Kahana S - Search Results

1

Chromosomal Microarray Analysis Compared With Noninvasive Prenatal Testing in Pregnancies With Abnormal Maternal Serum Screening.

Sagi-Dain L, Salzer Sheelo L, Brabbing-Goldstein D, Matar R, Kahana S, Agmon-Fishman I, Klein C, Gurevitch M, Basel-Salmon L, Maya I. Sagi-Dain L, et al. Among authors: kahana s. Obstet Gynecol. 2022 May 1;139(5):877-887. doi: 10.1097/AOG.0000000000004758. Epub 2022 Apr 5. Obstet Gynecol. 2022. PMID: 35576346

2

A de-novo interstitial microduplication involving 2p16.1-p15 and mirroring 2p16.1-p15 microdeletion syndrome: Clinical and molecular analysis.

Mimouni-Bloch A, Yeshaya J, Kahana S, Maya I, Basel-Vanagaite L. Mimouni-Bloch A, et al. Among authors: kahana s. Eur J Paediatr Neurol. 2015 Nov;19(6):711-5. doi: 10.1016/j.ejpn.2015.07.013. Epub 2015 Aug 4. Eur J Paediatr Neurol. 2015. PMID: 26278498

3

Chromosomal microarray analysis in fetuses with aberrant right subclavian artery.

Maya I, Kahana S, Yeshaya J, Tenne T, Yacobson S, Agmon-Fishman I, Cohen-Vig L, Levi A, Reinstein E, Basel-Vanagaite L, Sharony R. Maya I, et al. Among authors: kahana s. Ultrasound Obstet Gynecol. 2017 Mar;49(3):337-341. doi: 10.1002/uog.15935. Ultrasound Obstet Gynecol. 2017. PMID: 27063194 Free article.

4

Cut-off value of nuchal translucency as indication for chromosomal microarray analysis.

Maya I, Yacobson S, Kahana S, Yeshaya J, Tenne T, Agmon-Fishman I, Cohen-Vig L, Shohat M, Basel-Vanagaite L, Sharony R. Maya I, et al. Among authors: kahana s. Ultrasound Obstet Gynecol. 2017 Sep;50(3):332-335. doi: 10.1002/uog.17421. Epub 2017 Jul 26. Ultrasound Obstet Gynecol. 2017. PMID: 28133835 Free article.

5

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.

Maya I, Sharony R, Yacobson S, Kahana S, Yeshaya J, Tenne T, Agmon-Fishman I, Cohen-Vig L, Goldberg Y, Berger R, Basel-Salmon L, Shohat M. Maya I, et al. Among authors: kahana s. Genet Med. 2018 Jan;20(1):128-131. doi: 10.1038/gim.2017.89. Epub 2017 Jul 20. Genet Med. 2018. PMID: 28726807 Free article.

6

Cytogenetic analysis in fetuses with late onset abnormal sonographic findings.

Bardin R, Hadar E, Haizler-Cohen L, Gabbay-Benziv R, Meizner I, Kahana S, Yeshaya J, Yacobson S, Cohen-Vig L, Agmon-Fishman I, Basel-Vanagaite L, Maya I. Bardin R, et al. Among authors: kahana s. J Perinat Med. 2018 Nov 27;46(9):975-982. doi: 10.1515/jpm-2017-0071. J Perinat Med. 2018. PMID: 28915119

7

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.

Sagi-Dain L, Cohen Vig L, Kahana S, Yacobson S, Tenne T, Agmon-Fishman I, Klein C, Matar R, Basel-Salmon L, Maya I. Sagi-Dain L, et al. Among authors: kahana s. Genet Med. 2019 Nov;21(11):2462-2467. doi: 10.1038/s41436-019-0550-x. Epub 2019 May 24. Genet Med. 2019. PMID: 31123319 Free article.

8

Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndrome.

Maya I, Kahana S, Agmon-Fishman I, Klein C, Matar R, Berger R, Shohat M, Basel-Salmon L, Sharony R, Sagi-Dain L. Maya I, et al. Among authors: kahana s. Eur J Med Genet. 2020 Oct;63(10):104008. doi: 10.1016/j.ejmg.2020.104008. Epub 2020 Jul 21. Eur J Med Genet. 2020. PMID: 32702406

9

Should We Report 15q11.2 BP1-BP2 Deletions and Duplications in the Prenatal Setting?

Maya I, Perlman S, Shohat M, Kahana S, Yacobson S, Tenne T, Agmon-Fishman I, Tomashov Matar R, Basel-Salmon L, Sukenik-Halevy R. Maya I, et al. Among authors: kahana s. J Clin Med. 2020 Aug 11;9(8):2602. doi: 10.3390/jcm9082602. J Clin Med. 2020. PMID: 32796639 Free PMC article.

10

A study of normal copy number variations in Israeli population.

Maya I, Smirin-Yosef P, Kahana S, Morag S, Yacobson S, Agmon-Fishman I, Matar R, Bitton E, Shohat M, Basel-Salmon L, Salmon-Divon M. Maya I, et al. Among authors: kahana s. Hum Genet. 2021 Mar;140(3):553-563. doi: 10.1007/s00439-020-02225-4. Epub 2020 Sep 27. Hum Genet. 2021. PMID: 32980975

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