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Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred.
Melhem NM, Hamdan S, Klei L, Wood S, Zelazny J, Frisch A, Weizman A, Carmel M, Michaelovsky E, Farbstein I, Wasserman D, El-Heib M, Ferrell R, Apter A, Devlin B, Brent D. Melhem NM, et al. Among authors: frisch a. Psychiatr Genet. 2017 Oct;27(5):169-177. doi: 10.1097/YPG.0000000000000177. Psychiatr Genet. 2017. PMID: 28570395 Free PMC article.
Genotype-phenotype correlation in 22q11.2 deletion syndrome.
Michaelovsky E, Frisch A, Carmel M, Patya M, Zarchi O, Green T, Basel-Vanagaite L, Weizman A, Gothelf D. Michaelovsky E, et al. Among authors: frisch a. BMC Med Genet. 2012 Dec 17;13:122. doi: 10.1186/1471-2350-13-122. BMC Med Genet. 2012. PMID: 23245648 Free PMC article.
Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family trios.
Michaelovsky E, Frisch A, Leor S, Stein D, Danziger Y, Carel C, Fennig S, Mimouni M, Klauck SM, Benner A, Poustka A, Apter A, Weizman A. Michaelovsky E, et al. Among authors: frisch a. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):45-50. doi: 10.1002/ajmg.b.30230. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16118784
Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca(2+)-activated K+ channel to genetic predisposition to anorexia nervosa.
Koronyo-Hamaoui M, Frisch A, Stein D, Denziger Y, Leor S, Michaelovsky E, Laufer N, Carel C, Fennig S, Mimouni M, Ram A, Zubery E, Jeczmien P, Apter A, Weizman A, Gak E. Koronyo-Hamaoui M, et al. Among authors: frisch a. J Psychiatr Res. 2007 Jan-Feb;41(1-2):160-7. doi: 10.1016/j.jpsychires.2005.07.010. Epub 2005 Sep 12. J Psychiatr Res. 2007. PMID: 16157352
312 results