Dvora Filon

1.6k total citations
44 papers, 1.1k citations indexed

About

Dvora Filon is a scholar working on Genetics, Hematology and Genetics. According to data from OpenAlex, Dvora Filon has authored 44 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 30 papers in Hematology and 15 papers in Genetics. Recurrent topics in Dvora Filon's work include Hemoglobinopathies and Related Disorders (31 papers), Iron Metabolism and Disorders (24 papers) and Forensic and Genetic Research (10 papers). Dvora Filon is often cited by papers focused on Hemoglobinopathies and Related Disorders (31 papers), Iron Metabolism and Disorders (24 papers) and Forensic and Genetic Research (10 papers). Dvora Filon collaborates with scholars based in Israel, United States and Germany. Dvora Filon's co-authors include Ariella Oppenheim, Deborah Rund, Marina Faerman, Almut Nebel, Varda Oron‐Karni, Patricia Smith, A Oppenheim, Charles L. Greenblatt, Bernd Brinkmann and Ada Goldfarb and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.

In The Last Decade

Dvora Filon

43 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dvora Filon Israel 19 533 475 416 185 151 44 1.1k
Liliana Maccioni Italy 15 634 1.2× 537 1.1× 394 0.9× 243 1.3× 122 0.8× 43 1.2k
D. Tills United Kingdom 17 157 0.3× 324 0.7× 286 0.7× 107 0.6× 26 0.2× 49 833
Pierangela Grignani Italy 14 98 0.2× 72 0.2× 313 0.8× 279 1.5× 103 0.7× 43 629
Goonnapa Fucharoen Thailand 32 2.9k 5.4× 2.6k 5.5× 420 1.0× 395 2.1× 95 0.6× 182 3.5k
Julie Di Cristofaro France 21 43 0.1× 134 0.3× 450 1.1× 294 1.6× 90 0.6× 52 1.4k
Hamid Sayar United States 11 71 0.1× 169 0.4× 269 0.6× 250 1.4× 125 0.8× 36 648
Pilar Martı́nez Spain 8 221 0.4× 181 0.4× 102 0.2× 171 0.9× 66 0.4× 23 638
Bjørnar Olaisen Norway 16 46 0.1× 76 0.2× 310 0.7× 352 1.9× 44 0.3× 32 769
Budsaba Rerkamnuaychoke Thailand 12 51 0.1× 84 0.2× 143 0.3× 176 1.0× 33 0.2× 52 351
Costanza Bosi Italy 13 210 0.4× 385 0.8× 35 0.1× 281 1.5× 4 0.0× 25 630

Countries citing papers authored by Dvora Filon

Since Specialization
Citations

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

Fields of papers citing papers by Dvora Filon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dvora Filon

