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Cdan1 Is Essential for Primitive Erythropoiesis.
Published in:
Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.685242
By:
- Noy-Lotan, Sharon;
- Dgany, Orly;
- Marcoux, Nathaly;
- Atkins, Ayelet;
- Kupfer, Gary M.;
- Bosques, Linette;
- Gottschalk, Christine;
- Steinberg-Shemer, Orna;
- Motro, Benny;
- Tamary, Hannah
Publication type:
Article
Biallelic hypomorphic variants in CAD cause uridine‐responsive macrocytic anaemia with elevated haemoglobin‐A2.
Published in:
British Journal of Haematology, 2024, v. 204, n. 3, p. 1067, doi. 10.1111/bjh.19215
By:
- Steinberg‐Shemer, Orna;
- Yacobovich, Joanne;
- Noy‐Lotan, Sharon;
- Dgany, Orly;
- Krasnov, Tanya;
- Barg, Assaf;
- Landau, Yuval E.;
- Kneller, Katya;
- Somech, Raz;
- Gilad, Oded;
- Brik Simon, Dafna;
- Orenstein, Naama;
- Izraeli, Shai;
- del Caño‐Ochoa, Francisco;
- Tamary, Hannah;
- Ramón‐Maiques, Santiago
Publication type:
Article
Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias.
Published in:
British Journal of Haematology, 2021, v. 193, n. 3, p. 570, doi. 10.1111/bjh.17285
By:
- Noy‐Lotan, Sharon;
- Krasnov, Tanya;
- Dgany, Orly;
- Jeison, Marta;
- Yanir, Asaf D.;
- Gilad, Oded;
- Toledano, Helen;
- Barzilai‐Birenboim, Shlomit;
- Yacobovich, Joanne;
- Izraeli, Shai;
- Tamary, Hannah;
- Steinberg‐Shemer, Orna
Publication type:
Article
Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.
Published in:
European Journal of Haematology, 2024, v. 113, n. 2, p. 146, doi. 10.1111/ejh.14197
By:
- Yeshareem, Lital;
- Yacobovich, Joanne;
- Lebel, Asaf;
- Noy‐Lotan, Sharon;
- Dgany, Orly;
- Krasnov, Tanya;
- Berger Pinto, Galit;
- Oniashvili, Nino;
- Mardoukh, Jacques;
- Bielorai, Bella;
- Laor, Ruth;
- Mandel‐Shorer, Noa;
- Ben Barak, Ayelet;
- Levin, Carina;
- Asleh, Mahdi;
- Miskin, Hagit;
- Revel‐Vilk, Shoshana;
- Levin, Dror;
- Benish, Marganit;
- Zuckerman, Tsila
Publication type:
Article
Characterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I disease.
Published in:
BMC Molecular & Cell Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12860-020-00258-1
By:
- Swickley, Grace;
- Bloch, Yehoshua;
- Malka, Lidor;
- Meiri, Adi;
- Noy-Lotan, Sharon;
- Yanai, Amiel;
- Tamary, Hannah;
- Motro, Benny
Publication type:
Article
Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias.
Published in:
European Journal of Haematology, 2018, v. 101, n. 3, p. 297, doi. 10.1111/ejh.13097
By:
- Shefer Averbuch, Noa;
- Steinberg‐Shemer, Orna;
- Dgany, Orly;
- Krasnov, Tanya;
- Noy‐Lotan, Sharon;
- Yacobovich, Joanne;
- Kuperman, Amir A.;
- Kattamis, Antonis;
- Ben Barak, Ayelet;
- Roth‐Jelinek, Batia;
- Chubar, Evgeni;
- Shabad, Evelyn;
- Dufort, Gustavo;
- Ellis, Martin;
- Wolach, Ofir;
- Pazgal, Idit;
- Abu Quider, Abed;
- Miskin, Hagit;
- Tamary, Hannah
Publication type:
Article
Molecular diagnosis of α-thalassemia in a multiethnic population.
Published in:
European Journal of Haematology, 2017, v. 98, n. 6, p. 553, doi. 10.1111/ejh.12866
By:
- Gilad, Oded;
- Shemer, Orna Steinberg;
- Dgany, Orly;
- Krasnov, Tanya;
- Nevo, Michal;
- Noy ‐ Lotan, Sharon;
- Rabinowicz, Ron;
- Amitai, Nofar;
- Ben ‐ Dor, Shifra;
- Yaniv, Isaac;
- Yacobovich, Joanne;
- Tamary, Hannah
Publication type:
Article
Alpha-Thalassemia Carrier due to –α<sup>3.7</sup> Deletion: Not So Silent.
Published in:
Acta Haematologica, 2020, v. 143, n. 5, p. 432, doi. 10.1159/000503023
By:
- Gilad, Oded;
- Steinberg-Shemer, Orna;
- Dgany, Orly;
- Krasnov, Tanya;
- Noy-Lotan, Sharon;
- Tamary, Hannah;
- Yacobovich, Joanne
Publication type:
Article

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