lardelli, M. (2011). Identification and expression analysis of the zebrafish orthologue of Klotho. Development Genes and Evolution, 221(3), 179-186. DOI Scopus11 WoS11 Europe PMC8
  2011	Wells, S., Nornes, S., & Lardelli, M. (2011). Transgenic zebrafish recapitulating tbx16 gene early developmental expression. PLoS One, 6(6), e21559-1-e21559-6. DOI Scopus11 WoS10 Europe PMC8
  2011	Moussavi Nik, S., Newman, M., & Lardelli, M. (2011). The response of HMGA1 to changes in oxygen availability is evolutionarily conserved. Experimental Cell Research, 317(11), 1503-1512. DOI Scopus19 WoS20 Europe PMC16
  2011	Newman, M., Verdile, G., Martins, R., & Lardelli, M. (2011). Zebrafish as a tool in Alzheimer's disease research. Biochimica et Biophysica Acta-Molecular Basis of Disease, 1812(3), 346-352. DOI Scopus50 WoS41 Europe PMC26
  2010	Newman, M., & Lardelli, M. (2010). A hyperactive sleeping beauty transposase enhances transgenesis in zebrafish embryos. BMC Research Notes, 3(1), 282-286. DOI Scopus7 Europe PMC5
  2010	Wells, S., Conran, J., Tamme, R., Gaudin, A., Webb, J., & Lardelli, M. (2010). Cryptic organisation within an apparently irregular rostrocaudal distribution of interneurons in the embryonic zebrafish spinal cord. Experimental Cell Research, 316(19), 3292-3303. DOI Scopus1 WoS1 Europe PMC1
  2010	Newman, M., Wilson, L., Camp-Dotlic, E., Verdile, G., Martins, R., & Lardelli, M. (2010). A zebrafish melanophore model of amyloidβ toxicity. Zebrafish, 7(2), 155-159. DOI Scopus19 WoS19 Europe PMC12
  2010	Aleklett, K., Hook, M., Jakobsson, K., Lardelli, M., Snowden, S., & Soderbergh, B. (2010). The peak of the oil age - Analyzing the world oil production reference scenario in world energy outlook 2008. Energy Policy, 38(3), 1398-1414. DOI Scopus251 WoS198
  2009	Chen, M., Martins, R., & Lardelli, M. (2009). Complex splicing and neural expression of duplicated Tau genes in zebrafish embryos. Journal of Alzheimer's Disease, 18(2), 305-317. DOI Scopus44 WoS38 Europe PMC26
  2009	Henshall, T., Tucker, B., Lumsden, A., Nornes, S., Lardelli, M., & Richards, R. (2009). Selective neuronal requirement for Huntingtin in the developing zebrafish. Human Molecular Genetics, 18(24), 4830-4842. DOI Scopus35 WoS34 Europe PMC27
  2009	Nornes, S., Newman, M., Wells, S., Verdile, G., Martins, R., & Lardelli, M. (2009). Independent and cooperative action of Psen2 with Psen1 in zebrafish embryos. Experimental Cell Research, 316(16), 2791-2801. DOI Scopus37 WoS36 Europe PMC21
  2009	Newman, M., Tucker, B., Nornes, S., Ward, A., & Lardelli, M. (2009). Altering presenilin gene activity in zebrafish embryos causes changes in expression of genes with potential involvement in Alzheimer's Disease pathogenesis. Journal of Alzheimer's Disease, 16(1), 133-147. DOI Scopus23 WoS23 Europe PMC15
  2009	Nornes, S., Tucker, B., & Lardelli, M. (2009). Zebrafish aplnra functions in epiboly. BMC Research Notes, 2(1), 1-6. DOI Scopus7 Europe PMC6
  2009	Lardelli, M. (2009). Mining the data on coal. Science, 324(5929), 880-881. DOI Scopus6 WoS5
  2009	Newman, M., Tucker, B., Nornes, S., Ward, A., & Lardelli, M. (2009). Erratum: Altering presenilin gene activity in zebrafish embryos causes changes in expression of genes with potential involvement in Alzheimer's disease pathogenesis (Journal of Alzheimer's Disease (2009) 16:1 (133-147)). Journal of Alzheimer's Disease, 18(4), 993. DOI
  2008	Nornes, S., Newman, M., Verdile, G., Wells, S., Stoick-Cooper, C., Tucker, B., . . . Lardelli, M. (2008). Interference with splicing of Presenilin transcripts has potent dominant negative effects on Presenilin activity. Human Molecular Genetics, 17(3), 402-412. DOI Scopus39 WoS37 Europe PMC24
