I Radford-Weiss

5.1k total citations
19 papers, 677 citations indexed

About

I Radford-Weiss is a scholar working on Hematology, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, I Radford-Weiss has authored 19 papers receiving a total of 677 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Hematology, 7 papers in Molecular Biology and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in I Radford-Weiss's work include Acute Myeloid Leukemia Research (8 papers), Acute Lymphoblastic Leukemia research (6 papers) and Retinoids in leukemia and cellular processes (3 papers). I Radford-Weiss is often cited by papers focused on Acute Myeloid Leukemia Research (8 papers), Acute Lymphoblastic Leukemia research (6 papers) and Retinoids in leukemia and cellular processes (3 papers). I Radford-Weiss collaborates with scholars based in France, United States and Switzerland. I Radford-Weiss's co-authors include Éric Delabesse, Georges Flandrin, Xavier Troussard, Katrina Rack, Françoise Picard, Hélène A. Poirel, D Leboeuf, M Lessard, Mårina Lafage‐Pochitaloff and Roland Berger and has published in prestigious journals such as Blood, British Journal of Haematology and British Journal of Dermatology.

In The Last Decade

I Radford-Weiss

17 papers receiving 667 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
I Radford-Weiss France 13 518 388 185 120 88 19 677
R Släter Netherlands 17 606 1.2× 395 1.0× 543 2.9× 120 1.0× 78 0.9× 24 983
MR Baer United States 11 569 1.1× 307 0.8× 194 1.0× 119 1.0× 30 0.3× 14 706
Jutta Bradtke Germany 13 375 0.7× 235 0.6× 301 1.6× 99 0.8× 104 1.2× 20 623
Petti Mc Italy 12 679 1.3× 596 1.5× 185 1.0× 86 0.7× 18 0.2× 24 786
Kristiina Heinonen Finland 16 714 1.4× 364 0.9× 369 2.0× 190 1.6× 68 0.8× 30 918
L Elia Italy 13 507 1.0× 216 0.6× 461 2.5× 114 0.9× 62 0.7× 29 691
Laurence Detourmignies France 9 237 0.5× 195 0.5× 86 0.5× 70 0.6× 87 1.0× 16 402
V. Shetty United States 7 505 1.0× 250 0.6× 105 0.6× 135 1.1× 23 0.3× 9 643
P Lemež Czechia 10 436 0.8× 174 0.4× 276 1.5× 96 0.8× 62 0.7× 27 575
Lovisa Wennström Sweden 11 618 1.2× 385 1.0× 192 1.0× 170 1.4× 16 0.2× 24 687

Countries citing papers authored by I Radford-Weiss

Since Specialization
Citations

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

Fields of papers citing papers by I Radford-Weiss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by I Radford-Weiss. 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 I Radford-Weiss. The network helps show where I Radford-Weiss may publish in the future.

