Michaelovsky E - Search Results

1

Thymic and bone marrow output in individuals with 22q11.2 deletion syndrome.

Dar N, Gothelf D, Korn D, Frisch A, Weizman A, Michaelovsky E, Carmel M, Yeshayahu Y, Dubnov-Raz G, Pessach IM, Simon AJ, Lev A, Somech R. Dar N, et al. Among authors: michaelovsky e. Pediatr Res. 2015 Apr;77(4):579-85. doi: 10.1038/pr.2015.14. Epub 2015 Jan 12. Pediatr Res. 2015. PMID: 25580739

2

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. Michaelovsky E, et al. Mol Psychiatry. 1999 Jan;4(1):97-9. doi: 10.1038/sj.mp.4000449. Mol Psychiatry. 1999. PMID: 10089018

3

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

Frisch A, Laufer N, Danziger Y, Michaelovsky E, Leor S, Carel C, Stein D, Fenig S, Mimouni M, Apter A, Weizman A. Frisch A, et al. Among authors: michaelovsky e. Mol Psychiatry. 2001 Mar;6(2):243-5. doi: 10.1038/sj.mp.4000830. Mol Psychiatry. 2001. PMID: 11317231

4

A rare short allele of the serotonin transporter promoter region (5-HTTLPR) found in an aggressive schizophrenic patient of Jewish Libyan origin.

Frisch A, Finkel B, Michaelovsky E, Sigal M, Laor N, Weizman R. Frisch A, et al. Among authors: michaelovsky e. Psychiatr Genet. 2000 Dec;10(4):179-83. doi: 10.1097/00041444-200010040-00005. Psychiatr Genet. 2000. PMID: 11324943

5

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. Zalsman G, et al. Among authors: michaelovsky e. Am J Med Genet. 2001 Apr 8;105(3):239-45. doi: 10.1002/ajmg.1261. Am J Med Genet. 2001. PMID: 11353442

6

Case control and family-based studies of tryptophan hydroxylase gene A218C polymorphism and suicidality in adolescents.

Zalsman G, Frisch A, King RA, Pauls DL, Grice DE, Gelernter J, Alsobrook J, Michaelovsky E, Apter A, Tyano S, Weizman A, Leckman JF. Zalsman G, et al. Among authors: michaelovsky e. Am J Med Genet. 2001 Jul 8;105(5):451-7. doi: 10.1002/ajmg.1406. Am J Med Genet. 2001. PMID: 11449398

7

DRD4 exon III polymorphism and response to risperidone in Israeli adolescents with schizophrenia: a pilot pharmacogenetic study.

Zalsman G, Frisch A, Lev-Ran S, Martin A, Michaelovsky E, Bensason D, Gothelf D, Nahshoni E, Tyano S, Weizman A. Zalsman G, et al. Among authors: michaelovsky e. Eur Neuropsychopharmacol. 2003 May;13(3):183-5. doi: 10.1016/s0924-977x(03)00006-3. Eur Neuropsychopharmacol. 2003. PMID: 12729944 Clinical Trial.

8

Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis.

Frisch A, Colombo R, Michaelovsky E, Karpati M, Goldman B, Peleg L. Frisch A, et al. Among authors: michaelovsky e. Hum Genet. 2004 Mar;114(4):366-76. doi: 10.1007/s00439-003-1072-8. Epub 2004 Jan 15. Hum Genet. 2004. PMID: 14727180

9

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 population.

Koronyo-Hamaoui M, Gak E, Stein D, Frisch A, Danziger Y, Leor S, Michaelovsky E, Laufer N, Carel C, Fennig S, Mimouni M, Apter A, Goldman B, Barkai G, Weizman A. Koronyo-Hamaoui M, et al. Among authors: michaelovsky e. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):76-80. doi: 10.1002/ajmg.b.20154. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389773

10

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. Zalsman G, et al. Among authors: michaelovsky e. J Neural Transm (Vienna). 2004 Dec;111(12):1593-603. doi: 10.1007/s00702-004-0182-3. Epub 2004 Jun 30. J Neural Transm (Vienna). 2004. PMID: 15565493

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