  2007	Khut, P., Tucker, B., Lardelli, M., & Wood, S. (2007). Evolutionary and expression analysis of the zebrafish deubiquitylating enzyme, Usp9. Zebrafish, 4(2), 95-101. DOI Scopus9 WoS8 Europe PMC7
  2007	Tucker, B., & Lardelli, M. (2007). A rapid apoptosis assay measuring relative acridine orange fluorescence in zebrafish embryos. Zebrafish, 4(2), 113-116. DOI Scopus92 WoS92 Europe PMC53
  2007	Belle, L., Wadham, C., Crocker, L., Lardelli, M., & Khew-Goodall, Y. (2007). The protein tyrosine phosphatase Pez regulates TGFβ, epithelial–mesenchymal transition, and organ development. Journal of Cell Biology, 178(7), 1223-1235. DOI Scopus70 WoS67 Europe PMC50
  2007	Lumsden, A., Henshall, T., Dayan, S., Lardelli, M., & Richards, R. (2007). Huntingtin-deficient zebrafish exhibit defects in iron utilization and development. Human Molecular Genetics, 16(16), 1905-1920. DOI Scopus125 WoS121 Europe PMC90
  2007	Newman, M., Musgrave, I., & Lardelli, M. (2007). Alzheimer disease: amyloidogenesis, the presenilins and animal models. Biochimica et Biophysica Acta-Molecular Basis of Disease, 1772(3), 285-297. DOI Scopus112 WoS100 Europe PMC64
  2007	Lardelli, M. (2007). Scientists need to confront economists about peak oil. Nature, 446(7133), 257. DOI Scopus3 WoS3 Europe PMC1
  2007	Tucker, B., Hepperle, C., Kortschak, R., Rainbird, B., Wells, S., Oates, A., & Lardelli, M. (2007). Zebrafish Angiotensin II receptor-like 1a (agtrl1a) is expressed in migrating hypoblast, vasculature, and in multiple embryonic epithelia. Gene Expression Patterns, 7(3), 258-265. DOI Scopus26 WoS27 Europe PMC23
  2007	Newman, M., Musgrave, I. F., & Lardelli, M. (2007). Corrigendum to "Alzheimer disease: Amyloidogenesis, the presenilins and animal models" [Biochim. Biophys. Acta 1772 (2007) 285-297] (DOI:10.1016/j.bbadis.2006.12.001). Biochimica et Biophysica Acta - Molecular Basis of Disease, 1772(9), 1118. DOI
  2006	Tucker, B., Richards, R., & Lardelli, M. (2006). Contribution of mGluR and Fmr1 functional pathways to neurite morphogenesis, craniofacial development and fragile X syndrome. Human Molecular Genetics, 15(23), 3446-3458. DOI Scopus105 WoS102 Europe PMC80
  2004	Tucker, B., Richards, R., & Lardelli, M. (2004). Expression of three zebrafish orthologs of human FMR1-related genes and their phylogenetic relationships. Development Genes and Evolution, 214(11), 567-574. DOI Scopus31 WoS28 Europe PMC20
  2004	Scholpp, S., Groth, C., Lohs, C., Lardelli, M., & Brand, M. (2004). Zebrafish fgfr1 is a member of the fgf8 synexpression group and is required for fgf8 signalling at the midbrain-hindbrain boundary. Development Genes and Evolution, 214(6), 285-295. DOI Scopus60 WoS52 Europe PMC46
  2003	Lardelli, M. (2003). The evolutionary relationships of zebrafish genes tbx6, tbx16/spadetail and mga. Development Genes and Evolution, 213(10), 519-522. DOI Scopus16 WoS16 Europe PMC15
  2003	Camp-Dotlic, E., Badhwar, P., Mann, G., & Lardelli, M. (2003). Expression analysis of a Tyrosinase promoter sequence in zebrafish. Pigment Cell Research, 16(2), 117-126. DOI Scopus14 WoS15 Europe PMC7
  2003	Camp-Dotlic, E., Hope, R., Kortschak, R., Cox, T., & Lardelli, M. (2003). Expression of three spalt (sal) gene homologues in zebrafish embryos. Development Genes and Evolution, 213(1), 35-43. DOI Scopus21 WoS20 Europe PMC18
  2003	Nornes, S., Groth, C., Camp-Dotlic, E., Ey, P., & Lardelli, M. (2003). Developmental control of Presenilin1 expression, endoproteolysis, and interaction in zebrafish embryos. Experimental Cell Research, 289(1), 124-132. DOI Scopus44 WoS40 Europe PMC27
  2003	Lardelli, M. (2003). Something fishy in 21st century genomics. Todays Life Science, 15, 20-23.
