Sarah Furlong

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Sarah Furlong

Dr

 https://orcid.org/0000-0001-5914-500X
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20172023

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Biography

Dr Furlong manages the Neurodegenerative Disease Biobank in the Centre for Motor Neuron Disease Research at Macquarie University.

After completing her PhD in molecular medicine from Trinity College Dublin in 2013, she gained a quality control position with an analytical science company. In 2014, she moved to Brisbane, and began working as a research officer in the University of Queensland, investigating the genetics of MND. Later that year, Sarah started as a research officer in a biobank in Queensland Institute of Molecular Medicine, working on next generation sequencing projects and organising biobank projects. In late 2015, Sarah took on the role of biobank manager at Macquarie, overseeing the clinical and laboratory operations, data management and governance of the facility.

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  • Riluzole is associated with decreasing neuritic plaque severity in amyotrophic lateral sclerosis

    Mazumder, S., McCann, H., D'Silva, S., Furlong, S., Shepherd, C. E., Kril, J. J., Halliday, G. M., Rowe, D. B., Kiernan, M. C. & Tan, R. H., 1 Mar 2023, In: Brain. 146, 3, p. e17-e19 3 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    File
    2 Citations (Scopus)
    8 Downloads (Pure)

  • Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS

    Hop, P. J., Zwamborn, R. A. J., Hannon, E., Shireby, G. L., Nabais, M. F., Walker, E. M., van Rheenen, W., van Vugt, J. J. F. A., Dekker, A. M., Westeneng, H-J., Tazelaar, G. H. P., van Eijk, K. R., Moisse, M., Baird, D., Al Khleifat, A., Iacoangeli, A., Ticozzi, N., Ratti, A., Cooper-Knock, J., Morrison, K. E., & 65 othersShaw, P. J., Basak, A. N., Chiò, A., Calvo, A., Moglia, C., Canosa, A., Brunetti, M., Grassano, M., Gotkine, M., Lerner, Y., Zabari, M., Vourc'h, P., Corcia, P., Couratier, P., Mora Pardina, J. S., Salas, T., Dion, P., Ross, J. P., Henderson, R. D., Mathers, S., McCombe, P. A., Needham, M., Nicholson, G., Rowe, D. B., Pamphlett, R., Mather, K. A., Sachdev, P. S., Furlong, S., Garton, F. C., Henders, A. K., Lin, T., Ngo, S. T., Steyn, F. J., Wallace, L., Williams, K. L., BIOS Consortium, Brain MEND Consortium, Neto, M. M., Cauchi, R. J., Blair, I. P., Kiernan, M. C., Drory, V., Povedano, M., de Carvalho, M., Pinto, S., Weber, M., Rouleau, G. A., Silani, V., Landers, J. E., Shaw, C. E., Andersen, P. M., McRae, A. F., van Es, M. A., Pasterkamp, R. J., Wray, N. R., McLaughlin, R. L., Hardiman, O., Kenna, K. P., Tsai, E., Runz, H., Al-Chalabi, A., van den Berg, L. H., Van Damme, P., Mill, J. & Veldink, J. H., 23 Feb 2022, In: Science Translational Medicine. 14, 633, p. 1-15 15 p., eabj0264.

