A comparative study of the neuropsychiatric and neurocognitive phenotype in two microdeletion syndromes: Velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes
Zarchi, O, Diamond, A, Weinberger, R, Abbott, D, Carmel, M, Frisch, A, Michaelovsky, E, Gruber, R, Green, T, Weizman, A, Gothelf, D
Published in European psychiatry (01.05.2014)
Published in European psychiatry (01.05.2014)
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Journal Article
Association of unipolar major depressive disorder with genes of the serotonergic and dopaminergic pathways
FRISCH, A, POSTILNICK, D, SCHNEIDMAN, M, MODAI, I, WEIZMAN, R, ROCKAH, R, MICHAELOVSKY, E, POSTILNICK, S, BIRMAN, E, LAOR, N, RAUCHVERGER, B, KREININ, A, POYUROVSKY, M
Published in Molecular psychiatry (01.07.1999)
Published in Molecular psychiatry (01.07.1999)
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Journal Article
Association of anorexia nervosa with the high activity allele of the COMT gene : a family-based study in israeli patients
FRISCH, A, LAUFER, N, WEIZMAN, A, DANZIGER, Y, MICHAELOVSKY, E, LEOR, S, CAREL, C, STEIN, D, FENIG, S, MIMOUNI, M, APTER, A
Published in Molecular psychiatry (01.03.2001)
Published in Molecular psychiatry (01.03.2001)
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Journal Article
Association between obsessive-compulsive disorder and polymorphisms of genes encoding components of the serotonergic and dopaminergic pathways
Frisch, A, Michaelovsky, E, Rockah, R, Amir, I, Hermesh, H, Laor, N, Fuchs, C, Zohar, J, Lerer, B, Buniak, S.F, Landa, S, Poyurovsky, M, Shapira, B, Weizman, R
Published in European neuropsychopharmacology (01.05.2000)
Published in European neuropsychopharmacology (01.05.2000)
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Journal Article
Relationships between serotonin transporter promoter polymorphism, platelet serotonin transporter binding and clinical phenotype in suicidal and non-suicidal adolescent inpatients
Zalsman, G, Anderson, G M, Peskin, M, Frisch, A, King, R A, Vekslerchik, M, Sommerfeld, E, Michaelovsky, E, Sher, L, Weizman, A, Apter, A
Published in Journal of Neural Transmission (01.02.2005)
Published in Journal of Neural Transmission (01.02.2005)
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Journal Article
Dopamine transporter haplotype and attention-deficit hyperactivity disorder
Galili-Weisstub, E, Levy, S, Frisch, A, Gross-Tsur, V, Michaelovsky, E, Kosov, A, Meltzer, A, Goltser, T, Serretti, A, Cusin, C, Darvasi, A, Inbar, E, Weizman, A, Segman, R H
Published in Molecular psychiatry (01.07.2005)
Published in Molecular psychiatry (01.07.2005)
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Journal Article
Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family trios
Michaelovsky, Elena, Frisch, Amos, Leor, Shani, Stein, Daniel, Danziger, Yardena, Carel, Cynthia, Fennig, Silvana, Mimouni, Marc, Klauck, Sabine M., Benner, Axel, Poustka, Annemarie, Apter, Alan, Weizman, Abraham
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.11.2005)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.11.2005)
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Journal Article
Search for association between suicide attempt and serotonergic polymorphisms
Geijer, T, Frisch, A, Persson, M L, Wasserman, D, Rockah, R, Michaelovsky, E, Apter, A, Jönsson, E G, Nöthen, M M, Weizman, A
Published in Psychiatric genetics (01.03.2000)
Published in Psychiatric genetics (01.03.2000)
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Journal Article
A novel allele in the promoter region of the human serotonin transporter gene
MICHAELOVSKY, E, FRISCH, A, ROCKAH, R, PELEG, L, MAGAL, N, SHOHAT, M, WEIZMAN, R
Published in Molecular psychiatry (1999)
Published in Molecular psychiatry (1999)
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Journal Article
DRD4 receptor gene exon III polymorphism in inpatient suicidal adolescents
Zalsman, G, Frisch, A, Lewis, R, Michaelovsky, E, Hermesh, H, Sher, L, Nahshoni, E, Wolovik, L, Tyano, S, Apter, A, Weizman, R, Weizman, A
Published in Journal of Neural Transmission (01.12.2004)
Published in Journal of Neural Transmission (01.12.2004)