  2002	Tamme, R., Wells, S., Conran, J., & Lardelli, M. (2002). The identity and distribution of neural cells expressing the mesodermal determinant spadetail. BMC Developmental Biology, 2(9), www 1-www 13. DOI
  2002	Groth, C., Nornes, S., Mc Carty, R., Tamme, R., & Lardelli, M. (2002). Identification of a second presenilin gene in zebrafish with similarity to the human Alzheimer's disease gene presenilin2. Development Genes and Evolution, 212(10), 486-490. DOI Scopus53 WoS50 Europe PMC32
  2002	Groth, C., & Lardelli, M. (2002). The structure and function of vertebrate fibroblast growth factor receptor 1. International Journal of Developmental Biology, 46(4 Special Issue SI), 393-400. Scopus72 WoS69 Europe PMC49
  2002	Tamme, R., Wells, S., Conran, J. G., & Lardelli, M. (2002). The identity and distribution of neural cells expressing the mesodermal determinant spadetail.. BMC developmental biology [electronic resource], 2(1), 9. DOI Scopus8 Europe PMC12
  2002	Tamme, R., Wells, S., Conran, J., & Lardelli, M. (2002). The identity and distribution of neural cells expressing the mesodermaldeterminant spadetail. BMC Developmental Biology, 2, 1-13. DOI Scopus14
  2002	Kortschak, R. D., Tamme, R., & Lardelli, M. (2002). Erratum: Evolutionary analysis of vertebrate Notch genes (Development Genes and Evolution (2001) vol. 211 (350-354)). Development Genes and Evolution, 212(3), 158. DOI
  2001	Holland, L. Z., Rached, L. A., Tamme, R., Holland, N. D., Kortschak, D., Inoko, H., . . . Lardelli, M. (2001). Erratum: Characterization and developmental expression of the amphioxus homolog of Notch (AmnphiNotch): Evolutionary conservation of multiple expression domains in amphioxus and vertebrates (Developmental Biology (2001) 232:2 (495-507)). Developmental Biology, 233(1), 238. DOI Scopus1
  2001	Jonsson, J., Xiang, Z., Pettersson, M., Lardelli, M., & Nilsson, G. (2001). Distinct and regulated expression of Notch receptors in hematopoietic lineages and during myeloid differentiation. European Journal of Immunology, 31(11), 3240-3247. DOI Scopus43 WoS43 Europe PMC32
  2001	Holland, L., Rached, L., Tamme, R., Holland, N., Inoko, H., Kortschak, R., . . . Lardelli, M. (2001). Characterization and developmental expression of the amphioxus homolog of Notch (AmphiNotch): Evolutionary conservation of multiple expression domains in amphioxus and vertebrates. Developmental Biology, 232(2), 493-507. DOI Scopus50 WoS48 Europe PMC33
  2001	Camp-Dotlic, E., & Lardelli, M. (2001). Tyrosinase gene expression in zebrafish embryos. Development Genes and Evolution, 211(3), 150-153. DOI Scopus60 WoS58 Europe PMC43
  2001	Kortschak, R., Tamme, R., & Lardelli, M. (2001). Evolutionary analysis of vertebrate Notch genes. Development Genes and Evolution, 211(7), 350-354. DOI Scopus27 WoS29 Europe PMC23
  2001	Tamme, R., Mills, K., Rainbird, B., Nornes, S., & Lardelli, M. (2001). Simple, directional cDNA cloning for in situ transcript hybridization screens. Biotechniques, 31(4), 938-946. DOI Scopus6 WoS5 Europe PMC5
  2000	Tamme, R., Camp-Dotlic, E., Kortschak, R., & Lardelli, M. (2000). Non-specific, nested suppression PCR method for isolation of unknown flanking DNA. Biotechniques, 28(5), 895-902. DOI Scopus10 WoS8 Europe PMC6
  1997	Westin, J., & Lardelli, M. (1997). Three novel Notch genes in zebrafish: Implications for vertebrate Notch gene evolution and function. Development Genes and Evolution, 207(1), 51-63. DOI Scopus118 WoS115 Europe PMC65
  1997	Zhang, H. Y., Lardelli, M., & Ekblom, P. (1997). Sequence of zebrafish fibulin-1 and its expression in developing heart and other embryonic organs. Development Genes and Evolution, 207(5), 340-351. DOI Scopus15 WoS14 Europe PMC8
