Publications by authors named "Russell L Mclaughlin"

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Putative mitochondrial components of frontotemporal lobar degeneration: topological correlations between mitochondrial density and atrophy in FTLD/FTD phenotypes.
Marlene Tahedl, Jana Kleinerova, Mary Clare McKenna, We Fong Siah, Orla Hardiman, Russell L McLaughlin

J Neurol· December 2025

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Sex-aware causal inference assessment of the immune system in complex neurodegenerative diseases.
Frida Lona-Durazo, Ross P Byrne, Marc-Olivier Pilon, Michael D Greicius, Marie-Pierre Dubé, Russell L McLaughlin

Brain· December 2025

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Anatomical Associations Between Focal Mitochondrial Metabolism and Patterns of Neurodegeneration in Amyotrophic Lateral Sclerosis.
Marlene Tahedl, We Fong Siah, Efstratios Karavasilis, Jennifer C Hengeveld, Mark A Doherty, Russell L McLaughlin

Ann Neurol· November 2025

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Extreme exercise in males is linked to mTOR signalling and onset of amyotrophic lateral sclerosis.
David O'Brien, Elham Alhathli, Ceryl Harwood, Debarati Bhattacharya, Kriti Gupta, Russell L McLaughlin

Brain· October 2025

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Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implications.
Alfredo Iacoangeli, Allison A Dilliott, Ahmad Al Khleifat, Peter M Andersen, Nazlı A Başak, Russell L McLaughlin

J Neurol Neurosurg Psychiatry· September 2025

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Progressive Thalamo-Cortical Disconnection in Amyotrophic Lateral Sclerosis Genotypes: Structural Degeneration and Network Dysfunction of Thalamus-Relayed Circuits.
Marlene Tahedl, Jana Kleinerova, Mark A Doherty, Jennifer C Hengeveld, Russell L McLaughlin

Eur J Neurol· May 2025

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A genetic perspective on the recent demographic history of Ireland and Britain.
Ashwini Shanmugam, Michael Merrigan, Seamus O'Reilly, Anne M Molloy, Lawrence Brody, Russell L McLaughlin

Eur J Hum Genet· April 2025

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Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis.
Olivia A Grant, Alfredo Iacoangeli, Ramona A J Zwamborn, Wouter van Rheenen, Ross Byrne, Russell L McLaughlin

bioRxiv· November 2024

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The role of genetically predicted serum iron levels on neurodegenerative and cardiovascular traits.
Wiame Belbellaj, Frida Lona-Durazo, Cinzia Bodano, David Busseuil, Marie-Christyne Cyr, Russell L McLaughlin

Sci Rep· October 2024

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Comparison of machine learning methods for genomic prediction of selected Arabidopsis thaliana traits.
Ciaran Michael Kelly, Russell Lewis McLaughlin

PLoS One· August 2024

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Progressive Cerebrocerebellar Uncoupling in Sporadic and Genetic Forms of Amyotrophic Lateral Sclerosis.
Marlene Tahedl, Ee Ling Tan, Jana Kleinerova, Siobhan Delaney, Jennifer C Hengeveld, Russell L Mclaughlin

Neurology· July 2024

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Limbic Network and Papez Circuit Involvement in ALS: Imaging and Clinical Profiles in GGGGCC Hexanucleotide Carriers in and -Negative Patients.
Foteini Christidi, Jana Kleinerova, Ee Ling Tan, Siobhan Delaney, Asya Tacheva, Russell L McLaughlin

Biology (Basel)· July 2024

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Supra- and infra-tentorial degeneration patterns in primary lateral sclerosis: a multimodal longitudinal neuroradiology study.
Jana Kleinerova, Marlene Tahedl, Ee Ling Tan, Siobhan Delaney, Jennifer C Hengeveld, Russell L McLaughlin

J Neurol· June 2024

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Repeat Expansion Discordance in 6 Multigenerational Kindreds.
Marie Ryan, Mark A Doherty, Ahmad Al Khleifat, Emmet Costello, Jennifer C Hengeveld, Russell L Mclaughlin

Neurol Genet· February 2024

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Language deficits in primary lateral sclerosis: cortical atrophy, white matter degeneration and functional disconnection between cerebral regions.
Ee Ling Tan, Marlene Tahedl, Jasmin Lope, Jennifer C Hengeveld, Mark A Doherty, Russell L McLaughlin

J Neurol· January 2024

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The involvement of language-associated networks, tracts, and cortical regions in frontotemporal dementia and amyotrophic lateral sclerosis: Structural and functional alterations.
Marlene Tahedl, Ee Ling Tan, Rangariroyashe H Chipika, Jasmin Lope, Jennifer C Hengeveld, Russell L McLaughlin

Brain Behav· November 2023

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Radiological correlates of pseudobulbar affect: Corticobulbar and cerebellar components in primary lateral sclerosis.
Marlene Tahedl, Ee Ling Tan, We Fong Siah, Jennifer C Hengeveld, Mark A Doherty, Russell L McLaughlin

J Neurol Sci· August 2023

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Brainstem-cortex disconnection in amyotrophic lateral sclerosis: bulbar impairment, genotype associations, asymptomatic changes and biomarker opportunities.
Marlene Tahedl, Ee Ling Tan, Rangariroyashe H Chipika, Jennifer C Hengeveld, Alice Vajda, Russell L McLaughlin

J Neurol· July 2023

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Not a benign motor neuron disease: longitudinal imaging captures relentless motor connectome disintegration in primary lateral sclerosis.
Marlene Tahedl, Ee Ling Tan, Stacey Li Hi Shing, Rangariroyashe H Chipika, We Fong Siah, Russell L McLaughlin

Eur J Neurol· May 2023

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Cognitive and neuropsychiatric endophenotypes in amyotrophic lateral sclerosis.
Emmet Costello, Marie Ryan, Bronagh Donohoe, Caoimhe Kavanagh, Marta Pinto-Grau, Russell Lewis McLaughlin

Brain Commun· May 2023

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Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis.
Gijs H P Tazelaar, Paul J Hop, Meinie Seelen, Joke J F A van Vugt, Wouter van Rheenen, Russell L McLaughlin

Neurobiol Aging· February 2023

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Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.
Ahmad Al Khleifat, Alfredo Iacoangeli, Ashley R Jones, Joke J F A van Vugt, Matthieu Moisse, Russell L McLaughlin

Front Cell Neurosci· December 2022

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Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
Wouter van Rheenen, Rick A A van der Spek, Mark K Bakker, Joke J F A van Vugt, Paul J Hop, Russell L McLaughlin

Nat Genet· March 2022

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Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS.
Paul J Hop, Ramona A J Zwamborn, Eilis Hannon, Gemma L Shireby, Marta F Nabais, Russell L McLaughlin

Sci Transl Med· February 2022

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Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.
Ahmad Al Khleifat, Alfredo Iacoangeli, Joke J F A van Vugt, Harry Bowles, Matthieu Moisse, Russell L McLaughlin

NPJ Genom Med· January 2022

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