Projects per year
Personal profile
Biography
Dr Lyndal Henden is a Postdoctoral Research Fellow and Senior Lecturer in the Genomics and Bioinformatic Team within the Centre for Motor Neuron Disease Research at Macquarie University. She completed her PhD in 2017 at the Walter and Eliza Hall Institute of Medical Research, where she developed statistical methods to identify cryptic relatedness in the human genome and the genomes of microorganisms that cause disease. Her methods have been successfully used to discover and quantify unknown or misspecified familial relatedness, and to identify loci containing disease susceptibility genes in disorders such as Autism, Epilepsy and Intellectual Disability. She has also identified loci under positive selection that are suspected of being associated with antimalarial drug resistance in a global Plasmodium falciparum cohort.
Dr Henden’s current research is focused on understanding the genetic basis of Motor Neuron Disease (MND) and Frontotemporal Dementia (FTD). Her expertise in cryptic relatedness analysis is being applied to large MND/FTD patient cohorts to identify candidate disease loci for gene screening in the hopes of identifying novel gene mutations that are causing disease. Her research findings will have significant genetic counselling implications for MND/FTD patients and their family members.
Teaching
Dr Henden is the unit convenor for MEDI2201 - Clinical Bioinformatics and Biostatistics, a compulsory unit in the Genomics and Medical Informatics major. She has also taught into the following units:
STAT1378, MEDI3200, MEDI3401, MEDI2400
Education/Academic qualification
PhD, Walter and Eliza Hall Institute of Medical Research
Award Date: 15 Dec 2017
Mathematics and Statistics, BSc (Honours I), Massey University
Award Date: 6 Nov 2012
External positions
Visiting Scholar, University Medical Center Utrecht
Feb 2025 → Mar 2025
Adjunct Fellow, The University of Queensland
May 2022 → May 2024
Postdoctoral Researcher, Walter and Eliza Hall Institute of Medical Research
Mar 2017 → Mar 2018
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Collaborations and top research areas from the last five years
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MND 24: Investigating the molecular origin of a “C9orf72-like” patient subgroup of sporadic ALS
Grima, N. (Primary Chief Investigator), Henden, L. (Chief Investigator) & Williams, K. (Chief Investigator)
1/01/25 → 31/12/25
Project: Research
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FightMND IMPACT: Delving deep into the ALS genome to reveal somatic mosaicism
Henden, L. (Primary Chief Investigator), Williams, K. (Chief Investigator), Blair, I. (Associate Investigator), Smith, A. (Associate Investigator) & Chan Moi Fat, S. K. K. (Other)
1/02/24 → 31/01/26
Project: Research
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When sporadic disease is not sporadic - exploiting cryptic relatedness to unravel MND genetics
Williams, K. (Primary Chief Investigator), Henden, L. (Chief Investigator), Berkovsky, S. (Chief Investigator), Blair, I. (Associate Investigator), Iacoangeli, A. (Associate Investigator), Smith, B. (Associate Investigator), Dobson-Stone, C. (Associate Investigator), Kwok, J. B. (Associate Investigator), Halliday, G. (Associate Investigator), Nicholson, G. (Associate Investigator), Rowe, D. (Associate Investigator) & Scotter, E. L. (Associate Investigator)
1/10/22 → 30/09/26
Project: Research
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Comprehensive transcriptome analysis of neuroanatomical regions with variable pTDP-43 pathology in sporadic ALS patients
Williams, K. (Primary Chief Investigator), Henden, L. (Chief Investigator) & Blair, I. (Chief Investigator)
28/01/20 → 27/01/21
Project: Other
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Multi-region brain transcriptomic analysis of amyotrophic lateral sclerosis reveals widespread RNA alterations and substantial cerebellum involvement
Grima, N., Smith, A. N., Shepherd, C. E., Henden, L., Winn, T., Carroll, L., Rowe, D. B., Kiernan, M. C., Blair, I. P. & Williams, K. L., 25 Apr 2025, In: Molecular Neurodegeneration. 20, 1, p. 1-19 19 p., 40.Research output: Contribution to journal › Article › peer-review
Open AccessFile1 Citation (Scopus)24 Downloads (Pure) -
The genetics of motor neuron disease in New Zealand
Mrkela, M., Rodrigues, M., Naidoo, S., Devaux, J. B. L., Kirk, S. E., Vinnakota, C., Buchanan, C. M., Mulroy, D., Fraser, H., Jacobsen, J. C., Wyatt, H., Drake, K., Parker, E., Potter, H., Henden, L., McCann, E. P., Williams, K. L., Henders, A. K., Roxburgh, R. H. & Scotter, E. L., 15 Jul 2025, In: Journal of the Neurological Sciences. 474, p. 1-13 13 p., 123472.Research output: Contribution to journal › Article › peer-review
Open AccessFile2 Downloads (Pure) -
Hippocampal aggregation signatures of pathogenic UBQLN2 in amyotrophic lateral sclerosis and frontotemporal dementia
Thumbadoo, K. M., Dieriks, B. V., Murray, H. C., Swanson, M. E. V., Yoo, J. H., Mehrabi, N. F., Turner, C., Dragunow, M., Faull, R. L. M., Curtis, M. A., Siddique, T., Shaw, C. E., Newell, K. L., Henden, L., Williams, K. L., Nicholson, G. A. & Scotter, E. L., 3 Oct 2024, In: Brain. 147, 10, p. 3547-3561 15 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile4 Citations (Scopus)14 Downloads (Pure) -
Integration is the foundation for discovery: Macquarie Neurodegenerative Diseases Biobank
Zussa, Z. N., Heads, J. A., Henden, L., Grima, N., D'Silva, S., Poynter, D., Rowe, D. B., Blair, I. P. & Williams, K. L., 2024, (Unpublished). 1 p.Research output: Contribution to conference › Poster
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Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry
Henden, L., Fearnley, L. G., Southwood, D., Smith, A., Rowe, D. B., Kiernan, M. C., Pamphlett, R., Bahlo, M., Blair, I. P. & Williams, K. L., Aug 2024, In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 25, 5-6, p. 644-647 4 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile1 Citation (Scopus)20 Downloads (Pure)