How High are Carrier Frequencies of Rare Recessive Syndromes? Contemporary Estimates for Fanconi Anemia in the United States and Israel

by Rosenberg, Philip S., Tamary, Hannah, Alter, Blanche P.
Published 2011

Congenital dyserythropoietic anemias: molecular insights and diagnostic approach

by Iolascon, Achille, Heimpel, Hermann, Wahlin, Anders, Tamary, Hannah
Published 2013

Consensus Paper—ICIS Expert Meeting Basel 2009 treatment milestones in immune thrombocytopenia

by Tamary, Hannah, Roganovic, Jelena, Chitlur, Meera, Nugent, Diane J.
Published 2010

Heparin-Induced Thrombocytopenia and Extracorporeal Membrane Oxygenation: A Case Report and Review of the Literature

by Pollak, Uri, Yacobobich, Joanne, Tamary, Hannah, Dagan, Ovdi, Manor-Shulman, Orit
Published in J Extra Corpor Technol (2011)

Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome

by Marrone, Anna, Walne, Amanda, Tamary, Hannah, Masunari, Yuka, Kirwan, Michael, Beswick, Richard, Vulliamy, Tom, Dokal, Inderjeet
Published 2007

Characterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I disease

by Swickley, Grace, Bloch, Yehoshua, Malka, Lidor, Meiri, Adi, Noy-Lotan, Sharon, Yanai, Amiel, Tamary, Hannah, Motro, Benny
Published in BMC Mol Cell Biol (2020)

Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I

by Tamary, Hannah, Shalev, Hanna, Perez-Avraham, Galit, Zoldan, Meira, Levi, Itai, Swinkels, Dorine W., Tanno, Toshihiko, Miller, Jeffery L.
Published 2008

Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia

by Steinberg-Shemer, Orna, Ulirsch, Jacob C., Noy-Lotan, Sharon, Krasnov, Tanya, Attias, Dina, Dgany, Orly, Laor, Ruth, Sankaran, Vijay G., Tamary, Hannah
Published in Cold Spring Harb Mol Case Stud (2017)

Newly diagnosed immune thrombocytopenia in children and adults: a comparative prospective observational registry of the Intercontinental Cooperative Immune Thrombocytopenia Study G...

by Kühne, Thomas, Berchtold, Willi, Michaels, Lisa A., Wu, Runhui, Donato, Hugo, Espina, Bibiana, Tamary, Hannah, Rodeghiero, Francesco, Chitlur, Meera, Rischewski, Johannes, Imbach, Paul
Published 2011

Cdan1 Is Essential for Primitive Erythropoiesis

by Noy-Lotan, Sharon, Dgany, Orly, Marcoux, Nathaly, Atkins, Ayelet, Kupfer, Gary M., Bosques, Linette, Gottschalk, Christine, Steinberg-Shemer, Orna, Motro, Benny, Tamary, Hannah
Published in Front Physiol (2021)

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

by Russo, Roberta, Gambale, Antonella, Esposito, Maria Rosaria, Serra, Maria Luisa, Troiano, Annaelena, De Maggio, Ilaria, Capasso, Mario, Luzzatto, Lucio, Delaunay, Jean, Tamary, Hannah, Iolascon, Achille
Published 2011

Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1

by Seo, Aaron, Steinberg-Shemer, Orna, Unal, Sule, Casadei, Silvia, Walsh, Tom, Gumruk, Fatma, Shalev, Stavit, Shimamura, Akiko, Akarsu, Nurten Ayse, Tamary, Hannah, King, Mary-Claire
Published in Proc Natl Acad Sci U S A (2018)

Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated

by Noy-Lotan, Sharon, Dgany, Orly, Lahmi, Roxane, Marcoux, Nathaly, Krasnov, Tanya, Yissachar, Nissan, Ginsberg, Doron, Motro, Benny, Resnitzky, Peretz, Yaniv, Isaac, Kupfer, Gary M., Tamary, Hannah
Published 2009

Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)

by Seo, Aaron, Gulsuner, Suleyman, Pierce, Sarah, Ben-Harosh, Miri, Shalev, Hanna, Walsh, Tom, Krasnov, Tanya, Dgany, Orly, Doulatov, Sergei, Tamary, Hannah, Shimamura, Akiko, King, Mary-Claire
Published in Hum Mol Genet (2019)

Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis

by Steinberg-Shemer, Orna, Keel, Siobán, Dgany, Orly, Walsh, Tom, Noy-Lotan, Sharon, Krasnov, Tanya, Yacobovich, Joanne, Quarello, Paola, Ramenghi, Ugo, King, Mary-Claire, Shimamura, Akiko, Tamary, Hannah
Published in J Pediatr Hematol Oncol (2016)

Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition

by Grabowski, Piotr, Hesse, Sebastian, Hollizeck, Sebastian, Rohlfs, Meino, Behrends, Uta, Sherkat, Roya, Tamary, Hannah, Ünal, Ekrem, Somech, Raz, Patıroğlu, Türkan, Canzar, Stefan, van der Werff Ten Bosch, Jutte, Klein, Christoph, Rappsilber, Juri
Published in Mol Cell Proteomics (2019)

Triallelic and epigenetic-like inheritance in human disorders of telomerase

by Collopy, Laura C., Walne, Amanda J., Cardoso, Shirleny, de la Fuente, Josu, Mohamed, Mahfuzah, Toriello, Helga, Tamary, Hannah, Ling, Adam J. Y. V., Lloyd, Timothy, Kassam, Rebecca, Tummala, Hemanth, Vulliamy, Thomas J., Dokal, Inderjeet
Published in Blood (2015)

Effects of eltrombopag on platelet count and platelet activation in Wiskott-Aldrich syndrome/X-linked thrombocytopenia

by Gerrits, Anja J., Leven, Emily A., Frelinger, Andrew L., Brigstocke, Sophie L., Berny-Lang, Michelle A., Mitchell, W. Beau, Revel-Vilk, Shoshana, Tamary, Hannah, Carmichael, Sabrina L., Barnard, Marc R., Michelson, Alan D., Bussel, James B.
Published in Blood (2015)

Outcome and management of pregnancies in severe chronic neutropenia patients by the European Branch of the Severe Chronic Neutropenia International Registry

by Zeidler, Cornelia, Grote, Ulrike A.H., Nickel, Anna, Brand, Beate, Carlsson, Göran, Cortesão, Emília, Dufour, Carlo, Duhem, Caroline, Notheis, Gundula, Papadaki, Helen A., Tamary, Hannah, Tjønnfjord, Geir E., Tucci, Fabio, Van Droogenbroeck, Jan, Vermylen, Christiane, Voglova, Jaroslava, Xicoy, Blanca, Welte, Karl
Published 2014

Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population

by Steinberg-Shemer, Orna, Goldberg, Tracie A., Yacobovich, Joanne, Levin, Carina, Koren, Ariel, Revel-Vilk, Shoshana, Ben-Ami, Tal, Kuperman, Amir A., Zemer, Vered Shkalim, Toren, Amos, Kapelushnik, Joseph, Ben-Barak, Ayelet, Miskin, Hagit, Krasnov, Tanya, Noy-Lotan, Sharon, Dgany, Orly, Tamary, Hannah
Published in Haematologica (2020)