All Stories

  1. Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes

    Article • Neurobiology of Aging, November 2014, Elsevier

    Jordi Clarimon

  2. Frontotemporal dementia and its subtypes: a genome-wide association study

    Article • The Lancet Neurology, July 2014, Elsevier

    Dr Christopher M Morris, Jordi Clarimon

  3. Cerebrospinal fluid β-amyloid and phospho-tau biomarker interactions affecting brain structure in preclinical Alzheimer disease

    Article • Annals of Neurology, June 2014, Wiley

    Jordi Clarimon

  4. Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease

    Article • PLoS ONE, June 2014, PLOS

    Jordi Clarimon, Francesco Panza

  5. Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

    Article • Acta Neuropathologica, June 2014, Springer Science + Business Media

    Jordi Clarimon

  6. Methylglyoxal Produced by Amyloid-β Peptide-Induced Nitrotyrosination of Triosephosphate Isomerase Triggers Neuronal Death in Alzheimer's Disease

    Article • Journal of Alzheimer s Disease, June 2014, IOS Press

    Jordi Clarimon

  7. Parkinson's Disease: From Genetics to Clinical Practice

    Article • Current Genomics, February 2014, Bentham Science Publishers

    Jordi Clarimon

  8. Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia

    Article • Neurobiology of Aging, February 2014, Elsevier

    Jordi Clarimon

  9. Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation

    Article • Journal of Neurology Neurosurgery & Psychiatry, December 2013, BMJ

    Jordi Clarimon

  10. Confluence of α-Synuclein, Tau, and β-Amyloid Pathologies in Dementia With Lewy Bodies

    Article • Journal of Neuropathology & Experimental Neurology, December 2013, Oxford University Press (OUP)

    Jordi Clarimon

  11. Reelin Signaling Pathway Genotypes and Alzheimer Disease in a Spanish Population

    Article • Alzheimer Disease & Associated Disorders, December 2013, Wolters Kluwer Health

    Jordi Clarimon

  12. Autosomal-dominant Alzheimer's disease mutations at the same codon of amyloid precursor protein differentially alter Aβ production

    Article • Journal of Neurochemistry, October 2013, Wiley

    Jordi Clarimon

  13. Fused in Sarcoma (FUS) gene mutations are not a frequent cause of essential tremor in Europeans

    Article • Neurobiology of Aging, October 2013, Elsevier

    Jordi Clarimon

  14. Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia

    Article • Human Molecular Genetics, September 2013, Oxford University Press (OUP)

    Jordi Clarimon

  15. Rare Variants in Calcium Homeostasis Modulator 1 (CALHM1) Found in Early Onset Alzheimer’s Disease Patients Alter Calcium Homeostasis

    Article • PLoS ONE, September 2013, PLOS

    Jordi Clarimon

  16. Comparison of 2 Diagnostic Criteria for the Behavioral Variant of Frontotemporal Dementia

    Article • American Journal of Alzheimer s Disease & Other Dementias®, May 2013, SAGE Publications

    Jordi Clarimon

  17. MAPT H1 haplotype is associated with enhanced α-synuclein deposition in dementia with Lewy bodies

    Article • Neurobiology of Aging, March 2013, Elsevier

    Jordi Clarimon

  18. Distinct patterns of APP processing in the CNS in autosomal-dominant and sporadic Alzheimer disease

    Article • Acta Neuropathologica, December 2012, Springer Science + Business Media

    Jordi Clarimon

  19. Using the Neandertal and Denisova Genetic Data to Understand the Common MAPT 17q21 Inversion in Modern Humans

    Article • Human Biology, December 2012, Human Biology (The International Journal of Population Biology and Genetics)

    Jordi Clarimon

  20. Investigation of C9orf72 in 4 Neurodegenerative Disorders

    Article • Archives of Neurology, December 2012, American Medical Association (AMA)

    Jordi Clarimon

  21. Genetic risk score predicting accelerated progression from mild cognitive impairment to Alzheimer’s disease

    Article • Journal of Neural Transmission, November 2012, Springer Science + Business Media

    Jordi Clarimon

  22. Analysis of theC9orf72Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide

    Article • Human Mutation, October 2012, Wiley

    Jordi Clarimon

  23. Genetic variability of the gene cluster CALHM1–3 in sporadic Creutzfeldt-Jakob disease

    Article • Prion, September 2012, Taylor & Francis

    Jordi Clarimon

  24. Phenotypic Variability Within the Inclusion Body Spectrum of Basophilic Inclusion Body Disease and Neuronal Intermediate Filament Inclusion Disease in Frontotemporal Lobar Degenerations With FUS-Positive Inclusions

    Article • Journal of Neuropathology & Experimental Neurology, September 2012, Oxford University Press (OUP)

