פרופ' חנה תמרי

Noy-Lotan S, Dgany O, Lahmi R, Marcoux N, Krasnov T, Yissachar N, Ginsberg D, Motro B, Resnitzky P, Yaniv I, Kupfer GM, Tamary H
Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated.
Haematologica. 94:629-37, 2009 If 6.461

Crétien A, Proust A, Delaunay J, Rincé P, Leblanc T, Ducrocq R, Simansour M, Marie I, Tamary H, Meerpohl J, Niemeyer C, Gazda H, Sieff C, Ball S, Tchernia G, Mohandas N, Da Costa L.
Genetic variants in the noncoding region of RPS19 gene in Diamond-Blackfan anemia: Potential implications for phenotypic heterogeneity.
Am J Hematol. 85:111-6, 2010 IF-2.61

Malcov M, Reches A, Ben-Yosef D, Cohen T, Amit A, Dgany O, Tamary H, Yaron Y
Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia.
Prenat Diagn. 30(3):207-11, 2010. IF-1.707

Tamary H, Nishri D, Yacobovich J, Zilber R, Dgany O, Krasnov T, Aviner S, Stepensky P, Ravel-Vilk S, Bitan M, Kaplinsky C, Ben Barak A, Elhasid R, Kapelusnik J, Koren A, Levin C, Attias D, Laor R, Yaniv I, Rosenberg PS, Alter BP
Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry.
Haematologica. 95:1300-7, 2010 IF- 6.461

Arnaud L, Saison C, Helias V, Lucien N, Steschenko D, Giarratana MC, Prehu C, Foliguet B, Montout L, de Brevern AG, Francina A, Ripoche P, Fenneteau O, Da Costa L, Peyrard T, Coghlan G, Illum N, Birgens H, Tamary H, Iolascon A, Delaunay J, Tchernia G, Cartron JP.
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia
Am J Hum Genet. 12:87:721-7, 2010. IF-12.303

Amir A, Dgany O,  Krasnov T, Resnitzky P, Mor-Cohen R, Bennett M Berrebi A, Tamary H
E109K is a SEC23B Founder Mutation Among Israeli Moroccan Jewish Patients With Congenital Dyserythropoietic Anemia Type II
Acta Haematologica 2011 125:202-207, 2011 IF-1.069

Rosenberg PS, Tamary H, Alter BP

How high are carrier frequencies of rare recessive syndromes? Contemporary estimates for Fanconi Anemia in the United States and Israel

Am J Med Genet A. 155A(8):1877-83,  2011

Russo R, Gambale A, Esposito MR, Serra ML, Troiano A, De Maggio I, Capasso M, Luzzatto L, Delaunay J, Tamary H, Iolascon A. Russo R, Gambale A, Esposito MR, Serra ML, Troiano A, De Maggio I, Capasso M, Luzzatto L, Delaunay J, Tamary H, Iolascon A.

Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population

Am J Hematol86(9):727-32, 2011.

2010-2013

Congenital neutropenia with ELA-2 mutations: identification of genetic co-factors and molecular underlying clinical heterogeneity- European Research Projects on Rare diseases.

2010-2014

Binational Science Foundation (BSF) Grant for Analysis of congenital dyserythropoietic anemia (CDA) through creation and manipulation of patient-derived induced pluripotent stem cells (iPSCs)