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Journal Article
Dopamine D4 receptor gene polymorphism and personality traits in healthy volunteers
Persson, M L, Wasserman, D, Geijer, T, Frisch, A, Rockah, R, Michaelovsky, E, Apter, A, Weizman, A, Jönsson, E G, Bergman, H
Published in European archives of psychiatry and clinical neuroscience (2000)
Published in European archives of psychiatry and clinical neuroscience (2000)
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Journal Article
Lack of association between suicide attempt and a polymorphism at the dopamine receptor D4 locus
Persson, M L, Geijer, T, Wasserman, D, Rockah, R, Frisch, A, Michaelovsky, E, Jönsson, E G, Apter, A, Weizman, A
Published in Psychiatric genetics (01.06.1999)
Published in Psychiatric genetics (01.06.1999)
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Journal Article
Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred
Melhem, Nadine M, Hamdan, Sami, Klei, Lambertus, Wood, Shawn, Zelazny, Jamie, Frisch, Amos, Weizman, Abraham, Carmel, Miri, Michaelovsky, Elena, Farbstein, Ilana, Wasserman, Danuta, El-Heib, Muhammad, Ferrell, Robert, Apter, Alan, Devlin, Bernie, Brent, David
Published in Psychiatric genetics (01.10.2017)
Published in Psychiatric genetics (01.10.2017)
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Journal Article
Association of the serotonin transporter promotor polymorphism with suicide attempters with a high medical damage
Wasserman, Danuta, Geijer, Thomas, Sokolowski, Marcus, Frisch, Amos, Michaelovsky, Elena, Weizman, Abraham, Rozanov, Vsevolod, Wasserman, Jerzy
Published in European neuropsychopharmacology (01.02.2007)
Published in European neuropsychopharmacology (01.02.2007)
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Journal Article
Family-based association study of serotonin transporter promoter in suicidal adolescents: no association with suicidality but possible role in violence traits
Zalsman, G, Frisch, A, Bromberg, M, Gelernter, J, Michaelovsky, E, Campino, A, Erlich, Z, Tyano, S, Apter, A, Weizman, A
Published in American journal of medical genetics (08.04.2001)
Published in American journal of medical genetics (08.04.2001)
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Journal Article
Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca2+ -activated K+ channel to genetic predisposition to anorexia nervosa
Koronyo-Hamaoui, Maya, Frisch, Amos, Stein, Daniel, Denziger, Yardena, Leor, Shani, Michaelovsky, Elena, Laufer, Neil, Carel, Cynthia, Fennig, Silvana, Mimouni, Mark, Ram, Anca, Zubery, Eynat, Jeczmien, Pablo, Apter, Alan, Weizman, Abraham, Gak, Eva
Published in Journal of psychiatric research (01.01.2007)
Published in Journal of psychiatric research (01.01.2007)
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Journal Article
Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca(2+)-activated K+ channel to genetic predisposition to anorexia nervosa
Koronyo-Hamaoui, Maya, Frisch, Amos, Stein, Daniel, Denziger, Yardena, Leor, Shani, Michaelovsky, Elena, Laufer, Neil, Carel, Cynthia, Fennig, Silvana, Mimouni, Mark, Ram, Anca, Zubery, Eynat, Jeczmien, Pablo, Apter, Alan, Weizman, Abraham, Gak, Eva
Published in Journal of psychiatric research (01.01.2007)
Published in Journal of psychiatric research (01.01.2007)
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Journal Article
Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis
FRISCH, Amos, COLOMBO, Roberto, MICHAELOVSKY, Elena, KARPATI, Mazal, GOLDMAN, Boleslaw, PELEG, Leah
Published in Human genetics (01.03.2004)
Published in Human genetics (01.03.2004)
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Journal Article
DRD4 exon III polymorphism and response to risperidone in Israeli adolescents with schizophrenia: a pilot pharmacogenetic study
Zalsman, Gil, Frisch, Amos, Lev-Ran, Shaul, Martin, Andrés, Michaelovsky, Elena, Bensason, Daniela, Gothelf, Doron, Nahshoni, Eitan, Tyano, Samuel, Weizman, Abraham
Published in European neuropsychopharmacology (01.05.2003)
Published in European neuropsychopharmacology (01.05.2003)
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