I. Bouchardy

Most-cited papers

1. Breast cancer and active and passive smoking: the role of the N-acetyltransferase 2 genotype.

   A. Morabia, M. Bernstein, I. Bouchardy, Jaime L. Kurtz +1 more

   2000American Journal of Epidemiology89 citations Open access

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2. Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.

   M. Neerman-Arbez, D. Vũ, B. Abu-Libdeh, I. Bouchardy +1 more

   2003Blood55 citations Open access

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3. MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother.

   A. Dayer, A. Bottani, I. Bouchardy, J. Fluss +3 more

   2007Brain & development (Tokyo. 1979)47 citations Open access

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4. Elicited repetitive daily blindness

   D. Le Fort, A. Safran, F. Picard, I. Bouchardy +1 more

   2004Neurology17 citations Open access

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5. Combined factor V – factor VIII deficiency (F5F8D): Compound heterozygosity for two novel truncating mutations in LMAN1 in a consanguineous patient

   R. Farah, P. de Moerloose, I. Bouchardy, M. Morris +3 more

   2006Thrombosis and Haemostasis13 citations Open access

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6. New Horizons in Industry, Business and Education

   M. Allan, C. Chisholm, S. Jerrams, T. Betts +3 more

   200710 citations

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7. [R74W;R1070W;D1270N]: a new complex allele responsible for cystic fibrosis.

   Ana de Prada Merino, F. N. Bütschi, I. Bouchardy, J. Beckmann +3 more

   2010Journal of Cystic Fibrosis9 citations Open access

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8. No major contribution of the TGFBR1‐ and TGFBR2‐mediated pathway to Kabuki syndrome

   A. Bottani, B. Pardo, I. Bouchardy, J. Schoumans +2 more

   2006American Journal of Medical Genetics. Part A6 citations

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9. Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE

   I. Bouchardy, O. Steinlein, Romina Combi, Luigi Ferini-Strambi +4 more

   2011Neurology1 citations Open access

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10. QUALITY STRATEGIES: WHAT ARE FRENCH UNIVERSITIES LOOKING FOR?

    I. Bouchardy

    20101 citations

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11. The sustainable city: between symbols and paradoxes

    I. Bouchardy, M. Méquignon

    20140 citations

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12. Indicators and benchmarks: how to articulate information and decision support systems in a French university in the process of autonomy?

    I. Bouchardy

    20130 citations Open access

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13. nonsense mutation in the FGB gene in a Palestinian family Prenatal diagnosis for congenital afibrinogenemia caused by a novel

    M. Neerman-Arbez, D. Vũ, B. Abu-Libdeh, I. Bouchardy +1 more

    20130 citations

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14. Study of the genetic basis of autosomal dominant nocturnal frontal lobe epilepsy

    Sansoni, I. Bouchardy, F. Picard, R. Combi

    20100 citations

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