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  1. No Access

    Article

    Dopamine transporter haplotype and attention-deficit hyperactivity disorder

    E Galili-Weisstub, S Levy, A Frisch, V Gross-Tsur, E Michaelovsky… in Molecular Psychiatry (2005)

  2. No Access

    Article

    Preferential transmission of interleukin-1 receptor antagonist alleles in attention deficit hyperactivity disorder

    Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, where family data support substantial heritability.1 To date, association studies focussed mainly on genes regulating dopam...

    R H Segman, A Meltzer, V Gross-Tsur, A Kosov, A Frisch, E Inbar… in Molecular Psychiatry (2002)

  3. No Access

    Article

    Association between anorexia nervosa and the hsKCa3 gene: a family-based and case control study

    Familial and twin studies have suggested that anorexia nervosa (AN) is a multifactorial disorder with a substantial genetic contribution.1–5 The hSKCa3 potassium channel gene, which contains polymorphic CAG repea...

    M Koronyo-Hamaoui, Y Danziger, A Frisch, D Stein, S Leor, N Laufer… in Molecular Psychiatry (2002)

  4. No Access

    Article

    Association of anorexia nervosa with the high activity allele of the COMT gene: a family-based study in Israeli patients

    Anorexia nervosa (AN) is a common, severe and disabling psychiatric disorder, characterized by profound weight loss and body image disturbance.1 Family and twin studies indicate a significant genetic contribution

    A Frisch, N Laufer, Y Danziger, E Michaelovsky, S Leor, C Carel… in Molecular Psychiatry (2001)

  5. No Access

    Article

    Association of unipolar major depressive disorder with genes of the serotonergic and dopaminergic pathways

    Major depressive disorder (MDD) is a severe psychiatric disorder with a lifetime prevalence of about 15%.1 The importance of the genetic component is well accepted,2 but the mode of inheritance is complex and non...

    A Frisch, D Postilnick, R Rockah, E Michaelovsky, S Postilnick… in Molecular Psychiatry (1999)

  6. No Access

    Article

    A novel allele in the promoter region of the human serotonin transporter gene

    The human serotonin transporter (hSERT) gene is a promising candidate for mediating the genetic susceptibility for various psychiatric conditions such as mood1 and obsessive-compulsive disorders.2 Two polymorphic...

    E Michaelovsky, A Frisch, R Rockah, L Peleg, N Magal, M Shohat… in Molecular Psychiatry (1999)

  7. No Access

    Article

    No association between the serotonin transporter gene regulatory region polymorphism and the Tridimensional Personality Questionnaire (TPQ) temperament of harm avoidance

    A functional polymorphism in the upstream regulatory region of the serotonin transporter gene has been recently reported to be associated with anxiety-related traits assessed by the NEO-PI-R. Individuals both ...

    R P Ebstein, I Gritsenko, L Nemanov, A Frisch, Y Osher… in Molecular Psychiatry (1997)