Nathalie Nadal

1.8k total citations
23 papers, 414 citations indexed

About

Nathalie Nadal is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Nathalie Nadal has authored 23 papers receiving a total of 414 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Hematology, 8 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Nathalie Nadal's work include Acute Myeloid Leukemia Research (10 papers), Lymphoma Diagnosis and Treatment (8 papers) and Chronic Lymphocytic Leukemia Research (5 papers). Nathalie Nadal is often cited by papers focused on Acute Myeloid Leukemia Research (10 papers), Lymphoma Diagnosis and Treatment (8 papers) and Chronic Lymphocytic Leukemia Research (5 papers). Nathalie Nadal collaborates with scholars based in France, Belgium and United Kingdom. Nathalie Nadal's co-authors include Pascale Flandrin‐Gresta, Lydia Campos, Denis Guyotat, Jérôme Cornillon, Emmanuelle Tavernier, Lennart Angervall, M. Kœnig, B Gunterberg, Göran Stenman and Jean‐Louis Mandel and has published in prestigious journals such as Journal of Clinical Oncology, Blood and Human Molecular Genetics.

In The Last Decade

Nathalie Nadal

20 papers receiving 407 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nathalie Nadal France 12 179 135 102 86 84 23 414
Anthony D. Pomicter United States 15 258 1.4× 291 2.2× 224 2.2× 52 0.6× 65 0.8× 40 588
Frank J.G. Scherpen Netherlands 14 363 2.0× 149 1.1× 103 1.0× 37 0.4× 146 1.7× 33 592
Melissa Stafford United States 10 305 1.7× 185 1.4× 87 0.9× 29 0.3× 117 1.4× 11 610
Philip Vlummens Belgium 13 323 1.8× 137 1.0× 39 0.4× 33 0.4× 124 1.5× 33 503
Martine Guillier France 15 388 2.2× 166 1.2× 123 1.2× 34 0.4× 177 2.1× 27 628
Francesco Acquadro Spain 13 241 1.3× 125 0.9× 60 0.6× 70 0.8× 129 1.5× 19 536
Joshua Sasine United States 13 279 1.6× 229 1.7× 90 0.9× 22 0.3× 165 2.0× 27 596
Ludger Klewes Canada 15 437 2.4× 52 0.4× 104 1.0× 45 0.5× 80 1.0× 18 634
Tihomira I. Todorova United States 10 362 2.0× 307 2.3× 103 1.0× 61 0.7× 64 0.8× 15 661
Martina Podleschny Germany 8 180 1.0× 111 0.8× 109 1.1× 24 0.3× 73 0.9× 9 329

Countries citing papers authored by Nathalie Nadal

Since Specialization
Citations

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

Fields of papers citing papers by Nathalie Nadal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nathalie Nadal