Co-authorship network of co-authors of I Radford-Weiss

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

All Works

19 of 19 papers shown
2.
Chapuis, Nicolas, Camille Debord, Alexandra Rouquette, et al.. (2013). Flow cytometric detection of dyserythropoiesis: a sensitive and powerful diagnostic tool for myelodysplastic syndromes. Leukemia. 27(10). 1981–1987. 58 indexed citations
3.
Petit, Arnaud, Christine Ragu, Chris Ottolenghi, et al.. (2011). Functional analysis of the NUP98-CCDC28A fusion protein. Haematologica. 97(3). 379–387. 14 indexed citations
4.
Su, Xiaoyang, Véronique Della-Valle, Isabelle André‐Schmutz, et al.. (2006). HOX11L2/TLX3 is transcriptionally activated through T-cell regulatory elements downstream of BCL11B as a result of the t(5;14)(q35;q32). Blood. 108(13). 4198–4201. 39 indexed citations
5.
Al‐Mousa, Hamoud, Capucine Pïcard, I Radford-Weiss, et al.. (2005). Transient familial haemophagocytic lymphohistiocytosis reactivation post‐CD34 haematopoietic stem cell transplantation. British Journal of Haematology. 130(3). 404–408. 4 indexed citations
6.
Letestu, Rémi, Valérie Ugo, Françoise Valensi, et al.. (2004). Prognostic impact of p27KIP1 expression in cyclin D1 positive lymphoproliferative disorders. Leukemia. 18(5). 953–961. 15 indexed citations
7.
Lesca, Gaëtan, et al.. (2003). T-cell prolymphocytic leukemia with autoimmune manifestations in Nijmegen breakage syndrome. Annals of Hematology. 82(8). 515–517. 16 indexed citations
8.
Belaud‐Rotureau, Marc‐Antoine, Hatem Elghezal, Damien Sanlaville, et al.. (2003). [Spectral karyotyping (SKY) principle, avantages and limitations].. PubMed. 61(2). 139–46.
9.
Damaj, Gandhi, D. Canioni, Marie Thérèse Rubio, et al.. (2002). Remission of transformed myelodysplastic syndrome with fibrosis after danazol therapy. European Journal Of Haematology. 68(4). 233–235. 2 indexed citations
10.
Damaj, Gandhi, Éric Delabesse, Christine Le Bihan-Benjamin, et al.. (2002). Typical essential thrombocythaemia does not express bcr–abelson fusion transcript. British Journal of Haematology. 116(4). 812–816. 16 indexed citations
11.
Elghezal, Hatem, et al.. (2001). Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis. Genes Chromosomes and Cancer. 30(4). 383–392. 23 indexed citations
12.
Grimwade, David, Antonio Biondi, Julien Mozziconacci, et al.. (2000). Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): results of the European Working Party. Groupe Francais de Cytogenetique Hematologique, Groupe de Francais d'Hematologie Cellulaire, UK Cancer Cytogenetics Group and BIOMED 1 European Community-Concerted Action "Molecular Cytogenetic Diagnosis in Haematological Malignancies". SPIRE - Sciences Po Institutional REpository. 30 indexed citations
13.
Mégarbane, Bruno, Christine Bodemer, Françoise Valensi, et al.. (2000). Association of acute neutrophilic dermatosis and myelodysplastic syndrome with (6; 9) chromosome translocation: a case report and review of the literature. British Journal of Dermatology. 143(6). 1322–1324. 8 indexed citations
14.
Grimwade, David, Andrea Biondi, Julien Mozziconacci, et al.. (2000). Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17):. Radboud Repository (Radboud University). 224 indexed citations
15.
Rack, Katrina, Éric Delabesse, I Radford-Weiss, et al.. (1998). Simultaneous detection of MYC, BVR1, and PVT1 translocations in lymphoid malignancies by fluorescence in situ hybridization. Genes Chromosomes and Cancer. 23(3). 220–226.
16.
Mauvieux, Laurent, Danielle Canioni, Olivier Hermine, et al.. (1998). Quantitative RNA slot-blot analysis of CCND1/cyclin D1 expression in suspected mantle cell lymphoma. Leukemia. 12(1). 78–85. 12 indexed citations
17.
Rack, Katrina, François Cornélis, I Radford-Weiss, et al.. (1997). A Chromosome 14q11/TCRα/δ Specific Yeast Artificial Chromosome Improves the Detection Rate and Characterization of Chromosome Abnormalities in T-Lymphoproliferative Disorders. Blood. 90(3). 1233–1240. 9 indexed citations
18.
Poirel, Hélène A., Katrina Rack, Éric Delabesse, et al.. (1996). Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5. Blood. 87(6). 2496–2505. 82 indexed citations
19.
Poirel, Hélène A., I Radford-Weiss, Katrina Rack, et al.. (1995). Detection of the chromosome 16 CBF beta-MYH11 fusion transcript in myelomonocytic leukemias. Blood. 85(5). 1313–1322. 82 indexed citations

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