Shay Ben Shachar
Overview
Explore the profile of Shay Ben Shachar including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
84
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Recent Articles
1.
Michaeli O, Ladany H, Erez A, Ben Shachar S, Izraeli S, Lidzbarsky G, et al.
Clin Genet
. 2021 Dec;
101(4):442-447.
PMID: 34967012
Polymerase proofreading-associated polyposis (PPAP) and Lynch syndrome, caused by mutated POLE and mismatch repair (MMR) genes, respectively, are associated with adult-onset cancer. PPAP and MMR-deficient tumors are both hypermutated, and...
2.
Ben Shachar S, Barda N, Manor S, Israeli S, Dagan N, Carmi S, et al.
J Clin Immunol
. 2021 May;
41(6):1154-1161.
PMID: 34050837
HLA haplotypes were found to be associated with increased risk for viral infections or disease severity in various diseases, including SARS. Several genetic variants are associated with COVID-19 severity. Studies...
3.
Sagi-Dain L, Singer A, Falik-Zaccai T, Peleg A, Bar-Shira A, Feingold-Zadok M, et al.
Arch Gynecol Obstet
. 2021 Feb;
304(3):649-656.
PMID: 33591382
Purpose: To analyze the risk for clinically significant microarray aberrations in pregnancies with polyhydramnios. Methods: Data from all chromosomal microarray analyses (CMA) performed due to polyhydramnios between January 2013 and...
4.
Sagi-Dain L, Singer A, Ben Shachar S, Josefsberg Ben Yehoshua S, Feingold-Zadok M, Greenbaum L, et al.
Obstet Gynecol
. 2020 Dec;
137(1):126-131.
PMID: 33278279
Objective: To examine the risk of clinically significant chromosomal microarray analysis findings in fetuses with nuchal translucency from 3.0-3.4 mm. In addition, we aimed to define the yield of noninvasive...
5.
Singer A, Maya I, Banne E, Feldman H, Vinkler C, Ben Shachar S, et al.
Early Hum Dev
. 2020 Apr;
145:105047.
PMID: 32339917
Objective: To examine the detection rate of clinically significant chromosomal microarray analysis (CMA) results in singleton pregnancies with clubfoot. Methods: Data from all CMA tests in singleton pregnancies with sonographic...
6.
Singer A, Maya I, Sukenik-Halevy R, Tenne T, Lev D, Ben Shachar S, et al.
J Perinat Med
. 2019 Dec;
48(1):53-58.
PMID: 31811807
Objective To explore the risk for abnormal chromosomal microarray analysis (CMA) findings in pregnancies with oligohydramnios. Methods Data from all CMA analyses performed due to oligohydramnios between 2013 and 2017...
7.
Maya I, Singer A, Yonath H, Reches A, Rienstein S, Zeligson S, et al.
Acta Obstet Gynecol Scand
. 2019 Aug;
99(6):757-764.
PMID: 31424084
Introduction: Ventricular septal defect (VSD) represents the most common type of congenital cardiac anomaly, affecting more than 1 in 300 live births. The objective of this study was to examine...
8.
Singer A, Maya I, Frumkin A, Zeligson S, Josefsberg S, Berger R, et al.
J Matern Fetal Neonatal Med
. 2019 Apr;
34(5):696-700.
PMID: 31032679
Duplication of the renal collecting system is one of the most common variants of urinary tract anatomy. The objective of our study was to examine the risk for chromosomal aberrations...
9.
Sagi-Dain L, Singer A, Frumkin A, Shalata A, Koifman A, Segel R, et al.
J Perinat Med
. 2018 May;
47(1):30-34.
PMID: 29813032
Objective To examine the risk for abnormal chromosomal microarray analysis (CMA) results among fetuses with an apparently isolated pelvic kidney. Methods Data from all CMA analyses performed due to an...
10.
Singer A, Maya I, Koifman A, Samra N, Baris H, Falik-Zaccai T, et al.
Early Hum Dev
. 2018 Mar;
119:25-28.
PMID: 29522884
Introduction: Fetal echogenic bowel is a frequent sonographic finding, demonstrated in about 1% of pregnancies. The advised evaluation of fetal echogenic bowel includes maternal serology, genetic testing for cystic fibrosis,...