M. Periquet

Most-cited papers

1. Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse.

   J. Itier, P. Ibáñez, M. Mena, N. Abbas +23 more

   2003Human Molecular Genetics515 citations Open access

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2. How much phenotypic variation can be attributed to parkin genotype?

   E. Lohmann, M. Periquet, V. Bonifati, Nick W. Wood +19 more

   2003Annals of Neurology333 citations

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3. Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

   M. Periquet, M. Latouche, E. Lohmann, N. Rawal +13 more

   2003Brain : a journal of neurology314 citations Open access

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4. Complex relationship between Parkin mutations and Parkinson disease.

   A. West, M. Periquet, S. Lincoln, C. Lücking +13 more

   2002American journal of medical genetics211 citations

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5. Proteomic analysis of parkin knockout mice: alterations in energy metabolism, protein handling and synaptic function

   M. Periquet, O. Corti, Sandrine Jacquier, A. Brice

   2005Journal of Neurochemistry162 citations Open access

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6. Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects.

   M. Periquet, C. Lücking, J. Vaughan, V. Bonifati +15 more

   2001American Journal of Human Genetics121 citations Open access

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7. New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism

   N. Rawal, M. Periquet, E. Lohmann, C. Lücking +17 more

   2003Neurology60 citations

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8. The wild-type conformation of the Mos-1 Inverted Terminal Repeats is suboptimal for transposition in bacteria

   C. Augé-Gouillou, M. Hamelin, M. Demattéi, M. Periquet +1 more

   2001Zeitschrift für Induktive Abstammungs- und Vererbungslehre53 citations

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9. Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations

   C. Lücking, V. Bonifati, M. Periquet, N. Vanacore +2 more

   2001Neurology47 citations

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10. Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism

    S. Illarioshkin, M. Periquet, N. Rawal, C. Lücking +7 more

    2003Movement Disorders33 citations

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11. Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism

    V. Bonifati, C. Lücking, E. Fabrizio, M. Periquet +2 more

    2001Journal of Neurology Neurosurgery & Psychiatry22 citations Open access

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12. Exclusion of the Nurr1 gene in autosomal recessive Parkinson’s disease

    N. Rawal, M. Periquet, A. Dürr, G. De Michele +6 more

    2002Journal of Neurology8 citations

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13. Phenotype/genotype correlations in Parkinson's disease

    A. Brice, E. Lohmann, P. Ibáñez, M. Periquet +4 more

    20051 citations Open access

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14. Erratum: Complex relationship between Parkin mutations and Parkinson disease (American Journal of Medical Genetics-Neuropsychocetric (2002) 114-(584-591))

    A. West, M. Periquet, S. Lincoln, C. Lücking +13 more

    20021 citations

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15. Etudes génétique et fonctionnelle de la Parkine : un gène responsable d'une Maladie de Parkinson à début précoce et de transmission autosomique récessive

    M. Periquet

    20030 citations

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16. Origin of parkin gene mutations in Europe

    M. Periquet, C. Lücking, J. Vaughan, V. Bonifati +11 more

    20010 citations

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