Neurociencias
Departamento
Assistance Publique -Hopitaux De Paris
París, FranciaPublicaciones en colaboración con investigadoras/es de Assistance Publique -Hopitaux De Paris (20)
2023
2021
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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores
Nature communications, Vol. 12, Núm. 1, pp. 3417
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Corrigendum to “Translating big data to better treatment in bipolar disorder - a manifesto for coordinated action [European Neuropsychopharmacology (2020) 36, 121–136]” (European Neuropsychopharmacology (2020) 36 (121–136), (S0924977X20301802), (10.1016/j.euroneuro.2020.05.006))
European Neuropsychopharmacology
2019
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Association between solar insolation and a history of suicide attempts in bipolar I disorder
Journal of Psychiatric Research, Vol. 113, pp. 1-9
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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
The Lancet Neurology, Vol. 18, Núm. 12, pp. 1091-1102
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Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy
Brain, Vol. 142, Núm. 9, pp. 2605-2616
2017
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Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry
Movement Disorders, Vol. 32, Núm. 10, pp. 1432-1438
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Solar insolation in springtime influences age of onset of bipolar I disorder
Acta Psychiatrica Scandinavica, Vol. 136, Núm. 6, pp. 571-582
2015
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Generalizability of pharmacological and psychotherapy clinical trial results for borderline personality disorder to community samples
Personality Disorders: Theory, Research, and Treatment, Vol. 6, Núm. 1, pp. 81-87
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Influence of birth cohort on age of onset cluster analysis in bipolar I disorder
European Psychiatry, Vol. 30, Núm. 1, pp. 99-105
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Influence of light exposure during early life on the age of onset of bipolar disorder
Journal of Psychiatric Research, Vol. 64, pp. 1-8
2014
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Early netrin-1 expression impairs central nervous system remyelination
Annals of Neurology, Vol. 76, Núm. 2, pp. 252-268
2013
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SOX17 is expressed in regenerating oligodendrocytes in experimental models of demyelination and in multiple sclerosis
GLIA, Vol. 61, Núm. 10, pp. 1659-1672
2011
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Eosinophilic infiltration related to CAPN3 mutations: A pathophysiological component of primary calpainopathy?
Clinical Genetics
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Erratum to 'Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia' [Neuromuscular Disorders 19 (2009) 316-323]
Neuromuscular Disorders
2010
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Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1
Psychological Medicine, Vol. 40, Núm. 3, pp. 487-495
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Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
Nature Genetics, Vol. 42, Núm. 3, pp. 234-239
2009
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Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia
Neuromuscular Disorders, Vol. 19, Núm. 5, pp. 316-323
2007
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Functional impairment in patients with mania: Baseline results of the EMBLEM study
Bipolar Disorders, Vol. 9, Núm. 1-2, pp. 45-52
2006
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CAPN3 mutations in patients with idiopathic eosinophilic myositis
Annals of Neurology, Vol. 59, Núm. 6, pp. 905-911