Teltsh O - Search Results

1

Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.

Teltsh O, Kanyas K, Karni O, Levi A, Korner M, Ben-Asher E, Lancet D, Hamdan A, Lerer B, Kohn Y. Teltsh O, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):209-15. doi: 10.1002/ajmg.b.30591. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 17823922

2

Oxytocin and vasopressin genes are significantly associated with schizophrenia in a large Arab-Israeli pedigree.

Teltsh O, Kanyas-Sarner K, Rigbi A, Greenbaum L, Lerer B, Kohn Y. Teltsh O, et al. Int J Neuropsychopharmacol. 2012 Apr;15(3):309-19. doi: 10.1017/S1461145711001374. Epub 2011 Sep 7. Int J Neuropsychopharmacol. 2012. PMID: 21899794 Free article.

3

Involvement of PTPN5, the gene encoding the striatal-enriched protein tyrosine phosphatase, in schizophrenia and cognition.

Pelov I, Teltsh O, Greenbaum L, Rigbi A, Kanyas-Sarner K, Lerer B, Lombroso P, Kohn Y. Pelov I, et al. Among authors: teltsh o. Psychiatr Genet. 2012 Aug;22(4):168-76. doi: 10.1097/YPG.0b013e3283518586. Psychiatr Genet. 2012. PMID: 22555153 Free PMC article.

4

Further evidence for association of the RGS2 gene with antipsychotic-induced parkinsonism: protective role of a functional polymorphism in the 3'-untranslated region.

Greenbaum L, Smith RC, Rigbi A, Strous R, Teltsh O, Kanyas K, Korner M, Lancet D, Ben-Asher E, Lerer B. Greenbaum L, et al. Among authors: teltsh o. Pharmacogenomics J. 2009 Apr;9(2):103-10. doi: 10.1038/tpj.2008.6. Epub 2008 Mar 18. Pharmacogenomics J. 2009. PMID: 18347610

5

No association between regulator of G-protein signaling 9 (RGS9) and schizophrenia in a Jewish population.

Greenbaum L, Pelov I, Teltsh O, Lerer B, Kohn Y. Greenbaum L, et al. Among authors: teltsh o. Psychiatr Genet. 2010 Feb;20(1):47-8. doi: 10.1097/YPG.0b013e3283351234. Psychiatr Genet. 2010. PMID: 20016399 No abstract available.

6

Oxytocin and vasopressin genes are significantly associated with schizophrenia in a large Arab-Israeli pedigree - CORRIGENDUM.

Teltsh O, Kanyas-Sarner K, Rigbi A, Greenbaum L, Lerer B, Kohn Y. Teltsh O, et al. Int J Neuropsychopharmacol. 2013 Jun 1;16(5):1183. doi: 10.1017/S1461145712001162. Int J Neuropsychopharmacol. 2013. PMID: 31615168 Free article. No abstract available.

7

Optimizing prediction of response to antidepressant medications using machine learning and integrated genetic, clinical, and demographic data.

Taliaz D, Spinrad A, Barzilay R, Barnett-Itzhaki Z, Averbuch D, Teltsh O, Schurr R, Darki-Morag S, Lerer B. Taliaz D, et al. Among authors: teltsh o. Transl Psychiatry. 2021 Jul 8;11(1):381. doi: 10.1038/s41398-021-01488-3. Transl Psychiatry. 2021. PMID: 34238923 Free PMC article.

8

Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegia.

Lossos A, Teltsh O, Milman T, Meiner V, Rozen R, Leclerc D, Schwahn BC, Karp N, Rosenblatt DS, Watkins D, Shaag A, Korman SH, Heyman SN, Gal A, Newman JP, Steiner-Birmanns B, Abramsky O, Kohn Y. Lossos A, et al. Among authors: teltsh o. JAMA Neurol. 2014 Jul 1;71(7):901-4. doi: 10.1001/jamaneurol.2014.116. JAMA Neurol. 2014. PMID: 24797679

9

Additional support for the association of SLITRK1 var321 and Tourette syndrome.

O'Roak BJ, Morgan TM, Fishman DO, Saus E, Alonso P, Gratacòs M, Estivill X, Teltsh O, Kohn Y, Kidd KK, Cho J, Lifton RP, State MW. O'Roak BJ, et al. Among authors: teltsh o. Mol Psychiatry. 2010 May;15(5):447-50. doi: 10.1038/mp.2009.105. Epub 2010 Mar 30. Mol Psychiatry. 2010. PMID: 20351724 Free PMC article. No abstract available.

10

Role of genetic variants in the CHRNA5-CHRNA3-CHRNB4 cluster in nicotine dependence risk: importance of gene-environment interplay.

Greenbaum L, Rigbi A, Teltsh O, Lerer B. Greenbaum L, et al. Among authors: teltsh o. Mol Psychiatry. 2009 Sep;14(9):828-30. doi: 10.1038/mp.2009.25. Mol Psychiatry. 2009. PMID: 19696770 No abstract available.

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