  1997	Lardelli, M. (1997). Generation and PCR screening of bacteriophage gamma sublibraries enriched for rare clones (the "sublibrary method").. Methods in molecular biology (Clifton, N.J.), 67, 345-355. DOI Scopus3 Europe PMC1
  1996	Lardelli, M., Williams, R., Mitsiadis, T., & Lendahl, U. (1996). Expression of the Notch 3 intracellular domain in mouse central nervous system progenitor cells is lethal and leads to disturbed neural tube development. Mechanisms of Development, 59(2), 177-190. DOI Scopus93 WoS91 Europe PMC68
  1995	Dahlstrand, J., Lardelli, M., & Lendahl, U. (1995). Nestin mRNA expression correlates with the central nervous system progenitor cell state in many, but not all, regions of developing central nervous system. Developmental Brain Research, 84(1), 109-129. DOI Scopus440 WoS420 Europe PMC332
  1995	Mitsiadis, T. A., Lardelli, M., Lendahl, U., & Thesleff, I. (1995). Expression of Notch 1, 2, and 3 is regulated by epithelial-mesenchymal interactions and retinoic acid in the developing mouse tooth and associated with determination of ameloblast cell fate. Journal of Cell Biology, 130(2), 407-418. DOI Scopus153 WoS150 Europe PMC112
  1995	Williams, R., Lendahl, U., & Lardelli, M. (1995). Complementary and combinatorial patterns of Notch gene family expression during early mouse development. Mechanisms of Development, 53(3), 357-368. DOI Scopus143 WoS145 Europe PMC98
  1995	Lardelli, M. (1995). Residents’ rights. Nature, 378(6555), 330. DOI
  1995	Lardelli, M., Williams, R., & Lendahl, U. (1995). Notch-related genes in animal development. International Journal of Developmental Biology, 39(5), 769-780. Scopus50 WoS50 Europe PMC31
  1995	Lardelli, M. (1995). Discriminatory frontier policy. Nature, 376(6535), 12. DOI
  1994	Lardelli, M., Dahlstrand, J., & Lendahl, U. (1994). The novel Notch homologue mouse Notch 3 lacks specific epidermal growth factor-repeats and is expressed in proliferating neuroepithelium. Mechanisms of Development, 46(2), 123-136. DOI Scopus260 WoS275 Europe PMC184
  1994	Larsson, C., Lardelli, M., White, I., & Lendahl, U. (1994). The human NOTCH1, 2, and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated translocation. Genomics, 24(2), 253-258. DOI Scopus84 WoS90 Europe PMC55
  1994	Barlow, C., Meister, B., Lardelli, M., Lendahl, U., & Vennström, B. (1994). Thyroid abnormalities and hepatocellular carcinoma in mice transgenic for v-erbA. EMBO Journal, 13(18), 4241-4250. DOI Scopus74 WoS76 Europe PMC48
  1994	Lardelli, M., & Lendahl, U. (1994). Generating bacteriophage λ sublibraries enriched for rare clones. BioTechniques, 16(3), 420-422. Scopus10 WoS10 Europe PMC7
  1993	Lardelli, M., & Ish-Horowicz, D. (1993). Drosophila hairy pair-rule gene regulates embryonic patterning outside its apparent stripe domains. Development, 118(1), 255-266. DOI Scopus12 WoS12 Europe PMC9
  1993	Lardelli, M., & Lendahl, U. (1993). Motch A and Motch B — Two mouse Notch homologues coexpressed in a wide variety of tissues. Experimental Cell Research, 204(2), 364-372. DOI Scopus120 WoS132 Europe PMC72
  1989	Rushlow, C. A., Hogan, A., Pinchin, S. M., Howe, K. M., Lardelli, M., & Ish-Horowicz, D. (1989). The Drosophila hairy protein acts in both segmentation and bristle patterning and shows homology to N-myc.. The EMBO journal, 8(10), 3095-3103. DOI Scopus164 WoS232 Europe PMC134
  1989	Johnson, M. A., Misra, R. M., Lardelli, M., Messina, M., Ephraums, C., Reeves, P. R., . . . Holmes, I. H. (1989). Synthesis in Escherichia coli of the major glycoprotein of human rotavirus: analysis of the antigenic regions. Gene, 84(1), 73-81. DOI Scopus9 WoS9 Europe PMC9

