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Plos One|August 1, 2015
TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) RepairInbal Gazy, David A Zeevi, Paul Renbaum, et al.
Molecular Biology International|January 16, 2013
Prevention of lysosomal storage diseases and derivation of mutant stem cell lines by preimplantation genetic diagnosisGheona Altarescu, Rachel Beeri, Rachel Eiges, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 23, 2015
The spinal muscular atrophy with pontocerebellar hypoplasia gene VRK1 regulates neuronal migration through an amyloid-β precursor protein-dependent mechanismHadar Vinograd-Byk, Tamar Sapir, Lara Cantarero, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 18, 2015
Rac1 Polymorphisms and Thiopurine Efficacy in Children With Inflammatory Bowel DiseaseRaffi Lev-Tzion, Paul Renbaum, Rachel Beeri, et al.
Plos One|October 17, 2015
Establishment of Homozygote Mutant Human Embryonic Stem Cells by ParthenogenesisSilvina Epsztejn-Litman, Yaara Cohen-Hadad, Shira Aharoni, et al.
Human Mutation|February 20, 2013
Preimplantation genetic diagnosis in genomic regions with duplications and pseudogenes: long-range PCR in the single-cell assayDavid A Zeevi, Paul Renbaum, Raphael Ron-El, et al.
Scientific Reports|October 21, 2023
SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testingDaniel Backenroth, Gheona Altarescu, Fouad Zahdeh, et al.
European Journal of Endocrinology|September 23, 2023
Loss of function of FIGNL1, a DNA damage response gene, causes human ovarian dysgenesisNatan Florsheim, Larisa Naugolni, Fouad Zahdeh, et al.
Obstetrics and Gynecology|January 25, 2012
Preimplantation genetic diagnosis for fetal neonatal alloimmune thrombocytopenia due to antihuman platelet antigen maternal antibodiesGheona Altarescu, T Eldar-Geva, T Eldar Geva, et al.
Journal of Medical Genetics|June 14, 2015
Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stressAriella Weinberg-Shukron, Abdulsalam Abu-Libdeh, Fouad Zhadeh, et al.
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