    Research output: Contribution to journal › Article › peer-review

    24 Citations (Scopus)

  • Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

    van Rheenen, W., van der Spek, R. A. A., Bakker, M. K., van Vugt, J. J. F. A., Hop, P. J., Zwamborn, R. A. J., de Klein, N., Westra, H-J., Bakker, O. B., Deelen, P., Shireby, G., Hannon, E., Moisse, M., Baird, D., Restuadi, R., Dolzhenko, E., Dekker, A. M., Gawor, K., Westeneng, H-J., Tazelaar, G. H. P., & 176 othersvan Eijk, K. R., Kooyman, M., Byrne, R. P., Doherty, M., Heverin, M., Al Khleifat, A., Iacoangeli, A., Shatunov, A., Ticozzi, N., Cooper-Knock, J., Smith, B. N., Gromicho, M., Chandran, S., Pal, S., Morrison, K. E., Shaw, P. J., Hardy, J., Orrell, R. W., Sendtner, M., Meyer, T., Başak, N., van der Kooi, A. J., Ratti, A., Fogh, I., Gellera, C., Lauria, G., Corti, S., Cereda, C., Sproviero, D., D'Alfonso, S., Sorarù, G., Siciliano, G., Filosto, M., Padovani, A., Chiò, A., Calvo, A., Moglia, C., Brunetti, M., Canosa, A., Grassano, M., Beghi, E., Pupillo, E., Logroscino, G., Nefussy, B., Osmanovic, A., Nordin, A., Lerner, Y., Zabari, M., Gotkine, M., Baloh, R. H., Bell, S., Vourc'h, P., Corcia, P., Couratier, P., Millecamps, S., Meininger, V., Salachas, F., Mora Pardina, J. S., Assialioui, A., Rojas-García, R., Dion, P. A., Ross, J. P., Ludolph, A. C., Weishaupt, J. H., Brenner, D., Freischmidt, A., Bensimon, G., Brice, A., Durr, A., Payan, C. A. M., Saker-Delye, S., Wood, N. W., Topp, S., Rademakers, R., Tittmann, L., Lieb, W., Franke, A., Ripke, S., Braun, A., Kraft, J., Whiteman, D. C., Olsen, C. M., Uitterlinden, A. G., Hofman, A., Rietschel, M., Cichon, S., Nöthen, M. M., Amouyel, P., SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, Traynor, B. J., Singleton, A. B., Mitne Neto, M., Cauchi, R. J., Ophoff, R. A., Wiedau-Pazos, M., Lomen-Hoerth, C., van Deerlin, V. M., Grosskreutz, J., Roediger, A., Gaur, N., Jörk, A., Barthel, T., Theele, E., Ilse, B., Stubendorff, B., Witte, O. W., Steinbach, R., Hübner, C. A., Graff, C., Brylev, L., Fominykh, V., Demeshonok, V., Ataulina, A., Rogelj, B., Koritnik, B., Zidar, J., Ravnik-Glavač, M., Glavač, D., Stević, Z., Drory, V., Povedano, M., Blair, I. P., Kiernan, M. C., Benyamin, B., Henderson, R. D., Furlong, S., Mathers, S., McCombe, P. A., Needham, M., Ngo, S. T., Nicholson, G. A., Pamphlett, R., Rowe, D. B., Steyn, F. J., Williams, K. L., Mather, K. A., Sachdev, P. S., Henders, A. K., Wallace, L., de Carvalho, M., Pinto, S., Petri, S., Weber, M., Rouleau, G. A., Silani, V., Curtis, C. J., Breen, G., Glass, J. D., Brown, R. H., Landers, J. E., Shaw, C. E., Andersen, P. M., Groen, E. J. N., van Es, M. A., Pasterkamp, R. J., Fan, D., Garton, F. C., McRae, A. F., Davey Smith, G., Gaunt, T. R., Eberle, M. A., Mill, J., McLaughlin, R. L., Hardiman, O., Kenna, K. P., Wray, N. R., Tsai, E., Runz, H., Franke, L., Al-Chalabi, A., Van Damme, P., van den Berg, L. H. & Veldink, J. H., Dec 2021, In: Nature Genetics. 53, 12, p. 1636-1648 32 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    File
    123 Citations (Scopus)
    6 Downloads (Pure)

  • Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

    Nabais, M. F., Laws, S. M., Lin, T., Vallerga, C. L., Armstrong, N. J., Blair, I. P., Kwok, J. B., Mather, K. A., Mellick, G. D., Sachdev, P. S., Wallace, L., Henders, A. K., Zwamborn, R. A. J., Hop, P. J., Lunnon, K., Pishva, E., Roubroeks, J. A. Y., Soininen, H., Tsolaki, M., Mecocci, P., & 52 othersLovestone, S., Kłoszewska, I., Vellas, B., Australian Imaging Biomarkers and Lifestyle study, Alzheimer's Disease Neuroimaging Initiative, Furlong, S., Garton, F. C., Henderson, R. D., Mathers, S., McCombe, P. A., Needham, M., Ngo, S. T., Nicholson, G., Pamphlett, R., Rowe, D. B., Steyn, F. J., Williams, K. L., Anderson, T. J., Bentley, S. R., Dalrymple-Alford, J., Fowder, J., Gratten, J., Halliday, G., Hickie, I. B., Kennedy, M., Lewis, S. J. G., Montgomery, G. W., Pearson, J., Pitcher, T. L., Silburn, P., Zhang, F., Visscher, P. M., Yang, J., Stevenson, A. J., Hillary, R. F., Marioni, R. E., Harris, S. E., Deary, I. J., Jones, A. R., Shatunov, A., Iacoangeli, A., van Rheenen, W., van den Berg, L. H., Shaw, P. J., Shaw, C. E., Morrison, K. E., Al-Chalabi, A., Veldink, J. H., Hannon, E., Mill, J., Wray, N. R. & McRae, A. F., 26 Mar 2021, In: Genome biology. 22, 1, p. 1-30 30 p., 90.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    File
    26 Citations (Scopus)
    8 Downloads (Pure)

  • Metabolite profiling reveals predictive biomarkers and the absence of β-methyl amino-l-alanine in plasma from individuals diagnosed with amyotrophic lateral sclerosis

    Bereman, M. S., Kirkwood, K. I., Sabaretnam, T., Furlong, S., Rowe, D. B., Guillemin, G. J., Mellinger, A. L. & Muddiman, D. C., 7 Aug 2020, In: Journal of Proteome Research. 19, 8, p. 3276-3285 10 p.

    Research output: Contribution to journal › Article › peer-review

    15 Citations (Scopus)
View all 7 research outputs