• Books

  Year	Citation
  2013	Aleklett, K., Lardelli, M., & Qvennerstedt, O. (2013). Peeking at peak oil (Vol. 9781461434245). Springer. DOI Scopus54

• Book Chapters

  Year	Citation
  2017	Newman, M., Kretzschmar, D., Khan, I., Chen, M., Verdile, G., & Lardelli, M. (2017). Animal models of Alzheimer's disease. In M. Conn (Ed.), Animal Models for the Study of Human Disease (2 ed., pp. 1031-1085). United States: Academic Press. DOI Scopus13
  2013	Chen, M., Kretzschmar, D., Verdile, G., & Lardelli, M. (2013). Models of Alzheimer's disease. In P. Conn (Ed.), Animal Models for the Study of Human Disease (1 ed., pp. 595-633). United Kingdom: Elsevier. DOI Scopus1
  2002	Lardelli, M. (2002). Generation and PCR screening of bacteriophage lambda sublibraries enriched for rare clones (the "sublibrary method"). In PCR Cloning Protocols Second Edition, Ch 41 (Vol. 192, 2 ed., pp. 391-399). Totowa, N.J: Humana Press. DOI Scopus1 Europe PMC1
  2002	Lardelli, M. (2002). Nonspecific, nested suppression PCR method for isolation of unknown flanking DNA ("Cold-start method"). In PCR Cloning Protocols Second Edition, Ch 25 (Vol. 192, pp. 285-292). Totowa, New Jersey: Humana Press. DOI Scopus1

• Conference Papers

  Year	Citation
  2015	Lardelli, M., Ebrahimie, E., Newman, M., Nik, S. M., & Hoek, M. V. D. (2015). Transcriptome analyses using human and zebrafish brain data reveal hypoxia as an important element in Alzheimer's disease. In JOURNAL OF NEUROCHEMISTRY Vol. 134 (pp. 324). Cairns, AUSTRALIA: WILEY-BLACKWELL.
  2006	Henshall, T. L., Lumsden, A. L., Lardelli, M. T., & Richards, R. I. (2006). A critical role for huntingtin in neural development. In INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE Vol. 24 (pp. 511). Banff, CANADA: PERGAMON-ELSEVIER SCIENCE LTD. DOI

• Conference Items

  Year	Citation
  2012	Moussavi Nik, S. H., Verdile, G., Sharman, M., Chen, M., Ong, D., Wijaya, L., . . . Martins, R. (2012). The impact of cholesterol intake on expression of Alzheimer's disease–related genes in the guinea pig brain. Poster session presented at the meeting of Alzheimer's and Dementia. Vancouver, British Columbia: Elsevier. DOI

• Theses

  Year	Citation
  1991	Lardelli, M. (1991). Regulation and function of the pair-rule gene hairy in Drosophila melanogaster..

