Onofre Combarros

Medicine · Health Sciences

52h-index19.5kcitations222works0.02yr avg
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Research Topics

Alzheimer's disease research and treatments(67), Genetic Neurodegenerative Diseases(39), Hereditary Neurological Disorders(34), Mitochondrial Function and Pathology(20), Neurological diseases and metabolism(20)

Publications212 total

MAPT H1 Haplotype is Associated with Late-Onset Alzheimer’s Disease Risk in APOE ɛ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium
Journal of Alzheimer s Disease·2015· 38 citedOpen Access
Assessing the role of TUBA4A gene in frontotemporal degeneration
Neurobiology of Aging·2015· 11 citedOpen Access
Comparative blood transcriptome analysis in idiopathic and LRRK2 G2019S–associated Parkinson's disease
Neurobiology of Aging·2015· 41 cited
Analysis of the<i>CHCHD10</i>gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain
Brain·2015· 59 citedOpen Access
A Genome Wide Association Study Links Glutamate Receptor Pathway to Sporadic Creutzfeldt-Jakob Disease Risk
PLoS ONE·2015· 33 citedOpen Access
Identification of candidate genes for Parkinson's disease through blood transcriptome analysis in LRRK2-G2019S carriers, idiopathic cases, and controls
Neurobiology of Aging·2014· 41 cited
Serum uric acid and risk of dementia in Parkinson's disease
Parkinsonism & Related Disorders·2014· 29 cited
Genetic Risk Factors for Alzheimer’s Disease
Neurodegenerative Diseases·2014· 1 cited
Rare Variants in Calcium Homeostasis Modulator 1 (CALHM1) Found in Early Onset Alzheimer’s Disease Patients Alter Calcium Homeostasis
PLoS ONE·2013· 31 citedOpen Access
Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia
Neurobiology of Aging·2013· 119 cited
Hereditary neuropathy with liability to pressure palsy: fulminant radicular dysfunction during anterolateral lumbar interbody fusion
Journal of Neurology·2013· 3 cited
The sex-specific associations of the aromatase gene with Alzheimer’s disease and its interaction with IL10 in the Epistasis Project
European Journal of Human Genetics·2013· 40 citedOpen Access
Genetic variability related to serum uric acid concentration and risk of Parkinson's disease
Movement Disorders·2013· 46 cited
Screening for progranulin mutations by serum protein dosage in common neurodegenerative disorders
Parkinsonism & Related Disorders·2013· 4 cited
Neurodegenerative Disease Phenotypes in Carriers of MAPT p.A152T, A Risk Factor for Frontotemporal Dementia Spectrum Disorders and Alzheimer Disease
Alzheimer Disease & Associated Disorders·2013· 43 citedOpen Access
Reduced serum progranulin level might be associated with Parkinson's disease risk
European Journal of Neurology·2013· 30 cited
Olfaction and imaging biomarkers in premotor <i>LRRK2</i> G2019S-associated Parkinson disease
Neurology·2013· 80 cited
Genetic risk score predicting accelerated progression from mild cognitive impairment to Alzheimer’s disease
Journal of Neural Transmission·2012· 73 cited
Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease
Neurobiology of Aging·2012· 30 citedOpen Access
Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease
Molecular Psychiatry·2012· 10 citedOpen Access
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Frequent Co-authors

José Berciano(19), Ignacio Mateo(16), Jon Infante(16), Victoria Álvarez(11), Javier Llorca(10), Eliécer Coto(9), Eloy Rodríguez‐Rodríguez(9), J. M. Polo(8), Jesús Calleja(8), José Berciano(8), Pascual Sánchez‐Juan(8), María J. Bullido(7), Jean‐Charles Lambert(6), Benedetta Nacmias(6), Philippe Amouyel(6), Paolo Bosco(5), Michelangelo Mancuso(5), Francesco Panza(5), Paola Bossù(5), Davide Seripa(5)