Miguel A Martin

Cited by

	All	Since 2019
Citations	9725	3865
h-index	50	30
i10-index	159	106

860

430

215

645

1999200020012002200320042005200620072008200920102011201220132014201520162017201820192020202120222023202436 50 54 56 79 81 103 170 221 251 365 324 359 441 467 519 491 519 577 561 563 705 846 798 720 227

Public access

View all

88 articles

16 articles

available

not available

Based on funding mandates

Co-authors

Campos YResearch Scientist, Mitochondrial Pathology Unit, Instituto de Salud Carlos IIIVerified email at isciii.es
Gisela Nogales-GadeaInstitut d'Investigació en Ciències de la Salut Germans Trias i PujolVerified email at igtp.cat
Margarita Perez RuizUniversidad Politécnica de MadridVerified email at upm.es
Aitor Delmiro MagdalenaHospital Universitario 12 de Octubre - Instituto de Investigación i+12Verified email at h12o.es
Cristina Domínguez-González 0000-0...Adjunto de Neurología. Hospital 12 de Octubre.Verified email at salud.madrid.org
Felix Gomez-GallegoDepartamento de Ciencias Básicas de la Salud. Universidad Rey Juan CarlosVerified email at urjc.es
Francisco J BlancoINIBIC-Hospital Universitario A Coruña. Universidad de A CoruñaVerified email at sergas.es
Pablo Serrano-LorenzoInvestigador CIBERER. Fundación Investigación i+12. Hospital 12 de OctubreVerified email at h12o.es
M. Esther Gallardo PerezHead of Traslational Research with iPS Cells Group, Research Institute Hospital 12 de Octubre, i+12Verified email at h12o.es
Jaume Coll CantíUnivesitat Autònoma de Barcelona. Hospital Germans TriasVerified email at gencat.cat
Prof. dr. Jan A.M. SmeitinkProfessor in Mitochondrial MedicineVerified email at radboudumc.nl
María C de AndrésMiguel Servet ResearcherVerified email at sergas.es
Alejandro Santos-Lozanoi+HeALTH, Department of Health Sciences, Miguel de Cervantes European University, Valladolid (Spain)Verified email at uemc.es
Massimo Zeviani, MD, PhDUniversity of PadovaVerified email at unipd.it
john vissingProfessorVerified email at rh.dk
GUILLEM PINTOS-MORELLVall d'Hebron University Hospital & Research Institute, BarcelonaVerified email at vhir.org
Alfonsina Ballester-LopezFundació Institut Germans Trias i PujolVerified email at igtp.cat
Israel Fernandez CadenasPrincipal Investigator at the stroke pharmacogenomics and genetics group, Sant Pau Hospital Research Instiute.Verified email at santpau.cat
Antoni BarrientosUniversity of miamiVerified email at med.miami.edu
Marta González-FreireNational Institute on Aging, BaltimoreVerified email at nih.gov

