Lyndal Henden

716 total citations
17 papers, 204 citations indexed

About

Lyndal Henden is a scholar working on Neurology, Genetics and Neurology. According to data from OpenAlex, Lyndal Henden has authored 17 papers receiving a total of 204 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 8 papers in Genetics and 8 papers in Neurology. Recurrent topics in Lyndal Henden's work include Amyotrophic Lateral Sclerosis Research (11 papers), Neurological diseases and metabolism (8 papers) and Neurogenetic and Muscular Disorders Research (8 papers). Lyndal Henden is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (11 papers), Neurological diseases and metabolism (8 papers) and Neurogenetic and Muscular Disorders Research (8 papers). Lyndal Henden collaborates with scholars based in Australia, New Zealand and United States. Lyndal Henden's co-authors include Melanie Bahlo, Ivo Müeller, Alyssa E. Barry, Stuart Lee, Kelly L. Williams, Ian P. Blair, Emily P. McCann, Natalie Grima, Dominic B. Rowe and Matthew C. Kiernan and has published in prestigious journals such as Bioinformatics, PLoS ONE and Brain.

In The Last Decade

Lyndal Henden

12 papers receiving 202 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Lyndal Henden 92 63 61 55 38 17 204
Modibo Sangaré 36 0.4× 8 0.1× 40 0.7× 58 1.1× 19 0.5× 24 211
Romal Stewart 56 0.6× 24 0.4× 104 1.7× 52 0.9× 102 2.7× 21 345
Marcos Madruga‐Garrido 24 0.3× 21 0.3× 100 1.6× 8 0.1× 23 0.6× 15 201
Mengxiao Ma 60 0.7× 8 0.1× 145 2.4× 4 0.1× 27 0.7× 8 274
Virginie Roth 12 0.1× 35 0.6× 94 1.5× 10 0.2× 3 0.1× 9 180
Katrina M. Kutchko 17 0.2× 4 0.1× 195 3.2× 40 0.7× 19 0.5× 11 349
Víctor López Del Amo 9 0.1× 5 0.1× 215 3.5× 38 0.7× 13 0.3× 14 270
Sofia Esteves 38 0.4× 8 0.1× 194 3.2× 12 0.2× 4 0.1× 12 279
Katherine W. Snapinn 131 1.4× 2 0.0× 57 0.9× 88 1.6× 91 2.4× 8 305
Vasiliki Karalis 10 0.1× 6 0.1× 128 2.1× 27 0.5× 8 0.2× 7 285

Countries citing papers authored by Lyndal Henden

Since Specialization
Citations

This map shows the geographic impact of Lyndal Henden's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Lyndal Henden with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lyndal Henden more than expected).

Fields of papers citing papers by Lyndal Henden

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lyndal Henden. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Lyndal Henden. The network helps show where Lyndal Henden may publish in the future.

Co-authorship network of co-authors of Lyndal Henden

This figure shows the co-authorship network connecting the top 25 collaborators of Lyndal Henden. A scholar is included among the top collaborators of Lyndal Henden based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lyndal Henden. Lyndal Henden is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Rodrigues, Miriam, Chitra Vinnakota, Christina M. Buchanan, et al.. (2025). The genetics of motor neuron disease in New Zealand. Journal of the Neurological Sciences. 474. 123472–123472.
2.
Grima, Natalie, Claire E. Shepherd, Lyndal Henden, et al.. (2025). Multi-region brain transcriptomic analysis of amyotrophic lateral sclerosis reveals widespread RNA alterations and substantial cerebellum involvement. Molecular Neurodegeneration. 20(1). 40–40.
3.
Henden, Lyndal, Liam G. Fearnley, Dominic B. Rowe, et al.. (2024). Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 25(5-6). 644–647.
4.
Dieriks, Birger Victor, Helen C. Murray, Molly E. V. Swanson, et al.. (2024). Hippocampal aggregation signatures of pathogenic UBQLN2 in amyotrophic lateral sclerosis and frontotemporal dementia. Brain. 147(10). 3547–3561. 5 indexed citations
5.
McCann, Emily P., Natalie Grima, Jennifer A. Fifita, et al.. (2023). Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic Variants. Journal of Neuromuscular Diseases. 10(6). 1127–1141. 4 indexed citations
6.
Grima, Natalie, Sidong Liu, Lyndal Henden, et al.. (2023). RNA sequencing of peripheral blood in amyotrophic lateral sclerosis reveals distinct molecular subtypes: Considerations for biomarker discovery. Neuropathology and Applied Neurobiology. 49(6). e12943–e12943. 11 indexed citations
7.
Henden, Lyndal, et al.. (2022). Identity-by-descent analysis of CMTX3 links three families through a common founder. Journal of Human Genetics. 68(1). 47–49. 3 indexed citations
8.
Grima, Natalie, Lyndal Henden, Liam G. Fearnley, et al.. (2022). NEK1 and STMN2 short tandem repeat lengths are not associated with Australian amyotrophic lateral sclerosis risk. Neurobiology of Aging. 116. 92–95.
9.
Jacobs, Kelly R., et al.. (2021). Effects of stress associated with academic examination on the kynurenine pathway profile in healthy students. PLoS ONE. 16(6). e0252668–e0252668. 13 indexed citations
10.
McCann, Emily P., Kelly L. Williams, Lyndal Henden, et al.. (2021). Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 101. 297.e9–297.e11. 6 indexed citations
11.
Grima, Natalie, et al.. (2021). Simultaneous Isolation of High-Quality RNA and DNA From Postmortem Human Central Nervous System Tissues for Omics Studies. Journal of Neuropathology & Experimental Neurology. 81(2). 135–145. 6 indexed citations
12.
Henden, Lyndal, Natalie A. Twine, Emily P. McCann, et al.. (2020). Identity by descent analysis identifies founder events and links SOD1 familial and sporadic ALS cases. npj Genomic Medicine. 5(1). 32–32. 14 indexed citations
13.
McCann, Emily P., Lyndal Henden, Jennifer A. Fifita, et al.. (2020). Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis. Journal of Medical Genetics. 58(2). 87–95. 57 indexed citations
14.
Henden, Lyndal, Stuart Lee, Ivo Müeller, Alyssa E. Barry, & Melanie Bahlo. (2018). Identity-by-descent analyses for measuring population dynamics and selection in recombining pathogens. PLoS Genetics. 14(5). e1007279–e1007279. 61 indexed citations
15.
Henden, Lyndal, David Wakeham, & Melanie Bahlo. (2016). XIBD: software for inferring pairwise identity by descent on the X chromosome. Bioinformatics. 32(15). 2389–2391. 11 indexed citations
16.
Shaw, Marie, Lyndal Henden, Melanie Bahlo, et al.. (2015). Identical by descent L1CAM mutation in two apparently unrelated families with intellectual disability without L1 syndrome. European Journal of Medical Genetics. 58(6-7). 364–368. 13 indexed citations
17.
Henden, Lyndal. (2011). The Edge Slide Graph of the 3-cube. Rose-Hulman Scholar (Rose–Hulman Institute of Technology). 12(2). 6.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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2026