Acceptable applications of preimplantation genetic diagnosis (PGD) among Israeli PGD users

द्वारा Zuckerman, Shachar, Zeevi, David A, Gooldin, Sigal, Altarescu, Gheona
में प्रकाशित Eur J Hum Genet (2017)

The decision-making process, experience, and perceptions of preimplantation genetic testing (PGT) users

द्वारा Zuckerman, Shachar, Gooldin, Sigal, Zeevi, David A., Altarescu, Gheona
में प्रकाशित J Assist Reprod Genet (2020)

Heteromultimeric TRPML channel assemblies play a crucial role in the regulation of cell viability models and starvation-induced autophagy

द्वारा Zeevi, David A., Lev, Shaya, Frumkin, Ayala, Minke, Baruch, Bach, Gideon
प्रकाशित 2010

Off the street phasing (OTSP): no hassle haplotype phasing for molecular PGD applications

द्वारा Zeevi, David A., Zahdeh, Fouad, Kling, Yehuda, Carmi, Shai, Altarescu, Gheona
में प्रकाशित J Assist Reprod Genet (2019)

The utility of MALDI-TOF MS for outbreak investigation in the neonatal intensive care unit

द्वारा Bar-Meir, Maskit, Berliner, Elihay, Kashat, Livnat, Zeevi, David A., Assous, Marc V.
में प्रकाशित Eur J Pediatr (2020)

Constitutive Activity of the Human TRPML2 Channel Induces Cell Degeneration

द्वारा Lev, Shaya, Zeevi, David A., Frumkin, Ayala, Offen-Glasner, Vered, Bach, Gideon, Minke, Baruch
प्रकाशित 2010

TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair

द्वारा Gazy, Inbal, Zeevi, David A., Renbaum, Paul, Zeligson, Sharon, Eini, Lital, Bashari, Dana, Smith, Yoav, Lahad, Amnon, Goldberg, Michal, Ginsberg, Doron, Levy-Lahad, Ephrat
में प्रकाशित PLoS One (2015)

Noninvasive paternal exclusion testing for cystic fibrosis in the first five to eight weeks of gestation

द्वारा Zeevi, David A., Zahdeh, Fouad, Kling, Yehuda, Rosen, Tzvia, Renbaum, Paul, Ron-El, Raphael, Eldar-Geva, Talia, Holzer, Hananel E. G., Levy-Lahad, Ephrat, Altarescu, Gheona
में प्रकाशित Sci Rep (2018)

Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations

द्वारा Zeevi, David A., Altarescu, Gheona, Weinberg-Shukron, Ariella, Zahdeh, Fouad, Dinur, Tama, Chicco, Gaya, Herskovitz, Yair, Renbaum, Paul, Elstein, Deborah, Levy-Lahad, Ephrat, Rolfs, Arndt, Zimran, Ari
में प्रकाशित J Clin Invest (2015)

A founder deletion in the TRPM1 gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews

द्वारा Hirsch, Yoel, Zeevi, David A., Lam, Byron L., Scher, Sholem Y., Bringer, Rachel, Cherki, Bitya, Cohen, Cadina C., Muallem, Hagit, Chiang, John (Pei-Wen), Pantrangi, Madhulatha, Ekstein, Josef, Johansson, Martin M.
में प्रकाशित Hum Genome Var (2019)

Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities

द्वारा Muir, Alison M., Cohen, Jennifer L., Sheppard, Sarah E., Guttipatti, Pavithran, Lo, Tsz Y., Weed, Natalie, Doherty, Dan, DeMarzo, Danielle, Fagerberg, Christina R., Kjærsgaard, Lars, Larsen, Martin J., Rump, Patrick, Löhner, Katharina, Hirsch, Yoel, Zeevi, David A., Zackai, Elaine H., Bhoj, Elizabeth, Song, Yuanquan, Mefford, Heather C.
में प्रकाशित Am J Hum Genet (2020)