Lyndal Henden

13PUBLICATIONS
54CO-AUTHORS
Neurology and neuromuscular diseasesCancer diagnosisGenetics not elsewhere classifiedDevelopmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)
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Publications (13)

|Apr 24, 2025
Multi-region brain transcriptomic analysis of amyotrophic lateral sclerosis reveals widespread RNA alterations and substantial cerebellum involvement.

Natalie Grima, Andrew N Smith, Claire E Shepherd

|Jul 02, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp

|May 10, 2024
Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry.

Lyndal Henden, Liam G Fearnley, Dean Southwood

|May 04, 2024
Hippocampal aggregation signatures of pathogenic UBQLN2 in amyotrophic lateral sclerosis and frontotemporal dementia.

Kyrah M Thumbadoo, Birger V Dieriks, Helen C Murray

|Oct 11, 2023
RNA sequencing of peripheral blood in amyotrophic lateral sclerosis reveals distinct molecular subtypes: Considerations for biomarker discovery.

Natalie Grima, Sidong Liu, Dean Southwood

|May 05, 2023
Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia.

Lyndal Henden, Liam G Fearnley, Natalie Grima

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Frequent Collaborators

10 joint publications

Kelly Louise Williams

7 joint publications

Ian P Blair

6 joint publications

Dominic B Rowe

6 joint publications

Natalie Grima