C Cabrol

797 total citations
34 papers, 363 citations indexed

About

C Cabrol is a scholar working on Hematology, Genetics and Genetics. According to data from OpenAlex, C Cabrol has authored 34 papers receiving a total of 363 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Hematology, 10 papers in Genetics and 9 papers in Genetics. Recurrent topics in C Cabrol's work include Acute Myeloid Leukemia Research (11 papers), Genomic variations and chromosomal abnormalities (9 papers) and Chronic Myeloid Leukemia Treatments (7 papers). C Cabrol is often cited by papers focused on Acute Myeloid Leukemia Research (11 papers), Genomic variations and chromosomal abnormalities (9 papers) and Chronic Myeloid Leukemia Treatments (7 papers). C Cabrol collaborates with scholars based in Switzerland, France and United States. C Cabrol's co-authors include P Beris, B Chapuis, Christiane Werner‐Favre, Anne Hagemeijer, Étienne Roux, Eric Engel, Peter Marynen, Chrystèle Bilhou‐Nabera, Jan Cools and Pascaline Talmant and has published in prestigious journals such as Blood, Annals of Oncology and Transplantation.

In The Last Decade

C Cabrol

32 papers receiving 348 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C Cabrol Switzerland 11 201 104 76 66 65 34 363
E A Harden United States 7 148 0.7× 107 1.0× 111 1.5× 44 0.7× 70 1.1× 8 375
BR Blazar United States 10 355 1.8× 56 0.5× 207 2.7× 104 1.6× 49 0.8× 13 528
Henriëtte M. Goselink Netherlands 10 272 1.4× 80 0.8× 207 2.7× 83 1.3× 75 1.2× 18 464
JH Bourhis United States 8 437 2.2× 151 1.5× 119 1.6× 77 1.2× 59 0.9× 10 507
LD Notarangelo Italy 13 137 0.7× 97 0.9× 254 3.3× 100 1.5× 16 0.2× 19 534
JE Landegent Netherlands 8 237 1.2× 115 1.1× 145 1.9× 58 0.9× 35 0.5× 12 407
Lidia De Felice Italy 13 485 2.4× 222 2.1× 175 2.3× 161 2.4× 91 1.4× 33 701
R. Hintermeíer-Knabe Germany 6 314 1.6× 54 0.5× 319 4.2× 32 0.5× 18 0.3× 8 488
EM Bryant United States 11 435 2.2× 135 1.3× 234 3.1× 118 1.8× 134 2.1× 16 675
Laura Todt United States 6 264 1.3× 123 1.2× 147 1.9× 49 0.7× 22 0.3× 8 432

Countries citing papers authored by C Cabrol

Since Specialization
Citations

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

Fields of papers citing papers by C Cabrol

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C Cabrol

This figure shows the co-authorship network connecting the top 25 collaborators of C Cabrol. A scholar is included among the top collaborators of C Cabrol 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 C Cabrol. C Cabrol 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.
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
2.
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
3.
Meyer‐Monard, Sandrine, V. Parlier, Jakob Passweg, et al.. (2006). Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia. Leukemia. 20(2). 247–253. 12 indexed citations
4.
Mühlematter, Dominique, V. Parlier, C Cabrol, et al.. (2005). Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases. Cancer Genetics and Cytogenetics. 160(2). 97–119. 13 indexed citations
5.
Laurencet, France M., Gilbert B. Zulian, C Cabrol, & Daniel Betticher. (1997). Myelodysplastic syndrome with biclonal monosomy 7 and trisomy 8 after treatment with cladribine (2-chloro-2-deoxyadenosine) and involved field radiation therapy. Cancer Genetics and Cytogenetics. 99(1). 85–89. 11 indexed citations
6.
Cabrol, C, et al.. (1993). Etoposide and secondary haematological malignancies: Coincidence or causality?. Annals of Oncology. 4(7). 559–566. 14 indexed citations
7.
Ferran, Christiane, Michel Peuchmaur, Nicole Brousse, et al.. (1993). IMPLICATIONS OF DE NOVO ELAM-1 AND VCAM-1 EXPRESSION IN HUMAN CARDIAC ALLOGRAFT REJECTION. Transplantation. 55(3). 605–609. 51 indexed citations
8.
Lunel, F., et al.. (1990). Is postoperative HBV hepatitis in heart transplant recipients the fruit of hazard?. PubMed. 14(11). 848–9. 5 indexed citations
9.
Komajda, M, C Raffoux, Ephrem Salamé, et al.. (1987). [HLA A-B and DR in dilated myocardiopathies].. PubMed. 80(8). 1233–7. 14 indexed citations
10.
Cabrol, C, et al.. (1987). Modification in orthotopic heart transplantation: Surgical technique. Clinical Transplantation. 1(2). 95–98. 1 indexed citations
11.
Werner‐Favre, Christiane, C Cabrol, M Wyss, & Eric Engel. (1984). Translocation t(1;19)(q21;q13) in acute lymphoblastic leukemia. Cytogenetic and Genome Research. 38(3). 240–240. 4 indexed citations
12.
13.
Werner‐Favre, Christiane, C Cabrol, P Beris, & Eric Engel. (1983). Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemia.. PubMed. 26(4). 240–2. 4 indexed citations
14.
Cabrol, C, et al.. (1978). [Chromosome 5q-- in the medullar cells of a patient with anaemia which later developed into acute non-differentiated leukaemia (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 26(3). 195–202. 12 indexed citations
15.
Cabrol, C, et al.. (1976). [Triple Philadelphia chromosome during blastic crisis of a chronic myelocytic leukemia].. PubMed. 106(40). 1381–1381. 1 indexed citations
16.
Cox, Josephine H., et al.. (1975). [Anatomo-pathological and cytogenetic study of free trisomy 13 and a case of trisomy 13 due to a translocation 13q13q].. PubMed. 23 SUPPL. 71–6. 1 indexed citations
17.
Gilgenkrantz, S, et al.. (1973). [Chromosome mosaics 47, XYY-45, XO. 2 cases with different sex].. PubMed. 2(9). 563–7. 1 indexed citations
18.
Gilgenkrantz, S, et al.. (1972). Délétion du bras court du 18 par translocation t(22-;18p+) avec déficit en IgA. Etude cytogénétique avec autoradiographie et fluorescence.. Annales de Génétique. 15(4). 3 indexed citations
19.
Gilgenkrantz, S, et al.. (1970). [Syndrome 47, XXYY, 13-, 14-, t(13q14q)+].. PubMed. 13(3). 201–6. 5 indexed citations
20.
Fouquet, J, et al.. (1966). [Intrabronchial aspergillosis. Complication of tuberculous primary infection].. PubMed. 23(1). 37–45.

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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