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| Deterministic direct reprogramming of somatic cells to pluripotency Y Rais, A Zviran, S Geula, O Gafni, E Chomsky, S Viukov, AAF Mansour, ... Nature 502 (7469), 65, 2013 | 647 | 2013 |
| Context-dependent functional compensation between Ythdf m6A reader proteins L Lasman, V Krupalnik, S Viukov, N Mor, A Aguilera-Castrejon, D Schneir, ... Genes & Development, 2020 | 192 | 2020 |
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| Human non-olfactory cognition phase-locked with inhalation O Perl, A Ravia, M Rubinson, A Eisen, T Soroka, N Mor, L Secundo, ... Nature Human Behaviour, 1, 2019 | 131 | 2019 |
| Principles of signaling pathway modulation for enhancing human naive pluripotency induction J Bayerl, M Ayyash, T Shani, YS Manor, O Gafni, R Massarwa, Y Kalma, ... Cell Stem Cell, 2021 | 88 | 2021 |
| Neutralizing Gatad2a-Chd4-Mbd3/NuRD Complex Facilitates Deterministic Induction of Naive Pluripotency N Mor, Y Rais, D Sheban, S Peles, A Aguilera-Castrejon, A Zviran, ... Cell stem cell 23 (3), 412-425. e10, 2018 | 71 | 2018 |
| Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder A Lossos, N Elazar, I Lerer, O Schueler-Furman, Y Fellig, B Glick, ... Brain 138 (9), 2521-2536, 2015 | 53 | 2015 |
| Deterministic Somatic Cell Reprogramming Involves Continuous Transcriptional Changes Governed by Myc and Epigenetic-Driven Modules A Zviran, N Mor, Y Rais, H Gingold, S Peles, E Chomsky, S Viukov, ... Cell stem cell 24 (2), 328-341. e9, 2019 | 50 | 2019 |
| SUMOylation of linker histone H1 drives chromatin condensation and restriction of embryonic cell fate identity D Sheban, T Shani, R Maor, A Aguilera-Castrejon, N Mor, B Oldak, ... Molecular Cell, 2021 | 21 | 2021 |
| A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies B Pode-Shakked, O Barel, A Singer, M Regev, H Poran, A Eliyahu, ... Scientific Reports 11 (1), 1-8, 2021 | 13 | 2021 |
| A multidisciplinary nephrogenetic referral clinic for children and adults—diagnostic achievements and insights B Pode-Shakked, Y Ben-Moshe, O Barel, LC Regev, M Kagan, A Eliyahu, ... Pediatric Nephrology, 1-24, 2022 | 11 | 2022 |
| A multiplexed screening method for pluripotency A Plotnikov, N Kozer, V Krupalnik, S Peles, N Mor, Y Rais, JH Hanna, ... Stem cell research 23, 158-162, 2017 | 8 | 2017 |
| Tripartite Inhibition of SRC-WNT-PKC Signalling Consolidates Human Naïve Pluripotency J Bayerl, M Ayyash, T Shani, Y Manor, O Gafni, Y Kalma, ... bioRxiv, 2020 | 6 | 2020 |
| Mbd3/NuRD is a Key Inhibitory Module During the Induction and Maintenance of Naïve Pluripotency A Zviran, Y Rais, N Mor, N Novershtern, JH Hanna bioRxiv, 013961, 2015 | 5 | 2015 |
| GATA2 Deficiency in Adult Life Is Characterized by Phenotypic Diversity and Delayed Diagnosis O Shamriz, N Zahalka, AJ Simon, A Lev, O Barel, N Mor, Y Tal, MJ Segel, ... Frontiers in Immunology, 2105, 0 | 3 | |
| Adult-onset Alexander disease among patients of Jewish Syrian descent S Anis, T Fay-Karmon, S Lassman, F Shbat, O Lesman-Segev, N Mor, ... neurogenetics, 1-8, 2023 | 1 | 2023 |
| Intellectual disability syndrome associated with a homozygous founder variant in SGSM3 in Ashkenazi Jews R Birnbaum, S Ezer, NS Lotan, A Eilat, K Sternlicht, L Benyamini, O Reish, ... Journal of Medical Genetics, 2023 | | 2023 |
| Diagnostic utility of exome sequencing among Israeli children with kidney failure YB Moshe, O Shlomovitz, D Atias-Varon, O Haskin, E Ben-Shalom, ... Kidney International Reports, 2023 | | 2023 |
