Sharon Zeligson
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Explore the profile of Sharon Zeligson including associated specialties, affiliations and a list of published articles.
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37
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1010
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Recent Articles
1.
Backenroth D, Altarescu G, Zahdeh F, Mann T, Murik O, Renbaum P, et al.
Sci Rep
. 2023 Oct;
13(1):18036.
PMID: 37865712
Recent advances in genomic technologies expand the scope and efficiency of preimplantation genetic testing (PGT). We previously developed Haploseek, a clinically-validated, variant-agnostic comprehensive PGT solution. Haploseek is based on microarray...
2.
Michaelson-Cohen R, Murik O, Zeligson S, Lobel O, Weiss O, Picard E, et al.
Mol Genet Genomics
. 2022 Apr;
297(4):925-933.
PMID: 35488049
Complex chromosomal rearrangements (CCRs), a class of structural variants (SVs) involving more than two chromosome breaks, were classically thought to be extremely rare. As advanced technologies become more available, it...
3.
Daum H, Segel R, Meiner V, Goldberg Y, Zeligson S, Weiss O, et al.
J Med Genet
. 2022 Mar;
60(1):99-105.
PMID: 35264407
Background: Copy number variants (CNVs) associated with late-onset medical conditions are rare but important secondary findings in chromosomal microarray analysis (CMA) performed during pregnancy. Here, we critically review the cases...
4.
Yechieli M, Gulsuner S, Ben-Pazi H, Fattal A, Aran A, Kuzminsky A, et al.
J Med Genet
. 2021 Jul;
59(8):759-767.
PMID: 34321325
Objective: To determine the yield of genetic diagnoses using chromosomal microarray (CMA) and trio whole exome sequencing (WES), separately and combined, among patients with cryptogenic cerebral palsy (CP). Methods: Trio...
5.
Goldenstein H, Beni Shrem S, Weiss O, Zeligson S, Segel R, Mory A, et al.
Clin Dysmorphol
. 2021 Jul;
30(4):181-185.
PMID: 34232135
No abstract available.
6.
Zeevi D, Backenroth D, Hakam-Spector E, Renbaum P, Mann T, Zahdeh F, et al.
Genet Med
. 2021 Mar;
23(7):1334-1340.
PMID: 33772222
Purpose: We previously developed Haploseek, a method for comprehensive preimplantation genetic testing (PGT). However, some key features were missing, and the method has not yet been systematically validated. Methods: We...
7.
Rotshenker-Olshinka K, Srebnik Moshe N, Weiss O, Shaviv S, Freireich O, Segel R, et al.
J Assist Reprod Genet
. 2021 Jan;
38(3):719-725.
PMID: 33443723
Purpose: To review cases of couples presented to our PGT-unit with copy number variants (CNVs) classified as variants of uncertain significance (VUS) in order to better understand their needs. Methods:...
8.
Pasternak Y, Singer A, Maya I, Sagi-Dain L, Ben-Shachar S, Khayat M, et al.
J Perinat Med
. 2020 Jul;
48(6):553-558.
PMID: 32721143
Objectives: Chromosomal microarray analysis (CMA) is the method of choice for genetic work-up in cases of fetal malformations. We assessed the detection rate of CMA in cases of abnormal fetal...
9.
Segel R, Aran A, Gulsuner S, Nakamura H, Rosen T, Walsh T, et al.
Neurogenetics
. 2020 May;
21(4):259-267.
PMID: 32462292
Deficiency of the endoplasmic reticulum transmembrane protein ARV1 leads to epileptic encephalopathy in humans and in mice. ARV1 is highly conserved, but its function in human cells is unknown. Studies...
10.
Levy-Khademi F, Zeligson S, Lavi E, Klopstock T, Chertin B, Avnon-Ziv C, et al.
Endocrine
. 2020 May;
69(3):650-654.
PMID: 32372306
Purpose: Mutations in the gene HSD17B3 encoding the 17-beta hydroxysteroid dehydrogenase 3 enzyme cause testosterone insufficiency leading to XY disorders of sex development. In this study the clinical and molecular...