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Year Number of Results
2009 1
2014 1
2016 1
2017 2
2018 1
2019 1
2020 4
2021 3
2022 3
2023 1
2024 2

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17 results

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Page 1
Cdan1 Is Essential for Primitive Erythropoiesis.
Noy-Lotan S, Dgany O, Marcoux N, Atkins A, Kupfer GM, Bosques L, Gottschalk C, Steinberg-Shemer O, Motro B, Tamary H. Noy-Lotan S, et al. Front Physiol. 2021 Jun 21;12:685242. doi: 10.3389/fphys.2021.685242. eCollection 2021. Front Physiol. 2021. PMID: 34234691 Free PMC article.
Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children.
Gilad O, Dgany O, Noy-Lotan S, Krasnov T, Yacobovich J, Rabinowicz R, Goldberg T, Kuperman AA, Abu-Quider A, Miskin H, Kapelushnik N, Mandel-Shorer N, Shimony S, Harlev D, Ben-Ami T, Adam E, Levin C, Aviner S, Elhasid R, Berger-Achituv S, Chaitman-Yerushalmi L, Kodman Y, Oniashvilli N, Hameiri-Grosman M, Izraeli S, Tamary H, Steinberg-Shemer O. Gilad O, et al. Among authors: noy lotan s. Haematologica. 2022 Sep 1;107(9):2081-2095. doi: 10.3324/haematol.2021.280116. Haematologica. 2022. PMID: 35295078 Free PMC article.
ETV6-NCOA2 fusion induces T/myeloid mixed-phenotype leukemia through transformation of nonthymic hematopoietic progenitor cells.
Fishman H, Madiwale S, Geron I, Bari V, Van Loocke W, Kirschenbaum Y, Ganmore I, Kugler E, Rein-Gil A, Friedlander G, Schiby G, Birger Y, Strehl S, Soulier J, Knoechel B, Ferrando A, Noy-Lotan S, Nagler A, Mulloy JC, Van Vlierberghe P, Izraeli S. Fishman H, et al. Among authors: noy lotan s. Blood. 2022 Jan 20;139(3):399-412. doi: 10.1182/blood.2020010405. Blood. 2022. PMID: 34624096 Free PMC article.
Molecular diagnosis of α-thalassemia in a multiethnic population.
Gilad O, Shemer OS, Dgany O, Krasnov T, Nevo M, Noy-Lotan S, Rabinowicz R, Amitai N, Ben-Dor S, Yaniv I, Yacobovich J, Tamary H. Gilad O, et al. Among authors: noy lotan s. Eur J Haematol. 2017 Jun;98(6):553-562. doi: 10.1111/ejh.12866. Epub 2017 Apr 6. Eur J Haematol. 2017. PMID: 28160324
Alpha-Thalassemia Carrier due to -α3.7 Deletion: Not So Silent.
Gilad O, Steinberg-Shemer O, Dgany O, Krasnov T, Noy-Lotan S, Tamary H, Yacobovich J. Gilad O, et al. Among authors: noy lotan s. Acta Haematol. 2020;143(5):432-437. doi: 10.1159/000503023. Epub 2020 Jan 14. Acta Haematol. 2020. PMID: 31935715
Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population.
Steinberg-Shemer O, Goldberg TA, Yacobovich J, Levin C, Koren A, Revel-Vilk S, Ben-Ami T, Kuperman AA, Zemer VS, Toren A, Kapelushnik J, Ben-Barak A, Miskin H, Krasnov T, Noy-Lotan S, Dgany O, Tamary H. Steinberg-Shemer O, et al. Among authors: noy lotan s. Haematologica. 2020 Jul;105(7):1825-1834. doi: 10.3324/haematol.2019.222877. Epub 2019 Sep 26. Haematologica. 2020. PMID: 31558676 Free PMC article.
Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.
Yeshareem L, Yacobovich J, Lebel A, Noy-Lotan S, Dgany O, Krasnov T, Berger Pinto G, Oniashvili N, Mardoukh J, Bielorai B, Laor R, Mandel-Shorer N, Ben Barak A, Levin C, Asleh M, Miskin H, Revel-Vilk S, Levin D, Benish M, Zuckerman T, Wolach O, Pazgal I, Brik Simon D, Gilad O, Yanir AD, Goldberg TA, Izraeli S, Tamary H, Steinberg-Shemer O. Yeshareem L, et al. Among authors: noy lotan s. Eur J Haematol. 2024 Apr 11. doi: 10.1111/ejh.14197. Online ahead of print. Eur J Haematol. 2024. PMID: 38600884
Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2.
Steinberg-Shemer O, Yacobovich J, Noy-Lotan S, Dgany O, Krasnov T, Barg A, Landau YE, Kneller K, Somech R, Gilad O, Brik Simon D, Orenstein N, Izraeli S, Del Caño-Ochoa F, Tamary H, Ramón-Maiques S. Steinberg-Shemer O, et al. Among authors: noy lotan s. Br J Haematol. 2024 Mar;204(3):1067-1071. doi: 10.1111/bjh.19215. Epub 2023 Nov 20. Br J Haematol. 2024. PMID: 37984840
Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome.
Yanir AD, Krauss A, Stein J, Steinberg-Shemer O, Gilad O, Lotan SN, Dgany O, Krasnov T, Kodman Y, Feuerstein T, Mardoukh J, Fishman H, Geron I, Yacobovich J, Tamary H, Birger Y, Avrahami G, Izraeli S, Birenboim SB. Yanir AD, et al. Among authors: lotan sn. Pediatr Blood Cancer. 2021 Oct;68(10):e29138. doi: 10.1002/pbc.29138. Epub 2021 May 21. Pediatr Blood Cancer. 2021. PMID: 34019335
Congenital thrombocytopenia associated with a heterozygous variant in the MEIS1 gene encoding a transcription factor essential for megakaryopoiesis.
Steinberg-Shemer O, Orenstein N, Krasnov T, Noy-Lotan S, Marcoux N, Dgany O, Yacobovich J, Gilad O, Shabad E, Basel-Salmon L, Tamary H. Steinberg-Shemer O, et al. Among authors: noy lotan s. Platelets. 2022 May 19;33(4):645-648. doi: 10.1080/09537104.2021.1961704. Epub 2022 Feb 8. Platelets. 2022. PMID: 35130804
17 results