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Page 1
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: carmel m. Psychiatr Genet. 2017 Oct;27(5):169-177. doi: 10.1097/YPG.0000000000000177. Psychiatr Genet. 2017. PMID: 28570395 Free PMC article.
Effectiveness and tolerability of citalopram for the treatment of depression and anxiety disorders in children and adolescents: an open-label study.
Schirman S, Kronenberg S, Apter A, Brent D, Melhem N, Pick N, Carmel M, Frisch A, Weizman A, Gothelf D. Schirman S, et al. Among authors: carmel m. J Neural Transm (Vienna). 2010 Jan;117(1):139-45. doi: 10.1007/s00702-009-0330-x. Epub 2009 Oct 23. J Neural Transm (Vienna). 2010. PMID: 19851705 Clinical Trial.
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: carmel m. BMC Med Genet. 2012 Dec 17;13:122. doi: 10.1186/1471-2350-13-122. BMC Med Genet. 2012. PMID: 23245648 Free PMC article.
Additive effects of 5-HTTLPR (serotonin transporter) and tryptophan hydroxylase 2 G-703T gene polymorphisms on the clinical response to citalopram among children and adolescents with depression and anxiety disorders.
Rotberg B, Kronenberg S, Carmel M, Frisch A, Brent D, Zalsman G, Apter A, Weizman A. Rotberg B, et al. Among authors: carmel m. J Child Adolesc Psychopharmacol. 2013 Mar;23(2):117-22. doi: 10.1089/cap.2012.0020. J Child Adolesc Psychopharmacol. 2013. PMID: 23510446
Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.
Gothelf D, Law AJ, Frisch A, Chen J, Zarchi O, Michaelovsky E, Ren-Patterson R, Lipska BK, Carmel M, Kolachana B, Weizman A, Weinberger DR. Gothelf D, et al. Among authors: carmel m. Biol Psychiatry. 2014 Mar 1;75(5):406-13. doi: 10.1016/j.biopsych.2013.07.021. Epub 2013 Aug 28. Biol Psychiatry. 2014. PMID: 23992923 Free PMC article.
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. Zarchi O, et al. Among authors: carmel m. Eur Psychiatry. 2014 May;29(4):203-10. doi: 10.1016/j.eurpsy.2013.07.001. Epub 2013 Sep 17. Eur Psychiatry. 2014. PMID: 24054518
127 results