Orly Dgany

1.3k total citations
39 papers, 511 citations indexed

About

Orly Dgany is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Orly Dgany has authored 39 papers receiving a total of 511 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Hematology, 14 papers in Molecular Biology and 14 papers in Genetics. Recurrent topics in Orly Dgany's work include Erythrocyte Function and Pathophysiology (13 papers), Hemoglobinopathies and Related Disorders (11 papers) and Blood groups and transfusion (9 papers). Orly Dgany is often cited by papers focused on Erythrocyte Function and Pathophysiology (13 papers), Hemoglobinopathies and Related Disorders (11 papers) and Blood groups and transfusion (9 papers). Orly Dgany collaborates with scholars based in Israel, United States and France. Orly Dgany's co-authors include Hannah Tamary, Tatyana Krasnov, Ron Wides, Joanne Yacobovich, Ariel Koren, Joseph Kapelushnik, Isaac Yaniv, Hanna Shalev, Carina Levin and Orna Steinberg‐Shemer and has published in prestigious journals such as Nucleic Acids Research, Blood and Biochemical Journal.

In The Last Decade

Orly Dgany

38 papers receiving 496 citations

Peers

Orly Dgany

HEMAT

GENET

PHYSI

GENET

Milena Batchvarova United States

Merlin Nithya Gnanapragasam United States

Tatjana Kilo Australia

Mirosława Siatecka United States

V. Bony France

Peter Hillmen United Kingdom

EM Alderman United States

Prashanth Porayette United States

Flávia Roche Moreira Latini Brazil

PN Porter United States

Milena Batchvarova United States

Orly Dgany

228 ×1.0

HEMAT

244 ×1.1

GENET

145 ×0.9

PHYSI

105 ×0.7

40 ×0.3

GENET

Citations per year, relative to Orly Dgany Orly Dgany (= 1×) peers Milena Batchvarova

Countries citing papers authored by Orly Dgany

Since Specialization

Citations

This map shows the geographic impact of Orly Dgany's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Orly Dgany with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Orly Dgany more than expected).

Fields of papers citing papers by Orly Dgany

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Orly Dgany. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Orly Dgany. The network helps show where Orly Dgany may publish in the future.

Co-authorship network of co-authors of Orly Dgany

This figure shows the co-authorship network connecting the top 25 collaborators of Orly Dgany. A scholar is included among the top collaborators of Orly Dgany based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Orly Dgany. Orly Dgany is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Filon, Dvora, Vardiella Meiner, Orly Dgany, et al.. (2024). A Variable Clinical Presentation of Hemoglobin City of Hope. Clinical Genetics. 107(5). 552–558.

Krauss, Aviva C., Jerry Stein, Orna Steinberg‐Shemer, et al.. (2021). Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome. Pediatric Blood & Cancer. 68(10). e29138–e29138. 3 indexed citations

Dgany, Orly, Ayelet Atkins, Gary M. Kupfer, et al.. (2021). Cdan1 Is Essential for Primitive Erythropoiesis. Frontiers in Physiology. 12. 685242–685242. 7 indexed citations

Steinberg‐Shemer, Orna, Joanne Yacobovich, Carina Levin, et al.. (2019). Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population. Haematologica. 105(7). 1825–1834. 28 indexed citations

Gülsüner, Süleyman, Sarah B. Pierce, Hanna Shalev, et al.. (2018). Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE). Human Molecular Genetics. 28(1). 133–142. 32 indexed citations

Steinberg‐Shemer, Orna, Jacob C. Ulirsch, Dina Attias, et al.. (2017). Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia. Molecular Case Studies. 3(6). a001941–a001941. 14 indexed citations

Gilad, Oded, Orly Dgany, Sarah Elitzur, et al.. (2014). Characterization of Two Unique α-Globin Gene Cluster Deletions Causing α-Thalassemia in Israeli Arabs. Hemoglobin. 38(5). 319–324. 9 indexed citations

Dgany, Orly, et al.. (2013). MPL Baltimore Mutation and Thrombocytosis. Journal of Pediatric Hematology/Oncology. 35(3). e112–e114. 4 indexed citations

Elitzur, Sarah, Joanne Yacobovich, Orly Dgany, et al.. (2013). From Blood Smear to Lipid Disorder. Journal of Pediatric Hematology/Oncology. 35(8). e329–e331. 1 indexed citations

10.

Amir, Achiya, Orly Dgany, P Resnitzky, et al.. (2011). E109K Is a SEC23B Founder Mutation among Israeli Moroccan Jewish Patients with Congenital Dyserythropoietic Anemia Type II. Acta Haematologica. 125(4). 202–207. 14 indexed citations

11.

Malcov, Mira, Adi Reches, Dalit Ben‐Yosef, et al.. (2010). Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia. Prenatal Diagnosis. 30(3). 207–211. 6 indexed citations

12.

Dgany, Orly, Tatyana Krasnov, Nissan Yissachar, et al.. (2009). Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated. Haematologica. 94(5). 629–637. 24 indexed citations

13.

Gilad, Gil, Orly Dgany, Tatyana Krasnov, et al.. (2007). Congenital Amegakaryocytic Thrombocytopenia—3 Novel c-MPL Mutations and Their Phenotypic Correlations. Journal of Pediatric Hematology/Oncology. 29(12). 822–825. 21 indexed citations

14.

Tamary, Hannah, H Offret, Orly Dgany, et al.. (2007). Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous arg1042trp mutation in codanin‐1). European Journal Of Haematology. 80(3). 271–274. 13 indexed citations

15.

Kinel‐Tahan, Yael, Hanna Weiss, Orly Dgany, Anna Levine, & Ron Wides. (2007). Drosophila odz gene is required for multiple cell types in the compound retina. Developmental Dynamics. 236(9). 2541–2554. 19 indexed citations

16.

Arnon, Shmuel, Hannah Tamary, Orly Dgany, et al.. (2004). Hydrops fetalis associated with homozygosity for hemoglobin Taybe (α 38/39 THR deletion) in newborn triplets. American Journal of Hematology. 76(3). 263–266. 19 indexed citations

17.

Tamary, Hannah, Orly Dgany, Helen Toledano, et al.. (2004). Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs. European Journal Of Haematology. 72(5). 330–335. 21 indexed citations

18.

Tamary, Hannah, Isaac Yaniv, Joel Stein, et al.. (2003). A clinical and molecular study of a Bedouin family with dysmegakaryopoiesis, mild anemia, and neutropenia cured by bone marrow transplantation. European Journal Of Haematology. 71(3). 196–203. 8 indexed citations

19.

Dgany, Orly & Ron Wides. (2002). The Drosophila odz/ten-m gene encodes a type I, multiply cleaved heterodimeric transmembrane protein. Biochemical Journal. 363(3). 633–633. 12 indexed citations

20.

Katcoff, Don J., et al.. (1993). SIN1 interacts with a protein that binds the URS1 region of the yeastHOgene. Nucleic Acids Research. 21(22). 5101–5109. 8 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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