P Verpillat

Summary

Country: France

Publications

  1. ncbi Meta-analysis of family-based association studies between the dopamine transporter gene and attention deficit hyperactivity disorder
    D Purper-Ouakil
    CHU Robert Debré AP HP, Paris VII, Paris, France
    Psychiatr Genet 15:53-9. 2005
  2. ncbi Brain spect perfusion of frontotemporal dementia associated with motor neuron disease
    E Guedj
    , , Centre Hospitalo-Universitaire de la Timone, Marseille Cedex 5, France
    Neurology 69:488-90. 2007
  3. ncbi Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis
    Patrice Verpillat
    INSERM U535, Le Kremlin Bicetre, France, and Département d EpidAmiologie, de Biostatistique et de Recherche Clinique, Centre Hospitalier Universitaire Bichat Claude Bernard, AP HP Université Paris VII, Paris, France
    Eur J Hum Genet 10:399-405. 2002
  4. ncbi Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population
    P Verpillat
    INSERM U535, Le Kremlin Bicetre, France, and INSERM U289, Paris, France
    Eur J Hum Genet 9:464-8. 2001
  5. ncbi Association between the extended tau haplotype and frontotemporal dementia
    Patrice Verpillat
    Département d Epidémiologie, de Biostatistique, et de Recherche Clinique, Hopital Bichat Claude Bernard, 46 rue Henri Huchard, 75877 Paris Cedex 18, France
    Arch Neurol 59:935-9. 2002
  6. ncbi Aldosterone synthase (CYP11B2) gene polymorphism and cerebral white matter hyperintensities
    P Verpillat
    Institut National de la Santé et de la Recherche Médicale U360, Hopital Pitie Salpetriere, Paris, France
    Neurology 56:673-5. 2001
  7. ncbi Possible implication of thiopurine S-methyltransferase in occurrence of infectious episodes during maintenance therapy for childhood lymphoblastic leukemia with mercaptopurine
    T Dervieux
    , , Paris, France
    Leukemia 15:1706-12. 2001
  8. ncbi Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure
    E Matichard
    J Med Genet 41:e13. 2004
  9. ncbi Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism
    C Dumanchin
    Génétique et Hématologie Moléculaires JE 2006, Centre Hospitalo Universitaire de Rouen, 76031 Rouen, France and IFRMP, 76821 Mont Saint Aignon, France
    Hum Mol Genet 7:1825-9. 1998
  10. ncbi [Cutaneous necrosis is predictive of cancer in adult dermatomyositis]
    M Burnouf
    Service de Dermatologie, Groupe Hospitalier Bichat-Claude Bernard, , Paris
    Ann Dermatol Venereol 130:313-6. 2003

Collaborators

Detail Information

Publications12

  1. ncbi Meta-analysis of family-based association studies between the dopamine transporter gene and attention deficit hyperactivity disorder
    D Purper-Ouakil
    CHU Robert Debré AP HP, Paris VII, Paris, France
    Psychiatr Genet 15:53-9. 2005
    ..A recent meta-analysis showed that the DRD4 gene has a significant role in the vulnerability to ADHD...
  2. ncbi Brain spect perfusion of frontotemporal dementia associated with motor neuron disease
    E Guedj
    , , Centre Hospitalo-Universitaire de la Timone, Marseille Cedex 5, France
    Neurology 69:488-90. 2007
  3. ncbi Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis
    Patrice Verpillat
    INSERM U535, Le Kremlin Bicetre, France, and Département d EpidAmiologie, de Biostatistique et de Recherche Clinique, Centre Hospitalier Universitaire Bichat Claude Bernard, AP HP Université Paris VII, Paris, France
    Eur J Hum Genet 10:399-405. 2002
    ..If this finding was confirmed, it could provide new insights into the mechanisms of differential risk related to APOE in neurodegenerative diseases...
  4. ncbi Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population
    P Verpillat
    INSERM U535, Le Kremlin Bicetre, France, and INSERM U289, Paris, France
    Eur J Hum Genet 9:464-8. 2001
    ..One interest in this study is the use of the haplotype analysis, which can be used to combine information from several polymorphisms, taking into account their dependence...
  5. ncbi Association between the extended tau haplotype and frontotemporal dementia
    Patrice Verpillat
    Département d Epidémiologie, de Biostatistique, et de Recherche Clinique, Hopital Bichat Claude Bernard, 46 rue Henri Huchard, 75877 Paris Cedex 18, France
    Arch Neurol 59:935-9. 2002
    ..In FTD, the pathological accumulation of the microtubule-associated protein tau suggests that the tau gene may be a genetic risk factor for this disorder...
  6. ncbi Aldosterone synthase (CYP11B2) gene polymorphism and cerebral white matter hyperintensities
    P Verpillat
    Institut National de la Santé et de la Recherche Médicale U360, Hopital Pitie Salpetriere, Paris, France
    Neurology 56:673-5. 2001
    ..61 (95% CI, 1.46 to 14.55) for the TT genotype and 2.45 (95% CI, 0.81 to 7.46) for the TC genotype in men. This association was independent of hypertension...
  7. ncbi Possible implication of thiopurine S-methyltransferase in occurrence of infectious episodes during maintenance therapy for childhood lymphoblastic leukemia with mercaptopurine
    T Dervieux
    , , Paris, France
    Leukemia 15:1706-12. 2001
    ..001). In conclusion, during maintenance therapy of ALL, children with higher TPMT activity receive a higher 6-MP dosage and may have infectious episodes caused by metabolism of 6-MP into methylmercaptopurine nucleotides...
  8. ncbi Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure
    E Matichard
    J Med Genet 41:e13. 2004
  9. ncbi Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism
    C Dumanchin
    Génétique et Hématologie Moléculaires JE 2006, Centre Hospitalo Universitaire de Rouen, 76031 Rouen, France and IFRMP, 76821 Mont Saint Aignon, France
    Hum Mol Genet 7:1825-9. 1998
    ..The observation of this mutation in several FTDP families might suggest that disruption of binding of MAPT protein to the microtubule is a key event in the pathogenesis of FTDP...
  10. ncbi [Cutaneous necrosis is predictive of cancer in adult dermatomyositis]
    M Burnouf
    Service de Dermatologie, Groupe Hospitalier Bichat-Claude Bernard, , Paris
    Ann Dermatol Venereol 130:313-6. 2003
    ..The interest of elevation in muscular enzyme as a predictive factor of cancer is discussed...
  11. ncbi Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation
    G Raux
    INSERM EPI 9906 Campion, Rouen, France
    Neurology 55:1577-8. 2000
    ..Neuroimaging features were consistent with the diagnosis of frontotemporal dementia. The authors conclude that PSEN1 mutations can be associated with clinical features of frontotemporal dementia...
  12. ncbi [Correlation between the presence of type-2 anti-pemphigoid antibodies and dementia in elderly subjects with no clinical signs of pemphigoid]
    N Foureur
    , , Assistance Publique, , Ivry-sur-Seine
    Ann Dermatol Venereol 133:439-43. 2006
    ..The overall prevalence of antinuclear antibodies was 14.5% and the figure was similar between the two groups. DISCUSSION: The presence of anti-PBAg2 could be associated with the diagnosis of dementia in elderly subjects...