On the interpretive method of R. Raphael Berdugo: (Based on his exegesis of the former prophets)FRISCH, Amos.Revue des études juives. 2004, Vol 163, Num 3-4, pp 445-462, issn 0484-8616, 18 p.Article

Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesisFRISCH, Amos; COLOMBO, Roberto; MICHAELOVSKY, Elena et al.Human genetics. 2004, Vol 114, Num 4, pp 366-376, issn 0340-6717, 11 p.Article

Specific mutations in the HEXA gene among Iraqi Jewish Tay-Sachs disease carriers: dating of founder ancestorKARPATI, Mazal; GAZIT, Epbraim; GOLDMAN, Boleslaw et al.Neurogenetics (Oxford. Print). 2004, Vol 5, Num 1, pp 35-40, issn 1364-6745, 6 p.Article

Trauma exposure, posttraumatic stress disorder and risk for alcohol, nicotine, and marijuana dependence in IsraelWALSH, Kate; ELLIOT, Jennifer C; SHMULEWITZ, Dvora et al.Comprehensive psychiatry (Print). 2014, Vol 55, Num 3, pp 621-630, issn 0010-440X, 10 p.Article

Risk Factors and the Evolution of Psychosis in 22q11.2 Deletion Syndrome: A Longitudinal 2-Site StudyGOTHELF, Doron; SCHNEIDER, Maude; GREEN, Tamar et al.Journal of the American Academy of Child and Adolescent Psychiatry. 2013, Vol 52, Num 11, pp 1192-1203, issn 0890-8567, 12 p.Article

Effect of ADH1B genotype on alcohol consumption in young israeli jewsSPIVAK, Baruch; FRISCH, Amos; MAMAN, Ziyona et al.Alcoholism, clinical and experimental research. 2007, Vol 31, Num 8, pp 1297-1301, issn 0145-6008, 5 p.Article

COMT Val¹⁵⁸Met polymorphism in schizophrenia with obsessive-compulsive disorder : A case-control studyPOYUROVSKY, Michael; MICHAELOVSKY, Elena; FRISCH, Amos et al.Neuroscience letters. 2005, Vol 389, Num 1, pp 21-24, issn 0304-3940, 4 p.Article

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 populationKORONYO-HAMAOUI, Maya; GAK, Eva; MIMOUNI, Marc et al.American journal of medical genetics. 2004, Vol 131B, Num 1, pp 76-80, issn 0148-7299, 5 p.Article

Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjectsCARMEL, Miri; ZARCHI, Omer; MICHAELOVSKY, Elena et al.Journal of psychiatric research. 2014, Vol 56, pp 28-35, issn 0022-3956, 8 p.Article

Biological Effects of COMT Haplotypes and Psychosis Risk in 22q11.2 Deletion SyndromeGOTHELF, Doron; LAW, Amanda J; WEIZMAN, Abraham et al.Biological psychiatry (1969). 2014, Vol 75, Num 5, pp 406-413, issn 0006-3223, 8 p.Article

Nicotine dependence, abuse and craving: dimensionality in an Israeli sampleSHMULEWITZ, Dvora; KEYES, Katherine M; HASIN, Deborah et al.Addiction (Abingdon. Print). 2011, Vol 106, Num 9, pp 1675-1686, issn 0965-2140, 12 p.Article

Psychiatric Disorders and Intellectual Functioning Throughout Development in Velocardiofacial (22q11.2 Deletion) SyndromeGREEN, Tamar; GOTHELF, Doron; GLASER, Bronwyn et al.Journal of the American Academy of Child and Adolescent Psychiatry. 2009, Vol 48, Num 11, pp 1060-1068, issn 0890-8567, 9 p.Article

Family-based association study of serotonin transporter promoter in suicidal adolescents : No association with suicidality but possible role in violence traitsZALSMAN, Gil; FRISCH, Amos; BROMBERG, Michal et al.American journal of medical genetics. 2001, Vol 105, Num 3, pp 239-245, issn 0148-7299Conference Paper