Alberto García‐Redondo

Author

Centre for Biomedical Network Research on Rare Diseases ORCID

Also Known As

A García, A Garcı́a, A Redondo, A. Garcia-Redondo, A. García, A. García, A. García-Redondo, A. García‐Redondo, Adriana L. Vanegas García, Alberto G. Redondo

Publications

4.6K

Citations

H-Index

Concepts

All Affiliations

Centre for Biomedical Network Research on Rare Diseases Research Institute Hospital 12 de Octubre Centro de Investigación Biomédica en Red Hospital Universitario 12 De Octubre University of Massachusetts Chan Medical School

About

Alberto García‐Redondo is an author at Centre for Biomedical Network Research on Rare Diseases specializing in medicine, neurology, and neurodegenerative diseases.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	14	1K
2	Biochemistry	2	2	143
3	Natural Sciences	1	1	54
4	Public Health	1	1	95
5	Social Sciences	1	1	44

Alberto García‐Redondo

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis Kevin P. Kenna, Perry T.C. van Doormaal, Annelot M. Dekker, Nature Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderNeurologyNeuroscience	2016	278
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis Bradley Smith, Simon Topp, Claudia Fallini, Science Translational Medicine	2017	243
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia Kelly L. Williams, Simon Topp, Shu Yang, Nature Communications	2016	205
MicroRNA-206: A Potential Circulating Biomarker Candidate for Amyotrophic Lateral Sclerosis Janne M. Toivonen, Raquel Manzano, Sara Oliván, PLoS ONE	2014	184
Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia Oriol Dols‐Icardo, Alberto García‐Redondo, Ricard Rojas‐García, Human Molecular Genetics	2013	108
Analysis of the<i>C</i><i>9orf72</i>Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide Alberto García‐Redondo, Oriol Dols‐Icardo, Ricard Rojas‐García, Human Mutation Sporadic AlsGeneticsGenetic EpidemiologyDisease Gene IdentificationDifferent Populations Worldwide	2012	95
Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy Sabrina Sacconi, Eva Trevisson, Leonardo Salviati, Neuromuscular Disorders Mitochondrial MyopathyMuscle FunctionBiochemistryMitochondrial FunctionCoenzyme Q10	2009	89
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function Martina de Majo, Simon Topp, Bradley Smith, Neurobiology of Aging Protein FunctionSignal TransductionAmyotrophic Lateral SclerosisGenetic DisorderReceptor Tyrosine Kinase	2018	81
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis Ramita Dewan, Ruth Chia, Jinhui Ding, Neuron Amyotrophic Lateral SclerosisAlzheimer's DiseasePathologyDegenerative DiseaseFrontotemporal Dementia	2020	79
Association of Variants in the <i>SPTLC1</i> Gene With Juvenile Amyotrophic Lateral Sclerosis Janel O. Johnson, Ruth Chia, Danny E. Miller, JAMA Neurology	2021	78

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