Miguel A Martin

Hospital Universitario 12 de Octubre. Instituto de Investigación i+12

Verified email at h12o.es

mitochondrial disease McArdle exercise intolerance NGS genomics


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
Defective hepatic mitochondrial respiratory chain in patients with nonalcoholic steatohepatitis M Pérez‐Carreras, P Del Hoyo, MA Martín, JC Rubio, A Martín, ... Hepatology 38 (4), 999-1007, 2003	869	2003
OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes P Amati-Bonneau, ML Valentino, P Reynier, ME Gallardo, B Bornstein, ... Brain 131 (2), 338-351, 2008	562	2008
Mitochondrial complex I plays an essential role in human respirasome assembly D Moreno-Lastres, F Fontanesi, I García-Consuegra, MA Martín, J Arenas, ... Cell metabolism 15 (3), 324-335, 2012	307	2012
Mitochondrial respiration controls lysosomal function during inflammatory T cell responses F Baixauli, R Acín-Pérez, C Villarroya-Beltrí, C Mazzeo, N Nuñez-Andrade, ... Cell metabolism 22 (3), 485-498, 2015	295	2015
Mitochondrial respiratory activity is altered in osteoarthritic human articular chondrocytes E Maneiro, MA Martín, MC de Andres, MJ López‐Armada, ... Arthritis & Rheumatism 48 (3), 700-708, 2003	254	2003
Complex I defect in muscle from patients with Huntington's disease J Arenas, Y Campos, R Ribacoba, MA Martín, JC Rubio, P Ablanedo, ... Annals of neurology 43 (3), 397-400, 1998	220	1998
McArdle disease: what do neurologists need to know? A Lucia, G Nogales-Gadea, M Perez, MA Martin, AL Andreu, J Arenas Nature Clinical Practice Neurology 4 (10), 568-577, 2008	201	2008
Mitochondrial respiratory chain dysfunction: implications in neurodegeneration M Morán, D Moreno-Lastres, L Marín-Buera, J Arenas, MA Martín, ... Free Radical Biology and Medicine 53 (3), 595-609, 2012	181	2012
Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease R Pello, MA Martín, V Carelli, LG Nijtmans, A Achilli, M Pala, A Torroni, ... Human molecular genetics 17 (24), 4001-4011, 2008	178	2008
Mitochondrial activity is modulated by TNFα and IL-1β in normal human chondrocyte cells MJ López-Armada, B Carames, MA Martin, B Cillero-Pastor, M Lires-Dean, ... Osteoarthritis and cartilage 14 (10), 1011-1022, 2006	178	2006
Effect of nitric oxide on mitochondrial respiratory activity of human articular chondrocytes E Maneiro, MJ Lopez-Armada, MC De Andres, B Carames, MA Martin, ... Annals of the rheumatic diseases 64 (3), 388-395, 2005	164	2005
Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry A Lucia, JR Ruiz, A Santalla, G Nogales-Gadea, JC Rubio, ... Journal of Neurology, Neurosurgery & Psychiatry 83 (3), 322-328, 2012	162	2012
X‐linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy D Fernandez‐Moreira, C Ugalde, R Smeets, RJT Rodenburg, ... Annals of neurology 61 (1), 73-83, 2007	156	2007
Frequency of the C34T mutation of the AMPD1 gene in world-class endurance athletes: does this mutation impair performance? JC Rubio, MA Martin, M Rabadán, F Gómez-Gallego, AF San Juan, ... Journal of applied physiology 98 (6), 2108-2112, 2005	148	2005
Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases S Koene, RJ Rodenburg, MS Van der Knaap, M Willemsen, W Sperl, ... Journal of inherited metabolic disease 35, 737-747, 2012	145	2012
Renal pathology in children with mitochondrial diseases E Martín-Hernández, MT García-Silva, J Vara, Y Campos, A Cabello, ... Pediatric nephrology 20, 1299-1305, 2005	120	2005
Favorable responses to acute and chronic exercise in McArdle patients JL Maté-Munoz, M Moran, M Pérez, C Chamorro-Vina, F Gómez-Gallego, ... Clinical Journal of Sport Medicine 17 (4), 297-303, 2007	116	2007
Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): a genotype‐phenotype correlation study MA Martín, JC Rubio, J Buchbinder, R Fernández‐Hojas, P Del Hoyo, ... Annals of Neurology: Official Journal of the American Neurological …, 2001	114	2001
COX7A2L is a mitochondrial complex III binding protein that stabilizes the III2+ IV supercomplex without affecting respirasome formation R Pérez-Pérez, T Lobo-Jarne, D Milenkovic, A Mourier, A Bratic, ... Cell reports 16 (9), 2387-2398, 2016	112	2016
World-class performance in lightweight rowing: is it genetically influenced? A comparison with cyclists, runners and non-athletes CA Muniesa, M González-Freire, C Santiago, JI Lao, A Buxens, JC Rubio, ... British journal of sports medicine 44 (12), 898-901, 2010	110	2010

The system can't perform the operation now. Try again later.

Articles 1–20

Citations per year

Duplicate citations

Merged citations

Add co-authorsCo-authors

Follow

Cited by

Co-authors