This figure shows the co-authorship network connecting the top 25 collaborators of Nathalie Nadal. A scholar is included among the top collaborators of Nathalie Nadal 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 Nathalie Nadal. Nathalie Nadal 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.
Chapiro, Élise, Agnès Daudignon, Nathalie Nadal, et al.. (2023). Cytogenetics in the management of mature T-cell and NK-cell neoplasms: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH). Current Research in Translational Medicine. 71(4). 103428–103428.
2.
Nadal, Nathalie, Nathalie Auger, Audrey Bidet, & Florence Nguyen‐Khac. (2023). Cytogenetics in the management of clonal chromosomal abnormalities of undetermined significance and persistent polyclonal B-cell lymphocytosis: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH). Current Research in Translational Medicine. 71(4). 103426–103426.
3.
Lefebvre, Christine, Lauren Véronèse, Nathalie Nadal, et al.. (2023). Cytogenetics in the management of mature B-cell non-Hodgkin lymphomas: Guidelines from the Groupe Francophone de Cytogénétique Hematologique (GFCH). Current Research in Translational Medicine. 71(4). 103425–103425.
4.
Nguyen‐Khac, Florence, Audrey Bidet, Agnès Daudignon, et al.. (2022). The complex karyotype in hematological malignancies: a comprehensive overview by the Francophone Group of Hematological Cytogenetics (GFCH). Leukemia. 36(6). 1451–1466. 17 indexed citations
5.
Gouill, Steven Le, Franck Morschhauser, David Chiron, et al.. (2020). Ibrutinib, obinutuzumab, and venetoclax in relapsed and untreated patients with mantle cell lymphoma: a phase 1/2 trial. Blood. 137(7). 877–887. 75 indexed citations
6.
Magné, Julien, Adrien Chauchet, Olivier Casasnovas, et al.. (2018). Potential added value of a RT-qPCR method of SOX 11 expression, in the context of a multidisciplinary diagnostic assessment of B cell malignancies. Experimental Hematology and Oncology. 7(1). 5–5. 2 indexed citations
7.
8.
Duhoux, François P., Geneviève Ameye, Iwona Włodarska, et al.. (2011). PRDM16 (1p36) translocations define a distinct entity of myeloid malignancies with poor prognosis but may also occur in lymphoid malignancies.. Journal of Clinical Oncology. 29(15_suppl). 6531–6531. 5 indexed citations
9.
Campos, Lydia, Nathalie Nadal, Pascale Flandrin‐Gresta, et al.. (2010). Congenital acute leukemia with initial indolent presentation—A case report. Cytometry Part B Clinical Cytometry. 80B(2). 130–133. 2 indexed citations
10.
Flandrin‐Gresta, Pascale, Karine Augeul-Meunier, Emmanuelle Tavernier, et al.. (2010). CD133+ Acute Myeloid Leukemia (AML) Cells Exhibit Higher Clonogenic Capacity and Higher Levels of pAKT and Bcl-2 Proteins Than Their Negative Counterpart. Blood. 116(21). 1721–1721. 1 indexed citations
11.
Nguyen‐Khac, Florence, Claude Lesty, Virginie Éclache, et al.. (2010). Chromosomal abnormalities in transformed Ph‐negative myeloproliferative neoplasms are associated to the transformation subtype and independent of JAK2 and the TET2 mutations. Genes Chromosomes and Cancer. 49(10). 919–927. 15 indexed citations
12.
Nguyen‐Khac, Florence, Lucile Couronné, Virginie Éclache, et al.. (2009). Chromosomal Abnormalities in Transformed Ph-Negative Myeloproliferative Neoplasm Are Independent of the JAK2 and the TET2 Statuses.. Blood. 114(22). 2900–2900. 1 indexed citations
13.
Flandrin‐Gresta, Pascale, Denis Guyotat, Jérôme Cornillon, et al.. (2008). Significance of heat-shock protein (HSP) 90 expression in acute myeloid leukemia cells. Cell Stress and Chaperones. 13(3). 357–364. 65 indexed citations
14.
Tavernier, Emmanuelle, Jérôme Cornillon, Lydia Campos, et al.. (2008). Prognostic value of CXCR4 and FAK expression in acute myelogenous leukemia. Leukemia Research. 33(6). 764–768. 55 indexed citations
15.
Campos, Lydia, et al.. (2007). Multiparametric analysis of normal and postchemotherapy bone marrow: Implication for the detection of leukemia‐associated immunophenotypes. Cytometry Part B Clinical Cytometry. 74B(1). 17–24. 29 indexed citations
16.
Campos, Lydia, et al.. (2006). Expression and prognostic significance of heat-shock proteins in myelodysplastic syndromes.. Haematologica. 91(5). 713–4. 21 indexed citations
17.
Armstrong, Judith, I Bonaventura, Ana I. Rojo, et al.. (2005). Spinocerebellar ataxia type 2 (SCA2) with white matter involvement. Neuroscience Letters. 381(3). 247–251. 16 indexed citations
18.
Stenman, Göran, Nathalie Nadal, Stellan Persson, B Gunterberg, & Lennart Angervall. (1999). del(6)(q12q15) as the sole cytogenetic anomaly in a case of solitary infantile myofibromatosis.. Oncology Reports. 6(5). 1101–4. 26 indexed citations
19.
Hamida, C. Ben, L Cavalier, Samir Belal, et al.. (1997). Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1. Neurogenetics. 1(2). 129–133. 39 indexed citations
20.
Nadal, Nathalie, Marie-Odile Rolland, Christine Tranchant, et al.. (1995). Localization of Refsum disease with increased pipecolic acidaemia to chromosome 10p by homozygosity mapping and carrier testing in a single nuclear family. Human Molecular Genetics. 4(10). 1963–1966. 17 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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