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F. Garton · SciRah

Researcher profile · Semantic Scholar

F. Garton

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F. Garton — researcher profile on SciRah

h-index: 26
Works: 68
Citations: 2,872

Most-cited papers

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
W. van Rheenen, R. V. D. van der Spek, M. Bakker, L. H. van den Berg +188 more
2021Nature Genetics446 citations Open access
Semantic Scholar
Genes for Elite Power and Sprint Performance: ACTN3 Leads the Way
N. Eynon, Erik D. Hanson, A. Lucia, P. Houweling +3 more
2013Sports Medicine208 citations
Semantic Scholar
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness
Sara M. Willems, Daniel J. Wright, F. Day, K. Trajanoska +72 more
2017Nature Communications186 citations Open access
Semantic Scholar
ACTN3 R577X and ACE I/D gene variants influence performance in elite sprinters: a multi-cohort study
I. Papadimitriou, A. Lucia, Y. Pitsiladis, V. Pushkarev +23 more
2016BMC Genomics169 citations Open access
Semantic Scholar
No Evidence of a Common DNA Variant Profile Specific to World Class Endurance Athletes
T. Rankinen, N. Fuku, B. Wolfarth, Guan Wang +35 more
2016PLoS ONE168 citations Open access
Semantic Scholar
Direct-to-consumer genetic testing for predicting sports performance and talent identification: Consensus statement
N. Webborn, A. Williams, M. McNamee, C. Bouchard +20 more
2015British Journal of Sports Medicine147 citations Open access
Semantic Scholar
ACTN3 genotype influences muscle performance through the regulation of calcineurin signaling.
J. Seto, K. Quinlan, Monkol Lek, X. Zheng +9 more
2013Journal of Clinical Investigation143 citations Open access
Semantic Scholar
Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodeling.
J. Seto, Monkol Lek, K. Quinlan, P. Houweling +9 more
2011Human Molecular Genetics112 citations Open access
Semantic Scholar
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis
B. Benyamin, Ji He, Qiongyi Zhao, J. Gratten +60 more
2017Nature Communications97 citations Open access
Semantic Scholar
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS
P. Hop, R. Zwamborn, E. Hannon, Gemma Shireby +79 more
2022Science Translational Medicine90 citations Open access
Semantic Scholar
Loss of IL-15 receptor α alters the endurance, fatigability, and metabolic characteristics of mouse fast skeletal muscles.
E. Pistilli, S. Bogdanovich, F. Garton, N. Yang +7 more
2011Journal of Clinical Investigation89 citations Open access
Semantic Scholar
Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders
Marta F. Nabais, S. Laws, Tian Lin, C. Vallerga +66 more
2021Genome Biology79 citations Open access
Semantic Scholar
alpha-actinin-3 and performance.
N. Yang, F. Garton, K. North
2009Medicine and Sport Science78 citations
Semantic Scholar
Comprehensive cell type decomposition of circulating cell-free DNA with CelFiE
C. Caggiano, Barbara Celona, F. Garton, J. Mefford +5 more
2021Nature Communications73 citations Open access
Semantic Scholar
No association between ACTN3 R577X and ACE I/D polymorphisms and endurance running times in 698 Caucasian athletes
I. Papadimitriou, S. Lockey, S. Voisin, A. Herbert +21 more
2018BMC Genomics68 citations Open access
Semantic Scholar
Altered skeletal muscle glucose–fatty acid flux in amyotrophic lateral sclerosis
F. Steyn, Rui Li, Siobhan E. Kirk, T. W. Tefera +16 more
2020Brain Communications63 citations Open access
Semantic Scholar
Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics
A. Iacoangeli, Tian Lin, A. Al Khleifat, A. Jones +27 more
2020Cell Reports59 citations Open access
Semantic Scholar
Analysis of the ACTN3 heterozygous genotype suggests that α-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashion.
M. Hogarth, F. Garton, P. Houweling, T. Tukiainen +7 more
2016Human Molecular Genetics53 citations Open access
Semantic Scholar
NF1 is a critical regulator of muscle development and metabolism.
Kate Sullivan, J. El‐Hoss, K. Quinlan, N. Deo +9 more
2014Human Molecular Genetics52 citations Open access
Semantic Scholar
Progression and survival of patients with motor neuron disease relative to their fecal microbiota
S. Ngo, Restuadi Restuadi, Allan F. McCrae, R. V. van Eijk +5 more
2020Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration48 citations
Semantic Scholar
α-Actinin-3 deficiency alters muscle adaptation in response to denervation and immobilization.
F. Garton, J. Seto, K. G. R. Quinlan, N. Yang +2 more
2014Human Molecular Genetics41 citations
Semantic Scholar
Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1
Restuadi Restuadi, F. Steyn, E. Kabashi, S. Ngo +26 more
2022Genome Medicine32 citations Open access
Semantic Scholar
Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis
Marta F. Nabais, Tian Lin, B. Benyamin, K. Williams +33 more
2020npj Genomic Medicine31 citations Open access
Semantic Scholar
The Effect of ACTN3 Gene Doping on Skeletal Muscle Performance.
F. Garton, P. Houweling, Damjan Vukcevic, Lyra R. Meehan +12 more
2018American Journal of Human Genetics30 citations Open access
Semantic Scholar
Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese
J. Gratten, Qiongyi Zhao, B. Benyamin, F. Garton +34 more
2017Genome Medicine28 citations Open access
Semantic Scholar
Validation of an automated computational method for skeletal muscle fibre morphometry analysis.
