Zobrazeno 1 - 10
of 46
pro vyhledávání: '"David A, Zeevi"'
Autor:
Daniel Backenroth, Gheona Altarescu, Fouad Zahdeh, Tzvia Mann, Omer Murik, Paul Renbaum, Reeval Segel, Sharon Zeligson, Elinor Hakam-Spector, Shai Carmi, David A. Zeevi
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract 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 m
Externí odkaz:
https://doaj.org/article/69a704d99591414cb15f84c5e26fb2de
Autor:
Mor Rubinstein, Andrei Makhon, Yelena Losev, Gal Zizelski Valenci, Yair E. Gatt, Hanah Margalit, Ephraim Fass, Ina Kutikov, Omer Murik, David A. Zeevi, Michal Savyon, Luba Tau, Hasia Kaidar Shwartz, Zeev Dveyrin, Efrat Rorman, Israel Nissan
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
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 outcome for TB patient
Externí odkaz:
https://doaj.org/article/796d15d07df242cb80b578e11bdb0b03
Autor:
Omer Murik, David A. Zeevi, Tzvia Mann, Livnat Kashat, Marc V. Assous, Orli Megged, Pablo Yagupsky
Publikováno v:
Microbiology Spectrum, Vol 11, Iss 3 (2023)
ABSTRACT 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 asymptomatic oropharyngeal colonization to
Externí odkaz:
https://doaj.org/article/bcaff41474b6493dab7f3d3f6d68dad0
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
Abstract 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 classical Sanger sequence. We aimed to design and validate a method for se
Externí odkaz:
https://doaj.org/article/d6d1074245474c7a9812c07b568074f0
Autor:
David A. Zeevi, Wendy K. Chung, Chaim Levi, Sholem Y. Scher, Rachel Bringer, Yael Kahan, Hagit Muallem, Rinat Benel, Yoel Hirsch, Tzvi Weiden, Ahron Ekstein, Josef Ekstein
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 8, Pp n/a-n/a (2021)
Abstract 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 group of autosomal recessive c
Externí odkaz:
https://doaj.org/article/565f0f112a554ed790fd8cfda85b3719
Autor:
Paul S, Appelbaum, Wylie, Burke, Erik, Parens, David A, Zeevi, Laura, Arbour, Nanibaa' A, Garrison, Vence L, Bonham, Wendy K, Chung
Publikováno v:
Am J Hum Genet
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 findings can frust
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ae7610ac51ab7b5f7f22a2c5da6226a
https://doi.org/10.1016/j.ajhg.2022.04.012
https://doi.org/10.1016/j.ajhg.2022.04.012
Autor:
Rachel Michaelson-Cohen, Omer Murik, Sharon Zeligson, Orit Lobel, Omri Weiss, Elie Picard, Tzvia Mann, Hagar Mor-Shaked, David A. Zeevi, Reeval Segel
Publikováno v:
Molecular Genetics and Genomics. 297:925-933
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 has become apparent that CCRs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13e0c70f97f41c5fca01a72867851d99
https://doi.org/10.1007/s00438-022-01898-y
https://doi.org/10.1007/s00438-022-01898-y
Autor:
Esra Yıldız Bölükbaşı, Justyna A. Karolak, Przemyslaw Szafranski, Tomasz Gambin, Omer Murik, David A. Zeevi, Gheona Altarescu, Paweł Stankiewicz
Publikováno v:
American Journal of Medical Genetics Part A. 188:1420-1425
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61e2d24c90dd824a3aa87d99cda544b5
https://doi.org/10.1002/ajmg.a.62656
https://doi.org/10.1002/ajmg.a.62656
Autor:
Elinor Hakam-Spector, Tzvia Mann, Gheona Altarescu, Shai Carmi, Paul Renbaum, Fouad Zahdeh, Adi Ben-Yehuda, Reeval Segel, David A. Zeevi, Ido Ben-Ami, Daniel Backenroth, Talia Eldar-Geva, Sharon Zeligson
Publikováno v:
Genetics in Medicine. 23:1334-1340
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 extended Haploseek to incorpora
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f16a2f5627410208f0a9dff5b54fd38
https://doi.org/10.1038/s41436-021-01145-6
https://doi.org/10.1038/s41436-021-01145-6
Publikováno v:
J Assist Reprod Genet
PURPOSE: The decision to undergo preimplantation genetic testing (PGT) entails a variety of personal and societal variables. Although PGT technology is widely accepted and used, few studies have queried the motives and concerns of PGT users; moreover
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::def10a83bd4eb7409bdeffae59199679
https://doi.org/10.1007/s10815-020-01840-4
https://doi.org/10.1007/s10815-020-01840-4