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Page 1
STR data for 21 loci in northwestern Africa.
Bosch E, Clarimón J, Pérez-Lezaun A, Calafell F. Bosch E, et al. Among authors: clarimon j. Forensic Sci Int. 2001 Feb 1;116(1):41-51. doi: 10.1016/s0379-0738(00)00344-3. Forensic Sci Int. 2001. PMID: 11118752 No abstract available.
Dementia risk in Parkinson disease: disentangling the role of MAPT haplotypes.
Setó-Salvia N, Clarimón J, Pagonabarraga J, Pascual-Sedano B, Campolongo A, Combarros O, Mateo JI, Regaña D, Martínez-Corral M, Marquié M, Alcolea D, Suárez-Calvet M, Molina-Porcel L, Dols O, Gómez-Isla T, Blesa R, Lleó A, Kulisevsky J. Setó-Salvia N, et al. Among authors: clarimon j. Arch Neurol. 2011 Mar;68(3):359-64. doi: 10.1001/archneurol.2011.17. Arch Neurol. 2011. PMID: 21403021
Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course.
Setó-Salvia N, Pagonabarraga J, Houlden H, Pascual-Sedano B, Dols-Icardo O, Tucci A, Paisán-Ruiz C, Campolongo A, Antón-Aguirre S, Martín I, Muñoz L, Bufill E, Vilageliu L, Grinberg D, Cozar M, Blesa R, Lleó A, Hardy J, Kulisevsky J, Clarimón J. Setó-Salvia N, et al. Among authors: clarimon j. Mov Disord. 2012 Mar;27(3):393-9. doi: 10.1002/mds.24045. Epub 2011 Dec 15. Mov Disord. 2012. PMID: 22173904
Mendelian genes for Parkinson's disease contribute to the sporadic forms of the disease.
Spataro N, Calafell F, Cervera-Carles L, Casals F, Pagonabarraga J, Pascual-Sedano B, Campolongo A, Kulisevsky J, Lleó A, Navarro A, Clarimón J, Bosch E. Spataro N, et al. Among authors: clarimon j. Hum Mol Genet. 2015 Apr 1;24(7):2023-34. doi: 10.1093/hmg/ddu616. Epub 2014 Dec 11. Hum Mol Genet. 2015. PMID: 25504046
MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium.
Pastor P, Moreno F, Clarimón J, Ruiz A, Combarros O, Calero M, López de Munain A, Bullido MJ, de Pancorbo MM, Carro E, Antonell A, Coto E, Ortega-Cubero S, Hernandez I, Tárraga L, Boada M, Lleó A, Dols-Icardo O, Kulisevsky J, Vázquez-Higuera JL, Infante J, Rábano A, Fernández-Blázquez MÁ, Valentí M, Indakoetxea B, Barandiarán M, Gorostidi A, Frank-García A, Sastre I, Lorenzo E, Pastor MA, Elcoroaristizabal X, Lennarz M, Maier W, Rámirez A, Serrano-Ríos M, Lee SE, Sánchez-Juan P; Dementia Genetic Spanish Consortium (DEGESCO). Pastor P, et al. Among authors: clarimon j. J Alzheimers Dis. 2016;49(2):343-52. doi: 10.3233/JAD-150555. J Alzheimers Dis. 2016. PMID: 26444794 Free article.
Copy number variation analysis of the 17q21.31 region and its role in neurodegenerative diseases.
Cervera-Carles L, Pagonabarraga J, Pascual-Sedano B, Pastor P, Campolongo A, Fortea J, Blesa R, Alcolea D, Morenas-Rodríguez E, Sala I, Lleó A, Kulisevsky J, Clarimón J. Cervera-Carles L, et al. Among authors: clarimon j. Am J Med Genet B Neuropsychiatr Genet. 2016 Mar;171B(2):175-80. doi: 10.1002/ajmg.b.32390. Epub 2015 Oct 9. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 26453547
245 results