Michael Lardelli teaches at all levels of genetics but specialising in developmental genetics, genetic manipulation of model organisms, and the genetics of Alzheimers' disease.

• Current Higher Degree by Research Supervision (University of Adelaide)

  Date	Role	Research Topic	Program	Degree Type	Student Load	Student Name
  2023	Principal Supervisor	Investigating Early Molecular Drivers of Neurodegeneration by Modelling Parkinson's Disease in Zebrafish	Master of Philosophy	Master	Full Time	Miss Angel Grace Allen
  2022	Principal Supervisor	Investigating Alzheimer's disease and MPS III mutant gene using Zebrafish and Drosophila genetic models	Doctor of Philosophy	Doctorate	Full Time	Mr Kaijing Xu
  2021	Co-Supervisor	Exogenous Ketogenic Therapy to Inhibit the Symptoms Caused by BACE1 in Drosophila and Protect Mitochondria	Doctor of Philosophy	Doctorate	Full Time	Mr Hao Huang
  2020	Principal Supervisor	Bioinformatics analyses of familial Alzheimer's disease mutation models in zebrafish	Doctor of Philosophy	Doctorate	Full Time	Mr Lachlan Warren William Baer
  2020	Principal Supervisor	Molecular and bioinformatic studies of Alzheimer's and MPS III disease-linked genes in Zebrafish	Doctor of Philosophy	Doctorate	Full Time	Mr Ewan Gerken

• Past Higher Degree by Research Supervision (University of Adelaide)