This figure shows the co-authorship network connecting the top 25 collaborators of Dvora Filon. A scholar is included among the top collaborators of Dvora Filon 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 Dvora Filon. Dvora Filon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Filon, Dvora, Vardiella Meiner, Orly Dgany, et al.. (2024). A Variable Clinical Presentation of Hemoglobin City of Hope. Clinical Genetics. 107(5). 552–558.
2.
Shaulov, Adir, Deborah Rund, Dvora Filon, et al.. (2023). Successful treatment with plasma exchange in life‐threatening hyperhemolytic syndrome unrelated to sickle cell disease. Transfusion. 63(5). 1100–1106. 5 indexed citations
3.
Nachmias, Boaz, Svetlana Krichevsky, Dvora Filon, et al.. (2022). Monitoring Minimal Residual Disease in <b><i>RUNX1</i></b>-Mutated Acute Myeloid Leukemia. Acta Haematologica. 145(6). 642–649. 4 indexed citations
4.
Shaulov, Adir, Dvora Filon, & Deborah Rund. (2016). Haplotype analysis of α-thalassemia chromosomes reveals heterogeneity and multiple founders in Ashkenazi Jews. European Journal of Medical Genetics. 59(11). 555–558. 3 indexed citations
5.
Gesundheit, Benjamin, Reuven Or, Avraham Amar, Dvora Filon, & Gail Amir. (2006). Gaucher-like Cells in β-Thalassemia Patient After Bone Marrow Transplantation. Journal of Pediatric Hematology/Oncology. 28(4). 203–204. 1 indexed citations
6.
Nebel, Almut, Dvora Filon, Marina Faerman, Himla Soodyall, & Ariella Oppenheim. (2004). Y chromosome evidence for a founder effect in Ashkenazi Jews. European Journal of Human Genetics. 13(3). 388–391. 15 indexed citations
7.
8.
Nebel, Almut, Dvora Filon, Bernd Brinkmann, et al.. (2001). The Y Chromosome Pool of Jews as Part of the Genetic Landscape of the Middle East. The American Journal of Human Genetics. 69(5). 1095–1112. 105 indexed citations
9.
Nebel, Almut, Dvora Filon, Carsten Hohoff, et al.. (2001). Haplogroup-specific deviation from the stepwise mutation model at the microsatellite loci DYS388 and DYS392. European Journal of Human Genetics. 9(1). 22–26. 18 indexed citations
10.
Faerman, Marina, Almut Nebel, Dvora Filon, et al.. (2000). From a dry bone to a genetic portrait: A case study of sickle cell anemia. American Journal of Physical Anthropology. 111(2). 153–163. 14 indexed citations
11.
Nebel, Almut, Dvora Filon, Michael E. Weale, et al.. (2000). High-resolution Y chromosome haplotypes of Israeli and Palestinian Arabs reveal geographic substructure and substantial overlap with haplotypes of Jews. Human Genetics. 107(6). 630–641. 59 indexed citations
12.
Oron‐Karni, Varda, et al.. (2000). Diversity of ?-globin mutations and clinical presentation of ?-thalassemia in Israel. American Journal of Hematology. 65(3). 196–203. 45 indexed citations
13.
Rund, Deborah, Varda Oron‐Karni, Dvora Filon, & A Oppenheim. (1998). α‐Globin Mutations and Rearrangements in Israel: PCR‐Based Analysis Reveals Ethnic Diversitya. Annals of the New York Academy of Sciences. 850(1). 426–428. 1 indexed citations
14.
Rund, Deborah, Varda Oron‐Karni, Dvora Filon, et al.. (1997). Genetic analysis of β-thalassemia intermedia in Israel: Diversity of mechanisms and unpredictability of phenotype. American Journal of Hematology. 54(1). 16–22. 49 indexed citations
15.
Oron‐Karni, Varda, Dvora Filon, Deborah Rund, & Ariella Oppenheim. (1997). A Novel Mechanism Generating Short Deletion/Insertions Following Slippage is Suggested by a Mutation in the Human α2-Globin Gene. Human Molecular Genetics. 6(6). 881–885. 27 indexed citations
16.
Or, Reuven, Joseph Kapelushnik, Elizabeth Naparstek, et al.. (1996). Second transplantation using allogeneic peripheral blood stem cells in a β‐thalassaemia major patient featuring stable mixed chimaerism. British Journal of Haematology. 94(2). 285–287. 12 indexed citations
17.
Filon, Dvora, Marina Faerman, Patricia Smith, & Ariella Oppenheim. (1995). Sequence analysis reveals a β–thalassaemia mutation in the DNA of skeletal remains from the archaeological site of Akhziv, Israel. Nature Genetics. 9(4). 365–368. 39 indexed citations
18.
Faerman, Marina, et al.. (1995). Sex identification of archaeological human remains based on amplification of the X and Y amelogenin alleles. Gene. 167(1-2). 327–332. 90 indexed citations
19.
Filon, Dvora, et al.. (1995). Spectrum of β-thalassemia mutations in the Gaza area. Human Mutation. 5(4). 351–353. 14 indexed citations
20.
Rund, Deborah, Dvora Filon, A Oppenheim, & Ayala Abramov. (1993). Silent carrier β-thalassaemia due to a severe β-globin mutation interacting with other genetic elements. European Journal of Pediatrics. 152(7). 574–576. 6 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Liliana Maccioni Breakdown of academic impact, for papers by D. Tills Breakdown of academic impact, for papers by Pierangela Grignani Breakdown of academic impact, for papers by Goonnapa Fucharoen Breakdown of academic impact, for papers by Julie Di Cristofaro Breakdown of academic impact, for papers by Hamid Sayar Breakdown of academic impact, for papers by Pilar Martı́nez Breakdown of academic impact, for papers by Bjørnar Olaisen Breakdown of academic impact, for papers by Budsaba Rerkamnuaychoke Breakdown of academic impact, for papers by Costanza Bosi
Rankless by CCL
2026