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Journal of Studies on Alcohol and Drugs|July 3, 2014
Alcohol consumption mediates the relationship between ADH1B and DSM-IV alcohol use disorder and criteriaBari Kilcoyne, Dvora Shmulewitz, Jacquelyn L Meyers, et al.
Archives of Women'S Mental Health|June 19, 2013
Association between a common CYP17A1 haplotype and anxiety in female anorexia nervosaEfrat Czerniak, Michael Korostishevsky, Amos Frisch, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 25, 2005
Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family triosElena Michaelovsky, Amos Frisch, Shani Leor, et al.
Biological Psychiatry|September 3, 2013
Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndromeDoron Gothelf, Amanda J Law, Amos Frisch, et al.
The International Journal of Neuropsychopharmacology|June 1, 2006
Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndromeDoron Gothelf, Elena Michaelovsky, Amos Frisch, et al.
Addiction Biology|October 30, 2013
Childhood adversity moderates the effect of ADH1B on risk for alcohol-related phenotypes in Jewish Israeli drinkersJacquelyn L Meyers, Dvora Shmulewitz, Melanie M Wall, et al.
Pediatric Research|January 13, 2015
Thymic and bone marrow output in individuals with 22q11.2 deletion syndromeNina Dar, Doron Gothelf, David Korn, et al.
International Journal of Adolescent Medicine and Health|October 20, 2005
Family-based association study of 5-HT(2A) receptor T102C polymorphism and suicidal behavior in Ashkenazi inpatient adolescentsGil Zalsman, Amos Frisch, Ruth Baruch-Movshovits, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish populationMaya Koronyo-Hamaoui, Eva Gak, Daniel Stein, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 30, 2004
Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndromeDoron Gothelf, Gadi Presburger, Ada H Zohar, et al.
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