    Jordi Clarimon

  25. A Common BACE1 Polymorphism Is a Risk Factor for Sporadic Creutzfeldt-Jakob Disease

    Article • PLoS ONE, August 2012, PLOS

    Jordi Clarimon

  26. Expansion mutation in C9ORF72 does not influence plasma progranulin levels in frontotemporal dementia

    Article • Neurobiology of Aging, August 2012, Elsevier

    Jordi Clarimon

  27. Lack of Association Between CX3CR1 V249I and T280M Polymorphisms and Risk of Parkinson's Disease in a Greek Population

    Article • Genetic Testing and Molecular Biomarkers, August 2012, Mary Ann Liebert Inc

    Jordi Clarimon

  28. Lack of Association of thePICALMrs3851179 Polymorphism With Parkinson's Disease in the Greek Population

    Article • International Journal of Neuroscience, January 2012, Taylor & Francis

    Jordi Clarimon

  29. Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course

    Article • Movement Disorders, December 2011, Wiley

    Jordi Clarimon, Daniel Grinberg

  30. Unique post-exercise electrophysiological test results in a new Andersen–Tawil syndrome mutation

    Article • Clinical Neurophysiology, December 2011, Elsevier

    Jordi Clarimon

  31. Genetic variation in APOE cluster region and Alzheimer's disease risk

    Article • Neurobiology of Aging, November 2011, Elsevier

    Jordi Clarimon

  32. Tau Enhances α-Synuclein Aggregation and Toxicity in Cellular Models of Synucleinopathy

    Article • PLoS ONE, October 2011, PLOS

    Professor Tiago F Outeiro, Jordi Clarimon

  33. Genetic Cross-Interaction between APOE and PRNP in Sporadic Alzheimer's and Creutzfeldt-Jakob Diseases

    Article • PLoS ONE, July 2011, PLOS

    Jordi Clarimon

  34. Activation of PKR Causes Amyloid ß-Peptide Accumulation via De-Repression of BACE1 Expression

    Article • PLoS ONE, June 2011, PLOS

    Jordi Clarimon

  35. PICOGEN: experiencia de 5 años de un programa de asesoramiento genético en demencia

    Article • Neurología, April 2011, Elsevier

    Jordi Clarimon

  36. Dementia Risk in Parkinson Disease

    Article • Archives of Neurology, March 2011, American Medical Association (AMA)

    Jordi Clarimon

  37. GSK3β polymorphisms, MAPT H1 haplotype and Parkinson's disease in a Greek cohort

    Article • Neurobiology of Aging, March 2011, Elsevier

    Jordi Clarimon

  38. IGF-I gene variability is associated with an increased risk for AD

    Article • Neurobiology of Aging, March 2011, Elsevier

    Jordi Clarimon

  39. The Effect of MAPT H1 and APOE ε4 on Transition from Mild Cognitive Impairment to Dementia

    Article • Journal of Alzheimer s Disease, January 2011, IOS Press

    Jordi Clarimon

  40. Triflusal reduces dense-core plaque load, associated axonal alterations and inflammatory changes, and rescues cognition in a transgenic mouse model of Alzheimer's disease

    Article • Neurobiology of Disease, June 2010, Elsevier

    Jordi Clarimon

  41. Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP

    Article • Neurobiology of Aging, May 2010, Elsevier

    Jordi Clarimon, Dr. Rita Guerreiro

  42. A novel PSEN1 mutation (K239N) associated with Alzheimer’s disease with wide range age of onset and slow progression

    Article • European Journal of Neurology, February 2010, Wiley

    Jordi Clarimon

  43. A megalin polymorphism associated with promoter activity and Alzheimer's disease risk

    Article • American Journal of Medical Genetics Part B Neuropsychiatric Genetics, January 2010, Wiley

    Jordi Clarimon

  44. Clinical, Neuropathologic, and Biochemical Profile of the Amyloid Precursor Protein I716F Mutation

    Article • Journal of Neuropathology & Experimental Neurology, January 2010, Oxford University Press (OUP)

    Jordi Clarimon

  45. Whole genome analysis in a consanguineous family with early onset Alzheimer's disease

    Article • Neurobiology of Aging, December 2009, Elsevier

    Jordi Clarimon

  46. A novel GSK-3β inhibitor reduces Alzheimer's pathology and rescues neuronal loss in vivo

    Article • Neurobiology of Disease, September 2009, Elsevier

    Jordi Clarimon

  47. Mild cholesterol depletion reduces amyloid-β production by impairing APP trafficking to the cell surface

    Article • Journal of Neurochemistry, July 2009, Wiley

    Jordi Clarimon

  48. Early-Onset Familial Lewy Body Dementia With Extensive Tauopathy: A Clinical, Genetic, and Neuropathological Study

    Article • Journal of Neuropathology & Experimental Neurology, January 2009, Oxford University Press (OUP)

    Jordi Clarimon

  49. A Randomized, Double-blind, Placebo Controlled-trial of Triflusal in Mild Cognitive Impairment

    Article • Alzheimer Disease & Associated Disorders, January 2008, Wolters Kluwer Health

