Alberto García‐Redondo

Instituto de Salud Carlos III — Spain

Medicine · Health Sciences

32h-index4.7kcitations93works2.82yr avg
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Research Topics

Amyotrophic Lateral Sclerosis Research(56), Neurogenetic and Muscular Disorders Research(33), Mitochondrial Function and Pathology(13), Neurological diseases and metabolism(10), Metabolism and Genetic Disorders(9)

Publications89 total

Redefining periodic paralysis with CACNA1S mutation in a Spanish cohort
Neurología (English Edition)·2025Open Access
Circular RNA expression in ALS is progressively deregulated and tissue-dependent
BMC Genomics·2025· 5 citedOpen Access
LncRNA levels in the central nervous system as novel potential players and biomarkers in amyotrophic lateral sclerosis
Non-coding RNA Research·2025· 1 citedOpen Access
Redefining periodic paralysis with CACNA1S mutation in a Spanish cohort
Neurología·2024· 1 citedOpen Access
Differentially expressed lncRNAs in SOD1 <sup>G93A</sup> mice skeletal muscle: H19, Myhas and Neat1 as potential biomarkers in amyotrophic lateral sclerosis
Open Biology·2024· 8 citedOpen Access
Author response for "Differentially expressed lncRNAs in SOD1 &lt;sup&gt;G93A&lt;/sup&gt; mice skeletal muscle: H19, Myhas and Neat1 as potential biomarkers in amyotrophic lateral sclerosis"
2024
WITHDRAWN: Circular RNA expression in ALS is progressively deregulated and tissue-dependent
2024Open Access
Author response for "Differentially expressed lncRNAs in SOD1 &lt;sup&gt;G93A&lt;/sup&gt; mice skeletal muscle: H19, Myhas and Neat1 as potential biomarkers in amyotrophic lateral sclerosis"
2024
Intermediate Repeat Expansion in the ATXN2 Gene as a Risk Factor in the ALS and FTD Spanish Population
Biomedicines·2024· 10 citedOpen Access
Intermediate Repeat Expansion in ATXN2 Gene as a Risk Factor in ALS and FTD Spanish Population
Preprints.org·2023· 2 citedOpen Access
Enfermedades autoinmunes y embarazo
2023
WITHDRAWN: Circular RNA expression in ALS is progressively deregulated and tissue-dependent
2023· 1 citedOpen Access
Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies
Neurology Genetics·2023· 2 citedOpen Access
Cumulative Genetic Score and <i>C9orf72</i> Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies
Neurology Genetics·2023· 14 citedOpen Access
The E3 Ubiquitin Ligase SCF Cyclin F Promotes Sequestosome-1/p62 Insolubility and Foci Formation and is Dysregulated in ALS and FTD Pathogenesis
Molecular Neurobiology·2023· 10 citedOpen Access
Functional Characterization of a Familial ALS-Associated Missense TBK1 (p-Arg573Gly) Mutation in Patient-Derived Lymphoblasts
International Journal of Molecular Sciences·2023· 9 citedOpen Access
Characterizing <scp><i>SOD1</i></scp> mutations in Spain: The impact of genotype, age and sex in the natural history of the disease
European Journal of Neurology·2022· 9 citedOpen Access
Cumulative genetic risk and <i>C9orf72</i> repeat status independently associate with ALS status in two case-control studies
2022Open Access
<i>ATXN2</i> intermediate expansions in amyotrophic lateral sclerosis
Brain·2022· 45 citedOpen Access
TDP-43 is a ubiquitylation substrate of the SCFcyclin F complex
Neurobiology of Disease·2022· 21 citedOpen Access
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Frequent Co-authors

Jesús Esteban‐Pérez(19), Joaquı́n Arenas(15), Yolanda Campos(11), José Luís Muñoz-Blanco(10), Rosario Osta(10), Pilar del Hoyo(10), Kevin P. Kenna(9), Orla Hardiman(9), Daniel Borrego‐Hernández(9), Pamela J. Shaw(8), P. Zaragoza(8), Miguel A. Martı́n(8), Nicola Ticozzi(7), Ian P. Blair(7), Ana Cristina Calvo(7), Simon Topp(6), Jack W. Miller(6), Caroline Vance(6), Russell L. McLaughlin(6), Karen Morrison(6)