Hélène Zattara

906 total citations
13 papers, 85 citations indexed

About

Hélène Zattara is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Hélène Zattara has authored 13 papers receiving a total of 85 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Pathology and Forensic Medicine and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Hélène Zattara's work include Acute Lymphoblastic Leukemia research (5 papers), Acute Myeloid Leukemia Research (3 papers) and Tumors and Oncological Cases (2 papers). Hélène Zattara is often cited by papers focused on Acute Lymphoblastic Leukemia research (5 papers), Acute Myeloid Leukemia Research (3 papers) and Tumors and Oncological Cases (2 papers). Hélène Zattara collaborates with scholars based in France, Tunisia and Saudi Arabia. Hélène Zattara's co-authors include Violaine Bourdon, Frédérique Keslair, Hagay Sobol, Carla Fernandez, Esma Saâda, G. Héry, Florence Pédeutour, Abderrahim Khélif, Laurence Faivre and Hélène Dreyfus and has published in prestigious journals such as BMC Cancer, Genes Chromosomes and Cancer and Clinical Genetics.

In The Last Decade

Hélène Zattara

10 papers receiving 83 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hélène Zattara France 7 27 25 22 20 17 13 85
Sunkyu Kim South Korea 3 32 1.2× 17 0.7× 18 0.8× 20 1.0× 17 1.0× 7 93
Yasuhito Nanya Japan 6 22 0.8× 24 1.0× 10 0.5× 55 2.8× 18 1.1× 9 115
Méryem-Maud Farhat France 5 47 1.7× 33 1.3× 16 0.7× 41 2.0× 8 0.5× 15 107
Yoshiaki Usui Japan 7 38 1.4× 42 1.7× 14 0.6× 51 2.5× 20 1.2× 22 119
Zsolt Nagy Hungary 5 32 1.2× 31 1.2× 9 0.4× 14 0.7× 13 0.8× 15 85
R. Scott Mead Australia 5 28 1.0× 15 0.6× 16 0.7× 14 0.7× 5 0.3× 5 91
Cemre Celen United States 4 73 2.7× 23 0.9× 8 0.4× 14 0.7× 11 0.6× 4 102
Lesley Ann Sutton Sweden 5 33 1.2× 43 1.7× 7 0.3× 31 1.6× 57 3.4× 8 113
Nikita Mehta United States 6 21 0.8× 12 0.5× 42 1.9× 22 1.1× 15 0.9× 13 131
Bevan Tandon United States 5 47 1.7× 52 2.1× 12 0.5× 43 2.1× 56 3.3× 6 131

Countries citing papers authored by Hélène Zattara

Since Specialization
Citations

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

Fields of papers citing papers by Hélène Zattara

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hélène Zattara

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

All Works

13 of 13 papers shown
1.
Bouras, Ahmed, Aurélie Fabre, Hélène Zattara, et al.. (2024). Hereditary Colorectal Cancer and Polyposis Syndromes Caused by Variants in Uncommon Genes. Genes Chromosomes and Cancer. 63(8). e23263–e23263. 1 indexed citations
2.
Coze, S., C. d’Ercole, Nicoleta Panait, et al.. (2023). The role of pediatric oncologist in prenatal diagnosis: A 10-year retrospective study at Assistance Publique Hôpitaux de Marseille (AP-HM). Pediatric Hematology and Oncology. 41(1). 30–40.
3.
Hamadou, Walid Sabri, Nouha Bouali, Violaine Bourdon, et al.. (2021). Mutational analysis of apoptotic genes in familial aggregation of hematological malignancies. Bulletin du Cancer. 108(9). 798–805.
4.
Hamadou, Walid Sabri, Violaine Bourdon, Yosra Ben Youssef, et al.. (2017). GATA2 gene analysis in several forms of hematological malignancies including familial aggregations. Annals of Hematology. 96(10). 1635–1639. 6 indexed citations
5.
6.
Hamadou, Walid Sabri, Violaine Bourdon, Yosra Ben Youssef, et al.. (2016). ARLTS1, potential candidate gene in familial aggregation of hematological malignancies. Bulletin du Cancer. 104(2). 123–127. 9 indexed citations
7.
Zattara, Hélène, et al.. (2016). Molecular combing: A new tool in diagnosing leukemia. Cancer Biomarkers. 17(4). 405–409. 3 indexed citations
8.
Hamadou, Walid Sabri, Souhail Besbes, Violaine Bourdon, et al.. (2015). Familial hematological malignancies: ASXL1 gene investigation. Clinical & Translational Oncology. 18(4). 385–390. 11 indexed citations
9.
Rouleau, Étienne, Hélène Zattara, Cédrick Lefol, et al.. (2011). First large rearrangement in the MUTYH gene and attenuated familial adenomatous polyposis syndrome. Clinical Genetics. 80(3). 301–303. 12 indexed citations
10.
Quilichini, Benoît, et al.. (2011). A new case of t(8;14)(q11;q32) in an acute lymphoblastic leukemia. Atlas of Genetics and Cytogenetics in Oncology and Haematology.
11.
Bourdon, Violaine, Laëtitia Huiart, François Eisinger, et al.. (2009). Molecular study of CEPBA in familial hematological malignancies. Familial Cancer. 8(4). 581–584. 4 indexed citations
12.
Fernandez, Carla, Esma Saâda, Frédérique Keslair, et al.. (2009). HMGA2–NFIB fusion in a pediatric intramuscular lipoma: a novel case of NFIB alteration in a large deep-seated adipocytic tumor. Cancer Genetics and Cytogenetics. 195(1). 66–70. 24 indexed citations
13.
Quilichini, Benoît, Nicolás André, M Chrestian, et al.. (2006). Hidden chromosomal abnormalities in pleuropulmonary blastomas identified by multiplex FISH. BMC Cancer. 6(1). 4–4. 7 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 Sunkyu Kim Breakdown of academic impact, for papers by Yasuhito Nanya Breakdown of academic impact, for papers by Méryem-Maud Farhat Breakdown of academic impact, for papers by Yoshiaki Usui Breakdown of academic impact, for papers by Zsolt Nagy Breakdown of academic impact, for papers by R. Scott Mead Breakdown of academic impact, for papers by Cemre Celen Breakdown of academic impact, for papers by Lesley Ann Sutton Breakdown of academic impact, for papers by Nikita Mehta Breakdown of academic impact, for papers by Bevan Tandon
Rankless by CCL
2026