David A Zeevi
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Explore the profile of David A Zeevi including associated specialties, affiliations and a list of published articles.
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29
Citations
295
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Recent Articles
1.
Rubinstein M, Makhon A, Losev Y, Valenci G, Gatt Y, Margalit H, et al.
Front Med (Lausanne)
. 2023 Nov;
10:1292665.
PMID: 38020140
Coinfection of HIV and multidrug-resistant tuberculosis (MDR-TB) presents significant challenges in terms of the treatment and prognosis of tuberculosis, leading to complexities in managing the disease and impacting the overall...
2.
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...
3.
Murik O, Zeevi D, Mann T, Kashat L, Assous M, Megged O, et al.
Microbiol Spectr
. 2023 May;
11(3):e0389522.
PMID: 37195188
As a result of the increasing use of sensitive nucleic acid amplification tests, Kingella kingae is being recognized as a common pathogen of early childhood, causing medical conditions ranging from...
4.
Appelbaum P, Burke W, Parens E, Zeevi D, Arbour L, Garrison N, et al.
Am J Hum Genet
. 2022 Jun;
109(6):981-988.
PMID: 35659933
The underrepresentation of non-European ancestry groups in current genomic databases complicates interpretation of their genetic test results, yielding a much higher prevalence of variants of uncertain significance (VUSs). Such VUS...
5.
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...
6.
Yildiz Bolukbasi E, Karolak J, Szafranski P, Gambin T, Murik O, Zeevi D, et al.
Am J Med Genet A
. 2022 Jan;
188(5):1420-1425.
PMID: 35075769
Variants involving TBX4 are associated with a wide variety of disorders, including pulmonary arterial hypertension, ischiocoxopodopatellar syndrome (ICPPS)/small patella syndrome (SPS), lethal lung developmental disorders (LLDDs) in neonates, heart defects,...
7.
Nowak A, Murik O, Mann T, Zeevi D, Altarescu G
Sci Rep
. 2021 Nov;
11(1):22372.
PMID: 34785703
More than 900 variants have been described in the GLA gene. Some intronic variants and copy number variants in GLA can cause Fabry disease but will not be detected by...
8.
Zeevi D, Chung W, Levi C, Scher S, Bringer R, Kahan Y, et al.
Mol Genet Genomic Med
. 2021 Jul;
9(8):e1756.
PMID: 34288589
Background: There is a paucity of information available regarding the carrier frequency for autosomal recessive pathogenic variants among Syrian Jews. This report provides data to support carrier screening for a...
9.
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...
10.
Ben-Chetrit E, Assous M, Wiener-Well Y, Katz D, Kashat L, Zeevi D, et al.
World Neurosurg
. 2020 Sep;
144:258-261.e1.
PMID: 32889191
Background: Sinorhizobium meliloti is a phytobacterium found in the root nodules of plants, where it is involved in fixing nitrogen for delivery to the roots in exchange for a photosynthate...