Hannah Tamary

6.9k total citations · 1 hit paper
154 papers, 3.6k citations indexed

About

Hannah Tamary is a scholar working on Hematology, Genetics and Physiology. According to data from OpenAlex, Hannah Tamary has authored 154 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 79 papers in Hematology, 58 papers in Genetics and 47 papers in Physiology. Recurrent topics in Hannah Tamary's work include Hemoglobinopathies and Related Disorders (52 papers), Erythrocyte Function and Pathophysiology (40 papers) and Blood groups and transfusion (29 papers). Hannah Tamary is often cited by papers focused on Hemoglobinopathies and Related Disorders (52 papers), Erythrocyte Function and Pathophysiology (40 papers) and Blood groups and transfusion (29 papers). Hannah Tamary collaborates with scholars based in Israel, United States and France. Hannah Tamary's co-authors include Isaac Yaniv, Joanne Yacobovich, Hanna Shalev, Orly Dgany, Shoshana Revel‐Vilk, E Vilmer, Jérôme Feldmann, Alain Fischer, Cécile Dumont and Isabelle Callebaut and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Blood.

In The Last Decade

Hannah Tamary

151 papers receiving 3.5k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)

2003 684 citations Hannah Tamary et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Hannah Tamary Israel	33	1.9k	1.1k	862	688	660	154	3.6k
Aytemiz Gürgey Türkiye	33	2.4k 1.3×	1.4k 1.3×	313 0.4×	541 0.8×	586 0.9×	219	3.9k
E. C. Gordon‐Smith United Kingdom	31	2.8k 1.5×	1.0k 0.9×	439 0.5×	1.1k 1.5×	516 0.8×	124	4.1k
Gordon L. Phillips United States	26	1.6k 0.8×	514 0.5×	437 0.5×	643 0.9×	476 0.7×	87	3.8k
O. Fain France	37	815 0.4×	978 0.9×	397 0.5×	888 1.3×	377 0.6×	203	4.2k
Hélène Espérou France	36	2.9k 1.5×	1.1k 1.0×	215 0.2×	1.0k 1.5×	743 1.1×	90	4.6k
Brigitte Bader‐Meunier France	43	1.9k 1.0×	447 0.4×	476 0.6×	1.9k 2.8×	1.6k 2.4×	212	5.8k
Alina Ferster Belgium	30	1.9k 1.0×	1.6k 1.5×	203 0.2×	654 1.0×	521 0.8×	151	3.8k
Pietro Leoni Italy	34	1.7k 0.9×	989 0.9×	228 0.3×	463 0.7×	778 1.2×	128	3.4k
Frank Bridoux France	39	1.6k 0.9×	1.4k 1.3×	320 0.4×	1.0k 1.5×	3.3k 5.1×	165	5.8k
Christoph Licht Canada	38	1.3k 0.7×	561 0.5×	288 0.3×	3.1k 4.5×	666 1.0×	177	4.9k

Countries citing papers authored by Hannah Tamary

Since Specialization

Citations

This map shows the geographic impact of Hannah Tamary'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 Hannah Tamary with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hannah Tamary more than expected).

Fields of papers citing papers by Hannah Tamary

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hannah Tamary. 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 Hannah Tamary. The network helps show where Hannah Tamary may publish in the future.

Co-authorship network of co-authors of Hannah Tamary

This figure shows the co-authorship network connecting the top 25 collaborators of Hannah Tamary. A scholar is included among the top collaborators of Hannah Tamary 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 Hannah Tamary. Hannah Tamary 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

Zadik, Yehuda, et al.. (2025). Fanconi anemia patients with head and neck squamous cell carcinoma - a multi-center study. European Archives of Oto-Rhino-Laryngology. 282(9). 4745–4754. 1 indexed citations

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

Fioredda, Francesca, Julia Skokowa, Hannah Tamary, et al.. (2023). The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action. HemaSphere. 7(4). e872–e872. 22 indexed citations

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

Vulliamy, Tom, Inderjeet Dokal, Jean Soulier, et al.. (2021). Multinational Study on the Clinical and Genetic Features of the ERCC6L2-Disease. Blood. 138(Supplement 1). 864–864. 1 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

Włodarski, Marcin W., Lydie Da Costa, Marie-Françoise O’Donohue, et al.. (2017). Mutations in Ribosomal Protein Genes L9 and L15 Link to DBA with Specific Clinical Phenotypes. Blood. 130. 1172–1172. 1 indexed citations

Yacobovich, Joanne, Meira Zoldan, Yoseph Horovitz, et al.. (2017). Evaluating platelet function disorders in children with bleeding tendency – A single center study. Platelets. 28(7). 676–681. 7 indexed citations

Gerrits, Anja J., Emily Leven, Andrew L. Frelinger, et al.. (2015). Effects of eltrombopag on platelet count and platelet activation in Wiskott-Aldrich syndrome/X-linked thrombocytopenia. Blood. 126(11). 1367–1378. 58 indexed citations

10.

Collopy, Laura C., Amanda J. Walne, Shirleny Cardoso, et al.. (2015). Triallelic and epigenetic-like inheritance in human disorders of telomerase. Blood. 126(2). 176–184. 33 indexed citations

11.

Revel‐Vilk, Shoshana, et al.. (2013). Age and Duration of Bleeding Symptoms at Diagnosis Best Predict Resolution of Childhood Immune Thrombocytopenia at 3, 6, and 12 Months. The Journal of Pediatrics. 163(5). 1335–1339.e2. 27 indexed citations

12.

Levin, Carina, et al.. (2013). Small‐platelet thrombocytopenia in a family with autosomal recessive inheritance pattern. Pediatric Blood & Cancer. 60(10). E128–30. 5 indexed citations

13.

Russo, Roberta, Antonella Gambale, Maria Rosaria Esposito, et al.. (2011). Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population. American Journal of Hematology. 86(9). 727–732. 19 indexed citations

14.

Tamary, Hannah, Jelena Roganović, Meera Chitlur, & Diane J. Nugent. (2010). Consensus Paper—ICIS Expert Meeting Basel 2009 treatment milestones in immune thrombocytopenia. Annals of Hematology. 89(S1). 5–10. 6 indexed citations

15.

Marrone, Anna, Amanda J. Walne, Hannah Tamary, et al.. (2007). Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome. Blood. 110(13). 4198–4205. 119 indexed citations

16.

Zivelin, Ariella, et al.. (2004). Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients. Journal of Thrombosis and Haemostasis. 2(10). 1774–1781. 35 indexed citations

17.

Tamary, Hannah, et al.. (1999). NO RESPONSE TO RECOMBINANT HUMAN ERYTHROPOIETIN THERAPY IN PATIENTS WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I. Pediatric Hematology and Oncology. 16(2). 165–168. 11 indexed citations

18.

Tamary, Hannah, Lea Shalmon, Hanna Shalev, et al.. (1998). Localization of the Gene for Congenital Dyserythropoietic Anemia Type I to a <1-cM Interval on Chromosome 15q15.1-15.3. The American Journal of Human Genetics. 62(5). 1062–1069. 42 indexed citations

19.

Tamary, Hannah, Gil Klinger, Lea Shalmon, et al.. (1997). α-Thalassemia Caused by a 16 BP Deletion in the 3′ Untranslated Region of the α2-Globin Gene Including the First Nucleotide of the Poly a Signal Sequence. Hemoglobin. 21(2). 121–130. 7 indexed citations

20.

Tamary, Hannah, et al.. (1982). GM1 gangliosidosis presenting as neonatal ascites. The Journal of Pediatrics. 100(6). 940–943. 19 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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