Publications by authors named "David A Zeevi"

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Genomic features and alkane-metabolism profiles of three new Alcanivoracaceae bacteria isolates from the Eastern Mediterranean Sea.
Sheli Shlomo Itzahri, Aiswarya Kartha, Keren Davidov, Meti Gizaw Dhiba, Omer Murik, David A Zeevi

Mar Pollut Bull· December 2025

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Prolonged survival of a patient with active MDR-TB HIV co-morbidity: insights from a strain with a unique genomic deletion.
Mor Rubinstein, Andrei Makhon, Yelena Losev, Gal Zizelski Valenci, Yair E Gatt, David A Zeevi

Front Med (Lausanne)· November 2023

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SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testing.
Daniel Backenroth, Gheona Altarescu, Fouad Zahdeh, Tzvia Mann, Omer Murik, David A Zeevi

Sci Rep· October 2023

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Whole-Genome Sequencing Reveals Differences among Kingella kingae Strains from Carriers and Patients with Invasive Infections.
Omer Murik, David A Zeevi, Tzvia Mann, Livnat Kashat, Marc V Assous

Microbiol Spectr· June 2023

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Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangements.
Rachel Michaelson-Cohen, Omer Murik, Sharon Zeligson, Orit Lobel, Omri Weiss, David A Zeevi

Mol Genet Genomics· July 2022

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Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?
Paul S Appelbaum, Wylie Burke, Erik Parens, David A Zeevi, Laura Arbour

Am J Hum Genet· June 2022

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Exacerbation of mild lung disorders to lethal pulmonary hypoplasia by a noncoding hypomorphic SNV in a lung-specific enhancer in trans to the frameshifting TBX4 variant.
Esra Yıldız Bölükbaşı, Justyna A Karolak, Przemyslaw Szafranski, Tomasz Gambin, Omer Murik, David A Zeevi

Am J Med Genet A· May 2022

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Detection of single nucleotide and copy number variants in the Fabry disease-associated GLA gene using nanopore sequencing.
Albina Nowak, Omer Murik, Tzvia Mann, David A Zeevi, Gheona Altarescu

Sci Rep· November 2021

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Recommendation of premarital genetic screening in the Syrian Jewish community based on mutation carrier frequencies within Syrian Jewish cohorts.
David A Zeevi, Wendy K Chung, Chaim Levi, Sholem Y Scher, Rachel Bringer

Mol Genet Genomic Med· August 2021

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Expanded clinical validation of Haploseek for comprehensive preimplantation genetic testing.
David A Zeevi, Daniel Backenroth, Elinor Hakam-Spector, Paul Renbaum, Tzvia Mann

Genet Med· July 2021

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The utility of MALDI-TOF MS for outbreak investigation in the neonatal intensive care unit.
Maskit Bar-Meir, Elihay Berliner, Livnat Kashat, David A Zeevi, Marc V Assous

Eur J Pediatr· December 2020

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When a Root Is the Cause of Infection.
Eli Ben-Chetrit, Marc V Assous, Yonit Wiener-Well, David E Katz, Livnat Kashat, David A Zeevi

World Neurosurg· December 2020

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The decision-making process, experience, and perceptions of preimplantation genetic testing (PGT) users.
Shachar Zuckerman, Sigal Gooldin, David A Zeevi, Gheona Altarescu

J Assist Reprod Genet· August 2020

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Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities.
Alison M Muir, Jennifer L Cohen, Sarah E Sheppard, Pavithran Guttipatti, Tsz Y Lo, David A Zeevi

Am J Hum Genet· May 2020

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A Cluster of Bacillus cereus Infections in the Neonatal Intensive Care Unit: Epidemiologic and Whole-genome Sequencing Analysis.
Maskit Bar-Meir, Livnat Kashat, David A Zeevi, Yonit Wiener Well, Marc V Assous

Pediatr Infect Dis J· November 2019

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Study of carrier frequency of Warsaw breakage syndrome in the Ashkenazi Jewish population and presentation of two cases.
Rachel Rabin, Yoel Hirsch, Martin M Johansson, Joseph Ekstein, David A Zeevi

Am J Med Genet A· October 2019

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A founder deletion in the gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews.
Yoel Hirsch, David A Zeevi, Byron L Lam, Sholem Y Scher, Rachel Bringer

Hum Genome Var· September 2019

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Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy.
Daniel Backenroth, Fouad Zahdeh, Yehuda Kling, Aharon Peretz, Tzvia Rosen, David A Zeevi

Genet Med· June 2019

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Off the street phasing (OTSP): no hassle haplotype phasing for molecular PGD applications.
David A Zeevi, Fouad Zahdeh, Yehuda Kling, Shai Carmi, Gheona Altarescu

J Assist Reprod Genet· April 2019

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Noninvasive paternal exclusion testing for cystic fibrosis in the first five to eight weeks of gestation.
David A Zeevi, Fouad Zahdeh, Yehuda Kling, Tzvia Rosen, Paul Renbaum

Sci Rep· October 2018

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Acceptable applications of preimplantation genetic diagnosis (PGD) among Israeli PGD users.
Shachar Zuckerman, David A Zeevi, Sigal Gooldin, Gheona Altarescu

Eur J Hum Genet· October 2017

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TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair.
Inbal Gazy, David A Zeevi, Paul Renbaum, Sharon Zeligson, Lital Eini

PLoS One· May 2016

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Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations.
David A Zeevi, Gheona Altarescu, Ariella Weinberg-Shukron, Fouad Zahdeh, Tama Dinur

J Clin Invest· October 2015

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An intronic haplotype in α galactosidase A is associated with reduced mRNA expression in males with cryptogenic stroke.
David A Zeevi, Elinor Hakam-Spector, Yair Herskovitz, Rachel Beeri, Deborah Elstein

Gene· October 2014

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Preimplantation genetic diagnosis in genomic regions with duplications and pseudogenes: long-range PCR in the single-cell assay.
David A Zeevi, Paul Renbaum, Raphael Ron-El, Talia Eldar-Geva, Arieh Raziel

Hum Mutat· May 2013

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