    Jordi Clarimon

  50. Homocysteine and Cognitive Impairment

    Article • Dementia and Geriatric Cognitive Disorders, January 2008, Karger Publishers

    Jordi Clarimon

  51. Tremor dominant parkinsonism: Clinical description andLRRK2 mutation screening

    Article • Movement Disorders, January 2008, Wiley

    Jordi Clarimon

  52. Association of phosphodiesterase 4D gene G0 haplotype and ischaemic stroke in a Greek population

    Article • European Journal of Neurology, July 2007, Wiley

    Jordi Clarimon

  53. Linkage Disequilibrium and Association Analysis of ?-Synuclein and Alcohol and Drug Dependence in Two American Indian Populations

    Article • Alcoholism Clinical and Experimental Research, February 2007, Wiley

    Jordi Clarimon

  54. Assessing the role ofDRD5 andDYT1 in two different case–control series with primary blepharospasm

    Article • Movement Disorders, January 2007, Wiley

    Jordi Clarimon

  55. Assessment of PINK1 (PARK6) polymorphisms in Finnish PD

    Article • Neurobiology of Aging, June 2006, Elsevier

    Jordi Clarimon

  56. Conflicting Results Regarding the Semaphorin Gene (SEMA5A) and the Risk for Parkinson Disease

    Article • The American Journal of Human Genetics, June 2006, Elsevier

    Jordi Clarimon

  57. Lack of association with TorsinA haplotype in German patients with sporadic dystonia

    Article • Neurology, March 2006, Wolters Kluwer Health

    Jordi Clarimon

  58. Association of theTauhaplotype with Parkinson's disease in the Greek population

    Article • Movement Disorders, March 2006, Wiley

    Jordi Clarimon

  59. Dystonia and the Nuclear Envelope

    Article • Neuron, December 2005, Elsevier

    Jordi Clarimon

  60. Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease

    Article • Neuroscience Letters, July 2005, Elsevier

    Jordi Clarimon

  61. Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients

    Article • BMC Neurology, June 2005, Springer Science + Business Media

    Jordi Clarimon

  62. Tyrosinase exacerbates dopamine toxicity but is not genetically associated with Parkinson's disease

    Article • Journal of Neurochemistry, April 2005, Wiley

    Jordi Clarimon

  63. Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease

    Article • American Journal of Medical Genetics Part B Neuropsychiatric Genetics, January 2005, Wiley

    Jordi Clarimon

  64. Mutation of the Parkin gene in a Persian family: Clinical progression over a 40-year period

    Article • Movement Disorders, January 2005, Wiley

    Jordi Clarimon

  65. Torsin A haplotype predisposes to idiopathic dystonia

    Article • Annals of Neurology, January 2005, Wiley

    Jordi Clarimon

  66. Paraoxonase 1 (PON1) gene polymorphisms and Parkinson’s disease in a Finnish population

    Article • Neuroscience Letters, September 2004, Elsevier

    Jordi Clarimon

  67. Comparative Analysis of Alu Insertion Sequences in the APP 5′ FlankingRegion in Humans and Other Primates

    Article • Journal of Molecular Evolution, June 2004, Springer Science + Business Media

    Professor Jaume Bertranpetit, Jordi Clarimon

  68. HSP70-2 (HSPA1B) is Associated with Noncognitive Symptoms in Late-Onset Alzheimer's Disease

    Article • Journal of Geriatric Psychiatry and Neurology, September 2003, SAGE Publications

    Professor Jaume Bertranpetit, Jordi Clarimon

  69. Association study between Alzheimer?s disease and genes involved in A? biosynthesis, aggregation and degradation: suggestive results with BACE1

    Article • Deutsche Zeitschrift für Nervenheilkunde, August 2003, Springer Science + Business Media

    Professor Jaume Bertranpetit, Jordi Clarimon

  70. Possible increased risk for Alzheimer's disease associated with neprilysin gene

    Article • Journal of Neural Transmission, June 2003, Springer Science + Business Media

    Professor Jaume Bertranpetit, Jordi Clarimon

  71. Article • Psychiatric Genetics, June 2003, Wolters Kluwer Health

    Jordi Clarimon

  72. Genetic structure of north-west Africa revealed by STR analysis

    Article • European Journal of Human Genetics, May 2000, Nature

    Professor Jaume Bertranpetit, Jordi Clarimon

  73. Sex-Specific Migration Patterns in Central Asian Populations, Revealed by Analysis of Y-Chromosome Short Tandem Repeats and mtDNA

    Article • The American Journal of Human Genetics, July 1999, Elsevier

    Professor Jaume Bertranpetit, Jordi Clarimon

  74. Trading Genes along the Silk Road: mtDNA Sequences and the Origin of Central Asian Populations

    Article • The American Journal of Human Genetics, December 1998, Elsevier

    Professor Jaume Bertranpetit, Jordi Clarimon