  Date	Role	Research Topic	Program	Degree Type	Student Load	Student Name
  2018 - 2020	Principal Supervisor	Transcriptome Analysis of Zebrafish Genetic Models to Reveal Early Molecular Drivers of Alzheimer's Disease	Doctor of Philosophy	Doctorate	Full Time	Miss Nhi Hin
  2017 - 2021	Principal Supervisor	Investigating Alzheimer’s disease using zebrafish genetic models	Doctor of Philosophy	Doctorate	Full Time	Mr Yang Dong
  2017 - 2021	Principal Supervisor	Investigating the effects of mutations causative for early-onset familial Alzheimer’s disease using zebrafish as a model organism	Doctor of Philosophy	Doctorate	Full Time	Miss Karissa Barthelson
  2014 - 2018	Principal Supervisor	Identifying the pathological changes caused by familial Alzheimer’s disease-like mutations in zebrafish psen2	Doctor of Philosophy	Doctorate	Full Time	Ms Haowei Jiang
  2014 - 2020	Principal Supervisor	Investigations of y-secretase substrates Amyloid precursor protein and p75 neurotrophin receptor in zebrafish	Doctor of Philosophy	Doctorate	Full Time	Tanya Jayne
  2012 - 2016	Co-Supervisor	An Investigation of the Role of CreB Deubiquitinating Enzyme in the Regulation of Carbon Metabolism in Aspergillus nidulans	Doctor of Philosophy	Doctorate	Part Time	Mr Md Ashiqul Alam
  2011 - 2015	Principal Supervisor	Analysing the Biological Function of PS2V: An Aberrant Splicing Phenomenon or Evolutionarily Conserved Mechanism in Alzheimer's Disease	Doctor of Philosophy	Doctorate	Full Time	Dr Seyyed Hani Moussavi Nik
  2011 - 2015	Principal Supervisor	ANALYSING THE ROLE OF AUTOPHAGY IN ALZHEIMER'S DISEASE PATHOGENESIS USING THE ZEBRAFISH MODEL SYSTEM	Doctor of Philosophy	Doctorate	Full Time	Mr Swamynathan Ganesan
  2011 - 2015	Principal Supervisor	Analysis of the Subcellular Localization of Proteins Implicated in Alzheimer's Disease	Doctor of Philosophy	Doctorate	Full Time	Miss Anne Hwee Ling Lim
  2010 - 2011	Principal Supervisor	Characterization of the zebrafish Orthologue of Klotho	Master of Science	Master	Full Time	Mr Yuya Sugano
  2009 - 2012	Co-Supervisor	Function and Evolution of the piRNA Pathway in the Amniote Gonad and Human Ovarian Cancer	Doctor of Philosophy	Doctorate	Full Time	Miss Shu Ly Lim
  2009 - 2011	Principal Supervisor	Molecular Responses to Low Oxygen Levels/Oxidative Stress in Zebrafish	Master of Science	Master	Full Time	Dr Seyyed Hani Moussavi Nik
  2008 - 2009	Principal Supervisor	Identification and Analysis of the Two Tau Paralogues in Zebrafish	Master of Science	Master	Full Time	Miss Mengqi Chen
  2008 - 2013	Principal Supervisor	The analysis of Presenilin processing and activity with a focus on its implications for Alzheimer's disease pathogenesis using Danio Rerio as a model organism	Doctor of Philosophy	Doctorate	Full Time	Mr Lachlan James Wilson
  2008 - 2011	Co-Supervisor	From Model Organism to Industrial Workhorse	Doctor of Philosophy	Doctorate	Part Time	Mr Jai Denton
  2006 - 2010	Co-Supervisor	Investigation of RNA-Mediated Pathogenic Pathways in a Drosophila Model of Expanded Repeat Disease	Doctor of Philosophy	Doctorate	Full Time	Dr Clare van Eyk
  2006 - 2011	Co-Supervisor	Tyrosine Phosphatase Pez: A Novel Regulator of TGFß Signalling, Epithelial-Mesenchymal Transition and Protein Secretion in Development and Cancer	Doctor of Philosophy	Doctorate	Full Time	Mrs Leila Belle
  2005 - 2008	Principal Supervisor	Analysis of Genes Implicated in Alzheimer's Disease Pathogenesis Using Danio Rerio as a Model Organism	Doctor of Philosophy	Doctorate	Full Time	Dr Morgan Newman
  2004 - 2010	Co-Supervisor	Huntingtin Function During Zebrafish (Danio rerio) Development	Doctor of Philosophy	Doctorate	Full Time	Miss Tanya Henshall
  2003 - 2008	Co-Supervisor	The Genetic and Biochemical Analysis of Drosophila Wwox Protein Function	Doctor of Philosophy	Doctorate	Full Time	Mr Alexander Colella
  2003 - 2008	Principal Supervisor	Zebrafish as a Model of Genetic Disease	Doctor of Philosophy	Doctorate	Full Time	Dr Ben Tucker
  2002 - 2007	Co-Supervisor	Investigating the Role of Huntingtin in Development and Disease using the Zebrafish Model Organism	Doctor of Philosophy	Doctorate	Full Time	Ms Amanda Lumsden
  2001 - 2011	Principal Supervisor	An Investigation into the Development and Patterning of Dorsal Longitudinal Ascending Interneurons in Danio Rerio	Doctor of Philosophy	Doctorate	Full Time	Dr Simon Wells
  2000 - 2004	Principal Supervisor	Alzheimer's disease genes in zebrafish (Danio rerio)	Doctor of Philosophy	Doctorate	Full Time	Mr Casper Groth
  1999 - 2003	Principal Supervisor	Development of a Transgenic Strategy for Facilitated Modifier Mutation Screening in Zebrafish	Doctor of Philosophy	Doctorate	Part Time	Dr Esther Camp-Dotlic
  1998 - 2004	Principal Supervisor	Development and application of novel cloning strategies for analysis of genes controlling embryo development	Doctor of Philosophy	Doctorate	Full Time	Mr Richard Tamme

• Position: Associate Professor
• Phone: 83133212
• Email: michael.lardelli@adelaide.edu.au
• Fax: 83137534
• Campus: North Terrace
• Building: Molecular Life Sciences, floor 1
• Org Unit: Molecular and Biomedical Science