F. Garton, J. Seto, K. North, N. Yang
2010Neuromuscular Disorders28 citations
Semantic Scholar
Rodent models for resolving extremes of exercise and health.
F. Garton, K. North, L. Koch, S. Britton +2 more
2016Physiological Genomics26 citations Open access
Semantic Scholar
Large-scale drug screening in iPSC-derived motor neurons from sporadic ALS patients identifies a potential combinatorial therapy
C. Bye, Elizabeth Qian, K. Lim, Maciej S Daniszewski +26 more
2025Nature Neuroscience25 citations
Semantic Scholar
Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia
Restuadi Restuadi, F. Garton, B. Benyamin, Tian Lin +22 more
2021European Journal of Human Genetics25 citations Open access
Semantic Scholar
Cardiovascular disease, psychiatric diagnosis and sex differences in the multistep hypothesis of amyotrophic lateral sclerosis
F. Garton, B. Trabjerg, N. Wray, E. Agerbo
2020European Journal of Neurology23 citations Open access
Semantic Scholar
ALS in Danish Registries
B. Trabjerg, F. Garton, W. van Rheenen, F. Fang +4 more
2020Neurology: Genetics22 citations Open access
Semantic Scholar
Human cerebral evolution and the clinical syndrome of amyotrophic lateral sclerosis
R. Henderson, F. Garton, M. Kiernan, M. Turner +1 more
2018Journal of Neurology Neurosurgery & Psychiatry18 citations Open access
Semantic Scholar
Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort
F. Garton, B. Benyamin, Qiongyi Zhao, Zhi-Jun Liu +19 more
2017Molecular Genetics & Genomic Medicine18 citations Open access
Semantic Scholar
Mutations in heat shock protein beta-1 (HSPB1) are associated with a range of clinical phenotypes related to different patterns of motor neuron dysfunction: A case series.
M. Katz, Mark Davis, F. Garton, R. Henderson +3 more
2020Journal of Neurological Sciences15 citations
Semantic Scholar
The Effect of Heterozygosity for the ACTN3 Null Allele on Human Muscle Performance.
F. Garton, K. North
2016Medicine & Science in Sports & Exercise14 citations
Semantic Scholar
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis
Paul J. Hop, M. Kooyman, Brendan J. Kenna, R. Zwamborn +81 more
2026Nature Genetics13 citations Open access
Semantic Scholar
Multi-phase, multi-ethnic GWAS uncovers putative loci in predisposition to elite sprint and power performance, health and disease
Guan Wang, N. Fuku, E. Miyamoto-Mikami, Masashi Tanaka +17 more
2025Biology of Sport12 citations Open access
Semantic Scholar
What do we know about the variability in survival of patients with amyotrophic lateral sclerosis?
P. Mccombe, F. Garton, M. Katz, N. Wray +1 more
2020Expert Review of Neurotherapeutics10 citations
Semantic Scholar
Genome-wide study of DNA methylation in Amyotrophic Lateral Sclerosis identifies differentially methylated loci and implicates metabolic, inflammatory and cholesterol pathways
P. Hop, R. Zwamborn, E. Hannon, Gemma Shireby +79 more
2021medRxiv9 citations Open access
Semantic Scholar
Estimating the rate of cell type degeneration from epigenetic sequencing of cell-free DNA
C. Caggiano, Barbara Celona, F. Garton, J. Mefford +4 more
2020bioRxiv6 citations Open access
Semantic Scholar
Epigenetic profiles of tissue informative CpGs inform ALS disease status and progression
C. Caggiano, M. Morselli, X. Qian, B. Celona +22 more
2025Genome Medicine5 citations Open access
Semantic Scholar
Tissue informative cell-free DNA methylation sites in amyotrophic lateral sclerosis
C. Caggiano, M. Morselli, X. Qian, B. Celona +22 more
2024medRxiv5 citations Open access
Semantic Scholar
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 Rheenen, Rick A. A. Spek, M. Bakker, Joke J. F. A. Vugt +192 more
2022Nature Genetics4 citations Open access
Semantic Scholar
Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis
Olivia A. Grant, A. Iacoangeli, R. Zwamborn, W. van Rheenen +35 more
2024bioRxiv2 citations Open access
Semantic Scholar
Arylamine N-acetyltransferase-1 reveals a subpopulation of ALS patients with altered metabolic capacity
C. Choudhury, Sally Allen, Melinder K. Gill, F. Garton +5 more
2023bioRxiv2 citations Open access
Semantic Scholar
ReFIT study (reversing frailty in transplantation): protocol for a longitudinal study to assess clinical and biomedical changes in frailty through kidney transplantation
Trent Payne, A. Shaw, L. Hanjani, Ryan Homes +14 more
2026BMJ Open1 citations Open access
Semantic Scholar
Strategic Amyotrophic Lateral Sclerosis Australia–Systems Genomics Consortium (SALSA-SGC): cohort profile
Anjali K. Henders, L. Ziser, F. Garton, Lorel Adams +38 more
2026BMJ Open1 citations Open access
Semantic Scholar
A Blood Transcriptomic Resource for ALS Highlights Disease-Associated Signatures and Alternative Splicing Events
Cheong W. Wong, L. Ziser, L. Sparke, Ruolan Zhao +10 more
2025medRxiv1 citations Open access
Semantic Scholar
The roles of human endogenous retrovirus in neurodegenerative diseases: A systematic review.
L. Geleta, Caitlin Doyle, F. Garton, Megan Fowler +6 more
2025Brain, behavior, and immunity1 citations Open access
Semantic Scholar
Genomic and Functional studies identify RPSA as a risk gene for ALS and other neurological diseases
X. Qian, B. Stringer, Cheong W. Wong, Ang Li +11 more
2025medRxiv1 citations Open access
Semantic Scholar

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