Zeligson S - Search Results

1

Microarray analysis has no additional value in fetal aberrant right subclavian artery: description of 268 pregnancies and systematic literature review.

Sagi-Dain L, Singer A, Josefsberg S, Peleg A, Lev D, Samra NN, Bar-Shira A, Zeligson S, Maya I, Ben-Shachar S. Sagi-Dain L, et al. Among authors: zeligson s. Ultrasound Obstet Gynecol. 2019 Jun;53(6):810-815. doi: 10.1002/uog.20208. Ultrasound Obstet Gynecol. 2019. PMID: 30584678 Free article.

2

The spinal muscular atrophy with pontocerebellar hypoplasia gene VRK1 regulates neuronal migration through an amyloid-β precursor protein-dependent mechanism.

Vinograd-Byk H, Sapir T, Cantarero L, Lazo PA, Zeligson S, Lev D, Lerman-Sagie T, Renbaum P, Reiner O, Levy-Lahad E. Vinograd-Byk H, et al. Among authors: zeligson s. J Neurosci. 2015 Jan 21;35(3):936-42. doi: 10.1523/JNEUROSCI.1998-14.2015. J Neurosci. 2015. PMID: 25609612 Free PMC article.

3

Copy number variations in cryptogenic cerebral palsy.

Segel R, Ben-Pazi H, Zeligson S, Fatal-Valevski A, Aran A, Gross-Tsur V, Schneebaum-Sender N, Shmueli D, Lev D, Perlberg S, Blumkin L, Deutsch L, Levy-Lahad E. Segel R, et al. Among authors: zeligson s. Neurology. 2015 Apr 21;84(16):1660-8. doi: 10.1212/WNL.0000000000001494. Epub 2015 Mar 27. Neurology. 2015. PMID: 25817843

4

Is fetal isolated double renal collecting system an indication for chromosomal microarray?

Singer A, Maya I, Frumkin A, Zeligson S, Josefsberg SBY, Berger R, Shachar SB, Sagi-Dain L. Singer A, et al. Among authors: zeligson s. J Matern Fetal Neonatal Med. 2021 Mar;34(5):696-700. doi: 10.1080/14767058.2019.1613364. Epub 2019 May 15. J Matern Fetal Neonatal Med. 2021. PMID: 31032679 Free article.

5

What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?

Maya I, Singer A, Yonath H, Reches A, Rienstein S, Zeligson S, Ben Shachar S, Sagi-Dain L. Maya I, et al. Among authors: zeligson s. Acta Obstet Gynecol Scand. 2020 Jun;99(6):757-764. doi: 10.1111/aogs.13708. Epub 2019 Sep 9. Acta Obstet Gynecol Scand. 2020. PMID: 31424084 Free article.

6

The yield of chromosomal microarray testing for cases of abnormal fetal head circumference.

Pasternak Y, Singer A, Maya I, Sagi-Dain L, Ben-Shachar S, Khayat M, Greenbaum L, Feingold-Zadok M, Zeligson S, Sukenik Halevy R. Pasternak Y, et al. Among authors: zeligson s. J Perinat Med. 2020 Apr 28;48(6):553-558. doi: 10.1515/jpm-2020-0048. J Perinat Med. 2020. PMID: 32721143

7

Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy.

Yechieli M, Gulsuner S, Ben-Pazi H, Fattal A, Aran A, Kuzminsky A, Sagi L, Guttman D, Schneebaum Sender N, Gross-Tsur V, Klopstock T, Walsh T, Renbaum P, Zeligson S, Shemer Meiri L, Lev D, Shmueli D, Blumkin L, Lahad A, King MC, Levy EL, Segel R. Yechieli M, et al. Among authors: zeligson s. J Med Genet. 2022 Aug;59(8):759-767. doi: 10.1136/jmedgenet-2021-107884. Epub 2021 Jul 28. J Med Genet. 2022. PMID: 34321325

8

Detection of copy number variants associated with late-onset conditions in ~16 200 pregnancies: parameters for disclosure and pregnancy outcome.

Daum H, Segel R, Meiner V, Goldberg Y, Zeligson S, Weiss O, Stern S, Frumkin A, Zenvirt S, Ganz G, Shkedi-Rafid S. Daum H, et al. Among authors: zeligson s. J Med Genet. 2023 Jan;60(1):99-105. doi: 10.1136/jmedgenet-2021-107890. Epub 2022 Mar 9. J Med Genet. 2023. PMID: 35264407

9

A rare rearrangement of 5q31.2 in a child with a neurodevelopmental syndrome.

Goldenstein H, Shrem SB, Weiss O, Zeligson S, Segel R, Mory A, Weiss K. Goldenstein H, et al. Among authors: zeligson s. Clin Dysmorphol. 2021 Oct 1;30(4):181-185. doi: 10.1097/MCD.0000000000000380. Clin Dysmorphol. 2021. PMID: 34232135 No abstract available.

10

Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome.

Belostotsky R, Ben-Shalom E, Rinat C, Becker-Cohen R, Feinstein S, Zeligson S, Segel R, Elpeleg O, Nassar S, Frishberg Y. Belostotsky R, et al. Among authors: zeligson s. Am J Hum Genet. 2011 Feb 11;88(2):193-200. doi: 10.1016/j.ajhg.2010.12.010. Epub 2011 Jan 20. Am J Hum Genet. 2011. PMID: 21255763 Free PMC article.

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